KEGG   Felis catus (domestic cat): 101082635
Entry
101082635         CDS       T02385                                 
Symbol
SLC25A5
Name
(RefSeq) ADP/ATP translocase 2
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05164  Influenza A
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101082635 (SLC25A5)
   04022 cGMP-PKG signaling pathway
    101082635 (SLC25A5)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101082635 (SLC25A5)
   04218 Cellular senescence
    101082635 (SLC25A5)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101082635 (SLC25A5)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101082635 (SLC25A5)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101082635 (SLC25A5)
   05164 Influenza A
    101082635 (SLC25A5)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101082635 (SLC25A5)
   05012 Parkinson disease
    101082635 (SLC25A5)
   05016 Huntington disease
    101082635 (SLC25A5)
   05017 Spinocerebellar ataxia
    101082635 (SLC25A5)
   05020 Prion disease
    101082635 (SLC25A5)
   05022 Pathways of neurodegeneration - multiple diseases
    101082635 (SLC25A5)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101082635 (SLC25A5)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101082635 (SLC25A5)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:fca02000]
    101082635 (SLC25A5)
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    101082635 (SLC25A5)
Transporters [BR:fca02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   101082635 (SLC25A5)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 101082635
NCBI-ProteinID: XP_011277743
UniProt: M3VW78
LinkDB
Position
X:97387023..97390201
AA seq 298 aa
MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLGDCLVKIYKSDGIKGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTLDCWRKIARDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacagatgccgctgtgtccttcgccaaggacttcctggcgggtggagtggcggcggcc
atctccaagaccgcggtcgcgcccatcgagcgggtcaagctgctgctgcaggtgcagcat
gccagcaagcaaatcaccgcagataagcaatacaagggcatcatagactgcgtggttcgt
atccccaaggagcagggagtcctgtccttctggcgcggtaacctggccaatgtcatcaga
tacttccccacccaggccctcaacttcgccttcaaagataaatacaagcagatcttcctg
ggtggcgtggacaagagaacccagttttggcgctactttgcagggaatctggcatcgggt
ggcgccgctggggccacatccttgtgttttgtgtatcctctggattttgcccgtacccgt
ctagcggccgatgtgggcaaagccggagcggaaagggaattccgaggccttggtgactgc
ctggttaagatctacaaatctgatgggattaagggcctgtaccaaggctttaatgtgtct
gtgcagggcattatcatctaccgagctgcctacttcggtatctatgataccgcaaagggc
atgcttccggatcccaagaacactcacatcttcatcagctggatgatcgcacagtccgtc
acagcggttgccgggttgacttcctatccctttgacactgttcgtcgccgaatgatgatg
cagtcggggcgcaaaggaaccgacatcatgtacacaggcacgcttgactgctggaggaag
attgctcgtgacgaaggggccaaagcttttttcaagggggcgtggtccaatgttctcaga
ggcatgggtggtgccttcgtgcttgtcttgtatgatgaaatcaagaagttcacataa

KEGG   Felis catus (domestic cat): 101086294
Entry
101086294         CDS       T02385                                 
Symbol
SLC25A31
Name
(RefSeq) ADP/ATP translocase 4
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05164  Influenza A
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101086294 (SLC25A31)
   04022 cGMP-PKG signaling pathway
    101086294 (SLC25A31)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101086294 (SLC25A31)
   04218 Cellular senescence
    101086294 (SLC25A31)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101086294 (SLC25A31)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101086294 (SLC25A31)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101086294 (SLC25A31)
   05164 Influenza A
    101086294 (SLC25A31)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101086294 (SLC25A31)
   05012 Parkinson disease
    101086294 (SLC25A31)
   05016 Huntington disease
    101086294 (SLC25A31)
   05017 Spinocerebellar ataxia
    101086294 (SLC25A31)
   05020 Prion disease
    101086294 (SLC25A31)
   05022 Pathways of neurodegeneration - multiple diseases
    101086294 (SLC25A31)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101086294 (SLC25A31)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101086294 (SLC25A31)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:fca02000]
    101086294 (SLC25A31)
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    101086294 (SLC25A31)
Transporters [BR:fca02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   101086294 (SLC25A31)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 101086294
NCBI-ProteinID: XP_004001144
UniProt: M3W759
LinkDB
Position
B1:complement(96798053..96826669)
AA seq 323 aa
MQREPPKGRQGKKSEKRLFDPVSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSRQ
ISAESQYKGMVDCLVRIPREQGFFSYWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN
KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGADIGKGPEERQFKGLGDCIIKI
AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLVSFFIAQVVTTCS
GILSYPFDTVRRRMMMQSGEAERQYKGTLDCFVKIYQQEGINAFFRGAFSNILRGTGGAL
VLVLYDKIKELLNIDIGGSSSGD
NT seq 972 nt   +upstreamnt  +downstreamnt
atgcagcgtgaacctccgaaggggaggcaggggaagaagtcggaaaagcggctctttgac
cccgtgtccttcgggaaggacctactggccggcggggtcgcagcggctgtgtccaagaca
gccgtggcgcccatcgagcgggtgaagctgctgctgcaggtgcaggcgtcgtcccgacag
atcagcgccgagtctcagtacaaaggcatggtggattgcctggtgcggattccccgcgag
cagggtttcttcagttattggcgtggcaatttggcaaatgttatccggtattttccaaca
caagctctaaactttgcttttaaggacaaatacaaacaacttttcatgtctggagttaat
aaagaaaaacagttctggaggtggtttttggcaaacctggcctctggtggagctgctgga
gcaacatccttatgtgtagtttatccattagactttgcccgaacccgattaggtgctgat
attggaaaaggtcctgaagagcggcaattcaagggtttaggtgactgtattataaaaata
gcaaaatcggatggaattgttggtttgtaccaagggtttggtgtttcagttcagggcatc
attgtgtaccgagcctcctattttggagcatatgacaccgttaagggcttattaccaaaa
ccaaaggaaaccccgtttcttgtctcctttttcattgctcaagttgtgaccacatgctct
ggaattctctcttatccctttgacacagttagaagacgcatgatgatgcagagtggtgag
gctgaacggcaatataaaggaactttagactgctttgtgaagatataccaacaggaagga
atcaatgcattttttcgtggtgccttctccaatatccttcgtggtacagggggtgctttg
gtgttagtactatatgataaaattaaagaactccttaatattgatattggaggtagttca
tcaggagattaa

KEGG   Felis catus (domestic cat): 101092793
Entry
101092793         CDS       T02385                                 
Symbol
VDAC2
Name
(RefSeq) voltage-dependent anion-selective channel protein 2
  KO
K15040  voltage-dependent anion channel protein 2
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04216  Ferroptosis
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca04621  NOD-like receptor signaling pathway
fca04979  Cholesterol metabolism
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101092793 (VDAC2)
   04022 cGMP-PKG signaling pathway
    101092793 (VDAC2)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    101092793 (VDAC2)
   04217 Necroptosis
    101092793 (VDAC2)
   04218 Cellular senescence
    101092793 (VDAC2)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101092793 (VDAC2)
   04621 NOD-like receptor signaling pathway
    101092793 (VDAC2)
  09154 Digestive system
   04979 Cholesterol metabolism
    101092793 (VDAC2)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101092793 (VDAC2)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101092793 (VDAC2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101092793 (VDAC2)
   05012 Parkinson disease
    101092793 (VDAC2)
   05016 Huntington disease
    101092793 (VDAC2)
   05017 Spinocerebellar ataxia
    101092793 (VDAC2)
   05020 Prion disease
    101092793 (VDAC2)
   05022 Pathways of neurodegeneration - multiple diseases
    101092793 (VDAC2)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101092793 (VDAC2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101092793 (VDAC2)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:fca04040]
    101092793 (VDAC2)
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    101092793 (VDAC2)
Ion channels [BR:fca04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   101092793 (VDAC2)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 101092793
NCBI-ProteinID: XP_011285609
Ensembl: ENSFCAG00000026943
UniProt: M3X2J1
LinkDB
Position
D2:35588355..35600624
AA seq 294 aa
MATYGQSCARPMCIPPSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVEFSTSGSSNT
DTGKVTGTLETKYKWCEYGLTFTEKWNTDNTLGTEIAIEDQICQGLKLTFDTTFSPNTGK
KSGKIKSSYKRECINLGCDVDFDFAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRNNF
AVGYRTGDFQLHTNVNDGTEFGGSIYQKVCEDLDTSVNLAWTSGTNCTRFGIAAKYQLDP
TASISAKVNNSSLIGVGYTQTLRPGVKLTLSALVDGKSINAGGHKLGLALELEA
NT seq 885 nt   +upstreamnt  +downstreamnt
atggcgacctatggacagagctgcgcgcggccaatgtgtattcctccatcatatgctgac
cttggcaaagctgccagagatattttcaacaagggatttggttttgggttggtgaaactg
gatgtgaaaacaaagtcatgcagtggtgtggaattctcaacatctggttcatctaacaca
gacactggtaaagttactggaaccttggagaccaaatataaatggtgtgagtatggtctg
actttcacagaaaagtggaacactgataacactctgggaacagaaatagcaattgaagac
cagatttgtcaaggtttgaaactgacatttgatactaccttttcaccaaacacgggaaag
aaaagtggtaaaatcaagtcttcttacaagagggagtgtataaacctcggttgtgatgtt
gactttgattttgctggacctgcaatccatggttcagctgtctttggttatgagggctgg
cttgctgggtaccagatgacctttgacagtgccaaatcaaagctgacaagaaacaacttt
gcagtgggctacaggactggggatttccagctacacactaatgtcaatgatgggacagaa
tttggaggttcaatttatcagaaagtatgtgaagatcttgacacttcagtaaaccttgct
tggacatcaggtaccaactgcactcgctttggcattgcagccaaatatcagttggacccc
actgcttccatttctgcaaaagtcaacaactctagtttaattggagtgggctatactcag
actctgaggcctggtgtcaagcttacactgtctgctctggtagatgggaagagcattaat
gctggaggccacaaacttgggcttgccctggagttggaggcttaa

KEGG   Felis catus (domestic cat): 101095941
Entry
101095941         CDS       T02385                                 
Name
(RefSeq) ADP/ATP translocase 2-like
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05164  Influenza A
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101095941
   04022 cGMP-PKG signaling pathway
    101095941
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101095941
   04218 Cellular senescence
    101095941
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101095941
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101095941
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101095941
   05164 Influenza A
    101095941
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101095941
   05012 Parkinson disease
    101095941
   05016 Huntington disease
    101095941
   05017 Spinocerebellar ataxia
    101095941
   05020 Prion disease
    101095941
   05022 Pathways of neurodegeneration - multiple diseases
    101095941
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101095941
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101095941
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:fca02000]
    101095941
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    101095941
Transporters [BR:fca02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   101095941
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 101095941
NCBI-ProteinID: XP_044903278
LinkDB
Position
E3:complement(26756794..26757921)
AA seq 293 aa
MTDAAVSFAKDSLVCGVVVAISKTTVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPREQGVLSFWRGNLANVIRYFPTQALNFSFKDKYKIFLGGVDKRTQFWRYFAGNLASGG
AAGATSLCFVYPLDFARTCLAADVGKAGPEREFRGLVKIYKSDGIKGLYRGFNVSVQGII
IYRAAYFGIYDTAKGMLPDPKNTHIYISWMIAQSLTAVAGLTSYPFDTVRRRMMTQPGRK
GTDIMYTRMLDCWRKIAPNEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq 882 nt   +upstreamnt  +downstreamnt
atgacagatgctgctgtgtccttcgccaaggactccctggtgtgtggagtggtggtggcc
atctccaagaccacggtagcgcccatcgagcgggtcaagctgctgctgcaggtgcagcat
gccagcaagcaaatcaccgcagataagcaatacaagggcattatagactgcgtggttcgt
atcccccgggagcagggagtcctgtccttctggcgcggtaacctggccaatgtcatcaga
tacttccccacccaggccctcaacttctccttcaaagataaatacaagatcttcctgggt
ggcgtggacaagagaacccagttttggcgctactttgcagggaatctggcatcgggtggc
gccgctggggccacatccttgtgttttgtgtatcctctggattttgcccgtacctgtcta
gcagccgatgtgggcaaggctggaccagaaagggaattccgaggcctggttaagatctac
aaatctgatgggattaagggcctgtaccgaggctttaatgtgtctgtgcagggcattatc
atctaccgagctgcctacttcggtatctatgatactgcaaagggcatgcttccggatccc
aagaacactcacatctacatcagttggatgatcgcacagtccctcacagcggttgccggg
ttgacttcctatccctttgacactgttcgtcgccgaatgatgacgcagccggggcgcaaa
ggaaccgacatcatgtacacacgcatgcttgactgctggaggaagattgctcctaacgaa
ggggccaaagcttttttcaagggggcgtggtccaatgttctcagaggcatgggtggtgcc
ttcgtgcttgtcttgtatgatgaaatcaagaagttcacataa

KEGG   Felis catus (domestic cat): 101096309
Entry
101096309         CDS       T02385                                 
Symbol
SLC25A4
Name
(RefSeq) ADP/ATP translocase 1
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05164  Influenza A
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101096309 (SLC25A4)
   04022 cGMP-PKG signaling pathway
    101096309 (SLC25A4)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101096309 (SLC25A4)
   04218 Cellular senescence
    101096309 (SLC25A4)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101096309 (SLC25A4)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101096309 (SLC25A4)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101096309 (SLC25A4)
   05164 Influenza A
    101096309 (SLC25A4)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101096309 (SLC25A4)
   05012 Parkinson disease
    101096309 (SLC25A4)
   05016 Huntington disease
    101096309 (SLC25A4)
   05017 Spinocerebellar ataxia
    101096309 (SLC25A4)
   05020 Prion disease
    101096309 (SLC25A4)
   05022 Pathways of neurodegeneration - multiple diseases
    101096309 (SLC25A4)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101096309 (SLC25A4)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101096309 (SLC25A4)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:fca02000]
    101096309 (SLC25A4)
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    101096309 (SLC25A4)
Transporters [BR:fca02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   101096309 (SLC25A4)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 101096309
NCBI-ProteinID: XP_023108091
LinkDB
Position
B1:16048488..16052488
AA seq 298 aa
MTDHALSFLKDFLAGGVAAAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVR
IPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDRHKQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKGAAQREFSGLGDCLTKIFKSDGLKGLYQGFSVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNVHIIVSWMIAQSVTAVAGLVSYPFDTVRRRMMM
QSGRKGADIMYTGTVDCWRKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV
NT seq 897 nt   +upstreamnt  +downstreamnt
atgactgatcacgccttgagcttcctgaaggatttcctggccggcggcgtcgccgctgcc
gtgtccaagaccgcggtcgccccaatcgagagggtcaaactgctgctgcaggtccagcat
gccagcaaacagatcagtgctgagaagcagtacaaagggatcattgattgtgtggtgaga
atccccaaggagcagggctttctctccttctggaggggtaacctggccaacgtgatccgt
tacttccccacccaagctctcaacttcgccttcaaggacaagtacaagcagatcttcctg
gggggcgtcgaccggcataagcaattctggcgctactttgccggtaacctggcttccggt
ggggcagctggggccacctccctctgctttgtctacccactggactttgctaggaccagg
ttggctgccgacgtgggcaagggtgctgcccagcgtgagttcagtggtctgggcgactgt
ctcaccaagatcttcaagtctgatggcctgaagggtctctaccagggtttcagcgtctct
gtccagggcatcattatctacagagctgcctactttggagtttatgatactgccaagggg
atgttgcctgaccccaagaatgtgcacattattgtgagctggatgattgcccagagcgtg
acagcggtcgcagggctggtgtcctacccctttgacactgtccgccgtaggatgatgatg
cagtctggccggaaaggggcggatattatgtacactgggacggtggactgctggaggaag
attgcaaaagatgagggagccaaggctttcttcaaaggtgcctggtccaatgtgttgaga
ggcatgggcggagctttcgtattggtattgtatgatgagatcaaaaaatacgtctag

KEGG   Felis catus (domestic cat): 101098515
Entry
101098515         CDS       T02385                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca04621  NOD-like receptor signaling pathway
fca04979  Cholesterol metabolism
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05014  Amyotrophic lateral sclerosis
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05164  Influenza A
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101098515 (VDAC1)
   04022 cGMP-PKG signaling pathway
    101098515 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101098515 (VDAC1)
   04218 Cellular senescence
    101098515 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101098515 (VDAC1)
   04621 NOD-like receptor signaling pathway
    101098515 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    101098515 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101098515 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101098515 (VDAC1)
   05164 Influenza A
    101098515 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101098515 (VDAC1)
   05012 Parkinson disease
    101098515 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    101098515 (VDAC1)
   05016 Huntington disease
    101098515 (VDAC1)
   05017 Spinocerebellar ataxia
    101098515 (VDAC1)
   05020 Prion disease
    101098515 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    101098515 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101098515 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101098515 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:fca04040]
    101098515 (VDAC1)
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    101098515 (VDAC1)
Ion channels [BR:fca04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   101098515 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 101098515
NCBI-ProteinID: XP_023110926
LinkDB
Position
A1:complement(110680513..110708394)
AA seq 283 aa
MAVPPTYADLGKCARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacgtatgctgatcttggcaaatgtgccagggatgtcttcaccaag
ggttatggatttggcttaatcaaactcgatttgaagacaaaatctgagaatggactggaa
tttacgagctcaggttctgccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacagatggactgaatacggtctgacgtttacggagaaatggaacactgacaacaca
ttaggcacagagattactgtggaggatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacacagggaaaaaaaatgctaaaatcaagacagggtataagcgg
gagcacatcaacctgggctgtgacgtggatttcgacatcgccggcccttcaatccggggt
gctctggtgctgggctatgagggctggctggctggctaccagatgaattttgagactgca
aagtctcgagtgacccagagcaactttgcagttggctacaagactgacgaattccagctc
cacactaatgtaaacgatgggacagagtttggtggctccatttatcagaaggtgaacaag
aagttagagaccgctgttaatctggcctggacagcaggaaatagtaacactcgctttgga
atagcggccaagtatcagatcgatcctgacgcctgcttctcggctaaagtgaacaactcc
agcctgataggtttaggatacactcagaccctaaagccaggtatcaaactgacgctctca
gctttgctggatggcaagaatgtcaatgctggtggccacaagcttggtctaggactggaa
tttcaggcataa

KEGG   Felis catus (domestic cat): 101099117
Entry
101099117         CDS       T02385                                 
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3 isoform X1
  KO
K15041  voltage-dependent anion channel protein 3
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04216  Ferroptosis
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca04621  NOD-like receptor signaling pathway
fca04979  Cholesterol metabolism
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05161  Hepatitis B
fca05166  Human T-cell leukemia virus 1 infection
fca05203  Viral carcinogenesis
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101099117 (VDAC3)
   04022 cGMP-PKG signaling pathway
    101099117 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    101099117 (VDAC3)
   04217 Necroptosis
    101099117 (VDAC3)
   04218 Cellular senescence
    101099117 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101099117 (VDAC3)
   04621 NOD-like receptor signaling pathway
    101099117 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    101099117 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101099117 (VDAC3)
   05203 Viral carcinogenesis
    101099117 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101099117 (VDAC3)
   05161 Hepatitis B
    101099117 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101099117 (VDAC3)
   05012 Parkinson disease
    101099117 (VDAC3)
   05016 Huntington disease
    101099117 (VDAC3)
   05017 Spinocerebellar ataxia
    101099117 (VDAC3)
   05020 Prion disease
    101099117 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    101099117 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101099117 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101099117 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:fca04040]
    101099117 (VDAC3)
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    101099117 (VDAC3)
Ion channels [BR:fca04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   101099117 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 101099117
NCBI-ProteinID: XP_023108333
LinkDB
Position
B1:complement(40401610..40415928)
AA seq 284 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVMEFSTSGHAYTDTGKASGNLE
TKYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYK
RECFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQ
LHTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNN
ASLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 855 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccaacttactgtgacctaggaaaggccgccaaggatgtcttcaacaaa
ggatacggatttggcatggtcaaaatagacctgagaaccaagtcttgtagtggagtgatg
gaattttctacttctggtcatgcttacactgatacaggaaaagcgtcaggcaacctagag
accaaatataaggtctgtaactatggacttaccttcactcagaaatggaacacagataac
actcttggaacagaaatctctttggagaataagttggctgaagggttgaaactgactctt
gataccatatttgtaccgaacacaggaaagaagagtggaaaattgaaggcctcctataag
cgggaatgtttcagtctcggcagcaatgttgatatagatttttctggaccaaccatctat
ggctgggctgtgttagcctttgaaggttggcttgctggctatcagatgagtttcgacaca
gccaaatccaaactgtcacagaataatttcgctctgggttacaaggccgcagacttccag
ctgcacactcatgtgaatgacggcactgaatttggagggtctatctaccagaaggttaat
gagaagattgaaacatcaataaaccttgcttggacggctggcagtaacaatacccgtttt
ggcatcgctgctaaatacaagctggactgtagaacttctctatctgctaaagtaaataat
gccagcctgattggactgggttatactcagactcttcgaccaggagtcaaactgacccta
tcagctttaatcgacggaaagaacttcaatgcaggaggtcacaaggttgggttgggattt
gagctagaagcttaa

KEGG   Felis catus (domestic cat): 101099589
Entry
101099589         CDS       T02385                                 
Symbol
PPIF
Name
(RefSeq) peptidyl-prolyl cis-trans isomerase F, mitochondrial isoform X4
  KO
K09565  peptidyl-prolyl isomerase F (cyclophilin D) [EC:5.2.1.8]
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04613  Neutrophil extracellular trap formation
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05145  Toxoplasmosis
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101099589 (PPIF)
   04022 cGMP-PKG signaling pathway
    101099589 (PPIF)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101099589 (PPIF)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101099589 (PPIF)
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    101099589 (PPIF)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101099589 (PPIF)
   05012 Parkinson disease
    101099589 (PPIF)
   05016 Huntington disease
    101099589 (PPIF)
   05017 Spinocerebellar ataxia
    101099589 (PPIF)
   05020 Prion disease
    101099589 (PPIF)
   05022 Pathways of neurodegeneration - multiple diseases
    101099589 (PPIF)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101099589 (PPIF)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03110 Chaperones and folding catalysts [BR:fca03110]
    101099589 (PPIF)
Enzymes [BR:fca01000]
 5. Isomerases
  5.2  cis-trans-Isomerases
   5.2.1  cis-trans Isomerases (only sub-subclass identified to date)
    5.2.1.8  peptidylprolyl isomerase
     101099589 (PPIF)
Chaperones and folding catalysts [BR:fca03110]
 Protein folding catalysts
  Peptidyl prolyl isomerase
   Cyclophilin
    101099589 (PPIF)
SSDB
Motif
Pfam: Pro_isomerase
Other DBs
NCBI-GeneID: 101099589
NCBI-ProteinID: XP_003994158
Ensembl: ENSFCAG00000025543
UniProt: M3XFI8
LinkDB
Position
D2:39313953..39320716
AA seq 204 aa
MLALRCGPRLLGLLRVPRSAPLRLPAARACSGVGDPSPSSRNPLVYLDVGADGEPLGRVV
LELKADVVPKTAENFRALCTGEKGFGYKGSTFHRVIPSFMCQAGDFTNHNGTGGKSIYGS
RFPDENFTLKHVGPGVLSMANAGPNTNGSQFFICTIKTDWLDGKHVVFGHVKEGMDVVKK
IESFGSRSGKTSKKIVITDCGQLS
NT seq 615 nt   +upstreamnt  +downstreamnt
atgctggctctacgctgcggcccccgcctgctcggcctgctccgggtcccgcgctccgca
ccgctgcgcctccccgcggcccgcgcctgcagcggcgtcggcgacccgtccccttcctcc
cggaacccgctcgtgtacctggacgtgggcgccgacggggagccgctcggccgcgtggtg
ctggagctgaaggcagatgtcgtcccgaagacagcagagaacttcagagccctgtgtacc
ggggagaagggcttcggctacaaaggctccacctttcacagagtgattccgtccttcatg
tgccaggcgggcgacttcaccaaccacaatggcaccgggggaaagtccatctacggaagc
cgctttcctgatgagaacttcacactgaagcacgtgggaccaggtgtcctctccatggcg
aacgcaggccccaacaccaacggctcccagttcttcatctgcaccataaagacagactgg
ttggatggcaagcatgttgtgtttggccatgtcaaagagggcatggatgtcgtgaagaaa
atagaatctttcggttccaggagtgggaagacgtccaagaagatcgtcatcacagactgc
ggccagttgagctga

KEGG   Felis catus (domestic cat): 101100868
Entry
101100868         CDS       T02385                                 
Symbol
SLC25A6
Name
(RefSeq) ADP/ATP translocase 3
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05164  Influenza A
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    101100868 (SLC25A6)
   04022 cGMP-PKG signaling pathway
    101100868 (SLC25A6)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    101100868 (SLC25A6)
   04218 Cellular senescence
    101100868 (SLC25A6)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    101100868 (SLC25A6)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    101100868 (SLC25A6)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    101100868 (SLC25A6)
   05164 Influenza A
    101100868 (SLC25A6)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    101100868 (SLC25A6)
   05012 Parkinson disease
    101100868 (SLC25A6)
   05016 Huntington disease
    101100868 (SLC25A6)
   05017 Spinocerebellar ataxia
    101100868 (SLC25A6)
   05020 Prion disease
    101100868 (SLC25A6)
   05022 Pathways of neurodegeneration - multiple diseases
    101100868 (SLC25A6)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    101100868 (SLC25A6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    101100868 (SLC25A6)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:fca02000]
    101100868 (SLC25A6)
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    101100868 (SLC25A6)
Transporters [BR:fca02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   101100868 (SLC25A6)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 101100868
NCBI-ProteinID: XP_023104656
Ensembl: ENSFCAG00000045843
LinkDB
Position
X:complement(975364..978773)
AA seq 298 aa
MTEQAISFAKDFLAGGIAAAISKTAVAPIERVKLLLQVQHASKQIAADKQYKGIVDCIVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKHTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKSGTEREFKGLGDCLVKITKSDGIRGLYQGFNVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNTHIVVSWMIAQTVTAVAGVVSYPFDTVRRRMMM
QSGRKGADIMYKGTLDCWRKIFKDEGGKAFFKGAWSNVLRGMGGAFVLVLYDELKKVL
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacggaacaggccatctctttcgccaaggacttcctggccggaggcatcgccgccgcc
atctccaagacggcggtggccccgatcgagcgggttaagctgctgctgcaggtgcagcac
gccagcaagcagatcgccgccgacaagcagtacaagggcatcgtggactgcatcgtgcgc
atccccaaggagcagggcgtcctgtccttctggaggggcaacctggccaacgtcatccgc
tacttccccacgcaagcgctcaacttcgctttcaaggataagtacaagcagatcttcctg
gggggcgtggacaagcacacgcagttctggaggtacttcgccggcaacctggcgtcgggc
ggggcggccggagccacgtcgctgtgcttcgtgtacccgctggatttcgccaggacccgt
ctggccgccgacgtgggcaagtcgggcaccgagcgggagttcaagggcctgggagactgc
ctggtcaagatcaccaagtctgacggcatccggggcctgtaccagggcttcaacgtgtcg
gtgcagggcatcatcatctaccgggcggcctacttcggcgtgtacgacacggccaagggc
atgctcccggaccccaagaacacgcacatcgtggtgagctggatgatcgcgcagacggtg
acggctgtggcgggcgtggtctcctacccctttgacaccgtgcggaggcgcatgatgatg
cagtcggggcgcaaaggagccgacatcatgtacaaggggaccctcgactgctggcggaag
atcttcaaagacgaagggggcaaagccttcttcaagggtgcgtggtccaacgtcctgcgg
ggcatggggggcgcctttgtgctcgtgctgtatgatgagctgaagaaagtcctctag

KEGG   Felis catus (domestic cat): 102899304
Entry
102899304         CDS       T02385                                 
Name
(RefSeq) LOW QUALITY PROTEIN: voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
fca  Felis catus (domestic cat)
Pathway
fca04020  Calcium signaling pathway
fca04022  cGMP-PKG signaling pathway
fca04217  Necroptosis
fca04218  Cellular senescence
fca04613  Neutrophil extracellular trap formation
fca04621  NOD-like receptor signaling pathway
fca04979  Cholesterol metabolism
fca05010  Alzheimer disease
fca05012  Parkinson disease
fca05014  Amyotrophic lateral sclerosis
fca05016  Huntington disease
fca05017  Spinocerebellar ataxia
fca05020  Prion disease
fca05022  Pathways of neurodegeneration - multiple diseases
fca05164  Influenza A
fca05166  Human T-cell leukemia virus 1 infection
fca05208  Chemical carcinogenesis - reactive oxygen species
fca05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:fca00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    102899304
   04022 cGMP-PKG signaling pathway
    102899304
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    102899304
   04218 Cellular senescence
    102899304
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    102899304
   04621 NOD-like receptor signaling pathway
    102899304
  09154 Digestive system
   04979 Cholesterol metabolism
    102899304
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    102899304
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    102899304
   05164 Influenza A
    102899304
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    102899304
   05012 Parkinson disease
    102899304
   05014 Amyotrophic lateral sclerosis
    102899304
   05016 Huntington disease
    102899304
   05017 Spinocerebellar ataxia
    102899304
   05020 Prion disease
    102899304
   05022 Pathways of neurodegeneration - multiple diseases
    102899304
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    102899304
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:fca03029]
    102899304
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:fca04040]
    102899304
Mitochondrial biogenesis [BR:fca03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    102899304
Ion channels [BR:fca04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   102899304
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 102899304
NCBI-ProteinID: XP_044895278
LinkDB
Position
D1:complement(103761106..103762671)
AA seq 286 aa
MAVPPTYADLGKCARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTKTTKVTGSLET
KYRWTEYGLTFTEKXNTDDTLGTEITVEDQLARGLKLTFDSSFSPNRGGGGNAKIKIKTG
YKREHINLGRDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDE
FQLHTNVSDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKV
NNSSLIGLGYTQTLKPGIKLMLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 861 nt   +upstreamnt  +downstreamnt
atggctgtgcctcccacatatgctgatcttggcaaatgtgccagggatgtcttcaccaag
ggttatggatttggcttaatcaaactcgatttgaagacaaaatctgagaatggactggaa
tttacgagctcaggttccgccaacactaagaccaccaaagtgacgggcagtctggaaacc
aagtacagatggactgaatatggtctgacgtttacggagaaantgaacactgacgacaca
ctaggcacagagattactgtggaggatcagcttgcacgtggactgaagctgacctttgat
tcatccttctcaccaaacaggggggggggggggaatgctaaaatcaaaatcaagacaggg
tataagcgggagcacatcaacctgggccgtgacgtggatttcgacatcgccggcccttca
atccgcggcgctctggtgctgggctatgagggctggctggcaggctaccagatgaatttt
gagactgcaaagtctcgagtgacccagagcaactttgcagttggctacaagactgacgaa
ttccagctccacacgaacgtaagcgatgggacagagtttggtggctccatttatcagaag
gtgaacaagaagttagagaccgccgttaatctggcctggacagcaggaaatagtaacact
cgctttggaatagcggccaagtatcagatcgatcctgatgcctgcttctcggctaaagtg
aacaactccagcctgataggtttaggatacactcagaccctaaagccaggtatcaaactg
atgctctcagctttgctggatggcaagaatgtcaatgctggtggccacaagcttggtcta
ggactggaatttcaggcataa

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