KEGG   Oryctolagus cuniculus (rabbit): 100008751
Entry
100008751         CDS       T03373                                 
Symbol
VDAC1
Name
(RefSeq) voltage-dependent anion-selective channel protein 1
  KO
K05862  voltage-dependent anion channel protein 1
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu04621  NOD-like receptor signaling pathway
ocu04979  Cholesterol metabolism
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05014  Amyotrophic lateral sclerosis
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100008751 (VDAC1)
   04022 cGMP-PKG signaling pathway
    100008751 (VDAC1)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100008751 (VDAC1)
   04218 Cellular senescence
    100008751 (VDAC1)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100008751 (VDAC1)
   04621 NOD-like receptor signaling pathway
    100008751 (VDAC1)
  09154 Digestive system
   04979 Cholesterol metabolism
    100008751 (VDAC1)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100008751 (VDAC1)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100008751 (VDAC1)
   05164 Influenza A
    100008751 (VDAC1)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100008751 (VDAC1)
   05012 Parkinson disease
    100008751 (VDAC1)
   05014 Amyotrophic lateral sclerosis
    100008751 (VDAC1)
   05016 Huntington disease
    100008751 (VDAC1)
   05017 Spinocerebellar ataxia
    100008751 (VDAC1)
   05020 Prion disease
    100008751 (VDAC1)
   05022 Pathways of neurodegeneration - multiple diseases
    100008751 (VDAC1)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100008751 (VDAC1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100008751 (VDAC1)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ocu04040]
    100008751 (VDAC1)
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    100008751 (VDAC1)
Ion channels [BR:ocu04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   100008751 (VDAC1)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 100008751
NCBI-ProteinID: NP_001075544
Ensembl: ENSOCUG00000009369
UniProt: Q9TT15
LinkDB
Position
3:complement(16793192..16820937)
AA seq 283 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKSENGLEFTSSGSANTETTKVTGSLET
KYRWTEYGLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGKKNAKIKTGYKR
EHINLGCDVDFDIAGPSIRGALVLGYEGWLAGYQMNFETAKSRVTQSNFAVGYKTDEFQL
HTNVNDGTEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNS
SLIGLGYTQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 852 nt   +upstreamnt  +downstreamnt
atggctgtacctcccacgtatgccgatcttggcaaatctgccagggatgtcttcaccaag
ggctacggatttggcttaataaagcttgatttgaaaacaaagtccgagaatggattggaa
tttacaagctcaggctcagccaacactgagaccaccaaagtgacgggcagtctggaaacc
aagtacaggtggactgagtacgggctgacgtttacggagaaatggaacaccgacaacacg
ctgggcaccgagatcaccgtggaagaccagcttgcacgtggactgaagctgaccttcgat
tcctccttctcgcctaacactgggaaaaaaaatgctaaaatcaagacaggctacaagcgg
gagcacatcaacctgggctgcgacgtggatttcgacatcgctgggccctccatccggggt
gctctggtgctgggttatgagggctggctggctggctaccagatgaactttgagactgcc
aagtcccgagtcacccagagcaactttgccgtcggctacaagaccgatgaattccagctc
cacactaatgtgaacgacggaacggagtttggcggctccatttaccagaaggtgaacaag
aagctggagacggccgtcaatcttgcctggacagcaggaaacagtaacactcgcttcgga
atagcagccaagtatcagatcgaccctgacgcctgcttctcggcaaaagtgaacaactcc
agcctgataggattaggatacactcagaccctaaagccaggtatcaaactgacgctctca
gctctgctggatggcaagaacgtcaacgctggcggccacaagcttggtctaggactggaa
tttcaagcataa

KEGG   Oryctolagus cuniculus (rabbit): 100008752
Entry
100008752         CDS       T03373                                 
Symbol
VDAC3
Name
(RefSeq) voltage-dependent anion-selective channel protein 3
  KO
K15041  voltage-dependent anion channel protein 3
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04216  Ferroptosis
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu04621  NOD-like receptor signaling pathway
ocu04979  Cholesterol metabolism
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05161  Hepatitis B
ocu05166  Human T-cell leukemia virus 1 infection
ocu05203  Viral carcinogenesis
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100008752 (VDAC3)
   04022 cGMP-PKG signaling pathway
    100008752 (VDAC3)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    100008752 (VDAC3)
   04217 Necroptosis
    100008752 (VDAC3)
   04218 Cellular senescence
    100008752 (VDAC3)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100008752 (VDAC3)
   04621 NOD-like receptor signaling pathway
    100008752 (VDAC3)
  09154 Digestive system
   04979 Cholesterol metabolism
    100008752 (VDAC3)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100008752 (VDAC3)
   05203 Viral carcinogenesis
    100008752 (VDAC3)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100008752 (VDAC3)
   05161 Hepatitis B
    100008752 (VDAC3)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100008752 (VDAC3)
   05012 Parkinson disease
    100008752 (VDAC3)
   05016 Huntington disease
    100008752 (VDAC3)
   05017 Spinocerebellar ataxia
    100008752 (VDAC3)
   05020 Prion disease
    100008752 (VDAC3)
   05022 Pathways of neurodegeneration - multiple diseases
    100008752 (VDAC3)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100008752 (VDAC3)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100008752 (VDAC3)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ocu04040]
    100008752 (VDAC3)
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    100008752 (VDAC3)
Ion channels [BR:ocu04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   100008752 (VDAC3)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 100008752
NCBI-ProteinID: NP_001075545
Ensembl: ENSOCUG00000024318
UniProt: Q9TT13
LinkDB
AA seq 283 aa
MCNTPTYCDLGKAAKDVFNKGYGFGMVKIDLRTKSCSGVEFSTSGHAYTDTGKASGNLET
KYKVCNYGLTFTQKWNTDNTLGTEISLENKLAEGLKLTLDTIFVPNTGKKSGKLKASYKR
DCFSLGSNVDIDFSGPTIYGWAVLAFEGWLAGYQMSFDTAKSKLSQNNFALGYKAADFQL
HTHVNDGTEFGGSIYQKVNEKIETSINLAWTAGSNNTRFGIAAKYKLDCRTSLSAKVNNA
SLIGLGYTQTLRPGVKLTLSALIDGKNFNAGGHKVGLGFELEA
NT seq 852 nt   +upstreamnt  +downstreamnt
atgtgtaacacaccaacgtactgtgacctaggaaaggctgccaaggatgtcttcaacaaa
ggatacgggtttggcatggtcaaaatagacctgagaaccaagtcttgtagtggagtggaa
ttttctacttctggtcatgcttacactgatacaggaaaagcgtcaggcaacctagagacc
aaatataaggtctgtaactatggactcaccttcacccagaaatggaacacagacaacact
ctggggacagaaatctctctggagaataagttggctgaaggattgaaactgactcttgac
accatatttgtaccaaacacaggaaagaagagtgggaaattgaaggcctcctataaacgg
gattgttttagtcttggaagtaatgttgatatagatttttctggaccaaccatctatggc
tgggctgtgttggcttttgaaggttggcttgctggctatcagatgagttttgacacagcc
aaatccaaactgtcacagaataattttgccctgggttacaaggctgcagacttccagctg
cacactcatgtaaacgatggcactgaattcggaggctccatctaccagaaggtcaacgag
aagattgaaacgtcaataaacctcgcatggacggctggcagtaacaacacgcgttttggc
atcgcagctaaatacaagctggattgtagaacttctctctctgccaaagtaaataacgcc
agcctgattggactgggttatacgcagacccttcgaccaggagtcaaattgaccctgtcc
gctttaatcgacgggaagaacttcaacgcaggaggccataaggttgggctgggatttgag
ctggaagcctaa

KEGG   Oryctolagus cuniculus (rabbit): 100009414
Entry
100009414         CDS       T03373                                 
Symbol
SLC25A4
Name
(RefSeq) ADP/ATP translocase 1
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100009414 (SLC25A4)
   04022 cGMP-PKG signaling pathway
    100009414 (SLC25A4)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100009414 (SLC25A4)
   04218 Cellular senescence
    100009414 (SLC25A4)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100009414 (SLC25A4)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100009414 (SLC25A4)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100009414 (SLC25A4)
   05164 Influenza A
    100009414 (SLC25A4)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100009414 (SLC25A4)
   05012 Parkinson disease
    100009414 (SLC25A4)
   05016 Huntington disease
    100009414 (SLC25A4)
   05017 Spinocerebellar ataxia
    100009414 (SLC25A4)
   05020 Prion disease
    100009414 (SLC25A4)
   05022 Pathways of neurodegeneration - multiple diseases
    100009414 (SLC25A4)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100009414 (SLC25A4)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100009414 (SLC25A4)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ocu02000]
    100009414 (SLC25A4)
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    100009414 (SLC25A4)
Transporters [BR:ocu02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   100009414 (SLC25A4)
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 100009414
NCBI-ProteinID: NP_001076155
Ensembl: ENSOCUG00000002594
UniProt: O46373
LinkDB
Position
2:63060621..63064145
AA seq 298 aa
MSDQALSFLKDFLAGGVAAAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVR
IPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDRHKQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKGAAQREFSGLGNCLTKIFKSDGLRGLYQGFNVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNVHIIVSWMIAQTVTAVAGLVSYPFDTVRRRMMM
QSGRKGADIMYTGTVDCWKKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV
NT seq 897 nt   +upstreamnt  +downstreamnt
atgagtgatcaggctttgagcttcctcaaggacttcctggcaggtggcgtcgccgctgcc
gtctccaagactgcggtcgcccccatcgagagggtcaaactgctgctgcaggtccagcat
gccagcaaacagatcagcgctgagaagcagtacaaagggatcattgattgtgtggtgagg
atccccaaggagcagggctttctctccttctggaggggtaacctggccaacgtgatccgg
tacttccccacccaagctctcaacttcgccttcaaggacaagtacaagcagatcttcttg
gggggcgtggatcggcataagcagttctggcgctacttcgctggtaacctggcctccggt
ggggcagctggggccacctccctctgctttgtctacccgctggactttgccaggaccagg
ttggctgccgacgtgggcaagggtgccgcccagcgtgagttcagtggtctgggcaactgt
ctcaccaagatcttcaagtctgatggcctgaggggtctctaccagggtttcaatgtctct
gtgcaaggcatcattatctacagagctgcctacttcggagtctatgatactgccaagggg
atgttgcctgaccccaagaacgtgcacattatcgtgagctggatgatcgcccagaccgtg
acggcagtggccgggctggtgtcctacccctttgacactgttcgtcgtaggatgatgatg
cagtctggccggaaaggggctgacattatgtacacggggacagttgactgctggaagaag
attgcaaaagatgaaggagccaaggctttcttcaaaggtgcctggtccaatgtgttgaga
ggcatgggtggcgcttttgtattggtgttgtatgatgagatcaaaaaatatgtctaa

KEGG   Oryctolagus cuniculus (rabbit): 100009473
Entry
100009473         CDS       T03373                                 
Symbol
VDAC2
Name
(RefSeq) voltage-dependent anion-selective channel protein 2
  KO
K15040  voltage-dependent anion channel protein 2
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04216  Ferroptosis
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu04621  NOD-like receptor signaling pathway
ocu04979  Cholesterol metabolism
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100009473 (VDAC2)
   04022 cGMP-PKG signaling pathway
    100009473 (VDAC2)
 09140 Cellular Processes
  09143 Cell growth and death
   04216 Ferroptosis
    100009473 (VDAC2)
   04217 Necroptosis
    100009473 (VDAC2)
   04218 Cellular senescence
    100009473 (VDAC2)
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100009473 (VDAC2)
   04621 NOD-like receptor signaling pathway
    100009473 (VDAC2)
  09154 Digestive system
   04979 Cholesterol metabolism
    100009473 (VDAC2)
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100009473 (VDAC2)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100009473 (VDAC2)
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100009473 (VDAC2)
   05012 Parkinson disease
    100009473 (VDAC2)
   05016 Huntington disease
    100009473 (VDAC2)
   05017 Spinocerebellar ataxia
    100009473 (VDAC2)
   05020 Prion disease
    100009473 (VDAC2)
   05022 Pathways of neurodegeneration - multiple diseases
    100009473 (VDAC2)
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100009473 (VDAC2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100009473 (VDAC2)
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ocu04040]
    100009473 (VDAC2)
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    100009473 (VDAC2)
Ion channels [BR:ocu04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   100009473 (VDAC2)
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 100009473
NCBI-ProteinID: NP_001076187
Ensembl: ENSOCUG00000009082
UniProt: P68003
LinkDB
Position
18:complement(9236716..9248983)
AA seq 294 aa
MATHGQTCARPMCIPPSYADLGKAARDIFNKGFGFGLVKLDVKTKSCSGVEFSTSGSSNT
DTGKVTGTLETKYKWCEYGLTFTEKWNTDNTLGTEIAIEDQICQGLKLTFDTTFSPNTGK
KSGKIKSSYKRECINLGCDVDFDFAGPAIHGSAVFGYEGWLAGYQMTFDSAKSKLTRNNF
AVGYRTGDFQLHTNVNDGTEFGGSIYQKVCEDLDTSVNLAWTSGTNCTRFGIAAKYQLDP
TASISAKVNNSSLIGVGYTQTLRPGVKLTLSALVDGKSINAGGHKLGLALELEA
NT seq 885 nt   +upstreamnt  +downstreamnt
atggcgacccacggacagacttgcgcgcggccaatgtgtattcctccatcatacgccgac
cttggcaaagctgccagagatattttcaacaaaggatttggttttgggttggtgaaactg
gatgtgaaaacaaagtcctgcagtggtgtggaattctcaacatctggttcatctaataca
gatactggtaaagttactgggaccttggagaccaaatataaatggtgtgagtatggtctg
actttcacagaaaaatggaacactgataacactctgggaacagaaattgcaattgaagac
cagatttgtcagggtttgaagctgacgtttgatactaccttttcaccaaatacaggaaag
aaaagtggtaaaatcaagtcctcttacaagagggagtgtataaaccttggttgtgacgtt
gactttgattttgctgggcctgcaatccatggttcagctgtctttggttatgagggctgg
cttgctgggtaccagatgacctttgacagtgccaaatcaaagctgacaaggaataacttt
gcagtaggctacaggactggggacttccagctacacactaatgtcaatgatgggacagaa
tttggaggatcaatttatcagaaagtatgtgaagatcttgacacttcagtaaaccttgct
tggacatcaggtaccaactgcactcgttttggcattgcagcgaaatatcagctggatccc
actgcttccatttctgcaaaagtcaacaactctagtttaattggagtgggctacactcag
actctgaggcctggagtgaagctcacgctgtctgctctggtagatgggaagagcattaat
gctggaggccacaaacttgggcttgccctggagttggaggcttaa

KEGG   Oryctolagus cuniculus (rabbit): 100337764
Entry
100337764         CDS       T03373                                 
Name
(RefSeq) ADP/ATP translocase 2
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100337764
   04022 cGMP-PKG signaling pathway
    100337764
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100337764
   04218 Cellular senescence
    100337764
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100337764
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100337764
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100337764
   05164 Influenza A
    100337764
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100337764
   05012 Parkinson disease
    100337764
   05016 Huntington disease
    100337764
   05017 Spinocerebellar ataxia
    100337764
   05020 Prion disease
    100337764
   05022 Pathways of neurodegeneration - multiple diseases
    100337764
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100337764
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100337764
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ocu02000]
    100337764
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    100337764
Transporters [BR:ocu02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   100337764
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 100337764
NCBI-ProteinID: XP_002720308
Ensembl: ENSOCUG00000013268
UniProt: G1T524
LinkDB
Position
X:68173406..68176220
AA seq 298 aa
MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLGDCLVKIYKSDGIRGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTLDCWRKIARDEGGKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacagatgccgctgtgtccttcgccaaggactttctggcaggtggagtggctgcggcc
atctccaagaccgcggtagcgcccatcgagagggtcaagctgctgctgcaggtgcagcat
gccagcaagcaaatcactgccgataagcaatacaagggcattatagactgcgtggttcgt
atccccaaggagcagggagtcctgtccttctggcgtggtaacctggccaatgtcatcaga
tacttccccacccaggctctcaactttgccttcaaagataaatacaagcagatctttctg
ggtggcgtggacaagaggacccagttttggcgctactttgcaggaaatctggcatcaggt
ggtgctgctggagccacatccttgtgtttcgtgtaccctcttgattttgcccgtacccgt
ctagcagctgacgtgggcaaagctggagctgaaagggaattcagaggcctcggcgactgc
ctggttaagatctacaaatctgatgggattaggggcctgtaccaaggctttaatgtgtct
gtacagggcattatcatctaccgggctgcctacttcggtatctatgacaccgcaaaagga
atgcttccagatcccaagaacacacacatcttcatcagctggatgattgcgcagtctgtc
actgctgttgctgggttgacttcctatccatttgacactgttcgtcggcgcatgatgatg
cagtcggggcgtaaaggaactgatatcatgtacacaggcacacttgactgctggaggaag
attgctcgtgatgaaggaggcaaagcgtttttcaagggtgcatggtccaacgtcctcaga
ggcatgggtggtgcttttgtgcttgtcttgtatgatgaaatcaagaagttcacataa

KEGG   Oryctolagus cuniculus (rabbit): 100338362
Entry
100338362         CDS       T03373                                 
Name
(RefSeq) peptidyl-prolyl cis-trans isomerase F, mitochondrial
  KO
K09565  peptidyl-prolyl isomerase F (cyclophilin D) [EC:5.2.1.8]
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04613  Neutrophil extracellular trap formation
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05145  Toxoplasmosis
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100338362
   04022 cGMP-PKG signaling pathway
    100338362
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100338362
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100338362
  09174 Infectious disease: parasitic
   05145 Toxoplasmosis
    100338362
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100338362
   05012 Parkinson disease
    100338362
   05016 Huntington disease
    100338362
   05017 Spinocerebellar ataxia
    100338362
   05020 Prion disease
    100338362
   05022 Pathways of neurodegeneration - multiple diseases
    100338362
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100338362
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03110 Chaperones and folding catalysts [BR:ocu03110]
    100338362
Enzymes [BR:ocu01000]
 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
     100338362
Chaperones and folding catalysts [BR:ocu03110]
 Protein folding catalysts
  Peptidyl prolyl isomerase
   Cyclophilin
    100338362
SSDB
Motif
Pfam: Pro_isomerase
Other DBs
NCBI-GeneID: 100338362
NCBI-ProteinID: XP_051687516
Ensembl: ENSOCUG00000012345
LinkDB
Position
Unknown
AA seq 206 aa
MLALRRGPRLLGLLPARCAAPPGPAARAYSSDGARDSSSSAPGNPLVYLDVGADGQPLGR
VVLELKADVVPKTAENFRALCTGEKGFGYKGSTFHRVIPSFMCQAGDFTNHNGTGGKSIY
GSRFPDENFTLKHVGPGVLSMANAGPNTNGSQFFICTIKTDWLDGKHVVFGHVKEGMDVV
KKIESFGSRSGKTSKKIVITDCGQLS
NT seq 621 nt   +upstreamnt  +downstreamnt
atgctggcgctgcgccgcggcccccgcctgctcggcctgctcccggcccggtgcgcggcg
ccgccgggcccagcggcccgcgcctacagcagcgacggcgcccgcgactcgtcctcttcc
gccccggggaacccgctcgtgtacctggacgtgggcgccgacgggcagccgctcggccgc
gtggtgctggagctgaaggctgatgttgtcccaaagacagcagagaacttccgggccctg
tgcaccggggagaaaggcttcggctacaagggctccacgttccacagagtgatcccgtcc
ttcatgtgccaggctggcgacttcaccaaccacaacggcacagggggcaagtccatctac
ggaagccgctttcctgatgagaacttcacgctgaagcacgtgggaccaggtgtcctgtcc
atggcgaatgcaggccccaacaccaatggttcccagttcttcatttgcaccataaagaca
gactggctggacggcaagcacgtggtgttcggccacgtcaaagagggcatggacgtcgtg
aagaagatcgagtcctttggctcccggagcgggaagacgtccaagaagatcgtcatcacg
gactgcggccagctgagctaa

KEGG   Oryctolagus cuniculus (rabbit): 100342972
Entry
100342972         CDS       T03373                                 
Name
(RefSeq) ADP/ATP translocase 2-like
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100342972
   04022 cGMP-PKG signaling pathway
    100342972
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100342972
   04218 Cellular senescence
    100342972
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100342972
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100342972
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100342972
   05164 Influenza A
    100342972
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100342972
   05012 Parkinson disease
    100342972
   05016 Huntington disease
    100342972
   05017 Spinocerebellar ataxia
    100342972
   05020 Prion disease
    100342972
   05022 Pathways of neurodegeneration - multiple diseases
    100342972
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100342972
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100342972
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ocu02000]
    100342972
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    100342972
Transporters [BR:ocu02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   100342972
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 100342972
NCBI-ProteinID: XP_051713327
LinkDB
Position
13:49653894..49655066
AA seq 298 aa
MTDATVSFTKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLGDCLVKIYKSDGIRGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTLDCWRKIARDEGGKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacagatgccactgtgtccttcaccaaggactttctggcaggtggagtggctgcggcc
atctccaagaccgcggtagcgcccatcgagagggtcaagctgctgctgcaggtgcagcat
gccagcaagcaaatcactgccgataagcaatacaagggcattatagactgcgtggttcgt
atccccaaggagcagggagtcctgtccttctggcgtggtaacctggccaatgtcatcaga
tacttccccacccaggctctcaactttgccttcaaagataaatacaagcagatctttctg
ggtggcgtggacaagaggacccagttttggcgctactttgcaggaaatctggcatcaggt
ggtgctgctggagccacatccttgtgttttgtgtaccctcttgattttgcccgtacccgt
ctagcagctgacgtgggcaaagctggagctgaaagggaattcagaggcctcggcgactgc
ctggttaagatctacaaatctgatgggattaggggcctgtaccaaggctttaatgtgtct
gtacagggcattatcatctaccgggctgcctacttcggtatctatgacaccgcaaaagga
atgcttccagatcccaagaacacgcacatcttcatcagctggatgatcgcgcagtctgtc
actgctgttgctgggttgacttcctatccatttgacactgttcgtcggcgcatgatgatg
cagtcggggcgtaaaggaactgatatcatgtacacaggcacacttgactgctggaggaag
attgctcgtgatgaaggaggcaaagcgtttttcaagggtgcatggtccaacgtcctcaga
ggcatgggtggtgcttttgtgcttgtcttgtatgatgaaatcaagaagttcacataa

KEGG   Oryctolagus cuniculus (rabbit): 100346477
Entry
100346477         CDS       T03373                                 
Name
(RefSeq) ADP/ATP translocase 4 isoform X1
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100346477
   04022 cGMP-PKG signaling pathway
    100346477
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100346477
   04218 Cellular senescence
    100346477
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100346477
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100346477
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100346477
   05164 Influenza A
    100346477
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100346477
   05012 Parkinson disease
    100346477
   05016 Huntington disease
    100346477
   05017 Spinocerebellar ataxia
    100346477
   05020 Prion disease
    100346477
   05022 Pathways of neurodegeneration - multiple diseases
    100346477
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100346477
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100346477
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ocu02000]
    100346477
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    100346477
Transporters [BR:ocu02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   100346477
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 100346477
NCBI-ProteinID: XP_002717308
Ensembl: ENSOCUG00000015617
LinkDB
Position
15:100413497..100441859
AA seq 322 aa
MQREPAKKKPEKKAEKRLFDAASFGRDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQ
ISPETRYKGMVDCLVRIPREQGFFSYWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVN
KEKQFWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKI
AKSDGIVGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKETPFLISFFIAQVVTTCS
GILSYPFDTVRRRMMMQSGEAERQYKGTLDCFVKIYQHEGINAFFRGAFSNILRGTGGAL
VLVLYDKIKEFLKIDIGGGSSD
NT seq 969 nt   +upstreamnt  +downstreamnt
atgcagcgtgagcctgccaagaagaagccggagaagaaggctgagaagcggctgtttgac
gccgcatccttcggaagggacctgctggccggcggggtcgcggcggctgtgtccaagacg
gcagtggcgcccatcgagcgggtgaagctcctcctgcaggtgcaggcgtcgtccaagcag
atcagccccgagacgcgctacaagggcatggtggactgcctggtgcggattccccgcgag
cagggtttctttagttattggcgaggcaatttggcaaatgttatccggtactttccaaca
caagctctaaattttgcttttaaagacaaatacaaacaacttttcatgtctggagttaat
aaagaaaaacagttctggaggtggtttttggcaaacctggcttctggtggagctgccgga
gcaacatctttgtgtgtggtttatcctctagattttgcccgaactcggttaggtgttgac
attggaaaaggtcctgaagagcgacaattcaagggtctaggtgactgcattatgaaaata
gcaaaatcagatggcatagttggtttataccaagggtttggtgtttcagttcagggaatc
attgtgtaccgagcctcttactttggagcttatgacacagttaagggcttattaccaaaa
ccaaaagaaactccatttcttatctcctttttcattgctcaagttgtgactacatgctct
ggaatactctcttacccctttgatacagtgagaagacgcatgatgatgcagagtggtgaa
gctgaacggcagtataaaggaaccttagactgctttgtgaagatataccaacatgaggga
atcaatgcattttttcgtggtgccttctccaatatccttcgtggtacagggggtgctttg
gtgttggtgttatatgataaaattaaagaattccttaaaattgatattggaggtggttca
tcagattaa

KEGG   Oryctolagus cuniculus (rabbit): 100348057
Entry
100348057         CDS       T03373                                 
Name
(RefSeq) ADP/ATP translocase 2-like
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100348057
   04022 cGMP-PKG signaling pathway
    100348057
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100348057
   04218 Cellular senescence
    100348057
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100348057
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100348057
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100348057
   05164 Influenza A
    100348057
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100348057
   05012 Parkinson disease
    100348057
   05016 Huntington disease
    100348057
   05017 Spinocerebellar ataxia
    100348057
   05020 Prion disease
    100348057
   05022 Pathways of neurodegeneration - multiple diseases
    100348057
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100348057
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100348057
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:ocu02000]
    100348057
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    100348057
Transporters [BR:ocu02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   100348057
SSDB
Motif
Pfam: Mito_carr
Other DBs
NCBI-GeneID: 100348057
NCBI-ProteinID: XP_051702424
LinkDB
Position
4:63299323..63300687
AA seq 298 aa
MTDASVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
NPKEQGILSFWRGNLASVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLSDCLVKIYKSDGIRGLYQGFNVS
VQGIIIYRAAYFGIYDTTKGMLPDPKNTHIFISWMIAQSVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTLDCWRKIAHDEGGKAFFKGAWSNVLRGMGGAFVLVLYDEIKKFT
NT seq 897 nt   +upstreamnt  +downstreamnt
atgacagatgcctctgtgtccttcgccaaggactttctggcaggtggagtggctgcggcc
atctccaagaccgcggtagcgcccatcgagagggtcaagctgctgctgcaggtgcagcat
gccagcaagcaaatcactgccgataagcaatacaagggcattatagactgcgtggttcgt
aaccccaaggagcagggaatcctgtccttctggcgtggtaacctggccagtgtcatcaga
tacttccccacccaggctctcaactttgccttcaaagataaatacaagcagatctttctg
ggtggcgtggacaagaggacccagttttggcgctactttgcaggaaatctggcatcaggt
ggtgctgctggagccacatccttgtgttttgtgtaccctcttgattttgcccgtacccgt
ctagcagctgacgtgggcaaagctggagctgaaagggaattcagaggcctcagtgactgc
ctggttaagatctacaaatctgatgggattaggggcctgtaccaaggctttaatgtgtct
gtacagggcattatcatctaccgggctgcctactttggtatctatgacaccacaaaagga
atgcttccagatcccaagaacacgcacatcttcatcagctggatgatcgcgcagtctgtc
actgctgttgctgggttgacttcctatccatttgacactgttcgtcggcgcatgatgatg
cagtcggggcgtaaaggaactgatatcatgtacacaggcacacttgactgctggaggaag
attgctcatgatgaaggaggcaaagcgtttttcaagggtgcatggtccaacgtcctcaga
ggcatgggtggtgcttttgtgcttgtcttgtatgatgaaatcaagaagttcacataa

KEGG   Oryctolagus cuniculus (rabbit): 100349506
Entry
100349506         CDS       T03373                                 
Name
(RefSeq) LOW QUALITY PROTEIN: voltage-dependent anion-selective channel protein 1-like
  KO
K05862  voltage-dependent anion channel protein 1
Organism
ocu  Oryctolagus cuniculus (rabbit)
Pathway
ocu04020  Calcium signaling pathway
ocu04022  cGMP-PKG signaling pathway
ocu04217  Necroptosis
ocu04218  Cellular senescence
ocu04613  Neutrophil extracellular trap formation
ocu04621  NOD-like receptor signaling pathway
ocu04979  Cholesterol metabolism
ocu05010  Alzheimer disease
ocu05012  Parkinson disease
ocu05014  Amyotrophic lateral sclerosis
ocu05016  Huntington disease
ocu05017  Spinocerebellar ataxia
ocu05020  Prion disease
ocu05022  Pathways of neurodegeneration - multiple diseases
ocu05164  Influenza A
ocu05166  Human T-cell leukemia virus 1 infection
ocu05208  Chemical carcinogenesis - reactive oxygen species
ocu05415  Diabetic cardiomyopathy
Brite
KEGG Orthology (KO) [BR:ocu00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    100349506
   04022 cGMP-PKG signaling pathway
    100349506
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    100349506
   04218 Cellular senescence
    100349506
 09150 Organismal Systems
  09151 Immune system
   04613 Neutrophil extracellular trap formation
    100349506
   04621 NOD-like receptor signaling pathway
    100349506
  09154 Digestive system
   04979 Cholesterol metabolism
    100349506
 09160 Human Diseases
  09161 Cancer: overview
   05208 Chemical carcinogenesis - reactive oxygen species
    100349506
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    100349506
   05164 Influenza A
    100349506
  09164 Neurodegenerative disease
   05010 Alzheimer disease
    100349506
   05012 Parkinson disease
    100349506
   05014 Amyotrophic lateral sclerosis
    100349506
   05016 Huntington disease
    100349506
   05017 Spinocerebellar ataxia
    100349506
   05020 Prion disease
    100349506
   05022 Pathways of neurodegeneration - multiple diseases
    100349506
  09166 Cardiovascular disease
   05415 Diabetic cardiomyopathy
    100349506
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:ocu03029]
    100349506
  09183 Protein families: signaling and cellular processes
   04040 Ion channels [BR:ocu04040]
    100349506
Mitochondrial biogenesis [BR:ocu03029]
 Mitochondrial protein import machinery
  Outer membrane
   Porin
    100349506
Ion channels [BR:ocu04040]
 Chloride channels
  Maxi chloride channel (VDAC)
   100349506
SSDB
Motif
Pfam: Porin_3
Other DBs
NCBI-GeneID: 100349506
NCBI-ProteinID: XP_051710262
LinkDB
Position
12:28453080..28454788
AA seq 276 aa
MAVPPTYADLGKSARDVFTKGYGFGLIKLDLKTKXSSGSANTETTKVTGSLETKYRWTEY
GLTFTEKWNTDNTLGTEITVEDQLARGLKLTFDSSFSPNTGEKNAKIKTGYKREHINLGC
DVDFDIAGPSIRGALVLGYEGWLADYQMNFETAKSRVTQSNFAVGYKTDEFQLHTNVNDG
TEFGGSIYQKVNKKLETAVNLAWTAGNSNTRFGIAAKYQIDPDACFSAKVNNSSLIGLGY
TQTLKPGIKLTLSALLDGKNVNAGGHKLGLGLEFQA
NT seq 831 nt   +upstreamnt  +downstreamnt
atggctgtacctcccacgtatgccgatcttggcaaatctgccagggatgtcttcaccaag
ggctacggatttggcttaataaagcttgatttgaaaacaaaancaagctcaggctcagcc
aacactgagaccaccaaagtgacgggcagtctggaaaccaagtacaggtggaccgagtat
gggctgacgtttacggagaaatggaacaccgacaacacgctgggcaccgagatcaccgtg
gaagaccagcttgcacgtggactgaagctgaccttcgattcctccttctcgcctaacact
ggggaaaaaaatgctaaaatcaagacaggctacaagcgggagcacatcaacctgggctgc
gacgtggatttcgacatcgctgggccctccatccggggcgctctggtgctgggttacgag
ggctggctggctgactaccagatgaactttgagactgccaagtcccgagtcacccagagc
aactttgccgtcggctacaagaccgacgaattccagctccacactaatgtgaacgatgga
acggagtttggcggctccatttaccagaaggtgaacaagaagctggagacggccgtcaat
cttgcctggacagcaggaaacagtaacactcgctttggaatagcagccaagtatcagatc
gaccctgacgcctgcttctcggcaaaagtgaacaactccagcctgataggattaggatac
actcagaccctaaagccaggtatcaaactgacgctctcagctctgctggatggcaagaac
gtcaacgctggcggccacaagcttggtctaggactggagtttcaggcataa

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