KEGG   Homo sapiens (human): 291Help
Entry
291               CDS       T01001                                 

Gene name
SLC25A4, AAC1, ANT, ANT_1, ANT1, MTDPS12, MTDPS12A, PEO2, PEO3, PEOA2, T1
Definition
(RefSeq) solute carrier family 25 member 4
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
hsa  Homo sapiens (human)
Pathway
hsa04020  Calcium signaling pathway
hsa04022  cGMP-PKG signaling pathway
hsa04217  Necroptosis
hsa04218  Cellular senescence
hsa05012  Parkinson disease
hsa05016  Huntington disease
hsa05164  Influenza A
hsa05166  Human T-cell leukemia virus 1 infection
Disease
H00469  Mitochondrial DNA depletion syndrome
H01118  Progressive external ophthalmoplegia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    291 (SLC25A4)
   04022 cGMP-PKG signaling pathway
    291 (SLC25A4)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    291 (SLC25A4)
   04218 Cellular senescence
    291 (SLC25A4)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05012 Parkinson disease
    291 (SLC25A4)
   05016 Huntington disease
    291 (SLC25A4)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    291 (SLC25A4)
   05164 Influenza A
    291 (SLC25A4)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    291 (SLC25A4)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    291 (SLC25A4)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    291 (SLC25A4)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   291 (SLC25A4)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: Mito_carr
Motif
Other DBs
NCBI-GeneID: 291
NCBI-ProteinID: NP_001142
OMIM: 103220
HGNC: 10990
Ensembl: ENSG00000151729
Vega: OTTHUMG00000134299
Pharos: P12235(Tbio)
UniProt: P12235 A0A0S2Z3H3
LinkDB All DBs
Position
4q35.1
AA seq 298 aa AA seqDB search
MGDHAWSFLKDFLAGGVAAAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVR
IPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQLFLGGVDRHKQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKGAAQREFHGLGDCIIKIFKSDGLRGLYQGFNVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNVHIFVSWMIAQSVTAVAGLVSYPFDTVRRRMMM
QSGRKGADIMYTGTVDCWRKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV
NT seq 897 nt NT seq  +upstreamnt  +downstreamnt
atgggtgatcacgcttggagcttcctaaaggacttcctggccgggggcgtcgccgctgcc
gtctccaagaccgcggtcgcccccatcgagagggtcaaactgctgctgcaggtccagcat
gccagcaaacagatcagtgctgagaagcagtacaaagggatcattgattgtgtggtgaga
atccctaaggagcagggcttcctctccttctggaggggtaacctggccaacgtgatccgt
tacttccccacccaagctctcaacttcgccttcaaggacaagtacaagcagctcttctta
gggggtgtggatcggcataagcagttctggcgctactttgctggtaacctggcgtccggt
ggggccgctggggccacctccctttgctttgtctacccgctggactttgctaggaccagg
ttggctgctgatgtgggcaagggcgccgcccagcgtgagttccatggtctgggcgactgt
atcatcaagatcttcaagtctgatggcctgagggggctctaccagggtttcaacgtctct
gtccaaggcatcattatctatagagctgcctacttcggagtctatgatactgccaagggg
atgctgcctgaccccaagaacgtgcacatttttgtgagctggatgattgcccagagtgtg
acggcagtcgcagggctggtgtcctacccctttgacactgttcgtcgtagaatgatgatg
cagtccggccggaaaggggccgatattatgtacacggggacagttgactgctggaggaag
attgcaaaagacgaaggagccaaggccttcttcaaaggtgcctggtccaatgtgctgaga
ggcatgggcggtgcttttgtattggtgttgtatgatgagatcaaaaaatatgtctaa

KEGG   Homo sapiens (human): 292Help
Entry
292               CDS       T01001                                 

Gene name
SLC25A5, 2F1, AAC2, ANT2, T2, T3
Definition
(RefSeq) solute carrier family 25 member 5
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
hsa  Homo sapiens (human)
Pathway
hsa04020  Calcium signaling pathway
hsa04022  cGMP-PKG signaling pathway
hsa04217  Necroptosis
hsa04218  Cellular senescence
hsa05012  Parkinson disease
hsa05016  Huntington disease
hsa05164  Influenza A
hsa05166  Human T-cell leukemia virus 1 infection
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    292 (SLC25A5)
   04022 cGMP-PKG signaling pathway
    292 (SLC25A5)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    292 (SLC25A5)
   04218 Cellular senescence
    292 (SLC25A5)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05012 Parkinson disease
    292 (SLC25A5)
   05016 Huntington disease
    292 (SLC25A5)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    292 (SLC25A5)
   05164 Influenza A
    292 (SLC25A5)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    292 (SLC25A5)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    292 (SLC25A5)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    292 (SLC25A5)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   292 (SLC25A5)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: Mito_carr Fuseless
Motif
Other DBs
NCBI-GeneID: 292
NCBI-ProteinID: NP_001143
OMIM: 300150
HGNC: 10991
Ensembl: ENSG00000005022
Vega: OTTHUMG00000022715
Pharos: P05141(Tbio)
UniProt: P05141 Q6NVC0
LinkDB All DBs
Position
Xq24
AA seq 298 aa AA seqDB search
MTDAAVSFAKDFLAGGVAAAISKTAVAPIERVKLLLQVQHASKQITADKQYKGIIDCVVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKRTQFWLYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKAGAEREFRGLGDCLVKIYKSDGIKGLYQGFNVS
VQGIIIYRAAYFGIYDTAKGMLPDPKNTHIVISWMIAQTVTAVAGLTSYPFDTVRRRMMM
QSGRKGTDIMYTGTLDCWRKIARDEGGKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYT
NT seq 897 nt NT seq  +upstreamnt  +downstreamnt
atgacagatgccgctgtgtccttcgccaaggacttcctggcaggtggagtggccgcagcc
atctccaagacggcggtagcgcccatcgagcgggtcaagctgctgctgcaggtgcagcat
gccagcaagcagatcactgcagataagcaatacaaaggcattatagactgcgtggtccgt
attcccaaggagcagggagttctgtccttctggcgcggtaacctggccaatgtcatcaga
tacttccccacccaggctcttaacttcgccttcaaagataaatacaagcagatcttcctg
ggtggtgtggacaagagaacccagttttggctctactttgcagggaatctggcatcgggt
ggtgccgcaggggccacatccctgtgttttgtgtaccctcttgattttgcccgtacccgt
ctagcagctgatgtgggtaaagctggagctgaaagggaattccgaggcctcggtgactgc
ctggttaagatctacaaatctgatgggattaagggcctgtaccaaggctttaacgtgtct
gtgcagggtattatcatctaccgagccgcctacttcggtatctatgacactgcaaaggga
atgcttccggatcccaagaacactcacatcgtcatcagctggatgatcgcacagactgtc
actgctgttgccgggttgacttcctatccatttgacactgttcgccgccgcatgatgatg
cagtcagggcgcaaaggaactgacatcatgtacacaggcacgcttgactgctggcggaag
attgctcgtgatgaaggaggcaaagcttttttcaagggtgcatggtccaatgttctcaga
ggcatgggtggtgcttttgtgcttgtcttgtatgatgaaatcaagaagtacacataa

KEGG   Homo sapiens (human): 293Help
Entry
293               CDS       T01001                                 

Gene name
SLC25A6, AAC3, ANT, ANT_2, ANT_3, ANT3, ANT3Y
Definition
(RefSeq) solute carrier family 25 member 6
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
hsa  Homo sapiens (human)
Pathway
hsa04020  Calcium signaling pathway
hsa04022  cGMP-PKG signaling pathway
hsa04217  Necroptosis
hsa04218  Cellular senescence
hsa05012  Parkinson disease
hsa05016  Huntington disease
hsa05164  Influenza A
hsa05166  Human T-cell leukemia virus 1 infection
Network
nt06131  Apoptosis (virus)
nt06170  Influenza A virus (IAV)
  Element
N00745  IAV PB1-F2 to intrinsic apoptotic pathway
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    293 (SLC25A6)
   04022 cGMP-PKG signaling pathway
    293 (SLC25A6)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    293 (SLC25A6)
   04218 Cellular senescence
    293 (SLC25A6)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05012 Parkinson disease
    293 (SLC25A6)
   05016 Huntington disease
    293 (SLC25A6)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    293 (SLC25A6)
   05164 Influenza A
    293 (SLC25A6)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    293 (SLC25A6)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    293 (SLC25A6)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    293 (SLC25A6)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   293 (SLC25A6)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: Mito_carr Fuseless
Motif
Other DBs
NCBI-GeneID: 293
NCBI-ProteinID: NP_001627
OMIM: 300151 403000
HGNC: 10992
Ensembl: ENSG00000169100
Vega: OTTHUMG00000021058
Pharos: P12236(Tbio)
UniProt: P12236 Q6I9V5
LinkDB All DBs
Position
Xp22.33 and Yp11.2
AA seq 298 aa AA seqDB search
MTEQAISFAKDFLAGGIAAAISKTAVAPIERVKLLLQVQHASKQIAADKQYKGIVDCIVR
IPKEQGVLSFWRGNLANVIRYFPTQALNFAFKDKYKQIFLGGVDKHTQFWRYFAGNLASG
GAAGATSLCFVYPLDFARTRLAADVGKSGTEREFRGLGDCLVKITKSDGIRGLYQGFSVS
VQGIIIYRAAYFGVYDTAKGMLPDPKNTHIVVSWMIAQTVTAVAGVVSYPFDTVRRRMMM
QSGRKGADIMYTGTVDCWRKIFRDEGGKAFFKGAWSNVLRGMGGAFVLVLYDELKKVI
NT seq 897 nt NT seq  +upstreamnt  +downstreamnt
atgacggaacaggccatctccttcgccaaagacttcttggccggaggcatcgccgccgcc
atctccaagacggccgtggctccgatcgagcgggtcaagctgctgctgcaggtccagcac
gccagcaagcagatcgccgccgacaagcagtacaagggcatcgtggactgcattgtccgc
atccccaaggagcagggcgtgctgtccttctggaggggcaaccttgccaacgtcattcgc
tacttccccactcaagccctcaacttcgccttcaaggataagtacaagcagatcttcctg
gggggcgtggacaagcacacgcagttctggaggtactttgcgggcaacctggcctccggc
ggtgcggccggcgcgacctccctctgcttcgtgtacccgctggatttcgccagaacccgc
ctggcagcggacgtgggaaagtcaggcacagagcgcgagttccgaggcctgggagactgc
ctggtgaagatcaccaagtccgacggcatccggggcctgtaccagggcttcagtgtctcc
gtgcagggcatcatcatctaccgggcggcctacttcggcgtgtacgatacggccaagggc
atgctccccgaccccaagaacacgcacatcgtggtgagctggatgatcgcgcagaccgtg
acggccgtggccggcgtggtgtcctaccccttcgacacggtgcggcggcgcatgatgatg
cagtccgggcgcaaaggagctgacatcatgtacacgggcaccgtcgactgttggaggaag
atcttcagagatgaggggggcaaggccttcttcaagggtgcgtggtccaacgtcctgcgg
ggcatggggggcgccttcgtgctggtcctgtacgacgagctcaagaaggtgatctaa

KEGG   Homo sapiens (human): 83447Help
Entry
83447             CDS       T01001                                 

Gene name
SLC25A31, AAC4, ANT_4, ANT4, SFEC35kDa
Definition
(RefSeq) solute carrier family 25 member 31
  KO
K05863  solute carrier family 25 (mitochondrial adenine nucleotide translocator), member 4/5/6/31
Organism
hsa  Homo sapiens (human)
Pathway
hsa04020  Calcium signaling pathway
hsa04022  cGMP-PKG signaling pathway
hsa04217  Necroptosis
hsa04218  Cellular senescence
hsa05012  Parkinson disease
hsa05016  Huntington disease
hsa05164  Influenza A
hsa05166  Human T-cell leukemia virus 1 infection
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04020 Calcium signaling pathway
    83447 (SLC25A31)
   04022 cGMP-PKG signaling pathway
    83447 (SLC25A31)
 09140 Cellular Processes
  09143 Cell growth and death
   04217 Necroptosis
    83447 (SLC25A31)
   04218 Cellular senescence
    83447 (SLC25A31)
 09160 Human Diseases
  09164 Neurodegenerative disease
   05012 Parkinson disease
    83447 (SLC25A31)
   05016 Huntington disease
    83447 (SLC25A31)
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    83447 (SLC25A31)
   05164 Influenza A
    83447 (SLC25A31)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03029 Mitochondrial biogenesis [BR:hsa03029]
    83447 (SLC25A31)
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    83447 (SLC25A31)
Mitochondrial biogenesis [BR:hsa03029]
 Mitochondrial DNA transcription, translation, and replication factors
  Mitochondrial transcription and translation factors
   Other mitochondrial DNA transcription and translation factors
    83447 (SLC25A31)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC25: Mitochondrial carrier
   83447 (SLC25A31)
BRITE hierarchy
SSDB OrthologParalogGFIT
Motif
Pfam: Mito_carr
Motif
Other DBs
NCBI-GeneID: 83447
NCBI-ProteinID: NP_112581
OMIM: 610796
HGNC: 25319
Ensembl: ENSG00000151475
Vega: OTTHUMG00000133300
Pharos: Q9H0C2(Tbio)
UniProt: Q9H0C2
LinkDB All DBs
Position
4q28.1
AA seq 315 aa AA seqDB search
MHREPAKKKAEKRLFDASSFGKDLLAGGVAAAVSKTAVAPIERVKLLLQVQASSKQISPE
ARYKGMVDCLVRIPREQGFFSFWRGNLANVIRYFPTQALNFAFKDKYKQLFMSGVNKEKQ
FWRWFLANLASGGAAGATSLCVVYPLDFARTRLGVDIGKGPEERQFKGLGDCIMKIAKSD
GIAGLYQGFGVSVQGIIVYRASYFGAYDTVKGLLPKPKKTPFLVSFFIAQVVTTCSGILS
YPFDTVRRRMMMQSGEAKRQYKGTLDCFVKIYQHEGISSFFRGAFSNVLRGTGGALVLVL
YDKIKEFFHIDIGGR
NT seq 948 nt NT seq  +upstreamnt  +downstreamnt
atgcatcgtgagcctgcgaaaaagaaggcagaaaagcggctgtttgacgcctcatccttc
gggaaggaccttctggccggcggagtcgcggcagctgtgtccaagacagcggtggcgccc
atcgagcgggtgaagctgctgctgcaggtgcaggcgtcgtcgaagcagatcagccccgag
gcgcggtacaaaggcatggtggactgcctggtgcggattcctcgcgagcagggtttcttc
agtttttggcgtggcaatttggcaaatgttattcggtattttccaacacaagctctaaac
tttgcttttaaggacaaatacaagcagctattcatgtctggagttaataaagaaaaacag
ttctggaggtggtttttggcaaacctggcttctggtggagctgctggggcaacatcctta
tgtgtagtatatcctctagattttgcccgaacccgattaggtgtcgatattggaaaaggt
cctgaggagcgacaattcaagggtttaggtgactgtattatgaaaatagcaaaatcagat
ggaattgctggtttataccaagggtttggtgtttcagtacagggcatcattgtgtaccga
gcctcttattttggagcttatgacacagttaagggtttattaccaaagccaaagaaaact
ccatttcttgtctcctttttcattgctcaagttgtgactacatgctctggaatactttct
tatccctttgacacagttagaagacgtatgatgatgcagagtggtgaggctaaacggcaa
tataaaggaaccttagactgctttgtgaagatataccaacatgaaggaatcagttccttt
tttcgtggcgccttctccaatgttcttcgcggtacagggggtgctttggtgttggtatta
tatgataaaattaaagaattctttcatattgatattggtggtaggtaa

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