Homo sapiens (human): 123096 Help Entry 123096            CDS       T01001                                  Symbol SLC25A29, C14orf69, CACL, ORNT3 Name (RefSeq) solute carrier family 25 member 29   KO K15109   solute carrier family 25 (mitochondrial carnitine/acylcarnitine transporter), member 20/29 Organism hsa  Homo sapiens (human) Pathway hsa04714   Thermogenesis Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     123096 (SLC25A29)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     123096 (SLC25A29) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    123096 (SLC25A29) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr HTH_26 Motif Other DBs NCBI-GeneID:  123096 NCBI-ProteinID:  NP_001034444 OMIM:  615064 HGNC:  20116 Ensembl:  ENSG00000197119 Pharos:  Q8N8R3(Tbio) UniProt:  Q8N8R3 LinkDB All DBs Position 14:complement(100278567..100306444) Genome browser AA seq 303 aa AA seqDB search MALDFLAGCAGGVAGVLVGHPFDTVKVRLQVQSVEKPQYRGTLHCFKSIIKQESVLGLYK GLGSPLMGLTFINALVFGVQGNTLRALGHDSPLNQFLAGAAAGAIQCVICCPMELAKTRL QLQDAGPARTYKGSLDCLAQIYGHEGLRGVNRGMVSTLLRETPSFGVYFLTYDALTRALG CEPGDRLLVPKLLLAGGTSGIVSWLSTYPVDVVKSRLQADGLRGAPRYRGILDCVHQSYR AEGWRVFTRGLASTLLRAFPVNAATFATVTVVLTYARGEEAGPEGEAVPAAPAGPALAQP SSL NT seq 912 nt NT seq  +upstreamnt  +downstreamnt atggcgctggacttcttggctggatgcgcggggggtgtggcaggcgtgcttgtgggacac ccgtttgacacggtcaaggtacggcttcaggtccagagcgtggagaagcctcagtaccgc gggacgttgcactgcttcaagtccatcatcaagcaagagagcgtgctgggcctgtacaag ggcctgggctcgccgctcatggggctcaccttcatcaacgcgctggtgttcggggtgcag ggcaacaccctccgggccctgggccacgactcgcccctcaaccagttcctggcaggtgcg gcggcgggcgccatccagtgcgtcatctgctgccccatggagctggccaagacgcggctg cagctgcaggacgcgggcccagcgcgcacctacaagggctcgctggactgcctcgcgcag atctacgggcacgagggtctgcgtggcgtcaaccggggcatggtgtccacgttgctgcgt gagacgcccagcttcggcgtctacttcctcacctatgacgctctcacgcgggcgctgggc tgcgagccgggcgaccgcctgctggtgcccaagctgctgttggcgggcggtacgtcaggc atcgtgtcctggctctctacctatcctgtggacgtggtcaagtcgcggctgcaggcggac ggactgcggggcgccccgcgctaccgcggcatcctggactgcgtgcaccagagctaccgc gccgagggctggcgcgtcttcacacgggggctggcgtccacgctgctgcgcgccttcccc gtcaacgctgccaccttcgccaccgtcacggtggtgctcacctacgcgcgcggcgaggag gccgggcccgagggcgaggctgtgcccgccgcccctgcggggcctgccctggcgcagccc tccagcctgtga

Homo sapiens (human): 788 Help Entry 788               CDS       T01001                                  Symbol SLC25A20, CAC, CACT Name (RefSeq) solute carrier family 25 member 20   KO K15109   solute carrier family 25 (mitochondrial carnitine/acylcarnitine transporter), member 20/29 Organism hsa  Homo sapiens (human) Pathway hsa04714   Thermogenesis Network nt06020  beta-Oxidation in mitochondria   Element N00814   Transport of L-palmitoylcarnitine Disease H00525   Disorders of mitochondrial fatty-acid oxidation H01400   Secondary hyperammonemia H01983   Carnitine-acylcarnitine translocase deficiency H02596   Disorders of carnitine transport and the carnitine cycle Brite KEGG Orthology (KO) [BR:hsa00001]  09150 Organismal Systems   09159 Environmental adaptation    04714 Thermogenesis     788 (SLC25A20)  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    02000 Transporters [BR:hsa02000]     788 (SLC25A20) Transporters [BR:hsa02000]  Solute carrier family (SLC)   SLC25: Mitochondrial carrier    788 (SLC25A20) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Mito_carr Motif Other DBs NCBI-GeneID:  788 NCBI-ProteinID:  NP_000378 OMIM:  613698 HGNC:  1421 Ensembl:  ENSG00000178537 Pharos:  O43772(Tbio) UniProt:  O43772 LinkDB All DBs Position 3:complement(48856926..48898882) Genome browser AA seq 301 aa AA seqDB search MADQPKPISPLKNLLAGGFGGVCLVFVGHPLDTVKVRLQTQPPSLPGQPPMYSGTFDCFR KTLFREGITGLYRGMAAPIIGVTPMFAVCFFGFGLGKKLQQKHPEDVLSYPQLFAAGMLS GVFTTGIMTPGERIKCLLQIQASSGESKYTGTLDCAKKLYQEFGIRGIYKGTVLTLMRDV PASGMYFMTYEWLKNIFTPEGKRVSELSAPRILVAGGIAGIFNWAVAIPPDVLKSRFQTA PPGKYPNGFRDVLRELIRDEGVTSLYKGFNAVMIRAFPANAACFLGFEVAMKFLNWATPN L NT seq 906 nt NT seq  +upstreamnt  +downstreamnt atggccgaccagccaaaacccatcagcccgctcaagaacctgctggccggcggctttggc ggcgtgtgcctggtgttcgtcggtcaccctctggacacggtcaaggtccgactgcagaca cagccaccgagtttgcctggacaacctcccatgtactctgggacctttgactgtttccgg aagactctttttagagagggcatcacggggctatatcggggaatggctgcccctatcatc ggggtcactcccatgtttgccgtgtgcttctttgggtttggtttggggaagaaactacaa cagaaacacccagaagatgtgctcagctatccccagctttttgcagctgggatgttatct ggcgtattcaccacaggaatcatgactcctggagaacggatcaagtgcttattacagatt caggcttcttcaggagaaagcaagtacactggtaccttggactgtgcaaagaagctgtac caggagtttgggatccgaggcatctacaaagggactgtgcttacccttatgcgagatgtc ccagctagtggaatgtatttcatgacatatgaatggctgaaaaatatcttcactccggag ggaaagagggtcagtgagctcagtgcccctcggatcttggtggctgggggcattgcaggg atcttcaactgggctgtggcaatccccccagatgtgctcaagtctcgattccagactgca cctcctgggaaatatcctaatggtttcagagatgtgctgagggagctgatccgggatgaa ggagtcacatccttgtacaaagggttcaatgcagtgatgatccgagccttcccagccaat gcggcctgtttccttggctttgaagttgccatgaagttccttaattgggccacccccaac ttgtga

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