Homo sapiens (human): 123096 Help Entry 123096            CDS       T01001                                  Symbol SLC25A29, C14orf69, CACL, ORNT3 Name (RefSeq) solute carrier family 25 member 29   KO K28105   solute carrier family 25 (mitochondrial basic amino acids transporter), member 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 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 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 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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