Homo sapiens (human): 84233 Help Entry 84233             CDS       T01001                                  Symbol TMEM126A, OPA7 Name (RefSeq) transmembrane protein 126A   KO K18157   transmembrane protein 126A Organism hsa  Homo sapiens (human) Disease H01020   Optic atrophy Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03029 Mitochondrial biogenesis [BR:hsa03029]     84233 (TMEM126A) Mitochondrial biogenesis [BR:hsa03029]  Mitochondrial protein import machinery   Inner mambrane    Other inner membrane factors     84233 (TMEM126A) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TMEM126 TMEM126_like Motif Other DBs NCBI-GeneID:  84233 NCBI-ProteinID:  NP_115649 OMIM:  612988 HGNC:  25382 Ensembl:  ENSG00000171202 UniProt:  Q9H061 LinkDB All DBs Position 11:85647967..85656542 Genome browser AA seq 195 aa AA seqDB search MENHKSNNKENITIVDISRKINQLPEAERNLLENGSVYVGLNAALCGLIANSLFRRILNV TKARIAAGLPMAGIPFLTTDLTYRCFVSFPLNTGDLDCETCTITRSGLTGLVIGGLYPVF LAIPVNGGLAARYQSALLPHKGNILSYWIRTSKPVFRKMLFPILLQTMFSAYLGSEQYKL LIKALQLSEPGKEIH NT seq 588 nt NT seq  +upstreamnt  +downstreamnt atggaaaatcataaatccaataataaggaaaacataacaattgttgatatatccagaaaa attaaccagcttccagaagcagaaaggaatctacttgaaaatggatcggtttatgttgga ttaaatgctgctctttgtggcctcatagcaaacagtctttttcgacgcatcttgaatgtg acaaaggctcgcatagctgctggcttaccaatggcagggataccttttcttacaacagac ttaacttacagatgttttgtaagttttcctttgaatacaggtgatttggattgtgaaacc tgtaccataacacggagtggactgactggtcttgttattggtggtctataccctgttttc ttggctatacctgtaaatggtggtctagcagccaggtatcaatcagctctgttaccacac aaagggaacatcttaagttactggattagaacttctaagcctgtctttagaaagatgtta tttcctattttgctccagactatgttttcagcataccttgggtctgaacaatataaacta cttataaaggcccttcagttatctgaacctggcaaagaaattcactga

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