Homo sapiens (human): 65062 Help Entry 65062             CDS       T01001                                  Symbol TMEM237, ALS2CR4, JBTS14 Name (RefSeq) transmembrane protein 237   KO K22765   transmembrane protein 237 Organism hsa  Homo sapiens (human) Disease H00530   Joubert syndrome and related disorders Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     65062 (TMEM237) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   MKS complex    65062 (TMEM237) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TMEM237 Motif Other DBs NCBI-GeneID:  65062 NCBI-ProteinID:  NP_001037850 OMIM:  614423 HGNC:  14432 Ensembl:  ENSG00000155755 UniProt:  Q96Q45 LinkDB All DBs Position 2:complement(201620186..201643503) Genome browser AA seq 408 aa AA seqDB search MRTDSGARLEEGHLRPPRALPPVPSQDDIPLSRPKKKKPRTKNTPASASLEGLAQTAGRR PSEGNEPSTKELKEHPEAPVQRRQKKTRLPLELETSSTQKKSSSSSLLRNENGIDAEPAE EAVIQKPRRKTKKTQPAELQYANELGVEDEDIITDEQTTVEQQSVFTAPTGISQPVGKVF VEKSRRFQAADRSELIKTTENIDVSMDVKPSWTTRDVALTVHRAFRMIGLFSHGFLAGCA VWNIVVIYVLAGDQLSNLSNLLQQYKTLAYPFQSLLYLLLALSTISAFDRIDFAKISVAI RNFLALDPTALASFLYFTALILSLSQQMTSDRIHLYTPSSVNGSLWEAGIEEQILQPWIV VNLVVALLVGLSWLFLSYRPGMDLSEELMFSSEVEEYPDKEKEIKASS NT seq 1227 nt NT seq  +upstreamnt  +downstreamnt atgaggactgactcgggggctcggctggaggagggccacctgcgtcctccacgagctctt ccacctgtgccaagtcaagatgatattccacttagtcgtcctaagaaaaagaagcccaga acaaaaaacacaccagcaagtgcttctttggaaggccttgctcagactgctggtcgaagg ccctctgagggcaatgagccatcaactaaagaactcaaagagcacccagaggctcctgtt caaagaagacagaaaaagacaaggctacctcttgaattggagacttcctccacccaaaag aagtcatctagttcatctttattacgaaatgaaaatggtattgatgcggagccagctgag gaggcagttattcaaaaacctcggaggaagacaaagaaaacccagccagcagaattacag tatgccaatgagctaggagtagaagatgaagacataatcactgatgagcaaactactgtg gaacagcagtctgtattcactgcacccactggcattagccagcctgtaggcaaagtattt gtggaaaaaagccggagattccaggctgctgatcgttcagagttgataaagaccacagaa aacatagatgtgtcaatggacgtgaagccttcctggaccaccagagatgtggcacttaca gtgcaccgggctttcaggatgattggtctcttttctcatggattcttggctggctgtgct gtgtggaatattgttgtgatatatgttctagcaggagatcagctatccaacctctcaaac cttctgcaacaatacaagaccctagcgtatccattccagagtcttctgtacttgcttttg gctctgagtacaatttcagcttttgacaggattgactttgctaaaatatcagtagcaatc cgaaattttttggccctggatcctacagctttagcatctttcttgtactttactgctctt atactatctctgagtcagcaaatgacaagtgacagaatccacctttacacaccttcttct gttaatggtagcctctgggaagcaggaattgaggaacagattctccagccatggattgtg gtgaatctcgtggtggctcttctggttggattatcttggctatttttgtcttataggcca ggcatggatcttagtgaagagttaatgttctcctcagaggtggaagaatatcctgataaa gagaaagaaatcaaagcctcttcataa

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