Homo sapiens (human): 51524 Help Entry 51524             CDS       T01001                                  Symbol TMEM138, HSPC196 Name (RefSeq) transmembrane protein 138   KO K22867   transmembrane protein 138 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]     51524 (TMEM138) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   Other primary cilia associated proteins    51524 (TMEM138) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TMEM138 Motif Other DBs NCBI-GeneID:  51524 NCBI-ProteinID:  NP_057548 OMIM:  614459 HGNC:  26944 Ensembl:  ENSG00000149483 UniProt:  Q9NPI0 LinkDB All DBs Position 11:61362374..61376870 Genome browser AA seq 162 aa AA seqDB search MLQTSNYSLVLSLQFLLLSYDLFVNSFSELLQKTPVIQLVLFIIQDIAVLFNIIIIFLMF FNTFVFQAGLVNLLFHKFKGTIILTAVYFALSISLHVWVMNLRWKNSNSFIWTDGLQMLF VFQRLAAVLYCYFYKRTAVRLGDPHFYQDSLWLRKEFMQVRR NT seq 489 nt NT seq  +upstreamnt  +downstreamnt atgctccagaccagtaactacagcctggtgctctctctgcagttcctgctgctgtcctat gacctctttgtcaattccttctcagaactgctccaaaagactcctgtcatccagcttgtg ctcttcatcatccaggatattgcagtcctcttcaacatcatcatcattttcctcatgttc ttcaacaccttcgtcttccaggctggcctggtcaacctcctattccataagttcaaaggg accatcatcctgacagctgtgtactttgccctcagcatctcccttcatgtctgggtcatg aacttacgctggaaaaactccaacagcttcatatggacagatggacttcaaatgctgttt gtattccagagactagcagcagtgttgtactgctacttctataaacggacagccgtaaga ctaggcgatcctcacttctaccaggactctttgtggctgcgcaaggagttcatgcaagtt cgaaggtga

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