Homo sapiens (human): 51259 Help Entry 51259             CDS       T01001                                  Symbol TMEM216, HSPC244, RP98, CORS2, MKS2 Name (RefSeq) transmembrane protein 216   KO K19385   transmembrane protein 216 Organism hsa  Homo sapiens (human) Disease H00261   Meckel syndrome H00527   Retinitis pigmentosa 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]     51259 (TMEM216) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   MKS complex    51259 (TMEM216) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Transmemb_17 Motif Other DBs NCBI-GeneID:  51259 NCBI-ProteinID:  NP_001167461 OMIM:  613277 HGNC:  25018 Ensembl:  ENSG00000187049 UniProt:  Q9P0N5 LinkDB All DBs Position 11:61392587..61398846 Genome browser AA seq 145 aa AA seqDB search MLPRGLKMAPRGKRLSSTPLEILFFLNGWYNATYFLLELFIFLYKGVLLPYPTANLVLDV VMLLLYLGIEVIRLFFGTKGNLCQRKMPLSISVALTFPSAMMASYYLLLQTYVLRLEAIM NGILLFFCGSELLLEVLTLAAFSRI NT seq 438 nt NT seq  +upstreamnt  +downstreamnt atgctgccacggggactgaagatggcgccgcgaggtaaacggttgtcctccaccccgctg gaaatcctgttctttctgaacgggtggtataatgctacctatttcctgctggaacttttc atatttctgtataaaggtgtcctgctaccatatccaacagctaacctagtactggatgtg gtgatgctcctcctttatcttggaattgaagtaattcgcctgttttttggtacaaaggga aacctctgccagcgaaagatgccgctcagtattagcgtggccttgaccttcccatctgcc atgatggcctcctattacctgctgctgcagacctacgtactccgcctggaagccatcatg aatggcatcttgctcttcttctgtggctcagagcttttacttgaggtgctcaccttggct gctttctccaggatttga

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