Homo sapiens (human): 95681 Help Entry 95681             CDS       T01001                                  Symbol CEP41, JBTS15, TSGA14 Name (RefSeq) centrosomal protein 41   KO K16455   centrosomal protein CEP41 Organism hsa  Homo sapiens (human) Disease H00530   Joubert syndrome and related disorders Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09182 Protein families: genetic information processing    03036 Chromosome and associated proteins [BR:hsa03036]     95681 (CEP41)   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     95681 (CEP41) Chromosome and associated proteins [BR:hsa03036]  Eukaryotic type   Centrosome formation proteins    Centriole proteins     95681 (CEP41) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   Other primary cilia associated proteins    95681 (CEP41) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Rhodanese Motif Other DBs NCBI-GeneID:  95681 NCBI-ProteinID:  NP_061188 OMIM:  610523 HGNC:  12370 Ensembl:  ENSG00000106477 UniProt:  Q9BYV8 LinkDB All DBs Position 7:complement(130393771..130441741) Genome browser AA seq 373 aa AA seqDB search MSLRRHIGNPEYLMKRIPQNPRYQHIKSRLDTGNSMTKYTEKLEEIKKNYRYKKDELFKR LKVTTFAQLIIQVASLSDQTLEVTAEEIQRLEDNDSAASDPDAETTARTNGKGNPGEQSP SPEQFINNAGAGDSSRSTLQSVISGVGELDLDKGPVKKAEPHTKDKPYPDCPFLLLDVRD RDSYQQCHIVGAYSYPIATLSRTMNPYSNDILEYKNAHGKIIILYDDDERLASQAATTMC ERGFENLFMLSGGLKVLAQKFPEGLITGSLPASCQQALPPGSARKRSSPKGPPLPAENKW RFTPEDLKKIEYYLEEEQGPADHPSRLNQANSSGRESKVPGARSAQNLPGGGPASHSNPR SLSSGHLQGKPWK NT seq 1122 nt NT seq  +upstreamnt  +downstreamnt atgtccctccggaggcacattgggaaccctgagtatctgatgaaaaggataccacagaac ccaagataccagcatatcaaatcaagactggacactggtaacagtatgactaaatatact gagaagctcgaagagattaagaaaaattatagatacaaaaaagatgagcttttcaagaga ctaaaagttacaacttttgcccagctgatcatccaagttgcttccctctctgatcaaaca ctggaagtgacagctgaggagattcaaaggctggaagacaatgattctgcagcttcagac cctgatgctgaaaccactgccaggaccaatgggaaaggaaatccaggtgagcagtcgccg agccctgagcagttcataaacaacgcaggagcaggggactccagccgctcaactcttcag agtgtcatcagtggtgttggggaactggatctagacaaagggccagtgaagaaagcagag ccccataccaaagacaaaccttatcctgactgccccttcctgctgctagatgtgcgtgat agagattcttaccagcagtgccacattgttggagcttacagttacccaattgcaactctg tctagaacaatgaacccttattcaaatgatattcttgaatataaaaatgcccatggcaag atcatcattctgtatgacgatgatgaaaggctggccagtcaggcggccaccaccatgtgc gagcgtggatttgaaaacctcttcatgctttccggaggtctaaaagtcttagctcagaaa ttcccggaaggactgattactggttccctgccagcatcttgccagcaggcccttcctcct gggtctgcccggaaacgatccagccccaaagggccacccctaccagctgagaataaatgg agatttaccccagaagacttaaaaaagatagaatattatctggaagaggagcaagggcct gcagatcatcctagccgactgaaccaagctaactcctccggaagagagtccaaggtgcct ggtgcccgaagcgctcagaatctgccaggtggcggccccgccagccactcaaacccccgc tccctcagcagtggtcacctgcaaggcaaaccctggaagtaa

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