Homo sapiens (human): 7401 Help Entry 7401              CDS       T01001                                  Symbol CLRN1, RP61, USH3, USH3A Name (RefSeq) clarin 1   KO K23841   clarin Organism hsa  Homo sapiens (human) Disease H00527   Retinitis pigmentosa H00779   Usher syndrome Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09183 Protein families: signaling and cellular processes    03037 Cilium and associated proteins [BR:hsa03037]     7401 (CLRN1) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   USH complex and associated proteins    7401 (CLRN1) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  PsbN MORN Motif Other DBs NCBI-GeneID:  7401 NCBI-ProteinID:  NP_777367 OMIM:  606397 HGNC:  12605 Ensembl:  ENSG00000163646 UniProt:  P58418 LinkDB All DBs Position 3:complement(150926163..150972999) Genome browser AA seq 232 aa AA seqDB search MPSQQKKIIFCMAGVFSFACALGVVTALGTPLWIKATVLCKTGALLVNASGQELDKFMGE MQYGLFHGEGVRQCGLGARPFRFSFFPDLLKAIPVSIHVNVILFSAILIVLTMVGTAFFM YNAFGKPFETLHGPLGLYLLSFISGSCGCLVMILFASEVKIHHLSEKIANYKEGTYVYKT QSEKYTTSFWVIFFCFFVHFLNGLLIRLAGFQFPFAKSKDAETTNVAADLMY NT seq 699 nt NT seq  +upstreamnt  +downstreamnt atgccaagccaacagaagaaaatcattttttgcatggccggagtgttcagttttgcatgt gccctcggagttgtgacagccttggggacaccgttgtggatcaaagccactgtcctctgc aaaacgggagctctgctcgtcaatgcctcagggcaggagctggacaagtttatgggtgaa atgcagtacgggcttttccacggagagggtgtgaggcagtgtgggttgggagcaaggccc tttcggttctcattttttccagatttgctcaaagcaatcccagtgagcatccacgtcaat gtcattctcttctctgccatccttattgtgttaaccatggtggggacagccttcttcatg tacaatgcttttggaaaaccttttgaaactctgcatggtcccctagggctgtaccttttg agcttcatttcaggctcctgtggctgtcttgtcatgatattgtttgcctctgaagtgaaa atccatcacctctcagaaaaaattgcaaattataaagaagggacttatgtctacaaaacg caaagtgaaaaatataccacctcattctgggtcattttcttttgcttttttgttcatttt ctgaatgggctcctaatacgacttgctggatttcagttcccttttgcaaaatctaaagac gcagaaacaactaatgtagctgcagatctaatgtactga

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