Homo sapiens (human): 84314 Help Entry 84314             CDS       T01001                                  Symbol TMEM107, GRVS638, JBTS29, MKS13, PRO1268 Name (RefSeq) transmembrane protein 107   KO K22764   transmembrane protein 107 Organism hsa  Homo sapiens (human) Disease H00261   Meckel syndrome H00454   Oral-facial-digital syndrome 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]     84314 (TMEM107) Cilium and associated proteins [BR:hsa03037]  Primary cilia and associated proteins   MKS complex    84314 (TMEM107) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  TMEM107 Motif Other DBs NCBI-GeneID:  84314 NCBI-ProteinID:  NP_898888 OMIM:  616183 HGNC:  28128 Ensembl:  ENSG00000179029 UniProt:  Q6UX40 LinkDB All DBs Position 17:complement(8172457..8176380) Genome browser AA seq 140 aa AA seqDB search MGRVSGLVPSRFLTLLAHLVVVITLFWSRDSNIQACLPLTFTPEEYDKQDIQLVAALSVT LGLFAVELAGFLSGVSMFNSTQSLISIGAHCSASVALSFFIFERWECTTYWYIFVFCSAL PAVTEMALFVTVFGLKKKPF NT seq 423 nt NT seq  +upstreamnt  +downstreamnt atgggccgggtctcagggcttgtgccctctcgcttcctgacgctcctggcgcatctggtg gtcgtcatcaccttattctggtcccgggacagcaacatacaggcctgcctgcctctcacg ttcacccccgaggagtatgacaagcaggacattcagctggtggccgcgctctctgtcacc ctgggcctctttgcagtggagctggccggtttcctctcaggagtctccatgttcaacagc acccagagcctcatctccattggggctcactgtagtgcatccgtggccctgtccttcttc atattcgagcgttgggagtgcactacgtattggtacatttttgtcttctgcagtgccctt ccagctgtcactgaaatggctttattcgtcaccgtctttgggctgaaaaagaaacccttc tga

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