| Entrez gene ID | | 91147 |
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| Official gene symbol | | TMEM67 |
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| Full name | | transmembrane protein 67 |
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| Aliases | | ,JBTS6,MECKELIN,MGC26979,MKS3,TNEM67, |
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| Gene summary | | The protein encoded by this gene localizes to the primary cilium and to the plasma membrane. The gene functions in centriole migration to the apical membrane and formation of the primary cilium. Multiple transcript variants encoding different isoforms have been found for this gene. Defects in this gene are a cause of Meckel syndrome type 3 (MKS3) and Joubert syndrome type 6 (JBTS6). [provided by RefSeq] |
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| Location | | Chromosome: 8 Locus: 8q22.1 |
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| Gene position | | 94767072 - 94831462 Map Viewer |
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| Gene orientation | | plus |
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| Gene size | | 64391 bp |
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| Gene sequence |
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| OMIM ID | | 609884 |
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