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TMEM107

transmembrane protein 107
2 disorders 1 causative 1 no genetic record 17p13.1 gene with protein product
HGNC:28128MonarchNCBI Gene 84314ENSG00000179029UniProt Q6UX40OMIM 616183

Aliases: MGC10744, JBTS29, MKS13.

In the knowledge base · computed from kb/ at build time

Disorders

Relationship is the entry's genetic[].relationship_type. untyped means the entry has a genetic record for the gene but does not type it; its free-text association is shown instead.

DisorderRelationshipWhere the gene appears
Meckel Syndrome causative germline
mechanism: Basal body localization without proper ciliogenesis
subtype: Meckel syndrome 13
Orofaciodigital Syndrome no genetic record
mechanism: Ciliary and Centriolar Gene Defect
subtype: OFD 16
Mechanism modules · computed from kb/

Identity from HGNC (snapshot 2026-10-01). Page layers are described in the gene pages documentation.