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Pathways
Genes search result for Homo sapiens
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3 records found for search term Tmco1
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RGD IDSymbolNameDescriptionChrStartStopSpeciesAnnotationsMatchType
1601866TMCO1transmembrane and coiled-coil domains 1This locus encodes a transmembrane protein. Mutations at this locus have been associated with craniofacial dysmorphism, skeletal anomalies, and cognitive disability. Mutations at this locus have also been associated with open angle glaucoma blindness. Alternatively spliced transcript variants have b1165724291165768922Human208symbol , old_gene_name , COSMIC , Human Proteome Mapgene, protein-coding, REVIEWED [RefSeq]
13793130TMCO1-AS1TMCO1 antisense RNA 11165768929165775449Humansymbol , COSMIC , name , Human Proteome Mapgene, ncrna, VALIDATED [RefSeq]
1317125RAB5IFRAB5 interacting factorInvolved in mitochondrial respirasome assembly and multi-pass transmembrane protein insertion into ER membrane. Located in mitochondrion. Part of multi-pass translocon complex. Implicated in craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 2. [provided by 203660577936612557Human76old_gene_namegene, protein-coding, VALIDATED [RefSeq]