POMT2 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | POMT2 , LGMD2N, MDDGA2, MDDGB2, MDDGC2, protein O-mannosyltransferase 2, LGMDR14 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 607439; MGI: 2444430; HomoloGene: 5297; GeneCards: POMT2; OMA:POMT2 - orthologs | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Protein O-mannosyl-transferase 2 is an enzyme that in humans is encoded by the POMT2 gene. [5] [6] [7]
POMT2 encodes an integral membrane protein of the endoplasmic reticulum (ER) that shares significant sequence similarity with a family of protein O-mannosyltransferases of S. cerevisiae. For additional background information, see POMT1 (MIM 607423).[supplied by OMIM] [7]
Fukutin is a eukaryotic protein necessary for the maintenance of muscle integrity, cortical histogenesis, and normal ocular development. Mutations in the fukutin gene have been shown to result in Fukuyama congenital muscular dystrophy (FCMD) characterised by brain malformation - one of the most common autosomal-recessive disorders in Japan. In humans this protein is encoded by the FCMD gene, located on chromosome 9q31. Human fukutin exhibits a length of 461 amino acids and a predicted molecular mass of 53.7 kDa.
Protein O-linked-mannose beta-1,2-N-acetylglucosaminyltransferase 1 is an enzyme that in humans is encoded by the POMGNT1 gene.
Alpha-1,2-mannosyltransferase ALG9 is an enzyme that in humans is encoded by the ALG9 gene.
Protein O-mannosyl-transferase 1 is an enzyme that in humans is encoded by the POMT1 gene. It is a member of the dolichyl-phosphate-mannose-protein mannosyltransferases.
Bardet–Biedl syndrome 5 protein is a protein that in humans is encoded by the BBS5 gene.
Protein CLN8 is a protein that in humans is encoded by the CLN8 gene.
Visual system homeobox 1 is a protein that in humans is encoded by the VSX1 gene.
NUAK family SNF1-like kinase 2 also known as SNF1/AMP kinase-related kinase (SNARK) is an enzyme that in humans is encoded by the NUAK2 gene. Its deficiency in humans causes anencephaly, a severe form of anterior neural tube defect that curtails brain development.
Pogo transposable element with ZNF domain is a protein that in humans is encoded by the POGZ gene.
Choline transporter-like protein 4 is a protein that in humans is encoded by the SLC44A4 gene.
Conserved oligomeric Golgi complex subunit 4 is a protein that in humans is encoded by the COG4 gene.
39S ribosomal protein L15, mitochondrial is a protein that in humans is encoded by the MRPL15 gene.
Dolichyl-P-Man:Man(7)GlcNAc(2)-PP-dolichyl-alpha-1,6-mannosyltransferase is an enzyme that in humans is encoded by the ALG12 gene.
Glycosyltransferase-like protein LARGE1 is an enzyme that in humans is encoded by the LARGE gene.
Stress-associated endoplasmic reticulum protein 1 is a protein that in humans is encoded by the SERP1 gene.
Zinc finger protein 346 is a protein that in humans is encoded by the ZNF346 gene.
Chitobiosyldiphosphodolichol beta-mannosyltransferase is an enzyme that is encoded by ALG1 whose structure and function has been conserved from lower to higher organisms.
39S ribosomal protein L17, mitochondrial is a protein that in humans is encoded by the MRPL17 gene.
Sarcoglycan zeta also known as SGCZ is a protein which in humans is encoded by the SGCZ gene.
Dolichol phosphate-mannose biosynthesis regulatory protein is a protein that in humans is encoded by the DPM2 gene.