PIGH

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Phosphatidylinositol N-acetylglucosaminyltransferase subunit H is an enzyme that in humans is encoded by the PIGH gene.[5][6] The PIGH gene is located on the reverse strand of chromosome 14 in humans, and is neighbored by TMEM229B.[7]

AliasesPIGH, GPI-H, phosphatidylinositol glycan anchor biosynthesis class H
End67,600,286 bp[1]
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PIGH
Identifiers
AliasesPIGH, GPI-H, phosphatidylinositol glycan anchor biosynthesis class H
External IDsOMIM: 600154; MGI: 99463; HomoloGene: 3361; GeneCards: PIGH; OMA:PIGH - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004569
NM_001363694

NM_029988

RefSeq (protein)

NP_004560
NP_001350623

NP_084264

Location (UCSC)Chr 14: 67.58 – 67.6 MbChr 12: 79.13 – 79.14 Mb
PubMed search[3][4]
Wikidata
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This gene encodes an endoplasmic reticulum associated protein that is involved in glycosylphosphatidylinositol (GPI)-anchor biosynthesis. The GPI anchor is a glycolipid found on many blood cells and which serves to anchor proteins to the cell surface. The protein encoded by this gene is a subunit of the GPI N-acetylglucosaminyl (GlcNAc) transferase that transfers GlcNAc to phosphatidylinositol (PI) on the cytoplasmic side of the endoplasmic reticulum.[6]

Interactions

PIGH has been shown to interact with PIGQ.[8]

References

Further reading

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