CMAHP Gene Summary [Human]

Sialic acids are terminal components of the carbohydrate chains of glycoconjugates involved in ligand-receptor, cell-cell, and cell-pathogen interactions. The two most common forms of sialic acid found in mammalian cells are N-acetylneuraminic acid (Neu5Ac) and its hydroxylated derivative, N-glycolylneuraminic acid (Neu5Gc). Studies of sialic acid distribution show that Neu5Gc is not detectable in normal human tissues although it was an abundant sialic acid in other mammals. Neu5Gc is, in actuality, immunogenic in humans. The absense of Neu5Gc in humans is due to a deletion within the human gene CMAH encoding cytidine monophosphate-N-acetylneuraminic acid hydroxylase, an enzyme responsible for Neu5Gc biosynthesis. Sequences encoding the mouse, pig, and chimpanzee hydroxylase enzymes were obtained by cDNA cloning and found to be highly homologous. However, the homologous human cDNA differs from these cDNAs by a 92-bp deletion in the 5' region. This deletion, corresponding to exon 6 of the mouse hydroxylase gene, causes a frameshift mutation and premature termination of the polypeptide chain in human. It seems unlikely that the truncated human hydroxylase mRNA encodes for an active enzyme explaining why Neu5Gc is undetectable in normal human tissues. Human genomic DNA also shows evidence of this deletion which does not occur in the genomes of African great apes. Nonetheless, the CMAH gene maps to 6p21.32 in humans and great apes indicating that mutation of the CMAH gene occurred following human divergence from chimpanzees and bonobos. [provided by RefSeq, Jul 2008]

Details

Type
Processed Transcript
Official Symbol
CMAHP
Official Name
cytidine monophospho-N-acetylneuraminic acid hydroxylase, pseudogene [Source:HGNC Symbol;Acc:HGNC:2098]
Ensembl ID
ENSG00000168405
Bio databases IDs NCBI: 8418 Ensembl: ENSG00000168405
Aliases cytidine monophospho-N-acetylneuraminic acid hydroxylase, pseudogene
Synonyms CMAH, CMP-NeuAc Hydroxylase-Like, CSAH, cytidine monophospho-N-acetylneuraminic acid hydroxylase, pseudogene, ENSG00000293489
Species
Human, Homo sapiens

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • COVID-19
  • psoriasis
  • schizophrenia
  • systemic lupus erythematosus
  • inflammatory bowel disease
  • thrombocytopenia
  • insulin-dependent diabetes mellitus
  • angina pectoris
  • gastric cancer
regulates
role in cell
  • migration
  • invasion by
  • tubulation by

Subcellular Expression

Locations within the cell where the protein is known or predicted to be active, providing insight into its function and cellular context.
  • Cytoplasm
  • cytoskeleton
  • cellular membrane
  • Nucleus

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human CMAHP gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • CMP-N-acetylneuraminate metabolic process
  • regulation of Wnt receptor signaling pathway

Cellular Component

Where in the cell the gene product is active
  • nucleus
  • cytoskeleton
  • cytoplasm
  • membrane

Molecular Function

What the gene product does at the molecular level
  • CMP-N-acetylneuraminate monooxygenase activity

Gene-Specific Assays for Results You Can Trust

Streamline your workflow with assays designed for this gene. Our targeted dPCR and qPCR assays help you generate meaningful data – efficiently and accurately.