KRTCAP3 Gene Summary [Human]

Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

Details

Type
Protein Coding
Official Symbol
KRTCAP3
Official Name
keratinocyte associated protein 3 [Source:HGNC Symbol;Acc:HGNC:28943]
Ensembl ID
ENSG00000157992
Bio databases IDs NCBI: 200634 Ensembl: ENSG00000157992
Aliases keratinocyte associated protein 3
Synonyms 2010001C09Rik, KCP3, keratinocyte associated protein 3
Species
Human, Homo sapiens
OrthologiesMouseRat

Protein Domains

A protein domain is a distinct structural or functional region within a protein that can evolve, function, and exist independently of the rest of the protein chain. These domains in human KRTCAP3 often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • protein binding
  • Beta-casein like protein

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
disease
  • short-rib thoracic dysplasia type 10
  • Bardet-Biedl syndrome type 20
  • retinitis pigmentosa
  • retinitis pigmentosa type 71
  • retinal dystrophy

Subcellular Expression

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

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the human KRTCAP3 gene, providing context for its role in the cell.

Cellular Component

Where in the cell the gene product is active
  • membrane

Molecular Function

What the gene product does at the molecular level
  • protein binding

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.