4933434E20Rik Gene Summary [Mouse]

Involved in phagocytosis. Acts upstream of or within in utero embryonic development. Predicted to be located in Golgi apparatus; cytosol; and mitochondrion. Orthologous to human C1orf43 (chromosome 1 open reading frame 43). [provided by Alliance of Genome Resources, Jul 2025]

Details

Type
Protein Coding
Official Symbol
4933434E20Rik
Official Name
RIKEN cDNA 4933434E20 gene [Source:MGI Symbol;Acc:MGI:1914027]
Ensembl ID
ENSMUSG00000027942
Bio databases IDs NCBI: 99650 Ensembl: ENSMUSG00000027942
Aliases RIKEN cDNA 4933434E20 gene
Synonyms 4933434E20Rik, 5730552F22Rik, AC163616.1, chromosome 1 open reading frame 43, HSPC012, NICE-3, NS5ATP4, NS5A transactivated protein 4, RIKEN cDNA 4933434E20 gene, S863-3
Species
Mouse, Mus musculus
OrthologiesHumanRat

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 mouse 4933434e20rik often fold into stable, three-dimensional structures and are associated with specific biological functions, such as binding to DNA, other proteins, or small molecules.
  • NICE-3 protein

Top Findings

The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
  • decreased circulating HDL cholesterol level
  • decreased circulating cholesterol level
  • decreased circulating fructosamine level
  • decreased circulating serum albumin level
  • decreased circulating triglyceride level
  • decreased total body fat amount
  • increased bone mineral content
  • increased bone mineral density
  • increased food intake
  • preweaning lethality complete penetrance
  • abnormal Mullerian duct morphology
  • abnormal Wolffian duct connection
  • abnormal aortic valve cusp morphology
  • abnormal atrioventricular cushion morphology
  • abnormal brain internal capsule morphology
  • abnormal cerebral cortex morphology
  • abnormal ductus venosus valve morphology
  • abnormal ductus venosus valve topology
  • abnormal dural venous sinus morphology
  • abnormal eye muscle morphology
  • abnormal forebrain morphology
  • abnormal heart atrium morphology
  • abnormal heart position or orientation
  • abnormal heart right atrium morphology
  • abnormal hindbrain morphology
  • abnormal hypoglossal nerve topology
  • abnormal inferior vena cava valve morphology
  • abnormal infrahyoid muscle connection
  • abnormal interatrial septum morphology
  • abnormal larynx morphology
  • abnormal lens morphology
  • abnormal pectinate muscle morphology
  • abnormal pineal gland morphology
  • abnormal pulmonary valve cusp morphology
  • abnormal vertebral arch morphology
  • abnormal vertebral artery topology
  • abnormal vertebral body morphology
  • abnormal vitelline vein connection
  • absent costovertebral joint
  • absent ductus venosus valve
  • absent hypoglossal canal
  • absent hypoglossal nerve
  • absent lobe of thyroid gland
  • absent segment of posterior cerebral artery
  • absent vertebral arch
  • anal atresia
  • arteriovenous malformation
  • blood in lymph vessels
  • dorsal root ganglion hypoplasia
  • double ureter
  • embryo cyst
  • enlarged liver sinusoidal spaces
  • enlarged lymphatic vessel
  • fused dorsal root ganglion
  • fusion of vertebral arches
  • herniated liver
  • heterochrony
  • intestinal/bowel diverticulum
  • muscular ventricular septal defect
  • overriding aortic valve
  • perimembraneous ventricular septal defect
  • persistent trigeminal artery
  • reduced sympathetic cervical ganglion size
  • retro-esophageal left subclavian artery
  • retroesophageal right subclavian artery
  • right aortic arch
  • small superior cervical ganglion
  • subcutaneous edema
  • thin hypoglossal nerve
  • urinary bladder hypoplasia
role in cell
  • phagocytosis 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.
  • Golgi Apparatus
  • Mitochondria
  • cytosol

Gene Ontology Annotations

Describes the biological processes, cellular components, and molecular functions associated with the mouse 4933434e20rik gene, providing context for its role in the cell.

Biological Process

Functions and activities the gene product is involved in
  • in utero embryonic development
  • phagocytosis

Cellular Component

Where in the cell the gene product is active
  • membrane
  • mitochondrion
  • cytosol
  • Golgi apparatus

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.