Fam172a - family with sequence similarity 172, member A Gene

Also Known as 53-E6; pEN87; 1110033M05Rik; 2610318O14Rik; 9430037D06Rik

Species: Mus musculus

Gene Type: protein coding
Gene ID: 68675

Summary

Predicted to contribute to siRNA binding activity. Involved in neural crest cell development and regulation of alternative mRNA splicing, via spliceosome. Located in endoplasmic reticulum and nucleus. Is expressed in telencephalon ventricular layer. Orthologous to human FAM172A (family with sequence similarity 172 member A). [provided by Alliance of Genome Resources, Apr 2022]

Fam172a Products (3)

mRNA Protein Name
NM_001163419.1 NP_001156891.1 cotranscriptional regulator FAM172A isoform 2
NM_001163420.1 NP_001156892.1 cotranscriptional regulator FAM172A isoform 3
NM_138312.1 NP_612185.1 cotranscriptional regulator FAM172A isoform 1 precursor

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
29311329 MGI
Biological Process GO Annotation Evidence References Source
involved in neural crest cell development IMP
IMP: Inferred from mutant phenotype
29311329 MGI
involved in regulation of alternative mRNA splicing, via spliceosome IDA
IDA: Inferred from direct assay
29311329 MGI
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
29311329 MGI
located in endoplasmic reticulum IDA
IDA: Inferred from direct assay
29311329 MGI
located in nucleus IDA
IDA: Inferred from direct assay
29311329 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

cotranscriptional regulator FAM172A

  • protein FAM172A

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS04696 FAM172A Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Fam172a NCBI NCBI:83989