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Protein Coding Gene : Fam111a family with sequence similarity 111, member A
Primary Identifier  MGI:1915508 Organism  mouse, laboratory
Chromosome  19 NCBI Gene Number  107373
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable single-stranded DNA binding activity. Predicted to be involved in DNA metabolic process; negative regulation of viral genome replication; and protein autoprocessing. Predicted to be located in chromatin; cytoplasm; and nuclear lumen. Predicted to be active in nucleus. Is expressed in alimentary system; brain ventricular layer; liver lobe; and orbito-sphenoid. Human ortholog(s) of this gene implicated in Kenny-Caffey syndrome type 2. Orthologous to human FAM111A (FAM111 trypsin like peptidase A).
PHENOTYPE: Mice homozygous for a null allele exhibit normal electrolyte homeostasis and bone phenotype. [provided by MGI curators]
  • synonyms:
  • MGI:2147729,
  • Fam111a,
  • expressed sequence AW413625,
  • family with sequence similarity 111, member A,
  • RIKEN cDNA 4632417K18 gene,
  • 4632417K18Rik,
  • AW413625
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