ITFG3

FAM234A
Identifiers
AliasesFAM234A, C16orf9, gs19, ITFG3, family with sequence similarity 234 member A
External IDsMGI: 2146854; HomoloGene: 12932; GeneCards: FAM234A; OMA:FAM234A - orthologs
Orthologs
SpeciesHumanMouse
Entrez

83986

106581

Ensembl

ENSG00000167930

ENSMUSG00000024187

UniProt

Q9H0X4

Q8C0Z1

RefSeq (mRNA)

NM_001284497
NM_032039

NM_001206335
NM_207217
NM_001357894
NM_001374603

RefSeq (protein)

NP_001271426
NP_114428

NP_001193264
NP_997100
NP_001344823

Location (UCSC)Chr 16: 0.23 – 0.27 MbChr 17: 26.21 – 26.24 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Protein ITFG3 also known as family with sequence similarity 234 member A (FAM234A) is a protein that in humans is encoded by the ITFG3 gene. Here, the gene is explored as encoded by mRNA found in Homo sapiens. The FAM234A gene is conserved in mice, rats, chickens, zebrafish, dogs, cows, frogs, chimpanzees, and rhesus monkeys. Orthologs of the gene can be found in at least 220 organisms including the tropical clawed frog, pandas, and Chinese hamsters. The gene is located at 16p13.3 and has a total of 19 exons. The mRNA has a total of 3224 bp and the protein has 552 aa. The molecular mass of the protein produced by this gene is 59660 Da. It is expressed in at least 27 tissue types in humans, with the greatest presence in the duodenum, fat, small intestine, and heart.

A “Newfoundland deletion” or a0-thalassemia deletion has been found within the second intervening sequence of the FAM234A gene. The gene is associated with multiple red blood cell phenotypes in African Americans – though the exact function or effect of the gene was not entirely clear. Review of GeneCards’ current database on the FAM234A gene provided no additional elucidation on the function of the gene.