FAM162A - family with sequence similarity 162 member A Gene

Homo sapiens

Also known as E2IG5; HGTD-P; C3orf28

Gene ID: 26355 | Gene type: protein coding

About FAM162A

Cytogenetic location: 3q21.1 Genomic coordinates (GRCh38): 3:122,384,182-122,412,334 (from NCBI)

This gene has 14 transcripts (splice variants), 131 orthologues and 1 paralogue. Ubiquitous expression in colon (RPKM 86.7), esophagus (RPKM 60.9) and 25 other tissues.

Summary

Involved in several processes, including activation of cysteine-type endopeptidase activity involved in apoptotic process; cellular response to hypoxia; and positive regulation of release of cytochrome c from mitochondria. Located in cytosol and mitochondrion. [provided by Alliance of Genome Resources, Apr 2022]

FAM162A Products(1)

mRNA	Protein	Name
NM_014367.4	NP_055182.3	protein FAM162A

FAM162A Protein Structure

DUF1075

0
100
154 a.a.

Protein Preferred Names

Protein Names

protein FAM162A

E2-induced gene 5 protein

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS04689	FAM162A Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	FAM162A	MGD	MGI:1917436
Macaca mulatta	FAM162A	VGNC	VGNC:72291
Canis familiaris	FAM162A	VGNC	VGNC:40612
Rattus norvegicus	FAM162A	RGD	RGD:1590883
Felis catus	FAM162A	VGNC	VGNC:102695
Bos taurus	FAM162A	VGNC	VGNC:28744

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