VCF2

VCF2
Identifiers
Aliases	VCF2, CXorf44, family with sequence similarity 104 member B, FAM104B, VCP nuclear cofactor family member 2
External IDs	GeneCards: VCF2
Gene location (Human)
Chr.	X chromosome (human)
End	55,161,310 bp
RNA expression pattern
	Top expressed in
	right uterine tube; ; olfactory zone of nasal mucosa; ; C1 segment; ; testicle; ; muscle of thigh; ; islet of Langerhans; ; ganglionic eminence; ; hypothalamus; ; cingulate gyrus; ; anterior cingulate cortex;
	n/a
	More reference expression data
	n/a
Orthologs
Databases	NCBI: entry; OMA: entry
	90736
	n/a
	ENSG00000182518
	n/a
	Q5XKR9
	n/a
NM_001166699; NM_001166700; NM_001166701; NM_001166702; NM_001166703;
	NM_001166704; NM_138362
	n/a
NP_001160171; NP_001160172; NP_001160173; NP_001160174; NP_001160175;
	NP_001160176; NP_612371
	n/a
	Wikidata
View/Edit Human

VCP nuclear cofactor family member 2 is a protein that in humans is encoded by the VCF2 gene (previously FAM104B).^[3] Not much has been reported about this protein's function, but it has a paralog: VCF1.^[4]

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000182518 – Ensembl, May 2017
↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
↑ "Entrez Gene: Family with sequence similarity 104 member B". Retrieved 2017-06-07.
↑ "Q5XKR9 · VCF2_HUMAN". uniprot.org. UniProt consortium. Retrieved 2026-08-17.

This article on a gene on the human X chromosome and/or its associated protein is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000182518 – Ensembl, May 2017

[2] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-3] "Entrez Gene: Family with sequence similarity 104 member B". Retrieved 2017-06-07.

[4] "Q5XKR9 · VCF2_HUMAN". uniprot.org. UniProt consortium. Retrieved 2026-08-17.

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References