EFHD2

EFHD2
Identifiers
Aliases	EFHD2, SWS1, EF-hand domain family member D2
External IDs	OMIM: 616450; MGI: 106504; HomoloGene: 32580; GeneCards: EFHD2; OMA:EFHD2 - orthologs
Gene location (Human)
Chr.	Chromosome 1 (human)[1]
End	15,430,339 bp[1]
Gene location (Mouse)
Chr.	Chromosome 4 (mouse)[2]
End	141,602,231 bp[2]
RNA expression pattern
	Top expressed in
	monocyte; ; blood; ; pons; ; spleen; ; palpebral conjunctiva; ; sperm; ; Brodmann area 9; ; body of stomach; ; appendix; ; body of pancreas;
	Top expressed in
	Paneth cell; ; ciliary body; ; retinal pigment epithelium; ; iris; ; left colon; ; epithelium of stomach; ; conjunctival fornix; ; ileum; ; medial ganglionic eminence; ; semi-lunar valve;
	More reference expression data
	n/a
Gene ontology
Molecular function	metal ion binding; calcium ion binding; cadherin binding;
Cellular component	membrane; membrane raft;
Biological process	cell-cell adhesion;
	Sources:Amigo / QuickGO
Orthologs
	79180
	27984
	ENSG00000142634
	ENSMUSG00000040659
	Q96C19
	Q9D8Y0; Q8C845
	NM_024329
	NM_025994
	NP_077305
	NP_080270
	Wikidata
View/Edit Human	View/Edit Mouse

EF-hand domain family member D2 is a protein that in humans is encoded by the EFHD2 gene. [5]

References

GRCh38: Ensembl release 89: ENSG00000142634 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000040659 – Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Entrez Gene: EF-hand domain family member D2". Retrieved 2016-07-14.