MEI1

MEI1
Identifiers
Aliases	MEI1, SPATA38, meiotic double-stranded break formation protein 1, HYDM3
External IDs	OMIM: 608797; MGI: 3028590; HomoloGene: 46535; GeneCards: MEI1; OMA:MEI1 - orthologs
Gene location (Human)
Chr.	Chromosome 22 (human)
End	41,799,456 bp
Gene location (Mouse)
Chr.	Chromosome 15 (mouse)
End	82,011,015 bp
RNA expression pattern
	Top expressed in
	bone marrow cells; ; right testis; ; granulocyte; ; left testis; ; spleen; ; appendix; ; testicle; ; blood; ; lymph node; ; gonad;
	Top expressed in
	lumbar spinal ganglion; ; otolith organ; ; utricle; ; embryo; ; morula; ; gastrula; ; spermatid; ; superior frontal gyrus; ; primary visual cortex; ; seminiferous tubule;
	More reference expression data
	n/a
Orthologs
	150365
	74369
	ENSG00000167077
	ENSMUSG00000068117
	Q5TIA1; Q4G0I1
	Q9D4I2
	NM_152513
	NM_028897; NM_001310435
	NP_689726; NP_689726.3
	NP_001297364; NP_083173
	Wikidata
View/Edit Human	View/Edit Mouse

Meiotic double-stranded break formation protein 1 is a protein that in humans is encoded by the MEI1 gene. ^[5]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000167077 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000068117 – 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: Meiotic double-stranded break formation protein 1". Retrieved 2017-03-25.

Sato H, Miyamoto T, Yogev L, Namiki M, Koh E, Hayashi H, Sasaki Y, Ishikawa M, Lamb DJ, Matsumoto N, Birk OS, Niikawa N, Sengoku K (2006). "Polymorphic alleles of the human MEI1 gene are associated with human azoospermia by meiotic arrest". J. Hum. Genet. 51 (6): 533–40. doi:10.1007/s10038-006-0394-5. PMID 16683055.

This article on a gene on human chromosome 22 is a stub. You can help Wikipedia by expanding it.