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Gene id 23788
Gene Summary    Diseases    PubMed    

Gene Summary

Gene Symbol MTCH2   Gene   UCSC   Ensembl
Aliases HSPC032, MIMP, SLC25A50
Gene name mitochondrial carrier 2
Alternate names mitochondrial carrier homolog 2, 2310034D24Rik, met-induced mitochondrial protein, solute carrier family 25, member 50,
Gene location 11p11.2 (47642653: 47604308)     Exons: 14     NC_000011.10
Gene summary(Entrez) This gene encodes a member of the SLC25 family of nuclear-encoded transporters that are localized in the inner mitochondrial membrane. Members of this superfamily are involved in many metabolic pathways and cell functions. Genome-wide association studies
OMIM 613221
Associated diseases References
Obesity GAD: 19910938
Diabetes GAD: 19164386
Diabetes GAD: 19910641
Anorexia nervosa GAD: 19746409
Polycystic ovary syndrome (PCOS) INFBASE: 24498077
Associated with apoptosis of spermatocytes MIK: 25813787
Male infertility MIK: 25813787
Hypospermatogenesis MIK: 28361989
Spermatogenic defects MIK: 31037746
Teratozoospermia MIK: 17327269

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
25813787 Associated
with apop
tosis of s
permatocyt
es, Male i
nfertility


Male infertility
Show abstract
17327269 Teratozoos
permia

19 (6 controls
, 13 cases)
Male infertility GSE6872 analyzed by GEO2R (cutoff 1.5 fold)
Show abstract
28361989 Hyposperma
togenesis

6 (3 controls,
3 Klienfelter s
yndrome
Male infertility Microarray
Show abstract
31037746 Spermatoge
nic defect
s

28 men with az
oospermia
Male infertility Microarray
Show abstract