Gene id |
56606 |
Gene Summary Diseases PubMed |
Gene Summary
|
Gene Symbol |
SLC2A9 Gene UCSC Ensembl |
Aliases |
GLUT9, GLUTX, UAQTL2, URATv1 |
Gene name |
solute carrier family 2 member 9 |
Alternate names |
solute carrier family 2, facilitated glucose transporter member 9, GLUT-9, glucose transporter type 9, human glucose transporter-like protein-9, solute carrier family 2 (facilitated glucose transporter), member 9, urate transporter, urate voltage-driven efflux , |
Gene location |
4p16.1 (10040247: 9771124) Exons: 27 NC_000010.11
|
Gene summary(Entrez) |
This gene encodes a member of the SLC2A facilitative glucose transporter family. Members of this family play a significant role in maintaining glucose homeostasis. The encoded protein may play a role in the development and survival of chondrocytes in cart
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OMIM |
606142 |
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Associated diseases |
References |
Coronary heart disease | GAD: 18398472 |
Diabetes | GAD: 18487473 |
Alzheimer's disease | GAD: 22005930 |
Sperm maturation arrest | MIK: 22228739 |
Decreased spermatogenesis | MIK: 22228739 |
Hyperuricemia | GAD: 19833602 |
Renal hypouricemia | KEGG: H00948 |
Cryptorchidism | MIK: 28606200 |
Spermatogenic defects | MIK: 22228739 |
Teratozoospermia | MIK: 17327269 |
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PMID |
Condition |
Mutation |
Ethnicity |
Population details |
Infertility_type |
Associated_genes |
Abstract |
22228739 |
Decreased spermatoge nesis, spe rm maturat ion
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Male infertility |
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Show abstract |
17327269 |
Teratozoos permia
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13 (5 controls, 8 cases)
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Male infertility |
GSE6967 analyzed by GEO2R (cutoff 1.5 fold)
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Show abstract |
28606200 |
Cryptorchi dism
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Monozgotic twin s (1 control, I cwith cryptorc hidism)
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Male infertility |
MeDIP-Seq
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Show abstract |
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