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Gene id 6257
Gene Summary    Protein Summary    Gene ontology    KEGG pathways    Diseases    PubMed    

Gene Summary

Gene Symbol RXRB   Gene   UCSC   Ensembl
Aliases DAUDI6, H-2RIIBP, NR2B2, RCoR-1
Gene name retinoid X receptor beta
Alternate names retinoic acid receptor RXR-beta, MHC class I promoter binding protein, nuclear receptor subfamily 2 group B member 2,
Gene location 6p21.32 (33200990: 33193584)     Exons: 11     NC_000020.11
Gene summary(Entrez) This gene encodes a member of the retinoid X receptor (RXR) family of nuclear receptors which are involved in mediating the effects of retinoic acid (RA). The encoded protein forms homodimers with the retinoic acid, thyroid hormone, and vitamin D receptor
OMIM 180246

Protein Summary

Gene ontology

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GO accessionTerm nameEvidence codeGo category

KEGG pathways

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Pathway idPathway name
hsa04659Th17 cell differentiation
hsa04920Adipocytokine signaling pathway
hsa03320PPAR signaling pathway
hsa04919Thyroid hormone signaling pathway
hsa04928Parathyroid hormone synthesis, secretion and action
hsa05200Pathways in cancer
hsa05202Transcriptional misregulation in cancer
hsa05226Gastric cancer
hsa05216Thyroid cancer
hsa05222Small cell lung cancer
hsa05223Non-small cell lung cancer
hsa05200Pathways in cancer
hsa04928Parathyroid hormone synthesis, secretion and action
hsa05202Transcriptional misregulation in cancer
hsa04919Thyroid hormone signaling pathway
hsa05223Non-small cell lung cancer
hsa05226Gastric cancer
hsa04659Th17 cell differentiation
hsa04920Adipocytokine signaling pathway
hsa05222Small cell lung cancer
hsa03320PPAR signaling pathway
hsa05216Thyroid cancer
Associated diseases References
Cancer (lung) GAD: 19170196
Cancer (bladder) GAD: 19692168
Cancer (prostate) GAD: 19255064
Systemic lupus erythematosus (SLE) GAD: 19851445
Diabetes GAD: 17389020
Alzheimer's disease GAD: 19141999
Schizophrenia GAD: 11840500
Spontaneous abortion GAD: 20587610
Abnormal spermatogenesis MIK: 8557197
Chronic obstructive pulmonary disease (COPD) GAD: 19625176
Wegener granulomatosis GAD: 19223982
Aberrant CpGs in Low Motility Sperm MIK: 21674046
Abnormal spermatogenesis MIK: 8557197
Associated with spermatogenesis and epigenetic regulation MIK: 21674046
Unexplained infertility MIK: 25753583

PubMed references

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PMID Condition Mutation Ethnicity Population details Infertility_type Associated_genes Abstract
8557197 Abnormal s
permatogen
esis


Male infertility
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21674046 Aberrant C
pGs in Low
Motility
Sperm

18
Male infertility GSE26881
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25753583 Unexplaine
d infertil
ity

46 (17 fertile
men, 29 male pa
tients)
Male infertility Microarray
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