HOXA9, homeobox A9, 3205

N. diseases: 147; N. variants: 6
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs11773804
rs11773804
Entrez Id: 3205;100534589;100874323
Gene Symbol: HOXA9;HOXA10-HOXA9;HOXA10-AS
HOXA9;HOXA10-HOXA9;HOXA10-AS
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2071243
rs2071243
Entrez Id: 3205;100534589;100874323
Gene Symbol: HOXA9;HOXA10-HOXA9;HOXA10-AS
HOXA9;HOXA10-HOXA9;HOXA10-AS
CUI: C1261502
Disease:
Finding of Mean Corpuscular Hemoglobin 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3801776
rs3801776
Entrez Id: 3205;100534589
Gene Symbol: HOXA9;HOXA10-HOXA9
HOXA9;HOXA10-HOXA9
CUI: C0009081
Disease:
Congenital clubfoot 		0.010 GeneticVariation BEFREE The present study suggests that the rs3801776 G>A polymorphism is associated with CTEV risk in Chinese children; however, this conclusion should be validated in larger studies. 31424148 2019
dbSNP: rs1381537616
rs1381537616
Entrez Id: 3205;3206;100534589
Gene Symbol: HOXA9;HOXA10;HOXA10-HOXA9
HOXA9;HOXA10;HOXA10-HOXA9
CUI: C0017636
Disease:
Glioblastoma 		0.010 GeneticVariation BEFREE Gene expression profiles of three glioma stem cell line samples, three normal astrocyte samples, three astrocyte overexpressing 4 iPSC-inducing and oncogenic factors (myc(T58A), OCT-4, p53DD, and H-Ras(G12V)) samples, three astrocyte overexpressing 7 iPSC-inducing and oncogenic factors (OCT4, H-Ras(G12V), myc(T58A), p53DD, cyclin D1, CDK4(RC24) and hTERT) samples and three glioblastoma cell line samples were downloaded from the ArrayExpress database (accession: E-MTAB-4771). 28952134 2017
dbSNP: rs1381537616
rs1381537616
Entrez Id: 3205;3206;100534589
Gene Symbol: HOXA9;HOXA10;HOXA10-HOXA9
HOXA9;HOXA10;HOXA10-HOXA9
CUI: C0280474
Disease:
Childhood Glioblastoma 		0.010 GeneticVariation BEFREE Gene expression profiles of three glioma stem cell line samples, three normal astrocyte samples, three astrocyte overexpressing 4 iPSC-inducing and oncogenic factors (myc(T58A), OCT-4, p53DD, and H-Ras(G12V)) samples, three astrocyte overexpressing 7 iPSC-inducing and oncogenic factors (OCT4, H-Ras(G12V), myc(T58A), p53DD, cyclin D1, CDK4(RC24) and hTERT) samples and three glioblastoma cell line samples were downloaded from the ArrayExpress database (accession: E-MTAB-4771). 28952134 2017
dbSNP: rs1381537616
rs1381537616
Entrez Id: 3205;3206;100534589
Gene Symbol: HOXA9;HOXA10;HOXA10-HOXA9
HOXA9;HOXA10;HOXA10-HOXA9
CUI: C0278878
Disease:
Adult Glioblastoma 		0.010 GeneticVariation BEFREE Gene expression profiles of three glioma stem cell line samples, three normal astrocyte samples, three astrocyte overexpressing 4 iPSC-inducing and oncogenic factors (myc(T58A), OCT-4, p53DD, and H-Ras(G12V)) samples, three astrocyte overexpressing 7 iPSC-inducing and oncogenic factors (OCT4, H-Ras(G12V), myc(T58A), p53DD, cyclin D1, CDK4(RC24) and hTERT) samples and three glioblastoma cell line samples were downloaded from the ArrayExpress database (accession: E-MTAB-4771). 28952134 2017
dbSNP: rs1381537616
rs1381537616
Entrez Id: 3205;3206;100534589
Gene Symbol: HOXA9;HOXA10;HOXA10-HOXA9
HOXA9;HOXA10;HOXA10-HOXA9
CUI: C1621958
Disease:
Glioblastoma Multiforme 		0.010 GeneticVariation BEFREE Gene expression profiles of three glioma stem cell line samples, three normal astrocyte samples, three astrocyte overexpressing 4 iPSC-inducing and oncogenic factors (myc(T58A), OCT-4, p53DD, and H-Ras(G12V)) samples, three astrocyte overexpressing 7 iPSC-inducing and oncogenic factors (OCT4, H-Ras(G12V), myc(T58A), p53DD, cyclin D1, CDK4(RC24) and hTERT) samples and three glioblastoma cell line samples were downloaded from the ArrayExpress database (accession: E-MTAB-4771). 28952134 2017
dbSNP: rs761581039
rs761581039
Entrez Id: 3205;3206;100534589
Gene Symbol: HOXA9;HOXA10;HOXA10-HOXA9
HOXA9;HOXA10;HOXA10-HOXA9
CUI: C0431664
Disease:
Unilateral Cryptorchidism 		0.010 GeneticVariation BEFREE And we found a mutation (N27K) in a boy with unilateral cryptorchidism. 27108669 2017
dbSNP: rs776428407
rs776428407
Entrez Id: 3205;3206;100534589
Gene Symbol: HOXA9;HOXA10;HOXA10-HOXA9
HOXA9;HOXA10;HOXA10-HOXA9
CUI: C0010417
Disease:
Cryptorchidism 		0.010 GeneticVariation BEFREE A novel V39G INSL3 mutation in a patient with cryptorchidism was identified; however, the functional analysis of the mutant peptide did not reveal compromised function. 19416188 2009