• Gene id: 934

Gene Summary

• Gene Symbol: CD24   Gene   UCSC   Ensembl
• Aliases: CD24A
• Gene name: CD24 molecule
• Alternate names: CD24 antigen (small cell lung carcinoma cluster 4 antigen),
• Gene location: 6q21 (19614092: 19611913)     Exons: 1     NC_000024.8
• Gene summary(Entrez): This gene encodes a sialoglycoprotein that is expressed on mature granulocytes and in many B cells. The encoded protein is anchored via a glycosyl phosphatidylinositol (GPI) link to the cell surface. An alignment of this gene's sequence finds genomic loca

SNPs

rs875989885

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000010.11   g.133555706G>A
NC_000010.10   g.135369210G>A
NG_052008.1   g.17570C>T
NM_130784.3   c.613C>T
NM_130784.2   c.613C>T
NM_001143764.2   c.721C>T
NM_001143764.3   c.721C>T
NM_001143764.1   c.721C>T
NM_001143763.1   c.721C>T
NP_570140.1   p.Gln205Ter
NP_001137  

rs774225566

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000010.11   g.133558953T>C
NC_000010.10   g.135372457T>C
NG_052008.1   g.14323A>G|SEQ=[T/C]|GENE=SYCE1

rs1422627

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000019.10   g.45913480C>G
NC_000019.10   g.45913480C>T
NC_000019.9   g.46416738C>G
NC_000019.9   g.46416738C>T
NM_001029861.2   c.*797G>C
NM_001029861.2   c.*797G>A
NM_001029861.3   c.*797G>C
NM_001029861.3   c.*797G>A|SEQ=[C/G/T]|GENE=NANOS2

rs9304651

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000019.10   g.45916515A>G
NC_000019.9   g.46419773A>G|SEQ=[A/G]|GENE=NANOS2

rs2015728

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000019.10   g.45915628G>A
NC_000019.10   g.45915628G>T
NC_000019.9   g.46418886G>A
NC_000019.9   g.46418886G>T|SEQ=[G/A/T]|GENE=NANOS2

rs4506565

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000010.11   g.112996282A>G
NC_000010.11   g.112996282A>T
NC_000010.10   g.114756041A>G
NC_000010.10   g.114756041A>T
NG_012631.1   g.51033A>G
NG_012631.1   g.51033A>T|SEQ=[A/G/T]|GENE=TCF7L2

rs7903146

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000010.11   g.112998590C>G
NC_000010.11   g.112998590C>T
NC_000010.10   g.114758349C>G
NC_000010.10   g.114758349C>T
NG_012631.1   g.53341C>G
NG_012631.1   g.53341C>T
NG_054085.1   g.746C>G
NG_054085.1   g.746C>T|SEQ=[C/G/T]|GENE=TCF7L2

rs12243326

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000010.11   g.113029056T>C
NC_000010.10   g.114788815T>C
NG_012631.1   g.83807T>C|SEQ=[T/C]|GENE=TCF7L2

rs12255372

Strand:    Allele origin:   Allele change:   Mutation type: snv

NC_000010.11   g.113049143G>A
NC_000010.11   g.113049143G>T
NC_000010.10   g.114808902G>A
NC_000010.10   g.114808902G>T
NG_012631.1   g.103894G>A
NG_012631.1   g.103894G>T|SEQ=[G/A/T]|GENE=TCF7L2

Protein Summary

Gene ontology

GO accession	Term name	Evidence code	Go category

Diseases

Associated diseases	References
Multiple sclerosis	PMID:14657362
Spermatogenic defects	MIK: 31037746

PubMed references

PMID	Condition	Mutation	Ethnicity	Population details	Infertility_type	Associated_genes
31037746	Spermatogenic defects			16 (1 control, 15 cases)	Male infertility	GSE6023 analyzed using GEO2R