Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 84667
MIM: 608059
HGNC: 15977
Ensembl: ENSG00000179111
Variants:
dbSNP: 84667
ClinVar: 84667
TCGA: ENSG00000179111
COSMIC: HES7
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000179111 | ENST00000317814 | Q9BYE0 |
| ENSG00000179111 | ENST00000541682 | Q9BYE0 |
| ENSG00000179111 | ENST00000577735 | J3KSH6 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 32943519 | 2020 | Species-specific segmentation clock periods are due to differential biochemical reaction speeds. | 92 |
| 32943519 | 2020 | Species-specific segmentation clock periods are due to differential biochemical reaction speeds. | 92 |
| 25928698 | 2015 | Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. | 11 |
| 25928698 | 2015 | Whole exome sequencing in an Indian family links Coats plus syndrome and dextrocardia with a homozygous novel CTC1 and a rare HES7 variation. | 11 |
| 23897666 | 2013 | Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus. | 13 |
| 23897666 | 2013 | Mutation of HES7 in a large extended family with spondylocostal dysostosis and dextrocardia with situs inversus. | 13 |
| 22744456 | 2012 | Mutation analysis of MESP2, HES7 and DUSP6 gene exons in patients with congenital scoliosis. | 1 |
| 22744456 | 2012 | Mutation analysis of MESP2, HES7 and DUSP6 gene exons in patients with congenital scoliosis. | 1 |
| 20087400 | 2010 | Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis. | 33 |
| 20406964 | 2010 | Risk of meningioma and common variation in genes related to innate immunity. | 21 |
| 20438785 | 2010 | Polymorphisms in innate immunity genes and risk of childhood leukemia. | 12 |
| 20628086 | 2010 | Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study. | 15 |
| 20087400 | 2010 | Two novel missense mutations in HAIRY-AND-ENHANCER-OF-SPLIT-7 in a family with spondylocostal dysostosis. | 33 |
| 20406964 | 2010 | Risk of meningioma and common variation in genes related to innate immunity. | 21 |
| 20438785 | 2010 | Polymorphisms in innate immunity genes and risk of childhood leukemia. | 12 |
Citation
Dessen P
HES7 (hes family bHLH transcription factor 7)
Atlas Genet Cytogenet Oncol Haematol. 2007-04-01
Online version: http://atlasgeneticsoncology.org/gene/47219/hes7
