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: 4762
MIM: 601726
HGNC: 7764
Ensembl: ENSG00000181965
Variants:
dbSNP: 4762
ClinVar: 4762
TCGA: ENSG00000181965
COSMIC: NEUROG1
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000181965 | ENST00000314744 | Q92886 |
| ENSG00000181965 | ENST00000314744 | F1T0H3 |
Expression (GTEx)
Pathways
| Pathway | Source | External ID |
|---|---|---|
| Signaling pathways regulating pluripotency of stem cells | KEGG | hsa04550 |
| Signaling pathways regulating pluripotency of stem cells | KEGG | ko04550 |
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 33439489 | 2021 | Adding evidence to the role of NEUROG1 in congenital cranial dysinnervation disorders. | 2 |
| 33439489 | 2021 | Adding evidence to the role of NEUROG1 in congenital cranial dysinnervation disorders. | 2 |
| 26634621 | 2016 | The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformation. | 2 |
| 27423984 | 2016 | Induction of neuronal-like phenotype in human mesenchymal stem cells by overexpression of Neurogenin1 and treatment with neurotrophins. | 7 |
| 26634621 | 2016 | The role of transcription factors of neurosensory cells in non-syndromic sensorineural hearing loss with or without inner ear malformation. | 2 |
| 27423984 | 2016 | Induction of neuronal-like phenotype in human mesenchymal stem cells by overexpression of Neurogenin1 and treatment with neurotrophins. | 7 |
| 25403753 | 2014 | Rapid neurogenesis through transcriptional activation in human stem cells. | 128 |
| 25403753 | 2014 | Rapid neurogenesis through transcriptional activation in human stem cells. | 128 |
| 23034738 | 2013 | Methylation and microsatellite status and recurrence following adjuvant FOLFOX in colorectal cancer. | 26 |
| 23419067 | 2013 | A boy with homozygous microdeletion of NEUROG1 presents with a congenital cranial dysinnervation disorder [Moebius syndrome variant]. | 7 |
| 23034738 | 2013 | Methylation and microsatellite status and recurrence following adjuvant FOLFOX in colorectal cancer. | 26 |
| 23419067 | 2013 | A boy with homozygous microdeletion of NEUROG1 presents with a congenital cranial dysinnervation disorder [Moebius syndrome variant]. | 7 |
| 21326223 | 2011 | Methylation of NEUROG1 in serum is a sensitive marker for the detection of early colorectal cancer. | 59 |
| 21326223 | 2011 | Methylation of NEUROG1 in serum is a sensitive marker for the detection of early colorectal cancer. | 59 |
| 19813087 | 2010 | Stable expression of neurogenin 1 induces LGR5, a novel stem cell marker, in an immortalized human neural stem cell line HB1.F3. | 7 |
Citation
Dessen P
NEUROG1 (neurogenin 1)
Atlas Genet Cytogenet Oncol Haematol. 2011-08-01
Online version: http://atlasgeneticsoncology.org/gene/52332/neurog1
