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: 100131390
HGNC: 30690
Ensembl: ENSG00000217236
Variants:
dbSNP: 100131390
ClinVar: 100131390
TCGA: ENSG00000217236
COSMIC: SP9
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000217236 | ENST00000394967 | P0CG40 |
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 38288683 | 2024 | De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity. | 0 |
| 38288683 | 2024 | De novo variants in SP9 cause a novel form of interneuronopathy characterized by intellectual disability, autism spectrum disorder, and epilepsy with variable expressivity. | 0 |
Citation
Dessen P
SP9 (Sp9 transcription factor)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/74092/sp9-(sp9-transcription-factor)
