Identity
HGNC
LOCATION
11q13.1
LOCUSID
ALIAS
GKLP,HT019,NKTL,NTKL,P105,SCAR21,TAPK,TEIF,TRAP
FUSION GENES
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: 57410
MIM: 607982
HGNC: 14372
Ensembl: ENSG00000142186
Variants:
dbSNP: 57410
ClinVar: 57410
TCGA: ENSG00000142186
COSMIC: SCYL1
RNA/Proteins
Expression (GTEx)
Protein levels (Protein atlas)
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 36290821 | 2022 | Overexpression of SCYL1 Is Associated with Progression of Breast Cancer. | 1 |
| 36290821 | 2022 | Overexpression of SCYL1 Is Associated with Progression of Breast Cancer. | 1 |
| 33442927 | 2021 | SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1. | 1 |
| 33442927 | 2021 | SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1. | 1 |
| 32146038 | 2020 | Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review. | 8 |
| 32583741 | 2020 | SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. | 8 |
| 32146038 | 2020 | Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review. | 8 |
| 32583741 | 2020 | SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis. | 8 |
| 30258122 | 2019 | Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation. | 13 |
| 30258122 | 2019 | Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation. | 13 |
| 29419818 | 2018 | SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN). | 24 |
| 29419818 | 2018 | SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN). | 24 |
| 28570664 | 2017 | SCYL1 does not regulate REST expression and turnover. | 6 |
| 28570664 | 2017 | SCYL1 does not regulate REST expression and turnover. | 6 |
| 25575811 | 2015 | Overexpression of N-terminal kinase like gene promotes tumorigenicity of hepatocellular carcinoma by regulating cell cycle progression and cell motility. | 9 |
Citation
Dessen P
SCYL1 (SCY1 like pseudokinase 1)
Atlas Genet Cytogenet Oncol Haematol. 2006-10-01
Online version: http://atlasgeneticsoncology.org/gene/43486/scyl1
