SCYL1 (SCY1 like pseudokinase 1)

2006-10-01  

Identity

HGNC
LOCATION
11q13.1
LOCUSID
ALIAS
GKLP,HT019,NKTL,NTKL,P105,SCAR21,TAPK,TEIF,TRAP
FUSION GENES

Other Information

Locus ID:

NCBI: 57410
MIM: 607982
HGNC: 14372
Ensembl: ENSG00000142186

Variants:

dbSNP: 57410
ClinVar: 57410
TCGA: ENSG00000142186
COSMIC: SCYL1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000142186ENST00000270176Q96KG9
ENSG00000142186ENST00000279270A0A0A0MQX4
ENSG00000142186ENST00000420247Q96KG9
ENSG00000142186ENST00000524944E9PS17
ENSG00000142186ENST00000525364E9PK59
ENSG00000142186ENST00000527009E9PPN3
ENSG00000142186ENST00000528545H0YDH0
ENSG00000142186ENST00000531601H0YCI6
ENSG00000142186ENST00000533862Q96KG9

Expression (GTEx)

0
50
100
150

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
362908212022Overexpression of SCYL1 Is Associated with Progression of Breast Cancer.1
362908212022Overexpression of SCYL1 Is Associated with Progression of Breast Cancer.1
334429272021SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1.1
334429272021SCYL1 disease and liver transplantation diagnosed by reanalysis of exome sequencing and deletion/duplication analysis of SCYL1.1
321460382020Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review.8
325837412020SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis.8
321460382020Mutations in NBAS and SCYL1, genetic causes of recurrent liver failure in children: Three case reports and a literature review.8
325837412020SCYL1 arginine methylation by PRMT1 is essential for neurite outgrowth via Golgi morphogenesis.8
302581222019Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation.13
302581222019Variant in SCYL1 gene causes aberrant splicing in a family with cerebellar ataxia, recurrent episodes of liver failure, and growth retardation.13
294198182018SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN).24
294198182018SCYL1 variants cause a syndrome with low γ-glutamyl-transferase cholestasis, acute liver failure, and neurodegeneration (CALFAN).24
285706642017SCYL1 does not regulate REST expression and turnover.6
285706642017SCYL1 does not regulate REST expression and turnover.6
255758112015Overexpression 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