EVC (EvC ciliary complex subunit 1)

2014-11-01  

Identity

HGNC
LOCATION
4p16.2
LOCUSID
ALIAS
DWF-1,EVC1,EVCL
FUSION GENES

Other Information

Locus ID:

NCBI: 2121
MIM: 604831
HGNC: 3497
Ensembl: ENSG00000072840

Variants:

dbSNP: 2121
ClinVar: 2121
TCGA: ENSG00000072840
COSMIC: EVC

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000072840ENST00000264956P57679
ENSG00000072840ENST00000509451E9PCN4

Expression (GTEx)

0
5
10
15
20
25
30
35
40
45

Pathways

PathwaySourceExternal ID
Hedgehog signaling pathwayKEGGko04340
Hedgehog signaling pathwayKEGGhsa04340
Signal TransductionREACTOMER-HSA-162582
Signaling by HedgehogREACTOMER-HSA-5358351
Hedgehog 'on' stateREACTOMER-HSA-5632684
Activation of SMOREACTOMER-HSA-5635838

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
340373142021An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation.1
340373142021An intrafamilial phenotypic variability in Ellis-Van Creveld syndrome due to a novel 27 bps deletion mutation.1
292572162018Molecular mechanisms of Ellis‑van Creveld gene variations in ventricular septal defect.2
292572162018Molecular mechanisms of Ellis‑van Creveld gene variations in ventricular septal defect.2
292298992017Phenotypic Variation in Patients with Homozygous c.1678G>T Mutation in EVC Gene: Report of Two Mexican Families with Ellis-van Creveld Syndrome.4
293213602017Ellis-van Creveld syndrome and profound deafness resulted by sequence variants in the EVC/EVC2 and TMC1 genes.7
292298992017Phenotypic Variation in Patients with Homozygous c.1678G>T Mutation in EVC Gene: Report of Two Mexican Families with Ellis-van Creveld Syndrome.4
293213602017Ellis-van Creveld syndrome and profound deafness resulted by sequence variants in the EVC/EVC2 and TMC1 genes.7
265806852016Novel homozygous mutations in the EVC and EVC2 genes in two consanguineous families segregating autosomal recessive Ellis-van Creveld syndrome.3
266213682016Novel mutations in EVC cause aberrant splicing in Ellis-van Creveld syndrome.1
267485862016Truncation and microdeletion of EVC/EVC2 with missense mutation of EFCAB7 in Ellis-van Creveld syndrome.5
265806852016Novel homozygous mutations in the EVC and EVC2 genes in two consanguineous families segregating autosomal recessive Ellis-van Creveld syndrome.3
266213682016Novel mutations in EVC cause aberrant splicing in Ellis-van Creveld syndrome.1
267485862016Truncation and microdeletion of EVC/EVC2 with missense mutation of EFCAB7 in Ellis-van Creveld syndrome.5
249960032014Epigenetic deregulation of Ellis Van Creveld confers robust Hedgehog signaling in adult T-cell leukemia.7

Citation

Dessen P

EVC (EvC ciliary complex subunit 1)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/62934/js/lib/bootstrap.min.js