ZNF778 (zinc finger protein 778)

2014-11-01  

Identity

HGNC
LOCATION
16q24.3
LOCUSID
ALIAS
-

Other Information

Locus ID:

NCBI: 197320
HGNC: 26479
Ensembl: ENSG00000170100

Variants:

dbSNP: 197320
ClinVar: 197320
TCGA: ENSG00000170100
COSMIC: ZNF778

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000170100ENST00000306502Q96MU6
ENSG00000170100ENST00000433976A0A0A0MSW5
ENSG00000170100ENST00000564906H3BUU4
ENSG00000170100ENST00000567651H3BSD4
ENSG00000170100ENST00000620195Q96MU6

Expression (GTEx)

0
1
2
3
4
5
6
7
8
9
10

Pathways

PathwaySourceExternal ID
Gene ExpressionREACTOMER-HSA-74160
Generic Transcription PathwayREACTOMER-HSA-212436

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
199208532010Identification of ANKRD11 and ZNF778 as candidate genes for autism and variable cognitive impairment in the novel 16q24.3 microdeletion syndrome.26

Citation

Dessen P

ZNF778 (zinc finger protein 778)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/76396/znf778