ZNF469 (zinc finger protein 469)

2019-04-01  

Identity

HGNC
ZNF469
LOCATION
16q24.2
LOCUSID
84627
ALIAS
BCS,BCS1,Zfp469
FUSION GENES
Show Gene Fusions

Other Information

Locus ID:

NCBI: 84627
MIM: 612078
HGNC: 23216
Ensembl: ENSG00000225614

Variants:

dbSNP: 84627
ClinVar: 84627
TCGA: ENSG00000225614
COSMIC: ZNF469

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000225614ENST00000437464Q96JG9
ENSG00000225614ENST00000565624H3BS19

Expression (GTEx)

0
1
2
3
4
5
6
7
8
Adipose - Subcutaneous
Adipose - Visceral
Adrenal Gland
Artery - Aorta
Artery - Tibial
Bladder
Brain - Amygdala
Brain - Anterior cingulate cortex
Brain - Caudate
Brain - Cerebellar Hemisphere
Brain - Cerebellum
Brain - Cortex
Brain - Frontal Cortex
Brain - Hippocampus
Brain - Hypothalamus
Brain - Nucleus accumbens
Brain - Putamen
Brain - Spinal cord
Brain - Substantia nigra
Breast - Mammary Tissue
Cells - Cultured fibroblasts
Cells - EBV - transformed lymphocytes
Cervix - Ectocervix
Cervix - Endocervix
Colon - Sigmoid
Colon - Transverse
Esophagus - Gastroesophageal Junction
Esophagus - Mucosa
Esophagus - Muscularis
Fallopian Tube
Heart - Atrial Appendage
Heart - Left Ventricle
Kidney - Cortex
Kidney - Medulla
Liver
Lung
Minor Salivary Gland
Muscle - Skeletal
Nerve - Tibial
Ovary
Pancreas
Pituitary
Prostate
Skin - Not Sun Exposed
Skin - Sun Exposed
Small Intestine - Terminal Ileum
Spleen
Stomach
Testis
Thyroid
Uterus
Vagina
Whole Blood

References

Pubmed IDYearTitleCitations
382679122024Genetic variants in the FOXO1 and ZNF469 genes are associated with keratoconus in Sweden: a case-control study.0
382679122024Genetic variants in the FOXO1 and ZNF469 genes are associated with keratoconus in Sweden: a case-control study.0
370981122023New ZNF469 Mutations in Spanish Siblings With Brittle Cornea Syndrome.1
370981122023New ZNF469 Mutations in Spanish Siblings With Brittle Cornea Syndrome.1
337395562021More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome.12
337395562021More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome.12
308650452019Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome.6
311077612019Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations.6
308650452019Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome.6
311077612019Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations.6
297551272018A novel long non-coding RNA linc-ZNF469-3 promotes lung metastasis through miR-574-5p-ZEB1 axis in triple negative breast cancer.41
297551272018A novel long non-coding RNA linc-ZNF469-3 promotes lung metastasis through miR-574-5p-ZEB1 axis in triple negative breast cancer.41
284843092017Identification of seven novel ZNF469 mutations in keratoconus patients in a Han Chinese population.10
286220622017Novel Zinc Finger Protein Gene 469 (ZNF469) Variants in Advanced Keratoconus.11
291872502017Polymorphism rs13334190 in zinc finger protein 469 (ZNF469) is not a risk factor for keratoconus in a Saudi cohort.4

Citation

Dessen P

ZNF469 (zinc finger protein 469)

Atlas Genet Cytogenet Oncol Haematol. 2019-04-01

Online version: http://atlasgeneticsoncology.org/gene/57950/teaching-explorer/gene-fusions-explorer/