ZNF469 (zinc finger protein 469)

2019-04-01 Affiliation

Identity

HGNC

ZNF469

LOCATION

16q24.2

LOCUSID

84627

ALIAS

BCS,BCS1,Zfp469

FUSION GENES

Show Gene Fusions

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: 84627
MIM: 612078
HGNC: 23216
Ensembl: ENSG00000225614

Variants:

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

RNA/Proteins

Gene ID	Transcript ID	Uniprot
ENSG00000225614	ENST00000437464	Q96JG9
ENSG00000225614	ENST00000565624	H3BS19

Expression (GTEx)

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 ID	Year	Title	Citations
38267912	2024	Genetic variants in the FOXO1 and ZNF469 genes are associated with keratoconus in Sweden: a case-control study.	0
38267912	2024	Genetic variants in the FOXO1 and ZNF469 genes are associated with keratoconus in Sweden: a case-control study.	0
37098112	2023	New ZNF469 Mutations in Spanish Siblings With Brittle Cornea Syndrome.	1
37098112	2023	New ZNF469 Mutations in Spanish Siblings With Brittle Cornea Syndrome.	1
33739556	2021	More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome.	12
33739556	2021	More than meets the eye: Expanding and reviewing the clinical and mutational spectrum of brittle cornea syndrome.	12
30865045	2019	Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome.	6
31107761	2019	Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations.	6
30865045	2019	Identification of a Novel ZNF469 Mutation in a Pakistani Family With Brittle Cornea Syndrome.	6
31107761	2019	Corneal Perforation After Corneal Cross-Linking in Keratoconus Associated With Potentially Pathogenic ZNF469 Mutations.	6
29755127	2018	A novel long non-coding RNA linc-ZNF469-3 promotes lung metastasis through miR-574-5p-ZEB1 axis in triple negative breast cancer.	41
29755127	2018	A novel long non-coding RNA linc-ZNF469-3 promotes lung metastasis through miR-574-5p-ZEB1 axis in triple negative breast cancer.	41
28484309	2017	Identification of seven novel ZNF469 mutations in keratoconus patients in a Han Chinese population.	10
28622062	2017	Novel Zinc Finger Protein Gene 469 (ZNF469) Variants in Advanced Keratoconus.	11
29187250	2017	Polymorphism 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/znf469-(zinc-finger-protein-469)