FOXI1 (forkhead box I1)

2007-04-01  

Identity

HGNC
LOCATION
5q35.1
LOCUSID
ALIAS
FKH10,FKHL10,FREAC-6,FREAC6,HFH-3,HFH3

Other Information

Locus ID:

NCBI: 2299
MIM: 601093
HGNC: 3815
Ensembl: ENSG00000168269

Variants:

dbSNP: 2299
ClinVar: 2299
TCGA: ENSG00000168269
COSMIC: FOXI1

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000168269ENST00000306268Q12951
ENSG00000168269ENST00000306268E0XEN6
ENSG00000168269ENST00000449804Q12951

Expression (GTEx)

0
5
10
15
20
25
30
35

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
192142372009The forkhead transcription factor Foxi1 is a master regulator of vacuolar H-ATPase proton pump subunits in the inner ear, kidney and epididymis.47
126955462003Transcriptional regulation of human CYP3A4 basal expression by CCAAT enhancer-binding protein alpha and hepatocyte nuclear factor-3 gamma.21
185649212008Candidate gene analysis in primary lymphedema.16
206213672010Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct.13
206213672010Screening of SLC26A4, FOXI1 and KCNJ10 genes in unilateral hearing impairment with ipsilateral enlarged vestibular aqueduct.13
224121812012Screening of SLC26A4, FOXI1, KCNJ10, and GJB2 in bilateral deafness patients with inner ear malformation.13
283583742017miR-491-5p, mediated by Foxi1, functions as a tumor suppressor by targeting Wnt3a/β-catenin signaling in the development of gastric cancer.11
239650302013Lack of significant association between mutations of KCNJ10 or FOXI1 and SLC26A4 mutations in Pendred syndrome/enlarged vestibular aqueducts.10
292422492018Acidosis and Deafness in Patients with Recessive Mutations in FOXI1.9
311771142019FOXI1 Immunohistochemistry Differentiates Benign Renal Oncocytoma from Malignant Chromophobe Renal Cell Carcinoma.0

Citation

Dessen P

FOXI1 (forkhead box I1)

Atlas Genet Cytogenet Oncol Haematol. 2007-04-01

Online version: http://atlasgeneticsoncology.org/gene/46644/foxi1