BRN4 Products

Description

BRN4 encodes a member of the POU-III class of neural transcription factors. This gene may play a role in the mediation of epigenetic signals which induce striatal neuron-precursor differentiation. Mutations have been associated with X chromosome-linked nonsyndromic mixed deafness. [provided by RefSeq]

Bioinformatics

Entrez	5456 Human
Uniprot	AAI46552.1 Human NP_000298 Human
Product By Gene ID	5456
Alternate Names	brain-specific homeobox/POU domain protein 4 octamer-binding transcription factor 9 OTF9 POU class 3 homeobox 4 POU domain, class 3, transcription factor 4

Diseases related to BRN4

Discover more about diseases related to BRN4.

Complete Hearing Loss
Sensorineural Hearing Loss (disorder)
Hearing Loss, Mixed Conductive-sensorineural
Genetic Diseases, X-linked
Dysplasia
Deafness Congenital
Conductive Hearing Loss
Choroideremia
Sex Chromosome Aberrations
Nervousness
Neoplasms
Congenital Abnormality
Cytogenetic Abnormality
Hearing Problem
Hearing Loss, Bilateral
Chromosome Inversion
Congenital Ear Anomaly Nos (disorder)
Norrie Disease

Pathways for BRN4

View related products by pathway and learn more about each of the pathways below.

Ear Development
Inner Ear Development
Localization
Glucose Homeostasis
Methylation
Regeneration
Pathogenesis
Transport
Response To Camp
Stem Cell Differentiation
Neurogenesis
Regulation Of Gene Expression
Pancreatic Bud Formation
Reverse Transcription
Mrna Transcription
Cell Differentiation
Potassium Ion Homeostasis
Bone Mineralization
Cell Proliferation
Pancreas Development

PTMs for BRN4

Learn more about PTMs related to BRN4.

Methylation
Prenylation

Bioinformatics Tool for BRN4

Discover related pathways, diseases and genes to BRN4. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.