Gene

slc44a4

ID
ZDB-GENE-040426-1371
Name
solute carrier family 44 member 4
Symbol
slc44a4 Nomenclature History
Previous Names
  • zgc:64108 (1)
Type
protein_coding_gene
Location
Chr: 19 Mapping Details/Browsers
Description
Predicted to have choline transmembrane transporter activity and thiamine pyrophosphate transmembrane transporter activity. Involved in neuromast hair cell development and otolith formation. Predicted to localize to plasma membrane. Is expressed in several structures, including liver; midbrain; olfactory system; otic vesicle; and pronephric duct. Used to study sensorineural hearing loss. Human ortholog(s) of this gene implicated in autosomal dominant nonsyndromic deafness 72. Orthologous to human SLC44A4 (solute carrier family 44 member 4).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
6 figures from 3 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
1 Figure from Ma et al., 2017
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc44a4 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal dominant nonsyndromic deafness 72 Alliance ?Deafness, autosomal dominant 72 617606
Associated With slc44a4 Via Experimental Models
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR007603 Choline transporter-like
Domain Details Per Protein
Protein Length Choline transporter-like
UniProtKB:A0A0G2KUI9 703
UniProtKB:Q7T2B0 723
Transcripts
Genome Browsers
No data available
Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations