Gene

lhfpl5a

ID
ZDB-GENE-110131-8
Name
LHFPL tetraspan subfamily member 5a
Symbol
lhfpl5a Nomenclature History
Previous Names
  • asn (1)
  • astronaut (1)
Type
protein_coding_gene
Location
Chr: 11 Mapping Details/Browsers
Description
Involved in detection of mechanical stimulus involved in sensory perception and protein localization to cilium. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in autosomal recessive nonsyndromic deafness 67. Orthologous to human LHFPL5 (LHFPL tetraspan subfamily member 5).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Erickson et al., 2020
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
4 figures from 3 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With lhfpl5a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive nonsyndromic deafness 67 Alliance Deafness, autosomal recessive 67 610265
Associated With lhfpl5a Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR019372 Lipoma HMGIC fusion partner-like protein
Domain Details Per Protein
Protein Length Lipoma HMGIC fusion partner-like protein
UniProtKB:F1Q837 219
UniProtKB:A0A2R8QN41 226
Transcripts
Genome Browsers
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