Gene

snx10b

ID
ZDB-GENE-070628-1
Name
sorting nexin 10b
Symbol
snx10b Nomenclature History
Previous Names
None
Type
protein_coding_gene
Location
Chr: 16 Mapping Details/Browsers
Description
Predicted to have phosphatidylinositol binding activity. Predicted to be involved in protein transport. Predicted to localize to endosome membrane. Human ortholog(s) of this gene implicated in autosomal recessive osteopetrosis 8. Orthologous to human SNX10 (sorting nexin 10).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
1 figure from Chen et al., 2012
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With snx10b Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
autosomal recessive osteopetrosis 8 Alliance Osteopetrosis, autosomal recessive 8 615085
Associated With snx10b Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR001683 Phox homology
Family IPR043544 Sorting nexin-10/11
Homologous_superfamily IPR036871 PX domain superfamily
Domain Details Per Protein
Protein Length Phox homology PX domain superfamily Sorting nexin-10/11
UniProtKB:A8WG21 170
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA snx10b-201 (1) Havana 2241 nt
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