Gene

rab39bb

ID

ZDB-GENE-061215-104

Name

RAB39B, member RAS oncogene family b

Symbol

rab39bb Nomenclature History

Previous Names

rab39b
zgc:153068

Type

protein_coding_gene

Location

Chr: 7 Mapping Details/Browsers

Description

Predicted to have GTPase activity. Predicted to be involved in Rab protein signal transduction and intracellular protein transport. Predicted to localize to endomembrane system. Human ortholog(s) of this gene implicated in Waisman syndrome and non-syndromic X-linked intellectual disability. Orthologous to human RAB39B (RAB39B, member RAS oncogene family).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

No data available

Cross-Species Comparison

High Throughput Data

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

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 rab39bb Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
non-syndromic X-linked intellectual disability 72	Alliance	Intellectual developmental disorder, X-linked 72	300271
Waisman syndrome	Alliance	Waisman syndrome	311510

Associated With rab39bb Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Domain	IPR005225	Small GTP-binding protein domain
Family	IPR001806	Small GTPase
Family	IPR041818	Rab39
Homologous_superfamily	IPR027417	P-loop containing nucleoside triphosphate hydrolase