Gene

slc17a9b

ID

ZDB-GENE-040718-380

Name

solute carrier family 17 member 9b

Symbol

slc17a9b Nomenclature History

Previous Names

sb:cb849
wu:fa99h02
zgc:92222

Type

protein_coding_gene

Location

Chr: 23 Mapping Details/Browsers

Description

Predicted to have transmembrane transporter activity. Predicted to be involved in anion transport. Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in porokeratosis. Is expressed in several structures, including anterior axial hypoblast; axis; cranium; hatching gland; and polster. Orthologous to human SLC17A9 (solute carrier family 17 member 9).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

6 figures from Thisse et al., 2001

Cross-Species Comparison

High Throughput Data

GEO (1)

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Daniocell

Thisse Expression Data

cb849 (10 images)

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 slc17a9b Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
		Porokeratosis 8, disseminated superficial actinic type	616063

Associated With slc17a9b Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Conserved_site	IPR005829	Sugar transporter, conserved site
Domain	IPR020846	Major facilitator superfamily domain
Family	IPR011701	Major facilitator superfamily
Family	IPR044777	Solute carrier family 17 member 9-like
Family	IPR050382	Major Facilitator Superfamily Sodium/Anion Cotransporter
Homologous_superfamily	IPR036259	MFS transporter superfamily