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TBC1D9 - TBC1 domain family member 9 Gene

Also Known as MDR1; GRAMD9

Species: Homo sapiens

Gene Type: protein coding

Gene ID: 23158

About TBC1D9

Cytogenetic location: 4q31.21 Genomic coordinates (GRCh38): 4:140,620,782-140,756,385 (from NCBI)

This gene has 3 transcripts (splice variants), 209 orthologues and 45 paralogues. Ubiquitous expression in spleen (RPKM 19.8), brain (RPKM 12.2) and 23 other tissues.

Summary

Predicted to enable GTPase activator activity. Predicted to be involved in activation of GTPase activity and intracellular protein transport. [provided by Alliance of Genome Resources, Apr 2022]

TBC1D9 Products (1)

mRNA	Protein	Name
NM_015130.3	NP_055945.2	TBC1 domain family member 9

Gene Ontology

Molecular Function

Molecular Function GO Annotation	Evidence	References	Source
enables protein binding	IPI IPI: Inferred from physical interaction	22354992	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

TBC1D9 Protein Structure

GRAM

RabGAP-TBC

0
200
400
600
800
1000
1200
1266 a.a.

Protein Preferred Names	Protein Names
TBC1 domain family member 9	TBC1 domain family member 9A

Related Diseases

Diseases	Alias
Non-Proliferative Fibrocystic Change Of The Breast	Non-Proliferative Fibrocystic Change Breast Fibrocystic Change, Non-Proliferative Type
Proliferative Type Fibrocystic Change Of Breast	Fibrocystic Change, Proliferative Type With Atypia Fibrocystic Disease, Proliferative Type With Atypia Proliferating Lesion Of Breast Without Atypia Proliferating Lesion Of The Breast Without Atypia Proliferative Fibrocystic Change Breast Fibrocystic Change, Proliferative Type
Carotid Artery Dissection	Dissection Of Carotid Artery
Mirror Movements 1	Congenital Mirror Movement Disorder Bimanual Synergia Congenital Mirror Movements Familial Congenital Controlateral Synkinesia Familial Congenital Mirror Movements Hereditary Congenital Controlateral Synkinesia Hereditary Congenital Mirror Movements Isolated Congenital Controlateral Synkinesia Isolated Congenital Mirror Movements Mirror Movements MRMV1 Mirror Movements 1 And/Or Agenesis Of The Corpus Callosum Mirror Movements, Congenital Bimanual Synkinesis Cmm Mirror Movements, Type 1

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS14249	TBC1D9 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Mus musculus	TBC1D9	MGD	MGI:1918560
Bos taurus	TBC1D9	VGNC	VGNC:35646
Felis catus	TBC1D9	VGNC	VGNC:65991
Rattus norvegicus	TBC1D9	RGD	RGD:1308221
Macaca mulatta	TBC1D9	VGNC	VGNC:78193
Others	TBC1D9	NCBI