DBNDD1 - dysbindin domain containing 1 Gene

Homo sapiens

Gene ID: 79007 | Gene type: protein coding

About DBNDD1

This gene has 7 transcripts (splice variants), 205 orthologues and 2 paralogues. Ubiquitous expression in brain (RPKM 6.9), esophagus (RPKM 5.3) and 22 other tissues.

Summary

Predicted to be involved in negative regulation of protein kinase activity. Predicted to be located in cytoplasm. [provided by Alliance of Genome Resources, Apr 2022]

DBNDD1 Products(5)

mRNA	Protein	Name
NM_001042610.3	NP_001036075.1	dysbindin domain-containing protein 1 isoform 1
NM_001288708.2	NP_001275637.1	dysbindin domain-containing protein 1 isoform 3
NM_001288709.2	NP_001275638.2	dysbindin domain-containing protein 1 isoform 5
NM_001371581.1	NP_001358510.1	dysbindin domain-containing protein 1 isoform 5
NM_024043.4	NP_076948.2	dysbindin domain-containing protein 1 isoform 2

DBNDD1 Protein Structure

Dysbindin

0
100
158 a.a.

Protein Preferred Names

Protein Names

dysbindin domain-containing protein 1

dysbindin (dystrobrevin binding protein 1) domain containing 1

Related Diseases

Diseases

Alias

Hermansky-Pudlak Syndrome 7

HPS7	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial
Delta Storage Pool Disease	Hermansky-Pudlak Syndrome, Type 7
Platelet Storage Pool Deficiency	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells

Glycogen Storage Disease Vii

Glycogen Storage Disease Type Vii	Muscle Phosphofructokinase Deficiency
Tarui Disease	GSD7
Pfkm Deficiency	Gsd Vii
Glycogen Storage Disease, Type Vii	Glycogen Storage Disease Type 7
Phosphofructokinase Deficiency	Glycogenosis Type Vii
Phosphofructokinase Myopathy	Glycogenosis 7
Glycogen Storage Disease Due To Muscle Phosphofructokinase Deficiency	Gsd Due To Muscle Phosphofructokinase Deficiency
Gsd Type 7	Gsd Type Vii
Glycogenosis Due To Muscle Phosphofructokinase Deficiency	Glycogenosis Type 7
Glycogen Storage Disease 7	Gsd-Vii
Storage Disease, Glycogen, Type Vii

Hermansky-Pudlak Syndrome

Hps	Albinism With Hemorrhagic Diathesis And Pigmented Reticuloendothelial Cells
Hermanski-Pudlak Syndrome	Hermansky Pudlak Syndrome
Platelet Storage Pool Deficiency

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS03549	DBNDD1 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	DBNDD1	VGNC	VGNC:39784
Rattus norvegicus	DBNDD1	RGD	RGD:1310008
Felis catus	DBNDD1	VGNC	VGNC:61348
Bos taurus	DBNDD1	VGNC	VGNC:27891
Macaca mulatta	DBNDD1	VGNC	VGNC:71778
Mus musculus	DBNDD1	MGD	MGI:1919435

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