DBNDD1 - dysbindin domain containing 1 Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79007

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

Dysbindin: Dysbindin (Dystrobrevin binding protein 1) (11 - 153)

  • 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

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 Set / 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
Others DBNDD1 NCBI