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  3. DBNDD1 - dysbindin domain containing 1 Gene

DBNDD1 - dysbindin domain containing 1 Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：含 dysbindin 结构域 1

种属: Homo sapiens

基因 ID: 79007 | 基因类型: protein coding

关于 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.

功能概要

预计参与蛋白激酶活性的负调节。预计位于细胞质中。 [由基因组资源联盟提供，2022 年 4 月]

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 基因产物(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 蛋白结构

Dysbindin

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

  • 0
  • 100
  • 158 a.a.
蛋白主名 其他名称

dysbindin domain-containing protein 1

dysbindin (dystrobrevin binding protein 1) domain containing 1

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS03549 DBNDD1 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 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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