2. Gene
  3. TBC1D9 - TBC1 domain family member 9 Gene

TBC1D9 - TBC1 domain family member 9 Gene

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

中文名称：TBC1 域家族成员 9

种属: Homo sapiens

同用名: MDR1; GRAMD9

基因 ID: 23158 | 基因类型: protein coding

关于 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.

功能概要

预测启用 GTPase 激活剂活动。预计参与 GTPase 活性的激活和细胞内蛋白质转运。 [由基因组资源联盟提供，2022 年 4 月]

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 基因产物(1)

mRNA Protein Name
NM_015130.3 NP_055945.2 TBC1 domain family member 9
基因本体论
  • 分子功能
分子功能 GO 注释 逻辑证据 参考文献 来源
enables protein binding IPI
IPI: 通过物理相互作用推断
22354992 GOA
EXP：通过实验结果推断 IDA：通过直接分析推断 IPI：通过物理相互作用推断 IMP：通过突变表型推断 IGI：通过遗传相互作用推断 IEP：通过表达模式推断

TBC1D9 蛋白结构

GRAM

GRAM: GRAM domain (147 - 212)

GRAM

GRAM: GRAM domain (293 - 359)

RabGAP-TBC

RabGAP-TBC: Rab-GTPase-TBC domain (519 - 721)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1266 a.a.
蛋白主名 其他名称

TBC1 domain family member 9

TBC1 domain family member 9A

关联疾病

疾病名称 别名
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
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-RS14249 TBC1D9 Human Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 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
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