1. Gene
  2. SPIN3 - spindlin family member 3 Gene

SPIN3 - spindlin family member 3 Gene

中文名称:纺锤家族成员 3

种属: Homo sapiens

同用名: SPIN-3; TDRD27; bA445O16.1

基因 ID: 169981 | 基因类型: protein coding

关于 SPIN3

This gene has 45 transcripts (splice variants), 170 orthologues and 4 paralogues. Ubiquitous expression in brain (RPKM 4.7), prostate (RPKM 3.7) and 24 other tissues.

功能概要

启用甲基化组蛋白结合活性。预计参与转录调控,以 DNA 为模板。预计是膜的组成部分。预计在胞质溶胶和核质中具有活性。 [由基因组资源联盟提供,2022 年 4 月]

Enables methylated histone binding activity. Predicted to be involved in regulation of transcription, DNA-templated. Predicted to be integral component of membrane. Predicted to be active in cytosol and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

SPIN3 基因产物(1)

mRNA Protein Name
NM_001010862.3 NP_001010862.2 spindlin-3

SPIN3 蛋白结构

Spin-Ssty

Spin-Ssty: Spin/Ssty Family (50 - 99)

Spin-Ssty

Spin-Ssty: Spin/Ssty Family (129 - 178)

Spin-Ssty

Spin-Ssty: Spin/Ssty Family (210 - 255)

  • 0
  • 100
  • 200
  • 258 a.a.
蛋白主名 其他名称

spindlin-3

bA445O16.1 (DXF34)

关联疾病

疾病名称 别名
Patent Foramen Ovale

Atrial Septal Defect Within Oval Fossa

Foramen Ovale Patent

Ostium Secundum Atrial Septal Defect

Atrial Septal Defect, Ostium Secundum Type

Foramen Ovale, Patent

Defect, Patent Or Persistent, Ostium Secundum

Ostium Secundum Type Atrial Septal Defect

Persistent Ostium Secundum

Asd Ostium Secundum Type

Ostium Secundum Asd

Osasd

Asd, Ostium Secundum Type

Pfo - [Patent Foramen Ovale]

Open Foramen Ovale

Open Oval Foramen

Persistent Foramen Ovale

Secundum Atrial Septal Defect

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