1. Gene
  2. C1QTNF9 - C1q and TNF related 9 Gene

C1QTNF9 - C1q and TNF related 9 Gene

中文名称:C1q 和 TNF 相关 9

种属: Homo sapiens

同用名: AQL1; CTRP9; C1QTNF9A

基因 ID: 338872 | 基因类型: protein coding

关于 C1QTNF9

Cytogenetic location: 13q12.12 Genomic coordinates (GRCh38): 13:24,307,166-24,322,531 (from NCBI)

This gene has 2 transcripts (splice variants), 202 orthologues and 23 paralogues. Broad expression in testis (RPKM 1.7), heart (RPKM 1.5) and 21 other tissues.

功能概要

实现相同的蛋白质结合活性。预计参与信号转导。预测位于细胞外区域。预计是胶原蛋白三聚体的一部分。 [由基因组资源联盟提供,2022 年 4 月]

Enables identical protein binding activity. Predicted to be involved in signal transduction. Predicted to be located in extracellular region. Predicted to be part of collagen trimer. [provided by Alliance of Genome Resources, Apr 2022]

C1QTNF9 基因产物(3)

mRNA Protein Name
NM_001303137.2 NP_001290066.1 complement C1q and tumor necrosis factor-related protein 9A precursor
NM_001303138.2 NP_001290067.1 complement C1q and tumor necrosis factor-related protein 9A precursor
NM_178540.5 NP_848635.2 complement C1q and tumor necrosis factor-related protein 9A precursor
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 identical protein binding IPI
IPI: 通过物理相互作用推断
19666007 GOA
enables protein binding IPI
IPI: 通过物理相互作用推断
19666007 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

C1QTNF9 蛋白结构

Collagen

Collagen: Collagen triple helix repeat (20 copies) (25 - 81)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (90 - 146)

Collagen

Collagen: Collagen triple helix repeat (20 copies) (131 - 189)

C1q

C1q: C1q domain (203 - 329)

  • 0
  • 100
  • 200
  • 300
  • 333 a.a.
蛋白主名 其他名称

complement C1q and tumor necrosis factor-related protein 9A

C1q and tumor necrosis factor related protein 9

C1QTNF9 蛋白互作信息

分类
蛋白名称 蛋白编号 互作蛋白 互作蛋白种属 互作蛋白编号 实验方法 参考文献
种属内
C1QTNF9 P0C862 C1QTNF9B Homo sapiens B2RNN3
GMS
19666007
种属内
C1QTNF9 P0C862 C1QTNF9B Homo sapiens B2RNN3 33961781
种属内
C1QTNF9 P0C862 C1QTNF9B Homo sapiens B2RNN3 28514442
种属内
C1QTNF9 P0C862 C1QTNF9B Homo sapiens B2RNN3 19666007
种属内
C1QTNF9 P0C862 COL6A1 Homo sapiens P12109 33961781
种属内
C1QTNF9 P0C862 C1QTNF9 Homo sapiens P0C862
GMS
19666007
种属内
C1QTNF9 P0C862 C1QTNF9 Homo sapiens P0C862 19666007
种属内
C1QTNF9 P0C862 COL6A1 Homo sapiens P12109 28514442
种属内
C1QTNF9 P0C862 TSNAX Homo sapiens Q99598 33961781
种属内
C1QTNF9 P0C862 ADIPOQ Homo sapiens Q15848 19666007
种属内
C1QTNF9 P0C862 COLGALT2 Homo sapiens Q8IYK4 33961781
种属内
C1QTNF9 P0C862 COL6A2 Homo sapiens P12110 33961781
种属内
C1QTNF9 P0C862 TSNAX Homo sapiens Q99598 28514442
种属内
C1QTNF9 P0C862 P3H3 Homo sapiens Q8IVL6 33961781
种属内
C1QTNF9 P0C862 C1QL1 Homo sapiens O75973 33961781
种属内
C1QTNF9 P0C862 COLGALT2 Homo sapiens Q8IYK4 28514442
种属内
C1QTNF9 P0C862 COL6A2 Homo sapiens P12110 28514442
种属内
C1QTNF9 P0C862 P3H3 Homo sapiens Q8IVL6 28514442
种属内
C1QTNF9 P0C862 C1QL1 Homo sapiens O75973 28514442
种属内
C1QTNF9 P0C862 DHRS4 Homo sapiens Q9BTZ2 33961781
种属内
C1QTNF9 P0C862 DHRS4 Homo sapiens Q9BTZ2 28514442
种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称 别名
Late-Onset Retinal Degeneration

LORD

Retinal Degeneration, Late-Onset, Autosomal Dominant

Autosomal Dominant Late-Onset Retinal Degeneration

Pigmentary Retinopathy

Retinal Degeneration, Late-Onset

Retinitis Pigmentosa

Nonobstructive Coronary Artery Disease

Non-Cad

Non-Obstructive Coronary Artery Disease

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

直系同源

种属 基因名 来源 基因 ID
Mus musculus C1QTNF9 MGD MGI:3045252