1. Gene
  2. CLDN9 - claudin 9 Gene

CLDN9 - claudin 9 Gene

中文名称:密蛋白 9

种属: Homo sapiens

同用名: DFNB116

基因 ID: 9080 | 基因类型: protein coding

关于 CLDN9

Cytogenetic location: 16p13.3 Genomic coordinates (GRCh38): 16:3,012,923-3,014,505 (from NCBI)

This gene has 1 transcript (splice variant), 86 orthologues, 22 paralogues and is associated with 1 phenotype.

功能概要

该基因编码密蛋白家族的一个成员。 Claudins 是完整的膜蛋白和紧密连接链的组成部分。紧密连接链作为物理屏障,防止溶质和水自由通过上皮或内皮细胞片之间的细胞旁空间,并且在维持细胞极性和信号转导中也起着关键作用。这种蛋白质是丙型肝炎病毒的进入辅助因子之一。小鼠研究表明,该基因是保护听觉器官中感觉细胞所必需的,该基因缺陷与耳聋有关。[RefSeq 提供,2010 年 6 月]

This gene encodes a member of the Claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This protein is one of the entry cofactors for hepatitis C virus. Mouse studies revealed that this gene is required for the preservation of sensory cells in the hearing organ and the gene deficiency is associated with deafness. [provided by RefSeq, Jun 2010]

CLDN9 基因产物(1)

mRNA Protein Name
NM_020982.4 NP_066192.1 claudin-9
基因本体论
  • 分子功能
  • 细胞组分
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
20375010 GOA
enables virus receptor activity IMP
IMP: 通过突变表型推断
20375010 GOA
细胞组分 GO 注释 逻辑证据 参考文献 来源
located in plasma membrane IDA
IDA: 通过直接分析推断
20375010 GOA
located in plasma membrane IMP
IMP: 通过突变表型推断
31175426 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

CLDN9 蛋白结构

PMP22_Claudin

PMP22_Claudin: PMP-22/EMP/MP20/Claudin family (5 - 180)

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

claudin-9

CLDN9 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
CLDN9 O95484 GRM2 Homo sapiens Q14416 32296183
种属内
CLDN9 O95484 RPRM Homo sapiens Q9NS64 32296183
种属内
CLDN9 O95484 ADIPOQ Homo sapiens Q15848 32296183
种属内
CLDN9 O95484 ERMP1 Homo sapiens Q7Z2K6 32296183
种属内
CLDN9 O95484 PLPP6 Homo sapiens Q8IY26 32296183
种属内
CLDN9 O95484 C4orf3 Homo sapiens Q8WVX3-2 32296183
种属内
CLDN9 O95484 LPAR3 Homo sapiens Q9UBY5 32296183
种属内
CLDN9 O95484 VSTM1 Homo sapiens Q6UX27-3 32296183
种属内
CLDN9 O95484 PLPPR2 Homo sapiens Q96GM1 32296183
种属内
CLDN9 O95484 PLPPR2 Homo sapiens Q96GM1 32296183
种属内
CLDN9 O95484 PLPPR2 Homo sapiens Q96GM1 32296183
种属内
CLDN9 O95484 EXTL1 Homo sapiens Q92935 32296183
种属内
CLDN9 O95484 AMIGO1 Homo sapiens Q86WK6 32296183
种属内
CLDN9 O95484 AMIGO1 Homo sapiens Q86WK6 32296183
种属内
CLDN9 O95484 AMIGO1 Homo sapiens Q86WK6 32296183
种属内
CLDN9 O95484 AOC3 Homo sapiens Q16853 32296183
种属内
CLDN9 O95484 MAL Homo sapiens P21145 32296183
种属内
CLDN9 O95484 EMP1 Homo sapiens P54849 32296183
种属内
CLDN9 O95484 IGFBP5 Homo sapiens P24593 32296183
种属内
CLDN9 O95484 STX8 Homo sapiens Q9UNK0 32296183
种属内
CLDN9 O95484 BNIP3 Homo sapiens Q12983 32296183
种属内
CLDN9 O95484 MALL Homo sapiens Q13021 32296183
种属内
CLDN9 O95484 CYB561 Homo sapiens P49447 32296183
种属间: 跨种属相互作用 种属内: 同种属相互作用

重组 CLDN9 蛋白

目录号 产品名 蛋白编号 纯度
HY-P700407 Claudin-9/CLDN9 Protein-VLP, Human (HEK293, His) O95484 (M1-V217) /

关联疾病

疾病名称 别名
Deafness, Autosomal Recessive 116

DFNB116

Deafness, Autosomal Recessive, 116

Hepatitis C Virus

Hepatitis C Virus, Susceptibility To

Hepatitis C Virus Infection, Response To Therapy Of

Hcv

Hcv, Susceptibility To

Hepatitis C Virus, Resistance To

Hepatitis C Virus, Response To Therapy Of

Resistance To Hepatitis C Virus

Sacrum Chordoma
Hepatitis C

Chronic Hepatitis C

Hepatitis C Infection

Hepatitis Nona Nonb

Nanbh

Viral Hepatitis C

Hepatitis C Chronic

Hepatitis C, Chronic

Chronic Type C Viral Hepatitis

Chronic Hcv - [Hepatitis C Virus] Infection

Hepatitis C Nos

Hepatitis C Infection Nos

Hepatitis C-Related Cirrhosis

Type C Viral Hepatitis

Hep C Nos

Deafness, Autosomal Recessive 29

DFNB29

Autosomal Recessive Nonsyndromic Deafness 29

Autosomal Recessive Deafness 29

Deafness, Autosomal Recessive, 29

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 29

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 29

Deafness, Autosomal Recessive, Type 29

Hepatitis

Chronic Hepatitis

Chronic Persistent Hepatitis

Acute Hepatitis

Hepatitis, Chronic

Acute And Subacute Liver Necrosis

Acute/Subac. Necrosis Of Liver

Animal Hepatitis

Hepatitis Chronic

Hepatitis A

Hepatitis, Animal

Hepatitis Due To Toxoplasmosis

Hepatitis In Toxoplasmosis

Toxoplasmal Hepatitis

Chronic Hepatitis, Unspecified

Chronic Active Hepatitis Nec

Other Specified Chronic Hepatitis

Chronic Persistent Hepatitis Nec

Chronic Lobular Hepatitis Nec

Deafness, Autosomal Recessive 49

DFNB49

Autosomal Recessive Nonsyndromic Deafness 49

Autosomal Recessive Deafness 49

Deafness, Autosomal Recessive, 49

Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 49

Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 49

Deafness, Autosomal Recessive, Type 49

Deafness, Autosomal Recessive 86

DFNB86

Autosomal Recessive Nonsyndromic Deafness 86

Autosomal Recessive Deafness 86

Deafness, Autosomal Recessive, 86

Deafness, Nonsyndromic, Autosomal Recessive, Type 86

Sensorineural Hearing Loss

Sensory Hearing Loss

Sensorineural Deafness

Sensorineural Hearing Loss Disorder

Hearing Loss, Sensorineural

Central Hearing Loss

High Frequency Deafness

High Frequency Hearing Loss

High-Frequency Hearing Loss

Perceptive Deafness

Perceptive Hearing Loss

Perceptive Hearing Loss Or Deafness

Hearing Loss Sensorineural

Deafness Sensorineural

Hearing Loss High-Frequency

Hearing Loss, Central

Hearing Loss, High-Frequency

Autosomal Recessive Nonsyndromic Deafness

Deafness, Autosomal Recessive, Nonsyndromic

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
Bos taurus CLDN9 VGNC VGNC:27420
Canis familiaris CLDN9 VGNC VGNC:39323
Rattus norvegicus CLDN9 RGD RGD:1308999
Felis catus CLDN9 VGNC VGNC:60939
Mus musculus CLDN9 MGD MGI:1913100
Others CLDN9 NCBI