1. Gene
  2. CDH9 - cadherin 9 Gene

CDH9 - cadherin 9 Gene

中文名称:钙粘蛋白 9

种属: Homo sapiens

基因 ID: 1007 | 基因类型: protein coding

关于 CDH9

Cytogenetic location: 5p14.1 Genomic coordinates (GRCh38): 5:26,880,597-27,038,586 (from NCBI)

This gene has 5 transcripts (splice variants), 133 orthologues and 33 paralogues. Biased expression in brain (RPKM 3.5) and kidney (RPKM 1.9).

功能概要

该基因编码来自钙粘蛋白超家族的 II 型经典钙粘蛋白,即介导钙依赖性细胞粘附的整合膜蛋白。成熟的钙粘蛋白由一个大的 N 末端胞外结构域、一个单一的跨膜结构域和一个小的、高度保守的 C 末端胞质结构域组成。细胞外结构域由 5 个子结构域组成,每个子结构域包含一个钙粘蛋白基序,并且似乎决定了该蛋白质的嗜同细胞粘附活性的特异性。 II 型 (非典型) 钙粘蛋白是根据它们缺乏 I 型钙粘蛋白特有的 HAV 细胞粘附识别序列来定义的。[RefSeq 提供,2008 年 7 月]

This gene encodes a type II classical cadherin from the cadherin superfamily, integral membrane proteins that mediate calcium-dependent cell-cell adhesion. Mature cadherin proteins are composed of a large N-terminal extracellular domain, a single membrane-spanning domain, and a small, highly conserved C-terminal cytoplasmic domain. The extracellular domain consists of 5 subdomains, each containing a cadherin motif, and appears to determine the specificity of the protein's homophilic cell adhesion activity. Type II (atypical) Cadherins are defined based on their lack of a HAV cell adhesion recognition sequence specific to type I Cadherins. [provided by RefSeq, Jul 2008]

CDH9 基因产物(1)

mRNA Protein Name
NM_016279.4 NP_057363.3 cadherin-9 preproprotein

CDH9 蛋白结构

Cadherin

Cadherin: Cadherin domain (68 - 147)

Cadherin

Cadherin: Cadherin domain (164 - 258)

Cadherin

Cadherin: Cadherin domain (273 - 359)

Cadherin

Cadherin: Cadherin domain (388 - 478)

Cadherin

Cadherin: Cadherin domain (492 - 589)

Cadherin_C

Cadherin_C: Cadherin cytoplasmic region (639 - 783)

  • 0
  • 200
  • 400
  • 600
  • 789 a.a.
蛋白主名 其他名称

cadherin-9

T1-cadherin

重组 CDH9 蛋白

目录号 产品名 蛋白编号 纯度
HY-P78770 Cadherin-9/CDH9 Protein, Human (HEK293, His) Q9ULB4-1 (G54-A615) ≥95%

关联疾病

疾病名称 别名
Craniofacial-Deafness-Hand Syndrome

CDHS

Craniofacial Deafness Hand Syndrome

Sommer-Young-Wee-Frye Syndrome

Features Of Flat Facial Profile, Hypertelorism, Hypoplastic Nose With Slitlike Nares, And A Sensorineural Hearing Loss

Craniofacial-Hearing Loss-Hand Syndrome

Childhood Disintegrative Disease

Childhood Disintegrative Disorder

Disintegrative Psychosis

Heller'S Syndrome

Symbiotic Psychosis

Dementia Infantilis

Heller Syndrome

Shared Paranoid Disorder

Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Benign Epilepsy With Centrotemporal Spikes

Rolandic Epilepsy

Benign Rolandic Epilepsy

Epilepsy, Rolandic

Bcects

Benign Childhood Epilepsy With Centrotemporal Spike

Sylvan Seizures

Becrs

Bects

Bre

Benign Epilepsy Of Childhood With Centrotemporal Spikes

Benign Familial Epilepsy Of Childhood With Rolandic Spikes

Centrotemporal Epilepsy

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 CDH9 VGNC VGNC:27107
Mus musculus CDH9 MGD MGI:107433
Felis catus CDH9 VGNC VGNC:60687
Macaca mulatta CDH9 VGNC VGNC:70977
Canis familiaris CDH9 VGNC VGNC:39036
Rattus norvegicus CDH9 RGD RGD:1308343
Others CDH9 NCBI