CDH8 - cadherin 8 Gene

Also Known as Nbla04261

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 1006

About CDH8

Cytogenetic location: 16q21 Genomic coordinates (GRCh38): 16:61,647,250-62,036,438 (from NCBI)

This gene has 14 transcripts (splice variants), 213 orthologues and 33 paralogues. Biased expression in brain (RPKM 2.8) and ovary (RPKM 0.2).

Summary

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. This particular Cadherin is expressed in brain and is putatively involved in synaptic adhesion, axon outgrowth and guidance. [provided by RefSeq, Jul 2008]

CDH8 Products (2)

mRNA Protein Name
NM_001410893.1 NP_001397822.1 cadherin-8 isoform 2
NM_001796.5 NP_001787.2 cadherin-8 isoform 1 preproprotein

CDH8 Protein Structure

Cadherin

Cadherin: Cadherin domain (75 - 158)

Cadherin

Cadherin: Cadherin domain (172 - 266)

Cadherin

Cadherin: Cadherin domain (281 - 382)

Cadherin

Cadherin: Cadherin domain (397 - 487)

Cadherin

Cadherin: Cadherin domain (500 - 597)

Cadherin_C

Cadherin_C: Cadherin cytoplasmic region (646 - 791)

  • 0
  • 200
  • 400
  • 600
  • 799 a.a.
Protein Preferred Names Protein Names

cadherin-8

  • cadherin 8, type 2

Recombinant CDH8 Proteins

Cat. No. Product Name Accession Purity
HY-P7704 Cadherin-8 Protein, Human (HEK293, His) P55286 (A30-M621) ≥ 90%, as determined by reducing SDS-PAGE.

Related Diseases

Diseases Alias
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

Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy Syndrome
  • Eem Syndrome

  • Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy

  • EEMS

  • Ectodermal Dysplasia-Ectrodactyly-Macular Dystrophy Syndrome

  • Albrectsen-Svendsen Syndrome

  • Ohdo-Hirayama-Terawaki Syndrome

  • Dysplasia, Ectodermal, Ectrodactyly, And Macular Dystrophy

Diseases Alias
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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus CDH8 RGD RGD:69286
Macaca mulatta CDH8 VGNC VGNC:70976
Canis familiaris CDH8 VGNC VGNC:39035
Mus musculus CDH8 MGD MGI:107434
Bos taurus CDH8 VGNC VGNC:109398
Others CDH8 NCBI