1. Gene
  2. CADM4 - cell adhesion molecule 4 Gene

CADM4 - cell adhesion molecule 4 Gene

Homo sapiens

Also known as NECL4; TSLL2; IGSF4C; Necl-4; synCAM4

Gene ID: 199731 | Gene type: protein coding

About CADM4

Cytogenetic location: 19q13.31 Genomic coordinates (GRCh38): 19:43,622,368-43,641,984 (from NCBI)

This gene has 2 transcripts (splice variants), 191 orthologues and 14 paralogues. Biased expression in brain (RPKM 59.7), kidney (RPKM 14.7) and 8 other tissues.

Summary

Enables vascular endothelial growth factor receptor 2 binding activity. Involved in several processes, including negative regulation of protein phosphorylation; regulation of Rac protein signal transduction; and regulation of wound healing. Located in cell leading edge and cell-cell contact zone. [provided by Alliance of Genome Resources, Apr 2022]

CADM4 Products(1)

mRNA Protein Name
NM_145296.2 NP_660339.1 cell adhesion molecule 4 precursor

CADM4 Protein Structure

V-set

V-set: Immunoglobulin V-set domain (28 - 117)

C2-set_2

C2-set_2: CD80-like C2-set immunoglobulin domain (130 - 206)

Ig_2

Ig_2: Immunoglobulin domain (228 - 302)

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  • 388 a.a.
Protein Preferred Names Protein Names

cell adhesion molecule 4

TSLC1-like 2

Recombinant CADM4 Proteins

Cat. No. Product Name Accession Purity
HY-P76187 CADM4/IGSF4C Protein, Human (HEK293, His) Q8NFZ8 (M1-Y323) ≥95%
HY-P76188 CADM4/IGSF4C Protein, Human (HEK293, Fc) Q8NFZ8 (M1-Y323) ≥95%

Related Diseases

Diseases Alias
Ciliary Dyskinesia, Primary, 22

Primary Ciliary Dyskinesia 22

CILD22

Primary Ciliary Dyskinesia 22 With Or Without Situs Inversus

Ciliary Dyskinesia, Primary, 22, With Or Without Situs Inversus

Dyskinesia, Ciliary, Primary, 22

Spondylometaphyseal Dysplasia With Cone-Rod Dystrophy

Spondylometaphyseal Dysplasia-Cone-Rod Dystrophy Syndrome

SMDCRD

Smd-Crd

Dysplasia, Spondylometaphyseal, With Cone-Rod Dystrophy

Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive

Charcot-Marie-Tooth Disease Type 4

Charcot-Marie-Tooth Disease Type 4e

Hereditary Motor And Sensory Neuropathy

Cmt4e

CHN1

Hypomyelinating Neuropathy, Congenital, 1

Charcot-Marie-Tooth Neuropathy Type 4e

Neuropathy, Congenital Hypomyelinating, 1

Ar-Cmt1

Autosomal Recessive Demyelinating Charcot-Marie-Tooth

Cmt4

Neuropathy, Congenital Hypomyelinating Or Amyelinating, Autosomal Recessive

Hypomyelination, Severe Congenital

Charcot-Marie-Tooth Disease, Type 4e

Charcot-Marie-Tooth Neuropathy, Type 4e

Autosomal Recessive Congenital Hypomyelinating Or Amyelinating Neuropathy

Autosomal Recessive Congenital Hypomyelinating Neuropathy

Congenital Amyelinating Neuropathy

Congenital Hypomyelinating Neuropathy Autosomal Recessive

Neuropathy, Congenital Hypomyelinating Or Amyelinating

Severe Congenital Hypomyelination

Hereditary Sensory Motor Neuropathy

Charcot-Marie-Tooth Disease, Demyelinating, Autosomal Recessive

Neuropathy, Hypomyelinating, Congenital, Type 1

Neuropathy, Motor And Sensory, Hereditary

Congenital Hypomyelinating Neuropathy

Hereditary Motor And Sensory Neuropathies

Hereditary Sensorimotor Neuropathy

Hmsn - [Hereditary Motor And Sensory Neuropathy]

Hsmn - [Hereditary Sensory And Motor Neuropathy]

Hereditary Motor And Sensory Neuropathy, Types I-Iv

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
Canis familiaris CADM4 VGNC VGNC:53675
Mus musculus CADM4 MGD MGI:2449088
Macaca mulatta CADM4 VGNC VGNC:70681
Rattus norvegicus CADM4 RGD RGD:1304722
Bos taurus CADM4 VGNC VGNC:26697
Felis catus CADM4 VGNC VGNC:60315
Others CADM4 NCBI