CNTNAP3B - contactin associated protein family member 3B Gene

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 728577

About CNTNAP3B

This gene has 15 transcripts (splice variants), 289 orthologues and 35 paralogues. Ubiquitous expression in esophagus (RPKM 5.1), fat (RPKM 3.4) and 22 other tissues.

Summary

Predicted to be involved in cell adhesion. Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

CNTNAP3B Products (1)

mRNA Protein Name
NM_001201380.3 NP_001188309.2 contactin-associated protein-like 3B precursor

CNTNAP3B Protein Structure

F5_F8_type_C

F5_F8_type_C: F5/8 type C domain (45 - 174)

Laminin_G_2

Laminin_G_2: Laminin G domain (212 - 340)

Laminin_G_2

Laminin_G_2: Laminin G domain (398 - 521)

Laminin_G_2

Laminin_G_2: Laminin G domain (821 - 939)

Laminin_G_2

Laminin_G_2: Laminin G domain (1046 - 1174)

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  • 1288 a.a.
Protein Preferred Names Protein Names

contactin-associated protein-like 3B

  • cell recognition molecule Caspr3b

Related Diseases

Diseases Alias
Bladder Exstrophy

  • Exstrophy Of The Bladder

  • Classic Exstrophy Of The Bladder
Cloacal Exstrophy

  • Oeis Complex

  • Omphalocele-Cloacal Exstrophy-Imperforate Anus-Spinal Defect Syndrome

  • Omphalocele, Exstrophy Of The Cloaca, Imperforate Anus, And Spinal Defects Compl

  • Omphalocele, Exstrophy Of The Cloaca, Imperforate Anus, And Spinal Defects Complex

  • Cloacal Exstrophy Sequence

  • Omphalocele - Cloacal Exstrophy - Imperforate Anus - Spinal Defect

  • Omphalocele, Exstrophy Of The Cloaca, Imperforate Anus, And Spinal Defects

  • Omphalocele Exstrophy Imperforate Anus
Bladder Exstrophy-Epispadias-Cloacal Exstrophy Complex

  • Exstrophy-Epispadias Complex

  • Bladder Exstrophy-Epispadias-Cloacal Extrophy Complex

  • Beec

  • Eec

  • Exstrophy Of The Bladder

  • Bladder Exstrophy

  • Bladder Exstrophy And Epispadias Complex
Developmental And Epileptic Encephalopathy 76

  • DEE76

  • Epileptic Encephalopathy, Early Infantile, 76

  • Eiee76

  • Decam

  • Developmental And Epileptic Encephalopathy, 76

  • Developmental Delay, Epileptic Encephalopathy, Cerebral Atrophy, And Abnormal Myelination

  • Developmental Delay, Epileptic Endephalopathy, Cerebral Atrophy, And Abnormal Myelination

  • Early Infantile Epileptic Encephalopathy 76
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

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS02935 CNTNAP3B Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Mus musculus CNTNAP3B MGD MGI:3588199