DIP2C - disco interacting protein 2 homolog C Gene

Also Known as KIAA0934

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 22982

About DIP2C

Cytogenetic location: 10p15.3 Genomic coordinates (GRCh38): 10:274,201-689,668 (from NCBI)

This gene has 5 transcripts (splice variants), 282 orthologues and 2 paralogues. Ubiquitous expression in kidney (RPKM 7.7), brain (RPKM 6.6) and 24 other tissues.

Summary

This gene encodes a member of the disco-interacting protein homolog 2 family. The protein shares strong similarity with a Drosophila protein which interacts with the transcription factor disco and is expressed in the nervous system. [provided by RefSeq, Oct 2008]

DIP2C Products (1)

mRNA Protein Name
NM_014974.3 NP_055789.1 disco-interacting protein 2 homolog C

DIP2C Protein Structure

DMAP_binding

DMAP_binding: DMAP1-binding Domain (9 - 119)

AMP-binding

AMP-binding: AMP-binding enzyme (348 - 799)

AMP-binding

AMP-binding: AMP-binding enzyme (977 - 1422)

  • 0
  • 300
  • 600
  • 900
  • 1200
  • 1556 a.a.
Protein Preferred Names Protein Names

disco-interacting protein 2 homolog C

  • DIP2 disco-interacting protein 2 homolog C

Related Diseases

Diseases Alias
Spastic Hemiplegia

  • Spastic Hemiplegic Cerebral Palsy

  • Hemiplegic Cerebral Palsy

  • Congenital Hemiplegia

  • Hemiplegic Infantile Cerebral Palsy

  • Cerebral Palsy Spastic Hemiplegic

  • Spastic Hemiplegia Cerebral Palsy

  • Hemiplegia, Spastic
Familial Cold Autoinflammatory Syndrome 3

  • Plaid

  • Familial Atypical Cold Urticaria

  • Facu

  • FCAS3

  • Antibody Deficiency And Immune Dysregulation, Plcg2-Associated

  • Plcg2-Associated Antibody Deficiency And Immune Dysregulation

  • Familial Cold Urticaria With Common Variable Immunodeficiency

  • Plcg2 Associated Antibody Deficiency And Immune Dysregulation

  • Antibody Deficiency And Immune Dysregulation Placg2-Associated

  • Autoinflammatory Syndrome, Cold, Familial, Type 3
Middle Cerebral Artery Infarction

  • Infarction, Middle Cerebral Artery

  • Infarction Middle Cerebral Artery
Hypoparathyroidism-Deafness-Renal Disease Syndrome

  • Barakat Syndrome

  • Hypoparathyroidism, Deafness, Renal Disease Syndrome

  • Hdr Syndrome

  • Hypoparathyroidism, Sensorineural Deafness, And Renal Disease
Autism Spectrum Disorder

  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified
Autism

  • Autistic Disorder

  • Autism Susceptibility 1

  • Childhood Autism

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Kanner'S Syndrome

  • Autistic
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-RS03774 DIP2C Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Canis familiaris DIP2C VGNC VGNC:49864
Mus musculus DIP2C MGD MGI:1920179
Felis catus DIP2C VGNC VGNC:61494
Macaca mulatta DIP2C VGNC VGNC:71812
Bos taurus DIP2C VGNC VGNC:28068
Rattus norvegicus DIP2C RGD RGD:1560155
Others DIP2C NCBI