DIP2C - disco interacting protein 2 homolog C Gene

Homo sapiens

Also known as KIAA0934

Gene ID: 22982 | Gene type: protein coding

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

AMP-binding

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

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS03774	DIP2C Human Pre-designed siRNA Set A	Pre-designed Sets	/	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

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