CEBPD - CCAAT enhancer binding protein delta Gene

Homo sapiens

Also known as CELF; CRP3; C/EBP-delta; NF-IL6-beta

Gene ID: 1052 | Gene type: protein coding

About CEBPD

Cytogenetic location: 8q11.21 Genomic coordinates (GRCh38): 8:47,736,913-47,738,164 (from NCBI)

This gene has 1 transcript (splice variant), 158 orthologues and 4 paralogues.

Summary

The protein encoded by this intronless gene is a bZIP transcription factor which can bind as a homodimer to certain DNA regulatory regions. It can also form heterodimers with the related protein CEBP-alpha. The encoded protein is important in the regulation of genes involved in immune and inflammatory responses, and may be involved in the regulation of genes associated with activation and/or differentiation of macrophages. The cytogenetic location of this locus has been reported as both 8p11 and 8q11. [provided by RefSeq, Sep 2010]

CEBPD Products(1)

mRNA	Protein	Name
NM_005195.4	NP_005186.2	CCAAT/enhancer-binding protein delta

CEBPD Protein Structure

bZIP_2

0
100
200
269 a.a.

Protein Preferred Names

Protein Names

CCAAT/enhancer-binding protein delta

CCAAT/enhancer binding protein (C/EBP), delta

Recombinant CEBPD Proteins

Cat. No.	Product Name	Accession	Purity
HY-P72134	CEBP delta/CEBPD Protein, Human (His-Myc)	P49716 (S2-R269)	≥95%

Related Diseases

Diseases

Alias

Speech And Communication Disorders

Language Disorder	Communication Disorder
Language Disorders	Communication Disorders
Speech Language Disorder	Speech-Language Disorder
Communication Impairment	Speech And Language Disorder

Developmental Coordination Disorder

Motor Skills Disorders

Expressive Language Disorder

Developmental Expressive Language Disorder

Specific Language Impairment

Language Impairment, Specific

Mixed Receptive-Expressive Language Disorder

Myotonic Disease

Myotonic Disorders	Myotonic Syndrome
Symptomatic Myotonia

Reading Disorder

Specific Reading Disorder	Reading
Dyslexia	Developmental Reading Disorder

Dysgraphia

Agraphia

Learning Disability

Learning Disabilities	Learning Disorders
Academic Skill Disorder	Learning Disorder

Articulation Disorder

Phonological Disorder	Articulation Disorders
Articulation Impairment	Speech Sound Disorders

Speech Disorder

Speech Disorders

Myotonic Dystrophy 1

Myotonic Dystrophy	Dystrophia Myotonica
Steinert Disease	Myotonic Dystrophy Type 1
Myotonia Atrophica	DM1
Congenital Myotonic Dystrophy	Myotonia Dystrophica
Steinert Myotonic Dystrophy	Dystrophia Myotonica 1
Dm	Steinert'S Disease
Steinert Myotonic Dystrophy Syndrome	Myotonic Dystrophy Of Steinert
Dystrophia Myotonica Type 1	Myotonic Dystrophy Congenital
Dystrophy, Myotonic, Type 1	Dm - [Dystrophia Myotonica]
Myotonic Muscular Dystrophy

Echolalia

Spinocerebellar Ataxia 8

Spinocerebellar Ataxia Type 8	SCA8
Ataxia, Spinocerebellar, Type 8

Dyslexia

Stuttering

Stammering	Familial Persistent Stuttering
Stuttering, Familial Persistent 1

Attention Deficit-Hyperactivity Disorder

Attention Deficit Hyperactivity Disorder	ADHD
Attention Deficit Disorder	Attention Deficit-Hyperactivity Disorder, Susceptibility To
Attention Deficit Disorder With Hyperactivity	Hyperkinetic Disorder
Hyperactivity Of Childhood	Attention-Deficit/Hyperactivity Disorder
Add	Addh
Attention Deficit	Attention Deficit Disorder Of Childhood With Hyperactivity
Attention Deficit Disorder With Hyperactivity Syndrome	Hyperkinetic Syndrome
Attention-Deficit Hyperactivity Disorder	Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type
Disturbance Of Activity And Attention	Disorder Of Activity And Attention
Adhd - [Attention Deficit Hyperactivity Disorder]	Hyperkinetic Disorders
Disorder Of Activity And Attention With Hyperkinesia	Attention Deficit Syndrome With Hyperactivity

Benign Epilepsy With Centrotemporal Spikes

Rolandic Epilepsy	Benign Rolandic Epilepsy
Epilepsy, Rolandic	Bcects
Benign Childhood Epilepsy With Centrotemporal Spike	Sylvan Seizures
Becrs	Bects
Bre	Benign Epilepsy Of Childhood With Centrotemporal Spikes
Benign Familial Epilepsy Of Childhood With Rolandic Spikes	Centrotemporal Epilepsy

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-RS02447	CEBPD Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	CEBPD	VGNC	VGNC:106685
Rattus norvegicus	CEBPD	RGD	RGD:2328
Mus musculus	CEBPD	MGD	MGI:103573
Macaca mulatta	CEBPD	VGNC	VGNC:83988
Others	CEBPD	NCBI

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