2. Gene
  3. CEBPD - CCAAT enhancer binding protein delta Gene

CEBPD - CCAAT enhancer binding protein delta Gene

  • 基因
  • 蛋白
  • 疾病
  • 相关产品
  • 直系同源

中文名称：CCAAT 增强子结合蛋白 delta

种属: Homo sapiens

同用名: CELF; CRP3; C/EBP-delta; NF-IL6-beta

基因 ID: 1052 | 基因类型: protein coding

关于 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.

功能概要

由这种无内含子基因编码的蛋白质是一种 bZIP 转录因子，它可以作为同型二聚体与某些 DNA 调控区域结合。它还可以与相关蛋白 CEBP-alpha 形成异二聚体。编码的蛋白质在免疫和炎症反应相关基因的调节中很重要，并且可能参与与巨噬细胞活化和/或分化相关的基因的调节。该基因座的细胞遗传学位置已被报道为 8p11 和 8q11。[RefSeq 提供，2010 年 9 月]

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 基因产物(1)

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

CEBPD 蛋白结构

bZIP_2

bZIP_2: Basic region leucine zipper (191 - 242)

  • 0
  • 100
  • 200
  • 269 a.a.
蛋白主名 其他名称

CCAAT/enhancer-binding protein delta

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

重组 CEBPD 蛋白

目录号 产品名 蛋白编号 纯度
HY-P72134 CEBP delta/CEBPD Protein, Human (His-Myc) P49716 (S2-R269) ≥95%

关联疾病

疾病名称 别名
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
疾病名称 别名
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

相关产品

Pre-clinical Phase
生物活性分子 (1)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS02447 CEBPD Human Pre-designed siRNA Set A / 否

直系同源

种属 基因名 来源 基因 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
嗨！很高兴为您提供帮助！

尊敬的 MCE 客户您好，
请您选择所在区域，我们将转接对应客服为您服务！

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z

热 A B C F G H J L N Q S T X Y Z