2. Gene
  3. ELFN1 - extracellular leucine rich repeat and fibronectin type III domain containing 1 Gene

ELFN1 - extracellular leucine rich repeat and fibronectin type III domain containing 1 Gene

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

中文名称：含细胞外富亮氨酸的重复序列和纤连蛋白 III 型结构域 1

种属: Homo sapiens

同用名: PPP1R28

基因 ID: 392617 | 基因类型: protein coding

关于 ELFN1

Cytogenetic location: 7p22.3 Genomic coordinates (GRCh38): 7:1,666,064-1,747,946 (from NCBI)

This gene has 4 transcripts (splice variants), 247 orthologues, 22 paralogues and is associated with 1 phenotype. Broad expression in liver (RPKM 1.3), kidney (RPKM 0.9) and 14 other tissues.

功能概要

预测可启用蛋白磷酸酶抑制剂活性。预计参与突触组织。预测位于树突和兴奋性突触中。预计在细胞外基质和细胞外空间中具有活性。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable protein Phosphatase Inhibitor activity. Predicted to be involved in synapse organization. Predicted to be located in dendrite and excitatory synapse. Predicted to be active in extracellular matrix and extracellular space. [provided by Alliance of Genome Resources, Apr 2022]

ELFN1 基因产物(3)

mRNA Protein Name
NM_001128636.4 NP_001122108.1 protein ELFN1 precursor
NM_001394187.1 NP_001381116.1 protein ELFN1 precursor
NM_001394188.1 NP_001381117.1 protein ELFN1 precursor

ELFN1 蛋白结构

LRR_8

LRR_8: Leucine rich repeat (109 - 168)

  • 0
  • 200
  • 400
  • 600
  • 828 a.a.
蛋白主名 其他名称

protein ELFN1

extracellular leucine-rich repeat and fibronectin type III containing 1

关联疾病

疾病名称 别名
Congenital Stationary Night Blindness

Night Blindness, Congenital Stationary

Congenital Essential Nyctalopia

Oguchi Disease

Blindness, Night, Stationary, Congenital
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
Cone-Rod Dystrophy 2

Cone-Rod Dystrophy

CORD2

Cone-Rod Retinal Dystrophy

Rcrd2

Cone-Rod Retinal Dystrophy 2

Crd2

Cord

Crd

Retinal Cone-Rod Dystrophy

Cone-Rod Retinal Dystrophy-2

Retinal Cone-Rod Dystrophy 2

Tapetoretinal Degeneration

Cone-Rod Degeneration

Cone Rod Dystrophy

Dystrophy, Cone-Rod

Dystrophy, Cone-Rod, Type 2

Retinitis Pigmentosa

Retinitis Pigmentosa 2

Progressive Cone-Rod Dystrophy
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 (2)
Cat. No. 产品名 作用方式
纯度 是否罕见病
HY-RS04303 ELFN1 Human Pre-designed siRNA Set A Pre-designed Set / 否
HY-RS22483 Elfn1 Mouse Pre-designed siRNA Set A Pre-designed Set / 否

直系同源

种属 基因名 来源 基因 ID
Rattus norvegicus ELFN1 RGD RGD:1308787
Macaca mulatta ELFN1 VGNC VGNC:72204
Bos taurus ELFN1 VGNC VGNC:28431
Mus musculus ELFN1 MGD MGI:2442479
Felis catus ELFN1 VGNC VGNC:80569
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