2. Gene
  3. RERGL - RERG like Gene

RERGL - RERG like Gene

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

中文名称：样

种属: Homo sapiens

基因 ID: 79785 | 基因类型: protein coding

关于 RERGL

This gene has 5 transcripts (splice variants), 157 orthologues and 35 paralogues. Broad expression in endometrium (RPKM 13.0), fat (RPKM 12.7) and 18 other tissues.

功能概要

预测启用 G 蛋白活性和 GTP 结合活性。 [由基因组资源联盟提供，2022 年 4 月]

Predicted to enable G protein activity and GTP binding activity. [provided by Alliance of Genome Resources, Apr 2022]

RERGL 基因产物(2)

mRNA Protein Name
NM_001286201.2 NP_001273130.1 ras-related and estrogen-regulated growth inhibitor-like protein isoform b
NM_024730.4 NP_079006.1 ras-related and estrogen-regulated growth inhibitor-like protein isoform a

RERGL 蛋白结构

Ras

Ras: Ras family (19 - 173)

  • 0
  • 100
  • 205 a.a.
蛋白主名 其他名称

ras-related and estrogen-regulated growth inhibitor-like protein

RERG/RAS-like

关联疾病

疾病名称 别名
Viral Labyrinthitis

Epidemic Vertigo

Vestibular Neuronitis
Episodic Ataxia, Type 4

Episodic Ataxia Type 4

Periodic Vestibulocerebellar Ataxia

Patx

EA4

Ataxia, Periodic Vestibulocerebellar
Corneal Dystrophy, Subepithelial Mucinous

Subepithelial Mucinous Corneal Dystrophy

SMCD
Episodic Ataxia, Type 3

Episodic Ataxia Type 3

EA3

Ataxia, Episodic, With Vertigo And Tinnitus

Episodic Ataxia-Vertigo-Tinnitus-Myokymia Syndrome
Episodic Ataxia, Type 7

Episodic Ataxia Type 7

EA7
Temtamy Syndrome

TEMTYS

Craniofacial Dysmorphism With Ocular Coloboma Absent Corpus Callosum And Aortic Dilatation

Craniofacial Dysmorphism-Coloboma-Corpus Callosum Agenesis Syndrome

Dysmorphism, Corpus Callosum Agenesis And Colobomas

Temtamy-Shalash Syndrome

Mental Retardation With Or Without Craniofacial Dysmorphism, Ocular Coloboma, Or Abnormal Corpus Callosum
Episodic Ataxia, Type 5

Episodic Ataxia Type 5

EA5

Episodic Ataxia 5

Ea-5

Ataxia, Episodic, Type 5
Cantu Syndrome

Hypertrichotic Osteochondrodysplasia

Hypertrichotic Osteochondrodysplasia Cantu Type

Cantú Syndrome

Craniofaciocardioskeletal Syndrome

Hypertrichosis-Osteochondrodysplasia-Cardiomegaly Syndrome

Congenital Hypertrichosis-Acromegaloid Facial Features Spectrum

Congenital Hypertrichosis-Coarse Facial Features Spectrum

HTOCD

Osteochondrodysplasia, Hypertrichotic
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-RS11850 RERGL Human 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 RERGL RGD RGD:1560090
Bos taurus RERGL VGNC VGNC:33874
Canis familiaris RERGL VGNC VGNC:45479
Felis catus RERGL VGNC VGNC:64575
Macaca mulatta RERGL VGNC VGNC:100099
Mus musculus RERGL MGD MGI:3642998
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