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  2. IL31RA - interleukin 31 receptor A Gene

IL31RA - interleukin 31 receptor A Gene

中文名称:白介素 31 受体 A

种属: Homo sapiens

同用名: CRL; GPL; CRL3; GLMR; GLM-R; PLCA2; hGLM-R; IL-31RA; PRO21384; zcytoR17

基因 ID: 133396 | 基因类型: protein coding

关于 IL31RA

Cytogenetic location: 5q11.2 Genomic coordinates (GRCh38): 5:55,839,789-55,922,850 (from NCBI)

This gene has 13 transcripts (splice variants), 174 orthologues, 23 paralogues and is associated with 2 phenotypes. Low expression observed in reference dataset.

功能概要

该基因编码的蛋白质属于 I 型细胞因子受体家族。这种与 gp130 同源的受体在单核细胞上表达,并通过激活 STAT-3 和 STAT-5 参与 IL-31 信号传导。它既可以作为单体,也可以作为与制瘤素 M 受体 (OSMR) 形成的受体复合物的一部分。已经注意到该基因有几种编码不同亚型的可变剪接转录物变体。[RefSeq 提供,2011 年 6 月]

The protein encoded by this gene belongs to the type I cytokine receptor family. This receptor, with homology to gp130, is expressed on monocytes, and is involved in IL-31 signaling via activation of STAT-3 and STAT-5. It functions either as a monomer, or as part of a receptor complex with oncostatin M receptor (OSMR). Several alternatively spliced transcript variants encoding different isoforms have been noted for this gene.[provided by RefSeq, Jun 2011]

IL31RA 基因产物(6)

mRNA Protein Name
NM_001242636.2 NP_001229565.1 interleukin-31 receptor subunit alpha isoform 2 precursor
NM_001242637.2 NP_001229566.1 interleukin-31 receptor subunit alpha isoform 3
NM_001242638.2 NP_001229567.1 interleukin-31 receptor subunit alpha isoform 4 precursor
NM_001242639.2 NP_001229568.1 interleukin-31 receptor subunit alpha isoform 5
NM_001297570.3 NP_001284499.1 interleukin-31 receptor subunit alpha isoform 6
NM_139017.7 NP_620586.3 interleukin-31 receptor subunit alpha isoform 1
基因本体论
  • 生物过程
生物过程 GO 注释 逻辑证据 参考文献 来源
involved in cell surface receptor signaling pathway via JAK-STAT IEP
IEP: 通过表达模式推断
11877449 GOA
involved in monocyte differentiation IEP
IEP: 通过表达模式推断
11877449 GOA
involved in positive regulation of cell population proliferation IDA
IDA: 通过直接分析推断
11877449 GOA
involved in positive regulation of tyrosine phosphorylation of STAT protein IEP
IEP: 通过表达模式推断
11877449 GOA
EXP:通过实验结果推断 IDA:通过直接分析推断 IPI:通过物理相互作用推断 IMP:通过突变表型推断 IGI:通过遗传相互作用推断 IEP:通过表达模式推断

IL31RA 蛋白结构

IL6Ra-bind

IL6Ra-bind: Interleukin-6 receptor alpha chain, binding (56 - 151)

fn3

fn3: Fibronectin type III domain (157 - 246)

fn3

fn3: Fibronectin type III domain (460 - 533)

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

interleukin-31 receptor subunit alpha

IL-31 receptor subunit alpha

重组 IL31RA 蛋白

目录号 产品名 蛋白编号 纯度
HY-P75859 IL-31R alpha Protein, Human (HEK293, Fc) Q8NI17-1/EAW54932.1 (A20-S516) ≥95%
HY-P75860 IL-31R alpha Protein, Human (HEK293, His) Q8NI17-1/EAW54932.1 (A20-S516) ≥95%

关联疾病

疾病名称 别名
Amyloidosis, Primary Localized Cutaneous, 2

PLCA2

Primary Localized Cutaneous Amyloidosis 2

Primary Cutaneous Amyloidosis

Plca

Primary Localized Cutaneous Amyloidosis

Familial Primary Localized Cutaneous Amyloidosis

Amyloidosis Ix

Lichen Amyloidosis Familial

Amyloidosis, Primary Cutaneous

Pca

Amyloidosis 9

Amyloidosis Familial Cutaneous Lichen

Fplca

Familial Lichen Amyloidosis

Dermatitis

Eczema

Skin Inflammation

Inflammatory Dermatosis

Lichen Amyloidosis

Amyloid Lichen

Lichen Amyloidosus

Amyloidosis, Primary Cutaneous

Macular Amyloidosis

Amyloidosis, Macular

Amyloidosis

Amyloid Disease

Amyloid

Amyloid Degeneration

Amyloidosis Nos

Amyloid Deposition

Amyloid Infiltration

Idiopathic Amyloidosis

Hyaloid Degeneration

Lardaceous Degeneration

Amyloidosis, Primary Localized Cutaneous, 3

Amyloidosis Cutis Dyschromica

PLCA3

Acd

Primary Localized Cutaneous Amyloidosis 3

Amyloidosis Cutis Dyschromia

Neurodermatitis
Contact Dermatitis

Contact Dermatitis/Eczema

Contact Eczema

Dermatitis Venenata

Dermatitis, Venenata

Dermatitis Contact

Dermatitis, Contact

Allergic Contact Dermatitis

Dermatitis, Allergic Contact

Contact Dermatitis, Allergic

Dermatitis Allergic Contact

Allergic Contact Eczema

Acd - [Allergic Contact Dermatitis]

Allergic Contact Dermatitis, Unspecified Cause

Allergic Dermatitis

Allergic Eczema

Allergy Dermatitis

Allergy Eczema

Allergic Contact Eczema Due To Clothing Or Footwear

Perfume Allergic Contact Dermatitis

Allergic Contact Dermatitis Due To Cosmetics

Allergic Contact Eczema Due To Cosmetics Or Fragrances

Allergic Contact Eczema Due To Dental Materials

Allergic Contact Eczema Due To Food Flavours Or Additives

Allergic Contact Eczema Due To Hairdressing Products

Allergic Contact Eczema Due To Metals Or Metal Salts

Allergic Contact Eczema Due To Proteins

Allergic Contact Eczema Due To Plastics Or Resin Systems

Allergic Contact Eczema Due To Preservatives Or Biocides

Allergic Contact Eczema Due To Rubber Chemicals

Rubber Dermatitis

Allergic Contact Eczema Due To Systemic Medicaments

Allergic Contact Eczema Due To Topical Medicaments

Allergic Contact Dermatitis Due To Drugs In Contact With Skin

Dermatitis, Atopic

Atopic Dermatitis

Atopic Eczema

Dermatitis, Atopic, Susceptibility To, 1

Atod

Eczema, Atopic

Dermatitis, Atopic 1

Allergic Dermatitis

Atopic Neurodermatitis

Besnier'S Prurigo

Dermatitis, Atopic, 1

Dermatitis Atopic

Eczema

Besnier Prurigo

Congenital Central Hypoventilation Syndrome

Cchs

Haddad Syndrome

Ondine Curse

Ondine Syndrome

Congenital Central Hypoventilation

Congenital Central Alveolar Hypoventilation Syndrome

Congenital Failure Of Autonomic Control

Ondine'S Curse

Primary Alveolar Hypoventilation

Ondine-Hirschsprung Disease

Central Congenital Hypoventilation Syndrome

Congenital Ondine Curse

Idiopathic Congenital Central Alveolar Hypoventilation

Congenital Central Alveolar Hypoventilation-Hirschsprung Disease Syndrome

Ondine-Hirschsprung Syndrome

Noonan Syndrome 1

Noonan Syndrome

NS1

Male Turner Syndrome

Female Pseudo-Turner Syndrome

Turner Phenotype With Normal Karyotype

Noonan Syndrome With Pigmented Villonodular Synovitis

Turner'S Phenotype, Karyotype Normal

Familial Turner Syndrome

Noonan'S Syndrome

Noonan-Ehmke Syndrome

Ns

Pseudo-Ullrich-Turner Syndrome

Turner Syndrome In Female With X Chromosome

Turner-Like Syndrome

Ullrich-Noonan Syndrome

Noonan-Like/Multiple Giant Cell Lesion Syndrome

Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions

Pterygium Colli Syndrome

Noonan Syndrome, Type 1

Turner Syndrome, Male

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

直系同源

种属 基因名 来源 基因 ID
Mus musculus IL31RA MGD MGI:2180511
Rattus norvegicus IL31RA RGD RGD:1586478
Macaca mulatta IL31RA VGNC VGNC:73624
Bos taurus IL31RA VGNC VGNC:30154
Felis catus IL31RA VGNC VGNC:62911
Canis familiaris IL31RA VGNC VGNC:41981
Others IL31RA NCBI