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  2. GPR33 - G protein-coupled receptor 33 Gene

GPR33 - G protein-coupled receptor 33 Gene

中文名称:G 蛋白偶联受体 33

种属: Homo sapiens

基因 ID: 2856 | 基因类型: protein coding

关于 GPR33

Cytogenetic location: 14q12 Genomic coordinates (GRCh38): 14:31,482,875-31,488,039 (from NCBI)

This gene has 1 transcript (splice variant), 232 orthologues and 8 paralogues. Low expression observed in reference dataset.

功能概要

该基因已被鉴定为孤儿趋化 G 蛋白偶联受体 (GPCR) 假基因。研究表明,失活基因在人群中作为主要等位基因存在。已发现一小部分人群具有完整的等位基因。[RefSeq 提供,2010 年 10 月]

This gene has been identified as an orphan chemoattractant G-protein-coupled receptors (GPCR) pseudogene. Studies have shown that the inactivated gene is present as the predominant allele in the human population. A small fraction of the human population has been found to harbor an intact allele.[provided by RefSeq, Oct 2010]

GPR33 基因产物(1)

mRNA Protein Name
NM_001197184.3 NP_001184113.2 probable G-protein coupled receptor 33
蛋白主名 其他名称

probable G-protein coupled receptor 33

G protein-coupled receptor 33 pseudogene

关联疾病

疾病名称 别名
Epiphyseal Dysplasia, Multiple, 1

EDM1

Multiple Epiphyseal Dysplasia 1

Multiple Epiphyseal Dysplasia Type 1

Med1

Multiple Epiphyseal Dysplasia Comp-Related

Polyepiphyseal Dysplasia Type 1

Multiple Epiphyseal Dysplasia, Comp-Related

Epiphyseal Dysplasia Multiple 1

Epiphyseal Dysplasia, Multiple 1

Dysplasia, Epiphyseal, Multiple, Type 1

Epiphyseal Dysplasia, Multiple, 2

EDM2

Multiple Epiphyseal Dysplasia 2

Dysplasia, Epiphyseal, Multiple, Type 2

Multiple Epiphyseal Dysplasia Due To Collagen 9 Anomaly
Miles-Carpenter Syndrome

X-Linked Intellectual Disability, Miles-Carpenter Type

Mcs

Mental Retardation, X-Linked, Syndromic 4

Mental Retardation, X-Linked, With Congenital Contractures And Low Fingertip Arches

Mrxs4

Miles-Carpenter X-Linked Mental Retardation Syndrome

Multiple Epiphyseal Dysplasia

Med

Polyepiphyseal Dysplasia

Edm

Epiphyseal Dysplasia, Multiple, 1

Epiphyseal Dysplasia, Multiple, 2

Epiphyseal Dysplasia, Multiple, 3

Epiphyseal Dysplasia, Multiple, 4

Epiphyseal Dysplasia, Multiple, 5

Epiphyseal Dysplasia, Multiple

Edm1

Edm2

Edm3

Edm4

Edm5

Epiphyseal Dysplasia, Fairbank Type

Epiphyseal Dysplasia, Ribbing Type

Multiple Epiphyseal Dysplasia, Autosomal Dominant

Multiple Epiphyseal Dysplasia, Autosomal Recessive

Rmed

Dysplasia, Epiphyseal, Multiple

Osteochondrodysplasias

Nephrogenic Syndrome Of Inappropriate Antidiuresis

NSIAD

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
Felis catus GPR33 VGNC VGNC:103732
Mus musculus GPR33 MGD MGI:1277106
Bos taurus GPR33 VGNC VGNC:53938
Rattus norvegicus GPR33 RGD RGD:1306830
Canis familiaris GPR33 VGNC VGNC:53496
Macaca mulatta GPR33 VGNC VGNC:84344