GOLPH3 - golgi phosphoprotein 3 Gene

中文名称：高尔基磷蛋白 3

种属: Homo sapiens

同用名: GOPP1; GPP34; MIDAS; Vps74

基因 ID: 64083 | 基因类型: protein coding

关于 GOLPH3

Cytogenetic location: 5p13.3 Genomic coordinates (GRCh38): 5:32,124,716-32,174,319 (from NCBI)

This gene has 3 transcripts (splice variants), 142 orthologues and 1 paralogue. Ubiquitous expression in gall bladder (RPKM 38.1), prostate (RPKM 32.0) and 25 other tissues.

功能概要

高尔基复合体在内质网输出的蛋白质的分类和修饰中起着关键作用。由该基因编码的蛋白质是高尔基体堆栈的外周膜蛋白，可能在高尔基体运输中具有调节作用。已经描述了该基因的几种可变剪接的转录本变体，但尚未确定这些变体的全长性质。[RefSeq 提供，2008 年 7 月]

The Golgi complex plays a key role in the sorting and modification of proteins exported from the endoplasmic reticulum. The protein encoded by this gene is a peripheral membrane protein of the Golgi stack and may have a regulatory role in Golgi trafficking. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of these variants has not been determined. [provided by RefSeq, Jul 2008]

GOLPH3 基因产物(1)

mRNA	Protein	Name
NM_022130.4	NP_071413.1	Golgi phosphoprotein 3

GOLPH3 蛋白结构

GPP34

0
100
200
298 a.a.

蛋白主名

其他名称

Golgi phosphoprotein 3

coat protein GPP34

GOLPH3 蛋白互作信息

分类	蛋白名称	蛋白编号	互作蛋白	互作蛋白种属	互作蛋白编号	实验方法	参考文献
种属内	GOLPH3	Q9H4A6	XRCC5	Homo sapiens	P13010	Anti Bait CoIP	24485452
种属内	GOLPH3	Q9H4A6	ARL6IP1	Homo sapiens	Q15041	Y2H Array	25416956
种属内	GOLPH3	Q9H4A6	ARL6IP1	Homo sapiens	Q15041	Validated Y2H	25416956
种属内	GOLPH3	Q9H4A6	GCNT1	Homo sapiens	Q02742	Y2H	23027862
种属内	GOLPH3	Q9H4A6	GCNT1	Homo sapiens	Q02742	Confocal	23027862
种属内	GOLPH3	Q9H4A6	GCNT1	Homo sapiens	Q02742	Pull Down	23027862
种属内	GOLPH3	Q9H4A6	MYO18A	Homo sapiens	Q92614	Pull Down	19837035

种属间: 跨种属相互作用 种属内: 同种属相互作用

关联疾病

疾病名称

别名

Anemia, Congenital Dyserythropoietic, Type Ii

Congenital Dyserythropoietic Anemia Type Ii	CDAN2
Cda Ii	Hereditary Erythroblastic Multinuclearity With Positive Acidified-Serum Test
Cda Type Ii	Congenital Dyserythropoietic Anemia Type 2
Hereditary Erythroblastic Multinuclearity With A Positive Acidified-Serum Test	Sec23b-Cdg
Congenital Dyserythropoietic Anemia, Type Ii	Dyserythropoietic Anemia, Hempas Type
Hempas	Cda Type 2
Dyserythropoietic Anemia, Congenital, Type Ii	Cda, Type Ii
Congenital Dyserythropoietic Anaemia Type 2	Congenital Dyserythropoietic Anaemia Type Ii
Anemia, Dyserythropoietic, Congenital Type 2	Hempas Anemia
Dyserythropoietic Anemia, Congenital Type 2	Anemia, Congenital Dyserythropoietic, 2
Dyserythropoietic Anemia Hempas Type	Anemia, Dyserythropoietic Congenital, Type Ii
Anemia, Dyserythropoietic, Congenital, Type Ii

Dyggve-Melchior-Clausen Disease

Dyggve-Melchior-Clausen Syndrome	DMC
Dmc Disease	Pseudo-Morquio Disease Type I
Dmc Syndrome

Spondyloepiphyseal Dysplasia Tarda, X-Linked

Spondyloepiphyseal Dysplasia Tarda	X-Linked Spondyloepiphyseal Dysplasia Tarda
SEDT	Sed Tarda, X-Linked
Spondyloepiphyseal Dysplasia, Late	Spondyloepiphyseal Dysplasia Tarda X-Linked
Sed	X Linked Spondyloepiphyseal Dysplasia Tarda
X-Linked Spondyloepiphyseal Dysplasia	Late Onset Spondyloepiphyseal Dysplasia
Sed Tarda	X-Linked Sed
X-Linked Sedt	Dysplasia, Spondyloepiphyseal, Tarda
Spondyloepiphyseal Dysplasia

Craniolenticulosutural Dysplasia

Boyadjiev-Jabs Syndrome	CLSD
Cranio-Lenticulo-Sutural Dysplasia	Cranio-Lenticulo-Sutural Dysplasia, Clsd

Geroderma Osteodysplasticum

Gerodermia Osteodysplastica	Geroderma Osteodysplastica
GO	Walt Disney Dwarfism
Type Of Gerodermia Osteodysplastica

Chylomicron Retention Disease

CMRD	Anderson Disease
Lipid Transport Defect Of Intestine	Hypobetalipoproteinemia With Accumulation Of Apolipoprotein B-Like Protein In Intestinal Cells
Andd	Anderson Syndrome
Crd	Andersons Disease
Malabsorption Syndrome

Congenital Disorder Of Glycosylation, Type In

Congenital Disorder Of Glycosylation	CDG1N
Congenital Disorders Of Glycosylation	Cdg In
Cdgin	Congenital Disorder Of Glycosylation 1n
Carbohydrate-Deficient Glycoprotein Syndrome	Cdg
Rft1-Cdg	Cdg-In
Congenital Disorder Of Glycosylation Type In	Carbohydrate Deficient Glycoprotein Syndrome
Cdg Syndrome	Congenital Disorder Of Glycosylation In
Carbohydrate-Deficient Glycoprotein Syndromes	Cdg Syndrome Type In
Carbohydrate Deficient Glycoprotein Syndrome Type In	Congenital Disorder Of Glycosylation Type 1n
Man5glcnac2-Pp-Dol Flippase Deficiency	Glycosylation, Congenital Disorder Of
Glycosylation, Congenital Disorder Of, Type In

Hereditary Spastic Paraplegia

Familial Spastic Paraplegia	Hereditary Spastic Paraparesis
Strumpell-Lorrain Disease	Familial Spastic Paraparesis
Hsp	Spg
Strümpell-Lorrain Disease	Spastic Paraplegia, Hereditary
French Settlement Disease	Strumpell-Lorrain Syndrome
Fsp	Spastic Paraplegia, Familial
Spastic Paraplegia Hereditary	Spastic Paraplegia 3, Autosomal Dominant
Spastic Paraparesis	Hereditary Spastic Paralysis
Familial Spastic Paralysis	Hereditary Spastic Ataxia

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

Cat. No.	产品名	作用方式	纯度	是否罕见病
HY-RS05594	GOLPH3 Human Pre-designed siRNA Set A	Pre-designed Sets	/	否
HY-RS05595	GOLPH3L Human Pre-designed siRNA Set A	Pre-designed Sets	/	否

直系同源

种属	基因名	来源	基因 ID
Rattus norvegicus	GOLPH3	RGD	RGD:621226
Macaca mulatta	GOLPH3	VGNC	VGNC:72947
Bos taurus	GOLPH3	VGNC	VGNC:29492
Mus musculus	GOLPH3	MGD	MGI:1913879
Canis familiaris	GOLPH3	VGNC	VGNC:49691

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MedChemExpress (MCE) 只为有资质的科研机构、医药企业基于科学研究或药证申报的用途提供医药研发服务，不为任何个人或者非科研性质的、非用于药证申报使用等其他用途提供服务。

站点地图隐私声明

沪ICP备15051369号-4

上海工商

沪公网安备31011502019417

沪(浦)应急管危经许[2021]201709(QFYS)

营业执照（三证合一）

GOLPH3 - golgi phosphoprotein 3 Gene

关于 GOLPH3

功能概要

GOLPH3 基因产物(1)

GOLPH3 蛋白结构

GOLPH3 蛋白互作信息

关联疾病

直系同源

热门区域

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GOLPH3 - golgi phosphoprotein 3 Gene

关于 GOLPH3

功能概要

GOLPH3 基因产物(1)

GOLPH3 蛋白结构

GOLPH3 蛋白互作信息

关联疾病

相关产品

直系同源

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z