GOLIM4 - golgi integral membrane protein 4 Gene

Homo sapiens

Also known as P138; GIMPC; GOLPH4; GPP130

Gene ID: 27333 | Gene type: protein coding

About GOLIM4

Cytogenetic location: 3q26.2 Genomic coordinates (GRCh38): 3:168,008,689-168,095,924 (from NCBI)

This gene has 3 transcripts (splice variants) and 205 orthologues. Ubiquitous expression in small intestine (RPKM 37.0), colon (RPKM 33.7) and 24 other tissues.

Summary

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 type II Golgi-resident protein. It may process proteins synthesized in the rough endoplasmic reticulum and assist in the transport of protein cargo through the Golgi apparatus. [provided by RefSeq, Jul 2008]

GOLIM4 Products(2)

mRNA	Protein	Name
NM_001308155.2	NP_001295084.1	Golgi integral membrane protein 4 isoform 2
NM_014498.5	NP_055313.1	Golgi integral membrane protein 4 isoform 1

Protein Preferred Names

Protein Names

Golgi integral membrane protein 4

130 kDa golgi-localized phosphoprotein

Related Diseases

Diseases

Alias

Congenital Disorder Of Glycosylation, Type Iig

CDG2G	Congenital Disorder Of Glycosylation Type Iig
Cdg Iig	Cdgiig
Cdgii/Cog1 Cerebrocostomandibular-Like Syndrome	Carbohydrate Deficient Glycoprotein Syndrome Type Iig
Cdg-Iig	Congenital Disorder Of Glycosylation, Type 2g
Cog1-Cdg	Cdg Syndrome Type Iig
Congenital Disorder Of Glycosylation Type 2g	Congenital Disorder Of Glycosylation 2g
Cdg-Ii Caused By Cog1 Deficiency	Glycosylation, Congenital Disorder Of, Type Iig

Spinal Muscular Atrophy, Distal, Autosomal Recessive, 3

Distal Spinal Muscular Atrophy Type 3	DSMA3
Spinal Muscular Atrophy, Chronic Distal, Autosomal Recessive	Autosomal Recessive Distal Spinal Muscular Atrophy Type 3
Dhmn3 And Dhmn4	Distal Hereditary Motor Neuropathy Type 3 And Type 4
Neuronopathy, Distal Hereditary Motor, Type Iv	Hmn4
Dhmn4	Neuropathy, Distal Hereditary Motor, Type Iv
Hmn Iv	Neuronopathy, Distal Hereditary Motor, Type Iii
Hmn3	Dhmn3
Hmn Iii

Phosphoglycerate Dehydrogenase Deficiency

Phgdh Deficiency	3-Phosphoglycerate Dehydrogenase Deficiency
PHGDHD	3-Pgdh Deficiency
3-Phosphoglycerate Dehydrogenase Deficiency, Infantile/Juvenile Form	Phgdh Deficiency, Infantile/Juvenile Form
Deficiency, Phosphoglycerate Dehydrogenase

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

Diseases	Alias
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

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS05591	GOLIM4 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	GOLIM4	VGNC	VGNC:29490
Rattus norvegicus	GOLIM4	RGD	RGD:1310948
Felis catus	GOLIM4	VGNC	VGNC:62642
Mus musculus	GOLIM4	MGD	MGI:1920374
Canis familiaris	GOLIM4	VGNC	VGNC:41344
Macaca mulatta	GOLIM4	VGNC	VGNC:72945

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