GOLIM4 - golgi integral membrane protein 4 Gene

Also Known as P138; GIMPC; GOLPH4; GPP130

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 27333

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

Gene Ontology

  • Cellular Component
Cellular Component GO Annotation Evidence References Source
located in Golgi apparatus IDA
IDA: Inferred from direct assay
9201717 GOA
located in membrane IDA
IDA: Inferred from direct assay
9201717 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

Golgi integral membrane protein 4

  • 130 kDa golgi-localized phosphoprotein

GOLIM4 Antibodies

Cat. No. Product Name Application Reactivity
HY-P82494 GOLPH4 Antibody (YA2239) WB, IHC-P Human

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

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS05591 GOLIM4 Human Pre-designed siRNA Set A Pre-designed Set / 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
Others GOLIM4 NCBI