GLG1 - golgi glycoprotein 1 Gene

Homo sapiens

Also known as CFR-1; ESL-1; MG160; MG-160

Gene ID: 2734 | Gene type: protein coding

About GLG1

Cytogenetic location: 16q23.1 Genomic coordinates (GRCh38): 16:74,447,440-74,607,114 (from NCBI)

This gene has 14 transcripts (splice variants) and 284 orthologues. Ubiquitous expression in ovary (RPKM 26.0), testis (RPKM 23.5) and 25 other tissues.

Summary

Predicted to enable Fibroblast Growth Factor binding activity. Predicted to act upstream of or within several processes, including negative regulation of protein processing; negative regulation of transforming growth factor beta receptor signaling pathway; and regulation of chondrocyte differentiation. Located in Golgi apparatus. [provided by Alliance of Genome Resources, Apr 2022]

GLG1 Products(3)

mRNA	Protein	Name
NM_001145666.2	NP_001139138.1	Golgi apparatus protein 1 isoform 2 precursor
NM_001145667.2	NP_001139139.1	Golgi apparatus protein 1 isoform 3 precursor
NM_012201.6	NP_036333.2	Golgi apparatus protein 1 isoform 1 precursor

GLG1 Protein Structure

Cys_rich_FGFR

0
200
400
600
800
1000
1179 a.a.

Protein Preferred Names

Protein Names

Golgi apparatus protein 1

E-selectin ligand 1

Related Diseases

Diseases

Alias

Algoneurodystrophy

Reflex Sympathetic Dystrophy

Algoneurodystrophy, Site Unspecified

Pontocerebellar Hypoplasia, Type 2e

Pontocerebellar Hypoplasia Type 2	Pontocerebellar Hypoplasia Type 2e
Pch2	PCH2E
Progressive Microcephaly From Birth Extrapyramidal Dyskinesia Chorea Epilepsy	Pontocerebellar Hypoplasia 2e
Pcca2	Progressive Cerebello-Cerebral Atrophy Type 2
Doid:0112328	Hypoplasia, Pontocerebellar, Type 2e
Pontocerebellar Hypoplasia, Type 2d	Pontocerebellar Hypoplasia Type 2a

Trichinosis

Trichinellosis	Human Trichinellosis
Trichiniasis	Trichinella Spiralis Infection
Infection With Trichinella	Trichinelliasis
Trichinella Spiralis Infestation

Amyotrophic Lateral Sclerosis 1

Amyotrophic Lateral Sclerosis	ALS
Lou Gehrig Disease	Amyotrophic Lateral Sclerosis Type 1
Charcot Disease	ALS1
Amyotrophic Lateral Sclerosis, Susceptibility To	Fals
Lou Gehrig'S Disease	Mnd
Motor Neuron Disease	Familial Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 1, Familial	Amyotrophic Lateral Sclerosis 1, Autosomal Dominant
Motor Neuron Disease, Bulbar	Motor Neurone Disease
Amyotrophic Lateral Sclerosis With Dementia	Dementia With Amyotrophic Lateral Sclerosis
Motor Neuron Disease, Amyotrophic Lateral Sclerosis	Sclerosis, Lateral, Amyotrophic
Sclerosis, Lateral, Amyotrophic, Type 1	Amyotrophic Sclerosis
Als - [Amyotrophic Lateral Sclerosis]	Wasting Palsy
Amyotrophic Paralysis	Amyotrophy Lateral Sclerosis
Wasting Paralysis	Spinal Progressive Amyotrophy
Progressive Atrophic Paralysis

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

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS05471	GLG1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Bos taurus	GLG1	VGNC	VGNC:29398
Rattus norvegicus	GLG1	RGD	RGD:69345
Mus musculus	GLG1	MGD	MGI:104967
Macaca mulatta	GLG1	VGNC	VGNC:73068
Felis catus	GLG1	VGNC	VGNC:62577
Canis familiaris	GLG1	VGNC	VGNC:41255