GLT8D1 - glycosyltransferase 8 domain containing 1 Gene

Also Known as AD-017; MSTP139

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 55830

About GLT8D1

Cytogenetic location: 3p21.1 Genomic coordinates (GRCh38): 3:52,694,486-52,705,791 (from NCBI)

This gene has 15 transcripts (splice variants), 195 orthologues, 1 paralogue and is associated with 1 phenotype. Ubiquitous expression in thyroid (RPKM 29.7), testis (RPKM 28.8) and 25 other tissues.

Summary

This gene encodes a member of the Glycosyltransferase family. The specific function of this protein has not been determined. Alternative splicing results in multiple transcript variants of this gene [provided by RefSeq, May 2013]

GLT8D1 Products (5)

mRNA Protein Name
NM_001010983.3 NP_001010983.1 glycosyltransferase 8 domain-containing protein 1
NM_001278280.2 NP_001265209.1 glycosyltransferase 8 domain-containing protein 1
NM_001278281.2 NP_001265210.1 glycosyltransferase 8 domain-containing protein 1
NM_018446.4 NP_060916.1 glycosyltransferase 8 domain-containing protein 1
NM_152932.3 NP_690909.1 glycosyltransferase 8 domain-containing protein 1

GLT8D1 Protein Structure

Glyco_transf_8

Glyco_transf_8: Glycosyl transferase family 8 (67 - 339)

  • 0
  • 100
  • 200
  • 300
  • 371 a.a.
Protein Preferred Names Protein Names

glycosyltransferase 8 domain-containing protein 1

  • glycosyltransferase AD-017

Related Diseases

Diseases Alias
Frontotemporal Dementia

  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia
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
Spondylometaphyseal Dysplasia, Axial

  • Axial Spondylometaphyseal Dysplasia

  • SMDAX

  • Axial Smd

  • Smd Axial

  • Smd, Axial

  • Spondylometaphyseal Dysplasia Axial Type

  • Dysplasia, Spondylometaphyseal, Axial
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 2

  • FTDALS2

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-2

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 2
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 3

  • FTDALS3

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-3

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis, Type 3
Amyotrophic Lateral Sclerosis Type 22

  • Als 22

  • Amyotrohpic Lateral Sclerosis 22 With Or Without Frontotemporal Dementia

  • Amyotrophic Lateral Sclerosis 22
Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1

  • FTDALS1

  • Frontotemporal Dementia And/Or Motor Neuron Disease

  • Ftdmnd

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia

  • Alsftd

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1

  • Frontotemporal Dementia With Motor Neuron Disease

  • Ftdals

  • Ftd-Als

  • Ftd-Mnd

  • Frontotemporal Dementia With Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1

  • Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1

  • Frontotemporal Lobar Degeneration

  • Grn-Related Frontotemporal Dementia
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-RS05505 GLT8D1 Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Bos taurus GLT8D1 VGNC VGNC:29423
Macaca mulatta GLT8D1 VGNC VGNC:73001
Rattus norvegicus GLT8D1 RGD RGD:1359293
Mus musculus GLT8D1 MGD MGI:1923735
Felis catus GLT8D1 VGNC VGNC:62597
Canis familiaris GLT8D1 VGNC VGNC:41280
Others GLT8D1 NCBI