DSEL - dermatan sulfate epimerase like Gene

Also Known as C18orf4; DE-epi2

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 92126

About DSEL

Cytogenetic location: 18q22.1 Genomic coordinates (GRCh38): 18:67,506,587-67,516,720 (from NCBI)

This gene has 1 transcript (splice variant), 1 gene allele, 202 orthologues and 1 paralogue. Broad expression in brain (RPKM 4.8), kidney (RPKM 3.2) and 22 other tissues.

Summary

Predicted to enable chondroitin-glucuronate 5-epimerase activity. Predicted to be involved in chondroitin sulfate metabolic process and dermatan sulfate metabolic process. Predicted to be located in Golgi membrane. [provided by Alliance of Genome Resources, Apr 2022]

DSEL Products (1)

mRNA Protein Name
NM_032160.3 NP_115536.2 dermatan-sulfate epimerase-like protein precursor

DSEL Protein Structure

Sulfotransfer_1

Sulfotransfer_1: Sulfotransferase domain (863 - 1212)

  • 0
  • 200
  • 400
  • 600
  • 800
  • 1000
  • 1222 a.a.
Protein Preferred Names Protein Names

dermatan-sulfate epimerase-like protein

  • NCAG1

Related Diseases

Diseases Alias
Ehlers-Danlos Syndrome, Musculocontractural Type, 2

  • Ehlers-Danlos Syndrome, Musculocontractural Type 2

  • EDSMC2

  • Ehlers-Danlos Syndrome Musculocontractural Type 2

  • Ehlers-Danlos, Musculocontractural Syndrome, Type 2
Ehlers-Danlos Syndrome, Spondylodysplastic Type, 1

  • Xylosylprotein 4-Beta-Galactosyltransferase Deficiency

  • Xgpt Deficiency

  • EDSSPD1

  • Ehlers-Danlos Syndrome With Short Stature And Limb Anomalies

  • Edssla

  • Proteodermatan Sulfate, Defective Biosynthesis Of

  • Pds, Defective Biosynthesis Of

  • Dermatan Sulfate Proteoglycan

  • Galactosyltransferase I Deficiency

  • Ehlers-Danlos Syndrome Spondylodysplastic Type 1

  • Spondylodysplastic Ehlers-Danlos Syndrome

  • Ehlers-Danlos Syndrome, Progeroid Type, 1, Formerly

  • Edsp1, Formerly

  • Ehlers-Danlos Syndrome, Progeroid Type

  • Galactosyltransferase 1 Deficiency

  • Spondylodysplastic Eds

  • Speds

  • Defective Biosynthesis Of Pds

  • Defective Biosynthesis Of Proteodermatan Sulfate

  • Edsp1

  • Ehlers-Danlos Syndrome, Progeroid Type, 1

  • Proteodermatan Sulfate Defective Biosynthesis Of

  • Ehlers-Danlos, Spondylodysplastic Syndrome

  • Ehlers-Danlos Syndrome, Progeroid Form
Ehlers-Danlos Syndrome, Spondylodysplastic Type, 2

  • Ehlers-Danlos Syndrome Progeroid Type

  • Ehlers-Danlos Syndrome, Progeroid Type, 2

  • EDSSPD2

  • Ehlers-Danlos Syndrome Spondylodysplastic Type 2

  • Ehlers-Danlos Syndrome, Progeroid Type, 2, Formerly

  • Edsp2, Formerly

  • Defective Biosynthesis Of Proteodermatan Sulfate

  • Xgpt Deficiency

  • Xylosylprotein 4-Beta-Galactosyltransferase Deficiency

  • B3galt6-Related Spondylodysplastic Ehlers-Danlos Syndrome

  • B3galt6-Related Speds

  • B3galt6-Related Spondylodysplastic Eds

  • Beta3galt6-Deficient Eds

  • Ehlers-Danlos Syndrome Progeroid Type 2

  • Speds-B3galt6

  • Edsp2

  • Ehlers-Danlos, Spondylodysplastic Syndrome, Type 2

  • Ehlers-Danlos Syndrome, Progeroid Form
Ehlers-Danlos Syndrome, Musculocontractural Type, 1

  • Ehlers-Danlos Syndrome, Musculocontractural Type 1

  • EDSMC1

  • Edsmc

  • Adducted Thumb-Clubfoot Syndrome

  • Atcs

  • Dundar Syndrome

  • Arthrogryposis, Distal, With Peculiar Facies And Hydronephrosis

  • Ehlers-Danlos Syndrome Musculocontractural Type 1

  • Adducted Thumb, Clubfoot, And Progressive Joint And Skin Laxity Syndrome

  • Ehlers-Danlos Syndrome, Type Vib, Formerly

  • Eds6b, Formerly

  • Adducted Thumbs-Arthrogryposis Dundar Type

  • Arthrogryposis Distal With Peculiar Facies And Hydronephrosis

  • Eds6b Formerly

  • Ehlers-Danlos Syndrome Type Vib Formerly

  • Ehlers-Danlos, Musculocontractural Syndrome, Type 1
Temtamy Preaxial Brachydactyly Syndrome

  • Preaxial Brachydactyly Syndrome, Temtamy Type

  • TPBS

  • Intellectual Disability Syndrome With Preaxial Brachydactyly, Hyperphalangism, Deafness And Orodental Anomalies

  • Preaxial Brachydactyly Syndrome Temtamy Type
Schneckenbecken Dysplasia

  • SHNKND

  • Chondrodysplasia, Lethal Neonatal, With Snail-Like Pelvis

  • Chondrodysplasia Lethal Neonatal With Snail Like Pelvis

  • Chondrodysplasia With Snail-Like Pelvis

  • Slc35d1-Cdg

  • Dysplasia, Schneckenbecken
Diaphragmatic Hernia, Congenital

  • Congenital Diaphragmatic Hernia

  • Diaphragmatic Hernia

  • Cdh

  • Congenital Diaphragmatic Defect

  • Hernia, Diaphragmatic

  • Dih

  • Hernia, Congenital Diaphragmatic

  • Hcd

  • Diaphragmatic Defect, Congenital

  • Diaphragm, Unilateral Agenesis Of

  • Hemidiaphragm, Agenesis Of

  • Diaphragmatic Hernia 1

  • Agenesis Of Hemidiaphragm

  • Unilateral Agenesis Of Diaphragm

  • Hernia Diaphragmatic

  • Hernia Diaphragmatic Congenital

  • Hernia, Diaphragmatic, Type 1

  • Hiatus Hernia

  • Oesophageal Hiatus Hernia

  • Paraoesophageal Hernia

  • Sliding Hiatus Hernia

  • Congenital Diaphragm Hernia

  • Congenital Diaphragm Defect With Hernia

  • Gross Congenital Diaphragm Defect
Ehlers-Danlos Syndrome

  • Eds

  • Cutis Hyperelastica

  • Elastic Skin

  • Ehlers-Danlos Syndromes

  • Ed Syndrome

  • Ehlers Danlos Syndrome

  • Ehlers Danlos Disease

  • Eds - [Ehlers-Danlos Syndrome]
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-RS04020 DSEL Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Macaca mulatta DSEL VGNC VGNC:101438
Rattus norvegicus DSEL RGD RGD:1307724
Bos taurus DSEL VGNC VGNC:28219
Felis catus DSEL VGNC VGNC:82343
Mus musculus DSEL MGD MGI:2442948
Canis familiaris DSEL VGNC VGNC:40104
Others DSEL NCBI