NGLY1 - N-glycanase 1 Gene

Also Known as CDDG; PNG1; CDG1V; PNG-1; PNGase

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 55768

About NGLY1

Cytogenetic location: 3p24.2 Genomic coordinates (GRCh38): 3:25,718,944-25,790,039 (from NCBI)

This gene has 21 transcripts (splice variants), 215 orthologues and is associated with 3 phenotypes. Broad expression in testis (RPKM 28.0), lymph node (RPKM 11.3) and 25 other tissues.

Summary

This gene encodes an enzyme that catalyzes hydrolysis of an N(4)-(acetyl-beta-D-glucosaminyl) asparagine residue to N-acetyl-beta-D-glucosaminylamine and a peptide containing an aspartate residue. The encoded enzyme may play a role in the proteasome-mediated degradation of misfolded glycoproteins. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Feb 2009]

NGLY1 Products (4)

mRNA Protein Name
NM_001145293.2 NP_001138765.1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase isoform 2
NM_001145294.2 NP_001138766.1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase isoform 3
NM_001145295.2 NP_001138767.1 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase isoform 4
NM_018297.4 NP_060767.2 peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase isoform 1
Molecular Function GO Annotation Evidence References Source
enables peptide-N4-(N-acetyl-beta-glucosaminyl)asparagine amidase activity IGI
IGI: Inferred from genetic interaction
28826503 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
15358861 GOA
Biological Process GO Annotation Evidence References Source
involved in glycoprotein catabolic process IDA
IDA: Inferred from direct assay
15358861 GOA
Cellular Component GO Annotation Evidence References Source
located in cytoplasm IDA
IDA: Inferred from direct assay
15358861 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

NGLY1 Protein Structure

PUB

PUB: PUB domain (24 - 103)

Transglut_core

Transglut_core: Transglutaminase-like superfamily (269 - 354)

PAW

PAW: PNGase C-terminal domain, mannose-binding module PAW (497 - 556)

  • 0
  • 200
  • 400
  • 600
  • 654 a.a.
Protein Preferred Names Protein Names

peptide-N(4)-(N-acetyl-beta-glucosaminyl)asparagine amidase

  • hPNGase

NGLY1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
NGLY1 Q96IV0 BICRAL Homo sapiens Q6AI39 32296183
Intra
NGLY1 Q96IV0 BICRAL Homo sapiens Q6AI39 32296183
Intra
NGLY1 Q96IV0 UBQLN1 Homo sapiens Q9UMX0-2 25416956
Intra
NGLY1 Q96IV0 TCF12 Homo sapiens Q99081-3 32296183
Intra
NGLY1 Q96IV0 TCF12 Homo sapiens Q99081-3 32296183
Intra
NGLY1 Q96IV0 TCF12 Homo sapiens Q99081-3 32296183
Intra
NGLY1 Q96IV0 GUCD1 Homo sapiens Q96NT3-2 32296183
Intra
NGLY1 Q96IV0 TRAFD1 Homo sapiens O14545 32296183
Intra
NGLY1 Q96IV0 TRAFD1 Homo sapiens O14545 25416956
Intra
NGLY1 Q96IV0 TRAFD1 Homo sapiens O14545 32296183
Intra
NGLY1 Q96IV0 TRAFD1 Homo sapiens O14545 25416956
Intra
NGLY1 Q96IV0 UBXN2B Homo sapiens Q14CS0 31515488
Intra
NGLY1 Q96IV0 UBXN2B Homo sapiens Q14CS0 25416956
Intra
NGLY1 Q96IV0 UBXN2B Homo sapiens Q14CS0 25416956
Intra
NGLY1 Q96IV0 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
NGLY1 Q96IV0 TRIM54 Homo sapiens Q9BYV2 25416956
Intra
NGLY1 Q96IV0 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
NGLY1 Q96IV0 TRIM54 Homo sapiens Q9BYV2 32296183
Intra
NGLY1 Q96IV0 VMAC Homo sapiens Q2NL98 32296183
Intra
NGLY1 Q96IV0 VMAC Homo sapiens Q2NL98 32296183
Intra
NGLY1 Q96IV0 PAX5 Homo sapiens Q02548 32296183
Intra
NGLY1 Q96IV0 PAX5 Homo sapiens Q02548 32296183
Intra
NGLY1 Q96IV0 NPAS2 Homo sapiens Q99743 32296183
Intra
NGLY1 Q96IV0 NPAS2 Homo sapiens Q99743 32296183
Intra
NGLY1 Q96IV0 NPAS2 Homo sapiens Q99743 32296183
Intra
NGLY1 Q96IV0 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
NGLY1 Q96IV0 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
NGLY1 Q96IV0 UBQLN1 Homo sapiens Q9UMX0 25416956
Intra
NGLY1 Q96IV0 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
NGLY1 Q96IV0 RAD23A Homo sapiens P54725 32296183
Intra
NGLY1 Q96IV0 RAD23A Homo sapiens P54725 31515488
Intra
NGLY1 Q96IV0 RAD23A Homo sapiens P54725 25416956
Intra
NGLY1 Q96IV0 RAD23A Homo sapiens P54725 32296183
Intra
NGLY1 Q96IV0 PAX6 Homo sapiens P26367 32296183
Intra
NGLY1 Q96IV0 PAX6 Homo sapiens P26367 32296183
Intra
NGLY1 Q96IV0 GUCD1 Homo sapiens Q96NT3 25416956
Intra
NGLY1 Q96IV0 RAD23B Homo sapiens P54727 22119785
Intra
NGLY1 Q96IV0 RAD23B Homo sapiens P54727 32296183
Intra
NGLY1 Q96IV0 RAD23B Homo sapiens P54727 25416956
Intra
NGLY1 Q96IV0 RAD23B Homo sapiens P54727 32296183
Intra
NGLY1 Q96IV0 RAD23B Homo sapiens P54727 31515488
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Congenital Disorder Of Deglycosylation 1
  • Congenital Disorder Of Deglycosylation

  • CDDG1

  • Cddg

  • Congenital Disorder Of Glycosylation, Type Iv, Formerly

  • Cdg1v, Formerly

  • Cdg1v

  • Cdgiv

  • Congenital Disorder Of Glycosylation 1v

  • Congenital Disorder Of Glycosylation Type Iv

  • Deglycosylation, Congenital Disorder Of

Ngly1-Deficiency
  • Deficiency Of N-Glycanase 1

  • Ngly1-Cddg

  • Alacrimia-Choreoathetosis-Liver Dysfunction Syndrome

  • Ngly1 Deficiency

  • Congenital Disorder Of Deglycosylation

  • Congenital Disorder Of Glycosylation Type Iv

  • Congenital Disorder Of Deglycosylation

  • Cddg

  • Congenital Disorder Of Glycosylation Type Iv

  • Cdg1v

Peripheral Nervous System Disease
  • Peripheral Neuropathy

  • Peripheral Nerve Disease

  • Peripheral Nerve Disorders

  • Neuropathy, Peripheral

  • Peripheral Neuropathy Due To Vitamin Pyridoxine Hyperalimentation

Hypotonia
Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

Autoinflammation, Panniculitis, And Dermatosis Syndrome
  • Otulipenia

  • Otulin-Related Autoinflammatory Syndrome

  • AIPDS

  • Oras

  • Infantile-Onset Periodic Fever-Panniculitis-Dermatosis Syndrome

  • Autoinflammation, Panniculitis And Dermatosis Syndrome

  • Otulin Deficiency

Aspartylglucosaminuria
  • Aspartylglycosaminuria

  • Glycosylasparaginase Deficiency

  • Aspartylglucosaminidase Deficiency

  • Aga Deficiency

  • AGU

  • Aspartylglucosamidase Deficiency

  • Glycoasparaginase

  • Aspartylglucosamidase Deficiency

  • Hyperammonemia, Type Iii

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

Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

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

Orthologs Information

Species Symbol Source ID
Rattus norvegicus NGLY1 RGD RGD:1308518
Felis catus NGLY1 VGNC VGNC:63795
Bos taurus NGLY1 VGNC VGNC:32063
Macaca mulatta NGLY1 VGNC VGNC:75200
Mus musculus NGLY1 MGD MGI:1913276
Canis familiaris NGLY1 VGNC VGNC:43796
Others NGLY1 NCBI