ASNS - asparagine synthetase (glutamine-hydrolyzing) Gene

Also Known as TS11; ASNSD

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 440

About ASNS

Cytogenetic location: 7q21.3 Genomic coordinates (GRCh38): 7:97,851,677-97,928,441 (from NCBI)

This gene has 17 transcripts (splice variants), 218 orthologues, 1 paralogue and is associated with 3 phenotypes. Ubiquitous expression in brain (RPKM 19.6), testis (RPKM 14.4) and 24 other tissues.

Summary

The protein encoded by this gene is involved in the synthesis of asparagine. This gene complements a mutation in the temperature-sensitive hamster mutant ts11, which blocks progression through the G1 phase of the cell cycle at nonpermissive temperature. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010]

ASNS Products (7)

mRNA Protein Name
NM_001178075.2 NP_001171546.1 asparagine synthetase [glutamine-hydrolyzing] isoform b
NM_001178076.2 NP_001171547.1 asparagine synthetase [glutamine-hydrolyzing] isoform c
NM_001178077.1 NP_001171548.1 asparagine synthetase [glutamine-hydrolyzing] isoform c
NM_001352496.2 NP_001339425.1 asparagine synthetase [glutamine-hydrolyzing] isoform a
NM_001673.5 NP_001664.3 asparagine synthetase [glutamine-hydrolyzing] isoform a
NM_133436.3 NP_597680.2 asparagine synthetase [glutamine-hydrolyzing] isoform a
NM_183356.4 NP_899199.2 asparagine synthetase [glutamine-hydrolyzing] isoform a

ASNS Protein Structure

GATase_7

GATase_7: Glutamine amidotransferase domain (49 - 164)

Asn_synthase

Asn_synthase: Asparagine synthase (235 - 467)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 561 a.a.
Protein Preferred Names Protein Names

asparagine synthetase [glutamine-hydrolyzing]

  • TS11 cell cycle control protein

ASNS Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Verweise
Intra
ASNS P08243 TRIM69 Homo sapiens Q86WT6-2 32296183
Intra
ASNS P08243 TRIM69 Homo sapiens Q86WT6-2 32296183
Intra
ASNS P08243 TRIM69 Homo sapiens Q86WT6-2 32296183
Intra
ASNS P08243 TRIM69 Homo sapiens Q86WT6 25416956
Intra
ASNS P08243 TRIM69 Homo sapiens Q86WT6 25416956
Intra
ASNS P08243 WDR27 Homo sapiens A2RRH5 25416956
Intra
ASNS P08243 WDR27 Homo sapiens A2RRH5 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

ASNS Antibodies

Art. -Nr. Produktname Anwendung Reactivity
HY-P80550 Asparagine Synthetase Antibody (YA608) WB, IHC-P Human, Rat
HY-P80550A Asparagine Synthetase Antibody (YA608)(PBS only) WB, IHC-P Human, Rat

Related Diseases

Diseases Alias
Asparagine Synthetase Deficiency
  • Asns Deficiency

  • ASNSD

  • Congenital Microcephaly-Severe Encephalopathy-Progressive Cerebral Atrophy Syndrome

  • Disorder Of Asparagine Metabolism

  • Congenital Microcephaly - Severe Encephalopathy - Progressive Cerebral Atrophy Syndrome

Neuronal Migration Disorders
  • Abnormality Of Neuronal Migration

  • Malformations Of Cortical Development, Group Ii

  • Neuronal Dysmigration Syndromes

Childhood Acute Lymphocytic Leukemia
  • Childhood Acute Lymphoblastic Leukemia

  • Childhood All

  • Pediatric Acute Lymphoblastic Leukemia

  • Lymphoblastic Leukemia Acute Childhood

Leukemia, Acute Lymphoblastic
  • Acute Lymphoblastic Leukemia

  • ALL

  • Acute Lymphocytic Leukemia

  • Leukemia, Acute Lymphocytic, Susceptibility To, 1

  • Acute Lymphoblastic Leukaemia

  • Precursor Lymphoblastic Lymphoma/Leukemia

  • Precursor Lymphoid Neoplasm

  • Leukemia, Acute Lymphoblastic, Susceptibility To

  • B-Cell Acute Lymphoblastic Leukemia

  • Leukemia, Acute Lymphocytic 1

  • Acute Lymphocytic Leukaemia

  • Acute Lymphoblastic Leukemia/Lymphoma

  • All1

  • Childhood Acute Lymphoblastic Leukemia

  • Leukemia Acute Lymphoblastic 1

  • Leukemia Acute Lymphoblastic B-Hyperdiploid

  • Leukemia Acute Lymphocytic

  • Leukemia Acute Lymphocytic 1

  • Leukemia B-Cell Acute Lymphoblastic

  • Leukemia T-Cell Acute Lymphoblastic

  • Leukemia, Acute Lymphoblastic, 3

  • ALL3

  • Lymphoblastic Leukemia Acute

  • Leukemia, Acute, Lymphoblastic

  • Precursor Cell Lymphoblastic Leukemia Lymphoma

  • Leukemia, Lymphocytic, Acute, L1

  • Leukemia, Acute Lymphoblastic, Susceptibility To, 3

Microcephaly
  • Microencephaly

  • Microcephalus

  • Microcephalic

  • Nanocephaly

  • Congenital Microcephaly

  • Brain Hypoplasia

  • Brain Nondevelopment

  • Cephalic Hypoplasia

  • Undeveloped Cerebrum

  • Undeveloped Brain

  • Micrencephalon

  • Micrencephaly

Precursor T-Cell Acute Lymphoblastic Leukemia
  • T-All

  • Precursor T-Cell Acute Lymphoblastic Leukemia/Lymphoma

  • Precursor T-Cell Acute Lymphocytic Leukemia

  • Precursor T-Cell Acute Lymphocytic Leukemia/Lymphoma

  • Precursor T-Cell Lymphoblastic Leukemia-Lymphoma

  • Adult T-Cell Lymphoma/Leukemia

Adult Hepatocellular Carcinoma
  • Adult Primary Hepatocellular Carcinoma

  • Adult Hepatoma

  • Adult Hcc

Ovarian Cancer
  • Ovarian Carcinoma

  • Ovarian Neoplasm

  • Malignant Tumour Of Ovary

  • Cancer Of The Ovary

  • Epithelial Ovarian Cancer

  • Neoplasm Of Ovary

  • Ovarian Neoplasms

  • Ovarian Cancers

  • Malignant Neoplasm Of Ovary

  • Primary Malignant Neoplasm Of Ovary

  • Ovarian Cancer, Somatic

  • Malignant Ovarian Tumor

  • Ovary Neoplasm

  • Primary Ovarian Cancer

  • Tumor Of The Ovary

  • Malignant Neoplasm Of The Ovary

  • Malignant Tumor Of The Ovary

  • Ovarian Malignant Tumor

  • OC

  • Ovarian Carcinomas

  • Cancer, Ovarian

  • Cancer Of Ovary

  • Ovary Cancer

  • Ca Ovary

Hyperekplexia
  • Hereditary Hyperekplexia

  • Kok Disease

  • Congenital Stiff Man Syndrome

  • Familial Startle Disease

  • Sthe

  • Stiff-Baby Syndrome

  • Hereditary Hyperexplexia

  • Startle Disease

  • Exaggerated Startle Reaction

  • Hyperexplexia Hereditary

  • Startle Disease, Familial

  • Startle Reaction, Exaggerated

  • Stiff-Man Syndrome, Congenital

  • Stiff-Person Syndrome, Congenital

  • Congenital Stiff-Man Syndrome

  • Congenital Stiff-Person Syndrome

  • Familial Hyperekplexia

  • Startle Syndrome

  • Stiff Baby Syndrome

  • Hyperekplexia, Hereditary

  • Stiff-Person Syndrome

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 ASNS RGD RGD:2162
Mus musculus ASNS MGD MGI:1350929
Macaca mulatta ASNS VGNC VGNC:80798
Felis catus ASNS VGNC VGNC:69354
Canis familiaris ASNS VGNC VGNC:53542
Others ASNS NCBI