1. Gene
  2. ASNS - asparagine synthetase (glutamine-hydrolyzing) Gene

ASNS - asparagine synthetase (glutamine-hydrolyzing) Gene

Homo sapiens

Also known as TS11; ASNSD

Gene ID: 440 | Gene type: protein coding

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)

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  • 561 a.a.
Protein Preferred Names Protein Names

asparagine synthetase [glutamine-hydrolyzing]

TS11 cell cycle control protein

Recombinant ASNS Proteins

Cat. No. Product Name Accession Purity
HY-P78974 Asparagine Synthetase/ASNS Protein, Human (HEK293, His) P08243-1 (C2-A561) ≥95%

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