ENSMUSG00000025533


Mus musculus

Features
Gene ID: ENSMUSG00000025533
  
Biological name :Asl
  
Synonyms : Argininosuccinate lyase / Asl / Q91YI0
  
Possible biological names infered from orthology : AC068533.4 / P04424
  
Species: Mus musculus
  
Chr. number: 5
Strand: -1
Band: G1.3
Gene start: 130011258
Gene end: 130029247
  
Corresponding Affymetrix probe sets: 10534120 (MoGene1.0st)   1448350_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000124487
Ensembl peptide - ENSMUSP00000125143
Ensembl peptide - ENSMUSP00000124579
Ensembl peptide - ENSMUSP00000123799
Ensembl peptide - ENSMUSP00000123861
Ensembl peptide - ENSMUSP00000124274
NCBI entrez gene - 109900     See in Manteia.
MGI - MGI:88084
RefSeq - XM_017320601
RefSeq - NM_133768
RefSeq - XM_006504341
RefSeq Peptide - NP_598529
swissprot - E0CYV3
swissprot - Q91YI0
swissprot - F7D439
swissprot - E0CY49
Ensembl - ENSMUSG00000025533
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 aslENSDARG00000033361Danio rerio
 ASL1ENSGALG00000002558Gallus gallus
 ASL2ENSGALG00000002576Gallus gallus
 AC068533.4ENSG00000249319Homo sapiens
 ASLENSG00000126522Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR000362  Fumarate lyase family
 IPR008948  L-Aspartase-like
 IPR009049  Argininosuccinate lyase
 IPR020557  Fumarate lyase, conserved site
 IPR022761  Fumarate lyase, N-terminal
 IPR024083  Fumarase/histidase, N-terminal
 IPR029419  Argininosuccinate lyase, C-terminal


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000050 urea cycle IEA
 biological_processGO:0006520 cellular amino acid metabolic process IMP
 biological_processGO:0006526 arginine biosynthetic process IEA
 biological_processGO:0007626 locomotory behavior IMP
 biological_processGO:0008652 cellular amino acid biosynthetic process IEA
 biological_processGO:0009791 post-embryonic development IMP
 biological_processGO:0019676 ammonia assimilation cycle IMP
 biological_processGO:0042450 arginine biosynthetic process via ornithine IEA
 cellular_componentGO:0005737 cytoplasm IBA
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0004056 argininosuccinate lyase activity IEA
 molecular_functionGO:0016829 lyase activity IEA
 molecular_functionGO:0042802 identical protein binding ISO


Pathways (from Reactome)
Pathway description
Urea cycle


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000278 abnormal myocardial fiber morphology "malformed or poorly developed cardiac muscle fibers, the multinucleated muscle cells of the heart" [J:18048]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0000367 abnormal coat/ hair morphology "anomalous color, structure, growth, or texture of the hair" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0000377 abnormal hair follicle "malformed invagination of the epidermis from which the hair shaft develops" [J:65031]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0000380 small hair follicles "reduced size of the invagination of the epidermis from which the hair shaft develops" [J:56777]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0000711 thymic cortex hypoplasia "reduced cell number in the outer portion of the thymus" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0001221 epidermal atrophy "wasting of the epidermal layer of the skin" [J:65033]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0001243 abnormal dermal layer morphology "malformed or atypical condition of the dermal layer of the skin" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:56777]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0001262 decreased body weight "lower than normal average weight " [J:61295]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0001732 postnatal growth retardation "slow or limited development after birth " [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0002083 premature death "death after 3 weeks of age, but before normal life span" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0002169 no phenotype detected "normal, viable and fertile appearance and behavior; indistinguishable from controls" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0002447 abnormal erythrocyte morphology "structural anomaly of the cells in the blood that carry oxygen, red blood cells" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0002942 decreased circulating alanine transaminase level "decreased concentration in the blood of this enzyme, which transfers amino groups from l-alanine to 2 ketoglutarate, or the reverse (from l-glutamate to pyruvate); serum concentration is increased in viral hepatitis and myocardial infarction" [pvb:Pierre Vanden Borre , Mouse Genome Informatics Curator, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0003957 abnormal nitric oxide homeostasis "anomaly in the state of equilibrium in the body of nitric oxide, a free radical gas and a potent vasodilator" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0005016 decreased lymphocyte number "fewer than normal white blood cell numbers " [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Cdx2tm1Fbe/Cdx2tm2.1Fbe
Genetic Background: involves: 129P2/OlaHsd * 129S1/Sv * BALB/cJ

 MP:0005202 lethargy "mild impairment of consciousness resulting in reduced alertness and awareness; ultimately due to generalized brain dysfunction" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Large1myd/Large1myd
Genetic Background: B6.Cg-Large1myd/Pjn

 MP:0005309 increased circulating ammonia level "significantly elevated levels of ammonia or its compounds in blood; often associated with liver failure and hepatic encephalopathy " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:83263]
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Allelic Composition: Large1myd/Large1myd
Genetic Background: B6.Cg-Large1myd/Pjn

Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0005311 abnormal circulating amino acid level "aberrant concentration in the blood of these organic compounds, which, when polymerized, form proteins" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, J:83263]
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Allelic Composition: Large1myd/Large1myd
Genetic Background: B6.Cg-Large1myd/Pjn

Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0005325 abnormal glomerulus "anomalous structure of the capillary loops of the kidney that normally function as a filtration unit" [J:57971, cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0005425 increased macrophage count "greater than the normal numbers of macrophages" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, J:73418]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0005449 abnormal food intake "anomalous total number of calories taken in daily when compared to the norm" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
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Allelic Composition: Large1myd/Large1myd
Genetic Background: B6.Cg-Large1myd/Pjn

 MP:0005558 decreased creatinine clearance "less than the normal amount of this creatine metabolite filtered by the kidneys in a specific period of time; indicative of kidney function" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, RGD:Rat Genome Database submission]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0005584 abnormal enzyme/coenzyme activity "altered ability of any of these proteins, or their cofactors, to act as catalysts to induce chemical changes in other substances" [Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Large1myd/Large1myd
Genetic Background: B6.Cg-Large1myd/Pjn

 MP:0005591 decreased vasodilation "less than the expected or normal widening of the lumen of the blood vessels" [RGD:Rat Genome Database submission, Stedman s Medical Dictionary:ISBN 0-683-40008-8]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0005632 decreased circulating aspartate transaminase level "less than normal concentration in the blood of this enzyme, which catalyzes the reversible transfer of an amine group from l-glutamic acid to oxaloacetic acid, forming alpha-ketoglutaric acid and l-aspartic acid; aids in diagnosis of viral hepatitis and myocardial infarction" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, RGD:Rat Genome Database submission]
Show

Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0006143 increased diastolic blood pressure "abnormal increase in the pressure in the arteries between heart beats when the heart is relaxed" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0006144 increased systolic blood pressure "abnormal increase in the pressure in the arteries as the heart contracts and pumps blood into the arteries" [ncbi:Matthew Mailman, NCBI request, smb:Susan M Bello, Mouse Genome Informatics Curator]
Show

Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0006263 decreased diastolic blood pressure "abnormal decrease in the pressure in the arteries between heart beats when the heart is relaxed" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:21887]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0006264 decreased systolic blood pressure "abnormal decrease in the pressure in the arteries as the heart contracts and pumps blood into the arteries" [monikat:Monika Tomczuk, Mouse Genome Informatics Curator, J:21887]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0008476 increased spleen red pulp amount "increase in the quantity of the parenchymatous tissue network of the spleen that consists of loose plates or cords (sinuses) infiltrated with red blood cells where most of the blood filtration occurs and degenerate erythrocytes are removed from the circulation" [MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0008482 decreased spleen germinal center number "reduced number of spleen secondary B follicles where rapid B-cell proliferation, somatic hypermutation, and selection for antigen binding occurs" [PMID:17495967]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0010177 acanthocytosis "presence of erythrocytes characterized by multiple spiny (thorn-like) cytoplasmic projections" [MGI:anna "Anna V. Anagnostopoulos, Mouse Genome Informatics Curator"]
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Allelic Composition: Asltm1Brle/Asltm1Brle
Genetic Background: involves: 129S7/SvEvBrd

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
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Allelic Composition: Large1myd/Large1myd
Genetic Background: B6.Cg-Large1myd/Pjn

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000025533 Asl / Q91YI0 / Argininosuccinate lyase / P04424* / AC068533.4*  / complex






 

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