|  Help  |  About  |  Contact Us

Search our database by keyword

Examples

  • Search this entire website. Enter identifiers, names or keywords for genes, diseases, strains, ontology terms, etc. (e.g. Pax6, Parkinson, ataxia)
  • Use OR to search for either of two terms (e.g. OR mus) or quotation marks to search for phrases (e.g. "dna binding").
  • Boolean search syntax is supported: e.g. Balb* for partial matches or mus AND NOT embryo to exclude a term

Search results 1 to 100 out of 5463 for Tyr

<< First    < Previous  |  Next >    Last >>
0.051s

Categories

Hits by Pathway

Hits by Strain

Hits by Category

Type Details Score
Gene
Type: gene
Organism: Not Specified
Gene
Type: gene
Organism: human
Gene
Type: gene
Organism: zebrafish
Gene
Type: gene
Organism: macaque, rhesus
Gene
Type: gene
Organism: frog, western clawed
Gene
Type: gene
Organism: cattle
Gene
Type: gene
Organism: rat
Gene
Type: gene
Organism: dog, domestic
Gene
Type: gene
Organism: chimpanzee
Gene
Type: gene
Organism: chicken
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
SO Term
Publication  
First Author: Dickie MM
Year: 1969
Journal: Mouse News Lett
Title: Remutations: Tyr and Aw - white-bellied agouti.
Volume: 40
Pages: 29
Publication      
First Author: Arnold C
Year: 2010
Journal: MGI Direct Data Submission
Title: Pale rider is an allele of Tyr and causes albinism
Publication  
First Author: Whitmore S
Year: 1983
Journal: Mouse News Lett
Title: Coat color variant - Tyr
Volume: 69
Pages: 19
Publication
First Author: Lyon MF
Year: 1979
Journal: Mutat Res
Title: Dose-response curves for radiation-induced gene mutations in mouse oocytes and their interpretation.
Volume: 63
Issue: 1
Pages: 161-73
Publication
First Author: Wines ME
Year: 1998
Journal: Genomics
Title: Physical localization of the mouse aryl hydrocarbon receptor nuclear translocator-2 (Arnt2) gene within the c112K deletion.
Volume: 51
Issue: 2
Pages: 223-32
Publication
First Author: Wines ME
Year: 2001
Journal: Genomics
Title: Identification of mesoderm development (mesd) candidate genes by comparative mapping and genome sequence analysis.
Volume: 72
Issue: 1
Pages: 88-98
Publication
First Author: Gluecksohn-Waelsch S
Year: 1974
Journal: Proc Natl Acad Sci U S A
Title: Complementation studies of lethal alleles in the mouse causing deficiencies of glucose-6-phosphatase, tyrosine aminotransferase, and serine dehydratase.
Volume: 71
Issue: 3
Pages: 825-9
Publication
First Author: Wines ME
Year: 2000
Journal: Genomics
Title: Physical localization of the mesoderm development (mesd) functional region.
Volume: 68
Issue: 3
Pages: 322-9
Chromosome Structure Variation
Type: chromosomal_deletion
Organism: mouse, laboratory
Chromosome Structure Variation
Type: chromosomal_deletion
Organism: mouse, laboratory
Chromosome Structure Variation
Type: chromosomal_deletion
Organism: mouse, laboratory
Chromosome Structure Variation
Type: chromosomal_deletion
Organism: mouse, laboratory
Chromosome Structure Variation
Type: chromosomal_deletion
Organism: mouse, laboratory
Publication
First Author: Lavado A
Year: 2005
Journal: J Biol Chem
Title: Molecular basis of the extreme dilution mottled mouse mutation: a combination of coding and noncoding genomic alterations.
Volume: 280
Issue: 6
Pages: 4817-24
Publication
First Author: Juriloff DM
Year: 1994
Journal: Genome
Title: Three spontaneous mutations at the albino locus in SELH/Bc mice.
Volume: 37
Issue: 2
Pages: 190-7
Publication  
First Author: Phillips RJS
Year: 1970
Journal: Mouse News Lett
Title: Chinchilla-mottled
Volume: 42
Pages: 26
Publication  
First Author: Phillips RJS
Year: 1966
Journal: Mouse News Lett
Title: A mottled c-locus mutant, c22H
Volume: 34
Pages: 27
Publication
First Author: Miller DA
Year: 1974
Journal: Genetics
Title: Cytological detection of the c-25H deletion involving the albino (c) locus on chromosome 7 in the mouse.
Volume: 78
Issue: 3
Pages: 905-10
Publication
First Author: Beechey C
Year: 1995
Journal: Mouse Genome
Title: List of Chromosome anomalies
Volume: 93
Issue: 2
Pages: 407-20
Publication  
First Author: Nadijcka MD
Year: 1979
Journal: J Embryol Exp Morphol
Title: Ultrastructural studies of lethal c25H/C25H mouse embryos.
Volume: 52
Pages: 1-11
Publication
First Author: Wu M
Year: 1997
Journal: Proc Natl Acad Sci U S A
Title: Inherited somatic mosaicism caused by an intracisternal A particle insertion in the mouse tyrosinase gene.
Volume: 94
Issue: 3
Pages: 890-4
Publication
First Author: Porter S
Year: 1991
Journal: Dev Genet
Title: Mosaicism of tyrosinase-locus transcription and chromatin structure in dark vs. light melanocyte clones of homozygous chinchilla-mottled mice.
Volume: 12
Issue: 6
Pages: 393-402
Publication
First Author: Beermann F
Year: 2004
Journal: Mamm Genome
Title: The Tyr (albino) locus of the laboratory mouse.
Volume: 15
Issue: 10
Pages: 749-58
Publication      
First Author: Medical Research Council (MRC) Harwell
Year: 2012
Journal: MGI Direct Data Submission
Title: Direct Data Submission 2012/01/26
Publication
First Author: Porter S
Year: 1991
Journal: Gene
Title: Multiple alternatively spliced transcripts of the mouse tyrosinase-encoding gene.
Volume: 97
Issue: 2
Pages: 277-82
Publication
First Author: Diamond RP
Year: 1974
Journal: Nature
Title: Gene dosage in a deletion for a nuclear-coded, mitochondrial enzyme.
Volume: 248
Issue: 447
Pages: 418-9
Publication      
First Author: Beutler B
Year: 2011
Journal: MGI Direct Data Submission
Title: Direct Data Submission 2011/01/14
Publication
First Author: Peters J
Year: 1985
Journal: Genetics
Title: A mouse beta-globin mutant that is an exact model of hemoglobin Rainier in man.
Volume: 110
Issue: 4
Pages: 709-21
Publication
First Author: Rikke BA
Year: 1997
Journal: Genetics
Title: Murine albino-deletion complex: high-resolution microsatellite map and genetically anchored YAC framework map.
Volume: 147
Issue: 2
Pages: 787-99
Publication
First Author: Mizuno S
Year: 2014
Journal: Mamm Genome
Title: Simple generation of albino C57BL/6J mice with G291T mutation in the tyrosinase gene by the CRISPR/Cas9 system.
Volume: 25
Issue: 7-8
Pages: 327-34
Publication
First Author: Challa AK
Year: 2016
Journal: PLoS One
Title: Novel Hypomorphic Alleles of the Mouse Tyrosinase Gene Induced by CRISPR-Cas9 Nucleases Cause Non-Albino Pigmentation Phenotypes.
Volume: 11
Issue: 5
Pages: e0155812
Publication
First Author: Johnson LL
Year: 2024
Journal: Invest Ophthalmol Vis Sci
Title: Nystagmus in the B6(CG)Tyr(c-2J)/J Albino Mouse: A Functional and RNA-Seq Analysis.
Volume: 65
Issue: 1
Pages: 26
Publication
First Author: Libby RT
Year: 2003
Journal: Science
Title: Modification of ocular defects in mouse developmental glaucoma models by tyrosinase.
Volume: 299
Issue: 5612
Pages: 1578-81
Publication
First Author: Rikke BA
Year: 2001
Journal: Alcohol Clin Exp Res
Title: No effect of albinism on sedative-hypnotic sensitivity to ethanol and anesthetics.
Volume: 25
Issue: 2
Pages: 171-6
Publication
First Author: Parikh BA
Year: 2015
Journal: PLoS One
Title: Detailed phenotypic and molecular analyses of genetically modified mice generated by CRISPR-Cas9-mediated editing.
Volume: 10
Issue: 1
Pages: e0116484
Publication
First Author: Johnson BA
Year: 2010
Journal: Genetics
Title: Tyrosinase is the modifier of retinoschisis in mice.
Volume: 186
Issue: 4
Pages: 1337-44
Publication
First Author: Kobayashi T
Year: 2007
Journal: J Cell Sci
Title: Direct interaction of tyrosinase with Tyrp1 to form heterodimeric complexes in vivo.
Volume: 120
Issue: Pt 24
Pages: 4261-8
Publication
First Author: SILVERS WK
Year: 1958
Journal: Anat Rec
Title: Origin and identity of clear cells found in hair bulbs of albino mice.
Volume: 130
Issue: 2
Pages: 135-44
Publication
First Author: Thiessen DD
Year: 1970
Journal: Behav Genet
Title: Behavior and allelic variations in enzyme activity and coat color at the C locus of the mouse.
Volume: 1
Issue: 3
Pages: 257-67
Publication
First Author: Guillery RW
Year: 1974
Journal: Sci Am
Title: Visual pathways in albinos.
Volume: 230
Issue: 5
Pages: 44-54
Publication  
First Author: Cattanach BM
Year: 1988
Journal: Mouse News Lett
Title: Dark-eyed albinism, c44H.
Volume: 81
Pages: 64
Publication
First Author: Beermann F
Year: 1992
Journal: Proc Natl Acad Sci U S A
Title: Expression of the mouse tyrosinase gene during embryonic development: recapitulation of the temporal regulation in transgenic mice.
Volume: 89
Issue: 7
Pages: 2809-13
Publication  
First Author: Hamanaka T
Year: 2017
Journal: J Virol
Title: Melanin or a Melanin-Like Substance Interacts with the N-Terminal Portion of Prion Protein and Inhibits Abnormal Prion Protein Formation in Prion-Infected Cells.
Volume: 91
Issue: 6
Publication
First Author: Jeffery G
Year: 1994
Journal: Dev Biol
Title: Correction of abnormal retinal pathways found with albinism by introduction of a functional tyrosinase gene in transgenic mice.
Volume: 166
Issue: 2
Pages: 460-4
Publication
First Author: Jackson IJ
Year: 1990
Journal: Proc Natl Acad Sci U S A
Title: Identification of the albino mutation of mouse tyrosinase by analysis of an in vitro revertant.
Volume: 87
Issue: 18
Pages: 7010-4
Publication  
First Author: Dickie MM
Year: 1966
Journal: Mouse News Lett
Title: Platinum
Volume: 34
Pages: 30
Publication
First Author: Yokoyama T
Year: 1990
Journal: Nucleic Acids Res
Title: Conserved cysteine to serine mutation in tyrosinase is responsible for the classical albino mutation in laboratory mice.
Volume: 18
Issue: 24
Pages: 7293-8
Publication
First Author: Jeffery G
Year: 1997
Journal: Brain Res Dev Brain Res
Title: Correction of retinal abnormalities found in albinism by introduction of a functional tyrosinase gene in transgenic mice and rabbits.
Volume: 99
Issue: 1
Pages: 95-102
Publication
First Author: Tyler PA
Year: 1970
Journal: Behav Genet
Title: Coat color differences and runway learning in mice.
Volume: 1
Issue: 2
Pages: 149-55
Publication
First Author: Vemula SK
Year: 2022
Journal: Invest Ophthalmol Vis Sci
Title: Impaired Extraocular Muscle Innervation Is Present Before Eye Opening in a Mouse Model of Infantile Nystagmus Syndrome.
Volume: 63
Issue: 10
Pages: 4
Publication  
First Author: Silvers WK
Year: 1956
Journal: J Morphol
Title: Pigment cells: occurrence in hair follicles.
Volume: 99
Pages: 41-55
Publication
First Author: Hegmann JP
Year: 1974
Journal: Behav Genet
Title: Gene differences influencing visual system function and behavior.
Volume: 4
Issue: 2
Pages: 165-70
Publication
First Author: Qiao JH
Year: 1993
Journal: J Clin Invest
Title: Involvement of the tyrosinase gene in the deposition of cardiac lipofuscin in mice. Association with aortic fatty streak development.
Volume: 92
Issue: 5
Pages: 2386-93
Publication
First Author: Peissel B
Year: 2001
Journal: Mamm Genome
Title: Use of intercross outbred mice and single nucleotide polymorphisms to map skin cancer modifier loci.
Volume: 12
Issue: 4
Pages: 291-4
Publication
First Author: Ollendorff V
Year: 1992
Journal: Mamm Genome
Title: New gene in the homologous human 11q13-q14 and mouse 7F chromosomal regions.
Volume: 2
Issue: 3
Pages: 195-200
Publication
First Author: Simpson VJ
Year: 1998
Journal: Anesthesiology
Title: Identification of a genetic region in mice that specifies sensitivity to propofol.
Volume: 88
Issue: 2
Pages: 379-89
Publication
First Author: Rinchik EM
Year: 1993
Journal: Genetics
Title: Molecular analysis of radiation-induced albino (c)-locus mutations that cause death at preimplantation stages of development.
Volume: 135
Issue: 4
Pages: 1107-16
Publication
First Author: Whitney IE
Year: 2009
Journal: Invest Ophthalmol Vis Sci
Title: Multiple genes on chromosome 7 regulate dopaminergic amacrine cell number in the mouse retina.
Volume: 50
Issue: 5
Pages: 1996-2003
Publication
First Author: Lavado A
Year: 2005
Journal: BMC Cell Biol
Title: A strategy to study tyrosinase transgenes in mouse melanocytes.
Volume: 6
Issue: 1
Pages: 18
Publication
First Author: Ramesh V
Year: 1992
Journal: Mamm Genome
Title: Mapping of ornithine aminotransferase gene sequences to mouse chromosomes 7, X, and 3.
Volume: 3
Issue: 1
Pages: 17-22
Publication
First Author: Wallace ME
Year: 1976
Journal: J Hyg (Lond)
Title: A major gene controlling warfarin-resistance in the house mouse.
Volume: 76
Issue: 2
Pages: 173-81
Publication  
First Author: Detlefsen JA
Year: 1921
Journal: Am Naturalist
Title: A new mutation in the house mouse.
Volume: 55
Pages: 469-73
Publication
First Author: Townsend D
Year: 1981
Journal: J Exp Zool
Title: Tyrosinase subcellular distribution and kinetic parameters in wild type and C-locus mutant C57BL/6J mice.
Volume: 216
Issue: 1
Pages: 113-9
Publication
First Author: Juriloff DM
Year: 1992
Journal: Genome
Title: Studies of a spontaneous lethal mutation at the albino locus in SELH/Bc mice.
Volume: 35
Issue: 2
Pages: 342-6
Publication
First Author: Kobayashi T
Year: 1998
Journal: J Biol Chem
Title: Tyrosinase stabilization by Tyrp1 (the brown locus protein).
Volume: 273
Issue: 48
Pages: 31801-5
Publication
First Author: Cortese K
Year: 2005
Journal: Invest Ophthalmol Vis Sci
Title: The ocular albinism type 1 (OA1) gene controls melanosome maturation and size.
Volume: 46
Issue: 12
Pages: 4358-64
Publication
First Author: Klebig ML
Year: 1992
Journal: Mamm Genome
Title: Physical analysis of murine albino deletions that disrupt liver-specific gene regulation or mesoderm development.
Volume: 2
Issue: 1
Pages: 51-63
Publication
First Author: Keighren MA
Year: 2015
Journal: Transgenic Res
Title: Lessons from mouse chimaera experiments with a reiterated transgene marker: revised marker criteria and a review of chimaera markers.
Volume: 24
Issue: 4
Pages: 665-91
Publication      
First Author: Karst SY
Year: 2009
Journal: MGI Direct Data Submission
Title: Chick yellow: Mutation on Chromosome 3 causing eye and coat color abnormalties
Publication
First Author: Rinchik EM
Year: 1993
Journal: Mutat Res
Title: Molecular analysis of viable spontaneous and radiation-induced albino (c)-locus mutations in the mouse.
Volume: 286
Issue: 2
Pages: 199-207
Publication
First Author: Aponte JL
Year: 2001
Journal: Proc Natl Acad Sci U S A
Title: Point mutations in the murine fumarylacetoacetate hydrolase gene: Animal models for the human genetic disorder hereditary tyrosinemia type 1.
Volume: 98
Issue: 2
Pages: 641-5
Publication  
First Author: Wang H
Year: 2016
Journal: Sci Rep
Title: In vivo coherent Raman imaging of the melanomagenesis-associated pigment pheomelanin.
Volume: 6
Pages: 37986
Publication
First Author: Rios M
Year: 1999
Journal: J Neurosci
Title: Catecholamine synthesis is mediated by tyrosinase in the absence of tyrosine hydroxylase.
Volume: 19
Issue: 9
Pages: 3519-26
Publication
First Author: Erickson RP
Year: 1968
Journal: Proc Natl Acad Sci U S A
Title: Glucose-6-phosphatase deficiency caused by radiation-induced alleles at the albino locus in the mouse.
Volume: 59
Issue: 2
Pages: 437-44
Protein Domain
Type: Active_site
Description: Pectinesterase (pectin methylesterase) catalyses the de-esterification of pectin into pectate and methanol. Pectin is one of the main components of the plant cell wall. In plants, pectinesterase plays an important role in cell wall metabolism during fruit ripening. In plant bacterial pathogens such as Erwinia carotovora and in fungal pathogens such as Aspergillus niger, pectinesterase is involved in maceration and soft-rotting of plant tissue. Plant pectinesterases are regulated by pectinesterase inhibitors, which are ineffective against microbial enzymes [].Prokaryotic and eukaryotic pectinesterases share a few regions of sequence similarity. The crystal structure of pectinesterase from Erwinia chrysanthemi revealed a β-helix structure similar to that found in pectinolytic enzymes, though it is different from most structures of esterases []. The putative catalytic residues are in a similar location to those of the active site and substrate-binding cleft of pectate lyase.The entry represents a region found in the N-terminal section of these enzymes; it contains a conserved tyrosine which may play a role in the catalytic mechanism [].
Publication
First Author: Rinchik EM
Year: 1999
Journal: Genetics
Title: N-ethyl-N-nitrosourea mutagenesis of a 6- to 11-cM subregion of the Fah-Hbb interval of mouse chromosome 7: Completed testing of 4557 gametes and deletion mapping and complementation analysis of 31 mutations.
Volume: 152
Issue: 1
Pages: 373-83
Publication
First Author: Aydin IT
Year: 2012
Journal: Pigment Cell Melanoma Res
Title: Coat color dilution in mice because of inactivation of the melanoma antigen MART-1.
Volume: 25
Issue: 1
Pages: 37-46
Publication
First Author: Wakamatsu K
Year: 2007
Journal: Pigment Cell Res
Title: High levels of melanin-related metabolites in plasma from pink-eyed dilution mice.
Volume: 20
Issue: 3
Pages: 222-4
Publication
First Author: Russell LB
Year: 1992
Journal: Proc Natl Acad Sci U S A
Title: Genetic, cytogenetic, and molecular analyses of mutations induced by melphalan demonstrate high frequencies of heritable deletions and other rearrangements from exposure of postspermatogonial stages of the mouse.
Volume: 89
Issue: 13
Pages: 6182-6
Publication
First Author: Chen J
Year: 2005
Journal: Mamm Genome
Title: "Agouti NOD": identification of a CBA-derived Idd locus on Chromosome 7 and its use for chimera production with NOD embryonic stem cells.
Volume: 16
Issue: 10
Pages: 775-83
Publication
First Author: Potter CS
Year: 2015
Journal: Exp Mol Pathol
Title: Dysregulated expression of sterol O-acyltransferase 1 (Soat1) in the hair shaft of Hoxc13 null mice.
Volume: 99
Issue: 3
Pages: 441-4
Publication  
First Author: Sweet HO
Year: 1987
Journal: Mouse News Lett
Title: Acromelanic (ca).
Volume: 78
Pages: 56
Publication  
First Author: COLEMAN DL
Year: 1962
Journal: Arch Biochem Biophys
Title: Effect of genic substitution on the incorporation of tyrosine into the melanin of mouse skin.
Volume: 96
Pages: 562-8
Publication
First Author: Uehara S
Year: 2009
Journal: Pigment Cell Melanoma Res
Title: Specific expression of Gsta4 in mouse cochlear melanocytes: a novel role for hearing and melanocyte differentiation.
Volume: 22
Issue: 1
Pages: 111-9
Publication
First Author: Hearing VJ
Year: 1973
Journal: J Ultrastruct Res
Title: The fine structure of melanogenesis in coat color mutants of the mouse.
Volume: 43
Issue: 1
Pages: 88-106
Publication
First Author: Bharti K
Year: 2008
Journal: Development
Title: Alternative promoter use in eye development: the complex role and regulation of the transcription factor MITF.
Volume: 135
Issue: 6
Pages: 1169-78
Publication
First Author: Hirobe T
Year: 1998
Journal: Eur J Cell Biol
Title: Effects of genic substitution at the agouti, brown, albino, dilute, and pink-eyed dilution loci on the proliferation and differentiation of mouse epidermal melanocytes in serum-free culture.
Volume: 75
Issue: 2
Pages: 184-91
Publication
First Author: Lighthouse JK
Year: 2011
Journal: Dev Dyn
Title: MESD is essential for apical localization of megalin/LRP2 in the visceral endoderm.
Volume: 240
Issue: 3
Pages: 577-88