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Search results 301 to 318 out of 318 for Tcirg1

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0.019s
Type Details Score
Publication      
First Author: Mouse Genome Informatics Scientific Curators
Year: 2009
Journal: Database Download
Title: Mouse Microarray Data Integration in Mouse Genome Informatics, the Affymetrix GeneChip Mouse Genome 430 2.0 Array Platform
Publication      
First Author: Allen Institute for Brain Science
Year: 2004
Journal: Allen Institute
Title: Allen Brain Atlas: mouse riboprobes
Allele
Name: coiled-coil domain containing 154; new toothless
Allele Type: Spontaneous
Attribute String: Null/knockout
Allele
Name: T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3; targeted mutation 1, Yi Ping Li
Allele Type: Targeted
Attribute String: Null/knockout
Protein Coding Gene
Type: protein_coding_gene
Organism: mouse, laboratory
Genotype
Symbol: Tcirg1/Tcirg1
Background: B6C3Fe a/a-Tcirg1/J
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Tcirg1/Tcirg1
Background: involves: 129S4/SvJae * C57BL/6J
Zygosity: hm
Has Mutant Allele: true
Genotype
Symbol: Ccdc154/Ccdc154
Background: involves: 129S7/SvEvBrd * C57BL/6J
Zygosity: hm
Has Mutant Allele: true
DO Term
Allele  
Name: T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3; targeted mutation 1, Yoh Wada
Allele Type: Targeted
Allele  
Name: T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3; osteosclerotic
Allele Type: Spontaneous
Allele
Name: T cell, immune regulator 1, ATPase, H+ transporting, lysosomal V0 protein A3; targeted mutation 1.1, Yoh Wada
Allele Type: Targeted
Attribute String: Null/knockout, Reporter
Strain
Attribute String: mutant stock, targeted mutation
Genotype
Symbol: Tcirg1/?
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Zygosity: ot
Has Mutant Allele: true
Genotype
Symbol: Tcirg1/Tcirg1
Background: involves: 129S1/Sv * 129X1/SvJ * C57BL/6 * SJL
Zygosity: hm
Has Mutant Allele: true
Publication  
First Author: Schweikl C
Year: 2022
Journal: Int J Mol Sci
Title: Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity.
Volume: 23
Issue: 20
Publication
First Author: Pangrazio A
Year: 2006
Journal: J Bone Miner Res
Title: Mutations in OSTM1 (grey lethal) define a particularly severe form of autosomal recessive osteopetrosis with neural involvement.
Volume: 21
Issue: 7
Pages: 1098-105
Publication
First Author: Beranger GE
Year: 2008
Journal: J Bone Miner Res
Title: Poly(adp-ribose) polymerase-1 regulates Tracp gene promoter activity during RANKL-induced osteoclastogenesis.
Volume: 23
Issue: 4
Pages: 564-71