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Phenotypic Alleles
Query Results -- Summary
 Symbol
Name
ID
Col2a1
collagen, type II, alpha 1
MGI:88452

15 matching Alleles (1 Gene/Marker represented)
                                                Allele Symbol
Name Chr Synonyms Category Phenotypic Classes Human Diseases Col2a1Dmm
collagen, type II, alpha 1; disproportionate micromelia 15 Radiation induced craniofacial, digestive/alimentary, growth/size, limbs/digits/tail, mortality/aging, respiratory, skeleton Col2a1Lpk
collagen, type II, alpha 1; longpockets 15 Chemically induced (ENU) craniofacial, digestive/alimentary, growth/size, limbs/digits/tail, mortality/aging, skeleton Spondyloepiphyseal Dysplasia Congenita; SEDC 183900 Col2a1M2J
collagen, type II, alpha 1; mutation 2 Jackson 15 cleft Chemically induced (ENU) adipose, craniofacial, digestive/alimentary, growth/size, skeleton Col2a1M3J
collagen, type II, alpha 1; mutation 3 Jackson 15 Spontaneous craniofacial Col2a1Rgsc856
collagen, type II, alpha 1; RIKEN Genomic Sciences Center (GSC), 856 15 M100856 Chemically induced (ENU) craniofacial, growth/size, limbs/digits/tail, mortality/aging, skeleton Platyspondylic Lethal Skeletal Dysplasia, Torrance Type; PLSDT 151210 Col2a1sedc
collagen, type II, alpha 1; spondyloepiphyseal dysplasia congenita 15 Col2a1sed Spontaneous behavior, digestive/alimentary, growth/size, hearing/vestibular/ear, nervous system, vision/eye Spondyloepiphyseal Dysplasia Congenita; SEDC 183900 Col2a1tm1.1Ksec
collagen, type II, alpha 1; targeted mutation 1.1, Kathryn S E Cheah 15 IIA- Targeted (knock-out) craniofacial, embryogenesis, limbs/digits/tail, mortality/aging, nervous system, respiratory, skeleton, vision/eye Col2a1tm1.1Mcali
collagen, type II, alpha 1; targeted mutation 1.1, Audrey McAlinden 15 Col2a1+ex2 Targeted (knock-in) no abnormal phenotype observed Col2a1tm1Prc
collagen, type II, alpha 1; targeted mutation 1, Darwin J Prockop
images 15 Targeted (knock-out) cardiovascular, craniofacial, digestive/alimentary, embryogenesis, growth/size, limbs/digits/tail, mortality/aging, renal/urinary, respiratory, skeleton, vision/eye Achondrogenesis, Type II; ACG2 200610; Spondyloepiphyseal Dysplasia Congenita; SEDC 183900; Stickler Syndrome, Type I, Nonsyndromic Ocular 609508 Col2a1tm1(SOX9)Crm
collagen, type II, alpha 1; targeted mutation 1, Benoit de Crombrugghe 15 Targeted (knock-in) craniofacial, digestive/alimentary, growth/size, limbs/digits/tail, mortality/aging, respiratory, skeleton Col2a1Gt(317C02)Cmhd
collagen, type II, alpha 1; gene trap 317C02, Centre for Modeling Human Disease 15 Gene trapped
(Cell Line) Col2a1Gt(IST12518F2)Tigm
collagen, type II, alpha 1; gene trap IST12518F2, Texas A&M Institute for Genomic Medicine 15 Gene trapped
(Cell Line) Col2a1Gt(OST2945)Lex
collagen, type II, alpha 1; gene trap OST2945, Lexicon Genetics 15 Gene trapped
(Cell Line) Col2a1tm1a(EUCOMM)Wtsi
collagen, type II, alpha 1; targeted mutation 1a, Wellcome Trust Sanger Institute 15 Targeted (Floxed/Frt)
(Cell Line) Col2a1tm1e(EUCOMM)Wtsi
collagen, type II, alpha 1; targeted mutation 1e, Wellcome Trust Sanger Institute 15 Targeted (Reporter)
(Cell Line)

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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory