Phenotype: mammalian phenotype

Definition
the observable morphological, physiological, behavioral and other characteristics of mammalian organisms that are manifested through development and lifespan
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with mammalian phenotype

Total number of significant genotype-phenotype associations: 40

Gene / Allele Zygosity Sex Life Stage Phenotype Procedure | Parameter Phenotyping Center | Source P Value
Stx8
Stx8tm2a(EUCOMM)Wtsi
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 1.18×10-19
Vangl2
Vangl2Lp
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 2.42×10-18
Mysm1
Mysm1tm1a(KOMP)Wtsi
HOM Early adult mammalian phenotype Dysmorphology | adult mouse HMGU | EuroPhenome 3.46×10-17
Nfya
NfyaGt(EUCJ0004f10)Hmgu
HET Early adult mammalian phenotype Dysmorphology | adult mouse HMGU | EuroPhenome 5.20×10-17
Celsr1
Celsr1Scy
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 7.33×10-14
Ostes
Ostes
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 8.40×10-14
Celsr1
Celsr1Crsh
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 3.08×10-13
Sfrp2
Sfrp2tm1Aksh
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 1.78×10-12
Trpc3
Trpc3Mwk
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 3.52×10-12
Ctnnb1
Ctnnb1Bfc
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 9.73×10-11
Ankrd11
Ankrd11Yod
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 1.95×10-07
Brpf1
Brpf1tm1a(EUCOMM)Wtsi
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 8.51×10-07
Wdr47
Wdr47tm1a(EUCOMM)Wtsi
HOM Early adult mammalian phenotype Dysmorphology | adult mouse WTSI | EuroPhenome 2.28×10-06
Cyb561
Cyb561tm1a(EUCOMM)Wtsi
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 2.85×10-06
D430041D05Rik
D430041D05Riktm1a(EUCOMM)Hmgu
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 3.95×10-06
Kcnj16
Kcnj16tm1Sjtu
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 4.71×10-06
Phex
Phexnot yet available
HOM Early adult mammalian phenotype Dysmorphology | adult mouse HMGU | EuroPhenome 5.95×10-06
Sfrp2
Sfrp2C50F
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 7.05×10-06
Fam83g
Fam83gtm1a(EUCOMM)Wtsi
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 7.24×10-06
Grhl3
Grhl3tm1a(EUCOMM)Wtsi
HET Early adult mammalian phenotype Dysmorphology | adult mouse ICS | EuroPhenome 1.01×10-05
2310022B05Rik
2310022B05Riktm1a(EUCOMM)Hmgu
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 1.17×10-05
Ift20
Ift20tm1a(EUCOMM)Wtsi
HET Early adult mammalian phenotype Dysmorphology | adult mouse ICS | EuroPhenome 1.85×10-05
Kdm8
Kdm8tm1a(EUCOMM)Wtsi
HET Early adult mammalian phenotype Dysmorphology | adult mouse ICS | EuroPhenome 2.79×10-05
Smoc1
Smoc1tm1a(EUCOMM)Wtsi
HET Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 3.17×10-05
Cisd2
Cisd2tm1a(EUCOMM)Wtsi
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 3.40×10-05
Per2
Per2tm1a(EUCOMM)Hmgu
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 4.96×10-05
Epc2
Epc2tm1e(EUCOMM)Wtsi
HET Early adult mammalian phenotype Dysmorphology | adult mouse WTSI | EuroPhenome 7.41×10-05
Elmod1
Elmod1tm1a(EUCOMM)Hmgu
HOM Early adult mammalian phenotype Dysmorphology | adult mouse MRC Harwell | EuroPhenome 8.52×10-05

Download data as:   TSV   XLS

 The way we measure

Procedure
Dysmorphology

 Phenotype associations stats

7.47% of tested genes with null mutations on a B6N genetic background have a phenotype association to mammalian phenotype (26/348)

4.31% females (14/325) 5.07% males (17/335)

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