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T+
Allele Detail

Nomenclature
Symbol: T+
Name: brachyury; wild type
MGI ID: MGI:1857758
Gene: T   Location: Chr17:8627288-8635361 bp, + strand    Genetic Position: Chr17, 4.02 cM
Show the 1 image(s) involving this allele.
Mutation
origin
Strain of Origin: Not Specified
Mutation
description
Allele Type: Not Specified
Inheritance: Not Specified
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation: Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any T Mutation: 45 strains or lines available
Expression
In Mice Carrying this Mutation: 13 assay results
Phenotype
summary
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Phenotype Summary by Mammalian Phenotype terms

(show or hide all annotated terms)

Genotypes are listed in the next section.

      Key:  
hm homozygous ht heterozygous
cn conditional genotype  cx complex: > 1 genome feature
tg involves transgenes ot other: hemizygous, indeterminate,...
N normal phenotype expected model not found
Affected SystemsGenotypes:
 
ht1
 
ht2
 
ht3
 
ht4
 
ht5
 
ht6
 
ht7
 
ht8
 
ht9
 
ht10
 
ht11
 
ht12
 
ht13
 
ht14
 
ht15
 
ht16
 
ht17
 
ht18
 
ht19
 
ht20
 
ht21
 
cx22
 
cx23
 
cx24
 
cx25
 
cx26
 
cx27
 
cx28
 
cx29
 
cx30
 
cx31
 
cx32
 
cx33
 
cx34
 
cx35
 
cx36
 
cx37
 
cx38
 
cx39
 
cx40
 
cx41
 
cx42
 
cx43
 
cx44
 
cx45
 
cx46
 
cx47
 
tg48
 
tg49
 
tg50
 
tg51
 
tg52
 
tg53
  
behavior/neurological          
                                                 
  
cardiovascular system          
                                                    
  
embryogenesis          
                                              
  
endocrine/exocrine glands          
                                                    
  
growth/size          
                                                   
  
hearing/vestibular/ear          
                                                  
  
homeostasis/metabolism          
                                                   
  
lethality/postnatal          
                                                   
  
lethality/prenatal-perinatal          
                                            
  
life span/aging          
                                                    
  
limbs/digits/tail          
                          N
  
nervous system          
                                                 
  
other phenotype          
                                                    
  
reproductive system          
                    N             
  
skeleton          
                                                
Phenotypic
data by
genotype
Phenotypic Data by Genotype

(show or hide all phenotypic details)

GenotypeAllelic CompositionGenetic Background
  
 ht1   
TOrl/T+ B6.Cg-TOrl/EiJ
  
 ht2   
Tc-3H/T+ BALB/cOlaHsd
  
 ht3   
T40H/T+ C57BL/6J
  
 ht4   
T41H/T+ C57BL/6J
  
 ht5   
T9J/T+ C57BL/6J
  
 ht6   
T8J/T+ C57BL/6J-Apoetm1Unc
  
 ht7   
T7J/T+ C57BL/6J-T7J
  
 ht8   
T31H/T+ involves: 101/H * C3H/HeH * TFH
  
 ht9   
T33H/T+ involves: 101/H * C3H/HeH * TFH
  
 ht10   
T36H/T+ involves: 101/H * C3H/HeH * TFH
  
 ht11   
TWis/T+ involves: A/J
  
 ht12   
Thp/T+ involves: AKR/J * C57BL/Gr * CBA/Gr
  
 ht13   
T39H/T+ involves: BALB/c * C3H/HeN
  
 ht14   
T29H/T+ involves: BALB/c * TFH
  
 ht15   
TOrl/T+ involves: C57BL/6J * Orl:Swiss
  
 ht16   
T34H/T+ involves: STOCK T34H * TFH
  
 ht17   
Tc/T+ mixed
  
 ht18   
T/T+ Not Specified
  
 ht19   
Tc/T+ Not Specified
  
 ht20   
Th/T+ Not Specified
  
 ht21   
TJic/T+ Not Specified
  
 cx22   
T34H/T+
tw32/t+
involves: 101/H * C3H/HeH * STOCK T34H * TFH
  
 cx23   
Nox3het/Nox3het
T31H/T+
involves: 101/H * C3H/HeH * TFH
  
 cx24   
T31H/T+
tw32/t+
involves: 101/H * C3H/HeH * TFH
  
 cx25   
Nox3het/Nox3het
T33H/T+
involves: 101/H * C3H/HeH * TFH
  
 cx26   
T30H/T+
tw32/t+
involves: 101/H * C3H/HeH * TFH
  
 cx27   
T33H/T+
tw32/t+
involves: 101/H * C3H/HeH * TFH
  
 cx28   
Nox3het/Nox3het
T36H/T+
involves: 101/H * C3H/HeH * TFH
  
 cx29   
T36H/T+
tw32/t+
involves: 101/H * C3H/HeH * TFH
  
 cx30   
T32H/T+
th51/t+
involves: 101/H * C3H/HeH * TFH
  
 cx31   
T32H/T+
tw32/t+
involves: 101/H * C3H/HeH * TFH
  
 cx32   
T30H/T+
t6/t+
involves: 101/H * C3H/HeH * TFH
  
 cx33   
T32H/T+
t6/t+
involves: 101/H * C3H/HeH * TFH
  
 cx34   
T36H/T+
t6/t+
involves: 101/H * C3H/HeH * TFH
  
 cx35   
T22H/T+
tw32/t+
involves: 101/H * C3H/HeH * TFH
  
 cx36   
Igf2rtm2Wag/Igf2r+
Thp/T+
involves: 129/Sv * 129P2/OlaHsd * AKR/J * C57BL/6
  
 cx37   
Sp5tm1Rbe/Sp5tm1Rbe
T/T+
involves: 129P2/Ola * C57BL/6J
  
 cx38   
D17Aus9df13J/D17Aus9+
T7J/T+
involves: 129S4/SvJae * BALB/cJ * C57BL/6
  
 cx39   
D17Aus9df12J/D17Aus9+
T7J/T+
involves: 129S4/SvJae * BALB/cJ * C57BL/6
  
 cx40   
D17Aus9df10J/D17Aus9+
T7J/T+
involves: 129S4/SvJae * BALB/cJ * C57BL/6
  
 cx41   
Map3k4byg/Map3k4+
Thp/T+
involves: AKR/J * C3H/HeH * C57BL/6J
  
 cx42   
T29H/T+
tw32/t+
involves: BALB/c * TFH
  
 cx43   
T29H/T+
t6/t+
involves: BALB/c * TFH
  
 cx44   
TOrl/T+
Qkqk/Qk+
involves: C57BL/6J * Orl:Swiss