Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb8 |
T |
C |
5: 24,606,055 (GRCm39) |
S247P |
probably damaging |
Het |
Atg4b |
A |
G |
1: 93,695,984 (GRCm39) |
E41G |
probably benign |
Het |
Bckdk |
T |
C |
7: 127,504,502 (GRCm39) |
|
probably benign |
Het |
Cacna2d1 |
A |
G |
5: 16,507,246 (GRCm39) |
|
probably null |
Het |
Chaf1a |
A |
G |
17: 56,351,068 (GRCm39) |
D16G |
unknown |
Het |
Defb12 |
A |
G |
8: 19,162,737 (GRCm39) |
I65T |
probably benign |
Het |
Dnah7c |
T |
C |
1: 46,787,738 (GRCm39) |
Y3264H |
probably damaging |
Het |
Ehhadh |
C |
A |
16: 21,581,602 (GRCm39) |
K463N |
probably damaging |
Het |
Ehmt2 |
G |
A |
17: 35,127,724 (GRCm39) |
R901Q |
possibly damaging |
Het |
Entrep1 |
G |
A |
19: 23,952,993 (GRCm39) |
A439V |
probably damaging |
Het |
Entrep1 |
C |
T |
19: 23,953,002 (GRCm39) |
S436N |
probably damaging |
Het |
Ern2 |
T |
C |
7: 121,777,069 (GRCm39) |
|
probably null |
Het |
Esp6 |
A |
G |
17: 40,876,035 (GRCm39) |
T28A |
possibly damaging |
Het |
Gm17333 |
A |
C |
16: 77,649,767 (GRCm39) |
|
noncoding transcript |
Het |
Heatr5a |
T |
C |
12: 52,003,008 (GRCm39) |
T165A |
probably benign |
Het |
Hoxa5 |
T |
C |
6: 52,181,240 (GRCm39) |
S31G |
probably benign |
Het |
Ift80 |
A |
G |
3: 68,801,507 (GRCm39) |
I744T |
probably benign |
Het |
Kalrn |
T |
C |
16: 34,055,761 (GRCm39) |
K853E |
probably damaging |
Het |
Krt36 |
A |
T |
11: 99,994,239 (GRCm39) |
D279E |
possibly damaging |
Het |
Map3k11 |
T |
A |
19: 5,740,852 (GRCm39) |
V193E |
probably damaging |
Het |
Mrgpra4 |
T |
A |
7: 47,630,684 (GRCm39) |
M306L |
probably benign |
Het |
Myo1a |
A |
G |
10: 127,549,602 (GRCm39) |
T428A |
probably benign |
Het |
Nuggc |
A |
G |
14: 65,848,621 (GRCm39) |
H174R |
possibly damaging |
Het |
Or14c40 |
G |
A |
7: 86,313,163 (GRCm39) |
V98M |
probably benign |
Het |
Or1e29 |
A |
T |
11: 73,667,664 (GRCm39) |
M163K |
possibly damaging |
Het |
Pigr |
G |
A |
1: 130,769,554 (GRCm39) |
D122N |
probably benign |
Het |
Pik3ca |
C |
T |
3: 32,494,084 (GRCm39) |
R349* |
probably null |
Het |
Rfxank |
T |
C |
8: 70,588,862 (GRCm39) |
D89G |
probably damaging |
Het |
Rsf1 |
CGGCGGCGG |
CGGCGGCGGTGGCGGCGG |
7: 97,229,127 (GRCm39) |
|
probably benign |
Het |
Serpina1a |
A |
G |
12: 103,820,934 (GRCm39) |
L348P |
probably damaging |
Het |
Shank1 |
A |
G |
7: 43,991,898 (GRCm39) |
Y701C |
unknown |
Het |
Six4 |
G |
T |
12: 73,159,314 (GRCm39) |
D207E |
possibly damaging |
Het |
Slco3a1 |
G |
T |
7: 74,204,276 (GRCm39) |
D21E |
probably benign |
Het |
Sox6 |
C |
T |
7: 115,143,704 (GRCm39) |
|
probably null |
Het |
Spta1 |
A |
G |
1: 174,007,418 (GRCm39) |
N216S |
probably damaging |
Het |
Stard13 |
T |
C |
5: 150,986,334 (GRCm39) |
N392S |
possibly damaging |
Het |
Tax1bp1 |
T |
C |
6: 52,704,263 (GRCm39) |
V81A |
possibly damaging |
Het |
Vmn1r90 |
C |
T |
7: 14,295,495 (GRCm39) |
W201* |
probably null |
Het |
Wdr31 |
T |
A |
4: 62,378,626 (GRCm39) |
N7I |
probably damaging |
Het |
Ypel4 |
A |
G |
2: 84,567,151 (GRCm39) |
|
probably benign |
Het |
Zfp39 |
T |
C |
11: 58,780,843 (GRCm39) |
K640E |
probably damaging |
Het |
Zfp579 |
A |
G |
7: 4,996,072 (GRCm39) |
|
probably benign |
Het |
Zfp974 |
C |
A |
7: 27,609,657 (GRCm39) |
K689N |
possibly damaging |
Het |
|
Other mutations in Trim29 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02364:Trim29
|
APN |
9 |
43,222,599 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02387:Trim29
|
APN |
9 |
43,236,149 (GRCm39) |
missense |
probably benign |
0.02 |
R1770:Trim29
|
UTSW |
9 |
43,243,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R1883:Trim29
|
UTSW |
9 |
43,222,702 (GRCm39) |
missense |
probably damaging |
1.00 |
R1962:Trim29
|
UTSW |
9 |
43,222,615 (GRCm39) |
missense |
probably benign |
|
R4198:Trim29
|
UTSW |
9 |
43,222,677 (GRCm39) |
nonsense |
probably null |
|
R4200:Trim29
|
UTSW |
9 |
43,222,677 (GRCm39) |
nonsense |
probably null |
|
R4863:Trim29
|
UTSW |
9 |
43,240,872 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4934:Trim29
|
UTSW |
9 |
43,222,265 (GRCm39) |
missense |
probably benign |
0.36 |
R6171:Trim29
|
UTSW |
9 |
43,230,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R6737:Trim29
|
UTSW |
9 |
43,230,681 (GRCm39) |
missense |
probably benign |
0.01 |
R6972:Trim29
|
UTSW |
9 |
43,238,409 (GRCm39) |
missense |
probably benign |
0.01 |
R7191:Trim29
|
UTSW |
9 |
43,222,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R7434:Trim29
|
UTSW |
9 |
43,246,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R7588:Trim29
|
UTSW |
9 |
43,246,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R7590:Trim29
|
UTSW |
9 |
43,222,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R8781:Trim29
|
UTSW |
9 |
43,222,615 (GRCm39) |
missense |
probably benign |
0.27 |
R8866:Trim29
|
UTSW |
9 |
43,222,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R8922:Trim29
|
UTSW |
9 |
43,233,636 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9336:Trim29
|
UTSW |
9 |
43,238,350 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9709:Trim29
|
UTSW |
9 |
43,231,797 (GRCm39) |
missense |
probably benign |
0.12 |
X0065:Trim29
|
UTSW |
9 |
43,233,621 (GRCm39) |
missense |
probably benign |
0.06 |
|