Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap6 |
T |
C |
12: 53,057,250 (GRCm39) |
|
probably benign |
Het |
Ankrd11 |
G |
A |
8: 123,618,984 (GRCm39) |
R1602W |
probably damaging |
Het |
Arhgap23 |
G |
T |
11: 97,342,426 (GRCm39) |
R236L |
probably benign |
Het |
Aurkaip1 |
T |
C |
4: 155,917,028 (GRCm39) |
V92A |
probably benign |
Het |
Cdh20 |
A |
T |
1: 104,881,816 (GRCm39) |
|
probably benign |
Het |
Ctnnd2 |
A |
G |
15: 30,847,482 (GRCm39) |
N691S |
probably benign |
Het |
Ddx24 |
A |
C |
12: 103,390,717 (GRCm39) |
D2E |
possibly damaging |
Het |
Dennd5b |
A |
G |
6: 148,934,799 (GRCm39) |
S691P |
probably benign |
Het |
Dhrs3 |
C |
T |
4: 144,650,519 (GRCm39) |
R248W |
possibly damaging |
Het |
Dlgap1 |
T |
C |
17: 70,823,029 (GRCm39) |
S5P |
probably damaging |
Het |
Dnai4 |
A |
T |
4: 102,947,595 (GRCm39) |
I227K |
probably benign |
Het |
Ep300 |
A |
T |
15: 81,497,613 (GRCm39) |
M510L |
unknown |
Het |
Fbxo25 |
T |
C |
8: 13,973,922 (GRCm39) |
|
probably benign |
Het |
Gm3252 |
A |
T |
14: 4,743,741 (GRCm38) |
K193M |
possibly damaging |
Het |
Gtf3c1 |
T |
C |
7: 125,267,162 (GRCm39) |
|
probably null |
Het |
Helz2 |
T |
C |
2: 180,873,483 (GRCm39) |
D2337G |
probably damaging |
Het |
Idh1 |
A |
T |
1: 65,201,081 (GRCm39) |
M290K |
probably damaging |
Het |
Layn |
T |
C |
9: 50,985,317 (GRCm39) |
S80G |
probably damaging |
Het |
Ltbp4 |
C |
T |
7: 27,006,359 (GRCm39) |
E1440K |
probably damaging |
Het |
Mri1 |
T |
C |
8: 84,982,924 (GRCm39) |
T166A |
probably damaging |
Het |
Myod1 |
C |
T |
7: 46,027,730 (GRCm39) |
T290I |
probably benign |
Het |
Nfat5 |
T |
A |
8: 108,078,154 (GRCm39) |
L431* |
probably null |
Het |
Nle1 |
A |
T |
11: 82,795,133 (GRCm39) |
Y299* |
probably null |
Het |
Nlrp4c |
T |
A |
7: 6,069,828 (GRCm39) |
F576L |
possibly damaging |
Het |
Nudt21 |
G |
T |
8: 94,746,329 (GRCm39) |
S123* |
probably null |
Het |
Plekhg1 |
A |
C |
10: 3,895,916 (GRCm39) |
D436A |
probably damaging |
Het |
Plxna2 |
T |
C |
1: 194,326,732 (GRCm39) |
V222A |
probably damaging |
Het |
Rbm14 |
A |
G |
19: 4,851,745 (GRCm39) |
|
probably benign |
Het |
Scfd1 |
T |
A |
12: 51,436,164 (GRCm39) |
|
probably benign |
Het |
Slc34a2 |
A |
G |
5: 53,225,073 (GRCm39) |
T405A |
probably benign |
Het |
Slc39a9 |
T |
A |
12: 80,691,695 (GRCm39) |
M14K |
probably damaging |
Het |
Slc39a9 |
G |
A |
12: 80,691,696 (GRCm39) |
M14I |
probably damaging |
Het |
Spast |
G |
A |
17: 74,679,334 (GRCm39) |
|
probably benign |
Het |
Spen |
T |
C |
4: 141,205,457 (GRCm39) |
R1057G |
unknown |
Het |
Sptbn4 |
T |
G |
7: 27,065,132 (GRCm39) |
T2056P |
probably damaging |
Het |
Ssrp1 |
T |
C |
2: 84,870,705 (GRCm39) |
L148P |
probably damaging |
Het |
Tdrd6 |
T |
A |
17: 43,938,093 (GRCm39) |
H985L |
probably damaging |
Het |
Tmem44 |
A |
G |
16: 30,358,199 (GRCm39) |
|
probably benign |
Het |
Vmn2r116 |
T |
A |
17: 23,603,808 (GRCm39) |
L11Q |
probably null |
Het |
|
Other mutations in Ppp4r3c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02024:Ppp4r3c1
|
APN |
X |
88,975,129 (GRCm39) |
missense |
probably benign |
0.17 |
R1980:Ppp4r3c1
|
UTSW |
X |
88,975,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R1981:Ppp4r3c1
|
UTSW |
X |
88,975,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Ppp4r3c1
|
UTSW |
X |
88,975,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R2299:Ppp4r3c1
|
UTSW |
X |
88,976,005 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2381:Ppp4r3c1
|
UTSW |
X |
88,974,116 (GRCm39) |
missense |
probably benign |
0.34 |
R2895:Ppp4r3c1
|
UTSW |
X |
88,976,005 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2896:Ppp4r3c1
|
UTSW |
X |
88,976,005 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4001:Ppp4r3c1
|
UTSW |
X |
88,974,116 (GRCm39) |
missense |
probably benign |
0.34 |
R4003:Ppp4r3c1
|
UTSW |
X |
88,974,116 (GRCm39) |
missense |
probably benign |
0.34 |
R4042:Ppp4r3c1
|
UTSW |
X |
88,975,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Ppp4r3c1
|
UTSW |
X |
88,975,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R4280:Ppp4r3c1
|
UTSW |
X |
88,976,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R4281:Ppp4r3c1
|
UTSW |
X |
88,976,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R4282:Ppp4r3c1
|
UTSW |
X |
88,976,105 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Ppp4r3c1
|
UTSW |
X |
88,973,843 (GRCm39) |
missense |
unknown |
|
Z1088:Ppp4r3c1
|
UTSW |
X |
88,973,842 (GRCm39) |
missense |
unknown |
|
Z1176:Ppp4r3c1
|
UTSW |
X |
88,973,847 (GRCm39) |
missense |
unknown |
|
|