Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
T |
C |
4: 144,396,895 (GRCm39) |
K279R |
probably benign |
Het |
Aldoart2 |
A |
C |
12: 55,612,981 (GRCm39) |
Y302S |
probably damaging |
Het |
Arpp21 |
G |
T |
9: 111,945,821 (GRCm39) |
|
probably benign |
Het |
Camk1g |
C |
T |
1: 193,029,680 (GRCm39) |
|
probably null |
Het |
Cand2 |
G |
A |
6: 115,762,161 (GRCm39) |
V196I |
possibly damaging |
Het |
Cdc25b |
T |
A |
2: 131,035,567 (GRCm39) |
L381Q |
probably damaging |
Het |
Col17a1 |
C |
T |
19: 47,654,946 (GRCm39) |
G610E |
probably damaging |
Het |
Col19a1 |
C |
T |
1: 24,342,575 (GRCm39) |
E797K |
probably damaging |
Het |
Col3a1 |
A |
T |
1: 45,385,212 (GRCm39) |
I110L |
probably benign |
Het |
Col5a2 |
T |
A |
1: 45,445,440 (GRCm39) |
D506V |
possibly damaging |
Het |
Crp |
A |
T |
1: 172,525,676 (GRCm39) |
|
probably null |
Het |
Esco1 |
G |
T |
18: 10,574,886 (GRCm39) |
H729N |
probably damaging |
Het |
Evx2 |
A |
G |
2: 74,488,170 (GRCm39) |
S217P |
probably damaging |
Het |
Gabrb1 |
T |
C |
5: 72,279,364 (GRCm39) |
V303A |
possibly damaging |
Het |
Gcnt3 |
A |
G |
9: 69,941,471 (GRCm39) |
Y366H |
probably benign |
Het |
Gmpr2 |
A |
G |
14: 55,915,733 (GRCm39) |
T304A |
possibly damaging |
Het |
Golga3 |
C |
T |
5: 110,349,856 (GRCm39) |
Q656* |
probably null |
Het |
Gramd1b |
T |
A |
9: 40,366,951 (GRCm39) |
M6L |
probably damaging |
Het |
Kif17 |
T |
C |
4: 138,025,532 (GRCm39) |
Y945H |
probably damaging |
Het |
Klhl18 |
G |
C |
9: 110,265,195 (GRCm39) |
N335K |
possibly damaging |
Het |
Lrrk1 |
T |
A |
7: 65,920,545 (GRCm39) |
Q1486L |
probably benign |
Het |
Mboat7 |
G |
T |
7: 3,694,380 (GRCm39) |
H72N |
probably damaging |
Het |
Med12l |
G |
A |
3: 59,165,622 (GRCm39) |
V1447M |
probably damaging |
Het |
Mrpl3 |
T |
C |
9: 104,954,294 (GRCm39) |
F333L |
probably benign |
Het |
Nav3 |
T |
C |
10: 109,702,796 (GRCm39) |
T246A |
probably benign |
Het |
Neil3 |
A |
T |
8: 54,054,054 (GRCm39) |
V325E |
probably benign |
Het |
Nlrp4g |
A |
T |
9: 124,349,930 (GRCm38) |
|
noncoding transcript |
Het |
Onecut1 |
C |
T |
9: 74,796,738 (GRCm39) |
S419F |
probably damaging |
Het |
Or10n1 |
A |
T |
9: 39,524,991 (GRCm39) |
I43F |
probably damaging |
Het |
Ptp4a1 |
A |
T |
1: 30,984,044 (GRCm39) |
V58E |
probably benign |
Het |
Radil |
C |
T |
5: 142,493,970 (GRCm39) |
R49H |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,723,582 (GRCm39) |
E1648G |
possibly damaging |
Het |
Rnft2 |
C |
T |
5: 118,380,567 (GRCm39) |
M13I |
probably damaging |
Het |
Satb2 |
A |
G |
1: 56,987,309 (GRCm39) |
L92P |
probably damaging |
Het |
Scn4a |
T |
C |
11: 106,211,715 (GRCm39) |
Y1434C |
probably damaging |
Het |
Setx |
T |
A |
2: 29,035,486 (GRCm39) |
M657K |
probably benign |
Het |
Shd |
A |
G |
17: 56,280,936 (GRCm39) |
E204G |
probably damaging |
Het |
Shh |
T |
A |
5: 28,671,578 (GRCm39) |
R62* |
probably null |
Het |
Slc9a4 |
A |
G |
1: 40,646,954 (GRCm39) |
T483A |
probably benign |
Het |
Tbc1d7 |
A |
C |
13: 43,308,178 (GRCm39) |
S96A |
probably benign |
Het |
Tfcp2 |
T |
C |
15: 100,425,755 (GRCm39) |
|
probably null |
Het |
Tlk2 |
T |
A |
11: 105,131,201 (GRCm39) |
S182R |
probably damaging |
Het |
Trim65 |
T |
C |
11: 116,016,906 (GRCm39) |
T519A |
probably benign |
Het |
Trio |
T |
C |
15: 27,844,892 (GRCm39) |
|
probably null |
Het |
Usf3 |
G |
A |
16: 44,037,769 (GRCm39) |
V750I |
probably benign |
Het |
Utrn |
T |
A |
10: 12,556,369 (GRCm39) |
K1480N |
probably damaging |
Het |
Vmn1r58 |
T |
A |
7: 5,413,872 (GRCm39) |
R119S |
probably benign |
Het |
Xirp2 |
A |
G |
2: 67,341,313 (GRCm39) |
I1185V |
probably benign |
Het |
Zc3h7b |
A |
G |
15: 81,670,092 (GRCm39) |
H654R |
probably damaging |
Het |
Zfyve16 |
G |
T |
13: 92,636,792 (GRCm39) |
A1306E |
probably damaging |
Het |
|
Other mutations in Tppp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0032:Tppp2
|
UTSW |
14 |
52,156,866 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0032:Tppp2
|
UTSW |
14 |
52,156,866 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0352:Tppp2
|
UTSW |
14 |
52,156,807 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0932:Tppp2
|
UTSW |
14 |
52,157,881 (GRCm39) |
splice site |
probably benign |
|
R1860:Tppp2
|
UTSW |
14 |
52,158,062 (GRCm39) |
missense |
probably benign |
0.00 |
R1861:Tppp2
|
UTSW |
14 |
52,158,062 (GRCm39) |
missense |
probably benign |
0.00 |
R4087:Tppp2
|
UTSW |
14 |
52,156,957 (GRCm39) |
splice site |
probably null |
|
R4484:Tppp2
|
UTSW |
14 |
52,156,868 (GRCm39) |
missense |
probably damaging |
0.99 |
R4801:Tppp2
|
UTSW |
14 |
52,156,805 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Tppp2
|
UTSW |
14 |
52,156,805 (GRCm39) |
missense |
probably benign |
0.00 |
R5071:Tppp2
|
UTSW |
14 |
52,157,912 (GRCm39) |
missense |
probably benign |
0.01 |
R5073:Tppp2
|
UTSW |
14 |
52,157,912 (GRCm39) |
missense |
probably benign |
0.01 |
R5103:Tppp2
|
UTSW |
14 |
52,156,909 (GRCm39) |
missense |
probably benign |
0.05 |
R5992:Tppp2
|
UTSW |
14 |
52,156,392 (GRCm39) |
missense |
probably benign |
0.08 |
R6124:Tppp2
|
UTSW |
14 |
52,156,937 (GRCm39) |
missense |
probably benign |
0.12 |
R7372:Tppp2
|
UTSW |
14 |
52,156,865 (GRCm39) |
missense |
probably benign |
0.08 |
R7506:Tppp2
|
UTSW |
14 |
52,158,058 (GRCm39) |
missense |
possibly damaging |
0.74 |
|