Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002D01Rik |
CCTTCTCCTTCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
CCTTCTCCTTCTTCTCCTTCTTCTCCATCTTCTCCTTCTTC |
7: 28,947,048 (GRCm39) |
|
probably benign |
Het |
Aarsd1 |
A |
C |
11: 101,301,597 (GRCm39) |
S262A |
probably benign |
Het |
Abhd17c |
A |
G |
7: 83,763,637 (GRCm39) |
Y189H |
probably damaging |
Het |
Adam33 |
T |
C |
2: 130,895,606 (GRCm39) |
R570G |
possibly damaging |
Het |
Alpk2 |
G |
A |
18: 65,424,464 (GRCm39) |
R1441W |
probably damaging |
Het |
Arhgap21 |
A |
G |
2: 20,885,464 (GRCm39) |
V581A |
probably benign |
Het |
Bcat2 |
T |
C |
7: 45,234,980 (GRCm39) |
V226A |
possibly damaging |
Het |
Cdh10 |
A |
G |
15: 19,013,521 (GRCm39) |
N707S |
possibly damaging |
Het |
Chd9 |
T |
C |
8: 91,659,174 (GRCm39) |
F45L |
unknown |
Het |
Clec1a |
T |
C |
6: 129,428,606 (GRCm39) |
T25A |
probably benign |
Het |
Cps1 |
T |
C |
1: 67,259,671 (GRCm39) |
F1338L |
probably damaging |
Het |
Cthrc1 |
A |
G |
15: 38,947,868 (GRCm39) |
T196A |
probably benign |
Het |
Ctsm |
A |
T |
13: 61,686,299 (GRCm39) |
V228D |
probably damaging |
Het |
Dennd3 |
A |
T |
15: 73,429,477 (GRCm39) |
D920V |
probably damaging |
Het |
Dnah17 |
A |
G |
11: 117,987,452 (GRCm39) |
I1286T |
probably benign |
Het |
Dnah3 |
T |
A |
7: 119,551,473 (GRCm39) |
T2949S |
probably benign |
Het |
Dram1 |
C |
T |
10: 88,192,703 (GRCm39) |
V28M |
probably benign |
Het |
Eml5 |
A |
G |
12: 98,827,554 (GRCm39) |
Y559H |
probably damaging |
Het |
Ermard |
C |
T |
17: 15,273,554 (GRCm39) |
R380C |
possibly damaging |
Het |
Fam181a |
A |
G |
12: 103,282,107 (GRCm39) |
D4G |
probably damaging |
Het |
Gabrd |
C |
A |
4: 155,472,803 (GRCm39) |
V127L |
probably damaging |
Het |
Galnt12 |
T |
A |
4: 47,104,163 (GRCm39) |
Y140* |
probably null |
Het |
Gpr161 |
A |
T |
1: 165,146,389 (GRCm39) |
K442* |
probably null |
Het |
Haus6 |
A |
T |
4: 86,513,665 (GRCm39) |
N332K |
probably benign |
Het |
Igsf3 |
T |
A |
3: 101,358,322 (GRCm39) |
Y738N |
probably damaging |
Het |
Itsn1 |
T |
A |
16: 91,625,264 (GRCm39) |
*622R |
probably null |
Het |
Kcna2 |
T |
A |
3: 107,012,887 (GRCm39) |
Y489* |
probably null |
Het |
Limk1 |
A |
G |
5: 134,701,864 (GRCm39) |
|
probably null |
Het |
Manba |
A |
T |
3: 135,255,079 (GRCm39) |
D479V |
probably benign |
Het |
Myh6 |
A |
T |
14: 55,189,779 (GRCm39) |
I1089N |
possibly damaging |
Het |
Npas4 |
T |
A |
19: 5,038,492 (GRCm39) |
D142V |
probably damaging |
Het |
Nr4a1 |
T |
C |
15: 101,168,053 (GRCm39) |
F30L |
probably benign |
Het |
Or10x4 |
G |
A |
1: 174,218,742 (GRCm39) |
A36T |
probably benign |
Het |
Or5p4 |
T |
C |
7: 107,680,040 (GRCm39) |
I13T |
|
Het |
Parp9 |
T |
C |
16: 35,777,234 (GRCm39) |
S393P |
probably damaging |
Het |
Pcdha11 |
A |
G |
18: 37,145,484 (GRCm39) |
E525G |
probably damaging |
Het |
Pdia2 |
T |
C |
17: 26,416,174 (GRCm39) |
T298A |
probably benign |
Het |
Per3 |
G |
A |
4: 151,094,945 (GRCm39) |
T946I |
probably benign |
Het |
Pla2r1 |
A |
T |
2: 60,258,902 (GRCm39) |
V1162D |
probably damaging |
Het |
Plxnd1 |
T |
A |
6: 115,932,730 (GRCm39) |
N1917Y |
probably damaging |
Het |
Pole3 |
A |
T |
4: 62,442,277 (GRCm39) |
D114E |
unknown |
Het |
Ppil3 |
T |
C |
1: 58,470,397 (GRCm39) |
D151G |
probably benign |
Het |
Psd3 |
A |
T |
8: 68,165,833 (GRCm39) |
M365K |
unknown |
Het |
Psme2b |
T |
G |
11: 48,836,566 (GRCm39) |
H127P |
probably damaging |
Het |
Ric8a |
C |
G |
7: 140,437,393 (GRCm39) |
R4G |
probably benign |
Het |
Rock2 |
A |
T |
12: 17,027,763 (GRCm39) |
D1360V |
probably damaging |
Het |
Simc1 |
A |
G |
13: 54,674,192 (GRCm39) |
T847A |
probably benign |
Het |
Slc12a1 |
T |
A |
2: 125,028,144 (GRCm39) |
V480E |
probably damaging |
Het |
Slc32a1 |
T |
C |
2: 158,456,241 (GRCm39) |
F299L |
probably benign |
Het |
Slc44a2 |
A |
G |
9: 21,258,333 (GRCm39) |
Y500C |
|
Het |
Ssbp2 |
A |
G |
13: 91,823,157 (GRCm39) |
D192G |
probably benign |
Het |
Stat5b |
T |
C |
11: 100,681,674 (GRCm39) |
K527E |
probably benign |
Het |
Tm7sf3 |
C |
T |
6: 146,525,179 (GRCm39) |
D89N |
possibly damaging |
Het |
Usp50 |
A |
G |
2: 126,619,817 (GRCm39) |
|
probably null |
Het |
Vegfc |
A |
T |
8: 54,610,053 (GRCm39) |
M70L |
probably benign |
Het |
Vmn1r40 |
A |
G |
6: 89,691,854 (GRCm39) |
T224A |
probably benign |
Het |
Vmn2r116 |
A |
G |
17: 23,605,919 (GRCm39) |
D277G |
probably benign |
Het |
Vti1a |
T |
A |
19: 55,612,278 (GRCm39) |
I197N |
possibly damaging |
Het |
Zfyve9 |
C |
A |
4: 108,576,435 (GRCm39) |
L215F |
probably damaging |
Het |
Znrf3 |
A |
T |
11: 5,288,710 (GRCm39) |
Y19* |
probably null |
Het |
|
Other mutations in Numbl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00976:Numbl
|
APN |
7 |
26,968,235 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01389:Numbl
|
APN |
7 |
26,980,472 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02671:Numbl
|
APN |
7 |
26,964,327 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Numbl
|
UTSW |
7 |
26,979,027 (GRCm39) |
missense |
probably benign |
|
R0212:Numbl
|
UTSW |
7 |
26,980,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R0709:Numbl
|
UTSW |
7 |
26,973,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R1768:Numbl
|
UTSW |
7 |
26,980,379 (GRCm39) |
missense |
probably benign |
|
R2181:Numbl
|
UTSW |
7 |
26,968,346 (GRCm39) |
critical splice donor site |
probably null |
|
R5071:Numbl
|
UTSW |
7 |
26,980,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5072:Numbl
|
UTSW |
7 |
26,980,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Numbl
|
UTSW |
7 |
26,980,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R6134:Numbl
|
UTSW |
7 |
26,980,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R6387:Numbl
|
UTSW |
7 |
26,976,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R6989:Numbl
|
UTSW |
7 |
26,980,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R7510:Numbl
|
UTSW |
7 |
26,971,412 (GRCm39) |
splice site |
probably null |
|
R8093:Numbl
|
UTSW |
7 |
26,980,461 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8518:Numbl
|
UTSW |
7 |
26,964,361 (GRCm39) |
missense |
probably benign |
0.12 |
V7580:Numbl
|
UTSW |
7 |
26,979,027 (GRCm39) |
missense |
probably benign |
|
V7583:Numbl
|
UTSW |
7 |
26,979,027 (GRCm39) |
missense |
probably benign |
|
|