Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4fm4 |
C |
T |
4: 144,396,698 (GRCm39) |
E345K |
probably damaging |
Het |
Bpifb1 |
A |
G |
2: 154,057,242 (GRCm39) |
N400S |
possibly damaging |
Het |
Cep250 |
G |
A |
2: 155,834,552 (GRCm39) |
R2159K |
probably damaging |
Het |
Crhr1 |
T |
A |
11: 104,044,377 (GRCm39) |
S22T |
probably benign |
Het |
Cyp4a10 |
G |
T |
4: 115,381,980 (GRCm39) |
V221L |
probably benign |
Het |
D1Pas1 |
G |
T |
1: 186,700,477 (GRCm39) |
W135C |
probably damaging |
Het |
Dcbld2 |
T |
C |
16: 58,285,701 (GRCm39) |
L620P |
probably damaging |
Het |
Dnah17 |
C |
T |
11: 117,971,675 (GRCm39) |
|
probably benign |
Het |
Dnm3 |
T |
C |
1: 161,911,699 (GRCm39) |
D66G |
probably damaging |
Het |
Fzd10 |
G |
A |
5: 128,679,476 (GRCm39) |
V399M |
probably damaging |
Het |
Gm10801 |
T |
A |
2: 98,494,361 (GRCm39) |
I146N |
possibly damaging |
Het |
Gm525 |
T |
A |
11: 88,965,830 (GRCm39) |
|
probably null |
Het |
Gpr37l1 |
T |
C |
1: 135,089,100 (GRCm39) |
I322V |
probably benign |
Het |
Grid2ip |
T |
G |
5: 143,371,794 (GRCm39) |
S679R |
probably damaging |
Het |
Gyg1 |
A |
T |
3: 20,209,189 (GRCm39) |
S15T |
probably benign |
Het |
Hace1 |
G |
A |
10: 45,587,604 (GRCm39) |
C901Y |
probably benign |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hp1bp3 |
C |
T |
4: 137,949,018 (GRCm39) |
A27V |
probably benign |
Het |
Hsf5 |
A |
G |
11: 87,522,508 (GRCm39) |
Y367C |
probably damaging |
Het |
Igf2r |
T |
C |
17: 12,924,716 (GRCm39) |
I1034V |
probably benign |
Het |
Itpr1 |
A |
G |
6: 108,371,802 (GRCm39) |
T1159A |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lrrc14 |
T |
C |
15: 76,597,765 (GRCm39) |
V165A |
probably benign |
Het |
Lrrc45 |
C |
T |
11: 120,609,503 (GRCm39) |
A422V |
probably benign |
Het |
Lrrk2 |
T |
A |
15: 91,651,664 (GRCm39) |
|
probably null |
Het |
Map3k4 |
T |
C |
17: 12,454,880 (GRCm39) |
H1370R |
possibly damaging |
Het |
Mpo |
A |
G |
11: 87,691,866 (GRCm39) |
Y433C |
probably damaging |
Het |
Nfkbil1 |
G |
T |
17: 35,439,932 (GRCm39) |
Q194K |
probably benign |
Het |
Nin |
C |
T |
12: 70,125,016 (GRCm39) |
G102E |
probably damaging |
Het |
Nmt1 |
T |
C |
11: 102,943,059 (GRCm39) |
V138A |
probably benign |
Het |
Optc |
T |
A |
1: 133,828,920 (GRCm39) |
R176* |
probably null |
Het |
Or10aa3 |
A |
T |
1: 173,878,076 (GRCm39) |
I46F |
probably damaging |
Het |
Or4c110 |
A |
G |
2: 88,832,377 (GRCm39) |
F85S |
probably benign |
Het |
Or52ae9 |
A |
C |
7: 103,389,794 (GRCm39) |
Y218D |
probably damaging |
Het |
Or6n2 |
T |
A |
1: 173,897,147 (GRCm39) |
F94L |
probably damaging |
Het |
Oxct1 |
T |
A |
15: 4,066,601 (GRCm39) |
N72K |
possibly damaging |
Het |
Plxna2 |
G |
A |
1: 194,477,218 (GRCm39) |
A1243T |
probably benign |
Het |
Rin1 |
G |
T |
19: 5,103,002 (GRCm39) |
L430F |
probably benign |
Het |
Ros1 |
A |
T |
10: 52,070,944 (GRCm39) |
S37T |
possibly damaging |
Het |
Rrp36 |
G |
T |
17: 46,983,732 (GRCm39) |
Q27K |
probably damaging |
Het |
Sez6 |
T |
C |
11: 77,867,708 (GRCm39) |
I875T |
probably damaging |
Het |
Sfrp5 |
T |
G |
19: 42,190,257 (GRCm39) |
Y65S |
probably damaging |
Het |
Slc25a54 |
T |
A |
3: 109,023,820 (GRCm39) |
L472I |
probably benign |
Het |
Slc35d3 |
T |
C |
10: 19,724,605 (GRCm39) |
E417G |
probably damaging |
Het |
Sumf2 |
A |
G |
5: 129,878,820 (GRCm39) |
D52G |
probably benign |
Het |
Sympk |
A |
G |
7: 18,781,447 (GRCm39) |
N801S |
possibly damaging |
Het |
Tcstv2c |
G |
A |
13: 120,616,368 (GRCm39) |
C69Y |
probably damaging |
Het |
Tmem38b |
T |
C |
4: 53,854,398 (GRCm39) |
F210S |
probably damaging |
Het |
Tnks |
T |
A |
8: 35,407,966 (GRCm39) |
H254L |
probably damaging |
Het |
Trappc10 |
A |
T |
10: 78,046,237 (GRCm39) |
V451E |
probably benign |
Het |
Trim43a |
A |
T |
9: 88,465,131 (GRCm39) |
I153F |
probably benign |
Het |
Tulp1 |
T |
C |
17: 28,572,683 (GRCm39) |
N213S |
probably damaging |
Het |
Ubr1 |
T |
C |
2: 120,746,951 (GRCm39) |
D830G |
probably benign |
Het |
Uqcc3 |
C |
T |
19: 8,858,069 (GRCm39) |
|
probably null |
Het |
Vmn2r26 |
T |
A |
6: 124,002,938 (GRCm39) |
M116K |
probably benign |
Het |
Zscan12 |
A |
G |
13: 21,552,800 (GRCm39) |
Q208R |
probably benign |
Het |
|
Other mutations in Taf7l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00730:Taf7l2
|
APN |
10 |
115,948,931 (GRCm39) |
missense |
probably benign |
0.13 |
IGL00942:Taf7l2
|
APN |
10 |
115,949,341 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0325:Taf7l2
|
UTSW |
10 |
115,949,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R0467:Taf7l2
|
UTSW |
10 |
115,949,058 (GRCm39) |
missense |
probably benign |
0.00 |
R0534:Taf7l2
|
UTSW |
10 |
115,948,707 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1068:Taf7l2
|
UTSW |
10 |
115,949,359 (GRCm39) |
missense |
probably damaging |
0.97 |
R1102:Taf7l2
|
UTSW |
10 |
115,949,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R1421:Taf7l2
|
UTSW |
10 |
115,949,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R1601:Taf7l2
|
UTSW |
10 |
115,949,521 (GRCm39) |
missense |
probably damaging |
0.99 |
R1834:Taf7l2
|
UTSW |
10 |
115,948,570 (GRCm39) |
missense |
probably benign |
0.15 |
R5799:Taf7l2
|
UTSW |
10 |
115,948,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R5908:Taf7l2
|
UTSW |
10 |
115,949,133 (GRCm39) |
missense |
probably benign |
0.04 |
R7765:Taf7l2
|
UTSW |
10 |
115,949,158 (GRCm39) |
nonsense |
probably null |
|
R8420:Taf7l2
|
UTSW |
10 |
115,948,440 (GRCm39) |
missense |
probably benign |
|
R9214:Taf7l2
|
UTSW |
10 |
115,948,903 (GRCm39) |
missense |
probably benign |
0.05 |
R9430:Taf7l2
|
UTSW |
10 |
115,949,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Taf7l2
|
UTSW |
10 |
115,948,931 (GRCm39) |
missense |
probably benign |
0.13 |
|