Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
A |
G |
8: 73,199,219 (GRCm39) |
S209G |
probably benign |
Het |
Aars1 |
T |
C |
8: 111,772,160 (GRCm39) |
L450P |
possibly damaging |
Het |
Acsbg1 |
G |
A |
9: 54,523,268 (GRCm39) |
T453M |
probably benign |
Het |
Aff3 |
A |
G |
1: 38,220,742 (GRCm39) |
S1100P |
possibly damaging |
Het |
B4galt5 |
G |
A |
2: 167,190,849 (GRCm39) |
A35V |
probably benign |
Het |
C1qtnf1 |
T |
C |
11: 118,338,683 (GRCm39) |
S118P |
probably benign |
Het |
Ceacam20 |
A |
T |
7: 19,705,628 (GRCm39) |
E206D |
probably damaging |
Het |
Celsr3 |
T |
C |
9: 108,725,993 (GRCm39) |
L3066P |
probably damaging |
Het |
Cers3 |
T |
G |
7: 66,439,386 (GRCm39) |
L299R |
probably damaging |
Het |
Cfhr2 |
G |
T |
1: 139,738,696 (GRCm39) |
H288Q |
probably benign |
Het |
Cnot1 |
A |
T |
8: 96,496,472 (GRCm39) |
M278K |
probably benign |
Het |
Cnot10 |
T |
C |
9: 114,456,537 (GRCm39) |
E166G |
probably damaging |
Het |
Ctsd |
T |
A |
7: 141,939,197 (GRCm39) |
D76V |
probably damaging |
Het |
Cyp1a1 |
T |
A |
9: 57,610,003 (GRCm39) |
F472L |
probably damaging |
Het |
Dusp19 |
T |
A |
2: 80,454,635 (GRCm39) |
D118E |
probably damaging |
Het |
Dusp29 |
A |
T |
14: 21,752,950 (GRCm39) |
D65E |
probably damaging |
Het |
Eif2ak3 |
C |
A |
6: 70,855,903 (GRCm39) |
R236S |
probably damaging |
Het |
Fam169a |
A |
G |
13: 97,259,260 (GRCm39) |
T439A |
probably benign |
Het |
Flg |
T |
C |
3: 93,191,639 (GRCm39) |
Y11H |
unknown |
Het |
Fn1 |
T |
A |
1: 71,667,618 (GRCm39) |
I792L |
probably benign |
Het |
Fzd7 |
T |
C |
1: 59,522,242 (GRCm39) |
S42P |
probably benign |
Het |
Gimap3 |
A |
G |
6: 48,742,370 (GRCm39) |
S187P |
possibly damaging |
Het |
Glt8d2 |
A |
T |
10: 82,498,037 (GRCm39) |
I124N |
probably damaging |
Het |
Hbp1 |
C |
T |
12: 31,983,387 (GRCm39) |
D356N |
probably damaging |
Het |
Hif1a |
T |
C |
12: 73,986,373 (GRCm39) |
S367P |
probably benign |
Het |
Hspg2 |
C |
G |
4: 137,246,290 (GRCm39) |
P1023A |
possibly damaging |
Het |
Itpr1 |
C |
A |
6: 108,365,190 (GRCm39) |
N880K |
probably benign |
Het |
Kank1 |
T |
C |
19: 25,355,842 (GRCm39) |
|
probably benign |
Het |
Kat2a |
T |
C |
11: 100,603,116 (GRCm39) |
T39A |
unknown |
Het |
Kcnk2 |
T |
A |
1: 189,072,046 (GRCm39) |
Q98L |
probably benign |
Het |
Kcnn4 |
G |
A |
7: 24,083,545 (GRCm39) |
G409S |
probably benign |
Het |
Klrb1 |
T |
A |
6: 128,690,576 (GRCm39) |
I49F |
probably damaging |
Het |
Larp4 |
G |
A |
15: 99,908,237 (GRCm39) |
V573I |
probably benign |
Het |
Lrpprc |
A |
G |
17: 85,047,496 (GRCm39) |
|
probably null |
Het |
Mybl1 |
A |
G |
1: 9,746,506 (GRCm39) |
S385P |
probably damaging |
Het |
Nup62 |
T |
C |
7: 44,478,440 (GRCm39) |
S152P |
possibly damaging |
Het |
Obi1 |
A |
T |
14: 104,717,091 (GRCm39) |
D427E |
probably damaging |
Het |
Or11a4 |
A |
G |
17: 37,536,241 (GRCm39) |
Y75C |
probably damaging |
Het |
Pcdh12 |
G |
A |
18: 38,414,630 (GRCm39) |
Q832* |
probably null |
Het |
Pcid2 |
A |
G |
8: 13,128,555 (GRCm39) |
I368T |
probably damaging |
Het |
Pcnx4 |
T |
A |
12: 72,603,437 (GRCm39) |
F492I |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,175,437 (GRCm39) |
Y464H |
|
Het |
Plekhg5 |
T |
G |
4: 152,189,201 (GRCm39) |
S260R |
possibly damaging |
Het |
Prkdc |
T |
A |
16: 15,532,005 (GRCm39) |
|
probably benign |
Het |
Prr14 |
A |
T |
7: 127,072,999 (GRCm39) |
E115D |
probably benign |
Het |
Rab3gap2 |
A |
T |
1: 184,978,877 (GRCm39) |
N285Y |
probably benign |
Het |
Rhot1 |
T |
A |
11: 80,148,386 (GRCm39) |
C609S |
possibly damaging |
Het |
Rnf123 |
T |
C |
9: 107,945,706 (GRCm39) |
Q360R |
probably benign |
Het |
Rrp12 |
T |
C |
19: 41,868,658 (GRCm39) |
T562A |
probably benign |
Het |
Rundc1 |
G |
A |
11: 101,322,992 (GRCm39) |
G317D |
probably benign |
Het |
Rusf1 |
C |
T |
7: 127,889,786 (GRCm39) |
R1H |
probably damaging |
Het |
Slc14a1 |
A |
T |
18: 78,145,656 (GRCm39) |
I426N |
possibly damaging |
Het |
Slc23a1 |
C |
T |
18: 35,755,588 (GRCm39) |
G436E |
probably damaging |
Het |
Slc45a3 |
A |
G |
1: 131,905,523 (GRCm39) |
D182G |
probably damaging |
Het |
Sos1 |
A |
T |
17: 80,715,728 (GRCm39) |
F1010I |
probably damaging |
Het |
Tap1 |
A |
G |
17: 34,412,163 (GRCm39) |
E456G |
probably damaging |
Het |
Tha1 |
A |
T |
11: 117,759,493 (GRCm39) |
V332E |
probably damaging |
Het |
Tmem18 |
T |
A |
12: 30,638,517 (GRCm39) |
I93N |
probably damaging |
Het |
Tnrc18 |
A |
G |
5: 142,711,767 (GRCm39) |
F2664S |
probably damaging |
Het |
Tpm3 |
T |
A |
3: 89,981,011 (GRCm39) |
|
probably benign |
Het |
Ttc3 |
A |
G |
16: 94,255,351 (GRCm39) |
E1615G |
probably damaging |
Het |
Ube3b |
A |
G |
5: 114,540,747 (GRCm39) |
T485A |
probably benign |
Het |
Vmn2r92 |
A |
G |
17: 18,386,886 (GRCm39) |
Y75C |
probably damaging |
Het |
Zfp169 |
T |
C |
13: 48,644,575 (GRCm39) |
D184G |
unknown |
Het |
|
Other mutations in Gli1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01543:Gli1
|
APN |
10 |
127,168,347 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01824:Gli1
|
APN |
10 |
127,172,396 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02134:Gli1
|
APN |
10 |
127,172,369 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02508:Gli1
|
APN |
10 |
127,172,961 (GRCm39) |
missense |
probably benign |
0.14 |
IGL02931:Gli1
|
APN |
10 |
127,168,279 (GRCm39) |
missense |
probably benign |
0.00 |
R0099:Gli1
|
UTSW |
10 |
127,171,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R0590:Gli1
|
UTSW |
10 |
127,167,432 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0792:Gli1
|
UTSW |
10 |
127,168,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R1169:Gli1
|
UTSW |
10 |
127,174,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R1519:Gli1
|
UTSW |
10 |
127,170,138 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1522:Gli1
|
UTSW |
10 |
127,168,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R1550:Gli1
|
UTSW |
10 |
127,174,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R1592:Gli1
|
UTSW |
10 |
127,167,198 (GRCm39) |
missense |
probably damaging |
0.97 |
R1879:Gli1
|
UTSW |
10 |
127,169,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1892:Gli1
|
UTSW |
10 |
127,165,975 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1934:Gli1
|
UTSW |
10 |
127,167,108 (GRCm39) |
missense |
possibly damaging |
0.65 |
R2049:Gli1
|
UTSW |
10 |
127,172,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R2088:Gli1
|
UTSW |
10 |
127,167,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R2141:Gli1
|
UTSW |
10 |
127,172,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R3803:Gli1
|
UTSW |
10 |
127,173,934 (GRCm39) |
splice site |
probably benign |
|
R3873:Gli1
|
UTSW |
10 |
127,167,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R3874:Gli1
|
UTSW |
10 |
127,166,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R3899:Gli1
|
UTSW |
10 |
127,172,535 (GRCm39) |
missense |
possibly damaging |
0.64 |
R4703:Gli1
|
UTSW |
10 |
127,166,724 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5552:Gli1
|
UTSW |
10 |
127,166,131 (GRCm39) |
missense |
probably benign |
0.00 |
R5686:Gli1
|
UTSW |
10 |
127,173,305 (GRCm39) |
missense |
probably benign |
0.01 |
R5812:Gli1
|
UTSW |
10 |
127,173,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R6053:Gli1
|
UTSW |
10 |
127,170,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Gli1
|
UTSW |
10 |
127,171,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R7162:Gli1
|
UTSW |
10 |
127,168,306 (GRCm39) |
missense |
probably benign |
|
R8229:Gli1
|
UTSW |
10 |
127,168,317 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8447:Gli1
|
UTSW |
10 |
127,166,106 (GRCm39) |
missense |
probably benign |
0.00 |
R8678:Gli1
|
UTSW |
10 |
127,173,260 (GRCm39) |
missense |
probably null |
0.65 |
R9123:Gli1
|
UTSW |
10 |
127,167,202 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9377:Gli1
|
UTSW |
10 |
127,173,359 (GRCm39) |
missense |
possibly damaging |
0.56 |
Z1177:Gli1
|
UTSW |
10 |
127,172,560 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Gli1
|
UTSW |
10 |
127,171,867 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Gli1
|
UTSW |
10 |
127,170,126 (GRCm39) |
missense |
probably damaging |
1.00 |
|