Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
A |
T |
7: 41,261,109 (GRCm39) |
|
probably benign |
Het |
9330182O14Rik |
A |
T |
15: 40,005,632 (GRCm39) |
K17* |
probably null |
Het |
Adamtsl3 |
A |
C |
7: 82,223,188 (GRCm39) |
I990L |
probably damaging |
Het |
Add1 |
T |
A |
5: 34,788,122 (GRCm39) |
S724T |
possibly damaging |
Het |
Afdn |
A |
G |
17: 14,072,627 (GRCm39) |
N865S |
probably benign |
Het |
Amot |
A |
T |
X: 144,244,745 (GRCm39) |
L435H |
|
Het |
Ap1m2 |
T |
A |
9: 21,223,523 (GRCm39) |
I8F |
probably benign |
Het |
Atp8a1 |
T |
C |
5: 67,824,944 (GRCm39) |
T811A |
|
Het |
Axin2 |
A |
G |
11: 108,822,378 (GRCm39) |
D310G |
probably damaging |
Het |
Bin1 |
T |
G |
18: 32,562,251 (GRCm39) |
F379L |
possibly damaging |
Het |
Bin2 |
C |
A |
15: 100,554,631 (GRCm39) |
S91I |
possibly damaging |
Het |
Birc5 |
A |
G |
11: 117,743,599 (GRCm39) |
N111S |
probably benign |
Het |
Blk |
T |
A |
14: 63,620,130 (GRCm39) |
N137Y |
probably damaging |
Het |
Cacna1d |
G |
A |
14: 29,796,873 (GRCm39) |
A1534V |
probably damaging |
Het |
Cacna2d1 |
T |
C |
5: 16,451,757 (GRCm39) |
V207A |
probably damaging |
Het |
Ccr3 |
A |
G |
9: 123,828,949 (GRCm39) |
I95V |
probably benign |
Het |
Celsr2 |
T |
C |
3: 108,309,862 (GRCm39) |
D1579G |
probably benign |
Het |
Cfap36 |
C |
A |
11: 29,196,541 (GRCm39) |
K19N |
probably benign |
Het |
Cfap52 |
C |
T |
11: 67,844,860 (GRCm39) |
V70M |
possibly damaging |
Het |
Chid1 |
A |
T |
7: 141,093,722 (GRCm39) |
I298N |
probably damaging |
Het |
Clstn1 |
G |
T |
4: 149,731,322 (GRCm39) |
R888L |
possibly damaging |
Het |
Col6a5 |
T |
A |
9: 105,822,596 (GRCm39) |
T254S |
unknown |
Het |
Coro6 |
C |
T |
11: 77,359,329 (GRCm39) |
P301S |
probably damaging |
Het |
Cstdc2 |
A |
G |
2: 148,692,589 (GRCm39) |
|
probably null |
Het |
Dchs1 |
T |
C |
7: 105,422,114 (GRCm39) |
D102G |
probably damaging |
Het |
Dnah14 |
T |
C |
1: 181,433,381 (GRCm39) |
F353L |
probably benign |
Het |
Dnajc10 |
A |
T |
2: 80,163,315 (GRCm39) |
I344L |
probably benign |
Het |
Dst |
T |
C |
1: 34,303,652 (GRCm39) |
V4026A |
probably damaging |
Het |
Exo1 |
A |
G |
1: 175,715,203 (GRCm39) |
E114G |
possibly damaging |
Het |
Fabp7 |
A |
G |
10: 57,662,439 (GRCm39) |
I109V |
probably benign |
Het |
Fars2 |
T |
C |
13: 36,416,109 (GRCm39) |
F206S |
probably damaging |
Het |
Gbp8 |
C |
T |
5: 105,179,155 (GRCm39) |
A115T |
possibly damaging |
Het |
Gm17067 |
T |
C |
7: 42,357,627 (GRCm39) |
T292A |
probably benign |
Het |
Gp2 |
T |
C |
7: 119,041,929 (GRCm39) |
D532G |
probably benign |
Het |
Gtf2i |
C |
A |
5: 134,271,534 (GRCm39) |
A917S |
probably damaging |
Het |
Guca1b |
A |
G |
17: 47,702,827 (GRCm39) |
E169G |
possibly damaging |
Het |
Hdac1 |
A |
T |
4: 129,428,499 (GRCm39) |
Y24N |
probably damaging |
Het |
Hepacam |
T |
C |
9: 37,293,693 (GRCm39) |
F251L |
probably damaging |
Het |
Hmcn1 |
G |
T |
1: 150,506,092 (GRCm39) |
N3811K |
probably damaging |
Het |
Htra4 |
A |
T |
8: 25,520,133 (GRCm39) |
M391K |
probably damaging |
Het |
Ino80d |
T |
C |
1: 63,097,930 (GRCm39) |
T760A |
probably benign |
Het |
Ints1 |
T |
G |
5: 139,748,586 (GRCm39) |
T1074P |
probably benign |
Het |
Itga6 |
A |
T |
2: 71,647,015 (GRCm39) |
Q75L |
possibly damaging |
Het |
Mapk14 |
A |
C |
17: 28,960,814 (GRCm39) |
N272T |
probably benign |
Het |
Meikin |
A |
T |
11: 54,285,517 (GRCm39) |
T185S |
possibly damaging |
Het |
Moxd2 |
C |
T |
6: 40,860,490 (GRCm39) |
G318D |
possibly damaging |
Het |
Mtmr3 |
G |
A |
11: 4,437,739 (GRCm39) |
T905I |
probably benign |
Het |
Muc16 |
A |
G |
9: 18,567,824 (GRCm39) |
I1565T |
unknown |
Het |
Myh14 |
A |
G |
7: 44,271,281 (GRCm39) |
S1500P |
possibly damaging |
Het |
Nfkb1 |
T |
C |
3: 135,310,874 (GRCm39) |
E475G |
probably benign |
Het |
Ngef |
C |
A |
1: 87,473,581 (GRCm39) |
R67L |
probably benign |
Het |
Olr1 |
T |
C |
6: 129,470,528 (GRCm39) |
E213G |
probably damaging |
Het |
Or13c3 |
T |
A |
4: 52,856,052 (GRCm39) |
I154F |
probably damaging |
Het |
Or5b124 |
A |
G |
19: 13,610,903 (GRCm39) |
I143V |
probably benign |
Het |
Or8g21 |
A |
G |
9: 38,906,573 (GRCm39) |
S53P |
probably benign |
Het |
Or9r3 |
A |
C |
10: 129,947,723 (GRCm39) |
I312R |
probably benign |
Het |
Pcdhga3 |
C |
T |
18: 37,809,088 (GRCm39) |
L514F |
probably damaging |
Het |
Pcnt |
A |
G |
10: 76,221,572 (GRCm39) |
M2018T |
possibly damaging |
Het |
Pde8a |
C |
T |
7: 80,982,619 (GRCm39) |
T746I |
probably damaging |
Het |
Pik3ca |
T |
C |
3: 32,503,755 (GRCm39) |
|
probably null |
Het |
Psapl1 |
A |
G |
5: 36,362,880 (GRCm39) |
S491G |
possibly damaging |
Het |
Psmf1 |
A |
T |
2: 151,577,457 (GRCm39) |
D73E |
probably benign |
Het |
Ptprcap |
A |
G |
19: 4,206,358 (GRCm39) |
D147G |
probably benign |
Het |
Ramacl |
T |
C |
13: 67,056,063 (GRCm39) |
F19L |
probably damaging |
Het |
Rdh8 |
T |
A |
9: 20,736,935 (GRCm39) |
V309E |
possibly damaging |
Het |
Rhobtb3 |
T |
A |
13: 76,041,121 (GRCm39) |
T396S |
probably benign |
Het |
Rpa1 |
A |
T |
11: 75,200,999 (GRCm39) |
L475* |
probably null |
Het |
Rtkn |
T |
A |
6: 83,129,190 (GRCm39) |
S562T |
probably damaging |
Het |
Saxo5 |
A |
T |
8: 3,525,967 (GRCm39) |
Y40F |
possibly damaging |
Het |
Scamp1 |
C |
T |
13: 94,389,533 (GRCm39) |
D35N |
probably benign |
Het |
Scarb1 |
C |
T |
5: 125,371,146 (GRCm39) |
A309T |
probably damaging |
Het |
Scube1 |
G |
A |
15: 83,543,298 (GRCm39) |
T180M |
possibly damaging |
Het |
Sez6 |
T |
G |
11: 77,868,473 (GRCm39) |
F945V |
probably damaging |
Het |
Sf3a1 |
C |
T |
11: 4,116,681 (GRCm39) |
T124M |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,722,659 (GRCm39) |
K759E |
probably damaging |
Het |
Sort1 |
C |
A |
3: 108,247,994 (GRCm39) |
C446* |
probably null |
Het |
Sun1 |
T |
A |
5: 139,219,273 (GRCm39) |
S360T |
probably benign |
Het |
Supv3l1 |
A |
G |
10: 62,268,238 (GRCm39) |
F536L |
probably damaging |
Het |
Taar6 |
A |
C |
10: 23,861,273 (GRCm39) |
V91G |
probably damaging |
Het |
Themis |
C |
A |
10: 28,658,233 (GRCm39) |
T420N |
probably benign |
Het |
Thoc2l |
T |
A |
5: 104,666,348 (GRCm39) |
L290H |
probably damaging |
Het |
Tmc2 |
T |
A |
2: 130,083,516 (GRCm39) |
I491N |
probably damaging |
Het |
Trmt112 |
T |
C |
19: 6,888,187 (GRCm39) |
I113T |
probably damaging |
Het |
Txndc16 |
T |
A |
14: 45,373,385 (GRCm39) |
D748V |
probably damaging |
Het |
Xkr6 |
A |
G |
14: 63,844,067 (GRCm39) |
D30G |
possibly damaging |
Het |
Zc3h14 |
C |
T |
12: 98,745,505 (GRCm39) |
S498L |
probably damaging |
Het |
Zc3h7b |
A |
C |
15: 81,661,184 (GRCm39) |
D341A |
probably benign |
Het |
Zfp108 |
T |
A |
7: 23,960,923 (GRCm39) |
C505S |
probably damaging |
Het |
Zfp354c |
A |
C |
11: 50,706,088 (GRCm39) |
L329R |
probably damaging |
Het |
Zfyve16 |
T |
A |
13: 92,657,871 (GRCm39) |
D680V |
probably damaging |
Het |
Znfx1 |
A |
G |
2: 166,897,185 (GRCm39) |
F580L |
probably benign |
Het |
|
Other mutations in Ttc14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01154:Ttc14
|
APN |
3 |
33,857,248 (GRCm39) |
missense |
probably benign |
0.35 |
IGL01326:Ttc14
|
APN |
3 |
33,855,507 (GRCm39) |
missense |
probably benign |
0.14 |
R0196:Ttc14
|
UTSW |
3 |
33,863,403 (GRCm39) |
unclassified |
probably benign |
|
R0427:Ttc14
|
UTSW |
3 |
33,857,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Ttc14
|
UTSW |
3 |
33,857,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R2312:Ttc14
|
UTSW |
3 |
33,861,984 (GRCm39) |
splice site |
probably null |
|
R2434:Ttc14
|
UTSW |
3 |
33,855,227 (GRCm39) |
missense |
probably benign |
0.40 |
R4794:Ttc14
|
UTSW |
3 |
33,857,298 (GRCm39) |
missense |
probably benign |
0.00 |
R4825:Ttc14
|
UTSW |
3 |
33,855,518 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4888:Ttc14
|
UTSW |
3 |
33,861,024 (GRCm39) |
nonsense |
probably null |
|
R5143:Ttc14
|
UTSW |
3 |
33,863,050 (GRCm39) |
unclassified |
probably benign |
|
R6051:Ttc14
|
UTSW |
3 |
33,863,073 (GRCm39) |
unclassified |
probably benign |
|
R6270:Ttc14
|
UTSW |
3 |
33,854,537 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6415:Ttc14
|
UTSW |
3 |
33,857,724 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6439:Ttc14
|
UTSW |
3 |
33,862,968 (GRCm39) |
unclassified |
probably benign |
|
R7021:Ttc14
|
UTSW |
3 |
33,857,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R7571:Ttc14
|
UTSW |
3 |
33,863,400 (GRCm39) |
missense |
unknown |
|
R7751:Ttc14
|
UTSW |
3 |
33,863,590 (GRCm39) |
missense |
unknown |
|
R8021:Ttc14
|
UTSW |
3 |
33,863,270 (GRCm39) |
nonsense |
probably null |
|
R8388:Ttc14
|
UTSW |
3 |
33,854,735 (GRCm39) |
missense |
probably benign |
0.01 |
R8884:Ttc14
|
UTSW |
3 |
33,854,696 (GRCm39) |
missense |
unknown |
|
R9399:Ttc14
|
UTSW |
3 |
33,858,856 (GRCm39) |
missense |
possibly damaging |
0.62 |
R9438:Ttc14
|
UTSW |
3 |
33,858,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R9537:Ttc14
|
UTSW |
3 |
33,857,347 (GRCm39) |
missense |
probably damaging |
0.96 |
R9663:Ttc14
|
UTSW |
3 |
33,855,537 (GRCm39) |
missense |
probably benign |
0.01 |
|