Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310016G11Rik |
T |
C |
7: 44,326,580 (GRCm39) |
|
noncoding transcript |
Het |
Casc3 |
C |
A |
11: 98,713,857 (GRCm39) |
P363Q |
possibly damaging |
Het |
Cep162 |
C |
A |
9: 87,082,056 (GRCm39) |
R1283L |
probably damaging |
Het |
Clk3 |
C |
A |
9: 57,659,075 (GRCm39) |
W562L |
probably damaging |
Het |
Col17a1 |
G |
A |
19: 47,645,529 (GRCm39) |
T844M |
possibly damaging |
Het |
Dntt |
G |
C |
19: 41,041,672 (GRCm39) |
G452A |
probably damaging |
Het |
Dop1b |
G |
A |
16: 93,513,120 (GRCm39) |
V20I |
possibly damaging |
Het |
Dst |
T |
C |
1: 34,202,316 (GRCm39) |
S215P |
probably damaging |
Het |
Dync1li2 |
A |
T |
8: 105,154,798 (GRCm39) |
I270N |
probably damaging |
Het |
Egflam |
A |
T |
15: 7,273,350 (GRCm39) |
I575N |
possibly damaging |
Het |
Gldc |
G |
T |
19: 30,138,168 (GRCm39) |
|
probably benign |
Het |
Gm17067 |
C |
A |
7: 42,357,462 (GRCm39) |
V347L |
probably benign |
Het |
Gmds |
T |
A |
13: 32,101,679 (GRCm39) |
N304I |
probably benign |
Het |
Grm7 |
G |
T |
6: 110,623,309 (GRCm39) |
V161F |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,895,509 (GRCm39) |
T1686A |
probably benign |
Het |
Lamb3 |
A |
T |
1: 193,013,683 (GRCm39) |
Q519L |
probably benign |
Het |
Lrp10 |
C |
T |
14: 54,705,823 (GRCm39) |
R338C |
probably damaging |
Het |
Macf1 |
A |
G |
4: 123,248,285 (GRCm39) |
|
probably benign |
Het |
Mcfd2 |
C |
G |
17: 87,565,387 (GRCm39) |
G39R |
possibly damaging |
Het |
Mecom |
T |
C |
3: 30,041,219 (GRCm39) |
H125R |
probably damaging |
Het |
Nme7 |
A |
G |
1: 164,172,807 (GRCm39) |
T173A |
probably benign |
Het |
Or4s2b |
A |
G |
2: 88,508,615 (GRCm39) |
T132A |
possibly damaging |
Het |
Or5ac15 |
C |
T |
16: 58,940,027 (GRCm39) |
M135I |
probably benign |
Het |
Pde1c |
T |
A |
6: 56,049,263 (GRCm39) |
R683S |
probably null |
Het |
Pkn2 |
A |
T |
3: 142,536,217 (GRCm39) |
|
probably benign |
Het |
Plppr4 |
T |
G |
3: 117,116,046 (GRCm39) |
T604P |
probably benign |
Het |
Pramel23 |
T |
A |
4: 143,424,856 (GRCm39) |
I196F |
probably benign |
Het |
Slc34a2 |
C |
T |
5: 53,226,628 (GRCm39) |
P584S |
probably damaging |
Het |
Slco5a1 |
A |
T |
1: 13,009,392 (GRCm39) |
M361K |
probably damaging |
Het |
Snx4 |
T |
A |
16: 33,084,666 (GRCm39) |
I60N |
probably damaging |
Het |
Sp6 |
T |
C |
11: 96,912,572 (GRCm39) |
L95P |
probably damaging |
Het |
Stat5b |
A |
G |
11: 100,678,175 (GRCm39) |
F646S |
probably damaging |
Het |
Tbc1d1 |
T |
C |
5: 64,490,891 (GRCm39) |
M785T |
probably benign |
Het |
Tbc1d22a |
T |
A |
15: 86,235,935 (GRCm39) |
C365S |
probably damaging |
Het |
Tle1 |
ACAGGTTTCTTCAGGTTTCTT |
ACAGGTTTCTT |
4: 72,036,400 (GRCm39) |
|
probably benign |
Het |
Tnfsf8 |
A |
T |
4: 63,779,264 (GRCm39) |
C11* |
probably null |
Het |
Ttn |
A |
T |
2: 76,748,485 (GRCm39) |
V4188E |
probably damaging |
Het |
Ugt2b5 |
T |
A |
5: 87,275,753 (GRCm39) |
H366L |
probably damaging |
Het |
Wdr17 |
T |
C |
8: 55,101,442 (GRCm39) |
|
probably benign |
Het |
Zfhx3 |
A |
G |
8: 109,683,022 (GRCm39) |
Y3487C |
unknown |
Het |
Zfp28 |
C |
T |
7: 6,396,441 (GRCm39) |
T292I |
probably benign |
Het |
|
Other mutations in Klk14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0309:Klk14
|
UTSW |
7 |
43,343,769 (GRCm39) |
missense |
probably benign |
0.01 |
R0467:Klk14
|
UTSW |
7 |
43,343,534 (GRCm39) |
missense |
probably benign |
0.33 |
R1432:Klk14
|
UTSW |
7 |
43,344,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R1575:Klk14
|
UTSW |
7 |
43,343,377 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2160:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2185:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2188:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2189:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2472:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2474:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2961:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2962:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R2968:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3147:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3148:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3176:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3177:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3276:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3277:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3419:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3430:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R3956:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4080:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4081:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4152:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4153:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4169:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Klk14
|
UTSW |
7 |
43,344,358 (GRCm39) |
missense |
probably benign |
0.00 |
R4284:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4285:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4287:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4356:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4359:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4379:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4381:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Klk14
|
UTSW |
7 |
43,343,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Klk14
|
UTSW |
7 |
43,341,392 (GRCm39) |
missense |
probably benign |
|
R4784:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4793:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4825:Klk14
|
UTSW |
7 |
43,341,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R4844:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4847:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4884:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4898:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4941:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4942:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4943:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4972:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R4997:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5021:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5022:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5024:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5053:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5054:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5097:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5253:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5257:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5459:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5490:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5493:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5543:Klk14
|
UTSW |
7 |
43,341,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R6823:Klk14
|
UTSW |
7 |
43,343,880 (GRCm39) |
nonsense |
probably null |
|
R7960:Klk14
|
UTSW |
7 |
43,341,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R7993:Klk14
|
UTSW |
7 |
43,344,367 (GRCm39) |
missense |
probably benign |
0.01 |
R8220:Klk14
|
UTSW |
7 |
43,343,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R8701:Klk14
|
UTSW |
7 |
43,343,566 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8880:Klk14
|
UTSW |
7 |
43,343,459 (GRCm39) |
missense |
probably damaging |
0.99 |
X0064:Klk14
|
UTSW |
7 |
43,343,534 (GRCm39) |
missense |
probably benign |
0.33 |
|