Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
G |
C |
7: 78,747,839 (GRCm39) |
G870A |
probably damaging |
Het |
Adamtsl2 |
T |
C |
2: 26,971,750 (GRCm39) |
W12R |
probably benign |
Het |
Bsph1 |
G |
A |
7: 13,204,254 (GRCm39) |
|
probably null |
Het |
Celsr1 |
G |
T |
15: 85,863,431 (GRCm39) |
H1200Q |
possibly damaging |
Het |
Clptm1 |
A |
T |
7: 19,371,070 (GRCm39) |
Y355* |
probably null |
Het |
Cry2 |
T |
C |
2: 92,242,037 (GRCm39) |
E572G |
possibly damaging |
Het |
Dlk1 |
G |
A |
12: 109,420,975 (GRCm39) |
|
probably null |
Het |
Eral1 |
A |
G |
11: 77,966,657 (GRCm39) |
V201A |
probably benign |
Het |
Esrp1 |
A |
T |
4: 11,357,603 (GRCm39) |
M503K |
probably benign |
Het |
Fam83e |
G |
T |
7: 45,371,607 (GRCm39) |
M1I |
probably null |
Het |
Flt4 |
G |
A |
11: 49,526,525 (GRCm39) |
A835T |
probably benign |
Het |
H2bc15 |
A |
G |
13: 21,938,447 (GRCm39) |
D52G |
probably damaging |
Het |
Hdac4 |
T |
C |
1: 91,903,244 (GRCm39) |
S562G |
probably null |
Het |
Icosl |
A |
G |
10: 77,909,759 (GRCm39) |
T235A |
possibly damaging |
Het |
Itga6 |
A |
G |
2: 71,655,961 (GRCm39) |
D295G |
probably benign |
Het |
Lipa |
A |
T |
19: 34,502,199 (GRCm39) |
L15Q |
probably benign |
Het |
Mcc |
T |
C |
18: 44,667,297 (GRCm39) |
E218G |
possibly damaging |
Het |
Mdga2 |
A |
G |
12: 66,519,970 (GRCm39) |
|
probably null |
Het |
Mmadhc |
A |
C |
2: 50,178,958 (GRCm39) |
C153W |
probably damaging |
Het |
Myh1 |
A |
G |
11: 67,112,430 (GRCm39) |
D1799G |
probably damaging |
Het |
Nlrp1b |
T |
A |
11: 71,060,621 (GRCm39) |
Q729L |
probably damaging |
Het |
Ofcc1 |
T |
A |
13: 40,333,924 (GRCm39) |
Q389L |
probably benign |
Het |
Or52b2 |
A |
G |
7: 104,986,809 (GRCm39) |
V38A |
probably benign |
Het |
Or5m5 |
A |
G |
2: 85,814,412 (GRCm39) |
D76G |
probably damaging |
Het |
Or5p4 |
A |
T |
7: 107,680,243 (GRCm39) |
M81L |
possibly damaging |
Het |
Or5p50 |
T |
C |
7: 107,421,822 (GRCm39) |
I285V |
probably benign |
Het |
Pml |
T |
C |
9: 58,142,157 (GRCm39) |
N225S |
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,321,187 (GRCm39) |
E1215G |
probably benign |
Het |
Scap |
T |
A |
9: 110,206,761 (GRCm39) |
I402N |
probably damaging |
Het |
Sgsm2 |
A |
G |
11: 74,743,908 (GRCm39) |
L886P |
probably damaging |
Het |
Sugct |
T |
C |
13: 17,836,851 (GRCm39) |
I104V |
probably benign |
Het |
Tmem200c |
A |
G |
17: 69,147,681 (GRCm39) |
Q88R |
probably damaging |
Het |
Tnfrsf1a |
T |
A |
6: 125,334,768 (GRCm39) |
L14Q |
probably benign |
Het |
Tnk2 |
C |
T |
16: 32,490,239 (GRCm39) |
L381F |
probably damaging |
Het |
Ubr2 |
C |
T |
17: 47,254,290 (GRCm39) |
V1454I |
probably benign |
Het |
V1ra8 |
A |
C |
6: 90,179,944 (GRCm39) |
D49A |
probably damaging |
Het |
Vmn2r5 |
A |
C |
3: 64,417,014 (GRCm39) |
M48R |
probably benign |
Het |
Yars1 |
A |
G |
4: 129,099,982 (GRCm39) |
I227V |
probably damaging |
Het |
Zfp850 |
C |
A |
7: 27,688,480 (GRCm39) |
R576L |
probably benign |
Het |
Zfpm2 |
T |
A |
15: 40,964,579 (GRCm39) |
F223I |
possibly damaging |
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 |
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 |
R4380: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 |
|