Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
A |
G |
3: 59,843,993 (GRCm39) |
Y229C |
probably damaging |
Het |
Adgrd1 |
A |
G |
5: 129,192,119 (GRCm39) |
D63G |
probably damaging |
Het |
Ahnak |
A |
G |
19: 8,979,960 (GRCm39) |
T415A |
probably benign |
Het |
Antxr2 |
A |
G |
5: 98,151,937 (GRCm39) |
V178A |
probably damaging |
Het |
Ap1s1 |
A |
G |
5: 137,070,634 (GRCm39) |
Y127H |
possibly damaging |
Het |
Bbs2 |
A |
T |
8: 94,803,710 (GRCm39) |
M510K |
probably benign |
Het |
Cbfa2t2 |
A |
G |
2: 154,377,090 (GRCm39) |
N591S |
probably damaging |
Het |
Chd6 |
T |
A |
2: 160,861,536 (GRCm39) |
R504* |
probably null |
Het |
Cnpy3 |
A |
G |
17: 47,054,217 (GRCm39) |
|
probably benign |
Het |
Cntn2 |
T |
G |
1: 132,446,114 (GRCm39) |
K824T |
probably benign |
Het |
Cntnap3 |
T |
C |
13: 64,905,223 (GRCm39) |
T853A |
probably damaging |
Het |
Cog4 |
G |
A |
8: 111,593,221 (GRCm39) |
G444D |
possibly damaging |
Het |
Col18a1 |
A |
T |
10: 76,932,300 (GRCm39) |
I510N |
probably damaging |
Het |
Cxcr5 |
G |
A |
9: 44,425,403 (GRCm39) |
R85W |
probably damaging |
Het |
Cyth3 |
C |
A |
5: 143,672,259 (GRCm39) |
T58K |
probably damaging |
Het |
Dio3 |
T |
C |
12: 110,245,970 (GRCm39) |
V102A |
probably damaging |
Het |
Dmbx1 |
G |
A |
4: 115,775,204 (GRCm39) |
R359C |
probably damaging |
Het |
Fam3d |
C |
T |
14: 8,361,475 (GRCm38) |
|
probably null |
Het |
Fras1 |
C |
A |
5: 96,926,034 (GRCm39) |
P3746Q |
probably damaging |
Het |
Glt1d1 |
T |
A |
5: 127,721,409 (GRCm39) |
M32K |
probably benign |
Het |
Hunk |
A |
G |
16: 90,229,460 (GRCm39) |
N31S |
probably damaging |
Het |
Ints11 |
T |
C |
4: 155,959,761 (GRCm39) |
S123P |
probably benign |
Het |
Izumo2 |
T |
C |
7: 44,358,339 (GRCm39) |
L58S |
probably damaging |
Het |
Izumo4 |
A |
G |
10: 80,540,032 (GRCm39) |
|
probably benign |
Het |
Kcnh7 |
T |
A |
2: 62,618,029 (GRCm39) |
K487* |
probably null |
Het |
Lrp12 |
T |
C |
15: 39,741,971 (GRCm39) |
Y248C |
probably damaging |
Het |
Maco1 |
T |
C |
4: 134,555,697 (GRCm39) |
K259E |
probably benign |
Het |
Map3k4 |
T |
C |
17: 12,490,801 (GRCm39) |
D210G |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,890,740 (GRCm39) |
D1038G |
probably damaging |
Het |
Noa1 |
T |
C |
5: 77,442,338 (GRCm39) |
T651A |
probably benign |
Het |
Nop2 |
A |
C |
6: 125,121,048 (GRCm39) |
K610T |
possibly damaging |
Het |
Nop2 |
G |
T |
6: 125,121,033 (GRCm39) |
G605V |
probably benign |
Het |
Npvf |
G |
A |
6: 50,629,670 (GRCm39) |
R107W |
probably benign |
Het |
Or10ad1b |
A |
G |
15: 98,125,232 (GRCm39) |
V98A |
probably benign |
Het |
Or2h2c |
T |
C |
17: 37,422,865 (GRCm39) |
N3S |
probably benign |
Het |
Oxr1 |
A |
G |
15: 41,718,329 (GRCm39) |
T775A |
probably damaging |
Het |
P2ry13 |
C |
T |
3: 59,117,029 (GRCm39) |
A250T |
probably damaging |
Het |
Piezo2 |
G |
A |
18: 63,153,704 (GRCm39) |
S2547F |
probably benign |
Het |
Pinx1 |
A |
G |
14: 64,156,609 (GRCm39) |
T179A |
probably damaging |
Het |
Pjvk |
T |
C |
2: 76,488,795 (GRCm39) |
V322A |
possibly damaging |
Het |
Pla2r1 |
T |
A |
2: 60,332,413 (GRCm39) |
R476S |
probably benign |
Het |
Polb |
A |
G |
8: 23,138,277 (GRCm39) |
|
probably benign |
Het |
Polg2 |
C |
T |
11: 106,659,293 (GRCm39) |
D407N |
probably damaging |
Het |
Pou5f2 |
G |
A |
13: 78,173,178 (GRCm39) |
R40Q |
probably benign |
Het |
Sctr |
T |
C |
1: 119,972,393 (GRCm39) |
M193T |
possibly damaging |
Het |
Sctr |
T |
A |
1: 119,949,909 (GRCm39) |
C33S |
probably damaging |
Het |
Sema5b |
T |
C |
16: 35,480,885 (GRCm39) |
S819P |
probably benign |
Het |
Setd1b |
C |
T |
5: 123,286,652 (GRCm39) |
T566I |
unknown |
Het |
Sptbn4 |
G |
A |
7: 27,126,258 (GRCm39) |
R222C |
possibly damaging |
Het |
Taf5l |
A |
G |
8: 124,730,197 (GRCm39) |
V129A |
possibly damaging |
Het |
Tmem163 |
C |
T |
1: 127,427,984 (GRCm39) |
V201I |
probably benign |
Het |
Ube3b |
T |
C |
5: 114,544,310 (GRCm39) |
L569P |
probably damaging |
Het |
Vwa3a |
A |
G |
7: 120,372,515 (GRCm39) |
E301G |
probably benign |
Het |
Wnk1 |
T |
C |
6: 119,914,823 (GRCm39) |
I1660V |
probably benign |
Het |
Zbtb22 |
T |
A |
17: 34,135,987 (GRCm39) |
L44Q |
probably damaging |
Het |
Zfp691 |
T |
C |
4: 119,027,389 (GRCm39) |
D281G |
probably damaging |
Het |
Zfy2 |
C |
T |
Y: 2,106,894 (GRCm39) |
G580D |
probably benign |
Het |
Zfy2 |
T |
A |
Y: 2,117,188 (GRCm39) |
H213L |
probably benign |
Het |
|
Other mutations in Pcsk9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Pcsk9
|
APN |
4 |
106,311,843 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02709:Pcsk9
|
APN |
4 |
106,304,886 (GRCm39) |
splice site |
probably benign |
|
IGL02804:Pcsk9
|
APN |
4 |
106,314,161 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03009:Pcsk9
|
APN |
4 |
106,311,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Pcsk9
|
APN |
4 |
106,303,967 (GRCm39) |
missense |
probably benign |
|
R0271:Pcsk9
|
UTSW |
4 |
106,306,246 (GRCm39) |
splice site |
probably benign |
|
R0321:Pcsk9
|
UTSW |
4 |
106,301,891 (GRCm39) |
missense |
probably benign |
|
R0413:Pcsk9
|
UTSW |
4 |
106,311,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R0426:Pcsk9
|
UTSW |
4 |
106,307,274 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0783:Pcsk9
|
UTSW |
4 |
106,307,314 (GRCm39) |
missense |
probably benign |
0.00 |
R2136:Pcsk9
|
UTSW |
4 |
106,303,967 (GRCm39) |
missense |
probably benign |
0.00 |
R4056:Pcsk9
|
UTSW |
4 |
106,301,899 (GRCm39) |
missense |
probably benign |
0.02 |
R4438:Pcsk9
|
UTSW |
4 |
106,316,156 (GRCm39) |
missense |
probably benign |
0.00 |
R4683:Pcsk9
|
UTSW |
4 |
106,316,092 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4739:Pcsk9
|
UTSW |
4 |
106,304,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Pcsk9
|
UTSW |
4 |
106,304,766 (GRCm39) |
missense |
probably benign |
0.43 |
R4802:Pcsk9
|
UTSW |
4 |
106,304,766 (GRCm39) |
missense |
probably benign |
0.43 |
R5249:Pcsk9
|
UTSW |
4 |
106,320,950 (GRCm39) |
missense |
probably benign |
0.01 |
R5307:Pcsk9
|
UTSW |
4 |
106,304,371 (GRCm39) |
missense |
probably damaging |
1.00 |
R5320:Pcsk9
|
UTSW |
4 |
106,320,988 (GRCm39) |
missense |
probably benign |
0.00 |
R5653:Pcsk9
|
UTSW |
4 |
106,316,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R5827:Pcsk9
|
UTSW |
4 |
106,306,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R6010:Pcsk9
|
UTSW |
4 |
106,311,469 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6019:Pcsk9
|
UTSW |
4 |
106,314,073 (GRCm39) |
missense |
probably benign |
0.02 |
R6393:Pcsk9
|
UTSW |
4 |
106,304,793 (GRCm39) |
missense |
probably benign |
0.00 |
R7472:Pcsk9
|
UTSW |
4 |
106,316,094 (GRCm39) |
missense |
probably benign |
0.08 |
R7614:Pcsk9
|
UTSW |
4 |
106,304,763 (GRCm39) |
missense |
probably benign |
0.34 |
R7807:Pcsk9
|
UTSW |
4 |
106,321,092 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8036:Pcsk9
|
UTSW |
4 |
106,311,536 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8735:Pcsk9
|
UTSW |
4 |
106,311,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R9258:Pcsk9
|
UTSW |
4 |
106,316,047 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9404:Pcsk9
|
UTSW |
4 |
106,311,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R9684:Pcsk9
|
UTSW |
4 |
106,307,386 (GRCm39) |
missense |
probably benign |
0.29 |
Z1176:Pcsk9
|
UTSW |
4 |
106,316,138 (GRCm39) |
missense |
probably damaging |
0.96 |
|