Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930505A04Rik |
C |
T |
11: 30,376,349 (GRCm39) |
V173M |
probably damaging |
Het |
Abcg5 |
A |
G |
17: 84,965,992 (GRCm39) |
L628S |
probably damaging |
Het |
Acbd3 |
C |
T |
1: 180,564,297 (GRCm39) |
R201* |
probably null |
Het |
Adsl |
A |
G |
15: 80,833,106 (GRCm39) |
|
probably benign |
Het |
Asic1 |
GCACC |
GCACCACC |
15: 99,596,684 (GRCm39) |
|
probably benign |
Het |
Cachd1 |
T |
C |
4: 100,823,397 (GRCm39) |
V483A |
possibly damaging |
Het |
Calm1 |
T |
C |
12: 100,166,472 (GRCm39) |
S19P |
probably benign |
Het |
Casq1 |
T |
C |
1: 172,040,641 (GRCm39) |
N313S |
possibly damaging |
Het |
Cav2 |
G |
T |
6: 17,286,935 (GRCm39) |
A64S |
possibly damaging |
Het |
Ccdc167 |
C |
A |
17: 29,924,485 (GRCm39) |
A39S |
possibly damaging |
Het |
Cd274 |
T |
C |
19: 29,359,936 (GRCm39) |
L247P |
probably benign |
Het |
Cdhr5 |
T |
C |
7: 140,854,361 (GRCm39) |
E138G |
probably damaging |
Het |
Cltb |
C |
T |
13: 54,741,693 (GRCm39) |
C81Y |
probably benign |
Het |
Clvs1 |
T |
C |
4: 9,281,865 (GRCm39) |
L103P |
possibly damaging |
Het |
Cntrob |
G |
T |
11: 69,212,717 (GRCm39) |
Q106K |
possibly damaging |
Het |
Ctsh |
T |
C |
9: 89,936,643 (GRCm39) |
L14P |
probably damaging |
Het |
Cubn |
T |
C |
2: 13,292,379 (GRCm39) |
N3268S |
probably damaging |
Het |
Cyb5r4 |
T |
C |
9: 86,909,001 (GRCm39) |
V26A |
possibly damaging |
Het |
Ddx18 |
A |
G |
1: 121,489,857 (GRCm39) |
I184T |
probably damaging |
Het |
Ddx60 |
T |
A |
8: 62,427,222 (GRCm39) |
W766R |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,349,746 (GRCm39) |
R2399Q |
probably benign |
Het |
Dnah5 |
G |
A |
15: 28,272,318 (GRCm39) |
V1041I |
probably benign |
Het |
Dnajc21 |
A |
T |
15: 10,464,050 (GRCm39) |
N38K |
probably benign |
Het |
Ermap |
T |
C |
4: 119,043,015 (GRCm39) |
|
probably null |
Het |
Fryl |
A |
G |
5: 73,243,943 (GRCm39) |
L1209P |
possibly damaging |
Het |
Gm5093 |
T |
C |
17: 46,750,799 (GRCm39) |
E76G |
possibly damaging |
Het |
Grk6 |
T |
C |
13: 55,599,519 (GRCm39) |
C169R |
probably damaging |
Het |
Hmgn1 |
A |
T |
16: 95,923,627 (GRCm39) |
|
probably null |
Het |
Lpcat2b |
T |
A |
5: 107,582,001 (GRCm39) |
Y443* |
probably null |
Het |
Macf1 |
T |
A |
4: 123,365,882 (GRCm39) |
M1395L |
probably benign |
Het |
Mllt10 |
C |
T |
2: 18,213,585 (GRCm39) |
Q997* |
probably null |
Het |
Mocos |
T |
A |
18: 24,825,611 (GRCm39) |
V722E |
probably damaging |
Het |
Moxd2 |
A |
T |
6: 40,856,271 (GRCm39) |
L534M |
probably benign |
Het |
Mphosph10 |
T |
C |
7: 64,035,568 (GRCm39) |
M368V |
possibly damaging |
Het |
Myo15a |
G |
A |
11: 60,394,440 (GRCm39) |
G2383D |
probably damaging |
Het |
Myo5b |
T |
C |
18: 74,834,745 (GRCm39) |
I935T |
possibly damaging |
Het |
Ndst4 |
T |
A |
3: 125,231,560 (GRCm39) |
L43H |
probably damaging |
Het |
Niban1 |
T |
A |
1: 151,579,580 (GRCm39) |
L433Q |
possibly damaging |
Het |
Nsl1 |
A |
G |
1: 190,807,387 (GRCm39) |
N189D |
probably benign |
Het |
Odad1 |
A |
G |
7: 45,578,540 (GRCm39) |
I77V |
probably damaging |
Het |
Or51e1 |
A |
T |
7: 102,358,868 (GRCm39) |
H134L |
probably damaging |
Het |
Pcdh8 |
T |
C |
14: 80,007,594 (GRCm39) |
D323G |
probably damaging |
Het |
Pkhd1 |
A |
G |
1: 20,279,448 (GRCm39) |
S2957P |
possibly damaging |
Het |
Prdm9 |
T |
G |
17: 15,783,155 (GRCm39) |
E42D |
probably damaging |
Het |
Rasal1 |
C |
A |
5: 120,813,460 (GRCm39) |
H611Q |
probably benign |
Het |
Relch |
T |
A |
1: 105,646,534 (GRCm39) |
L620* |
probably null |
Het |
Rif1 |
T |
A |
2: 51,971,301 (GRCm39) |
W260R |
probably damaging |
Het |
Rpain |
A |
G |
11: 70,864,658 (GRCm39) |
D115G |
probably benign |
Het |
Rpl3l |
T |
C |
17: 24,951,429 (GRCm39) |
V110A |
possibly damaging |
Het |
Ryr2 |
T |
A |
13: 11,787,338 (GRCm39) |
I1012F |
probably damaging |
Het |
Sema4f |
A |
G |
6: 82,894,631 (GRCm39) |
V480A |
probably benign |
Het |
Slc35a3 |
T |
A |
3: 116,474,794 (GRCm39) |
K199N |
probably damaging |
Het |
Slc5a6 |
T |
C |
5: 31,200,322 (GRCm39) |
Y121C |
probably damaging |
Het |
Slc7a14 |
T |
C |
3: 31,291,514 (GRCm39) |
|
probably null |
Het |
Spink5 |
C |
A |
18: 44,122,518 (GRCm39) |
H328N |
probably damaging |
Het |
Tbl1xr1 |
A |
G |
3: 22,263,770 (GRCm39) |
D504G |
probably damaging |
Het |
Tcaf3 |
C |
T |
6: 42,573,954 (GRCm39) |
C86Y |
possibly damaging |
Het |
Tfap2e |
T |
C |
4: 126,628,434 (GRCm39) |
D174G |
probably benign |
Het |
Tmem42 |
T |
C |
9: 122,851,232 (GRCm39) |
V65A |
probably damaging |
Het |
Vmn1r225 |
C |
G |
17: 20,723,177 (GRCm39) |
T206R |
probably damaging |
Het |
Vmn2r38 |
A |
G |
7: 9,100,571 (GRCm39) |
F65S |
probably benign |
Het |
Vmn2r87 |
A |
T |
10: 130,333,208 (GRCm39) |
L14Q |
probably null |
Het |
Xirp2 |
T |
C |
2: 67,345,711 (GRCm39) |
S2651P |
probably benign |
Het |
Zfp429 |
G |
A |
13: 67,538,959 (GRCm39) |
L162F |
probably damaging |
Het |
Zhx1 |
A |
T |
15: 57,915,819 (GRCm39) |
M809K |
probably damaging |
Het |
|
Other mutations in Sort1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00227:Sort1
|
APN |
3 |
108,263,623 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01677:Sort1
|
APN |
3 |
108,252,201 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02532:Sort1
|
APN |
3 |
108,233,036 (GRCm39) |
missense |
probably benign |
0.44 |
IGL03354:Sort1
|
APN |
3 |
108,256,022 (GRCm39) |
missense |
probably benign |
0.00 |
R0266:Sort1
|
UTSW |
3 |
108,252,247 (GRCm39) |
missense |
probably benign |
0.09 |
R0277:Sort1
|
UTSW |
3 |
108,231,908 (GRCm39) |
splice site |
probably benign |
|
R0559:Sort1
|
UTSW |
3 |
108,263,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R0597:Sort1
|
UTSW |
3 |
108,246,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Sort1
|
UTSW |
3 |
108,255,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Sort1
|
UTSW |
3 |
108,233,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R1872:Sort1
|
UTSW |
3 |
108,248,011 (GRCm39) |
missense |
probably benign |
0.01 |
R1986:Sort1
|
UTSW |
3 |
108,253,043 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2130:Sort1
|
UTSW |
3 |
108,259,002 (GRCm39) |
missense |
probably benign |
|
R2131:Sort1
|
UTSW |
3 |
108,259,002 (GRCm39) |
missense |
probably benign |
|
R2133:Sort1
|
UTSW |
3 |
108,259,002 (GRCm39) |
missense |
probably benign |
|
R2362:Sort1
|
UTSW |
3 |
108,253,981 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3436:Sort1
|
UTSW |
3 |
108,245,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R3548:Sort1
|
UTSW |
3 |
108,245,225 (GRCm39) |
missense |
possibly damaging |
0.83 |
R3700:Sort1
|
UTSW |
3 |
108,263,955 (GRCm39) |
nonsense |
probably null |
|
R4496:Sort1
|
UTSW |
3 |
108,217,461 (GRCm39) |
missense |
probably benign |
0.17 |
R4616:Sort1
|
UTSW |
3 |
108,262,857 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4632:Sort1
|
UTSW |
3 |
108,253,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R4749:Sort1
|
UTSW |
3 |
108,263,639 (GRCm39) |
nonsense |
probably null |
|
R4994:Sort1
|
UTSW |
3 |
108,235,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5753:Sort1
|
UTSW |
3 |
108,253,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Sort1
|
UTSW |
3 |
108,264,549 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6262:Sort1
|
UTSW |
3 |
108,217,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7369:Sort1
|
UTSW |
3 |
108,258,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R7484:Sort1
|
UTSW |
3 |
108,246,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Sort1
|
UTSW |
3 |
108,233,323 (GRCm39) |
splice site |
probably null |
|
R8076:Sort1
|
UTSW |
3 |
108,246,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R8222:Sort1
|
UTSW |
3 |
108,241,951 (GRCm39) |
missense |
probably benign |
|
R8871:Sort1
|
UTSW |
3 |
108,262,887 (GRCm39) |
critical splice donor site |
probably null |
|
R8894:Sort1
|
UTSW |
3 |
108,246,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R9169:Sort1
|
UTSW |
3 |
108,247,994 (GRCm39) |
nonsense |
probably null |
|
Z1177:Sort1
|
UTSW |
3 |
108,191,696 (GRCm39) |
missense |
probably benign |
0.00 |
|