Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
T |
C |
4: 148,026,232 (GRCm39) |
S251P |
probably damaging |
Het |
Aaas |
C |
A |
15: 102,255,153 (GRCm39) |
R79L |
probably benign |
Het |
Acap2 |
C |
A |
16: 30,923,754 (GRCm39) |
E657* |
probably null |
Het |
Adgrg5 |
A |
T |
8: 95,668,258 (GRCm39) |
E441V |
probably benign |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
AY358078 |
C |
T |
14: 52,057,876 (GRCm39) |
|
probably null |
Het |
Bco2 |
A |
G |
9: 50,461,929 (GRCm39) |
V25A |
possibly damaging |
Het |
Bltp1 |
T |
C |
3: 36,924,205 (GRCm39) |
V10A |
possibly damaging |
Het |
Carf |
T |
A |
1: 60,165,195 (GRCm39) |
|
probably null |
Het |
Ccdc38 |
A |
T |
10: 93,401,741 (GRCm39) |
I134L |
probably benign |
Het |
Cgnl1 |
A |
G |
9: 71,633,097 (GRCm39) |
S85P |
probably benign |
Het |
Ctsl |
A |
G |
13: 64,515,693 (GRCm39) |
V126A |
probably damaging |
Het |
Cwc27 |
A |
C |
13: 104,938,693 (GRCm39) |
S206A |
probably damaging |
Het |
D630045J12Rik |
A |
G |
6: 38,167,590 (GRCm39) |
I1004T |
probably damaging |
Het |
Dgki |
A |
G |
6: 37,027,138 (GRCm39) |
V401A |
probably damaging |
Het |
Dpp8 |
C |
T |
9: 64,970,775 (GRCm39) |
H545Y |
possibly damaging |
Het |
Dpy19l1 |
A |
T |
9: 24,386,680 (GRCm39) |
C205S |
probably damaging |
Het |
Enpp2 |
C |
T |
15: 54,709,225 (GRCm39) |
E797K |
probably benign |
Het |
Ephb2 |
C |
T |
4: 136,498,320 (GRCm39) |
R253H |
probably damaging |
Het |
Esrra |
T |
C |
19: 6,897,665 (GRCm39) |
T31A |
probably benign |
Het |
Ewsr1 |
C |
A |
11: 5,028,574 (GRCm39) |
|
probably benign |
Het |
Flt4 |
G |
T |
11: 49,522,808 (GRCm39) |
R475L |
probably benign |
Het |
Gm13547 |
A |
G |
2: 29,653,921 (GRCm39) |
E138G |
possibly damaging |
Het |
Gm572 |
A |
T |
4: 148,751,276 (GRCm39) |
R216S |
possibly damaging |
Het |
H2ac8 |
A |
G |
13: 23,755,119 (GRCm39) |
V55A |
probably damaging |
Het |
Hapln2 |
T |
A |
3: 87,931,404 (GRCm39) |
Y37F |
probably benign |
Het |
Hcn1 |
ACAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC |
ACAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGC |
13: 118,112,302 (GRCm39) |
|
probably benign |
Het |
Hhla1 |
C |
T |
15: 65,805,176 (GRCm39) |
A369T |
probably benign |
Het |
Hmg20a |
T |
A |
9: 56,374,685 (GRCm39) |
F14I |
possibly damaging |
Het |
Iqca1l |
A |
T |
5: 24,760,426 (GRCm39) |
|
probably null |
Het |
Itga2 |
A |
T |
13: 114,985,956 (GRCm39) |
S940T |
possibly damaging |
Het |
Kcnt2 |
A |
G |
1: 140,359,116 (GRCm39) |
N377S |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Lhx6 |
A |
G |
2: 35,981,049 (GRCm39) |
S298P |
probably benign |
Het |
Lrp2 |
C |
T |
2: 69,332,954 (GRCm39) |
G1521D |
probably damaging |
Het |
Mogat2 |
A |
G |
7: 98,881,766 (GRCm39) |
W57R |
probably damaging |
Het |
Ms4a3 |
T |
C |
19: 11,610,271 (GRCm39) |
N97S |
probably benign |
Het |
Myo1a |
A |
G |
10: 127,548,493 (GRCm39) |
D380G |
probably damaging |
Het |
Nufip2 |
T |
A |
11: 77,582,432 (GRCm39) |
D115E |
probably damaging |
Het |
Ogn |
A |
T |
13: 49,762,809 (GRCm39) |
K50N |
probably benign |
Het |
Or5ac20 |
T |
C |
16: 59,104,366 (GRCm39) |
R165G |
probably damaging |
Het |
Or8c10 |
A |
T |
9: 38,278,844 (GRCm39) |
M1L |
probably benign |
Het |
Pde8b |
G |
A |
13: 95,182,951 (GRCm39) |
T269I |
probably damaging |
Het |
Ppargc1b |
A |
T |
18: 61,443,677 (GRCm39) |
D495E |
probably damaging |
Het |
Prdm16 |
C |
A |
4: 154,613,117 (GRCm39) |
K103N |
possibly damaging |
Het |
Pxk |
A |
G |
14: 8,164,091 (GRCm38) |
N561S |
probably damaging |
Het |
Rapgef5 |
A |
G |
12: 117,610,721 (GRCm39) |
N323S |
probably benign |
Het |
Slc6a13 |
T |
G |
6: 121,309,333 (GRCm39) |
D281E |
possibly damaging |
Het |
Slc8a1 |
T |
C |
17: 81,955,676 (GRCm39) |
Y454C |
probably damaging |
Het |
Sntg2 |
C |
A |
12: 30,338,295 (GRCm39) |
L115F |
probably damaging |
Het |
Spata13 |
A |
G |
14: 60,993,857 (GRCm39) |
D1103G |
probably damaging |
Het |
Supv3l1 |
G |
A |
10: 62,268,225 (GRCm39) |
A540V |
probably benign |
Het |
Tet1 |
A |
T |
10: 62,648,689 (GRCm39) |
D1914E |
probably damaging |
Het |
Tmem30a |
A |
G |
9: 79,678,570 (GRCm39) |
*329Q |
probably null |
Het |
Tspan5 |
A |
T |
3: 138,604,102 (GRCm39) |
L162F |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,549,396 (GRCm39) |
K31760N |
probably damaging |
Het |
Tyr |
A |
T |
7: 87,087,200 (GRCm39) |
D437E |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,144,238 (GRCm39) |
L1427* |
probably null |
Het |
Utrn |
C |
A |
10: 12,312,108 (GRCm39) |
D616Y |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,841,075 (GRCm39) |
S1490P |
probably damaging |
Het |
Vcl |
T |
A |
14: 21,059,018 (GRCm39) |
C545S |
probably damaging |
Het |
Vmn2r4 |
C |
T |
3: 64,314,309 (GRCm39) |
G224D |
probably damaging |
Het |
Vmn2r97 |
T |
A |
17: 19,168,110 (GRCm39) |
V788E |
probably damaging |
Het |
Vrtn |
G |
A |
12: 84,695,282 (GRCm39) |
V11M |
probably damaging |
Het |
Zbtb21 |
A |
T |
16: 97,753,227 (GRCm39) |
V380D |
probably damaging |
Het |
Zcchc14 |
G |
A |
8: 122,331,002 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Proc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00693:Proc
|
APN |
18 |
32,256,566 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01071:Proc
|
APN |
18 |
32,256,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01287:Proc
|
APN |
18 |
32,256,873 (GRCm39) |
splice site |
probably benign |
|
IGL01298:Proc
|
APN |
18 |
32,256,605 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01898:Proc
|
APN |
18 |
32,266,198 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01977:Proc
|
APN |
18 |
32,260,472 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02040:Proc
|
APN |
18 |
32,267,913 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02724:Proc
|
APN |
18 |
32,267,925 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02852:Proc
|
APN |
18 |
32,258,208 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02901:Proc
|
APN |
18 |
32,256,678 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL03401:Proc
|
APN |
18 |
32,256,326 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0110:Proc
|
UTSW |
18 |
32,258,171 (GRCm39) |
missense |
probably benign |
0.26 |
R0131:Proc
|
UTSW |
18 |
32,268,951 (GRCm39) |
missense |
probably benign |
0.01 |
R0510:Proc
|
UTSW |
18 |
32,258,171 (GRCm39) |
missense |
probably benign |
0.26 |
R0988:Proc
|
UTSW |
18 |
32,266,536 (GRCm39) |
missense |
probably benign |
|
R1455:Proc
|
UTSW |
18 |
32,256,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1463:Proc
|
UTSW |
18 |
32,266,491 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1711:Proc
|
UTSW |
18 |
32,260,459 (GRCm39) |
missense |
probably benign |
0.05 |
R3414:Proc
|
UTSW |
18 |
32,256,738 (GRCm39) |
missense |
probably benign |
0.00 |
R3911:Proc
|
UTSW |
18 |
32,256,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R4276:Proc
|
UTSW |
18 |
32,268,967 (GRCm39) |
missense |
probably benign |
0.00 |
R4598:Proc
|
UTSW |
18 |
32,256,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Proc
|
UTSW |
18 |
32,260,526 (GRCm39) |
missense |
probably benign |
0.32 |
R4758:Proc
|
UTSW |
18 |
32,256,863 (GRCm39) |
missense |
probably damaging |
0.97 |
R4941:Proc
|
UTSW |
18 |
32,258,166 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5917:Proc
|
UTSW |
18 |
32,260,513 (GRCm39) |
missense |
probably benign |
0.07 |
R6349:Proc
|
UTSW |
18 |
32,266,486 (GRCm39) |
missense |
probably benign |
0.00 |
R6636:Proc
|
UTSW |
18 |
32,256,813 (GRCm39) |
missense |
probably benign |
0.00 |
R6735:Proc
|
UTSW |
18 |
32,256,701 (GRCm39) |
missense |
probably benign |
0.01 |
R7110:Proc
|
UTSW |
18 |
32,266,441 (GRCm39) |
missense |
probably benign |
0.30 |
R7310:Proc
|
UTSW |
18 |
32,268,952 (GRCm39) |
missense |
probably benign |
0.03 |
R7409:Proc
|
UTSW |
18 |
32,260,513 (GRCm39) |
missense |
probably benign |
0.03 |
R7597:Proc
|
UTSW |
18 |
32,256,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R7598:Proc
|
UTSW |
18 |
32,268,929 (GRCm39) |
missense |
probably benign |
0.00 |
R7604:Proc
|
UTSW |
18 |
32,267,831 (GRCm39) |
splice site |
probably null |
|
R7738:Proc
|
UTSW |
18 |
32,260,532 (GRCm39) |
nonsense |
probably null |
|
R7921:Proc
|
UTSW |
18 |
32,256,470 (GRCm39) |
missense |
probably damaging |
1.00 |
R8425:Proc
|
UTSW |
18 |
32,256,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Proc
|
UTSW |
18 |
32,268,950 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9382:Proc
|
UTSW |
18 |
32,256,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R9690:Proc
|
UTSW |
18 |
32,256,371 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Proc
|
UTSW |
18 |
32,256,560 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Proc
|
UTSW |
18 |
32,268,032 (GRCm39) |
missense |
probably benign |
0.03 |
|