Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A3galt2 |
A |
G |
4: 128,660,941 (GRCm39) |
R197G |
possibly damaging |
Het |
Acacb |
A |
T |
5: 114,347,878 (GRCm39) |
H983L |
probably damaging |
Het |
Adal |
T |
A |
2: 120,978,798 (GRCm39) |
D139E |
probably benign |
Het |
Agap1 |
A |
G |
1: 89,598,934 (GRCm39) |
K331E |
probably damaging |
Het |
Alyref |
T |
C |
11: 120,489,133 (GRCm39) |
D11G |
probably damaging |
Het |
B3gat1 |
A |
G |
9: 26,667,377 (GRCm39) |
E203G |
probably damaging |
Het |
Bsn |
T |
C |
9: 107,993,595 (GRCm39) |
E719G |
possibly damaging |
Het |
Cap2 |
G |
C |
13: 46,791,498 (GRCm39) |
|
probably null |
Het |
Ccni |
A |
G |
5: 93,350,186 (GRCm39) |
V31A |
probably benign |
Het |
Cdcp3 |
T |
A |
7: 130,796,032 (GRCm39) |
|
probably null |
Het |
Cfap54 |
A |
T |
10: 92,735,022 (GRCm39) |
L2343* |
probably null |
Het |
Clns1a |
T |
A |
7: 97,363,239 (GRCm39) |
Y204N |
possibly damaging |
Het |
Cox11 |
C |
T |
11: 90,535,326 (GRCm39) |
T259I |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,371,869 (GRCm39) |
N940S |
probably benign |
Het |
Erbb2 |
T |
C |
11: 98,327,265 (GRCm39) |
V1181A |
probably benign |
Het |
Exoc4 |
T |
C |
6: 33,839,022 (GRCm39) |
V686A |
possibly damaging |
Het |
F830045P16Rik |
A |
G |
2: 129,305,384 (GRCm39) |
V330A |
possibly damaging |
Het |
Fbf1 |
A |
C |
11: 116,045,860 (GRCm39) |
F245V |
probably damaging |
Het |
Fut10 |
T |
A |
8: 31,726,225 (GRCm39) |
F327I |
probably damaging |
Het |
Galnt1 |
C |
T |
18: 24,387,690 (GRCm39) |
P144S |
probably damaging |
Het |
Garin4 |
T |
C |
1: 190,895,105 (GRCm39) |
S513G |
probably benign |
Het |
Ghrhr |
A |
T |
6: 55,356,171 (GRCm39) |
D88V |
possibly damaging |
Het |
Greb1l |
T |
A |
18: 10,560,331 (GRCm39) |
C1864S |
probably damaging |
Het |
H1f2 |
T |
C |
13: 23,923,106 (GRCm39) |
I92T |
probably benign |
Het |
Hps1 |
T |
C |
19: 42,750,992 (GRCm39) |
E336G |
probably damaging |
Het |
Ibsp |
GGAAGAAGAAGAAGAAGA |
GGAAGAAGAAGAAGA |
5: 104,457,935 (GRCm39) |
|
probably benign |
Het |
Irgc |
C |
A |
7: 24,132,753 (GRCm39) |
E21D |
possibly damaging |
Het |
Itsn1 |
A |
T |
16: 91,625,168 (GRCm39) |
R590* |
probably null |
Het |
Katnip |
T |
C |
7: 125,394,557 (GRCm39) |
V211A |
probably benign |
Het |
Lmln |
T |
C |
16: 32,886,694 (GRCm39) |
V67A |
probably damaging |
Het |
Lsm14a |
T |
C |
7: 34,065,042 (GRCm39) |
Q179R |
probably damaging |
Het |
Ltbr |
A |
C |
6: 125,289,836 (GRCm39) |
D119E |
probably benign |
Het |
Mrc1 |
A |
G |
2: 14,284,705 (GRCm39) |
T565A |
possibly damaging |
Het |
Muc6 |
A |
C |
7: 141,235,939 (GRCm39) |
N473K |
possibly damaging |
Het |
Myocd |
A |
T |
11: 65,078,066 (GRCm39) |
D448E |
probably benign |
Het |
Neil2 |
T |
A |
14: 63,420,975 (GRCm39) |
I239F |
probably damaging |
Het |
Npnt |
A |
G |
3: 132,620,175 (GRCm39) |
F123S |
possibly damaging |
Het |
Or2g25 |
T |
A |
17: 37,970,997 (GRCm39) |
I76F |
probably damaging |
Het |
Or4f15 |
T |
C |
2: 111,813,645 (GRCm39) |
Y258C |
probably damaging |
Het |
Or52x1 |
C |
A |
7: 104,852,821 (GRCm39) |
C243F |
probably damaging |
Het |
Or56a5 |
T |
C |
7: 104,793,281 (GRCm39) |
D73G |
probably damaging |
Het |
Or5d37 |
T |
A |
2: 87,923,366 (GRCm39) |
R305* |
probably null |
Het |
Or8d1b |
A |
C |
9: 38,887,547 (GRCm39) |
|
probably null |
Het |
Or9i2 |
C |
T |
19: 13,815,902 (GRCm39) |
V212M |
possibly damaging |
Het |
Pcnx3 |
T |
C |
19: 5,722,646 (GRCm39) |
T941A |
probably benign |
Het |
Phldb3 |
G |
A |
7: 24,312,004 (GRCm39) |
R106Q |
probably benign |
Het |
Pitrm1 |
C |
A |
13: 6,625,115 (GRCm39) |
Y864* |
probably null |
Het |
Plcb4 |
T |
C |
2: 135,823,995 (GRCm39) |
I844T |
probably benign |
Het |
Plekhg5 |
T |
C |
4: 152,196,676 (GRCm39) |
C695R |
probably damaging |
Het |
Ppp1r3b |
T |
A |
8: 35,851,655 (GRCm39) |
F165I |
probably damaging |
Het |
Prr5 |
T |
A |
15: 84,587,322 (GRCm39) |
F357L |
probably damaging |
Het |
Rasgrf1 |
A |
T |
9: 89,891,419 (GRCm39) |
I1046F |
probably damaging |
Het |
Rbm15b |
T |
C |
9: 106,762,563 (GRCm39) |
Y535C |
probably damaging |
Het |
Rbp3 |
A |
T |
14: 33,677,858 (GRCm39) |
E602V |
probably damaging |
Het |
Rimklb |
T |
C |
6: 122,433,292 (GRCm39) |
N343S |
probably benign |
Het |
Rrp12 |
A |
G |
19: 41,860,199 (GRCm39) |
L1008P |
probably damaging |
Het |
Sec63 |
C |
T |
10: 42,674,794 (GRCm39) |
R226C |
probably damaging |
Het |
Sirpa |
T |
C |
2: 129,457,388 (GRCm39) |
V154A |
probably damaging |
Het |
Slc13a5 |
C |
G |
11: 72,141,626 (GRCm39) |
V405L |
probably damaging |
Het |
Slc17a3 |
C |
T |
13: 24,039,841 (GRCm39) |
S293F |
probably damaging |
Het |
Slc22a23 |
G |
A |
13: 34,367,244 (GRCm39) |
T588I |
probably damaging |
Het |
Slc22a27 |
C |
A |
19: 7,904,156 (GRCm39) |
|
probably benign |
Het |
Slc4a4 |
A |
C |
5: 89,304,195 (GRCm39) |
H502P |
possibly damaging |
Het |
Slc5a5 |
A |
T |
8: 71,342,277 (GRCm39) |
M258K |
probably damaging |
Het |
Spry4 |
A |
G |
18: 38,723,142 (GRCm39) |
I207T |
possibly damaging |
Het |
Stk11ip |
A |
G |
1: 75,505,711 (GRCm39) |
D460G |
possibly damaging |
Het |
Syn3 |
T |
A |
10: 86,284,750 (GRCm39) |
I117F |
possibly damaging |
Het |
Tead4 |
C |
T |
6: 128,220,365 (GRCm39) |
A224T |
probably damaging |
Het |
Tmtc3 |
A |
T |
10: 100,286,184 (GRCm39) |
N546K |
probably benign |
Het |
Tnn |
T |
A |
1: 159,916,036 (GRCm39) |
H1227L |
probably damaging |
Het |
Tor2a |
G |
A |
2: 32,648,716 (GRCm39) |
G62D |
probably damaging |
Het |
Trf |
T |
C |
9: 103,104,078 (GRCm39) |
|
probably null |
Het |
Ubr5 |
T |
C |
15: 37,968,737 (GRCm39) |
T2727A |
probably damaging |
Het |
Vmn2r27 |
T |
A |
6: 124,208,578 (GRCm39) |
T56S |
probably benign |
Het |
Wipf3 |
T |
G |
6: 54,473,486 (GRCm39) |
L458R |
probably damaging |
Het |
Zfp236 |
T |
C |
18: 82,648,119 (GRCm39) |
K966R |
probably damaging |
Het |
Zfp27 |
T |
A |
7: 29,593,532 (GRCm39) |
H811L |
possibly damaging |
Het |
Zfp366 |
A |
G |
13: 99,370,768 (GRCm39) |
H496R |
probably damaging |
Het |
Zfp467 |
A |
T |
6: 48,415,689 (GRCm39) |
V321E |
probably damaging |
Het |
|
Other mutations in Adam6b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Adam6b
|
APN |
12 |
113,455,013 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00800:Adam6b
|
APN |
12 |
113,454,062 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01456:Adam6b
|
APN |
12 |
113,455,083 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02232:Adam6b
|
APN |
12 |
113,454,764 (GRCm39) |
missense |
probably benign |
0.06 |
IGL03039:Adam6b
|
APN |
12 |
113,454,502 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03399:Adam6b
|
APN |
12 |
113,454,728 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL03412:Adam6b
|
APN |
12 |
113,455,390 (GRCm39) |
nonsense |
probably null |
|
R0234:Adam6b
|
UTSW |
12 |
113,454,230 (GRCm39) |
missense |
probably damaging |
0.98 |
R0373:Adam6b
|
UTSW |
12 |
113,454,275 (GRCm39) |
missense |
probably benign |
0.15 |
R0402:Adam6b
|
UTSW |
12 |
113,453,615 (GRCm39) |
missense |
probably damaging |
0.96 |
R0420:Adam6b
|
UTSW |
12 |
113,453,614 (GRCm39) |
missense |
probably benign |
0.02 |
R0573:Adam6b
|
UTSW |
12 |
113,455,278 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0884:Adam6b
|
UTSW |
12 |
113,454,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R1489:Adam6b
|
UTSW |
12 |
113,455,071 (GRCm39) |
missense |
probably benign |
0.15 |
R1542:Adam6b
|
UTSW |
12 |
113,454,559 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1591:Adam6b
|
UTSW |
12 |
113,453,452 (GRCm39) |
missense |
probably benign |
0.07 |
R1596:Adam6b
|
UTSW |
12 |
113,454,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1675:Adam6b
|
UTSW |
12 |
113,454,664 (GRCm39) |
missense |
probably benign |
0.00 |
R1699:Adam6b
|
UTSW |
12 |
113,454,205 (GRCm39) |
missense |
probably benign |
0.02 |
R1818:Adam6b
|
UTSW |
12 |
113,454,876 (GRCm39) |
missense |
probably benign |
0.15 |
R1829:Adam6b
|
UTSW |
12 |
113,453,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1851:Adam6b
|
UTSW |
12 |
113,455,442 (GRCm39) |
missense |
probably benign |
0.44 |
R1955:Adam6b
|
UTSW |
12 |
113,455,436 (GRCm39) |
missense |
probably benign |
0.16 |
R2040:Adam6b
|
UTSW |
12 |
113,454,364 (GRCm39) |
missense |
probably benign |
0.34 |
R3820:Adam6b
|
UTSW |
12 |
113,453,984 (GRCm39) |
missense |
probably benign |
0.38 |
R4112:Adam6b
|
UTSW |
12 |
113,453,256 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4434:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4435:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4438:Adam6b
|
UTSW |
12 |
113,454,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4509:Adam6b
|
UTSW |
12 |
113,453,972 (GRCm39) |
missense |
probably benign |
0.02 |
R5034:Adam6b
|
UTSW |
12 |
113,454,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R5316:Adam6b
|
UTSW |
12 |
113,455,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Adam6b
|
UTSW |
12 |
113,454,200 (GRCm39) |
missense |
possibly damaging |
0.45 |
R5331:Adam6b
|
UTSW |
12 |
113,454,200 (GRCm39) |
missense |
possibly damaging |
0.45 |
R5604:Adam6b
|
UTSW |
12 |
113,454,420 (GRCm39) |
nonsense |
probably null |
|
R5698:Adam6b
|
UTSW |
12 |
113,455,083 (GRCm39) |
missense |
probably benign |
0.30 |
R5877:Adam6b
|
UTSW |
12 |
113,453,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Adam6b
|
UTSW |
12 |
113,455,330 (GRCm39) |
missense |
probably benign |
|
R6254:Adam6b
|
UTSW |
12 |
113,453,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R6371:Adam6b
|
UTSW |
12 |
113,453,894 (GRCm39) |
missense |
probably damaging |
0.99 |
R6617:Adam6b
|
UTSW |
12 |
113,454,152 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6768:Adam6b
|
UTSW |
12 |
113,453,863 (GRCm39) |
missense |
probably benign |
0.01 |
R7002:Adam6b
|
UTSW |
12 |
113,453,327 (GRCm39) |
nonsense |
probably null |
|
R7003:Adam6b
|
UTSW |
12 |
113,453,662 (GRCm39) |
nonsense |
probably null |
|
R7049:Adam6b
|
UTSW |
12 |
113,454,122 (GRCm39) |
missense |
probably damaging |
0.99 |
R7313:Adam6b
|
UTSW |
12 |
113,454,754 (GRCm39) |
missense |
probably benign |
0.00 |
R7372:Adam6b
|
UTSW |
12 |
113,453,784 (GRCm39) |
missense |
probably benign |
0.24 |
R7684:Adam6b
|
UTSW |
12 |
113,455,196 (GRCm39) |
nonsense |
probably null |
|
R7777:Adam6b
|
UTSW |
12 |
113,453,758 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7781:Adam6b
|
UTSW |
12 |
113,454,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R7857:Adam6b
|
UTSW |
12 |
113,454,104 (GRCm39) |
missense |
probably benign |
0.09 |
R8196:Adam6b
|
UTSW |
12 |
113,454,087 (GRCm39) |
missense |
probably benign |
0.19 |
R8423:Adam6b
|
UTSW |
12 |
113,454,530 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8680:Adam6b
|
UTSW |
12 |
113,454,371 (GRCm39) |
missense |
probably benign |
0.05 |
R8762:Adam6b
|
UTSW |
12 |
113,453,227 (GRCm39) |
missense |
probably damaging |
0.98 |
R8792:Adam6b
|
UTSW |
12 |
113,455,310 (GRCm39) |
missense |
possibly damaging |
0.75 |
R8806:Adam6b
|
UTSW |
12 |
113,455,418 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8880:Adam6b
|
UTSW |
12 |
113,454,764 (GRCm39) |
missense |
probably benign |
|
R8977:Adam6b
|
UTSW |
12 |
113,453,996 (GRCm39) |
missense |
probably benign |
0.02 |
R8987:Adam6b
|
UTSW |
12 |
113,454,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R9101:Adam6b
|
UTSW |
12 |
113,455,376 (GRCm39) |
missense |
probably benign |
0.22 |
R9103:Adam6b
|
UTSW |
12 |
113,454,558 (GRCm39) |
nonsense |
probably null |
|
R9334:Adam6b
|
UTSW |
12 |
113,454,768 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Adam6b
|
UTSW |
12 |
113,454,176 (GRCm39) |
missense |
probably benign |
|
R9683:Adam6b
|
UTSW |
12 |
113,454,176 (GRCm39) |
missense |
probably benign |
|
R9796:Adam6b
|
UTSW |
12 |
113,454,272 (GRCm39) |
missense |
probably damaging |
1.00 |
RF012:Adam6b
|
UTSW |
12 |
113,453,552 (GRCm39) |
missense |
probably damaging |
1.00 |
RF022:Adam6b
|
UTSW |
12 |
113,455,289 (GRCm39) |
missense |
possibly damaging |
0.90 |
T0722:Adam6b
|
UTSW |
12 |
113,454,888 (GRCm39) |
missense |
probably benign |
0.11 |
T0722:Adam6b
|
UTSW |
12 |
113,453,197 (GRCm39) |
missense |
possibly damaging |
0.91 |
|