Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
T |
C |
1: 138,781,380 (GRCm39) |
T90A |
probably damaging |
Het |
A930011G23Rik |
T |
C |
5: 99,381,784 (GRCm39) |
D326G |
possibly damaging |
Het |
Abcc2 |
A |
T |
19: 43,795,581 (GRCm39) |
I446F |
probably damaging |
Het |
Adamts14 |
A |
G |
10: 61,034,439 (GRCm39) |
Y1150H |
probably benign |
Het |
Adgrl2 |
A |
G |
3: 148,522,880 (GRCm39) |
I217T |
possibly damaging |
Het |
Afap1l1 |
A |
T |
18: 61,874,842 (GRCm39) |
Y446* |
probably null |
Het |
Aimp2 |
G |
A |
5: 143,843,548 (GRCm39) |
A14V |
probably damaging |
Het |
Akap8 |
G |
A |
17: 32,535,586 (GRCm39) |
H143Y |
probably damaging |
Het |
Aldh2 |
A |
T |
5: 121,714,026 (GRCm39) |
V207E |
possibly damaging |
Het |
Aoc1l2 |
T |
A |
6: 48,907,703 (GRCm39) |
H234Q |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Arpp21 |
T |
C |
9: 111,986,861 (GRCm39) |
E230G |
probably damaging |
Het |
Arrdc3 |
G |
A |
13: 81,031,808 (GRCm39) |
D14N |
probably damaging |
Het |
Atn1 |
A |
G |
6: 124,722,291 (GRCm39) |
|
probably benign |
Het |
Atxn7l1 |
G |
A |
12: 33,408,743 (GRCm39) |
D302N |
probably damaging |
Het |
Bbs1 |
T |
A |
19: 4,941,736 (GRCm39) |
H518L |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,054,181 (GRCm39) |
H3100L |
probably benign |
Het |
Bmpr1a |
C |
A |
14: 34,147,050 (GRCm39) |
G241C |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Calcrl |
T |
C |
2: 84,200,855 (GRCm39) |
Y63C |
probably damaging |
Het |
Cand2 |
A |
G |
6: 115,762,093 (GRCm39) |
H173R |
possibly damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Card14 |
A |
T |
11: 119,212,647 (GRCm39) |
|
probably null |
Het |
Cd3d |
T |
A |
9: 44,896,299 (GRCm39) |
Y29* |
probably null |
Het |
Cd4 |
A |
G |
6: 124,844,651 (GRCm39) |
V378A |
possibly damaging |
Het |
Cluh |
A |
T |
11: 74,550,828 (GRCm39) |
H318L |
probably damaging |
Het |
Clvs1 |
T |
A |
4: 9,281,899 (GRCm39) |
D114E |
probably benign |
Het |
Cnot4 |
T |
A |
6: 35,000,344 (GRCm39) |
T548S |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Crebbp |
A |
T |
16: 3,946,561 (GRCm39) |
|
probably null |
Het |
Dnah7a |
T |
G |
1: 53,621,835 (GRCm39) |
K1097Q |
possibly damaging |
Het |
Doc2a |
T |
A |
7: 126,450,979 (GRCm39) |
|
probably null |
Het |
Dpp10 |
A |
T |
1: 123,832,833 (GRCm39) |
V48E |
probably null |
Het |
Dsg2 |
A |
G |
18: 20,734,530 (GRCm39) |
K836R |
probably damaging |
Het |
Egr2 |
T |
C |
10: 67,375,857 (GRCm39) |
V164A |
probably damaging |
Het |
Erbin |
A |
T |
13: 103,970,221 (GRCm39) |
S1132T |
probably benign |
Het |
Espn |
T |
A |
4: 152,213,012 (GRCm39) |
|
probably null |
Het |
Fam83b |
A |
G |
9: 76,399,304 (GRCm39) |
S600P |
probably benign |
Het |
Fanca |
A |
T |
8: 124,024,551 (GRCm39) |
N425K |
possibly damaging |
Het |
Flot2 |
C |
T |
11: 77,949,445 (GRCm39) |
L294F |
probably damaging |
Het |
Frs2 |
A |
G |
10: 116,910,459 (GRCm39) |
V301A |
probably benign |
Het |
Fv1 |
T |
A |
4: 147,953,618 (GRCm39) |
N61K |
possibly damaging |
Het |
Fxr2 |
A |
G |
11: 69,540,659 (GRCm39) |
E339G |
possibly damaging |
Het |
Gck |
T |
C |
11: 5,856,515 (GRCm39) |
Y214C |
probably damaging |
Het |
Golga3 |
C |
G |
5: 110,340,839 (GRCm39) |
T551R |
probably damaging |
Het |
Gorab |
A |
G |
1: 163,224,625 (GRCm39) |
S59P |
probably damaging |
Het |
Gsdme |
C |
T |
6: 50,185,102 (GRCm39) |
V451M |
probably damaging |
Het |
H2-T13 |
A |
C |
17: 36,391,938 (GRCm39) |
I216S |
probably damaging |
Het |
Herc4 |
T |
A |
10: 63,081,743 (GRCm39) |
V22E |
possibly damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hoxa2 |
A |
T |
6: 52,141,576 (GRCm39) |
S17T |
probably damaging |
Het |
Hs3st5 |
A |
G |
10: 36,708,882 (GRCm39) |
Y139C |
probably damaging |
Het |
Ism1 |
G |
A |
2: 139,587,937 (GRCm39) |
V221I |
probably benign |
Het |
Kalrn |
T |
G |
16: 33,796,108 (GRCm39) |
L1222F |
probably damaging |
Het |
Katnip |
A |
G |
7: 125,419,261 (GRCm39) |
N476S |
probably benign |
Het |
Kdm4c |
A |
G |
4: 74,261,631 (GRCm39) |
D602G |
possibly damaging |
Het |
Ktn1 |
A |
G |
14: 47,932,978 (GRCm39) |
K711E |
probably damaging |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Macf1 |
A |
G |
4: 123,350,488 (GRCm39) |
S3792P |
probably damaging |
Het |
Maml3 |
C |
T |
3: 51,598,178 (GRCm39) |
M189I |
probably benign |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mep1a |
T |
G |
17: 43,813,573 (GRCm39) |
I13L |
probably benign |
Het |
Mkrn2 |
G |
T |
6: 115,586,562 (GRCm39) |
C16F |
probably damaging |
Het |
Mlh1 |
C |
T |
9: 111,057,631 (GRCm39) |
A727T |
probably damaging |
Het |
Muc21 |
A |
T |
17: 35,929,600 (GRCm39) |
S1529T |
probably benign |
Het |
Naa16 |
T |
C |
14: 79,593,931 (GRCm39) |
Y344C |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,752,628 (GRCm39) |
Y585F |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,587,753 (GRCm39) |
K149R |
probably damaging |
Het |
Nufip1 |
T |
A |
14: 76,372,287 (GRCm39) |
I467N |
probably damaging |
Het |
Nup133 |
A |
G |
8: 124,632,960 (GRCm39) |
I1057T |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,886,653 (GRCm39) |
|
probably benign |
Het |
Or10ag52 |
T |
A |
2: 87,043,588 (GRCm39) |
C117* |
probably null |
Het |
Or5k1 |
A |
G |
16: 58,617,309 (GRCm39) |
V300A |
probably benign |
Het |
Or5k14 |
A |
C |
16: 58,692,874 (GRCm39) |
I213R |
probably benign |
Het |
Pi4k2a |
A |
T |
19: 42,104,377 (GRCm39) |
I380F |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pik3cg |
A |
T |
12: 32,254,024 (GRCm39) |
D654E |
possibly damaging |
Het |
Poli |
G |
T |
18: 70,642,058 (GRCm39) |
P714Q |
probably damaging |
Het |
Polr3f |
A |
G |
2: 144,378,230 (GRCm39) |
N201D |
probably benign |
Het |
Prorp |
A |
G |
12: 55,384,991 (GRCm39) |
D89G |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 22,959,747 (GRCm39) |
K81N |
probably benign |
Het |
Rbm19 |
T |
C |
5: 120,271,948 (GRCm39) |
|
probably null |
Het |
Sec24a |
C |
T |
11: 51,627,190 (GRCm39) |
V241I |
probably benign |
Het |
Sgk3 |
A |
G |
1: 9,950,567 (GRCm39) |
T160A |
possibly damaging |
Het |
Slc1a4 |
A |
G |
11: 20,254,375 (GRCm39) |
I497T |
probably benign |
Het |
Slc26a9 |
A |
T |
1: 131,690,532 (GRCm39) |
D512V |
probably damaging |
Het |
Slc43a3 |
C |
T |
2: 84,788,084 (GRCm39) |
R489C |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,452,089 (GRCm39) |
F327L |
probably benign |
Het |
Slitrk3 |
A |
G |
3: 72,957,104 (GRCm39) |
V556A |
possibly damaging |
Het |
Spata6l |
A |
G |
19: 28,926,024 (GRCm39) |
F130L |
probably damaging |
Het |
Spib |
T |
C |
7: 44,178,281 (GRCm39) |
E180G |
probably benign |
Het |
Spint2 |
T |
A |
7: 28,958,833 (GRCm39) |
N128Y |
probably damaging |
Het |
Spx |
G |
A |
6: 142,364,245 (GRCm39) |
G102E |
probably benign |
Het |
Spz1 |
T |
A |
13: 92,712,166 (GRCm39) |
E103D |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,495 (GRCm39) |
I138T |
probably benign |
Het |
Sytl3 |
T |
A |
17: 7,000,448 (GRCm39) |
I206N |
possibly damaging |
Het |
Tcaf2 |
T |
C |
6: 42,606,791 (GRCm39) |
T388A |
probably benign |
Het |
Tdpoz8 |
G |
T |
3: 92,981,344 (GRCm39) |
A121S |
probably benign |
Het |
Thap12 |
T |
C |
7: 98,365,572 (GRCm39) |
V580A |
possibly damaging |
Het |
Tlr5 |
T |
A |
1: 182,801,912 (GRCm39) |
D405E |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,890,878 (GRCm39) |
V407A |
probably damaging |
Het |
Tpx2 |
T |
A |
2: 152,732,544 (GRCm39) |
M606K |
probably benign |
Het |
Trim43a |
T |
G |
9: 88,466,312 (GRCm39) |
L211R |
probably damaging |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,424,188 (GRCm39) |
S1485L |
probably benign |
Het |
Ttll8 |
T |
C |
15: 88,798,654 (GRCm39) |
T694A |
probably benign |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,953,535 (GRCm39) |
A823V |
probably damaging |
Het |
Ubqln5 |
C |
A |
7: 103,778,741 (GRCm39) |
V28F |
probably damaging |
Het |
Ulk1 |
T |
A |
5: 110,935,017 (GRCm39) |
Q972L |
probably damaging |
Het |
Unc93b1 |
T |
C |
19: 3,994,062 (GRCm39) |
Y398H |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,822,531 (GRCm39) |
D615G |
probably benign |
Het |
Utp15 |
A |
G |
13: 98,387,420 (GRCm39) |
C385R |
probably benign |
Het |
Vmn2r91 |
T |
A |
17: 18,356,142 (GRCm39) |
V603D |
probably damaging |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Yjefn3 |
A |
T |
8: 70,341,645 (GRCm39) |
|
probably null |
Het |
Ywhab |
A |
T |
2: 163,853,807 (GRCm39) |
I95F |
probably damaging |
Het |
Zfp143 |
C |
T |
7: 109,660,489 (GRCm39) |
|
probably benign |
Het |
Zfp607b |
C |
G |
7: 27,401,949 (GRCm39) |
T135R |
possibly damaging |
Het |
Zfp970 |
A |
G |
2: 177,166,663 (GRCm39) |
Q79R |
possibly damaging |
Het |
|
Other mutations in Adam34l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00321:Adam34l
|
APN |
8 |
44,078,418 (GRCm39) |
missense |
probably benign |
0.12 |
IGL00391:Adam34l
|
APN |
8 |
44,078,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00422:Adam34l
|
APN |
8 |
44,079,388 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00664:Adam34l
|
APN |
8 |
44,079,006 (GRCm39) |
missense |
probably benign |
|
IGL01095:Adam34l
|
APN |
8 |
44,079,133 (GRCm39) |
missense |
probably benign |
0.22 |
IGL01113:Adam34l
|
APN |
8 |
44,079,189 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01444:Adam34l
|
APN |
8 |
44,079,470 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01782:Adam34l
|
APN |
8 |
44,079,772 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01921:Adam34l
|
APN |
8 |
44,078,548 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01964:Adam34l
|
APN |
8 |
44,079,798 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02139:Adam34l
|
APN |
8 |
44,078,615 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02555:Adam34l
|
APN |
8 |
44,078,305 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02951:Adam34l
|
APN |
8 |
44,080,125 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0056:Adam34l
|
UTSW |
8 |
44,078,540 (GRCm39) |
nonsense |
probably null |
|
R0218:Adam34l
|
UTSW |
8 |
44,079,477 (GRCm39) |
missense |
probably benign |
0.00 |
R0530:Adam34l
|
UTSW |
8 |
44,079,568 (GRCm39) |
missense |
probably benign |
0.00 |
R0925:Adam34l
|
UTSW |
8 |
44,079,340 (GRCm39) |
missense |
probably benign |
0.11 |
R0927:Adam34l
|
UTSW |
8 |
44,078,160 (GRCm39) |
missense |
probably benign |
0.00 |
R0975:Adam34l
|
UTSW |
8 |
44,078,155 (GRCm39) |
missense |
probably benign |
|
R1300:Adam34l
|
UTSW |
8 |
44,079,881 (GRCm39) |
nonsense |
probably null |
|
R1728:Adam34l
|
UTSW |
8 |
44,078,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1729:Adam34l
|
UTSW |
8 |
44,078,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Adam34l
|
UTSW |
8 |
44,078,954 (GRCm39) |
nonsense |
probably null |
|
R1869:Adam34l
|
UTSW |
8 |
44,078,132 (GRCm39) |
nonsense |
probably null |
|
R1870:Adam34l
|
UTSW |
8 |
44,078,132 (GRCm39) |
nonsense |
probably null |
|
R1871:Adam34l
|
UTSW |
8 |
44,078,132 (GRCm39) |
nonsense |
probably null |
|
R2008:Adam34l
|
UTSW |
8 |
44,080,074 (GRCm39) |
missense |
probably benign |
0.00 |
R2013:Adam34l
|
UTSW |
8 |
44,079,442 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2022:Adam34l
|
UTSW |
8 |
44,078,954 (GRCm39) |
nonsense |
probably null |
|
R2175:Adam34l
|
UTSW |
8 |
44,078,475 (GRCm39) |
missense |
probably benign |
|
R2875:Adam34l
|
UTSW |
8 |
44,080,177 (GRCm39) |
nonsense |
probably null |
|
R3406:Adam34l
|
UTSW |
8 |
44,079,089 (GRCm39) |
nonsense |
probably null |
|
R3845:Adam34l
|
UTSW |
8 |
44,079,669 (GRCm39) |
missense |
probably benign |
0.00 |
R4033:Adam34l
|
UTSW |
8 |
44,079,710 (GRCm39) |
missense |
probably benign |
0.28 |
R4072:Adam34l
|
UTSW |
8 |
44,079,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4074:Adam34l
|
UTSW |
8 |
44,079,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4075:Adam34l
|
UTSW |
8 |
44,079,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4076:Adam34l
|
UTSW |
8 |
44,079,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R4153:Adam34l
|
UTSW |
8 |
44,079,564 (GRCm39) |
missense |
probably benign |
0.04 |
R4330:Adam34l
|
UTSW |
8 |
44,079,287 (GRCm39) |
missense |
probably benign |
|
R4612:Adam34l
|
UTSW |
8 |
44,079,587 (GRCm39) |
missense |
probably benign |
0.09 |
R4662:Adam34l
|
UTSW |
8 |
44,080,116 (GRCm39) |
missense |
probably benign |
0.26 |
R5032:Adam34l
|
UTSW |
8 |
44,079,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5077:Adam34l
|
UTSW |
8 |
44,080,200 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5504:Adam34l
|
UTSW |
8 |
44,078,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R5697:Adam34l
|
UTSW |
8 |
44,079,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Adam34l
|
UTSW |
8 |
44,078,949 (GRCm39) |
missense |
probably benign |
0.00 |
R6233:Adam34l
|
UTSW |
8 |
44,078,949 (GRCm39) |
missense |
probably benign |
0.00 |
R6234:Adam34l
|
UTSW |
8 |
44,078,949 (GRCm39) |
missense |
probably benign |
0.00 |
R6235:Adam34l
|
UTSW |
8 |
44,078,949 (GRCm39) |
missense |
probably benign |
0.00 |
R6241:Adam34l
|
UTSW |
8 |
44,079,133 (GRCm39) |
missense |
probably benign |
0.22 |
R6392:Adam34l
|
UTSW |
8 |
44,079,038 (GRCm39) |
missense |
probably benign |
0.09 |
R6439:Adam34l
|
UTSW |
8 |
44,078,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R6454:Adam34l
|
UTSW |
8 |
44,079,845 (GRCm39) |
missense |
probably damaging |
0.96 |
R6455:Adam34l
|
UTSW |
8 |
44,079,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R6767:Adam34l
|
UTSW |
8 |
44,079,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6774:Adam34l
|
UTSW |
8 |
44,078,220 (GRCm39) |
missense |
probably benign |
0.00 |
R6877:Adam34l
|
UTSW |
8 |
44,078,274 (GRCm39) |
missense |
probably benign |
0.02 |
R6911:Adam34l
|
UTSW |
8 |
44,078,146 (GRCm39) |
missense |
probably benign |
0.02 |
R7211:Adam34l
|
UTSW |
8 |
44,078,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R7597:Adam34l
|
UTSW |
8 |
44,078,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R7602:Adam34l
|
UTSW |
8 |
44,079,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R7797:Adam34l
|
UTSW |
8 |
44,079,411 (GRCm39) |
missense |
probably benign |
0.04 |
R7981:Adam34l
|
UTSW |
8 |
44,078,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Adam34l
|
UTSW |
8 |
44,078,424 (GRCm39) |
missense |
probably damaging |
0.97 |
R8215:Adam34l
|
UTSW |
8 |
44,079,538 (GRCm39) |
missense |
probably benign |
0.05 |
R9180:Adam34l
|
UTSW |
8 |
44,079,970 (GRCm39) |
nonsense |
probably null |
|
R9307:Adam34l
|
UTSW |
8 |
44,079,304 (GRCm39) |
missense |
probably benign |
0.00 |
R9733:Adam34l
|
UTSW |
8 |
44,079,186 (GRCm39) |
missense |
possibly damaging |
0.94 |
RF001:Adam34l
|
UTSW |
8 |
44,079,942 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1177:Adam34l
|
UTSW |
8 |
44,079,583 (GRCm39) |
missense |
probably damaging |
0.99 |
|