Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
A |
G |
7: 43,147,543 (GRCm39) |
I182T |
possibly damaging |
Het |
4933406P04Rik |
A |
G |
10: 20,187,105 (GRCm39) |
|
probably benign |
Het |
A730018C14Rik |
A |
G |
12: 112,381,924 (GRCm39) |
|
noncoding transcript |
Het |
Aacs |
A |
T |
5: 125,593,394 (GRCm39) |
I666F |
possibly damaging |
Het |
Abcb9 |
C |
T |
5: 124,221,694 (GRCm39) |
V227I |
probably benign |
Het |
Abcd3 |
T |
C |
3: 121,578,122 (GRCm39) |
Q168R |
probably benign |
Het |
Adamts4 |
A |
G |
1: 171,080,311 (GRCm39) |
Q288R |
probably benign |
Het |
Atad2 |
G |
A |
15: 57,966,760 (GRCm39) |
A611V |
probably damaging |
Het |
Aup1 |
T |
C |
6: 83,032,187 (GRCm39) |
V118A |
possibly damaging |
Het |
Bend7 |
T |
A |
2: 4,768,122 (GRCm39) |
|
probably benign |
Het |
Brd4 |
A |
G |
17: 32,417,646 (GRCm39) |
|
probably benign |
Het |
C4b |
C |
A |
17: 34,957,941 (GRCm39) |
R580L |
probably benign |
Het |
Cct8 |
G |
T |
16: 87,288,342 (GRCm39) |
|
probably benign |
Het |
Cfhr4 |
A |
T |
1: 139,664,608 (GRCm39) |
C484S |
probably damaging |
Het |
Cilp |
T |
C |
9: 65,183,127 (GRCm39) |
Y344H |
probably benign |
Het |
Clic6 |
A |
T |
16: 92,288,961 (GRCm39) |
|
probably benign |
Het |
Colgalt2 |
T |
C |
1: 152,360,703 (GRCm39) |
S247P |
probably damaging |
Het |
Csf2rb |
G |
T |
15: 78,224,955 (GRCm39) |
A212S |
probably benign |
Het |
Csmd3 |
A |
C |
15: 47,475,294 (GRCm39) |
|
probably null |
Het |
Cyp26c1 |
A |
G |
19: 37,679,393 (GRCm39) |
D366G |
probably benign |
Het |
Dhx33 |
A |
G |
11: 70,890,354 (GRCm39) |
S222P |
probably damaging |
Het |
Dhx40 |
T |
A |
11: 86,697,379 (GRCm39) |
I63F |
possibly damaging |
Het |
Dlgap2 |
T |
A |
8: 14,879,861 (GRCm39) |
|
probably null |
Het |
Dnah7b |
T |
A |
1: 46,105,957 (GRCm39) |
D20E |
unknown |
Het |
Dnase2b |
C |
A |
3: 146,290,312 (GRCm39) |
A220S |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,570,352 (GRCm39) |
E362G |
probably benign |
Het |
Ect2l |
C |
T |
10: 18,044,182 (GRCm39) |
V226I |
probably benign |
Het |
Epha10 |
C |
A |
4: 124,779,389 (GRCm39) |
N78K |
probably damaging |
Het |
Epha3 |
A |
G |
16: 63,593,416 (GRCm39) |
V224A |
probably damaging |
Het |
Fcgr4 |
C |
A |
1: 170,847,523 (GRCm39) |
D40E |
probably damaging |
Het |
Fer1l4 |
T |
C |
2: 155,887,553 (GRCm39) |
M548V |
probably benign |
Het |
Flii |
C |
T |
11: 60,610,518 (GRCm39) |
|
probably null |
Het |
Flnc |
A |
T |
6: 29,444,079 (GRCm39) |
Y631F |
probably benign |
Het |
Gm6871 |
A |
C |
7: 41,195,514 (GRCm39) |
|
probably null |
Het |
Gtf2ird1 |
A |
T |
5: 134,387,772 (GRCm39) |
S1028T |
possibly damaging |
Het |
Hycc1 |
A |
T |
5: 24,170,139 (GRCm39) |
D403E |
probably benign |
Het |
Hydin |
A |
G |
8: 111,301,486 (GRCm39) |
H3739R |
probably benign |
Het |
Iqcg |
A |
T |
16: 32,865,895 (GRCm39) |
N149K |
probably benign |
Het |
Iqgap3 |
A |
G |
3: 88,006,200 (GRCm39) |
D537G |
probably benign |
Het |
Itih2 |
T |
G |
2: 10,110,025 (GRCm39) |
D576A |
probably benign |
Het |
Kcmf1 |
T |
C |
6: 72,825,212 (GRCm39) |
T243A |
probably benign |
Het |
Kif1a |
A |
G |
1: 93,002,670 (GRCm39) |
|
probably benign |
Het |
Klf10 |
C |
T |
15: 38,297,030 (GRCm39) |
G337S |
probably damaging |
Het |
Krt31 |
T |
C |
11: 99,938,699 (GRCm39) |
N298S |
possibly damaging |
Het |
Lmnb1 |
A |
G |
18: 56,882,823 (GRCm39) |
E556G |
probably benign |
Het |
Mael |
A |
T |
1: 166,029,859 (GRCm39) |
S354T |
probably benign |
Het |
Mast3 |
T |
C |
8: 71,238,816 (GRCm39) |
D496G |
probably damaging |
Het |
Med12l |
A |
G |
3: 59,172,661 (GRCm39) |
T1806A |
possibly damaging |
Het |
Mms19 |
A |
G |
19: 41,944,260 (GRCm39) |
|
probably null |
Het |
Moap1 |
A |
T |
12: 102,709,504 (GRCm39) |
M15K |
possibly damaging |
Het |
Mpv17l |
G |
T |
16: 13,764,683 (GRCm39) |
W70L |
probably damaging |
Het |
Muc4 |
G |
C |
16: 32,753,919 (GRCm38) |
R1265P |
probably benign |
Het |
Myo7b |
T |
C |
18: 32,127,962 (GRCm39) |
I577V |
probably benign |
Het |
Myo9b |
T |
A |
8: 71,743,620 (GRCm39) |
L227Q |
probably damaging |
Het |
Myom2 |
T |
C |
8: 15,154,059 (GRCm39) |
|
probably benign |
Het |
Naip6 |
C |
A |
13: 100,452,983 (GRCm39) |
R26L |
probably benign |
Het |
Nbea |
T |
C |
3: 55,966,248 (GRCm39) |
T405A |
probably damaging |
Het |
Nrp2 |
T |
A |
1: 62,802,063 (GRCm39) |
I502N |
probably damaging |
Het |
Nt5el |
A |
T |
13: 105,246,129 (GRCm39) |
H230L |
probably benign |
Het |
Nufip2 |
G |
A |
11: 77,582,733 (GRCm39) |
E216K |
possibly damaging |
Het |
Oaf |
A |
G |
9: 43,133,930 (GRCm39) |
Y264H |
probably damaging |
Het |
Or51a42 |
A |
G |
7: 103,708,431 (GRCm39) |
V126A |
probably damaging |
Het |
Or5m10 |
T |
C |
2: 85,717,615 (GRCm39) |
L157P |
probably damaging |
Het |
Or6c217 |
A |
T |
10: 129,738,293 (GRCm39) |
C95* |
probably null |
Het |
Pax1 |
T |
C |
2: 147,210,321 (GRCm39) |
V352A |
probably damaging |
Het |
Pkd1l2 |
TGGG |
TGG |
8: 117,764,974 (GRCm39) |
|
probably null |
Het |
Plxna3 |
G |
A |
X: 73,383,772 (GRCm39) |
|
probably null |
Het |
Pnpla3 |
T |
C |
15: 84,065,247 (GRCm39) |
V347A |
probably benign |
Het |
Ppl |
T |
A |
16: 4,920,461 (GRCm39) |
K350* |
probably null |
Het |
Pramel28 |
T |
C |
4: 143,692,632 (GRCm39) |
D123G |
probably benign |
Het |
Prb1a |
T |
A |
6: 132,186,424 (GRCm39) |
|
probably null |
Het |
Prb1a |
C |
A |
6: 132,186,423 (GRCm39) |
|
probably null |
Het |
Ptpn11 |
G |
A |
5: 121,275,574 (GRCm39) |
H540Y |
probably benign |
Het |
Ptprz1 |
C |
A |
6: 23,000,747 (GRCm39) |
H946N |
possibly damaging |
Het |
Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Het |
Rad51b |
A |
G |
12: 79,349,317 (GRCm39) |
E51G |
possibly damaging |
Het |
Rin2 |
T |
C |
2: 145,700,366 (GRCm39) |
V181A |
probably damaging |
Het |
Rnf157 |
T |
A |
11: 116,245,188 (GRCm39) |
|
probably null |
Het |
Rnf207 |
A |
G |
4: 152,398,328 (GRCm39) |
|
probably benign |
Het |
Ror1 |
A |
T |
4: 100,299,183 (GRCm39) |
K852M |
probably damaging |
Het |
Sbp |
T |
A |
17: 24,164,043 (GRCm39) |
I102K |
probably benign |
Het |
Scaf8 |
T |
C |
17: 3,195,429 (GRCm39) |
I33T |
probably damaging |
Het |
Scn5a |
C |
T |
9: 119,315,699 (GRCm39) |
V1670I |
probably damaging |
Het |
Serhl |
C |
T |
15: 82,989,877 (GRCm39) |
T42M |
probably damaging |
Het |
Sin3a |
A |
G |
9: 57,011,281 (GRCm39) |
|
probably benign |
Het |
Slc12a2 |
A |
G |
18: 58,012,374 (GRCm39) |
S166G |
probably benign |
Het |
Slc15a4 |
G |
A |
5: 127,680,832 (GRCm39) |
H396Y |
probably benign |
Het |
Slc2a7 |
A |
T |
4: 150,239,143 (GRCm39) |
N123Y |
probably damaging |
Het |
Smpd3 |
G |
A |
8: 106,992,199 (GRCm39) |
T118M |
possibly damaging |
Het |
Spns2 |
A |
T |
11: 72,347,193 (GRCm39) |
I427N |
probably benign |
Het |
Ssmem1 |
T |
A |
6: 30,519,650 (GRCm39) |
S112T |
probably damaging |
Het |
Stard10 |
A |
T |
7: 100,993,233 (GRCm39) |
D190V |
probably damaging |
Het |
Stil |
A |
T |
4: 114,881,049 (GRCm39) |
K531M |
probably damaging |
Het |
Strc |
T |
C |
2: 121,203,219 (GRCm39) |
|
probably null |
Het |
Svil |
T |
A |
18: 5,046,817 (GRCm39) |
I21N |
possibly damaging |
Het |
Syt11 |
T |
C |
3: 88,656,110 (GRCm39) |
M14V |
probably benign |
Het |
Tasor2 |
A |
T |
13: 3,640,413 (GRCm39) |
H241Q |
possibly damaging |
Het |
Tg |
A |
T |
15: 66,577,081 (GRCm39) |
Q1468L |
probably benign |
Het |
Tjp1 |
A |
G |
7: 64,952,669 (GRCm39) |
V1555A |
probably benign |
Het |
Tmprss11d |
A |
C |
5: 86,486,658 (GRCm39) |
S77R |
probably damaging |
Het |
Tsnaxip1 |
A |
G |
8: 106,554,383 (GRCm39) |
|
probably benign |
Het |
Tyr |
C |
A |
7: 87,141,914 (GRCm39) |
L138F |
probably damaging |
Het |
Ubash3b |
A |
G |
9: 40,927,901 (GRCm39) |
V469A |
probably damaging |
Het |
Ugt8a |
T |
C |
3: 125,709,098 (GRCm39) |
Y4C |
probably benign |
Het |
Vmn1r201 |
A |
T |
13: 22,658,968 (GRCm39) |
T61S |
probably benign |
Het |
Vmn1r204 |
A |
G |
13: 22,740,465 (GRCm39) |
H32R |
probably benign |
Het |
Vmn1r228 |
T |
A |
17: 20,997,285 (GRCm39) |
I78L |
probably benign |
Het |
Wdr90 |
T |
C |
17: 26,068,284 (GRCm39) |
D1348G |
possibly damaging |
Het |
Zfp563 |
T |
A |
17: 33,324,187 (GRCm39) |
C261S |
probably benign |
Het |
Zfp809 |
T |
A |
9: 22,146,395 (GRCm39) |
L28Q |
probably damaging |
Het |
Znrf3 |
T |
A |
11: 5,239,066 (GRCm39) |
Q99L |
probably damaging |
Het |
|