Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
A |
G |
13: 77,471,493 (GRCm39) |
E966G |
probably benign |
Het |
9330159F19Rik |
T |
C |
10: 29,097,795 (GRCm39) |
V64A |
probably damaging |
Het |
Abcb5 |
G |
T |
12: 118,831,696 (GRCm39) |
Q1219K |
possibly damaging |
Het |
Acox2 |
A |
T |
14: 8,248,059 (GRCm38) |
C408S |
possibly damaging |
Het |
Acsf3 |
T |
A |
8: 123,506,922 (GRCm39) |
Y72N |
probably damaging |
Het |
Acss2 |
T |
A |
2: 155,400,550 (GRCm39) |
Y530N |
probably damaging |
Het |
Adam28 |
T |
C |
14: 68,886,870 (GRCm39) |
E48G |
possibly damaging |
Het |
Adgrv1 |
A |
C |
13: 81,652,232 (GRCm39) |
M2957R |
probably benign |
Het |
Adi1 |
C |
A |
12: 28,729,562 (GRCm39) |
D138E |
probably benign |
Het |
Alk |
A |
C |
17: 72,198,032 (GRCm39) |
L1228R |
probably damaging |
Het |
Alms1 |
T |
A |
6: 85,655,485 (GRCm39) |
S3344T |
possibly damaging |
Het |
Aox1 |
G |
A |
1: 58,348,150 (GRCm39) |
A623T |
probably benign |
Het |
Arhgef2 |
C |
T |
3: 88,546,766 (GRCm39) |
T545I |
probably damaging |
Het |
Atp8a2 |
T |
A |
14: 60,243,815 (GRCm39) |
N630I |
possibly damaging |
Het |
Bcl9 |
G |
T |
3: 97,113,186 (GRCm39) |
Q1090K |
probably damaging |
Het |
Bdp1 |
A |
G |
13: 100,171,653 (GRCm39) |
S2152P |
probably benign |
Het |
Birc6 |
T |
A |
17: 74,921,385 (GRCm39) |
S2155T |
probably benign |
Het |
Camk2b |
T |
C |
11: 5,922,384 (GRCm39) |
E488G |
probably damaging |
Het |
Capn9 |
T |
A |
8: 125,332,304 (GRCm39) |
|
probably null |
Het |
Cd209f |
A |
G |
8: 4,154,491 (GRCm39) |
S119P |
probably damaging |
Het |
Cep78 |
T |
C |
19: 15,946,533 (GRCm39) |
E433G |
probably damaging |
Het |
Chid1 |
G |
T |
7: 141,106,409 (GRCm39) |
|
probably null |
Het |
Cobll1 |
A |
T |
2: 64,956,580 (GRCm39) |
F289Y |
probably damaging |
Het |
Creb1 |
C |
T |
1: 64,590,109 (GRCm39) |
Q32* |
probably null |
Het |
Creb3l4 |
G |
T |
3: 90,146,210 (GRCm39) |
S182Y |
probably benign |
Het |
Dgcr2 |
A |
T |
16: 17,667,584 (GRCm39) |
C292S |
probably damaging |
Het |
Dnah8 |
T |
C |
17: 31,093,901 (GRCm39) |
V4665A |
possibly damaging |
Het |
Dnah9 |
A |
T |
11: 66,009,667 (GRCm39) |
M740K |
probably benign |
Het |
Dnmt1 |
G |
A |
9: 20,829,542 (GRCm39) |
T687I |
probably damaging |
Het |
Ece1 |
C |
T |
4: 137,685,312 (GRCm39) |
R601W |
probably damaging |
Het |
Echdc2 |
C |
A |
4: 108,022,732 (GRCm39) |
R3S |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,852,920 (GRCm39) |
L1275Q |
unknown |
Het |
Epha6 |
A |
T |
16: 60,026,108 (GRCm39) |
W445R |
probably damaging |
Het |
Ercc5 |
T |
A |
1: 44,220,035 (GRCm39) |
S1102R |
probably benign |
Het |
Fam228a |
T |
G |
12: 4,765,620 (GRCm39) |
T264P |
probably damaging |
Het |
Fzd6 |
T |
A |
15: 38,897,315 (GRCm39) |
I488N |
probably damaging |
Het |
Gabrg3 |
T |
G |
7: 56,379,389 (GRCm39) |
N338H |
probably damaging |
Het |
Gde1 |
A |
G |
7: 118,294,357 (GRCm39) |
F39L |
possibly damaging |
Het |
Gjb3 |
G |
A |
4: 127,220,224 (GRCm39) |
R103W |
probably damaging |
Het |
Gm4781 |
T |
A |
10: 100,232,582 (GRCm39) |
|
noncoding transcript |
Het |
Gm4846 |
T |
A |
1: 166,311,492 (GRCm39) |
T456S |
probably benign |
Het |
Gpx5 |
A |
G |
13: 21,471,624 (GRCm39) |
I193T |
probably benign |
Het |
H3c2 |
T |
A |
13: 23,936,715 (GRCm39) |
V118D |
probably damaging |
Het |
Herc2 |
A |
T |
7: 55,804,853 (GRCm39) |
K2294* |
probably null |
Het |
Iqgap3 |
T |
A |
3: 88,015,675 (GRCm39) |
V19D |
probably damaging |
Het |
Itga5 |
T |
C |
15: 103,254,441 (GRCm39) |
I1006V |
probably damaging |
Het |
Lamb1 |
C |
T |
12: 31,351,093 (GRCm39) |
T781I |
probably benign |
Het |
Lias |
A |
G |
5: 65,549,686 (GRCm39) |
T57A |
probably benign |
Het |
Lin37 |
C |
A |
7: 30,256,368 (GRCm39) |
R108L |
probably damaging |
Het |
Lrrd1 |
A |
T |
5: 3,915,709 (GRCm39) |
T769S |
probably benign |
Het |
Mamstr |
T |
C |
7: 45,294,387 (GRCm39) |
W414R |
probably damaging |
Het |
Mtmr11 |
T |
G |
3: 96,072,103 (GRCm39) |
S233R |
probably damaging |
Het |
Myh1 |
A |
T |
11: 67,095,648 (GRCm39) |
I266F |
probably damaging |
Het |
Myt1 |
C |
A |
2: 181,439,068 (GRCm39) |
Q197K |
probably benign |
Het |
Naip5 |
G |
T |
13: 100,356,195 (GRCm39) |
T1140K |
probably benign |
Het |
Ncf2 |
G |
A |
1: 152,683,822 (GRCm39) |
V14M |
probably damaging |
Het |
Ndufb11b |
T |
C |
15: 81,865,068 (GRCm39) |
V103A |
probably damaging |
Het |
Nhsl1 |
G |
T |
10: 18,400,653 (GRCm39) |
R626S |
possibly damaging |
Het |
Nol12 |
T |
A |
15: 78,822,089 (GRCm39) |
V108E |
probably damaging |
Het |
Nr1i2 |
G |
T |
16: 38,069,644 (GRCm39) |
P420Q |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,184,464 (GRCm39) |
I1286M |
possibly damaging |
Het |
Ocrl |
T |
A |
X: 47,050,993 (GRCm39) |
I74N |
probably damaging |
Het |
Or4c10b |
A |
C |
2: 89,711,629 (GRCm39) |
H153P |
probably damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,592 (GRCm39) |
S117P |
probably damaging |
Het |
Or5ak23 |
A |
G |
2: 85,244,749 (GRCm39) |
V158A |
probably benign |
Het |
Pard3b |
C |
T |
1: 62,676,763 (GRCm39) |
S999L |
probably benign |
Het |
Pax9 |
A |
G |
12: 56,746,839 (GRCm39) |
E225G |
probably benign |
Het |
Pdcd4 |
T |
G |
19: 53,914,650 (GRCm39) |
L335R |
probably damaging |
Het |
Pdgfra |
T |
A |
5: 75,343,675 (GRCm39) |
M732K |
possibly damaging |
Het |
Pkhd1 |
G |
T |
1: 20,187,293 (GRCm39) |
Q3672K |
probably benign |
Het |
Pold2 |
A |
G |
11: 5,823,454 (GRCm39) |
L325P |
possibly damaging |
Het |
Pom121l2 |
A |
T |
13: 22,167,954 (GRCm39) |
T742S |
probably benign |
Het |
Ppfia1 |
C |
T |
7: 144,073,368 (GRCm39) |
E208K |
probably benign |
Het |
Prex2 |
A |
T |
1: 11,207,004 (GRCm39) |
R521W |
probably damaging |
Het |
Prr23a4 |
C |
A |
9: 98,785,535 (GRCm39) |
R67S |
probably benign |
Het |
Rhpn2 |
T |
C |
7: 35,071,813 (GRCm39) |
L226P |
probably benign |
Het |
Rps12 |
C |
A |
10: 23,661,527 (GRCm39) |
D95Y |
probably damaging |
Het |
Sardh |
T |
A |
2: 27,105,194 (GRCm39) |
D643V |
possibly damaging |
Het |
Sars1 |
T |
C |
3: 108,343,260 (GRCm39) |
D77G |
probably benign |
Het |
Scin |
C |
A |
12: 40,174,697 (GRCm39) |
V129F |
probably damaging |
Het |
Semp2l1 |
T |
G |
1: 32,584,758 (GRCm39) |
D384A |
probably damaging |
Het |
Sftpa1 |
T |
A |
14: 40,854,803 (GRCm39) |
M66K |
possibly damaging |
Het |
Sgo1 |
T |
C |
17: 53,994,799 (GRCm39) |
K28E |
probably damaging |
Het |
Sim2 |
G |
T |
16: 93,924,436 (GRCm39) |
|
probably null |
Het |
Srp54b |
T |
A |
12: 55,296,945 (GRCm39) |
|
probably null |
Het |
Stard7 |
T |
C |
2: 127,137,480 (GRCm39) |
V310A |
probably benign |
Het |
Tasp1 |
T |
C |
2: 139,793,477 (GRCm39) |
D233G |
probably damaging |
Het |
Tdrd6 |
G |
T |
17: 43,936,480 (GRCm39) |
L1523M |
probably benign |
Het |
Tle3 |
A |
G |
9: 61,321,305 (GRCm39) |
D639G |
probably damaging |
Het |
Tmem128 |
A |
G |
5: 38,417,750 (GRCm39) |
D2G |
probably damaging |
Het |
Tmem163 |
A |
G |
1: 127,605,246 (GRCm39) |
S41P |
probably benign |
Het |
Ttn |
C |
T |
2: 76,559,505 (GRCm39) |
S29632N |
probably damaging |
Het |
Tuba4a |
A |
G |
1: 75,192,754 (GRCm39) |
S287P |
probably benign |
Het |
Ubn1 |
G |
C |
16: 4,895,255 (GRCm39) |
G767A |
probably benign |
Het |
Ugdh |
A |
T |
5: 65,577,634 (GRCm39) |
C288* |
probably null |
Het |
Upf2 |
T |
A |
2: 6,055,135 (GRCm39) |
|
probably null |
Het |
Vmn1r2 |
T |
C |
4: 3,172,836 (GRCm39) |
S252P |
probably damaging |
Het |
Vmn1r28 |
A |
C |
6: 58,242,237 (GRCm39) |
T27P |
probably damaging |
Het |
Vmn1r77 |
T |
C |
7: 11,775,338 (GRCm39) |
I38T |
probably benign |
Het |
Vmn2r51 |
C |
A |
7: 9,832,090 (GRCm39) |
E499* |
probably null |
Het |
Vmn2r51 |
G |
T |
7: 9,832,091 (GRCm39) |
Y498* |
probably null |
Het |
Vmn2r53 |
A |
T |
7: 12,334,812 (GRCm39) |
W283R |
probably damaging |
Het |
Vpreb1a |
T |
A |
16: 16,686,933 (GRCm39) |
T15S |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,910,378 (GRCm39) |
S3381P |
probably damaging |
Het |
Wnt2 |
A |
T |
6: 18,023,234 (GRCm39) |
D138E |
probably damaging |
Het |
Zdhhc22 |
A |
G |
12: 87,030,204 (GRCm39) |
V248A |
probably benign |
Het |
Zfp30 |
T |
A |
7: 29,492,805 (GRCm39) |
I434N |
probably damaging |
Het |
Zfp316 |
A |
G |
5: 143,239,178 (GRCm39) |
L947P |
probably damaging |
Het |
|