Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aak1 |
T |
A |
6: 86,902,059 (GRCm39) |
M76K |
probably null |
Het |
Abcc4 |
A |
G |
14: 118,766,414 (GRCm39) |
I886T |
probably benign |
Het |
Adam6a |
T |
C |
12: 113,507,992 (GRCm39) |
Y122H |
possibly damaging |
Het |
Adgre1 |
A |
G |
17: 57,787,947 (GRCm39) |
T905A |
probably benign |
Het |
Arap2 |
A |
G |
5: 62,827,312 (GRCm39) |
F969L |
possibly damaging |
Het |
Arhgef4 |
G |
T |
1: 34,845,113 (GRCm39) |
G1439V |
possibly damaging |
Het |
Atm |
A |
G |
9: 53,375,529 (GRCm39) |
W2097R |
probably benign |
Het |
Atmin |
A |
G |
8: 117,684,698 (GRCm39) |
D786G |
probably damaging |
Het |
AU016765 |
T |
A |
17: 64,826,916 (GRCm39) |
|
noncoding transcript |
Het |
Capn1 |
A |
T |
19: 6,061,045 (GRCm39) |
N253K |
probably benign |
Het |
Cdc42bpa |
A |
G |
1: 179,972,130 (GRCm39) |
T527A |
probably damaging |
Het |
Chmp7 |
A |
T |
14: 69,958,404 (GRCm39) |
V255D |
probably damaging |
Het |
Cldn12 |
A |
G |
5: 5,558,385 (GRCm39) |
F14S |
probably damaging |
Het |
Cpsf2 |
T |
C |
12: 101,949,466 (GRCm39) |
S61P |
probably damaging |
Het |
Cpvl |
C |
T |
6: 53,908,918 (GRCm39) |
E282K |
probably benign |
Het |
Crygn |
T |
A |
5: 24,956,019 (GRCm39) |
|
probably benign |
Het |
Csde1 |
C |
T |
3: 102,954,388 (GRCm39) |
T386M |
probably damaging |
Het |
Cux1 |
G |
A |
5: 136,315,653 (GRCm39) |
T1129I |
probably damaging |
Het |
Dcaf10 |
G |
A |
4: 45,372,769 (GRCm39) |
R394Q |
possibly damaging |
Het |
Dhx16 |
T |
C |
17: 36,190,835 (GRCm39) |
V11A |
probably damaging |
Het |
Dnah10 |
T |
C |
5: 124,905,536 (GRCm39) |
M4060T |
possibly damaging |
Het |
Duox1 |
C |
T |
2: 122,149,956 (GRCm39) |
P116S |
probably benign |
Het |
Eif5b |
A |
G |
1: 38,084,793 (GRCm39) |
E880G |
probably damaging |
Het |
Eml6 |
A |
T |
11: 29,769,007 (GRCm39) |
Y67* |
probably null |
Het |
Faim2 |
C |
A |
15: 99,422,581 (GRCm39) |
|
probably null |
Het |
Faim2 |
T |
G |
15: 99,422,582 (GRCm39) |
S72R |
probably benign |
Het |
Fanca |
T |
C |
8: 123,995,711 (GRCm39) |
T1364A |
probably damaging |
Het |
Fhip1a |
A |
T |
3: 85,637,988 (GRCm39) |
W104R |
probably damaging |
Het |
Gak |
A |
G |
5: 108,730,826 (GRCm39) |
I860T |
probably benign |
Het |
Garem2 |
C |
A |
5: 30,319,665 (GRCm39) |
R376S |
probably damaging |
Het |
Gdf2 |
A |
G |
14: 33,667,408 (GRCm39) |
T377A |
probably damaging |
Het |
Gm2431 |
A |
T |
7: 141,811,440 (GRCm39) |
C155S |
unknown |
Het |
Gm5814 |
A |
G |
17: 47,721,288 (GRCm39) |
M1V |
probably null |
Het |
Gm5901 |
C |
G |
7: 105,026,438 (GRCm39) |
Q69E |
possibly damaging |
Het |
Gm9945 |
A |
G |
11: 53,371,202 (GRCm39) |
|
probably benign |
Het |
Gmps |
T |
C |
3: 63,908,956 (GRCm39) |
V486A |
probably benign |
Het |
Gtf2ird1 |
T |
A |
5: 134,412,756 (GRCm39) |
E55V |
probably damaging |
Het |
Hoxa11 |
T |
A |
6: 52,220,483 (GRCm39) |
N267Y |
probably damaging |
Het |
Ifngr2 |
C |
A |
16: 91,356,926 (GRCm39) |
H153Q |
possibly damaging |
Het |
Ift172 |
G |
T |
5: 31,442,598 (GRCm39) |
Q190K |
possibly damaging |
Het |
Iqch |
A |
G |
9: 63,352,853 (GRCm39) |
V899A |
probably damaging |
Het |
Lactb2 |
T |
C |
1: 13,717,624 (GRCm39) |
E133G |
probably damaging |
Het |
Lig3 |
G |
A |
11: 82,691,076 (GRCm39) |
V110M |
probably damaging |
Het |
Lin54 |
C |
A |
5: 100,600,943 (GRCm39) |
Q262H |
possibly damaging |
Het |
Lingo3 |
G |
A |
10: 80,671,372 (GRCm39) |
T186I |
probably damaging |
Het |
Lrrc7 |
GAAGTTGTTTGGAGATTCTTATCTTA |
GA |
3: 158,024,045 (GRCm39) |
|
probably benign |
Het |
Ly86 |
T |
A |
13: 37,559,010 (GRCm39) |
F70I |
probably damaging |
Het |
Mospd2 |
A |
T |
X: 163,730,329 (GRCm39) |
S301T |
probably benign |
Het |
Mroh2a |
A |
C |
1: 88,169,340 (GRCm39) |
I672L |
probably benign |
Het |
Myo15a |
A |
T |
11: 60,395,705 (GRCm39) |
|
probably null |
Het |
Nme8 |
C |
G |
13: 19,858,605 (GRCm39) |
A78P |
probably damaging |
Het |
Obscn |
C |
T |
11: 59,015,578 (GRCm39) |
V965M |
probably damaging |
Het |
Parn |
T |
C |
16: 13,358,967 (GRCm39) |
K592E |
probably benign |
Het |
Pax6 |
C |
A |
2: 105,514,343 (GRCm39) |
|
probably benign |
Het |
Pdcd6 |
A |
T |
13: 74,465,325 (GRCm39) |
M1K |
probably null |
Het |
Pex11b |
T |
C |
3: 96,551,151 (GRCm39) |
L198P |
possibly damaging |
Het |
Phldb3 |
C |
T |
7: 24,310,852 (GRCm39) |
A28V |
probably benign |
Het |
Pkn3 |
C |
A |
2: 29,975,469 (GRCm39) |
|
probably benign |
Het |
Pknox1 |
T |
C |
17: 31,814,300 (GRCm39) |
|
probably null |
Het |
Ptprg |
A |
C |
14: 12,215,288 (GRCm38) |
I1092L |
possibly damaging |
Het |
Pxylp1 |
A |
C |
9: 96,707,338 (GRCm39) |
I281M |
probably damaging |
Het |
Ramac |
C |
T |
7: 81,418,178 (GRCm39) |
R78W |
probably damaging |
Het |
Retreg2 |
G |
T |
1: 75,121,310 (GRCm39) |
L195F |
probably damaging |
Het |
Rgs20 |
G |
C |
1: 5,091,231 (GRCm39) |
F66L |
probably benign |
Het |
Ripk4 |
C |
T |
16: 97,556,273 (GRCm39) |
V157I |
probably damaging |
Het |
Ryr2 |
T |
C |
13: 11,765,571 (GRCm39) |
|
probably null |
Het |
Scaper |
A |
T |
9: 55,819,339 (GRCm39) |
S125R |
probably damaging |
Het |
Sec16a |
C |
T |
2: 26,302,970 (GRCm39) |
|
probably benign |
Het |
Slc35f6 |
T |
C |
5: 30,812,957 (GRCm39) |
L37P |
probably damaging |
Het |
Slc6a12 |
T |
A |
6: 121,335,972 (GRCm39) |
|
probably benign |
Het |
Slc9a5 |
A |
G |
8: 106,094,760 (GRCm39) |
K784E |
probably damaging |
Het |
Snd1 |
T |
C |
6: 28,707,053 (GRCm39) |
V455A |
probably damaging |
Het |
Ssbp2 |
A |
T |
13: 91,687,454 (GRCm39) |
I46L |
possibly damaging |
Het |
Stil |
A |
G |
4: 114,898,841 (GRCm39) |
D1157G |
probably benign |
Het |
Tax1bp1 |
T |
A |
6: 52,714,116 (GRCm39) |
C271S |
probably benign |
Het |
Tdpoz6 |
G |
A |
3: 93,599,776 (GRCm39) |
H198Y |
probably damaging |
Het |
Tdrd6 |
T |
A |
17: 43,935,007 (GRCm39) |
M2014L |
probably benign |
Het |
Thsd7a |
T |
A |
6: 12,504,012 (GRCm39) |
I381F |
possibly damaging |
Het |
Thsd7a |
T |
A |
6: 12,337,313 (GRCm39) |
T1235S |
possibly damaging |
Het |
Tmprss11d |
T |
C |
5: 86,457,260 (GRCm39) |
D133G |
probably damaging |
Het |
Tpr |
C |
T |
1: 150,320,150 (GRCm39) |
R2233W |
probably damaging |
Het |
Ugt1a1 |
CAGAGAGAGAGAGA |
CAGAGAGAGAGA |
1: 88,139,706 (GRCm39) |
|
probably benign |
Het |
Vgll1 |
A |
G |
X: 56,137,792 (GRCm39) |
R54G |
possibly damaging |
Het |
Wdr72 |
A |
G |
9: 74,117,306 (GRCm39) |
T673A |
probably benign |
Het |
Zfp169 |
C |
T |
13: 48,644,339 (GRCm39) |
|
probably benign |
Het |
Zfp319 |
G |
A |
8: 96,052,201 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or10ag57 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01783:Or10ag57
|
APN |
2 |
87,218,182 (GRCm39) |
missense |
probably benign |
0.39 |
IGL01783:Or10ag57
|
APN |
2 |
87,218,187 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02396:Or10ag57
|
APN |
2 |
87,218,049 (GRCm39) |
utr 5 prime |
probably benign |
|
IGL03338:Or10ag57
|
APN |
2 |
87,218,470 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03373:Or10ag57
|
APN |
2 |
87,218,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:Or10ag57
|
UTSW |
2 |
87,218,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1245:Or10ag57
|
UTSW |
2 |
87,218,553 (GRCm39) |
missense |
probably benign |
0.00 |
R1376:Or10ag57
|
UTSW |
2 |
87,218,162 (GRCm39) |
missense |
probably benign |
0.00 |
R1376:Or10ag57
|
UTSW |
2 |
87,218,162 (GRCm39) |
missense |
probably benign |
0.00 |
R1471:Or10ag57
|
UTSW |
2 |
87,218,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R1681:Or10ag57
|
UTSW |
2 |
87,218,964 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1995:Or10ag57
|
UTSW |
2 |
87,218,175 (GRCm39) |
missense |
probably damaging |
0.97 |
R2246:Or10ag57
|
UTSW |
2 |
87,218,195 (GRCm39) |
missense |
probably benign |
0.00 |
R2341:Or10ag57
|
UTSW |
2 |
87,218,084 (GRCm39) |
missense |
probably benign |
|
R4008:Or10ag57
|
UTSW |
2 |
87,218,924 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4009:Or10ag57
|
UTSW |
2 |
87,218,924 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4011:Or10ag57
|
UTSW |
2 |
87,218,924 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4119:Or10ag57
|
UTSW |
2 |
87,218,187 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4547:Or10ag57
|
UTSW |
2 |
87,218,504 (GRCm39) |
missense |
probably benign |
0.07 |
R4666:Or10ag57
|
UTSW |
2 |
87,218,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R4801:Or10ag57
|
UTSW |
2 |
87,218,553 (GRCm39) |
missense |
probably benign |
0.00 |
R4802:Or10ag57
|
UTSW |
2 |
87,218,553 (GRCm39) |
missense |
probably benign |
0.00 |
R5049:Or10ag57
|
UTSW |
2 |
87,219,002 (GRCm39) |
missense |
probably benign |
0.00 |
R5070:Or10ag57
|
UTSW |
2 |
87,218,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R7594:Or10ag57
|
UTSW |
2 |
87,218,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R7684:Or10ag57
|
UTSW |
2 |
87,218,372 (GRCm39) |
missense |
probably damaging |
0.99 |
R8064:Or10ag57
|
UTSW |
2 |
87,218,853 (GRCm39) |
missense |
probably benign |
0.00 |
R8218:Or10ag57
|
UTSW |
2 |
87,218,922 (GRCm39) |
missense |
probably damaging |
0.99 |
R8282:Or10ag57
|
UTSW |
2 |
87,218,852 (GRCm39) |
missense |
probably benign |
0.01 |
R8335:Or10ag57
|
UTSW |
2 |
87,218,204 (GRCm39) |
missense |
probably benign |
0.02 |
R9800:Or10ag57
|
UTSW |
2 |
87,218,508 (GRCm39) |
missense |
probably damaging |
1.00 |
|