Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9530002B09Rik |
T |
A |
4: 122,583,115 (GRCm39) |
|
probably benign |
Het |
Abca2 |
A |
T |
2: 25,327,517 (GRCm39) |
I669F |
possibly damaging |
Het |
Acin1 |
T |
A |
14: 54,902,711 (GRCm39) |
Q360H |
probably damaging |
Het |
Aldh3b1 |
T |
A |
19: 3,971,755 (GRCm39) |
D72V |
probably benign |
Het |
Alox12e |
G |
A |
11: 70,206,828 (GRCm39) |
R620W |
probably damaging |
Het |
Alpl |
T |
C |
4: 137,476,856 (GRCm39) |
|
probably benign |
Het |
Amy2a1 |
T |
C |
3: 113,324,217 (GRCm39) |
I108V |
probably benign |
Het |
Ascc2 |
A |
T |
11: 4,631,496 (GRCm39) |
M646L |
probably benign |
Het |
Bod1l |
G |
A |
5: 41,974,429 (GRCm39) |
T2295M |
probably benign |
Het |
Ccdc9 |
A |
T |
7: 16,012,475 (GRCm39) |
|
probably null |
Het |
Clptm1l |
C |
T |
13: 73,755,842 (GRCm39) |
Q153* |
probably null |
Het |
Csmd1 |
A |
G |
8: 15,950,782 (GRCm39) |
S3476P |
probably benign |
Het |
Ddias |
A |
T |
7: 92,508,907 (GRCm39) |
M336K |
possibly damaging |
Het |
Ehd1 |
T |
C |
19: 6,348,108 (GRCm39) |
L362P |
probably benign |
Het |
Epha1 |
G |
T |
6: 42,342,987 (GRCm39) |
H187Q |
probably benign |
Het |
Espl1 |
T |
C |
15: 102,207,525 (GRCm39) |
S330P |
probably damaging |
Het |
Fbln7 |
G |
T |
2: 128,719,386 (GRCm39) |
R61L |
probably damaging |
Het |
Fbxo41 |
C |
T |
6: 85,455,453 (GRCm39) |
W577* |
probably null |
Het |
Fgb |
C |
A |
3: 82,956,996 (GRCm39) |
D25Y |
probably benign |
Het |
Gc |
T |
A |
5: 89,594,376 (GRCm39) |
K37N |
probably damaging |
Het |
Gfpt1 |
T |
C |
6: 87,034,736 (GRCm39) |
I178T |
probably benign |
Het |
Gm12695 |
T |
C |
4: 96,657,963 (GRCm39) |
T69A |
probably benign |
Het |
Gm3944 |
C |
A |
12: 18,903,895 (GRCm39) |
S8* |
probably null |
Het |
Gm9912 |
T |
C |
3: 148,890,795 (GRCm39) |
T113A |
unknown |
Het |
Gpr156 |
A |
G |
16: 37,799,113 (GRCm39) |
D109G |
probably benign |
Het |
Hoxd1 |
A |
T |
2: 74,593,710 (GRCm39) |
T89S |
probably benign |
Het |
Htt |
C |
T |
5: 34,983,326 (GRCm39) |
T975I |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,317,050 (GRCm39) |
M768I |
probably benign |
Het |
Krt4 |
C |
A |
15: 101,833,099 (GRCm39) |
A3S |
possibly damaging |
Het |
Mrto4 |
T |
C |
4: 139,076,334 (GRCm39) |
K86E |
probably benign |
Het |
Mup4 |
T |
A |
4: 59,960,622 (GRCm39) |
|
probably benign |
Het |
Myh1 |
G |
A |
11: 67,105,446 (GRCm39) |
D1079N |
possibly damaging |
Het |
Myo1a |
A |
G |
10: 127,541,347 (GRCm39) |
N43D |
probably benign |
Het |
Napa |
A |
T |
7: 15,849,203 (GRCm39) |
|
probably benign |
Het |
Ndufa12 |
A |
G |
10: 94,056,569 (GRCm39) |
D99G |
probably damaging |
Het |
Neb |
A |
G |
2: 52,174,275 (GRCm39) |
I1528T |
probably benign |
Het |
Nek1 |
T |
C |
8: 61,460,196 (GRCm39) |
S41P |
probably damaging |
Het |
Nolc1 |
C |
T |
19: 46,072,046 (GRCm39) |
T612M |
probably damaging |
Het |
Nsun5 |
T |
G |
5: 135,403,926 (GRCm39) |
Y301D |
probably damaging |
Het |
Oas1g |
T |
C |
5: 121,023,946 (GRCm39) |
E121G |
probably damaging |
Het |
Or1e1f |
A |
G |
11: 73,855,740 (GRCm39) |
Y102C |
probably damaging |
Het |
Or5d41 |
A |
G |
2: 88,054,818 (GRCm39) |
V186A |
possibly damaging |
Het |
Or6ae1 |
T |
A |
7: 139,742,822 (GRCm39) |
I14F |
possibly damaging |
Het |
Or8b46 |
T |
A |
9: 38,450,576 (GRCm39) |
N128K |
probably benign |
Het |
Or8k38 |
G |
T |
2: 86,488,781 (GRCm39) |
T7K |
probably damaging |
Het |
Osmr |
T |
C |
15: 6,844,896 (GRCm39) |
N957D |
probably benign |
Het |
Parn |
G |
A |
16: 13,420,933 (GRCm39) |
S473L |
probably damaging |
Het |
Phc2 |
T |
C |
4: 128,640,929 (GRCm39) |
F672S |
probably damaging |
Het |
Pik3c2b |
T |
C |
1: 133,027,349 (GRCm39) |
S1283P |
probably damaging |
Het |
Pole2 |
G |
A |
12: 69,274,926 (GRCm39) |
R5W |
probably benign |
Het |
Prl7a2 |
T |
A |
13: 27,844,870 (GRCm39) |
Y172F |
probably damaging |
Het |
Ptprz1 |
A |
G |
6: 23,050,388 (GRCm39) |
|
probably benign |
Het |
Rapgef3 |
C |
A |
15: 97,664,842 (GRCm39) |
G7V |
probably damaging |
Het |
Ripor1 |
T |
A |
8: 106,344,340 (GRCm39) |
S491R |
probably benign |
Het |
Rnf141 |
A |
G |
7: 110,420,572 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
C |
T |
2: 112,777,302 (GRCm39) |
R285Q |
probably damaging |
Het |
Sall4 |
T |
C |
2: 168,598,465 (GRCm39) |
N125S |
probably benign |
Het |
Schip1 |
A |
G |
3: 68,525,119 (GRCm39) |
K360R |
probably damaging |
Het |
Senp6 |
T |
A |
9: 79,997,151 (GRCm39) |
V55E |
probably benign |
Het |
Skint1 |
T |
A |
4: 111,882,730 (GRCm39) |
V258D |
probably benign |
Het |
Slc25a16 |
T |
A |
10: 62,768,530 (GRCm39) |
H130Q |
probably benign |
Het |
Styx |
T |
C |
14: 45,611,020 (GRCm39) |
V217A |
probably benign |
Het |
Syne2 |
G |
A |
12: 75,935,116 (GRCm39) |
|
probably null |
Het |
Tagap1 |
A |
G |
17: 7,224,259 (GRCm39) |
S146P |
probably benign |
Het |
Tatdn2 |
A |
G |
6: 113,681,103 (GRCm39) |
K379E |
probably benign |
Het |
Thrap3 |
T |
C |
4: 126,069,189 (GRCm39) |
Y654C |
possibly damaging |
Het |
Tle2 |
T |
C |
10: 81,416,385 (GRCm39) |
L135P |
probably damaging |
Het |
Tmc1 |
A |
G |
19: 20,801,673 (GRCm39) |
F451S |
possibly damaging |
Het |
Trpm7 |
G |
A |
2: 126,639,647 (GRCm39) |
P1650S |
probably damaging |
Het |
Ttll4 |
G |
A |
1: 74,719,541 (GRCm39) |
R16H |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,544,717 (GRCm39) |
N32795S |
probably damaging |
Het |
Tubgcp6 |
T |
C |
15: 88,988,692 (GRCm39) |
E803G |
probably benign |
Het |
Ubr2 |
A |
G |
17: 47,274,071 (GRCm39) |
|
probably null |
Het |
Ugt2b35 |
A |
G |
5: 87,149,412 (GRCm39) |
D221G |
probably damaging |
Het |
Unc45b |
G |
A |
11: 82,802,515 (GRCm39) |
A4T |
probably benign |
Het |
Vmn1r70 |
A |
T |
7: 10,368,264 (GRCm39) |
I251F |
possibly damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,553 (GRCm39) |
H412L |
possibly damaging |
Het |
Zfp59 |
A |
G |
7: 27,552,935 (GRCm39) |
N129S |
probably benign |
Het |
Zgrf1 |
T |
C |
3: 127,406,999 (GRCm39) |
C1589R |
probably damaging |
Het |
|
Other mutations in Or2ab1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02121:Or2ab1
|
APN |
11 |
58,488,408 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02261:Or2ab1
|
APN |
11 |
58,488,630 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02725:Or2ab1
|
APN |
11 |
58,488,690 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03290:Or2ab1
|
APN |
11 |
58,489,149 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03308:Or2ab1
|
APN |
11 |
58,488,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R0531:Or2ab1
|
UTSW |
11 |
58,488,674 (GRCm39) |
missense |
probably benign |
0.01 |
R1463:Or2ab1
|
UTSW |
11 |
58,488,947 (GRCm39) |
missense |
probably damaging |
0.98 |
R1813:Or2ab1
|
UTSW |
11 |
58,489,133 (GRCm39) |
missense |
probably damaging |
1.00 |
R2062:Or2ab1
|
UTSW |
11 |
58,488,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R2063:Or2ab1
|
UTSW |
11 |
58,488,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R2065:Or2ab1
|
UTSW |
11 |
58,488,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R2068:Or2ab1
|
UTSW |
11 |
58,488,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Or2ab1
|
UTSW |
11 |
58,488,830 (GRCm39) |
missense |
probably benign |
0.03 |
R6237:Or2ab1
|
UTSW |
11 |
58,488,831 (GRCm39) |
missense |
probably damaging |
0.97 |
R6397:Or2ab1
|
UTSW |
11 |
58,488,338 (GRCm39) |
missense |
probably benign |
0.00 |
R7056:Or2ab1
|
UTSW |
11 |
58,489,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R8048:Or2ab1
|
UTSW |
11 |
58,488,233 (GRCm39) |
missense |
unknown |
|
R8765:Or2ab1
|
UTSW |
11 |
58,488,785 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9044:Or2ab1
|
UTSW |
11 |
58,489,126 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9708:Or2ab1
|
UTSW |
11 |
58,488,927 (GRCm39) |
missense |
probably benign |
0.00 |
Z1186:Or2ab1
|
UTSW |
11 |
58,488,491 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1186:Or2ab1
|
UTSW |
11 |
58,488,776 (GRCm39) |
missense |
probably benign |
|
Z1186:Or2ab1
|
UTSW |
11 |
58,488,344 (GRCm39) |
missense |
probably benign |
0.02 |
Z1186:Or2ab1
|
UTSW |
11 |
58,488,356 (GRCm39) |
missense |
probably benign |
|
Z1187:Or2ab1
|
UTSW |
11 |
58,488,776 (GRCm39) |
missense |
probably benign |
|
Z1187:Or2ab1
|
UTSW |
11 |
58,488,344 (GRCm39) |
missense |
probably benign |
0.02 |
Z1187:Or2ab1
|
UTSW |
11 |
58,488,356 (GRCm39) |
missense |
probably benign |
|
Z1187:Or2ab1
|
UTSW |
11 |
58,488,491 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1188:Or2ab1
|
UTSW |
11 |
58,488,491 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1188:Or2ab1
|
UTSW |
11 |
58,488,356 (GRCm39) |
missense |
probably benign |
|
Z1188:Or2ab1
|
UTSW |
11 |
58,488,344 (GRCm39) |
missense |
probably benign |
0.02 |
Z1188:Or2ab1
|
UTSW |
11 |
58,488,776 (GRCm39) |
missense |
probably benign |
|
Z1189:Or2ab1
|
UTSW |
11 |
58,488,356 (GRCm39) |
missense |
probably benign |
|
Z1189:Or2ab1
|
UTSW |
11 |
58,488,344 (GRCm39) |
missense |
probably benign |
0.02 |
Z1189:Or2ab1
|
UTSW |
11 |
58,488,776 (GRCm39) |
missense |
probably benign |
|
Z1189:Or2ab1
|
UTSW |
11 |
58,488,491 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1190:Or2ab1
|
UTSW |
11 |
58,488,491 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1190:Or2ab1
|
UTSW |
11 |
58,488,356 (GRCm39) |
missense |
probably benign |
|
Z1190:Or2ab1
|
UTSW |
11 |
58,488,344 (GRCm39) |
missense |
probably benign |
0.02 |
Z1190:Or2ab1
|
UTSW |
11 |
58,488,776 (GRCm39) |
missense |
probably benign |
|
Z1191:Or2ab1
|
UTSW |
11 |
58,488,491 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1191:Or2ab1
|
UTSW |
11 |
58,488,356 (GRCm39) |
missense |
probably benign |
|
Z1191:Or2ab1
|
UTSW |
11 |
58,488,344 (GRCm39) |
missense |
probably benign |
0.02 |
Z1191:Or2ab1
|
UTSW |
11 |
58,488,776 (GRCm39) |
missense |
probably benign |
|
Z1192:Or2ab1
|
UTSW |
11 |
58,488,491 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1192:Or2ab1
|
UTSW |
11 |
58,488,356 (GRCm39) |
missense |
probably benign |
|
Z1192:Or2ab1
|
UTSW |
11 |
58,488,344 (GRCm39) |
missense |
probably benign |
0.02 |
Z1192:Or2ab1
|
UTSW |
11 |
58,488,776 (GRCm39) |
missense |
probably benign |
|
|