Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
T |
C |
6: 142,578,862 (GRCm39) |
R901G |
possibly damaging |
Het |
Abhd18 |
T |
A |
3: 40,885,401 (GRCm39) |
M262K |
probably benign |
Het |
Ano2 |
C |
A |
6: 125,689,309 (GRCm39) |
L145I |
probably benign |
Het |
Ckap5 |
T |
C |
2: 91,408,426 (GRCm39) |
W874R |
probably damaging |
Het |
Cox4i1 |
G |
T |
8: 121,396,102 (GRCm39) |
|
probably benign |
Het |
Cwc27 |
A |
T |
13: 104,943,259 (GRCm39) |
N94K |
probably damaging |
Het |
Dcaf11 |
T |
C |
14: 55,804,342 (GRCm39) |
S372P |
probably damaging |
Het |
Dpysl4 |
A |
G |
7: 138,676,681 (GRCm39) |
N356S |
probably damaging |
Het |
Dusp8 |
A |
G |
7: 141,635,701 (GRCm39) |
|
probably benign |
Het |
Erc2 |
G |
A |
14: 27,993,662 (GRCm39) |
V894M |
probably benign |
Het |
Fbxo28 |
T |
A |
1: 182,144,719 (GRCm39) |
I282F |
probably benign |
Het |
Fsd2 |
T |
C |
7: 81,195,608 (GRCm39) |
T434A |
probably damaging |
Het |
Gabra4 |
T |
C |
5: 71,729,421 (GRCm39) |
H453R |
probably benign |
Het |
Glrx |
T |
A |
13: 75,988,065 (GRCm39) |
|
probably null |
Het |
Gm11541 |
A |
T |
11: 94,586,441 (GRCm39) |
L102* |
probably null |
Het |
Gm5113 |
T |
A |
7: 29,878,150 (GRCm39) |
Y79* |
probably null |
Het |
Gpr87 |
T |
A |
3: 59,086,587 (GRCm39) |
N306I |
probably damaging |
Het |
Hydin |
T |
A |
8: 111,336,561 (GRCm39) |
Y5113N |
possibly damaging |
Het |
Iqsec3 |
C |
T |
6: 121,390,430 (GRCm39) |
|
probably benign |
Het |
Kbtbd8 |
C |
A |
6: 95,103,570 (GRCm39) |
Y406* |
probably null |
Het |
Lamb1 |
G |
T |
12: 31,348,882 (GRCm39) |
R590L |
probably benign |
Het |
Lin54 |
A |
T |
5: 100,628,109 (GRCm39) |
N31K |
probably damaging |
Het |
Lnpk |
T |
C |
2: 74,367,845 (GRCm39) |
E165G |
probably damaging |
Het |
Lrp4 |
C |
T |
2: 91,305,557 (GRCm39) |
R276C |
probably damaging |
Het |
Lrrc7 |
T |
A |
3: 157,841,028 (GRCm39) |
T1384S |
probably benign |
Het |
Mia2 |
T |
C |
12: 59,217,780 (GRCm39) |
|
probably null |
Het |
Morc2a |
T |
C |
11: 3,635,400 (GRCm39) |
V797A |
probably damaging |
Het |
Mrps23 |
T |
C |
11: 88,096,193 (GRCm39) |
|
probably benign |
Het |
Muc17 |
A |
T |
5: 137,175,484 (GRCm39) |
I62K |
probably damaging |
Het |
Nlrp4g |
T |
A |
9: 124,349,630 (GRCm38) |
|
noncoding transcript |
Het |
Nptx1 |
A |
T |
11: 119,435,669 (GRCm39) |
|
probably benign |
Het |
Pabpc1l |
T |
G |
2: 163,886,302 (GRCm39) |
|
probably null |
Het |
Pdcd6ip |
A |
T |
9: 113,503,575 (GRCm39) |
|
probably null |
Het |
Plcg1 |
A |
G |
2: 160,603,383 (GRCm39) |
T1185A |
possibly damaging |
Het |
Plcxd1 |
A |
G |
5: 110,250,349 (GRCm39) |
Q230R |
probably benign |
Het |
Psme4 |
T |
A |
11: 30,824,282 (GRCm39) |
|
probably null |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ptch1 |
T |
A |
13: 63,690,038 (GRCm39) |
N320Y |
probably damaging |
Het |
Qars1 |
G |
A |
9: 108,385,642 (GRCm39) |
V60I |
possibly damaging |
Het |
Rbp3 |
C |
T |
14: 33,677,975 (GRCm39) |
T641M |
probably damaging |
Het |
Rhag |
T |
C |
17: 41,147,367 (GRCm39) |
S410P |
probably damaging |
Het |
Rnf213 |
A |
G |
11: 119,300,970 (GRCm39) |
K297E |
probably benign |
Het |
Rps6ka4 |
T |
C |
19: 6,814,720 (GRCm39) |
E294G |
probably benign |
Het |
Scaf4 |
T |
A |
16: 90,041,244 (GRCm39) |
I695F |
unknown |
Het |
Scrn2 |
T |
C |
11: 96,923,122 (GRCm39) |
|
probably benign |
Het |
Scx |
T |
A |
15: 76,342,363 (GRCm39) |
C188S |
probably damaging |
Het |
Sdk1 |
G |
T |
5: 142,197,805 (GRCm39) |
V1893L |
possibly damaging |
Het |
Sema5a |
C |
A |
15: 32,673,546 (GRCm39) |
Q795K |
probably damaging |
Het |
Slc24a3 |
A |
G |
2: 145,455,487 (GRCm39) |
S459G |
probably benign |
Het |
Smurf1 |
A |
G |
5: 144,820,372 (GRCm39) |
|
probably benign |
Het |
Taar4 |
T |
C |
10: 23,837,328 (GRCm39) |
Y313H |
probably damaging |
Het |
Tmprss11c |
A |
G |
5: 86,419,322 (GRCm39) |
F79S |
probably damaging |
Het |
Tnfaip8l2 |
T |
A |
3: 95,047,672 (GRCm39) |
I64F |
possibly damaging |
Het |
Trbv13-1 |
A |
G |
6: 41,093,372 (GRCm39) |
T102A |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,976,222 (GRCm39) |
N160K |
probably damaging |
Het |
Ttc22 |
A |
G |
4: 106,496,435 (GRCm39) |
Y495C |
probably benign |
Het |
Usp50 |
A |
G |
2: 126,619,949 (GRCm39) |
I121T |
probably damaging |
Het |
Vmn2r117 |
A |
G |
17: 23,678,885 (GRCm39) |
S780P |
probably damaging |
Het |
Vmn2r66 |
A |
T |
7: 84,644,607 (GRCm39) |
V601D |
probably damaging |
Het |
Wapl |
G |
A |
14: 34,413,734 (GRCm39) |
A199T |
probably benign |
Het |
Zfp658 |
A |
G |
7: 43,222,969 (GRCm39) |
T415A |
possibly damaging |
Het |
Zfp760 |
C |
T |
17: 21,939,935 (GRCm39) |
T9I |
probably damaging |
Het |
Zfp998 |
A |
G |
13: 66,581,495 (GRCm39) |
S59P |
probably damaging |
Het |
|
Other mutations in Or1j20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00899:Or1j20
|
APN |
2 |
36,760,222 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01538:Or1j20
|
APN |
2 |
36,760,532 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01716:Or1j20
|
APN |
2 |
36,759,679 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01735:Or1j20
|
APN |
2 |
36,759,698 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01998:Or1j20
|
APN |
2 |
36,759,658 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02820:Or1j20
|
APN |
2 |
36,759,871 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03267:Or1j20
|
APN |
2 |
36,760,513 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03306:Or1j20
|
APN |
2 |
36,760,537 (GRCm39) |
utr 3 prime |
probably benign |
|
R0013:Or1j20
|
UTSW |
2 |
36,760,172 (GRCm39) |
missense |
probably damaging |
1.00 |
R0081:Or1j20
|
UTSW |
2 |
36,760,022 (GRCm39) |
missense |
possibly damaging |
0.58 |
R0421:Or1j20
|
UTSW |
2 |
36,759,653 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1613:Or1j20
|
UTSW |
2 |
36,760,405 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1842:Or1j20
|
UTSW |
2 |
36,759,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4463:Or1j20
|
UTSW |
2 |
36,760,205 (GRCm39) |
missense |
probably benign |
0.31 |
R4993:Or1j20
|
UTSW |
2 |
36,760,000 (GRCm39) |
missense |
probably benign |
0.30 |
R5553:Or1j20
|
UTSW |
2 |
36,760,477 (GRCm39) |
missense |
probably benign |
0.00 |
R5666:Or1j20
|
UTSW |
2 |
36,760,401 (GRCm39) |
missense |
probably benign |
0.11 |
R5934:Or1j20
|
UTSW |
2 |
36,760,280 (GRCm39) |
missense |
probably benign |
0.34 |
R6290:Or1j20
|
UTSW |
2 |
36,760,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R6312:Or1j20
|
UTSW |
2 |
36,760,477 (GRCm39) |
missense |
probably benign |
0.02 |
R7358:Or1j20
|
UTSW |
2 |
36,759,890 (GRCm39) |
missense |
probably benign |
|
R8383:Or1j20
|
UTSW |
2 |
36,760,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Or1j20
|
UTSW |
2 |
36,760,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R8967:Or1j20
|
UTSW |
2 |
36,760,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R9311:Or1j20
|
UTSW |
2 |
36,760,405 (GRCm39) |
missense |
probably damaging |
1.00 |
X0022:Or1j20
|
UTSW |
2 |
36,760,289 (GRCm39) |
missense |
probably damaging |
1.00 |
|