Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abraxas2 |
G |
A |
7: 132,476,694 (GRCm39) |
A145T |
probably damaging |
Het |
Adamts20 |
T |
C |
15: 94,236,596 (GRCm39) |
D808G |
probably benign |
Het |
Ankdd1a |
C |
T |
9: 65,415,343 (GRCm39) |
A227T |
possibly damaging |
Het |
Arsk |
T |
A |
13: 76,239,935 (GRCm39) |
Q46L |
unknown |
Het |
Asnsd1 |
A |
G |
1: 53,387,187 (GRCm39) |
F147L |
probably benign |
Het |
Atp5f1a |
T |
A |
18: 77,869,056 (GRCm39) |
S427T |
probably benign |
Het |
Atp6v1b2 |
A |
C |
8: 69,562,530 (GRCm39) |
|
probably null |
Het |
AU021092 |
T |
A |
16: 5,030,050 (GRCm39) |
T322S |
possibly damaging |
Het |
Bcl7c |
A |
T |
7: 127,307,698 (GRCm39) |
M1K |
probably null |
Het |
Cacna1i |
T |
C |
15: 80,273,333 (GRCm39) |
V1673A |
probably damaging |
Het |
Ccdc146 |
A |
T |
5: 21,522,900 (GRCm39) |
|
probably null |
Het |
Cdc7 |
A |
G |
5: 107,120,660 (GRCm39) |
D122G |
probably damaging |
Het |
Cfap46 |
CCTTCTTCT |
CCTTCT |
7: 139,218,816 (GRCm39) |
|
probably benign |
Het |
Chd3 |
T |
A |
11: 69,236,361 (GRCm39) |
Q1950L |
probably damaging |
Het |
Cutc |
T |
C |
19: 43,748,436 (GRCm39) |
L111S |
probably damaging |
Het |
Cyp2j6 |
A |
G |
4: 96,406,398 (GRCm39) |
F458L |
probably damaging |
Het |
Ddhd1 |
T |
C |
14: 45,856,971 (GRCm39) |
|
probably null |
Het |
Dstyk |
T |
C |
1: 132,387,677 (GRCm39) |
S804P |
probably damaging |
Het |
Ech1 |
A |
G |
7: 28,531,261 (GRCm39) |
D283G |
possibly damaging |
Het |
Exosc10 |
A |
G |
4: 148,666,768 (GRCm39) |
|
probably null |
Het |
Fancg |
A |
C |
4: 43,010,084 (GRCm39) |
V5G |
probably benign |
Het |
Fbxo11 |
A |
G |
17: 88,316,332 (GRCm39) |
V394A |
probably benign |
Het |
Fcmr |
C |
T |
1: 130,806,060 (GRCm39) |
R339W |
probably damaging |
Het |
Fhip2b |
T |
C |
14: 70,829,198 (GRCm39) |
|
probably null |
Het |
Fsip2 |
T |
A |
2: 82,818,762 (GRCm39) |
L4832M |
possibly damaging |
Het |
Gab1 |
A |
G |
8: 81,518,237 (GRCm39) |
V125A |
possibly damaging |
Het |
Gabrr1 |
A |
T |
4: 33,149,026 (GRCm39) |
|
probably null |
Het |
Gon4l |
T |
C |
3: 88,799,968 (GRCm39) |
V871A |
possibly damaging |
Het |
Hspg2 |
A |
G |
4: 137,267,559 (GRCm39) |
T2056A |
probably damaging |
Het |
Lrrc3 |
T |
A |
10: 77,736,843 (GRCm39) |
T198S |
probably benign |
Het |
Lsamp |
A |
T |
16: 41,954,675 (GRCm39) |
E174V |
possibly damaging |
Het |
Ltbr |
C |
T |
6: 125,284,417 (GRCm39) |
V342M |
probably damaging |
Het |
Muc16 |
A |
T |
9: 18,566,742 (GRCm39) |
S1926T |
unknown |
Het |
Ntn1 |
C |
A |
11: 68,104,158 (GRCm39) |
V497F |
possibly damaging |
Het |
Or2ag18 |
A |
T |
7: 106,405,279 (GRCm39) |
L130Q |
probably damaging |
Het |
Or5k17 |
T |
C |
16: 58,746,877 (GRCm39) |
D19G |
probably benign |
Het |
Osmr |
T |
C |
15: 6,853,047 (GRCm39) |
Y615C |
probably damaging |
Het |
Pcdhgb2 |
T |
C |
18: 37,823,054 (GRCm39) |
V15A |
possibly damaging |
Het |
Pkd2l2 |
A |
G |
18: 34,547,733 (GRCm39) |
N162S |
probably benign |
Het |
Ppp1r12a |
G |
A |
10: 108,076,045 (GRCm39) |
|
probably null |
Het |
Prss59 |
G |
A |
6: 40,903,019 (GRCm39) |
P118S |
possibly damaging |
Het |
Prtg |
C |
T |
9: 72,812,076 (GRCm39) |
P899S |
probably damaging |
Het |
Ptprn |
A |
T |
1: 75,224,810 (GRCm39) |
S912R |
probably damaging |
Het |
Rex2 |
A |
G |
4: 147,141,931 (GRCm39) |
T140A |
possibly damaging |
Het |
Ryr2 |
T |
G |
13: 11,848,964 (GRCm39) |
D339A |
probably damaging |
Het |
Sf3b1 |
C |
T |
1: 55,046,677 (GRCm39) |
R289H |
probably damaging |
Het |
Slc17a9 |
A |
G |
2: 180,379,455 (GRCm39) |
D309G |
probably benign |
Het |
Slc4a10 |
A |
G |
2: 62,134,295 (GRCm39) |
R1004G |
probably benign |
Het |
Sprr2f |
A |
T |
3: 92,273,366 (GRCm39) |
Q55L |
unknown |
Het |
Syne1 |
C |
T |
10: 5,243,761 (GRCm39) |
G2801D |
probably benign |
Het |
Tenm3 |
A |
T |
8: 48,746,700 (GRCm39) |
V1026D |
probably damaging |
Het |
Ticam1 |
A |
T |
17: 56,577,730 (GRCm39) |
I455N |
probably damaging |
Het |
Tmem161b |
A |
G |
13: 84,399,363 (GRCm39) |
I6M |
possibly damaging |
Het |
Ubn1 |
A |
G |
16: 4,895,096 (GRCm39) |
E714G |
probably damaging |
Het |
Ush2a |
T |
G |
1: 188,475,651 (GRCm39) |
|
probably null |
Het |
Usp19 |
G |
A |
9: 108,377,343 (GRCm39) |
V874M |
probably damaging |
Het |
Vmn2r106 |
T |
C |
17: 20,488,501 (GRCm39) |
T633A |
probably benign |
Het |
Vmn2r75 |
A |
T |
7: 85,815,375 (GRCm39) |
|
probably benign |
Het |
Zfyve27 |
T |
C |
19: 42,178,016 (GRCm39) |
V386A |
probably damaging |
Het |
Zscan20 |
A |
T |
4: 128,498,327 (GRCm39) |
W24R |
probably damaging |
Het |
|
Other mutations in Or8g22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01928:Or8g22
|
APN |
9 |
38,958,709 (GRCm39) |
missense |
unknown |
|
R0086:Or8g22
|
UTSW |
9 |
38,958,191 (GRCm39) |
missense |
probably benign |
0.00 |
R0561:Or8g22
|
UTSW |
9 |
38,958,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R0650:Or8g22
|
UTSW |
9 |
38,957,996 (GRCm39) |
missense |
probably benign |
0.01 |
R1221:Or8g22
|
UTSW |
9 |
38,958,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1384:Or8g22
|
UTSW |
9 |
38,958,200 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1680:Or8g22
|
UTSW |
9 |
38,958,296 (GRCm39) |
missense |
probably benign |
0.43 |
R1733:Or8g22
|
UTSW |
9 |
38,958,678 (GRCm39) |
missense |
unknown |
|
R3767:Or8g22
|
UTSW |
9 |
38,958,707 (GRCm39) |
missense |
unknown |
|
R4786:Or8g22
|
UTSW |
9 |
38,958,783 (GRCm39) |
nonsense |
probably null |
|
R4944:Or8g22
|
UTSW |
9 |
38,958,158 (GRCm39) |
missense |
probably damaging |
1.00 |
R5186:Or8g22
|
UTSW |
9 |
38,958,265 (GRCm39) |
nonsense |
probably null |
|
R5403:Or8g22
|
UTSW |
9 |
38,957,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R6037:Or8g22
|
UTSW |
9 |
38,958,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R6037:Or8g22
|
UTSW |
9 |
38,958,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R6156:Or8g22
|
UTSW |
9 |
38,958,671 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6711:Or8g22
|
UTSW |
9 |
38,958,162 (GRCm39) |
makesense |
probably null |
|
R6919:Or8g22
|
UTSW |
9 |
38,958,827 (GRCm39) |
utr 5 prime |
probably benign |
|
R7022:Or8g22
|
UTSW |
9 |
38,958,379 (GRCm39) |
nonsense |
probably null |
|
R7275:Or8g22
|
UTSW |
9 |
38,958,815 (GRCm39) |
utr 5 prime |
probably benign |
|
R7290:Or8g22
|
UTSW |
9 |
38,958,694 (GRCm39) |
missense |
unknown |
|
R7644:Or8g22
|
UTSW |
9 |
38,958,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8906:Or8g22
|
UTSW |
9 |
38,958,077 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9099:Or8g22
|
UTSW |
9 |
38,958,026 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Or8g22
|
UTSW |
9 |
38,958,215 (GRCm39) |
missense |
probably damaging |
0.98 |
|