Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
C |
T |
5: 36,024,124 (GRCm39) |
|
probably benign |
Het |
Aire |
T |
C |
10: 77,870,327 (GRCm39) |
|
probably benign |
Het |
Akap12 |
T |
C |
10: 4,303,315 (GRCm39) |
S42P |
probably benign |
Het |
Amigo1 |
T |
C |
3: 108,098,985 (GRCm39) |
|
probably benign |
Het |
Angptl3 |
A |
G |
4: 98,921,499 (GRCm39) |
T206A |
probably benign |
Het |
Ank1 |
T |
A |
8: 23,600,400 (GRCm39) |
|
probably benign |
Het |
Ano5 |
A |
T |
7: 51,224,558 (GRCm39) |
T472S |
probably damaging |
Het |
Arid3c |
T |
C |
4: 41,725,958 (GRCm39) |
D215G |
probably damaging |
Het |
Cd200 |
T |
C |
16: 45,217,473 (GRCm39) |
I73V |
probably benign |
Het |
Cd47 |
T |
C |
16: 49,727,162 (GRCm39) |
I318T |
possibly damaging |
Het |
Cep290 |
A |
G |
10: 100,404,675 (GRCm39) |
|
probably null |
Het |
Cep350 |
A |
G |
1: 155,835,499 (GRCm39) |
S66P |
possibly damaging |
Het |
Cfap46 |
C |
T |
7: 139,255,950 (GRCm39) |
C300Y |
probably damaging |
Het |
Chd1 |
T |
A |
17: 15,978,523 (GRCm39) |
|
probably benign |
Het |
Chd5 |
C |
A |
4: 152,470,407 (GRCm39) |
T1913K |
probably benign |
Het |
Cimip3 |
T |
C |
17: 47,724,701 (GRCm39) |
E140G |
probably benign |
Het |
Clec4b1 |
A |
G |
6: 123,048,405 (GRCm39) |
Y180C |
probably damaging |
Het |
Cntnap5c |
A |
T |
17: 58,341,990 (GRCm39) |
D227V |
probably damaging |
Het |
Col19a1 |
C |
G |
1: 24,614,536 (GRCm39) |
|
probably benign |
Het |
Csmd1 |
A |
T |
8: 16,208,145 (GRCm39) |
M1270K |
probably benign |
Het |
Cyp2c66 |
T |
A |
19: 39,175,060 (GRCm39) |
F487I |
possibly damaging |
Het |
Dpp8 |
T |
C |
9: 64,973,784 (GRCm39) |
|
probably benign |
Het |
Duoxa1 |
A |
T |
2: 122,136,861 (GRCm39) |
|
probably benign |
Het |
Edil3 |
A |
G |
13: 89,325,399 (GRCm39) |
K263E |
probably damaging |
Het |
Fat2 |
A |
G |
11: 55,200,035 (GRCm39) |
L1013P |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,815,246 (GRCm39) |
|
probably benign |
Het |
Gab1 |
A |
G |
8: 81,496,297 (GRCm39) |
S668P |
probably damaging |
Het |
Galnt14 |
T |
C |
17: 73,852,030 (GRCm39) |
T130A |
probably damaging |
Het |
Gm10192 |
G |
A |
4: 97,071,109 (GRCm39) |
H99Y |
unknown |
Het |
Gm5592 |
A |
G |
7: 40,938,811 (GRCm39) |
T698A |
possibly damaging |
Het |
Gm6605 |
C |
A |
7: 38,147,699 (GRCm39) |
|
noncoding transcript |
Het |
Gsdma3 |
A |
G |
11: 98,522,017 (GRCm39) |
K149R |
probably benign |
Het |
Igkv4-71 |
A |
G |
6: 69,220,411 (GRCm39) |
S29P |
probably damaging |
Het |
Igsf10 |
C |
T |
3: 59,236,015 (GRCm39) |
V1389I |
probably benign |
Het |
Ik |
T |
C |
18: 36,880,386 (GRCm39) |
|
probably benign |
Het |
Ino80 |
G |
A |
2: 119,213,962 (GRCm39) |
P1203S |
probably damaging |
Het |
Iqsec2 |
G |
A |
X: 150,987,120 (GRCm39) |
E398K |
possibly damaging |
Het |
Jmjd6 |
A |
G |
11: 116,731,353 (GRCm39) |
V232A |
probably damaging |
Het |
Klhdc9 |
G |
A |
1: 171,187,895 (GRCm39) |
T112M |
possibly damaging |
Het |
Marcks |
A |
G |
10: 37,017,181 (GRCm39) |
|
probably benign |
Het |
Mctp2 |
T |
A |
7: 71,732,918 (GRCm39) |
T829S |
probably damaging |
Het |
Mroh2a |
C |
A |
1: 88,156,102 (GRCm39) |
A78E |
probably damaging |
Het |
Mroh2a |
G |
A |
1: 88,178,064 (GRCm39) |
D1053N |
probably damaging |
Het |
Mtmr14 |
A |
T |
6: 113,247,608 (GRCm39) |
H518L |
probably damaging |
Het |
Myo5c |
T |
C |
9: 75,185,571 (GRCm39) |
M978T |
probably benign |
Het |
Nlrc3 |
T |
C |
16: 3,766,775 (GRCm39) |
I1015V |
probably benign |
Het |
Nlrp5 |
C |
A |
7: 23,116,842 (GRCm39) |
Q189K |
possibly damaging |
Het |
Or1e26 |
A |
C |
11: 73,480,078 (GRCm39) |
L162R |
probably damaging |
Het |
Or2h2c |
G |
C |
17: 37,422,347 (GRCm39) |
L176V |
probably benign |
Het |
Or51f1d |
A |
G |
7: 102,700,909 (GRCm39) |
I135V |
probably benign |
Het |
Otof |
T |
A |
5: 30,539,705 (GRCm39) |
Y1051F |
probably benign |
Het |
Pcdhb14 |
C |
A |
18: 37,581,392 (GRCm39) |
T166K |
possibly damaging |
Het |
Pla2g4e |
A |
G |
2: 120,030,679 (GRCm39) |
|
probably benign |
Het |
Polr3gl |
T |
C |
3: 96,489,471 (GRCm39) |
E20G |
probably damaging |
Het |
Psmd1 |
A |
G |
1: 86,009,761 (GRCm39) |
D295G |
probably benign |
Het |
Ptpn21 |
C |
A |
12: 98,654,475 (GRCm39) |
A831S |
probably benign |
Het |
Pwwp3a |
T |
A |
10: 80,065,914 (GRCm39) |
V56E |
probably damaging |
Het |
Rd3l |
T |
C |
12: 111,946,596 (GRCm39) |
D60G |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
G |
11: 119,332,660 (GRCm39) |
D2624G |
probably benign |
Het |
Sec31a |
T |
C |
5: 100,541,066 (GRCm39) |
D347G |
probably damaging |
Het |
Sema4g |
G |
A |
19: 44,986,026 (GRCm39) |
R289H |
probably damaging |
Het |
Sema5b |
C |
T |
16: 35,480,703 (GRCm39) |
T761I |
probably benign |
Het |
Septin1 |
A |
T |
7: 126,816,171 (GRCm39) |
F86L |
probably damaging |
Het |
Shank3 |
T |
C |
15: 89,415,591 (GRCm39) |
V627A |
possibly damaging |
Het |
Slc25a46 |
C |
A |
18: 31,742,641 (GRCm39) |
G75V |
probably benign |
Het |
Slc45a2 |
T |
A |
15: 11,025,864 (GRCm39) |
Y405N |
probably damaging |
Het |
Spidr |
T |
C |
16: 15,855,498 (GRCm39) |
E339G |
probably damaging |
Het |
Sptbn1 |
A |
T |
11: 30,067,903 (GRCm39) |
H1770Q |
probably damaging |
Het |
Srgap1 |
T |
C |
10: 121,628,140 (GRCm39) |
Y944C |
probably damaging |
Het |
Supt20 |
C |
T |
3: 54,614,390 (GRCm39) |
T169I |
probably damaging |
Het |
Tie1 |
G |
A |
4: 118,336,966 (GRCm39) |
Q587* |
probably null |
Het |
Tmem214 |
A |
G |
5: 31,029,169 (GRCm39) |
T203A |
possibly damaging |
Het |
Tmprss15 |
C |
A |
16: 78,782,838 (GRCm39) |
S742I |
probably damaging |
Het |
Wdr87-ps |
T |
C |
7: 29,231,942 (GRCm39) |
|
noncoding transcript |
Het |
Zfhx2 |
A |
G |
14: 55,300,620 (GRCm39) |
V2377A |
probably damaging |
Het |
Zfp763 |
G |
A |
17: 33,238,774 (GRCm39) |
H124Y |
possibly damaging |
Het |
Zfp846 |
T |
C |
9: 20,504,853 (GRCm39) |
S238P |
probably benign |
Het |
|
Other mutations in Or8k35 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0483:Or8k35
|
UTSW |
2 |
86,424,752 (GRCm39) |
missense |
probably benign |
0.07 |
R0718:Or8k35
|
UTSW |
2 |
86,424,425 (GRCm39) |
missense |
probably benign |
0.01 |
R0727:Or8k35
|
UTSW |
2 |
86,424,724 (GRCm39) |
nonsense |
probably null |
|
R1517:Or8k35
|
UTSW |
2 |
86,424,948 (GRCm39) |
missense |
probably damaging |
0.99 |
R1850:Or8k35
|
UTSW |
2 |
86,424,448 (GRCm39) |
nonsense |
probably null |
|
R2430:Or8k35
|
UTSW |
2 |
86,425,052 (GRCm39) |
missense |
probably benign |
0.00 |
R2474:Or8k35
|
UTSW |
2 |
86,424,957 (GRCm39) |
missense |
probably benign |
0.00 |
R3009:Or8k35
|
UTSW |
2 |
86,424,714 (GRCm39) |
missense |
probably benign |
0.07 |
R3122:Or8k35
|
UTSW |
2 |
86,424,954 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4006:Or8k35
|
UTSW |
2 |
86,424,908 (GRCm39) |
missense |
probably benign |
0.14 |
R4007:Or8k35
|
UTSW |
2 |
86,424,908 (GRCm39) |
missense |
probably benign |
0.14 |
R4581:Or8k35
|
UTSW |
2 |
86,424,572 (GRCm39) |
missense |
probably benign |
0.08 |
R4762:Or8k35
|
UTSW |
2 |
86,424,381 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5617:Or8k35
|
UTSW |
2 |
86,424,345 (GRCm39) |
missense |
probably benign |
0.07 |
R6118:Or8k35
|
UTSW |
2 |
86,424,758 (GRCm39) |
missense |
probably benign |
|
R6140:Or8k35
|
UTSW |
2 |
86,424,448 (GRCm39) |
nonsense |
probably null |
|
R6313:Or8k35
|
UTSW |
2 |
86,424,411 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6528:Or8k35
|
UTSW |
2 |
86,424,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R6785:Or8k35
|
UTSW |
2 |
86,424,765 (GRCm39) |
missense |
probably damaging |
0.98 |
R6792:Or8k35
|
UTSW |
2 |
86,424,283 (GRCm39) |
missense |
probably benign |
0.09 |
R6857:Or8k35
|
UTSW |
2 |
86,424,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6998:Or8k35
|
UTSW |
2 |
86,424,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R7241:Or8k35
|
UTSW |
2 |
86,424,498 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8790:Or8k35
|
UTSW |
2 |
86,424,278 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8865:Or8k35
|
UTSW |
2 |
86,424,744 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9521:Or8k35
|
UTSW |
2 |
86,424,771 (GRCm39) |
missense |
|
|
|