Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Albfm1 |
G |
T |
5: 90,720,642 (GRCm39) |
C271F |
probably damaging |
Het |
Arhgef39 |
C |
T |
4: 43,497,112 (GRCm39) |
G293E |
possibly damaging |
Het |
Atp8a1 |
A |
C |
5: 67,932,171 (GRCm39) |
I206S |
probably benign |
Het |
Cacnb2 |
A |
T |
2: 14,980,026 (GRCm39) |
R290* |
probably null |
Het |
Ccdc137 |
T |
C |
11: 120,351,074 (GRCm39) |
S159P |
probably damaging |
Het |
Chil5 |
A |
G |
3: 105,926,943 (GRCm39) |
S231P |
probably damaging |
Het |
Cic |
C |
T |
7: 24,993,433 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
A |
G |
15: 47,532,581 (GRCm39) |
V2434A |
possibly damaging |
Het |
Csnk1a1 |
A |
G |
18: 61,718,381 (GRCm39) |
|
probably benign |
Het |
Eif4e1b |
T |
C |
13: 54,932,296 (GRCm39) |
S49P |
probably benign |
Het |
Far1 |
C |
A |
7: 113,149,208 (GRCm39) |
P194Q |
probably benign |
Het |
Fut4 |
T |
C |
9: 14,662,677 (GRCm39) |
T206A |
possibly damaging |
Het |
Galnt7 |
G |
T |
8: 58,005,606 (GRCm39) |
S209* |
probably null |
Het |
Gas2l1 |
A |
G |
11: 5,013,908 (GRCm39) |
V184A |
probably benign |
Het |
Herc1 |
T |
C |
9: 66,403,287 (GRCm39) |
L4402P |
probably damaging |
Het |
Hoxa13 |
C |
A |
6: 52,237,714 (GRCm39) |
|
probably benign |
Het |
Ighv1-9 |
T |
A |
12: 114,547,416 (GRCm39) |
K42* |
probably null |
Het |
Kif20a |
C |
T |
18: 34,764,994 (GRCm39) |
R743W |
probably damaging |
Het |
Lama2 |
G |
A |
10: 27,298,554 (GRCm39) |
R181C |
probably damaging |
Het |
Lrp2 |
G |
T |
2: 69,336,692 (GRCm39) |
T1360K |
probably benign |
Het |
Map4k1 |
G |
A |
7: 28,688,020 (GRCm39) |
V177I |
probably damaging |
Het |
Nbea |
G |
A |
3: 55,989,800 (GRCm39) |
T352I |
probably damaging |
Het |
Nde1 |
A |
G |
16: 14,006,200 (GRCm39) |
T82A |
possibly damaging |
Het |
Nes |
A |
G |
3: 87,883,349 (GRCm39) |
E536G |
probably damaging |
Het |
Nms |
C |
T |
1: 38,978,377 (GRCm39) |
P4L |
probably benign |
Het |
Nrip1 |
T |
C |
16: 76,088,293 (GRCm39) |
Q1088R |
possibly damaging |
Het |
Nwd1 |
A |
G |
8: 73,393,423 (GRCm39) |
K229E |
probably damaging |
Het |
Or51f1d |
T |
C |
7: 102,701,018 (GRCm39) |
L171P |
probably damaging |
Het |
Pcdhac2 |
T |
A |
18: 37,277,796 (GRCm39) |
S259T |
probably benign |
Het |
Pdcd5 |
T |
C |
7: 35,345,605 (GRCm39) |
D102G |
possibly damaging |
Het |
Pgm1 |
T |
C |
4: 99,819,337 (GRCm39) |
V169A |
probably benign |
Het |
Pitpnm2 |
C |
T |
5: 124,280,186 (GRCm39) |
E121K |
probably benign |
Het |
Plin3 |
T |
C |
17: 56,593,555 (GRCm39) |
Y53C |
probably damaging |
Het |
Poc1b |
T |
C |
10: 98,991,001 (GRCm39) |
|
probably null |
Het |
Polr2c |
A |
T |
8: 95,590,090 (GRCm39) |
N232Y |
probably damaging |
Het |
Ppp1r9b |
A |
T |
11: 94,892,150 (GRCm39) |
R188S |
possibly damaging |
Het |
Rab36 |
G |
A |
10: 74,880,328 (GRCm39) |
V63I |
probably damaging |
Het |
Rab3gap2 |
G |
A |
1: 184,967,539 (GRCm39) |
S141N |
probably damaging |
Het |
Radx |
T |
C |
X: 138,381,645 (GRCm39) |
V134A |
possibly damaging |
Het |
Rap1gap2 |
C |
A |
11: 74,298,148 (GRCm39) |
A491S |
possibly damaging |
Het |
Rnf166 |
A |
G |
8: 123,196,979 (GRCm39) |
L91P |
probably damaging |
Het |
Robo2 |
T |
A |
16: 73,745,154 (GRCm39) |
M200L |
probably damaging |
Het |
Rp1 |
A |
T |
1: 4,418,147 (GRCm39) |
H988Q |
probably benign |
Het |
Sbno2 |
T |
C |
10: 79,908,192 (GRCm39) |
K69R |
probably null |
Het |
Sgce |
G |
A |
6: 4,691,459 (GRCm39) |
A295V |
probably damaging |
Het |
Shc3 |
C |
G |
13: 51,634,130 (GRCm39) |
|
probably null |
Het |
Slc44a1 |
T |
C |
4: 53,563,286 (GRCm39) |
V671A |
probably benign |
Het |
Sptbn4 |
A |
C |
7: 27,123,223 (GRCm39) |
L233R |
probably damaging |
Het |
Stx5a |
A |
G |
19: 8,727,104 (GRCm39) |
T252A |
probably benign |
Het |
Timd6 |
T |
A |
11: 46,475,247 (GRCm39) |
F147L |
probably benign |
Het |
Tmem87b |
C |
T |
2: 128,688,670 (GRCm39) |
A485V |
probably benign |
Het |
Tns1 |
A |
G |
1: 74,024,908 (GRCm39) |
I403T |
probably damaging |
Het |
Ttll10 |
G |
C |
4: 156,133,018 (GRCm39) |
T22R |
possibly damaging |
Het |
Uevld |
A |
T |
7: 46,589,890 (GRCm39) |
S293T |
probably benign |
Het |
Utp18 |
T |
C |
11: 93,757,264 (GRCm39) |
N467D |
probably damaging |
Het |
Vmn1r39 |
A |
T |
6: 66,782,345 (GRCm39) |
|
probably null |
Het |
Vmn2r106 |
A |
G |
17: 20,505,641 (GRCm39) |
S18P |
probably benign |
Het |
Vmn2r61 |
A |
T |
7: 41,950,157 (GRCm39) |
H859L |
probably benign |
Het |
Vmn2r61 |
T |
C |
7: 41,950,159 (GRCm39) |
S860P |
probably benign |
Het |
Vmn2r72 |
G |
A |
7: 85,387,036 (GRCm39) |
R843* |
probably null |
Het |
Vwc2 |
A |
G |
11: 11,104,235 (GRCm39) |
T256A |
probably damaging |
Het |
Zfp715 |
T |
C |
7: 42,960,516 (GRCm39) |
D25G |
probably damaging |
Het |
|
Other mutations in Or52ad1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01525:Or52ad1
|
APN |
7 |
102,995,386 (GRCm39) |
missense |
probably benign |
0.15 |
IGL02239:Or52ad1
|
APN |
7 |
102,995,805 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02285:Or52ad1
|
APN |
7 |
102,995,245 (GRCm39) |
nonsense |
probably null |
|
IGL02547:Or52ad1
|
APN |
7 |
102,995,451 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03149:Or52ad1
|
APN |
7 |
102,996,056 (GRCm39) |
missense |
probably benign |
0.00 |
R0193:Or52ad1
|
UTSW |
7 |
102,995,411 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0304:Or52ad1
|
UTSW |
7 |
102,995,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Or52ad1
|
UTSW |
7 |
102,996,085 (GRCm39) |
missense |
probably benign |
0.02 |
R0622:Or52ad1
|
UTSW |
7 |
102,996,064 (GRCm39) |
missense |
probably damaging |
0.97 |
R1988:Or52ad1
|
UTSW |
7 |
102,995,316 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1989:Or52ad1
|
UTSW |
7 |
102,995,316 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2937:Or52ad1
|
UTSW |
7 |
102,995,272 (GRCm39) |
missense |
probably benign |
0.18 |
R5362:Or52ad1
|
UTSW |
7 |
102,995,454 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Or52ad1
|
UTSW |
7 |
102,995,826 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6793:Or52ad1
|
UTSW |
7 |
102,995,473 (GRCm39) |
missense |
probably benign |
0.00 |
R6863:Or52ad1
|
UTSW |
7 |
102,996,123 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6935:Or52ad1
|
UTSW |
7 |
102,996,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6983:Or52ad1
|
UTSW |
7 |
102,996,022 (GRCm39) |
missense |
probably benign |
0.00 |
R7262:Or52ad1
|
UTSW |
7 |
102,995,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7313:Or52ad1
|
UTSW |
7 |
102,995,538 (GRCm39) |
missense |
probably benign |
0.06 |
R7774:Or52ad1
|
UTSW |
7 |
102,995,737 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9246:Or52ad1
|
UTSW |
7 |
102,995,908 (GRCm39) |
missense |
probably damaging |
0.96 |
R9542:Or52ad1
|
UTSW |
7 |
102,995,569 (GRCm39) |
missense |
probably benign |
0.00 |
X0018:Or52ad1
|
UTSW |
7 |
102,996,106 (GRCm39) |
missense |
probably benign |
0.01 |
|