Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
G |
A |
3: 36,120,331 (GRCm39) |
R25K |
probably benign |
Het |
Acap1 |
C |
T |
11: 69,776,177 (GRCm39) |
|
probably benign |
Het |
Aox1 |
T |
C |
1: 58,098,215 (GRCm39) |
L309P |
probably damaging |
Het |
Asap2 |
A |
G |
12: 21,162,094 (GRCm39) |
D17G |
probably damaging |
Het |
Atp8b1 |
A |
T |
18: 64,689,962 (GRCm39) |
V590D |
probably damaging |
Het |
Bace2 |
G |
A |
16: 97,223,180 (GRCm39) |
R368Q |
probably damaging |
Het |
Cad |
G |
A |
5: 31,215,477 (GRCm39) |
S96N |
possibly damaging |
Het |
Csmd3 |
T |
C |
15: 47,763,240 (GRCm39) |
T1303A |
probably benign |
Het |
Defa24 |
A |
G |
8: 22,224,523 (GRCm39) |
|
probably benign |
Het |
Dffb |
A |
G |
4: 154,049,913 (GRCm39) |
C317R |
probably damaging |
Het |
Erap1 |
T |
C |
13: 74,821,778 (GRCm39) |
V711A |
probably benign |
Het |
Esco1 |
A |
G |
18: 10,595,074 (GRCm39) |
S71P |
possibly damaging |
Het |
Evpl |
G |
A |
11: 116,124,225 (GRCm39) |
T198M |
possibly damaging |
Het |
Gm10797 |
A |
G |
10: 67,408,515 (GRCm39) |
|
noncoding transcript |
Het |
Gm10822 |
C |
T |
2: 73,729,833 (GRCm39) |
|
noncoding transcript |
Het |
Huwe1 |
A |
T |
X: 150,646,955 (GRCm39) |
I682F |
probably damaging |
Het |
Ift22 |
A |
G |
5: 136,941,724 (GRCm39) |
E152G |
probably benign |
Het |
Ighv3-5 |
T |
A |
12: 114,226,498 (GRCm39) |
T25S |
possibly damaging |
Het |
Ivl |
CCTGCTGCTGCT |
CCTGCTGCTGCTGCT |
3: 92,479,262 (GRCm39) |
|
probably benign |
Het |
Kcna5 |
T |
C |
6: 126,511,303 (GRCm39) |
H275R |
probably benign |
Het |
Kdm7a |
C |
T |
6: 39,129,757 (GRCm39) |
R473Q |
probably damaging |
Het |
Klf14 |
G |
A |
6: 30,935,394 (GRCm39) |
A80V |
probably damaging |
Het |
Lrrc71 |
T |
A |
3: 87,652,715 (GRCm39) |
|
probably benign |
Het |
Lypd8 |
T |
A |
11: 58,273,215 (GRCm39) |
|
probably null |
Het |
Mef2b |
G |
A |
8: 70,619,918 (GRCm39) |
D345N |
probably damaging |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Mtmr10 |
C |
T |
7: 63,963,907 (GRCm39) |
T214M |
possibly damaging |
Het |
Or10g9b |
A |
G |
9: 39,917,577 (GRCm39) |
S223P |
probably damaging |
Het |
Or4f4b |
A |
T |
2: 111,313,909 (GRCm39) |
M45L |
probably benign |
Het |
Orc1 |
T |
C |
4: 108,459,252 (GRCm39) |
|
probably null |
Het |
P4htm |
T |
C |
9: 108,459,195 (GRCm39) |
S246G |
probably null |
Het |
Pax2 |
A |
G |
19: 44,824,402 (GRCm39) |
Y374C |
unknown |
Het |
Pde6b |
A |
G |
5: 108,551,234 (GRCm39) |
K173E |
probably benign |
Het |
Pde8a |
T |
A |
7: 80,958,568 (GRCm39) |
Y315* |
probably null |
Het |
Plekhh2 |
A |
G |
17: 84,873,525 (GRCm39) |
D270G |
probably benign |
Het |
Prr5 |
A |
C |
15: 84,626,114 (GRCm39) |
D63A |
probably damaging |
Het |
Robo4 |
CGG |
CG |
9: 37,322,786 (GRCm39) |
|
probably null |
Het |
Ryr1 |
C |
A |
7: 28,774,005 (GRCm39) |
|
probably benign |
Het |
Slc4a1ap |
G |
A |
5: 31,689,373 (GRCm39) |
V347M |
probably damaging |
Het |
Tasor |
A |
G |
14: 27,188,265 (GRCm39) |
T904A |
possibly damaging |
Het |
Tln1 |
C |
A |
4: 43,533,598 (GRCm39) |
A2319S |
probably damaging |
Het |
Tm6sf1 |
G |
A |
7: 81,509,209 (GRCm39) |
A5T |
probably damaging |
Het |
Tmem117 |
A |
T |
15: 94,992,677 (GRCm39) |
M446L |
probably benign |
Het |
Tnfrsf22 |
C |
T |
7: 143,203,313 (GRCm39) |
R19Q |
unknown |
Het |
Tnfsf11 |
T |
C |
14: 78,516,020 (GRCm39) |
D316G |
probably damaging |
Het |
Trerf1 |
G |
A |
17: 47,637,997 (GRCm39) |
|
noncoding transcript |
Het |
Ttc13 |
A |
G |
8: 125,402,016 (GRCm39) |
L657P |
probably damaging |
Het |
Unc79 |
C |
T |
12: 102,957,720 (GRCm39) |
T45I |
probably damaging |
Het |
Usp3 |
G |
T |
9: 66,428,047 (GRCm39) |
|
probably benign |
Het |
Vmn2r-ps158 |
C |
T |
7: 42,672,986 (GRCm39) |
Q130* |
probably null |
Het |
Wdr31 |
A |
C |
4: 62,372,159 (GRCm39) |
L319W |
probably damaging |
Het |
Zfp947 |
G |
T |
17: 22,365,124 (GRCm39) |
Y183* |
probably null |
Het |
|
Other mutations in Or13g1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00886:Or13g1
|
APN |
7 |
85,956,259 (GRCm39) |
missense |
probably damaging |
1.00 |
R0370:Or13g1
|
UTSW |
7 |
85,956,057 (GRCm39) |
missense |
probably benign |
0.42 |
R1869:Or13g1
|
UTSW |
7 |
85,955,875 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2047:Or13g1
|
UTSW |
7 |
85,956,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R3939:Or13g1
|
UTSW |
7 |
85,955,437 (GRCm39) |
missense |
probably benign |
0.00 |
R4640:Or13g1
|
UTSW |
7 |
85,956,274 (GRCm39) |
missense |
probably benign |
0.01 |
R4811:Or13g1
|
UTSW |
7 |
85,956,166 (GRCm39) |
missense |
probably benign |
0.41 |
R4867:Or13g1
|
UTSW |
7 |
85,955,491 (GRCm39) |
missense |
probably benign |
0.00 |
R4954:Or13g1
|
UTSW |
7 |
85,955,809 (GRCm39) |
missense |
probably benign |
0.01 |
R5784:Or13g1
|
UTSW |
7 |
85,955,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R6043:Or13g1
|
UTSW |
7 |
85,955,547 (GRCm39) |
missense |
probably damaging |
0.97 |
R6498:Or13g1
|
UTSW |
7 |
85,956,226 (GRCm39) |
missense |
probably benign |
|
R6849:Or13g1
|
UTSW |
7 |
85,956,248 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7238:Or13g1
|
UTSW |
7 |
85,955,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Or13g1
|
UTSW |
7 |
85,955,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7917:Or13g1
|
UTSW |
7 |
85,955,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Or13g1
|
UTSW |
7 |
85,956,260 (GRCm39) |
missense |
probably benign |
0.24 |
R8271:Or13g1
|
UTSW |
7 |
85,955,962 (GRCm39) |
missense |
probably benign |
0.13 |
R9017:Or13g1
|
UTSW |
7 |
85,955,957 (GRCm39) |
nonsense |
probably null |
|
R9150:Or13g1
|
UTSW |
7 |
85,955,942 (GRCm39) |
missense |
probably damaging |
0.96 |
T0975:Or13g1
|
UTSW |
7 |
85,955,492 (GRCm39) |
nonsense |
probably null |
|
|