Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700031F05Rik |
G |
T |
X: 101,904,515 (GRCm39) |
N132K |
possibly damaging |
Het |
2010315B03Rik |
T |
A |
9: 124,056,228 (GRCm39) |
Y232F |
probably benign |
Het |
2310079G19Rik |
T |
C |
16: 88,424,255 (GRCm39) |
S79G |
probably benign |
Het |
4930568D16Rik |
T |
A |
2: 35,244,458 (GRCm39) |
Y298F |
probably damaging |
Het |
Alpk2 |
A |
G |
18: 65,482,953 (GRCm39) |
F352L |
probably damaging |
Het |
Angpt1 |
T |
A |
15: 42,539,580 (GRCm39) |
Y93F |
probably benign |
Het |
Ankrd33b |
T |
C |
15: 31,325,170 (GRCm39) |
*129W |
probably null |
Het |
Atp5pf |
T |
C |
16: 84,625,343 (GRCm39) |
M87V |
probably benign |
Het |
Atp8b3 |
A |
G |
10: 80,361,457 (GRCm39) |
S822P |
possibly damaging |
Het |
Bbs10 |
A |
G |
10: 111,136,995 (GRCm39) |
K703E |
probably benign |
Het |
Bbs2 |
A |
T |
8: 94,807,507 (GRCm39) |
V429E |
probably damaging |
Het |
Bccip |
C |
T |
7: 133,316,628 (GRCm39) |
L83F |
probably damaging |
Het |
Brd9 |
G |
A |
13: 74,088,895 (GRCm39) |
V198I |
probably benign |
Het |
C1galt1c1 |
A |
T |
X: 37,720,349 (GRCm39) |
S216T |
probably benign |
Het |
Calhm1 |
A |
G |
19: 47,132,240 (GRCm39) |
L125P |
probably damaging |
Het |
Ccdc110 |
A |
T |
8: 46,395,705 (GRCm39) |
Q532L |
possibly damaging |
Het |
Cdh19 |
G |
A |
1: 110,852,907 (GRCm39) |
L343F |
probably benign |
Het |
Cep350 |
A |
G |
1: 155,778,344 (GRCm39) |
S1653P |
possibly damaging |
Het |
Cmtm4 |
A |
G |
8: 105,082,952 (GRCm39) |
I135T |
possibly damaging |
Het |
Cmya5 |
A |
G |
13: 93,230,336 (GRCm39) |
L1584P |
possibly damaging |
Het |
Crocc2 |
G |
A |
1: 93,096,516 (GRCm39) |
V24M |
possibly damaging |
Het |
Crp |
A |
G |
1: 172,525,704 (GRCm39) |
M1V |
probably null |
Het |
Csmd1 |
G |
A |
8: 16,048,788 (GRCm39) |
Q2305* |
probably null |
Het |
Cyp2c38 |
T |
A |
19: 39,449,132 (GRCm39) |
I74F |
probably benign |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dcaf1 |
A |
T |
9: 106,742,876 (GRCm39) |
|
probably benign |
Het |
Dhx16 |
C |
G |
17: 36,196,527 (GRCm39) |
A565G |
probably benign |
Het |
Dock7 |
C |
A |
4: 98,857,881 (GRCm39) |
E1448* |
probably null |
Het |
Dpf2 |
C |
T |
19: 5,957,109 (GRCm39) |
R38H |
probably damaging |
Het |
E030030I06Rik |
T |
A |
10: 22,024,744 (GRCm39) |
R56S |
unknown |
Het |
Etnk1 |
A |
G |
6: 143,141,000 (GRCm39) |
Y248C |
probably damaging |
Het |
Ext1 |
A |
G |
15: 52,953,383 (GRCm39) |
S494P |
possibly damaging |
Het |
Gk2 |
T |
C |
5: 97,603,579 (GRCm39) |
S420G |
probably benign |
Het |
Gm26596 |
T |
C |
10: 112,765,064 (GRCm39) |
|
probably benign |
Het |
Gm5414 |
G |
T |
15: 101,536,543 (GRCm39) |
N27K |
possibly damaging |
Het |
Gskip |
A |
G |
12: 105,664,988 (GRCm39) |
D9G |
probably benign |
Het |
H2-K2 |
T |
A |
17: 34,194,989 (GRCm39) |
|
noncoding transcript |
Het |
Hk1 |
T |
G |
10: 62,140,558 (GRCm39) |
S105R |
probably benign |
Het |
Hmg20b |
T |
A |
10: 81,184,416 (GRCm39) |
Q129L |
probably damaging |
Het |
Idnk |
A |
G |
13: 58,310,683 (GRCm39) |
D67G |
probably benign |
Het |
Igfbp5 |
G |
T |
1: 72,903,222 (GRCm39) |
H118N |
probably benign |
Het |
Irf4 |
A |
T |
13: 30,947,580 (GRCm39) |
Y427F |
probably benign |
Het |
Khdc3 |
A |
G |
9: 73,009,868 (GRCm39) |
E26G |
possibly damaging |
Het |
Kif7 |
T |
C |
7: 79,358,939 (GRCm39) |
D512G |
probably damaging |
Het |
Lamb3 |
T |
A |
1: 193,013,665 (GRCm39) |
I513N |
probably damaging |
Het |
Lipo3 |
A |
G |
19: 33,760,860 (GRCm39) |
L174P |
probably damaging |
Het |
Lnx1 |
C |
T |
5: 74,771,457 (GRCm39) |
V350I |
probably benign |
Het |
Map3k21 |
A |
G |
8: 126,668,850 (GRCm39) |
D812G |
probably benign |
Het |
Mast2 |
G |
T |
4: 116,172,036 (GRCm39) |
Y637* |
probably null |
Het |
Matn2 |
T |
C |
15: 34,428,679 (GRCm39) |
I681T |
probably damaging |
Het |
Med18 |
A |
T |
4: 132,190,274 (GRCm39) |
V37D |
possibly damaging |
Het |
Mip |
T |
A |
10: 128,062,922 (GRCm39) |
H122Q |
probably benign |
Het |
Mmp13 |
A |
T |
9: 7,274,233 (GRCm39) |
D180V |
probably damaging |
Het |
Mpg |
C |
A |
11: 32,180,034 (GRCm39) |
C187* |
probably null |
Het |
Mtmr14 |
A |
G |
6: 113,237,567 (GRCm39) |
E256G |
probably benign |
Het |
Myo7b |
C |
T |
18: 32,100,178 (GRCm39) |
|
probably null |
Het |
Nhsl3 |
G |
T |
4: 129,115,733 (GRCm39) |
T977K |
probably benign |
Het |
Nmt1 |
T |
A |
11: 102,954,743 (GRCm39) |
V425D |
probably damaging |
Het |
Nynrin |
T |
A |
14: 56,110,351 (GRCm39) |
Y1819* |
probably null |
Het |
Or10ak16 |
A |
G |
4: 118,751,147 (GRCm39) |
N289S |
possibly damaging |
Het |
Or5i1 |
T |
C |
2: 87,613,565 (GRCm39) |
V227A |
possibly damaging |
Het |
Otof |
T |
C |
5: 30,540,914 (GRCm39) |
E875G |
possibly damaging |
Het |
Paqr3 |
T |
A |
5: 97,256,069 (GRCm39) |
R102* |
probably null |
Het |
Phc1 |
T |
C |
6: 122,298,872 (GRCm39) |
I699V |
possibly damaging |
Het |
Prkdc |
T |
G |
16: 15,634,638 (GRCm39) |
D3594E |
probably benign |
Het |
Pstpip1 |
A |
T |
9: 56,032,502 (GRCm39) |
D246V |
probably damaging |
Het |
Rbm46 |
A |
T |
3: 82,771,765 (GRCm39) |
D283E |
probably benign |
Het |
Ror2 |
A |
T |
13: 53,439,536 (GRCm39) |
C9* |
probably null |
Het |
Setd1b |
C |
T |
5: 123,286,175 (GRCm39) |
A407V |
unknown |
Het |
Slc26a4 |
T |
G |
12: 31,590,525 (GRCm39) |
D376A |
possibly damaging |
Het |
Smarcad1 |
A |
G |
6: 65,044,073 (GRCm39) |
E215G |
probably benign |
Het |
Spag16 |
G |
A |
1: 69,866,194 (GRCm39) |
R11Q |
probably null |
Het |
Sult1d1 |
T |
A |
5: 87,713,954 (GRCm39) |
Q30L |
probably benign |
Het |
Tbc1d5 |
A |
G |
17: 51,043,251 (GRCm39) |
C746R |
probably benign |
Het |
Tdh |
A |
G |
14: 63,731,205 (GRCm39) |
L323P |
possibly damaging |
Het |
Tet2 |
A |
T |
3: 133,193,843 (GRCm39) |
M197K |
probably benign |
Het |
Tnn |
T |
C |
1: 159,973,612 (GRCm39) |
M252V |
probably benign |
Het |
Trdn |
G |
T |
10: 33,071,977 (GRCm39) |
E215* |
probably null |
Het |
Trem1 |
G |
A |
17: 48,551,590 (GRCm39) |
V84I |
probably benign |
Het |
Tspan5 |
T |
C |
3: 138,604,076 (GRCm39) |
F154L |
probably damaging |
Het |
Usp45 |
A |
G |
4: 21,825,044 (GRCm39) |
R647G |
probably benign |
Het |
Usp50 |
T |
A |
2: 126,619,953 (GRCm39) |
I120F |
probably damaging |
Het |
Vil1 |
T |
C |
1: 74,471,457 (GRCm39) |
M746T |
probably benign |
Het |
Washc4 |
T |
A |
10: 83,410,407 (GRCm39) |
M665K |
possibly damaging |
Het |
Zfp750 |
T |
C |
11: 121,402,706 (GRCm39) |
T681A |
probably benign |
Het |
|
Other mutations in Or4c107 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00089:Or4c107
|
APN |
2 |
88,789,110 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01398:Or4c107
|
APN |
2 |
88,789,193 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01537:Or4c107
|
APN |
2 |
88,788,885 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02197:Or4c107
|
APN |
2 |
88,789,028 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02557:Or4c107
|
APN |
2 |
88,789,025 (GRCm39) |
missense |
probably benign |
0.00 |
R0276:Or4c107
|
UTSW |
2 |
88,789,099 (GRCm39) |
nonsense |
probably null |
|
R0568:Or4c107
|
UTSW |
2 |
88,789,387 (GRCm39) |
nonsense |
probably null |
|
R0699:Or4c107
|
UTSW |
2 |
88,788,960 (GRCm39) |
missense |
probably benign |
0.31 |
R1101:Or4c107
|
UTSW |
2 |
88,789,328 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1205:Or4c107
|
UTSW |
2 |
88,788,932 (GRCm39) |
missense |
probably benign |
0.00 |
R1468:Or4c107
|
UTSW |
2 |
88,789,387 (GRCm39) |
nonsense |
probably null |
|
R1468:Or4c107
|
UTSW |
2 |
88,789,387 (GRCm39) |
nonsense |
probably null |
|
R1845:Or4c107
|
UTSW |
2 |
88,789,211 (GRCm39) |
missense |
probably damaging |
0.99 |
R2031:Or4c107
|
UTSW |
2 |
88,789,643 (GRCm39) |
missense |
probably benign |
0.19 |
R2418:Or4c107
|
UTSW |
2 |
88,789,380 (GRCm39) |
missense |
probably benign |
0.01 |
R2419:Or4c107
|
UTSW |
2 |
88,789,380 (GRCm39) |
missense |
probably benign |
0.01 |
R3781:Or4c107
|
UTSW |
2 |
88,789,091 (GRCm39) |
nonsense |
probably null |
|
R4049:Or4c107
|
UTSW |
2 |
88,789,617 (GRCm39) |
missense |
probably benign |
0.09 |
R4440:Or4c107
|
UTSW |
2 |
88,789,685 (GRCm39) |
missense |
probably benign |
0.22 |
R4583:Or4c107
|
UTSW |
2 |
88,789,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R4646:Or4c107
|
UTSW |
2 |
88,789,556 (GRCm39) |
missense |
probably damaging |
0.99 |
R4674:Or4c107
|
UTSW |
2 |
88,789,216 (GRCm39) |
missense |
probably damaging |
0.98 |
R4851:Or4c107
|
UTSW |
2 |
88,788,930 (GRCm39) |
missense |
probably damaging |
1.00 |
R4971:Or4c107
|
UTSW |
2 |
88,788,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5610:Or4c107
|
UTSW |
2 |
88,789,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R5805:Or4c107
|
UTSW |
2 |
88,788,985 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5887:Or4c107
|
UTSW |
2 |
88,789,098 (GRCm39) |
missense |
possibly damaging |
0.60 |
R6023:Or4c107
|
UTSW |
2 |
88,789,059 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6118:Or4c107
|
UTSW |
2 |
88,789,462 (GRCm39) |
nonsense |
probably null |
|
R7490:Or4c107
|
UTSW |
2 |
88,789,392 (GRCm39) |
missense |
probably benign |
0.00 |
R7542:Or4c107
|
UTSW |
2 |
88,789,119 (GRCm39) |
missense |
probably benign |
0.01 |
R7612:Or4c107
|
UTSW |
2 |
88,788,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7972:Or4c107
|
UTSW |
2 |
88,789,177 (GRCm39) |
nonsense |
probably null |
|
R8422:Or4c107
|
UTSW |
2 |
88,789,341 (GRCm39) |
missense |
probably benign |
0.05 |
R9111:Or4c107
|
UTSW |
2 |
88,789,055 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Or4c107
|
UTSW |
2 |
88,789,721 (GRCm39) |
missense |
probably benign |
|
|