Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
T |
5: 77,036,515 (GRCm39) |
I342N |
probably damaging |
Het |
Alb |
A |
T |
5: 90,619,932 (GRCm39) |
N453I |
possibly damaging |
Het |
Aox4 |
C |
A |
1: 58,274,366 (GRCm39) |
S384Y |
probably damaging |
Het |
Ap1g1 |
C |
T |
8: 110,564,399 (GRCm39) |
R315* |
probably null |
Het |
Cachd1 |
T |
C |
4: 100,832,060 (GRCm39) |
Y741H |
probably damaging |
Het |
Cacna2d2 |
C |
G |
9: 107,395,456 (GRCm39) |
L661V |
probably benign |
Het |
Ccdc90b |
T |
A |
7: 92,216,921 (GRCm39) |
H64Q |
probably damaging |
Het |
Ccdc93 |
C |
A |
1: 121,426,960 (GRCm39) |
N582K |
possibly damaging |
Het |
Cdh20 |
A |
G |
1: 109,921,835 (GRCm39) |
|
probably benign |
Het |
Cnksr1 |
T |
C |
4: 133,963,342 (GRCm39) |
N78D |
probably damaging |
Het |
Cttnbp2nl |
A |
G |
3: 104,915,307 (GRCm39) |
V132A |
probably damaging |
Het |
Cwc25 |
G |
A |
11: 97,644,044 (GRCm39) |
Q230* |
probably null |
Het |
Dsel |
G |
A |
1: 111,787,449 (GRCm39) |
R1029* |
probably null |
Het |
Dspp |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
TGACAGCAGTGACAGCAGCGACAGCAGCGACAGCAGTGACAGCAGCGACAGCAGCAACAGCAGTGACAGCAG |
5: 104,326,227 (GRCm39) |
|
probably benign |
Het |
Fam120a |
T |
C |
13: 49,055,750 (GRCm39) |
Y646C |
probably damaging |
Het |
Hltf |
T |
C |
3: 20,146,968 (GRCm39) |
W576R |
probably damaging |
Het |
Hmcn2 |
A |
G |
2: 31,279,359 (GRCm39) |
N1787S |
probably benign |
Het |
Ift122 |
A |
G |
6: 115,897,313 (GRCm39) |
E904G |
probably benign |
Het |
Igkv17-121 |
C |
T |
6: 68,013,806 (GRCm39) |
T2I |
unknown |
Het |
Ino80 |
T |
G |
2: 119,269,874 (GRCm39) |
R590S |
possibly damaging |
Het |
Intu |
T |
A |
3: 40,652,069 (GRCm39) |
I842N |
probably damaging |
Het |
Itgae |
A |
T |
11: 73,024,913 (GRCm39) |
T1015S |
probably damaging |
Het |
Kank1 |
GCGAACG |
GCG |
19: 25,388,569 (GRCm39) |
|
probably null |
Het |
Kcna10 |
A |
G |
3: 107,101,663 (GRCm39) |
E98G |
probably damaging |
Het |
Kcnb2 |
T |
A |
1: 15,780,837 (GRCm39) |
Y570N |
probably benign |
Het |
Kmt2c |
T |
C |
5: 25,564,676 (GRCm39) |
I923V |
probably benign |
Het |
Kptn |
A |
G |
7: 15,859,697 (GRCm39) |
D307G |
probably damaging |
Het |
Myo3b |
T |
C |
2: 70,083,458 (GRCm39) |
Y704H |
probably damaging |
Het |
Or12d13 |
A |
G |
17: 37,647,392 (GRCm39) |
F244L |
probably benign |
Het |
Or4c58 |
A |
T |
2: 89,674,611 (GRCm39) |
C235* |
probably null |
Het |
Or4f59 |
T |
C |
2: 111,872,523 (GRCm39) |
T285A |
possibly damaging |
Het |
Pmel |
G |
A |
10: 128,551,819 (GRCm39) |
V218M |
probably damaging |
Het |
Prkar2b |
T |
C |
12: 32,013,024 (GRCm39) |
H364R |
possibly damaging |
Het |
Psd4 |
T |
C |
2: 24,294,867 (GRCm39) |
F809S |
probably damaging |
Het |
Rabgap1l |
A |
G |
1: 160,078,838 (GRCm39) |
S59P |
|
Het |
Rgr |
A |
G |
14: 36,766,645 (GRCm39) |
F134L |
probably benign |
Het |
Rspry1 |
G |
T |
8: 95,349,753 (GRCm39) |
R47L |
probably damaging |
Het |
Scd3 |
G |
T |
19: 44,222,688 (GRCm39) |
E113* |
probably null |
Het |
Slc22a12 |
G |
A |
19: 6,586,938 (GRCm39) |
A476V |
possibly damaging |
Het |
Smg1 |
T |
C |
7: 117,792,878 (GRCm39) |
E560G |
unknown |
Het |
Snx3 |
A |
G |
10: 42,378,346 (GRCm39) |
D7G |
probably benign |
Het |
Son |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
AGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCGCAGGAGCCGAACCCCCAGCCG |
16: 91,457,222 (GRCm39) |
|
probably benign |
Het |
Tbc1d12 |
A |
G |
19: 38,905,285 (GRCm39) |
M667V |
probably benign |
Het |
Tbc1d30 |
A |
T |
10: 121,142,104 (GRCm39) |
V81E |
probably damaging |
Het |
Tbc1d9 |
A |
T |
8: 83,966,583 (GRCm39) |
I395F |
probably damaging |
Het |
Tes |
C |
A |
6: 17,096,322 (GRCm39) |
N103K |
probably benign |
Het |
Tet2 |
T |
C |
3: 133,193,426 (GRCm39) |
Y336C |
possibly damaging |
Het |
Tgfbr3 |
T |
C |
5: 107,287,726 (GRCm39) |
N491S |
probably damaging |
Het |
Tomt |
T |
C |
7: 101,549,554 (GRCm39) |
I245V |
probably damaging |
Het |
Trbc1 |
T |
C |
6: 41,515,236 (GRCm39) |
L28P |
|
Het |
Trp63 |
T |
C |
16: 25,639,436 (GRCm39) |
V208A |
unknown |
Het |
Ttll8 |
G |
T |
15: 88,799,565 (GRCm39) |
N625K |
probably benign |
Het |
Ush2a |
T |
A |
1: 188,132,135 (GRCm39) |
W786R |
probably benign |
Het |
Vmn2r97 |
A |
T |
17: 19,167,854 (GRCm39) |
I703F |
probably damaging |
Het |
|
Other mutations in Or4c100 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01311:Or4c100
|
APN |
2 |
88,356,104 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01727:Or4c100
|
APN |
2 |
88,356,271 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01790:Or4c100
|
APN |
2 |
88,356,767 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01868:Or4c100
|
APN |
2 |
88,356,059 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL03146:Or4c100
|
APN |
2 |
88,356,488 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03378:Or4c100
|
APN |
2 |
88,356,498 (GRCm39) |
nonsense |
probably null |
|
R0053:Or4c100
|
UTSW |
2 |
88,356,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R0829:Or4c100
|
UTSW |
2 |
88,356,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1210:Or4c100
|
UTSW |
2 |
88,356,620 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1754:Or4c100
|
UTSW |
2 |
88,356,159 (GRCm39) |
missense |
probably damaging |
0.99 |
R2260:Or4c100
|
UTSW |
2 |
88,356,730 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3426:Or4c100
|
UTSW |
2 |
88,356,208 (GRCm39) |
missense |
probably damaging |
1.00 |
R3781:Or4c100
|
UTSW |
2 |
88,356,709 (GRCm39) |
missense |
probably benign |
0.23 |
R4737:Or4c100
|
UTSW |
2 |
88,356,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R4908:Or4c100
|
UTSW |
2 |
88,356,254 (GRCm39) |
missense |
probably damaging |
1.00 |
R4932:Or4c100
|
UTSW |
2 |
88,356,079 (GRCm39) |
missense |
probably benign |
0.02 |
R5071:Or4c100
|
UTSW |
2 |
88,356,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R5831:Or4c100
|
UTSW |
2 |
88,356,824 (GRCm39) |
nonsense |
probably null |
|
R6222:Or4c100
|
UTSW |
2 |
88,329,614 (GRCm39) |
missense |
probably benign |
0.34 |
R6370:Or4c100
|
UTSW |
2 |
88,329,712 (GRCm39) |
nonsense |
probably null |
|
R6802:Or4c100
|
UTSW |
2 |
88,355,941 (GRCm39) |
missense |
probably benign |
0.02 |
R6931:Or4c100
|
UTSW |
2 |
88,356,538 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7044:Or4c100
|
UTSW |
2 |
88,356,830 (GRCm39) |
missense |
probably benign |
|
R7121:Or4c100
|
UTSW |
2 |
88,356,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Or4c100
|
UTSW |
2 |
88,355,990 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7387:Or4c100
|
UTSW |
2 |
88,356,744 (GRCm39) |
nonsense |
probably null |
|
R7891:Or4c100
|
UTSW |
2 |
88,356,289 (GRCm39) |
missense |
probably benign |
0.04 |
R7951:Or4c100
|
UTSW |
2 |
88,356,148 (GRCm39) |
missense |
probably damaging |
0.98 |
R8016:Or4c100
|
UTSW |
2 |
88,356,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R8039:Or4c100
|
UTSW |
2 |
88,356,215 (GRCm39) |
missense |
probably benign |
0.07 |
R8389:Or4c100
|
UTSW |
2 |
88,355,931 (GRCm39) |
start codon destroyed |
probably null |
|
R9211:Or4c100
|
UTSW |
2 |
88,356,170 (GRCm39) |
missense |
probably benign |
0.08 |
R9279:Or4c100
|
UTSW |
2 |
88,356,211 (GRCm39) |
missense |
probably benign |
0.01 |
R9691:Or4c100
|
UTSW |
2 |
88,356,421 (GRCm39) |
missense |
probably benign |
0.39 |
R9782:Or4c100
|
UTSW |
2 |
88,356,835 (GRCm39) |
missense |
probably benign |
0.01 |
|