Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,349,388 (GRCm39) |
Y3654C |
probably damaging |
Het |
Aldh1l2 |
A |
C |
10: 83,328,448 (GRCm39) |
Y756* |
probably null |
Het |
Arhgef12 |
T |
C |
9: 42,903,859 (GRCm39) |
E733G |
probably damaging |
Het |
Art5 |
A |
T |
7: 101,748,699 (GRCm39) |
M1K |
probably null |
Het |
Atp1a2 |
A |
T |
1: 172,113,338 (GRCm39) |
D448E |
probably damaging |
Het |
Atp6v1b1 |
C |
T |
6: 83,733,837 (GRCm39) |
T356I |
possibly damaging |
Het |
Celsr1 |
A |
G |
15: 85,784,889 (GRCm39) |
|
probably benign |
Het |
Cep89 |
A |
G |
7: 35,134,990 (GRCm39) |
Y686C |
probably damaging |
Het |
Cgrrf1 |
T |
A |
14: 47,090,901 (GRCm39) |
Y212* |
probably null |
Het |
Chrnb1 |
T |
C |
11: 69,675,916 (GRCm39) |
Y442C |
probably damaging |
Het |
Clcn1 |
T |
C |
6: 42,284,007 (GRCm39) |
|
probably benign |
Het |
Clcn7 |
G |
A |
17: 25,363,443 (GRCm39) |
V40M |
probably damaging |
Het |
Cntn1 |
A |
G |
15: 92,148,860 (GRCm39) |
Y369C |
possibly damaging |
Het |
Csmd1 |
T |
C |
8: 17,584,992 (GRCm39) |
|
probably benign |
Het |
Dpy19l2 |
A |
T |
9: 24,542,563 (GRCm39) |
C446S |
probably benign |
Het |
Edem3 |
G |
A |
1: 151,687,407 (GRCm39) |
E782K |
probably benign |
Het |
Efcab15 |
T |
A |
11: 103,090,275 (GRCm39) |
Q287L |
probably damaging |
Het |
Ephb3 |
T |
A |
16: 21,039,389 (GRCm39) |
|
probably benign |
Het |
Fndc4 |
T |
C |
5: 31,452,090 (GRCm39) |
D109G |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,805,267 (GRCm39) |
V1303A |
possibly damaging |
Het |
Gcn1 |
T |
C |
5: 115,723,940 (GRCm39) |
L532P |
probably benign |
Het |
Gm5150 |
A |
G |
3: 16,017,485 (GRCm39) |
L262P |
probably damaging |
Het |
Hbb-bs |
T |
C |
7: 103,477,091 (GRCm39) |
|
probably benign |
Het |
Krt74 |
A |
G |
15: 101,669,059 (GRCm39) |
|
noncoding transcript |
Het |
Myo1a |
T |
C |
10: 127,548,478 (GRCm39) |
V375A |
probably damaging |
Het |
Nup160 |
A |
T |
2: 90,560,079 (GRCm39) |
Q1268L |
probably benign |
Het |
Or4k42 |
G |
A |
2: 111,319,768 (GRCm39) |
T245M |
possibly damaging |
Het |
Or5d16 |
G |
A |
2: 87,773,262 (GRCm39) |
R237* |
probably null |
Het |
Or9s27 |
T |
C |
1: 92,516,648 (GRCm39) |
S199P |
possibly damaging |
Het |
Pan3 |
T |
C |
5: 147,463,406 (GRCm39) |
S497P |
probably damaging |
Het |
Pex5 |
T |
C |
6: 124,390,264 (GRCm39) |
T138A |
probably benign |
Het |
Pik3ap1 |
A |
G |
19: 41,270,451 (GRCm39) |
|
probably benign |
Het |
Ptchd4 |
A |
T |
17: 42,627,764 (GRCm39) |
H75L |
possibly damaging |
Het |
Rag2 |
A |
T |
2: 101,461,055 (GRCm39) |
H455L |
probably damaging |
Het |
Rergl |
T |
A |
6: 139,470,351 (GRCm39) |
E159V |
probably damaging |
Het |
Rrn3 |
A |
G |
16: 13,606,721 (GRCm39) |
N109S |
probably benign |
Het |
Scn1a |
A |
T |
2: 66,108,157 (GRCm39) |
V1523D |
probably damaging |
Het |
Sec23a |
A |
G |
12: 59,053,884 (GRCm39) |
V38A |
probably benign |
Het |
Slc15a2 |
G |
A |
16: 36,602,021 (GRCm39) |
T92M |
possibly damaging |
Het |
Slc2a2 |
A |
G |
3: 28,781,260 (GRCm39) |
T433A |
probably benign |
Het |
Sptan1 |
A |
G |
2: 29,906,067 (GRCm39) |
D1671G |
probably damaging |
Het |
Stab1 |
A |
G |
14: 30,861,167 (GRCm39) |
|
probably benign |
Het |
Stau2 |
A |
T |
1: 16,556,293 (GRCm39) |
I22N |
possibly damaging |
Het |
Strn3 |
A |
T |
12: 51,708,410 (GRCm39) |
Y123* |
probably null |
Het |
Tmem205 |
A |
G |
9: 21,837,607 (GRCm39) |
V13A |
possibly damaging |
Het |
Trub1 |
G |
A |
19: 57,472,009 (GRCm39) |
|
probably benign |
Het |
Ttn |
A |
G |
2: 76,568,699 (GRCm39) |
V27398A |
possibly damaging |
Het |
Vill |
A |
G |
9: 118,899,845 (GRCm39) |
E343G |
possibly damaging |
Het |
Zgpat |
T |
C |
2: 181,008,029 (GRCm39) |
F189L |
probably damaging |
Het |
|
Other mutations in Or51ag1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01924:Or51ag1
|
APN |
7 |
103,156,003 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02179:Or51ag1
|
APN |
7 |
103,155,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02303:Or51ag1
|
APN |
7 |
103,155,295 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02562:Or51ag1
|
APN |
7 |
103,155,423 (GRCm39) |
nonsense |
probably null |
|
IGL02806:Or51ag1
|
APN |
7 |
103,155,210 (GRCm39) |
missense |
probably benign |
0.10 |
R0743:Or51ag1
|
UTSW |
7 |
103,156,069 (GRCm39) |
nonsense |
probably null |
|
R0884:Or51ag1
|
UTSW |
7 |
103,156,069 (GRCm39) |
nonsense |
probably null |
|
R1673:Or51ag1
|
UTSW |
7 |
103,155,896 (GRCm39) |
missense |
probably damaging |
0.99 |
R1752:Or51ag1
|
UTSW |
7 |
103,155,765 (GRCm39) |
missense |
probably benign |
0.02 |
R1800:Or51ag1
|
UTSW |
7 |
103,155,248 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2043:Or51ag1
|
UTSW |
7 |
103,156,150 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
R2254:Or51ag1
|
UTSW |
7 |
103,155,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Or51ag1
|
UTSW |
7 |
103,155,367 (GRCm39) |
missense |
probably benign |
0.08 |
R4433:Or51ag1
|
UTSW |
7 |
103,155,346 (GRCm39) |
missense |
probably benign |
0.04 |
R5206:Or51ag1
|
UTSW |
7 |
103,155,309 (GRCm39) |
nonsense |
probably null |
|
R5470:Or51ag1
|
UTSW |
7 |
103,155,716 (GRCm39) |
missense |
probably benign |
0.00 |
R6020:Or51ag1
|
UTSW |
7 |
103,156,006 (GRCm39) |
missense |
probably benign |
|
R6848:Or51ag1
|
UTSW |
7 |
103,155,664 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7222:Or51ag1
|
UTSW |
7 |
103,155,664 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7832:Or51ag1
|
UTSW |
7 |
103,155,586 (GRCm39) |
missense |
probably damaging |
1.00 |
R7837:Or51ag1
|
UTSW |
7 |
103,156,052 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7893:Or51ag1
|
UTSW |
7 |
103,155,817 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9293:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9335:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9567:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9615:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
R9653:Or51ag1
|
UTSW |
7 |
103,155,727 (GRCm39) |
missense |
probably benign |
0.00 |
|