Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam17 |
A |
T |
12: 21,383,953 (GRCm39) |
|
probably null |
Het |
Adgrf5 |
A |
C |
17: 43,756,930 (GRCm39) |
I675L |
probably benign |
Het |
Arhgap24 |
T |
A |
5: 103,026,323 (GRCm39) |
M248K |
probably benign |
Het |
Chl1 |
G |
A |
6: 103,672,456 (GRCm39) |
D566N |
possibly damaging |
Het |
Cntn4 |
A |
T |
6: 106,656,856 (GRCm39) |
I908F |
possibly damaging |
Het |
Cyld |
T |
C |
8: 89,468,930 (GRCm39) |
I752T |
probably benign |
Het |
Cyp26a1 |
C |
A |
19: 37,689,072 (GRCm39) |
L336I |
possibly damaging |
Het |
Dlg2 |
A |
G |
7: 92,087,364 (GRCm39) |
|
probably null |
Het |
Dmkn |
G |
A |
7: 30,477,034 (GRCm39) |
G446D |
probably damaging |
Het |
Dnajc25 |
T |
C |
4: 59,020,356 (GRCm39) |
Y260H |
probably damaging |
Het |
Dnm3 |
C |
A |
1: 161,839,399 (GRCm39) |
R186L |
probably damaging |
Het |
Dst |
C |
T |
1: 34,218,116 (GRCm39) |
H1519Y |
possibly damaging |
Het |
Efcab3 |
C |
T |
11: 104,642,737 (GRCm39) |
T1120I |
possibly damaging |
Het |
Eif1ad |
A |
G |
19: 5,418,243 (GRCm39) |
H9R |
probably damaging |
Het |
Epha3 |
A |
T |
16: 63,386,963 (GRCm39) |
I891N |
probably benign |
Het |
Epx |
T |
C |
11: 87,765,137 (GRCm39) |
T187A |
probably damaging |
Het |
Fbln2 |
T |
G |
6: 91,210,649 (GRCm39) |
Y198D |
probably damaging |
Het |
Fhod3 |
A |
G |
18: 25,135,001 (GRCm39) |
I371V |
probably benign |
Het |
Gm4922 |
C |
T |
10: 18,660,096 (GRCm39) |
V209I |
probably damaging |
Het |
Gucy1a2 |
G |
A |
9: 3,759,580 (GRCm39) |
G462D |
probably damaging |
Het |
Gzmd |
T |
C |
14: 56,368,709 (GRCm39) |
T62A |
probably damaging |
Het |
Hnrnpul1 |
A |
T |
7: 25,453,846 (GRCm39) |
L72Q |
probably damaging |
Het |
Ifi211 |
A |
T |
1: 173,727,020 (GRCm39) |
W375R |
probably damaging |
Het |
Il1rl2 |
C |
A |
1: 40,404,413 (GRCm39) |
H511Q |
probably damaging |
Het |
Kcnn2 |
A |
T |
18: 45,692,505 (GRCm39) |
H27L |
possibly damaging |
Het |
Kng2 |
A |
G |
16: 22,806,982 (GRCm39) |
Y406H |
probably damaging |
Het |
Lama1 |
A |
G |
17: 68,087,592 (GRCm39) |
E1491G |
|
Het |
Lmf1 |
T |
C |
17: 25,873,582 (GRCm39) |
|
probably null |
Het |
Med24 |
T |
C |
11: 98,603,990 (GRCm39) |
N417S |
possibly damaging |
Het |
Mfsd4b5 |
T |
C |
10: 39,850,796 (GRCm39) |
E60G |
probably benign |
Het |
Myo7b |
A |
G |
18: 32,094,958 (GRCm39) |
V1879A |
probably benign |
Het |
Myrfl |
T |
A |
10: 116,675,258 (GRCm39) |
N225I |
possibly damaging |
Het |
Naaladl2 |
A |
C |
3: 24,467,512 (GRCm39) |
|
probably null |
Het |
Ndrg1 |
C |
T |
15: 66,820,243 (GRCm39) |
D64N |
probably damaging |
Het |
Or6c33 |
T |
C |
10: 129,853,403 (GRCm39) |
Y58H |
probably damaging |
Het |
Rasa3 |
A |
C |
8: 13,638,015 (GRCm39) |
L343R |
probably benign |
Het |
Ros1 |
T |
G |
10: 52,040,067 (GRCm39) |
K308T |
probably damaging |
Het |
Rp1l1 |
A |
G |
14: 64,267,252 (GRCm39) |
Y946C |
probably benign |
Het |
Rpl13a |
A |
T |
7: 44,775,597 (GRCm39) |
L156Q |
probably damaging |
Het |
Samd9l |
A |
G |
6: 3,375,975 (GRCm39) |
F429L |
possibly damaging |
Het |
Slc25a25 |
A |
G |
2: 32,341,221 (GRCm39) |
V39A |
probably benign |
Het |
Snrnp27 |
A |
T |
6: 86,657,935 (GRCm39) |
I101K |
possibly damaging |
Het |
Sspo |
G |
A |
6: 48,452,305 (GRCm39) |
W2756* |
probably null |
Het |
Sult6b2 |
T |
A |
6: 142,732,085 (GRCm39) |
N274I |
probably benign |
Het |
Tbc1d14 |
G |
A |
5: 36,652,382 (GRCm39) |
R667W |
probably damaging |
Het |
Tg |
T |
C |
15: 66,587,012 (GRCm39) |
S1597P |
probably damaging |
Het |
Thy1 |
A |
G |
9: 43,958,732 (GRCm39) |
D158G |
probably damaging |
Het |
Tns4 |
T |
C |
11: 98,962,296 (GRCm39) |
Y567C |
probably damaging |
Het |
Vmn1r170 |
A |
G |
7: 23,306,473 (GRCm39) |
R292G |
probably damaging |
Het |
Vmn2r120 |
C |
A |
17: 57,843,657 (GRCm39) |
R62S |
probably benign |
Het |
Vmn2r88 |
T |
G |
14: 51,655,446 (GRCm39) |
C552G |
|
Het |
Xpo4 |
T |
A |
14: 57,827,416 (GRCm39) |
I927F |
probably damaging |
Het |
Zc3h7a |
A |
T |
16: 10,956,890 (GRCm39) |
C906* |
probably null |
Het |
Zdhhc22 |
T |
C |
12: 87,030,162 (GRCm39) |
D262G |
probably benign |
Het |
Zfc3h1 |
C |
T |
10: 115,246,606 (GRCm39) |
Q898* |
probably null |
Het |
Zfp280d |
T |
A |
9: 72,209,247 (GRCm39) |
S126T |
probably damaging |
Het |
Zfp652 |
G |
T |
11: 95,640,544 (GRCm39) |
E156D |
probably benign |
Het |
Zfp74 |
T |
C |
7: 29,634,608 (GRCm39) |
R367G |
probably damaging |
Het |
|
Other mutations in Or8j3b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02403:Or8j3b
|
APN |
2 |
86,204,867 (GRCm39) |
missense |
probably benign |
0.05 |
IGL03267:Or8j3b
|
APN |
2 |
86,204,978 (GRCm39) |
nonsense |
probably null |
|
R0133:Or8j3b
|
UTSW |
2 |
86,205,159 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0993:Or8j3b
|
UTSW |
2 |
86,205,222 (GRCm39) |
missense |
probably damaging |
0.99 |
R1386:Or8j3b
|
UTSW |
2 |
86,205,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R1830:Or8j3b
|
UTSW |
2 |
86,205,487 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2398:Or8j3b
|
UTSW |
2 |
86,205,183 (GRCm39) |
missense |
probably damaging |
0.98 |
R3753:Or8j3b
|
UTSW |
2 |
86,205,259 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4394:Or8j3b
|
UTSW |
2 |
86,205,523 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4605:Or8j3b
|
UTSW |
2 |
86,205,141 (GRCm39) |
missense |
probably benign |
0.01 |
R4835:Or8j3b
|
UTSW |
2 |
86,204,853 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5029:Or8j3b
|
UTSW |
2 |
86,205,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Or8j3b
|
UTSW |
2 |
86,205,094 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7487:Or8j3b
|
UTSW |
2 |
86,205,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R7770:Or8j3b
|
UTSW |
2 |
86,205,604 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7888:Or8j3b
|
UTSW |
2 |
86,205,270 (GRCm39) |
missense |
probably benign |
0.02 |
R8678:Or8j3b
|
UTSW |
2 |
86,205,069 (GRCm39) |
missense |
probably benign |
0.01 |
R9614:Or8j3b
|
UTSW |
2 |
86,205,012 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Or8j3b
|
UTSW |
2 |
86,205,459 (GRCm39) |
missense |
possibly damaging |
0.78 |
|