Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts14 |
T |
C |
10: 61,034,438 (GRCm39) |
Y1147C |
possibly damaging |
Het |
Adgrf5 |
T |
A |
17: 43,766,161 (GRCm39) |
S1328T |
unknown |
Het |
Aff4 |
A |
G |
11: 53,295,379 (GRCm39) |
K860E |
probably damaging |
Het |
Aox1 |
A |
C |
1: 58,115,250 (GRCm39) |
H745P |
probably damaging |
Het |
Bpifc |
T |
C |
10: 85,836,413 (GRCm39) |
T31A |
probably benign |
Het |
C3 |
C |
A |
17: 57,530,938 (GRCm39) |
V388L |
probably benign |
Het |
Celsr3 |
G |
T |
9: 108,723,612 (GRCm39) |
M2874I |
probably damaging |
Het |
Cnga4 |
T |
A |
7: 105,057,239 (GRCm39) |
D550E |
probably benign |
Het |
Dhx8 |
A |
G |
11: 101,648,455 (GRCm39) |
T918A |
probably damaging |
Het |
Dnah14 |
A |
C |
1: 181,601,376 (GRCm39) |
E3670A |
probably benign |
Het |
Fbxo31 |
T |
C |
8: 122,287,181 (GRCm39) |
I131V |
probably benign |
Het |
Ftcd |
T |
C |
10: 76,413,893 (GRCm39) |
V99A |
probably benign |
Het |
Gucy2e |
A |
G |
11: 69,123,177 (GRCm39) |
V471A |
probably benign |
Het |
H60b |
T |
A |
10: 22,162,971 (GRCm39) |
L182Q |
probably benign |
Het |
Hbp1 |
G |
A |
12: 31,987,625 (GRCm39) |
H188Y |
probably damaging |
Het |
Itga4 |
C |
T |
2: 79,151,783 (GRCm39) |
T862I |
probably benign |
Het |
Kcnmb4 |
T |
A |
10: 116,254,158 (GRCm39) |
K206N |
probably damaging |
Het |
Klra4 |
A |
G |
6: 130,042,243 (GRCm39) |
F8S |
possibly damaging |
Het |
Mrpl2 |
C |
A |
17: 46,958,435 (GRCm39) |
Y72* |
probably null |
Het |
Nars2 |
C |
A |
7: 96,600,845 (GRCm39) |
|
probably benign |
Het |
Nup214 |
T |
C |
2: 31,886,458 (GRCm39) |
S607P |
possibly damaging |
Het |
Oas1d |
C |
T |
5: 121,057,221 (GRCm39) |
R276* |
probably null |
Het |
Or12d13 |
C |
T |
17: 37,647,587 (GRCm39) |
V179I |
probably benign |
Het |
Or1l8 |
T |
A |
2: 36,818,018 (GRCm39) |
Y36F |
probably damaging |
Het |
Or2t1 |
T |
A |
14: 14,329,011 (GRCm38) |
L300Q |
possibly damaging |
Het |
Pex13 |
A |
G |
11: 23,605,685 (GRCm39) |
S182P |
possibly damaging |
Het |
Piwil4 |
G |
T |
9: 14,638,774 (GRCm39) |
N297K |
probably benign |
Het |
Plxna4 |
T |
C |
6: 32,129,789 (GRCm39) |
T1845A |
probably benign |
Het |
Pml |
T |
C |
9: 58,136,643 (GRCm39) |
N579D |
probably benign |
Het |
Ppl |
A |
G |
16: 4,950,201 (GRCm39) |
S3P |
probably damaging |
Het |
Pramel16 |
G |
T |
4: 143,676,695 (GRCm39) |
D136E |
possibly damaging |
Het |
Prss54 |
G |
A |
8: 96,285,994 (GRCm39) |
Q360* |
probably null |
Het |
Ralgps2 |
A |
G |
1: 156,655,718 (GRCm39) |
I402T |
probably benign |
Het |
Rnf213 |
T |
A |
11: 119,318,909 (GRCm39) |
D1123E |
|
Het |
Sdha |
A |
T |
13: 74,479,416 (GRCm39) |
|
probably null |
Het |
Senp8 |
G |
A |
9: 59,644,814 (GRCm39) |
T114I |
|
Het |
Setx |
C |
T |
2: 29,035,348 (GRCm39) |
T611I |
possibly damaging |
Het |
Shc1 |
T |
G |
3: 89,329,215 (GRCm39) |
S20A |
possibly damaging |
Het |
Slc15a1 |
T |
C |
14: 121,727,275 (GRCm39) |
I98V |
probably benign |
Het |
Snrk |
A |
G |
9: 121,989,538 (GRCm39) |
E294G |
probably damaging |
Het |
Sox18 |
G |
A |
2: 181,312,751 (GRCm39) |
P127S |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,007,387 (GRCm39) |
T206A |
probably benign |
Het |
Tcfl5 |
A |
G |
2: 180,280,330 (GRCm39) |
S358P |
probably benign |
Het |
Tecta |
T |
A |
9: 42,289,325 (GRCm39) |
L413F |
possibly damaging |
Het |
Tlk1 |
T |
C |
2: 70,544,365 (GRCm39) |
T757A |
probably benign |
Het |
Tmem232 |
T |
A |
17: 65,709,990 (GRCm39) |
I433F |
probably damaging |
Het |
Top1mt |
T |
A |
15: 75,539,712 (GRCm39) |
K300* |
probably null |
Het |
Trbv20 |
C |
T |
6: 41,165,782 (GRCm39) |
A69V |
probably damaging |
Het |
Trim12a |
A |
T |
7: 103,955,282 (GRCm39) |
L147Q |
probably damaging |
Het |
Tuba8 |
G |
A |
6: 121,199,736 (GRCm39) |
S140N |
probably damaging |
Het |
Vcan |
A |
T |
13: 89,852,454 (GRCm39) |
N835K |
possibly damaging |
Het |
Xrcc1 |
G |
A |
7: 24,271,703 (GRCm39) |
R562H |
probably damaging |
Het |
Yipf7 |
C |
T |
5: 69,674,539 (GRCm39) |
G202D |
probably benign |
Het |
Ythdc1 |
T |
G |
5: 86,964,325 (GRCm39) |
S45A |
probably benign |
Het |
Zfp1002 |
T |
C |
2: 150,097,276 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Or2y1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01349:Or2y1b
|
APN |
11 |
49,209,127 (GRCm39) |
nonsense |
probably null |
0.00 |
IGL02283:Or2y1b
|
APN |
11 |
49,209,162 (GRCm39) |
missense |
probably benign |
|
IGL03010:Or2y1b
|
APN |
11 |
49,208,973 (GRCm39) |
missense |
probably damaging |
0.99 |
R0575:Or2y1b
|
UTSW |
11 |
49,208,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Or2y1b
|
UTSW |
11 |
49,208,928 (GRCm39) |
splice site |
probably null |
|
R1891:Or2y1b
|
UTSW |
11 |
49,208,684 (GRCm39) |
missense |
probably benign |
0.00 |
R2509:Or2y1b
|
UTSW |
11 |
49,209,048 (GRCm39) |
missense |
probably damaging |
0.97 |
R2511:Or2y1b
|
UTSW |
11 |
49,209,048 (GRCm39) |
missense |
probably damaging |
0.97 |
R4942:Or2y1b
|
UTSW |
11 |
49,208,375 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R5080:Or2y1b
|
UTSW |
11 |
49,208,914 (GRCm39) |
missense |
probably benign |
0.03 |
R5413:Or2y1b
|
UTSW |
11 |
49,209,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R5843:Or2y1b
|
UTSW |
11 |
49,209,076 (GRCm39) |
missense |
probably benign |
0.34 |
R6354:Or2y1b
|
UTSW |
11 |
49,208,465 (GRCm39) |
missense |
probably damaging |
0.98 |
R6605:Or2y1b
|
UTSW |
11 |
49,208,541 (GRCm39) |
missense |
probably damaging |
0.97 |
R8005:Or2y1b
|
UTSW |
11 |
49,208,968 (GRCm39) |
missense |
probably benign |
0.12 |
R8902:Or2y1b
|
UTSW |
11 |
49,209,206 (GRCm39) |
missense |
probably benign |
0.03 |
R9003:Or2y1b
|
UTSW |
11 |
49,209,155 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9431:Or2y1b
|
UTSW |
11 |
49,208,459 (GRCm39) |
missense |
probably benign |
|
R9696:Or2y1b
|
UTSW |
11 |
49,208,390 (GRCm39) |
missense |
probably benign |
|
|