Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
T |
C |
16: 90,852,654 (GRCm39) |
S161G |
probably benign |
Het |
Ankfy1 |
G |
A |
11: 72,621,308 (GRCm39) |
R198Q |
possibly damaging |
Het |
Ankrd11 |
A |
G |
8: 123,616,919 (GRCm39) |
V2290A |
probably benign |
Het |
Aox4 |
A |
G |
1: 58,252,212 (GRCm39) |
N29S |
probably benign |
Het |
Arhgap17 |
T |
C |
7: 122,891,379 (GRCm39) |
R592G |
possibly damaging |
Het |
Caap1 |
A |
T |
4: 94,389,640 (GRCm39) |
D231E |
possibly damaging |
Het |
Cabp1 |
T |
A |
5: 115,307,193 (GRCm39) |
M165L |
possibly damaging |
Het |
Calhm4 |
T |
A |
10: 33,917,630 (GRCm39) |
R274* |
probably null |
Het |
Cep72 |
A |
T |
13: 74,206,582 (GRCm39) |
L73H |
probably damaging |
Het |
Cfap74 |
A |
G |
4: 155,525,743 (GRCm39) |
S731G |
probably null |
Het |
Dsc2 |
T |
C |
18: 20,179,295 (GRCm39) |
I258V |
probably benign |
Het |
Dsg1c |
T |
G |
18: 20,407,687 (GRCm39) |
N344K |
probably benign |
Het |
Enah |
A |
G |
1: 181,841,920 (GRCm39) |
|
probably benign |
Het |
Fbn1 |
T |
A |
2: 125,225,591 (GRCm39) |
S554C |
probably damaging |
Het |
Fkrp |
C |
A |
7: 16,545,037 (GRCm39) |
R275L |
possibly damaging |
Het |
Gbp4 |
C |
T |
5: 105,270,986 (GRCm39) |
G215D |
possibly damaging |
Het |
Gli2 |
G |
A |
1: 118,783,284 (GRCm39) |
L239F |
probably damaging |
Het |
Gpr146 |
A |
G |
5: 139,378,573 (GRCm39) |
D125G |
probably damaging |
Het |
Hectd4 |
C |
A |
5: 121,494,259 (GRCm39) |
|
probably null |
Het |
Invs |
G |
A |
4: 48,397,534 (GRCm39) |
V370I |
possibly damaging |
Het |
Kdm2b |
A |
G |
5: 123,018,302 (GRCm39) |
V1040A |
probably damaging |
Het |
Kidins220 |
T |
A |
12: 25,088,434 (GRCm39) |
V1059D |
possibly damaging |
Het |
Kif26a |
T |
A |
12: 112,141,926 (GRCm39) |
S727T |
probably damaging |
Het |
Kifbp |
T |
C |
10: 62,410,813 (GRCm39) |
|
probably null |
Het |
Klk1b27 |
A |
G |
7: 43,705,169 (GRCm39) |
H112R |
probably benign |
Het |
Krt72 |
T |
G |
15: 101,685,187 (GRCm39) |
|
probably null |
Het |
Lactb |
C |
T |
9: 66,878,172 (GRCm39) |
R219H |
probably damaging |
Het |
Lrig2 |
A |
T |
3: 104,373,045 (GRCm39) |
I612N |
probably damaging |
Het |
Meaf6 |
A |
C |
4: 124,983,697 (GRCm39) |
N51T |
probably damaging |
Het |
Mtap |
A |
G |
4: 89,066,498 (GRCm39) |
T36A |
possibly damaging |
Het |
Myo3a |
G |
A |
2: 22,412,143 (GRCm39) |
G713S |
probably damaging |
Het |
Nr4a3 |
C |
T |
4: 48,083,255 (GRCm39) |
T596I |
probably damaging |
Het |
Or10ak14 |
A |
T |
4: 118,611,224 (GRCm39) |
C172* |
probably null |
Het |
Or4f14 |
C |
G |
2: 111,743,228 (GRCm39) |
G16R |
possibly damaging |
Het |
Pam |
A |
G |
1: 97,765,752 (GRCm39) |
V759A |
possibly damaging |
Het |
Pcare |
T |
A |
17: 72,051,701 (GRCm39) |
E1217V |
probably damaging |
Het |
Pds5a |
T |
A |
5: 65,772,944 (GRCm39) |
I1220F |
probably benign |
Het |
Phldb2 |
T |
A |
16: 45,568,240 (GRCm39) |
M1222L |
possibly damaging |
Het |
Phospho1 |
C |
T |
11: 95,721,513 (GRCm39) |
A61V |
possibly damaging |
Het |
Pnpla7 |
G |
A |
2: 24,906,550 (GRCm39) |
V638I |
possibly damaging |
Het |
Pramel34 |
C |
A |
5: 93,785,391 (GRCm39) |
|
probably null |
Het |
Ptf1a |
T |
A |
2: 19,451,848 (GRCm39) |
D282E |
probably damaging |
Het |
Ptgs2 |
A |
T |
1: 149,975,879 (GRCm39) |
|
probably benign |
Het |
Racgap1 |
T |
C |
15: 99,522,156 (GRCm39) |
R471G |
probably damaging |
Het |
Rptn |
T |
C |
3: 93,303,419 (GRCm39) |
S251P |
possibly damaging |
Het |
Shcbp1 |
T |
C |
8: 4,794,507 (GRCm39) |
M429V |
probably benign |
Het |
Shprh |
T |
C |
10: 11,062,637 (GRCm39) |
L1248P |
probably damaging |
Het |
Sppl3 |
T |
C |
5: 115,233,995 (GRCm39) |
L355P |
probably damaging |
Het |
Tbc1d31 |
A |
T |
15: 57,818,778 (GRCm39) |
R794W |
probably damaging |
Het |
Telo2 |
T |
C |
17: 25,320,386 (GRCm39) |
Y766C |
probably damaging |
Het |
Tfr2 |
A |
G |
5: 137,572,793 (GRCm39) |
|
probably null |
Het |
Tle4 |
T |
C |
19: 14,429,056 (GRCm39) |
D722G |
probably damaging |
Het |
Tprg1l |
A |
G |
4: 154,243,862 (GRCm39) |
V98A |
probably benign |
Het |
Trak1 |
C |
T |
9: 121,272,822 (GRCm39) |
R237C |
probably benign |
Het |
Vmn2r113 |
T |
C |
17: 23,177,715 (GRCm39) |
I833T |
probably damaging |
Het |
Vmn2r118 |
T |
A |
17: 55,915,093 (GRCm39) |
S518C |
probably damaging |
Het |
Vmn2r49 |
A |
G |
7: 9,710,524 (GRCm39) |
I736T |
probably damaging |
Het |
Wdr38 |
T |
A |
2: 38,889,970 (GRCm39) |
|
probably null |
Het |
Wee2 |
A |
G |
6: 40,429,553 (GRCm39) |
E180G |
probably benign |
Het |
Zbtb1 |
T |
C |
12: 76,432,604 (GRCm39) |
S197P |
possibly damaging |
Het |
Zc3h7a |
T |
C |
16: 10,976,629 (GRCm39) |
|
probably null |
Het |
Zfp516 |
T |
A |
18: 82,973,835 (GRCm39) |
L11Q |
probably damaging |
Het |
Zfp623 |
G |
A |
15: 75,819,317 (GRCm39) |
R91H |
probably benign |
Het |
Zkscan7 |
G |
A |
9: 122,725,170 (GRCm39) |
R713Q |
probably benign |
Het |
|
Other mutations in Son |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00531:Son
|
APN |
16 |
91,461,210 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01024:Son
|
APN |
16 |
91,452,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01066:Son
|
APN |
16 |
91,457,024 (GRCm39) |
intron |
probably benign |
|
IGL01083:Son
|
APN |
16 |
91,454,279 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01115:Son
|
APN |
16 |
91,456,346 (GRCm39) |
missense |
probably benign |
0.31 |
IGL01467:Son
|
APN |
16 |
91,454,165 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01506:Son
|
APN |
16 |
91,454,174 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01933:Son
|
APN |
16 |
91,454,903 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02156:Son
|
APN |
16 |
91,452,992 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02473:Son
|
APN |
16 |
91,455,683 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02498:Son
|
APN |
16 |
91,453,713 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02517:Son
|
APN |
16 |
91,452,099 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02530:Son
|
APN |
16 |
91,455,359 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02865:Son
|
APN |
16 |
91,448,640 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03180:Son
|
APN |
16 |
91,453,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Son
|
UTSW |
16 |
91,448,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R0036:Son
|
UTSW |
16 |
91,457,054 (GRCm39) |
intron |
probably benign |
|
R0037:Son
|
UTSW |
16 |
91,461,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Son
|
UTSW |
16 |
91,456,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0048:Son
|
UTSW |
16 |
91,455,865 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0056:Son
|
UTSW |
16 |
91,475,043 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0227:Son
|
UTSW |
16 |
91,453,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R0256:Son
|
UTSW |
16 |
91,453,472 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0302:Son
|
UTSW |
16 |
91,453,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R0815:Son
|
UTSW |
16 |
91,452,372 (GRCm39) |
missense |
probably damaging |
0.98 |
R1225:Son
|
UTSW |
16 |
91,454,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R1255:Son
|
UTSW |
16 |
91,461,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1457:Son
|
UTSW |
16 |
91,453,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1459:Son
|
UTSW |
16 |
91,452,230 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1535:Son
|
UTSW |
16 |
91,456,622 (GRCm39) |
missense |
probably damaging |
0.99 |
R1587:Son
|
UTSW |
16 |
91,456,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R1605:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R1629:Son
|
UTSW |
16 |
91,454,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Son
|
UTSW |
16 |
91,457,114 (GRCm39) |
intron |
probably benign |
|
R2138:Son
|
UTSW |
16 |
91,456,260 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2245:Son
|
UTSW |
16 |
91,444,848 (GRCm39) |
splice site |
probably null |
|
R2351:Son
|
UTSW |
16 |
91,454,547 (GRCm39) |
missense |
probably damaging |
0.98 |
R2434:Son
|
UTSW |
16 |
91,451,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2871:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2872:Son
|
UTSW |
16 |
91,461,205 (GRCm39) |
splice site |
probably null |
|
R2889:Son
|
UTSW |
16 |
91,456,787 (GRCm39) |
unclassified |
probably benign |
|
R3712:Son
|
UTSW |
16 |
91,453,614 (GRCm39) |
missense |
probably damaging |
0.99 |
R3913:Son
|
UTSW |
16 |
91,456,999 (GRCm39) |
intron |
probably benign |
|
R4172:Son
|
UTSW |
16 |
91,456,250 (GRCm39) |
missense |
probably damaging |
1.00 |
R4301:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4302:Son
|
UTSW |
16 |
91,455,299 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4770:Son
|
UTSW |
16 |
91,455,756 (GRCm39) |
missense |
probably damaging |
0.96 |
R4881:Son
|
UTSW |
16 |
91,472,397 (GRCm39) |
missense |
probably benign |
0.31 |
R5020:Son
|
UTSW |
16 |
91,453,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Son
|
UTSW |
16 |
91,454,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R5151:Son
|
UTSW |
16 |
91,452,587 (GRCm39) |
missense |
probably damaging |
1.00 |
R5153:Son
|
UTSW |
16 |
91,451,910 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5215:Son
|
UTSW |
16 |
91,453,563 (GRCm39) |
missense |
probably damaging |
0.99 |
R5243:Son
|
UTSW |
16 |
91,451,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R5354:Son
|
UTSW |
16 |
91,452,627 (GRCm39) |
missense |
probably damaging |
0.99 |
R5529:Son
|
UTSW |
16 |
91,452,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R5696:Son
|
UTSW |
16 |
91,468,301 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5763:Son
|
UTSW |
16 |
91,454,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R5766:Son
|
UTSW |
16 |
91,461,875 (GRCm39) |
intron |
probably benign |
|
R5788:Son
|
UTSW |
16 |
91,456,940 (GRCm39) |
intron |
probably benign |
|
R5992:Son
|
UTSW |
16 |
91,455,792 (GRCm39) |
missense |
probably benign |
0.04 |
R6314:Son
|
UTSW |
16 |
91,457,298 (GRCm39) |
intron |
probably benign |
|
R6371:Son
|
UTSW |
16 |
91,471,629 (GRCm39) |
|
|
|
R6429:Son
|
UTSW |
16 |
91,455,054 (GRCm39) |
missense |
probably benign |
0.33 |
R6451:Son
|
UTSW |
16 |
91,454,490 (GRCm39) |
missense |
probably damaging |
0.99 |
R6489:Son
|
UTSW |
16 |
91,452,044 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6753:Son
|
UTSW |
16 |
91,454,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R6916:Son
|
UTSW |
16 |
91,451,673 (GRCm39) |
missense |
probably damaging |
0.97 |
R7070:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7079:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7110:Son
|
UTSW |
16 |
91,453,406 (GRCm39) |
missense |
probably benign |
0.01 |
R7120:Son
|
UTSW |
16 |
91,467,414 (GRCm39) |
missense |
unknown |
|
R7120:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7167:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7205:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7208:Son
|
UTSW |
16 |
91,458,990 (GRCm39) |
missense |
unknown |
|
R7219:Son
|
UTSW |
16 |
91,461,889 (GRCm39) |
missense |
unknown |
|
R7249:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7328:Son
|
UTSW |
16 |
91,455,278 (GRCm39) |
missense |
probably benign |
0.33 |
R7330:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7374:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7405:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7420:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7424:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7464:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7514:Son
|
UTSW |
16 |
91,451,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R7555:Son
|
UTSW |
16 |
91,455,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R7645:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R7716:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R7718:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7778:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7824:Son
|
UTSW |
16 |
91,453,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R7856:Son
|
UTSW |
16 |
91,456,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Son
|
UTSW |
16 |
91,453,486 (GRCm39) |
unclassified |
probably benign |
|
R7928:Son
|
UTSW |
16 |
91,453,729 (GRCm39) |
unclassified |
probably benign |
|
R7972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R7978:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8000:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8192:Son
|
UTSW |
16 |
91,452,437 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8221:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8227:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8233:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8255:Son
|
UTSW |
16 |
91,461,824 (GRCm39) |
missense |
unknown |
|
R8292:Son
|
UTSW |
16 |
91,453,545 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8407:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8468:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R8495:Son
|
UTSW |
16 |
91,457,183 (GRCm39) |
small deletion |
probably benign |
|
R8772:Son
|
UTSW |
16 |
91,454,826 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8796:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8862:Son
|
UTSW |
16 |
91,453,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8962:Son
|
UTSW |
16 |
91,455,057 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8972:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R8991:Son
|
UTSW |
16 |
91,453,608 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8991:Son
|
UTSW |
16 |
91,453,366 (GRCm39) |
missense |
probably benign |
0.04 |
R9086:Son
|
UTSW |
16 |
91,467,418 (GRCm39) |
missense |
unknown |
|
R9138:Son
|
UTSW |
16 |
91,452,006 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9232:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9241:Son
|
UTSW |
16 |
91,454,122 (GRCm39) |
missense |
probably damaging |
0.96 |
R9258:Son
|
UTSW |
16 |
91,474,570 (GRCm39) |
missense |
unknown |
|
R9328:Son
|
UTSW |
16 |
91,452,645 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9420:Son
|
UTSW |
16 |
91,454,508 (GRCm39) |
missense |
probably damaging |
0.98 |
R9468:Son
|
UTSW |
16 |
91,454,439 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9500:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9516:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9595:Son
|
UTSW |
16 |
91,454,241 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9679:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9719:Son
|
UTSW |
16 |
91,456,440 (GRCm39) |
missense |
probably damaging |
0.96 |
R9749:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
R9772:Son
|
UTSW |
16 |
91,457,222 (GRCm39) |
small deletion |
probably benign |
|
R9782:Son
|
UTSW |
16 |
91,444,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R9788:Son
|
UTSW |
16 |
91,453,699 (GRCm39) |
unclassified |
probably benign |
|
RF007:Son
|
UTSW |
16 |
91,456,257 (GRCm39) |
missense |
possibly damaging |
0.53 |
RF041:Son
|
UTSW |
16 |
91,453,579 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Son
|
UTSW |
16 |
91,452,689 (GRCm39) |
missense |
possibly damaging |
0.80 |
|