Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
A |
T |
16: 90,853,096 (GRCm39) |
S13R |
probably benign |
Het |
Amn1 |
A |
T |
6: 149,084,983 (GRCm39) |
D32E |
probably damaging |
Het |
Asph |
T |
C |
4: 9,635,927 (GRCm39) |
D108G |
probably damaging |
Het |
C1rb |
T |
C |
6: 124,557,336 (GRCm39) |
L491P |
probably damaging |
Het |
Cep120 |
G |
A |
18: 53,839,984 (GRCm39) |
R759* |
probably null |
Het |
Chmp6 |
C |
T |
11: 119,806,288 (GRCm39) |
T38M |
possibly damaging |
Het |
Comtd1 |
A |
G |
14: 21,898,867 (GRCm39) |
F25S |
possibly damaging |
Het |
Dthd1 |
G |
A |
5: 62,975,904 (GRCm39) |
G193R |
possibly damaging |
Het |
Dyrk1a |
T |
A |
16: 94,474,330 (GRCm39) |
S362R |
probably damaging |
Het |
Ecm2 |
A |
G |
13: 49,683,792 (GRCm39) |
D590G |
probably benign |
Het |
Exd1 |
A |
T |
2: 119,354,180 (GRCm39) |
W293R |
probably damaging |
Het |
Fam110a |
C |
T |
2: 151,812,116 (GRCm39) |
R218Q |
probably benign |
Het |
Fga |
A |
T |
3: 82,940,610 (GRCm39) |
N755Y |
probably damaging |
Het |
Fstl4 |
C |
A |
11: 52,891,102 (GRCm39) |
T80K |
probably benign |
Het |
Gbp5 |
A |
G |
3: 142,208,783 (GRCm39) |
K109E |
probably benign |
Het |
Gucy2g |
A |
G |
19: 55,190,607 (GRCm39) |
V1009A |
probably null |
Het |
Herc6 |
C |
T |
6: 57,602,955 (GRCm39) |
Q545* |
probably null |
Het |
Hpd |
T |
A |
5: 123,318,794 (GRCm39) |
|
probably null |
Het |
Il4 |
C |
T |
11: 53,504,837 (GRCm39) |
R76H |
probably damaging |
Het |
Inpp4b |
T |
C |
8: 82,497,522 (GRCm39) |
V114A |
probably damaging |
Het |
Ints14 |
A |
G |
9: 64,891,314 (GRCm39) |
T432A |
probably benign |
Het |
Isoc1 |
G |
A |
18: 58,804,350 (GRCm39) |
R126H |
probably damaging |
Het |
Klb |
G |
T |
5: 65,533,044 (GRCm39) |
R451L |
possibly damaging |
Het |
Lrtm2 |
C |
T |
6: 119,297,948 (GRCm39) |
C31Y |
probably benign |
Het |
Mkrn3 |
T |
C |
7: 62,069,288 (GRCm39) |
I168V |
probably benign |
Het |
Mlph |
C |
T |
1: 90,867,088 (GRCm39) |
T370I |
probably benign |
Het |
Naaladl1 |
A |
T |
19: 6,162,725 (GRCm39) |
I478F |
probably damaging |
Het |
Neb |
A |
T |
2: 52,065,157 (GRCm39) |
H6251Q |
probably benign |
Het |
Nom1 |
C |
T |
5: 29,639,766 (GRCm39) |
R31C |
probably benign |
Het |
Nup153 |
A |
C |
13: 46,840,642 (GRCm39) |
F989V |
probably damaging |
Het |
Nup188 |
T |
C |
2: 30,220,777 (GRCm39) |
|
probably null |
Het |
Or4c12 |
T |
C |
2: 89,773,569 (GRCm39) |
K297E |
probably benign |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Or6c210 |
A |
G |
10: 129,495,938 (GRCm39) |
T88A |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,893,883 (GRCm39) |
|
probably benign |
Het |
Pcare |
T |
C |
17: 72,057,983 (GRCm39) |
T565A |
probably benign |
Het |
Pcdhb4 |
T |
C |
18: 37,442,781 (GRCm39) |
V697A |
possibly damaging |
Het |
Pds5a |
G |
T |
5: 65,823,600 (GRCm39) |
Q64K |
probably benign |
Het |
Pmpcb |
T |
C |
5: 21,953,810 (GRCm39) |
F353L |
probably damaging |
Het |
Pus10 |
G |
A |
11: 23,656,937 (GRCm39) |
C221Y |
probably damaging |
Het |
Qrfp |
A |
G |
2: 31,698,749 (GRCm39) |
V61A |
possibly damaging |
Het |
Runx1t1 |
A |
G |
4: 13,865,932 (GRCm39) |
I393M |
probably benign |
Het |
Sh2d5 |
T |
G |
4: 137,985,481 (GRCm39) |
S310A |
probably benign |
Het |
Shisa9 |
A |
G |
16: 12,085,408 (GRCm39) |
E339G |
possibly damaging |
Het |
Slc26a10 |
C |
T |
10: 127,009,239 (GRCm39) |
E641K |
probably benign |
Het |
Slc5a6 |
A |
G |
5: 31,197,803 (GRCm39) |
V302A |
possibly damaging |
Het |
Tdrd7 |
T |
A |
4: 46,005,416 (GRCm39) |
D407E |
probably damaging |
Het |
Trp53 |
A |
T |
11: 69,478,394 (GRCm39) |
Q101L |
probably benign |
Het |
Tsc2 |
T |
A |
17: 24,823,824 (GRCm39) |
N994Y |
probably damaging |
Het |
Ttc16 |
T |
G |
2: 32,657,195 (GRCm39) |
K577Q |
possibly damaging |
Het |
Vmn1r195 |
A |
G |
13: 22,462,535 (GRCm39) |
I2V |
probably benign |
Het |
Vmn2r83 |
G |
T |
10: 79,317,322 (GRCm39) |
E522* |
probably null |
Het |
Wdr48 |
T |
A |
9: 119,746,245 (GRCm39) |
F450L |
probably benign |
Het |
Wnt9a |
G |
A |
11: 59,218,592 (GRCm39) |
E100K |
possibly damaging |
Het |
Zfp729b |
A |
T |
13: 67,739,182 (GRCm39) |
S1028T |
probably benign |
Het |
Zfp729b |
C |
T |
13: 67,742,014 (GRCm39) |
V84I |
possibly damaging |
Het |
|
Other mutations in Mga |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00551:Mga
|
APN |
2 |
119,750,295 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL00719:Mga
|
APN |
2 |
119,777,934 (GRCm39) |
nonsense |
probably null |
|
IGL01619:Mga
|
APN |
2 |
119,762,309 (GRCm39) |
missense |
possibly damaging |
0.46 |
IGL01721:Mga
|
APN |
2 |
119,765,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01759:Mga
|
APN |
2 |
119,781,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01785:Mga
|
APN |
2 |
119,733,393 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01786:Mga
|
APN |
2 |
119,733,393 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01950:Mga
|
APN |
2 |
119,772,135 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01960:Mga
|
APN |
2 |
119,769,138 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02086:Mga
|
APN |
2 |
119,754,517 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02364:Mga
|
APN |
2 |
119,794,535 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02602:Mga
|
APN |
2 |
119,762,365 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02751:Mga
|
APN |
2 |
119,778,251 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02794:Mga
|
APN |
2 |
119,776,770 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03247:Mga
|
APN |
2 |
119,765,994 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL03303:Mga
|
APN |
2 |
119,733,933 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4515001:Mga
|
UTSW |
2 |
119,746,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R0060:Mga
|
UTSW |
2 |
119,791,442 (GRCm39) |
critical splice donor site |
probably null |
|
R0060:Mga
|
UTSW |
2 |
119,791,442 (GRCm39) |
critical splice donor site |
probably null |
|
R0417:Mga
|
UTSW |
2 |
119,733,271 (GRCm39) |
missense |
probably damaging |
0.99 |
R0449:Mga
|
UTSW |
2 |
119,771,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R0457:Mga
|
UTSW |
2 |
119,746,969 (GRCm39) |
missense |
probably damaging |
0.98 |
R0538:Mga
|
UTSW |
2 |
119,750,187 (GRCm39) |
critical splice donor site |
probably null |
|
R0568:Mga
|
UTSW |
2 |
119,765,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Mga
|
UTSW |
2 |
119,794,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R0671:Mga
|
UTSW |
2 |
119,750,391 (GRCm39) |
splice site |
probably null |
|
R0811:Mga
|
UTSW |
2 |
119,778,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R0812:Mga
|
UTSW |
2 |
119,778,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R0948:Mga
|
UTSW |
2 |
119,772,140 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1177:Mga
|
UTSW |
2 |
119,756,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1445:Mga
|
UTSW |
2 |
119,733,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Mga
|
UTSW |
2 |
119,772,156 (GRCm39) |
missense |
probably damaging |
0.96 |
R1527:Mga
|
UTSW |
2 |
119,747,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R1583:Mga
|
UTSW |
2 |
119,794,441 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1592:Mga
|
UTSW |
2 |
119,795,147 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1627:Mga
|
UTSW |
2 |
119,795,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R1658:Mga
|
UTSW |
2 |
119,772,170 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1677:Mga
|
UTSW |
2 |
119,791,333 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1887:Mga
|
UTSW |
2 |
119,754,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Mga
|
UTSW |
2 |
119,757,075 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1909:Mga
|
UTSW |
2 |
119,757,075 (GRCm39) |
missense |
possibly damaging |
0.66 |
R2061:Mga
|
UTSW |
2 |
119,795,461 (GRCm39) |
unclassified |
probably benign |
|
R2145:Mga
|
UTSW |
2 |
119,794,638 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2159:Mga
|
UTSW |
2 |
119,750,124 (GRCm39) |
missense |
probably damaging |
0.96 |
R2179:Mga
|
UTSW |
2 |
119,790,923 (GRCm39) |
missense |
probably damaging |
0.99 |
R2281:Mga
|
UTSW |
2 |
119,734,204 (GRCm39) |
missense |
probably benign |
|
R2423:Mga
|
UTSW |
2 |
119,795,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R3620:Mga
|
UTSW |
2 |
119,747,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R3622:Mga
|
UTSW |
2 |
119,772,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R3624:Mga
|
UTSW |
2 |
119,772,245 (GRCm39) |
missense |
probably damaging |
1.00 |
R3802:Mga
|
UTSW |
2 |
119,777,820 (GRCm39) |
missense |
probably damaging |
0.96 |
R4011:Mga
|
UTSW |
2 |
119,762,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R4065:Mga
|
UTSW |
2 |
119,777,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R4520:Mga
|
UTSW |
2 |
119,778,579 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4649:Mga
|
UTSW |
2 |
119,771,974 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4660:Mga
|
UTSW |
2 |
119,769,104 (GRCm39) |
intron |
probably benign |
|
R4757:Mga
|
UTSW |
2 |
119,734,120 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4771:Mga
|
UTSW |
2 |
119,794,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R4784:Mga
|
UTSW |
2 |
119,733,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R4866:Mga
|
UTSW |
2 |
119,794,535 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4900:Mga
|
UTSW |
2 |
119,794,535 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4952:Mga
|
UTSW |
2 |
119,733,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R4995:Mga
|
UTSW |
2 |
119,763,063 (GRCm39) |
nonsense |
probably null |
|
R5020:Mga
|
UTSW |
2 |
119,781,654 (GRCm39) |
nonsense |
probably null |
|
R5082:Mga
|
UTSW |
2 |
119,733,825 (GRCm39) |
missense |
probably damaging |
0.98 |
R5208:Mga
|
UTSW |
2 |
119,778,462 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5454:Mga
|
UTSW |
2 |
119,733,810 (GRCm39) |
missense |
probably damaging |
0.99 |
R5466:Mga
|
UTSW |
2 |
119,733,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R5484:Mga
|
UTSW |
2 |
119,747,107 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5669:Mga
|
UTSW |
2 |
119,733,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R5819:Mga
|
UTSW |
2 |
119,771,744 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5916:Mga
|
UTSW |
2 |
119,794,793 (GRCm39) |
missense |
probably benign |
0.27 |
R5942:Mga
|
UTSW |
2 |
119,777,440 (GRCm39) |
missense |
probably benign |
0.41 |
R6305:Mga
|
UTSW |
2 |
119,778,179 (GRCm39) |
missense |
probably benign |
0.00 |
R6434:Mga
|
UTSW |
2 |
119,754,419 (GRCm39) |
missense |
probably damaging |
0.99 |
R6467:Mga
|
UTSW |
2 |
119,776,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6488:Mga
|
UTSW |
2 |
119,791,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R6630:Mga
|
UTSW |
2 |
119,754,140 (GRCm39) |
missense |
probably damaging |
0.99 |
R6790:Mga
|
UTSW |
2 |
119,754,235 (GRCm39) |
missense |
probably damaging |
0.99 |
R7029:Mga
|
UTSW |
2 |
119,754,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R7039:Mga
|
UTSW |
2 |
119,763,159 (GRCm39) |
missense |
probably benign |
0.28 |
R7088:Mga
|
UTSW |
2 |
119,792,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R7195:Mga
|
UTSW |
2 |
119,747,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R7273:Mga
|
UTSW |
2 |
119,765,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R7286:Mga
|
UTSW |
2 |
119,795,269 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7346:Mga
|
UTSW |
2 |
119,766,008 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7383:Mga
|
UTSW |
2 |
119,790,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R7469:Mga
|
UTSW |
2 |
119,733,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7484:Mga
|
UTSW |
2 |
119,776,710 (GRCm39) |
missense |
probably damaging |
0.99 |
R7537:Mga
|
UTSW |
2 |
119,766,032 (GRCm39) |
missense |
probably damaging |
0.97 |
R7781:Mga
|
UTSW |
2 |
119,747,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7921:Mga
|
UTSW |
2 |
119,750,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R8165:Mga
|
UTSW |
2 |
119,777,719 (GRCm39) |
missense |
probably benign |
0.12 |
R8226:Mga
|
UTSW |
2 |
119,790,866 (GRCm39) |
missense |
probably benign |
0.33 |
R8305:Mga
|
UTSW |
2 |
119,776,800 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8309:Mga
|
UTSW |
2 |
119,791,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R8363:Mga
|
UTSW |
2 |
119,794,407 (GRCm39) |
missense |
probably benign |
0.43 |
R8388:Mga
|
UTSW |
2 |
119,794,562 (GRCm39) |
missense |
probably benign |
0.00 |
R8524:Mga
|
UTSW |
2 |
119,771,997 (GRCm39) |
missense |
probably damaging |
0.97 |
R8693:Mga
|
UTSW |
2 |
119,794,407 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8837:Mga
|
UTSW |
2 |
119,769,272 (GRCm39) |
splice site |
probably benign |
|
R8916:Mga
|
UTSW |
2 |
119,788,819 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8936:Mga
|
UTSW |
2 |
119,794,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R9028:Mga
|
UTSW |
2 |
119,778,070 (GRCm39) |
missense |
probably benign |
|
R9145:Mga
|
UTSW |
2 |
119,794,493 (GRCm39) |
missense |
probably benign |
|
R9155:Mga
|
UTSW |
2 |
119,757,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R9308:Mga
|
UTSW |
2 |
119,754,369 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9342:Mga
|
UTSW |
2 |
119,778,656 (GRCm39) |
missense |
probably benign |
|
R9347:Mga
|
UTSW |
2 |
119,733,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R9408:Mga
|
UTSW |
2 |
119,765,999 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9488:Mga
|
UTSW |
2 |
119,795,304 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9495:Mga
|
UTSW |
2 |
119,781,676 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9521:Mga
|
UTSW |
2 |
119,794,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R9780:Mga
|
UTSW |
2 |
119,747,253 (GRCm39) |
missense |
probably benign |
0.26 |
|