Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl4 |
A |
T |
4: 144,349,550 (GRCm39) |
N269I |
possibly damaging |
Het |
Abcc1 |
G |
T |
16: 14,283,006 (GRCm39) |
V1161F |
possibly damaging |
Het |
Adam3 |
A |
T |
8: 25,174,555 (GRCm39) |
|
probably null |
Het |
Agt |
A |
T |
8: 125,290,597 (GRCm39) |
S237T |
possibly damaging |
Het |
Ano3 |
A |
T |
2: 110,512,181 (GRCm39) |
F674L |
probably benign |
Het |
Asb2 |
G |
T |
12: 103,290,135 (GRCm39) |
A504E |
probably damaging |
Het |
Atp13a1 |
T |
A |
8: 70,259,748 (GRCm39) |
I1113N |
probably damaging |
Het |
Atxn7l2 |
T |
C |
3: 108,112,978 (GRCm39) |
|
probably null |
Het |
Bambi |
A |
G |
18: 3,511,463 (GRCm39) |
T95A |
probably benign |
Het |
Cfap210 |
A |
T |
2: 69,619,806 (GRCm39) |
M1K |
probably null |
Het |
Clrn1 |
T |
C |
3: 58,753,783 (GRCm39) |
T193A |
probably benign |
Het |
Colgalt2 |
T |
A |
1: 152,379,873 (GRCm39) |
D437E |
probably damaging |
Het |
Dchs1 |
C |
A |
7: 105,408,373 (GRCm39) |
A1820S |
probably damaging |
Het |
Dnah12 |
T |
A |
14: 26,428,073 (GRCm39) |
I233N |
possibly damaging |
Het |
Dsc3 |
T |
C |
18: 20,120,077 (GRCm39) |
N194D |
probably damaging |
Het |
Dync2h1 |
A |
G |
9: 7,102,309 (GRCm39) |
|
probably null |
Het |
Erich3 |
A |
T |
3: 154,401,460 (GRCm39) |
R36S |
probably damaging |
Het |
Fam243 |
T |
A |
16: 92,117,559 (GRCm39) |
E243V |
probably damaging |
Het |
Fmnl3 |
A |
T |
15: 99,219,709 (GRCm39) |
C680S |
probably damaging |
Het |
Focad |
T |
C |
4: 88,275,778 (GRCm39) |
L1129P |
unknown |
Het |
Fzd3 |
G |
A |
14: 65,440,178 (GRCm39) |
T664I |
probably benign |
Het |
Glb1l3 |
T |
C |
9: 26,766,032 (GRCm39) |
I129V |
probably benign |
Het |
Heatr1 |
T |
C |
13: 12,449,352 (GRCm39) |
F1950S |
probably damaging |
Het |
Herc6 |
G |
A |
6: 57,623,188 (GRCm39) |
G597E |
probably benign |
Het |
Hmcn2 |
T |
A |
2: 31,286,151 (GRCm39) |
V2101D |
probably damaging |
Het |
Il17re |
T |
A |
6: 113,447,084 (GRCm39) |
C612S |
probably damaging |
Het |
Il36g |
T |
G |
2: 24,082,806 (GRCm39) |
*194E |
probably null |
Het |
Junb |
T |
C |
8: 85,704,505 (GRCm39) |
Y185C |
probably benign |
Het |
Lrriq1 |
G |
A |
10: 103,057,243 (GRCm39) |
Q186* |
probably null |
Het |
Lrrn2 |
T |
A |
1: 132,865,538 (GRCm39) |
V201E |
probably damaging |
Het |
Ly6l |
A |
T |
15: 75,323,027 (GRCm39) |
T68S |
probably benign |
Het |
Marchf1 |
G |
T |
8: 66,839,763 (GRCm39) |
R182L |
possibly damaging |
Het |
Megf6 |
A |
G |
4: 154,333,882 (GRCm39) |
|
probably null |
Het |
Mx1 |
T |
C |
16: 97,252,933 (GRCm39) |
T396A |
probably benign |
Het |
Naip5 |
A |
C |
13: 100,359,209 (GRCm39) |
S676A |
probably benign |
Het |
Npepl1 |
G |
T |
2: 173,963,337 (GRCm39) |
W456C |
probably benign |
Het |
Ntrk2 |
A |
G |
13: 58,956,543 (GRCm39) |
M1V |
probably null |
Het |
Nufip1 |
T |
C |
14: 76,372,340 (GRCm39) |
*485Q |
probably null |
Het |
Ocln |
T |
G |
13: 100,642,687 (GRCm39) |
D216A |
possibly damaging |
Het |
Or10x1 |
A |
T |
1: 174,196,698 (GRCm39) |
T72S |
probably damaging |
Het |
Or1o11 |
C |
T |
17: 37,756,570 (GRCm39) |
L53F |
probably benign |
Het |
Or4f57 |
A |
G |
2: 111,791,175 (GRCm39) |
M81T |
probably damaging |
Het |
Or55b4 |
G |
A |
7: 102,133,586 (GRCm39) |
S247F |
probably damaging |
Het |
Ptprq |
A |
T |
10: 107,359,374 (GRCm39) |
M2243K |
probably damaging |
Het |
Rad51b |
C |
T |
12: 79,371,856 (GRCm39) |
Q190* |
probably null |
Het |
Resf1 |
C |
T |
6: 149,228,076 (GRCm39) |
T374I |
probably damaging |
Het |
Rfx8 |
T |
C |
1: 39,727,779 (GRCm39) |
Y182C |
probably benign |
Het |
Rpgrip1l |
C |
A |
8: 91,979,541 (GRCm39) |
R967L |
possibly damaging |
Het |
Scube2 |
A |
G |
7: 109,430,931 (GRCm39) |
Y423H |
possibly damaging |
Het |
Sipa1l2 |
A |
T |
8: 126,195,312 (GRCm39) |
Y809N |
probably damaging |
Het |
Slc35f1 |
C |
A |
10: 52,809,317 (GRCm39) |
Y101* |
probably null |
Het |
Tbc1d22a |
A |
G |
15: 86,098,809 (GRCm39) |
K12E |
possibly damaging |
Het |
Tent2 |
T |
C |
13: 93,312,055 (GRCm39) |
D215G |
probably damaging |
Het |
Tmcc2 |
C |
T |
1: 132,285,429 (GRCm39) |
V646M |
probably damaging |
Het |
Tpp1 |
A |
T |
7: 105,398,587 (GRCm39) |
M243K |
probably damaging |
Het |
Trappc12 |
A |
G |
12: 28,741,513 (GRCm39) |
L732P |
probably damaging |
Het |
U2af2 |
A |
T |
7: 5,082,179 (GRCm39) |
|
probably null |
Het |
Utrn |
T |
A |
10: 12,540,795 (GRCm39) |
N1877Y |
probably damaging |
Het |
Vsir |
C |
T |
10: 60,193,816 (GRCm39) |
T93I |
probably damaging |
Het |
Zkscan5 |
T |
A |
5: 145,142,112 (GRCm39) |
M3K |
possibly damaging |
Het |
Zscan29 |
G |
T |
2: 120,994,518 (GRCm39) |
T489N |
probably 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 |
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 |
R9390:Mga
|
UTSW |
2 |
119,794,332 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|