Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,911,447 (GRCm39) |
T1344A |
probably benign |
Het |
Actrt3 |
T |
A |
3: 30,652,876 (GRCm39) |
I73F |
probably damaging |
Het |
Ankrd24 |
T |
C |
10: 81,482,196 (GRCm39) |
S915P |
possibly damaging |
Het |
Ano1 |
A |
T |
7: 144,209,358 (GRCm39) |
F281I |
probably damaging |
Het |
Arhgap42 |
A |
G |
9: 9,059,102 (GRCm39) |
V148A |
probably benign |
Het |
Arnt2 |
A |
G |
7: 83,954,426 (GRCm39) |
I256T |
probably benign |
Het |
Bloc1s3 |
G |
A |
7: 19,241,408 (GRCm39) |
S40L |
possibly damaging |
Het |
Cep68 |
G |
A |
11: 20,192,142 (GRCm39) |
P19L |
probably benign |
Het |
Chst9 |
T |
A |
18: 15,586,221 (GRCm39) |
Q114L |
probably benign |
Het |
Cpa2 |
T |
A |
6: 30,545,536 (GRCm39) |
F106I |
probably benign |
Het |
Cplane1 |
A |
G |
15: 8,258,123 (GRCm39) |
E2123G |
probably benign |
Het |
Crocc |
T |
C |
4: 140,756,556 (GRCm39) |
D1187G |
probably benign |
Het |
Dhx8 |
A |
T |
11: 101,632,403 (GRCm39) |
D454V |
possibly damaging |
Het |
Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 72,684,217 (GRCm39) |
|
probably benign |
Het |
Eif3a |
A |
T |
19: 60,766,398 (GRCm39) |
L310H |
probably damaging |
Het |
Ergic3 |
C |
A |
2: 155,853,164 (GRCm39) |
Y202* |
probably null |
Het |
Fam117a |
A |
T |
11: 95,268,309 (GRCm39) |
I237L |
possibly damaging |
Het |
Fcsk |
T |
C |
8: 111,613,743 (GRCm39) |
M773V |
probably benign |
Het |
Gcnt4 |
T |
A |
13: 97,083,948 (GRCm39) |
S415T |
probably benign |
Het |
Hacl1 |
C |
A |
14: 31,362,519 (GRCm39) |
V43L |
possibly damaging |
Het |
Hbb-bh2 |
A |
G |
7: 103,489,624 (GRCm39) |
L4P |
probably damaging |
Het |
Hmbs |
A |
G |
9: 44,247,985 (GRCm39) |
L357P |
probably damaging |
Het |
Hpcal1 |
A |
G |
12: 17,836,494 (GRCm39) |
Y108C |
probably damaging |
Het |
Hspa14 |
A |
T |
2: 3,490,741 (GRCm39) |
M482K |
probably damaging |
Het |
Ifi27l2b |
G |
T |
12: 103,417,461 (GRCm39) |
P242Q |
unknown |
Het |
Insyn1 |
A |
G |
9: 58,406,881 (GRCm39) |
N264D |
probably damaging |
Het |
Itpr1 |
T |
C |
6: 108,487,795 (GRCm39) |
V2407A |
probably benign |
Het |
Lcp1 |
T |
C |
14: 75,440,178 (GRCm39) |
F154S |
probably damaging |
Het |
Lmod2 |
T |
C |
6: 24,604,233 (GRCm39) |
S403P |
probably damaging |
Het |
Lrrc63 |
G |
A |
14: 75,360,500 (GRCm39) |
A334V |
probably damaging |
Het |
Lrriq1 |
T |
A |
10: 103,025,824 (GRCm39) |
T933S |
probably damaging |
Het |
Msh4 |
T |
C |
3: 153,582,342 (GRCm39) |
Y510C |
probably damaging |
Het |
Myh11 |
T |
C |
16: 14,064,613 (GRCm39) |
K235R |
|
Het |
Nek2 |
A |
T |
1: 191,554,738 (GRCm39) |
D150V |
probably damaging |
Het |
Nfkbil1 |
C |
A |
17: 35,439,898 (GRCm39) |
R205L |
possibly damaging |
Het |
Nox3 |
A |
G |
17: 3,736,260 (GRCm39) |
F122S |
possibly damaging |
Het |
Nrxn1 |
A |
G |
17: 90,931,042 (GRCm39) |
V718A |
possibly damaging |
Het |
Oplah |
A |
G |
15: 76,181,940 (GRCm39) |
I1061T |
probably damaging |
Het |
Or13e8 |
G |
A |
4: 43,697,193 (GRCm39) |
|
probably benign |
Het |
Or2y16 |
G |
A |
11: 49,335,014 (GRCm39) |
C112Y |
possibly damaging |
Het |
Or51b17 |
A |
G |
7: 103,542,631 (GRCm39) |
S104P |
probably damaging |
Het |
Or9m1 |
A |
G |
2: 87,733,426 (GRCm39) |
L198P |
probably damaging |
Het |
Pcf11 |
A |
T |
7: 92,313,313 (GRCm39) |
D123E |
possibly damaging |
Het |
Pcna |
C |
T |
2: 132,094,794 (GRCm39) |
E55K |
probably benign |
Het |
Pip5k1c |
T |
C |
10: 81,141,030 (GRCm39) |
V46A |
probably benign |
Het |
Plce1 |
T |
G |
19: 38,609,134 (GRCm39) |
L481R |
possibly damaging |
Het |
Psma7 |
A |
T |
2: 179,678,339 (GRCm39) |
Y228N |
unknown |
Het |
Rcbtb1 |
T |
A |
14: 59,465,796 (GRCm39) |
Y380N |
probably benign |
Het |
Rin2 |
A |
T |
2: 145,718,551 (GRCm39) |
E677V |
probably damaging |
Het |
Scgb2b11 |
A |
G |
7: 31,909,861 (GRCm39) |
L75P |
probably damaging |
Het |
Scn4a |
A |
G |
11: 106,226,235 (GRCm39) |
V775A |
probably damaging |
Het |
Setx |
A |
G |
2: 29,016,999 (GRCm39) |
D34G |
possibly damaging |
Het |
Slc38a9 |
A |
T |
13: 112,862,591 (GRCm39) |
D430V |
probably damaging |
Het |
Snapc4 |
A |
T |
2: 26,267,019 (GRCm39) |
N77K |
possibly damaging |
Het |
Stk32a |
T |
G |
18: 43,375,049 (GRCm39) |
F20V |
probably benign |
Het |
Taf1b |
G |
A |
12: 24,564,818 (GRCm39) |
G145D |
probably damaging |
Het |
Tomt |
G |
C |
7: 101,549,536 (GRCm39) |
Q251E |
probably benign |
Het |
Tsc1 |
G |
A |
2: 28,565,761 (GRCm39) |
E471K |
probably damaging |
Het |
Ttll9 |
G |
A |
2: 152,836,023 (GRCm39) |
A256T |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,774,289 (GRCm39) |
C2252S |
probably benign |
Het |
Ttn |
A |
T |
2: 76,785,035 (GRCm39) |
D797E |
unknown |
Het |
Usf3 |
T |
A |
16: 44,039,181 (GRCm39) |
N1220K |
possibly damaging |
Het |
Usp22 |
A |
T |
11: 61,050,069 (GRCm39) |
H355Q |
probably benign |
Het |
Virma |
T |
A |
4: 11,513,442 (GRCm39) |
V432E |
possibly damaging |
Het |
Vtn |
A |
C |
11: 78,393,003 (GRCm39) |
D456A |
probably damaging |
Het |
Zbbx |
A |
G |
3: 74,945,359 (GRCm39) |
S688P |
probably damaging |
Het |
Zfhx2 |
C |
A |
14: 55,312,494 (GRCm39) |
D67Y |
probably benign |
Het |
Zfp87 |
T |
C |
13: 67,665,241 (GRCm39) |
H407R |
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 |
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 |
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 |
|