Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
T |
A |
6: 128,536,032 (GRCm39) |
H720L |
probably benign |
Het |
Abca15 |
T |
C |
7: 119,987,388 (GRCm39) |
Y1225H |
probably benign |
Het |
Adck1 |
C |
A |
12: 88,335,193 (GRCm39) |
N26K |
probably benign |
Het |
Adcy3 |
A |
G |
12: 4,245,208 (GRCm39) |
D382G |
probably damaging |
Het |
Ahi1 |
T |
A |
10: 20,876,488 (GRCm39) |
C800S |
probably benign |
Het |
Ahnak |
G |
T |
19: 8,992,287 (GRCm39) |
V4524L |
probably benign |
Het |
Aoc1l1 |
C |
A |
6: 48,952,890 (GRCm39) |
R272S |
probably benign |
Het |
Apol11a |
C |
T |
15: 77,397,778 (GRCm39) |
A43V |
probably benign |
Het |
Arid1a |
T |
C |
4: 133,421,214 (GRCm39) |
M479V |
unknown |
Het |
Atp13a2 |
T |
A |
4: 140,724,056 (GRCm39) |
C324S |
probably damaging |
Het |
C2cd2 |
T |
G |
16: 97,677,486 (GRCm39) |
T413P |
probably damaging |
Het |
Cct5 |
A |
C |
15: 31,591,107 (GRCm39) |
D531E |
|
Het |
Chst1 |
A |
T |
2: 92,444,523 (GRCm39) |
I332F |
probably damaging |
Het |
Col12a1 |
A |
T |
9: 79,527,344 (GRCm39) |
V2662D |
probably benign |
Het |
Cts3 |
A |
G |
13: 61,712,800 (GRCm39) |
Y307H |
probably benign |
Het |
D630023F18Rik |
G |
A |
1: 65,160,371 (GRCm39) |
|
probably benign |
Het |
Dhx9 |
A |
G |
1: 153,336,826 (GRCm39) |
I807T |
probably damaging |
Het |
Exoc3l4 |
T |
C |
12: 111,388,586 (GRCm39) |
L25P |
probably benign |
Het |
Ggcx |
T |
A |
6: 72,402,905 (GRCm39) |
C288S |
probably benign |
Het |
Gjb3 |
A |
G |
4: 127,220,140 (GRCm39) |
Y131H |
probably damaging |
Het |
Hdhd3 |
A |
G |
4: 62,417,574 (GRCm39) |
S201P |
probably benign |
Het |
Helz2 |
A |
T |
2: 180,881,848 (GRCm39) |
V315E |
probably damaging |
Het |
Hsp90aa1 |
A |
G |
12: 110,662,684 (GRCm39) |
|
probably null |
Het |
Ift70a1 |
A |
T |
2: 75,810,423 (GRCm39) |
Y553* |
probably null |
Het |
Il12a |
C |
T |
3: 68,598,875 (GRCm39) |
R19W |
unknown |
Het |
Isoc1 |
C |
T |
18: 58,806,347 (GRCm39) |
A219V |
possibly damaging |
Het |
Jup |
T |
A |
11: 100,269,124 (GRCm39) |
T430S |
probably benign |
Het |
Klra5 |
C |
T |
6: 129,886,911 (GRCm39) |
C39Y |
probably benign |
Het |
Map4 |
A |
T |
9: 109,855,268 (GRCm39) |
Q131L |
probably damaging |
Het |
Mau2 |
T |
A |
8: 70,480,165 (GRCm39) |
K314M |
probably damaging |
Het |
Mgme1 |
G |
A |
2: 144,114,405 (GRCm39) |
|
probably null |
Het |
Msrb2 |
A |
G |
2: 19,399,066 (GRCm39) |
E143G |
probably benign |
Het |
Muc5b |
G |
T |
7: 141,411,350 (GRCm39) |
C1432F |
unknown |
Het |
Naglu |
T |
C |
11: 100,961,940 (GRCm39) |
Y138H |
probably damaging |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nlrp1b |
A |
G |
11: 71,109,193 (GRCm39) |
Y103H |
probably benign |
Het |
Nodal |
A |
G |
10: 61,259,459 (GRCm39) |
N299D |
probably damaging |
Het |
Notch1 |
T |
C |
2: 26,349,587 (GRCm39) |
T2518A |
probably benign |
Het |
Nr2e1 |
A |
C |
10: 42,448,948 (GRCm39) |
S97A |
probably benign |
Het |
Nuak1 |
A |
T |
10: 84,210,587 (GRCm39) |
S500R |
probably benign |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Nyap1 |
T |
C |
5: 137,736,175 (GRCm39) |
E104G |
probably benign |
Het |
Or3a1b |
C |
T |
11: 74,012,526 (GRCm39) |
T137I |
probably benign |
Het |
Or52e18 |
T |
A |
7: 104,609,204 (GRCm39) |
H245L |
probably damaging |
Het |
Palld |
T |
C |
8: 62,330,107 (GRCm39) |
T257A |
probably benign |
Het |
Pcnx4 |
C |
T |
12: 72,603,043 (GRCm39) |
P435L |
probably damaging |
Het |
Piezo1 |
T |
C |
8: 123,208,753 (GRCm39) |
T2538A |
unknown |
Het |
Plagl1 |
T |
C |
10: 13,003,872 (GRCm39) |
L380P |
unknown |
Het |
Polrmt |
G |
T |
10: 79,576,415 (GRCm39) |
Q514K |
probably benign |
Het |
Psg17 |
T |
G |
7: 18,553,851 (GRCm39) |
D133A |
probably benign |
Het |
Rab3b |
G |
A |
4: 108,797,903 (GRCm39) |
D185N |
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,291,736 (GRCm39) |
S248T |
probably benign |
Het |
Rdh10 |
C |
A |
1: 16,199,430 (GRCm39) |
A212D |
probably damaging |
Het |
Rinl |
A |
G |
7: 28,495,089 (GRCm39) |
H154R |
|
Het |
Selenbp1 |
T |
C |
3: 94,851,414 (GRCm39) |
M389T |
probably benign |
Het |
Serpina1c |
T |
A |
12: 103,862,400 (GRCm39) |
H305L |
possibly damaging |
Het |
Sh3rf2 |
T |
A |
18: 42,282,746 (GRCm39) |
S467T |
|
Het |
Sipa1l1 |
A |
G |
12: 82,443,335 (GRCm39) |
D875G |
probably benign |
Het |
Slc10a6 |
A |
T |
5: 103,776,800 (GRCm39) |
V100D |
probably damaging |
Het |
Slc13a4 |
T |
C |
6: 35,247,290 (GRCm39) |
I577V |
possibly damaging |
Het |
Slc20a2 |
T |
C |
8: 23,030,447 (GRCm39) |
F168L |
probably benign |
Het |
Slc25a1 |
A |
T |
16: 17,745,108 (GRCm39) |
|
probably null |
Het |
Slc5a12 |
A |
G |
2: 110,471,242 (GRCm39) |
S495G |
probably benign |
Het |
Smpdl3a |
A |
G |
10: 57,677,028 (GRCm39) |
D42G |
possibly damaging |
Het |
Spag16 |
G |
C |
1: 70,420,459 (GRCm39) |
L482F |
probably damaging |
Het |
Susd5 |
G |
A |
9: 113,925,289 (GRCm39) |
G391R |
probably damaging |
Het |
Sync |
G |
T |
4: 129,187,618 (GRCm39) |
A217S |
|
Het |
Tha1 |
T |
A |
11: 117,759,512 (GRCm39) |
N326Y |
probably damaging |
Het |
Tjp1 |
A |
T |
7: 64,952,564 (GRCm39) |
F1590Y |
probably benign |
Het |
Tle4 |
T |
C |
19: 14,445,583 (GRCm39) |
N221S |
probably benign |
Het |
Tln1 |
T |
C |
4: 43,536,024 (GRCm39) |
T2054A |
probably damaging |
Het |
Ttll4 |
A |
G |
1: 74,718,949 (GRCm39) |
K267E |
probably benign |
Het |
Usp32 |
C |
T |
11: 84,913,118 (GRCm39) |
G930D |
probably damaging |
Het |
Vmn2r75 |
T |
C |
7: 85,813,447 (GRCm39) |
N452D |
probably damaging |
Het |
Vmn2r81 |
T |
C |
10: 79,104,028 (GRCm39) |
L217P |
possibly damaging |
Het |
Wnt2 |
T |
A |
6: 18,030,397 (GRCm39) |
|
probably benign |
Het |
Zfp459 |
C |
T |
13: 67,556,735 (GRCm39) |
S116N |
probably benign |
Het |
Zfp981 |
C |
A |
4: 146,622,410 (GRCm39) |
T445N |
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 |
|
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 |
|