Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acvr1b |
T |
C |
15: 101,092,722 (GRCm39) |
W122R |
possibly damaging |
Het |
Adgrv1 |
C |
T |
13: 81,592,657 (GRCm39) |
R4294H |
probably benign |
Het |
Afdn |
A |
G |
17: 14,024,315 (GRCm39) |
T74A |
probably damaging |
Het |
Aff3 |
T |
A |
1: 38,247,098 (GRCm39) |
D829V |
probably benign |
Het |
Akr1c12 |
T |
C |
13: 4,325,772 (GRCm39) |
Q107R |
probably benign |
Het |
Apc |
T |
A |
18: 34,402,252 (GRCm39) |
F131I |
probably benign |
Het |
Atosb |
A |
T |
4: 43,033,687 (GRCm39) |
F489I |
probably damaging |
Het |
Atp13a1 |
T |
A |
8: 70,259,424 (GRCm39) |
L1036H |
probably damaging |
Het |
BC035044 |
A |
C |
6: 128,867,855 (GRCm39) |
|
probably benign |
Het |
C1rl |
A |
G |
6: 124,485,535 (GRCm39) |
D302G |
probably benign |
Het |
C2cd6 |
A |
C |
1: 59,117,093 (GRCm39) |
D133E |
probably benign |
Het |
Cacna1c |
T |
A |
6: 118,629,671 (GRCm39) |
Y1061F |
probably damaging |
Het |
Cav1 |
A |
G |
6: 17,308,034 (GRCm39) |
D62G |
probably damaging |
Het |
Ccdc77 |
T |
C |
6: 120,327,242 (GRCm39) |
M68V |
probably damaging |
Het |
Cd55 |
A |
T |
1: 130,375,348 (GRCm39) |
|
probably benign |
Het |
Cdc27 |
C |
A |
11: 104,413,602 (GRCm39) |
A380S |
probably damaging |
Het |
Cenpb |
A |
T |
2: 131,021,477 (GRCm39) |
I107K |
probably damaging |
Het |
Cep135 |
T |
G |
5: 76,769,187 (GRCm39) |
H612Q |
possibly damaging |
Het |
Chd1l |
A |
T |
3: 97,470,849 (GRCm39) |
N815K |
probably damaging |
Het |
Cldn20 |
C |
T |
17: 3,582,992 (GRCm39) |
T55M |
possibly damaging |
Het |
Depdc1a |
A |
T |
3: 159,221,679 (GRCm39) |
I208L |
probably benign |
Het |
Dgkb |
C |
T |
12: 38,134,223 (GRCm39) |
A43V |
possibly damaging |
Het |
Dgkb |
C |
T |
12: 38,654,104 (GRCm39) |
T741I |
probably damaging |
Het |
Dhx16 |
A |
G |
17: 36,197,076 (GRCm39) |
N653S |
probably damaging |
Het |
Dnah5 |
T |
A |
15: 28,438,329 (GRCm39) |
S3987T |
probably benign |
Het |
Dnai4 |
T |
C |
4: 102,906,758 (GRCm39) |
D685G |
probably damaging |
Het |
Dst |
T |
A |
1: 34,334,277 (GRCm39) |
I4835N |
probably damaging |
Het |
Esrrb |
A |
G |
12: 86,561,114 (GRCm39) |
I288V |
probably damaging |
Het |
Fnta |
C |
T |
8: 26,497,341 (GRCm39) |
W169* |
probably null |
Het |
Golga4 |
T |
C |
9: 118,365,860 (GRCm39) |
L304P |
probably damaging |
Het |
Hace1 |
A |
G |
10: 45,466,362 (GRCm39) |
|
probably null |
Het |
Ino80b |
G |
T |
6: 83,101,112 (GRCm39) |
|
probably null |
Het |
Kcmf1 |
G |
A |
6: 72,820,082 (GRCm39) |
R306C |
probably damaging |
Het |
Lrrc46 |
G |
A |
11: 96,927,305 (GRCm39) |
T92I |
possibly damaging |
Het |
Man2b1 |
T |
C |
8: 85,824,076 (GRCm39) |
V991A |
possibly damaging |
Het |
Mgat4e |
T |
C |
1: 134,468,944 (GRCm39) |
T367A |
probably benign |
Het |
Mtr |
A |
G |
13: 12,202,992 (GRCm39) |
S1204P |
probably damaging |
Het |
Myo15a |
G |
A |
11: 60,417,487 (GRCm39) |
|
probably null |
Het |
Nktr |
T |
C |
9: 121,560,585 (GRCm39) |
S74P |
probably damaging |
Het |
Noct |
T |
C |
3: 51,157,508 (GRCm39) |
V282A |
possibly damaging |
Het |
Nol11 |
A |
T |
11: 107,071,912 (GRCm39) |
I227K |
possibly damaging |
Het |
Nsd3 |
T |
A |
8: 26,130,646 (GRCm39) |
S4T |
probably damaging |
Het |
Or5m10b |
T |
A |
2: 85,699,714 (GRCm39) |
Y259* |
probably null |
Het |
Or5p64 |
A |
G |
7: 107,855,109 (GRCm39) |
S79P |
probably damaging |
Het |
Pds5a |
T |
A |
5: 65,809,782 (GRCm39) |
L393F |
probably damaging |
Het |
Prex2 |
C |
T |
1: 11,336,259 (GRCm39) |
R1486C |
probably damaging |
Het |
Rc3h2 |
T |
C |
2: 37,272,028 (GRCm39) |
T768A |
probably damaging |
Het |
Rin3 |
A |
T |
12: 102,335,584 (GRCm39) |
E418D |
probably benign |
Het |
Rnf214 |
G |
T |
9: 45,778,886 (GRCm39) |
T586N |
probably damaging |
Het |
Samd4b |
A |
G |
7: 28,101,285 (GRCm39) |
S667P |
probably damaging |
Het |
Sec14l2 |
T |
C |
11: 4,061,161 (GRCm39) |
Y100C |
probably damaging |
Het |
Slc46a2 |
T |
C |
4: 59,914,077 (GRCm39) |
E282G |
probably benign |
Het |
Themis |
A |
C |
10: 28,657,762 (GRCm39) |
N110T |
possibly damaging |
Het |
Tln1 |
C |
A |
4: 43,543,165 (GRCm39) |
S1333I |
probably benign |
Het |
Tmem53 |
T |
C |
4: 117,125,625 (GRCm39) |
V224A |
possibly damaging |
Het |
Tmtc4 |
T |
A |
14: 123,163,391 (GRCm39) |
K664N |
possibly damaging |
Het |
Tnni3k |
T |
C |
3: 154,674,922 (GRCm39) |
D201G |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,912,898 (GRCm39) |
E1681G |
probably damaging |
Het |
Trhde |
A |
T |
10: 114,340,103 (GRCm39) |
D567E |
probably damaging |
Het |
Tsc2 |
T |
C |
17: 24,828,101 (GRCm39) |
M788V |
probably benign |
Het |
Ube3a |
A |
G |
7: 58,926,650 (GRCm39) |
Y476C |
probably damaging |
Het |
Ubiad1 |
T |
C |
4: 148,520,682 (GRCm39) |
N314S |
possibly damaging |
Het |
Unc79 |
T |
A |
12: 103,139,771 (GRCm39) |
N2375K |
probably damaging |
Het |
Vmn2r107 |
A |
T |
17: 20,595,939 (GRCm39) |
I831F |
probably damaging |
Het |
Vwa3b |
T |
A |
1: 37,124,367 (GRCm39) |
C322S |
probably benign |
Het |
Wnk1 |
A |
T |
6: 119,939,916 (GRCm39) |
H238Q |
probably benign |
Het |
Wnk2 |
A |
G |
13: 49,300,081 (GRCm39) |
Y210H |
probably damaging |
Het |
Wwc2 |
T |
C |
8: 48,304,943 (GRCm39) |
D894G |
unknown |
Het |
Yes1 |
T |
A |
5: 32,810,381 (GRCm39) |
F180Y |
probably damaging |
Het |
Yju2b |
T |
C |
8: 84,985,318 (GRCm39) |
E317G |
probably benign |
Het |
Zbtb46 |
T |
C |
2: 181,033,062 (GRCm39) |
Y533C |
probably damaging |
Het |
Zfp57 |
T |
C |
17: 37,316,942 (GRCm39) |
S7P |
possibly damaging |
Het |
Zzef1 |
T |
C |
11: 72,802,090 (GRCm39) |
|
probably null |
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 |
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 |
|