Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adprs |
T |
C |
4: 126,211,185 (GRCm39) |
E244G |
probably benign |
Het |
Aldh1l2 |
G |
A |
10: 83,356,229 (GRCm39) |
P54S |
probably damaging |
Het |
Ankdd1a |
G |
A |
9: 65,416,924 (GRCm39) |
|
probably benign |
Het |
Ankra2 |
T |
A |
13: 98,408,200 (GRCm39) |
S216R |
probably damaging |
Het |
Asah2 |
A |
T |
19: 32,030,356 (GRCm39) |
N105K |
probably benign |
Het |
Ass1 |
A |
T |
2: 31,404,831 (GRCm39) |
N371Y |
probably damaging |
Het |
Cacna1s |
A |
G |
1: 136,028,342 (GRCm39) |
Y893C |
probably benign |
Het |
Capza2 |
G |
A |
6: 17,648,523 (GRCm39) |
R15H |
probably benign |
Het |
Cbfa2t2 |
T |
C |
2: 154,376,796 (GRCm39) |
|
probably benign |
Het |
Ccdc96 |
A |
T |
5: 36,643,445 (GRCm39) |
T484S |
possibly damaging |
Het |
Cckar |
GCTTAGCCTCTTCT |
GCT |
5: 53,857,641 (GRCm39) |
|
probably null |
Het |
Ccl4 |
T |
A |
11: 83,554,280 (GRCm39) |
|
probably benign |
Het |
Cpt1b |
A |
G |
15: 89,302,073 (GRCm39) |
Y702H |
probably benign |
Het |
Cr1l |
G |
A |
1: 194,800,101 (GRCm39) |
T153I |
probably damaging |
Het |
Cyth2 |
C |
A |
7: 45,460,009 (GRCm39) |
E57* |
probably null |
Het |
Daxx |
T |
A |
17: 34,132,594 (GRCm39) |
S575T |
probably damaging |
Het |
Depdc5 |
T |
C |
5: 33,061,890 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,521,956 (GRCm39) |
D1923G |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,162,937 (GRCm39) |
T428A |
probably benign |
Het |
Dnm2 |
G |
T |
9: 21,411,639 (GRCm39) |
A619S |
probably benign |
Het |
Enpp2 |
T |
C |
15: 54,723,457 (GRCm39) |
T639A |
probably benign |
Het |
Epsti1 |
A |
T |
14: 78,177,366 (GRCm39) |
H182L |
probably damaging |
Het |
Exoc3l |
C |
T |
8: 106,020,175 (GRCm39) |
R250Q |
probably benign |
Het |
Ggn |
G |
T |
7: 28,870,665 (GRCm39) |
|
probably null |
Het |
Il1rap |
A |
G |
16: 26,511,544 (GRCm39) |
N196S |
probably benign |
Het |
Ints6 |
T |
C |
14: 62,946,961 (GRCm39) |
T335A |
probably damaging |
Het |
Itga1 |
G |
A |
13: 115,148,854 (GRCm39) |
|
probably benign |
Het |
Kifc3 |
G |
T |
8: 95,830,098 (GRCm39) |
Q557K |
possibly damaging |
Het |
Krt23 |
A |
G |
11: 99,369,027 (GRCm39) |
I422T |
probably benign |
Het |
Lcn2 |
A |
G |
2: 32,274,901 (GRCm39) |
|
probably benign |
Het |
Lonp2 |
A |
G |
8: 87,364,619 (GRCm39) |
T326A |
possibly damaging |
Het |
Lrpprc |
T |
C |
17: 85,047,506 (GRCm39) |
I909V |
possibly damaging |
Het |
Lrrc14 |
G |
T |
15: 76,598,552 (GRCm39) |
R396L |
probably benign |
Het |
Lypd6 |
T |
G |
2: 50,055,679 (GRCm39) |
|
probably benign |
Het |
Man2b1 |
A |
G |
8: 85,819,645 (GRCm39) |
N610S |
probably damaging |
Het |
Mctp2 |
C |
T |
7: 71,740,012 (GRCm39) |
V793I |
possibly damaging |
Het |
Med25 |
A |
C |
7: 44,529,982 (GRCm39) |
|
probably benign |
Het |
Mfsd6 |
T |
C |
1: 52,748,616 (GRCm39) |
Y83C |
probably damaging |
Het |
Mtbp |
A |
T |
15: 55,488,820 (GRCm39) |
M499L |
probably damaging |
Het |
Mtmr10 |
A |
T |
7: 63,947,245 (GRCm39) |
K53N |
probably damaging |
Het |
Nfat5 |
T |
C |
8: 108,085,333 (GRCm39) |
I542T |
probably damaging |
Het |
Nr1h3 |
A |
G |
2: 91,022,358 (GRCm39) |
M90T |
probably damaging |
Het |
Nsmce4a |
A |
G |
7: 130,147,623 (GRCm39) |
|
probably benign |
Het |
Oprl1 |
G |
A |
2: 181,361,021 (GRCm39) |
C318Y |
probably benign |
Het |
Or5d40 |
T |
A |
2: 88,015,854 (GRCm39) |
I211N |
possibly damaging |
Het |
Pbx3 |
A |
T |
2: 34,114,572 (GRCm39) |
S46T |
probably benign |
Het |
Pign |
A |
T |
1: 105,516,818 (GRCm39) |
F575I |
possibly damaging |
Het |
Ptpn13 |
G |
T |
5: 103,713,091 (GRCm39) |
S1738I |
probably benign |
Het |
Rnf126 |
G |
T |
10: 79,595,057 (GRCm39) |
P269Q |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,477,468 (GRCm39) |
|
probably benign |
Het |
Slc2a7 |
C |
T |
4: 150,233,978 (GRCm39) |
A31V |
probably damaging |
Het |
Slc6a12 |
A |
G |
6: 121,340,218 (GRCm39) |
D487G |
probably damaging |
Het |
Son |
G |
T |
16: 91,453,032 (GRCm39) |
G593V |
probably damaging |
Het |
Spata31d1a |
T |
C |
13: 59,850,964 (GRCm39) |
N388S |
probably benign |
Het |
Spg11 |
A |
T |
2: 121,922,668 (GRCm39) |
M927K |
possibly damaging |
Het |
Taf13 |
A |
G |
3: 108,479,038 (GRCm39) |
M1V |
probably null |
Het |
Trim32 |
G |
A |
4: 65,531,491 (GRCm39) |
R16Q |
probably damaging |
Het |
Trio |
A |
G |
15: 27,902,603 (GRCm39) |
F286S |
probably damaging |
Het |
Trpm2 |
A |
C |
10: 77,779,824 (GRCm39) |
|
probably benign |
Het |
Ttc7b |
T |
C |
12: 100,353,438 (GRCm39) |
M390V |
possibly damaging |
Het |
Vmn1r184 |
A |
T |
7: 25,966,968 (GRCm39) |
Q238L |
probably damaging |
Het |
Zfp236 |
T |
C |
18: 82,676,213 (GRCm39) |
E368G |
probably damaging |
Het |
Zfr2 |
G |
T |
10: 81,087,170 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Map2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01518:Map2
|
APN |
1 |
66,464,490 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02135:Map2
|
APN |
1 |
66,419,920 (GRCm39) |
nonsense |
probably null |
|
IGL02526:Map2
|
APN |
1 |
66,419,876 (GRCm39) |
missense |
possibly damaging |
0.94 |
Annas
|
UTSW |
1 |
66,472,756 (GRCm39) |
critical splice donor site |
probably null |
|
calliope
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
carthage
|
UTSW |
1 |
66,453,807 (GRCm39) |
missense |
probably damaging |
1.00 |
costas
|
UTSW |
1 |
66,451,812 (GRCm39) |
missense |
possibly damaging |
0.94 |
Jacobin
|
UTSW |
1 |
66,438,578 (GRCm39) |
missense |
probably damaging |
1.00 |
Nectar
|
UTSW |
1 |
66,454,522 (GRCm39) |
nonsense |
probably null |
|
ruby_throat
|
UTSW |
1 |
66,454,043 (GRCm39) |
missense |
possibly damaging |
0.67 |
Rufous
|
UTSW |
1 |
66,419,927 (GRCm39) |
missense |
probably damaging |
1.00 |
Speckled
|
UTSW |
1 |
66,451,886 (GRCm39) |
nonsense |
probably null |
|
Sunbird
|
UTSW |
1 |
66,454,646 (GRCm39) |
missense |
probably benign |
0.01 |
swift
|
UTSW |
1 |
66,455,523 (GRCm39) |
missense |
probably damaging |
1.00 |
E0370:Map2
|
UTSW |
1 |
66,455,883 (GRCm39) |
unclassified |
probably benign |
|
PIT4362001:Map2
|
UTSW |
1 |
66,451,677 (GRCm39) |
missense |
probably benign |
0.05 |
R0067:Map2
|
UTSW |
1 |
66,452,322 (GRCm39) |
missense |
probably benign |
0.04 |
R0238:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Map2
|
UTSW |
1 |
66,455,265 (GRCm39) |
missense |
probably damaging |
1.00 |
R0268:Map2
|
UTSW |
1 |
66,419,881 (GRCm39) |
nonsense |
probably null |
|
R0305:Map2
|
UTSW |
1 |
66,452,253 (GRCm39) |
missense |
probably benign |
0.00 |
R0409:Map2
|
UTSW |
1 |
66,472,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R0561:Map2
|
UTSW |
1 |
66,464,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R0674:Map2
|
UTSW |
1 |
66,452,361 (GRCm39) |
missense |
probably damaging |
1.00 |
R0738:Map2
|
UTSW |
1 |
66,464,348 (GRCm39) |
splice site |
probably benign |
|
R0893:Map2
|
UTSW |
1 |
66,419,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R1305:Map2
|
UTSW |
1 |
66,464,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R1534:Map2
|
UTSW |
1 |
66,452,339 (GRCm39) |
missense |
probably benign |
0.33 |
R1632:Map2
|
UTSW |
1 |
66,454,245 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1682:Map2
|
UTSW |
1 |
66,454,781 (GRCm39) |
splice site |
probably null |
|
R1774:Map2
|
UTSW |
1 |
66,453,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R2014:Map2
|
UTSW |
1 |
66,455,295 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2017:Map2
|
UTSW |
1 |
66,451,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R2050:Map2
|
UTSW |
1 |
66,453,473 (GRCm39) |
missense |
probably damaging |
0.98 |
R2093:Map2
|
UTSW |
1 |
66,438,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R2214:Map2
|
UTSW |
1 |
66,459,345 (GRCm39) |
missense |
probably damaging |
0.99 |
R2284:Map2
|
UTSW |
1 |
66,453,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R3011:Map2
|
UTSW |
1 |
66,453,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R3105:Map2
|
UTSW |
1 |
66,472,756 (GRCm39) |
critical splice donor site |
probably null |
|
R3708:Map2
|
UTSW |
1 |
66,455,714 (GRCm39) |
unclassified |
probably benign |
|
R3709:Map2
|
UTSW |
1 |
66,455,015 (GRCm39) |
nonsense |
probably null |
|
R3729:Map2
|
UTSW |
1 |
66,451,605 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3760:Map2
|
UTSW |
1 |
66,478,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R3788:Map2
|
UTSW |
1 |
66,456,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R3789:Map2
|
UTSW |
1 |
66,456,022 (GRCm39) |
missense |
probably damaging |
0.99 |
R4003:Map2
|
UTSW |
1 |
66,454,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Map2
|
UTSW |
1 |
66,455,063 (GRCm39) |
missense |
probably damaging |
1.00 |
R4172:Map2
|
UTSW |
1 |
66,452,759 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4198:Map2
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4200:Map2
|
UTSW |
1 |
66,464,457 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Map2
|
UTSW |
1 |
66,464,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Map2
|
UTSW |
1 |
66,464,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R4700:Map2
|
UTSW |
1 |
66,449,796 (GRCm39) |
missense |
probably damaging |
0.96 |
R4974:Map2
|
UTSW |
1 |
66,452,664 (GRCm39) |
missense |
probably benign |
0.15 |
R5007:Map2
|
UTSW |
1 |
66,452,448 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5039:Map2
|
UTSW |
1 |
66,477,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R5237:Map2
|
UTSW |
1 |
66,478,169 (GRCm39) |
unclassified |
probably benign |
|
R5313:Map2
|
UTSW |
1 |
66,464,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Map2
|
UTSW |
1 |
66,438,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R5490:Map2
|
UTSW |
1 |
66,452,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Map2
|
UTSW |
1 |
66,454,415 (GRCm39) |
missense |
probably benign |
0.00 |
R5532:Map2
|
UTSW |
1 |
66,453,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R5583:Map2
|
UTSW |
1 |
66,455,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R5764:Map2
|
UTSW |
1 |
66,454,034 (GRCm39) |
missense |
probably damaging |
0.99 |
R5996:Map2
|
UTSW |
1 |
66,454,043 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6058:Map2
|
UTSW |
1 |
66,454,573 (GRCm39) |
missense |
probably benign |
0.05 |
R6199:Map2
|
UTSW |
1 |
66,464,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R6208:Map2
|
UTSW |
1 |
66,470,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R6276:Map2
|
UTSW |
1 |
66,438,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Map2
|
UTSW |
1 |
66,454,488 (GRCm39) |
missense |
probably damaging |
1.00 |
R6424:Map2
|
UTSW |
1 |
66,453,946 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6743:Map2
|
UTSW |
1 |
66,454,766 (GRCm39) |
missense |
probably benign |
0.04 |
R6837:Map2
|
UTSW |
1 |
66,453,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R6901:Map2
|
UTSW |
1 |
66,460,932 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6984:Map2
|
UTSW |
1 |
66,454,395 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6989:Map2
|
UTSW |
1 |
66,454,065 (GRCm39) |
missense |
probably benign |
0.00 |
R7001:Map2
|
UTSW |
1 |
66,454,646 (GRCm39) |
missense |
probably benign |
0.01 |
R7055:Map2
|
UTSW |
1 |
66,455,983 (GRCm39) |
missense |
probably damaging |
1.00 |
R7094:Map2
|
UTSW |
1 |
66,451,886 (GRCm39) |
nonsense |
probably null |
|
R7106:Map2
|
UTSW |
1 |
66,449,903 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7182:Map2
|
UTSW |
1 |
66,451,812 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7235:Map2
|
UTSW |
1 |
66,453,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R7424:Map2
|
UTSW |
1 |
66,453,983 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7473:Map2
|
UTSW |
1 |
66,454,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7642:Map2
|
UTSW |
1 |
66,452,466 (GRCm39) |
missense |
probably benign |
0.01 |
R7660:Map2
|
UTSW |
1 |
66,453,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R7673:Map2
|
UTSW |
1 |
66,452,933 (GRCm39) |
missense |
probably benign |
0.03 |
R7768:Map2
|
UTSW |
1 |
66,453,642 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7796:Map2
|
UTSW |
1 |
66,455,654 (GRCm39) |
splice site |
probably null |
|
R7834:Map2
|
UTSW |
1 |
66,455,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Map2
|
UTSW |
1 |
66,455,570 (GRCm39) |
missense |
probably benign |
|
R7955:Map2
|
UTSW |
1 |
66,452,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R8056:Map2
|
UTSW |
1 |
66,454,779 (GRCm39) |
missense |
probably damaging |
0.99 |
R8118:Map2
|
UTSW |
1 |
66,464,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R8135:Map2
|
UTSW |
1 |
66,452,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R8152:Map2
|
UTSW |
1 |
66,453,902 (GRCm39) |
missense |
probably benign |
0.00 |
R8223:Map2
|
UTSW |
1 |
66,464,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R8329:Map2
|
UTSW |
1 |
66,454,272 (GRCm39) |
missense |
probably benign |
0.01 |
R8344:Map2
|
UTSW |
1 |
66,460,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8475:Map2
|
UTSW |
1 |
66,453,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8548:Map2
|
UTSW |
1 |
66,452,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Map2
|
UTSW |
1 |
66,460,872 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Map2
|
UTSW |
1 |
66,453,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R8745:Map2
|
UTSW |
1 |
66,452,556 (GRCm39) |
missense |
probably benign |
0.00 |
R8786:Map2
|
UTSW |
1 |
66,472,755 (GRCm39) |
critical splice donor site |
probably benign |
|
R8790:Map2
|
UTSW |
1 |
66,477,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8874:Map2
|
UTSW |
1 |
66,455,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R8887:Map2
|
UTSW |
1 |
66,454,758 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8948:Map2
|
UTSW |
1 |
66,419,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8950:Map2
|
UTSW |
1 |
66,419,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R8998:Map2
|
UTSW |
1 |
66,452,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8999:Map2
|
UTSW |
1 |
66,452,473 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9072:Map2
|
UTSW |
1 |
66,453,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R9088:Map2
|
UTSW |
1 |
66,453,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R9089:Map2
|
UTSW |
1 |
66,452,098 (GRCm39) |
missense |
probably benign |
0.09 |
R9106:Map2
|
UTSW |
1 |
66,454,522 (GRCm39) |
nonsense |
probably null |
|
R9112:Map2
|
UTSW |
1 |
66,472,723 (GRCm39) |
nonsense |
probably null |
|
R9120:Map2
|
UTSW |
1 |
66,453,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R9161:Map2
|
UTSW |
1 |
66,477,503 (GRCm39) |
missense |
possibly damaging |
0.65 |
R9464:Map2
|
UTSW |
1 |
66,454,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R9589:Map2
|
UTSW |
1 |
66,449,753 (GRCm39) |
missense |
probably benign |
|
V8831:Map2
|
UTSW |
1 |
66,455,004 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Map2
|
UTSW |
1 |
66,477,520 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Map2
|
UTSW |
1 |
66,419,839 (GRCm39) |
missense |
probably benign |
0.01 |
|