Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
C |
3: 137,775,632 (GRCm39) |
L1607P |
probably damaging |
Het |
1700016H13Rik |
T |
C |
5: 103,796,687 (GRCm39) |
*118W |
probably null |
Het |
Abcc2 |
A |
T |
19: 43,815,053 (GRCm39) |
R1147* |
probably null |
Het |
Acsbg3 |
A |
T |
17: 57,190,835 (GRCm39) |
N468Y |
probably benign |
Het |
Agap2 |
A |
G |
10: 126,927,571 (GRCm39) |
T1131A |
possibly damaging |
Het |
Aldh9a1 |
A |
G |
1: 167,189,416 (GRCm39) |
D388G |
probably damaging |
Het |
Ap3d1 |
G |
T |
10: 80,565,876 (GRCm39) |
A97E |
probably damaging |
Het |
Arhgef10 |
T |
A |
8: 15,012,636 (GRCm39) |
V320E |
probably damaging |
Het |
Baiap2l1 |
C |
A |
5: 144,202,820 (GRCm39) |
V498L |
probably damaging |
Het |
Bltp2 |
A |
C |
11: 78,160,530 (GRCm39) |
|
probably benign |
Het |
Cdh2 |
T |
C |
18: 16,762,633 (GRCm39) |
N437S |
probably benign |
Het |
Cert1 |
T |
A |
13: 96,685,795 (GRCm39) |
Y63N |
probably benign |
Het |
Cfap119 |
T |
C |
7: 127,184,034 (GRCm39) |
E261G |
probably damaging |
Het |
Cfap20dc |
C |
T |
14: 8,518,695 (GRCm38) |
G254R |
probably damaging |
Het |
Chd1 |
C |
A |
17: 15,945,693 (GRCm39) |
N72K |
probably benign |
Het |
Cstf2t |
A |
T |
19: 31,062,026 (GRCm39) |
M521L |
probably benign |
Het |
Dlx5 |
T |
C |
6: 6,881,619 (GRCm39) |
K90E |
possibly damaging |
Het |
Dmp1 |
A |
G |
5: 104,355,496 (GRCm39) |
E32G |
possibly damaging |
Het |
Espnl |
T |
G |
1: 91,272,211 (GRCm39) |
Y524D |
probably damaging |
Het |
Fam20c |
T |
C |
5: 138,741,479 (GRCm39) |
L30P |
probably damaging |
Het |
Fat1 |
G |
T |
8: 45,479,590 (GRCm39) |
A2879S |
probably benign |
Het |
Gabrg1 |
A |
T |
5: 70,931,732 (GRCm39) |
V337D |
probably damaging |
Het |
Gart |
C |
A |
16: 91,420,291 (GRCm39) |
D851Y |
possibly damaging |
Het |
Gcc1 |
T |
C |
6: 28,420,615 (GRCm39) |
H234R |
probably damaging |
Het |
Gemin6 |
T |
A |
17: 80,535,524 (GRCm39) |
H161Q |
probably damaging |
Het |
Glt6d1 |
A |
G |
2: 25,684,082 (GRCm39) |
I308T |
probably benign |
Het |
Gm10320 |
T |
C |
13: 98,628,491 (GRCm39) |
T7A |
probably benign |
Het |
Gm10912 |
T |
C |
2: 103,896,875 (GRCm39) |
S5P |
probably benign |
Het |
Gmpr2 |
T |
A |
14: 55,910,192 (GRCm39) |
D7E |
possibly damaging |
Het |
Hoxa3 |
T |
C |
6: 52,147,123 (GRCm39) |
|
probably benign |
Het |
Ift140 |
A |
G |
17: 25,309,907 (GRCm39) |
T1105A |
probably benign |
Het |
Kdr |
G |
T |
5: 76,129,082 (GRCm39) |
T188N |
possibly damaging |
Het |
Lepr |
A |
T |
4: 101,609,349 (GRCm39) |
D312V |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,880,329 (GRCm39) |
V501A |
probably damaging |
Het |
Mcur1 |
T |
C |
13: 43,699,216 (GRCm39) |
Y267C |
probably damaging |
Het |
Med13 |
T |
A |
11: 86,197,864 (GRCm39) |
T736S |
probably benign |
Het |
Med13l |
T |
C |
5: 118,809,067 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
G |
C |
1: 88,173,764 (GRCm39) |
A871P |
probably damaging |
Het |
Ndrg2 |
T |
A |
14: 52,144,460 (GRCm39) |
|
probably benign |
Het |
Oas3 |
G |
A |
5: 120,894,210 (GRCm39) |
R39C |
probably damaging |
Het |
Onecut2 |
T |
A |
18: 64,474,543 (GRCm39) |
S365T |
possibly damaging |
Het |
Or13c25 |
G |
A |
4: 52,910,849 (GRCm39) |
T315M |
probably benign |
Het |
Or4c10 |
A |
G |
2: 89,760,545 (GRCm39) |
T131A |
probably benign |
Het |
Or4k48 |
C |
T |
2: 111,476,136 (GRCm39) |
V69I |
probably benign |
Het |
Or51e1 |
T |
A |
7: 102,359,202 (GRCm39) |
H245Q |
probably damaging |
Het |
Pds5b |
C |
A |
5: 150,677,896 (GRCm39) |
Q505K |
probably benign |
Het |
Pramel22 |
C |
T |
4: 143,383,010 (GRCm39) |
E70K |
possibly damaging |
Het |
Rfx2 |
T |
C |
17: 57,110,722 (GRCm39) |
Y88C |
probably damaging |
Het |
Rpl6 |
T |
C |
5: 121,346,541 (GRCm39) |
V214A |
probably benign |
Het |
Samd3 |
T |
A |
10: 26,147,752 (GRCm39) |
C476S |
possibly damaging |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Shank1 |
C |
T |
7: 44,001,718 (GRCm39) |
R1146W |
unknown |
Het |
Smcr8 |
T |
C |
11: 60,668,941 (GRCm39) |
Y30H |
probably damaging |
Het |
Smpd4 |
T |
A |
16: 17,459,461 (GRCm39) |
|
probably null |
Het |
Strip1 |
C |
A |
3: 107,521,929 (GRCm39) |
D750Y |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,070,851 (GRCm39) |
K2312E |
possibly damaging |
Het |
Taf1c |
A |
T |
8: 120,326,722 (GRCm39) |
I438N |
probably damaging |
Het |
Tnfaip1 |
A |
T |
11: 78,420,840 (GRCm39) |
|
probably benign |
Het |
Unc45b |
T |
A |
11: 82,831,031 (GRCm39) |
L797Q |
possibly damaging |
Het |
Usp24 |
T |
A |
4: 106,264,330 (GRCm39) |
W1754R |
probably damaging |
Het |
Utp20 |
G |
A |
10: 88,613,378 (GRCm39) |
P1301L |
probably benign |
Het |
Vmn2r115 |
T |
A |
17: 23,578,755 (GRCm39) |
S743T |
probably damaging |
Het |
Vps41 |
T |
G |
13: 19,038,833 (GRCm39) |
|
probably null |
Het |
Vps72 |
G |
T |
3: 95,029,894 (GRCm39) |
L304F |
probably damaging |
Het |
Wiz |
A |
T |
17: 32,575,415 (GRCm39) |
I907N |
probably damaging |
Het |
Zfp521 |
T |
C |
18: 13,978,119 (GRCm39) |
T765A |
probably benign |
Het |
Zfp616 |
A |
T |
11: 73,976,500 (GRCm39) |
H923L |
probably damaging |
Het |
Zp2 |
A |
T |
7: 119,742,799 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Hc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00694:Hc
|
APN |
2 |
34,881,641 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00922:Hc
|
APN |
2 |
34,881,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01523:Hc
|
APN |
2 |
34,929,250 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01746:Hc
|
APN |
2 |
34,947,338 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01793:Hc
|
APN |
2 |
34,918,202 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01972:Hc
|
APN |
2 |
34,873,784 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02037:Hc
|
APN |
2 |
34,903,531 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02048:Hc
|
APN |
2 |
34,886,039 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02227:Hc
|
APN |
2 |
34,899,923 (GRCm39) |
intron |
probably benign |
|
IGL02230:Hc
|
APN |
2 |
34,903,682 (GRCm39) |
missense |
probably benign |
|
IGL02254:Hc
|
APN |
2 |
34,874,836 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02363:Hc
|
APN |
2 |
34,890,847 (GRCm39) |
missense |
probably benign |
|
IGL02650:Hc
|
APN |
2 |
34,890,886 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03053:Hc
|
APN |
2 |
34,914,210 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03168:Hc
|
APN |
2 |
34,914,210 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03341:Hc
|
APN |
2 |
34,893,389 (GRCm39) |
missense |
probably damaging |
0.98 |
PIT4142001:Hc
|
UTSW |
2 |
34,921,833 (GRCm39) |
splice site |
probably benign |
|
PIT4378001:Hc
|
UTSW |
2 |
34,921,876 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4508001:Hc
|
UTSW |
2 |
34,874,816 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4812001:Hc
|
UTSW |
2 |
34,919,464 (GRCm39) |
missense |
probably benign |
0.16 |
R0025:Hc
|
UTSW |
2 |
34,876,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Hc
|
UTSW |
2 |
34,947,287 (GRCm39) |
missense |
probably benign |
0.32 |
R0218:Hc
|
UTSW |
2 |
34,918,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R0242:Hc
|
UTSW |
2 |
34,926,166 (GRCm39) |
splice site |
probably benign |
|
R0496:Hc
|
UTSW |
2 |
34,903,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Hc
|
UTSW |
2 |
34,893,536 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1468:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R1468:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R1574:Hc
|
UTSW |
2 |
34,890,777 (GRCm39) |
intron |
probably benign |
|
R1610:Hc
|
UTSW |
2 |
34,896,173 (GRCm39) |
missense |
probably benign |
0.44 |
R1640:Hc
|
UTSW |
2 |
34,947,336 (GRCm39) |
nonsense |
probably null |
|
R1887:Hc
|
UTSW |
2 |
34,924,623 (GRCm39) |
missense |
probably benign |
|
R1920:Hc
|
UTSW |
2 |
34,919,407 (GRCm39) |
splice site |
probably benign |
|
R2018:Hc
|
UTSW |
2 |
34,903,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2019:Hc
|
UTSW |
2 |
34,903,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Hc
|
UTSW |
2 |
34,881,115 (GRCm39) |
intron |
probably benign |
|
R2366:Hc
|
UTSW |
2 |
34,903,648 (GRCm39) |
missense |
probably benign |
|
R4093:Hc
|
UTSW |
2 |
34,873,819 (GRCm39) |
nonsense |
probably null |
|
R4288:Hc
|
UTSW |
2 |
34,920,414 (GRCm39) |
missense |
probably damaging |
0.98 |
R4501:Hc
|
UTSW |
2 |
34,887,488 (GRCm39) |
splice site |
probably null |
|
R4502:Hc
|
UTSW |
2 |
34,896,264 (GRCm39) |
missense |
probably benign |
0.00 |
R4508:Hc
|
UTSW |
2 |
34,903,077 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4583:Hc
|
UTSW |
2 |
34,918,189 (GRCm39) |
missense |
probably benign |
0.00 |
R4686:Hc
|
UTSW |
2 |
34,929,260 (GRCm39) |
missense |
possibly damaging |
0.49 |
R4776:Hc
|
UTSW |
2 |
34,929,746 (GRCm39) |
missense |
probably benign |
0.12 |
R4846:Hc
|
UTSW |
2 |
34,909,682 (GRCm39) |
missense |
probably benign |
0.00 |
R5032:Hc
|
UTSW |
2 |
34,903,544 (GRCm39) |
missense |
probably benign |
0.07 |
R5089:Hc
|
UTSW |
2 |
34,914,902 (GRCm39) |
missense |
probably benign |
0.01 |
R5289:Hc
|
UTSW |
2 |
34,886,026 (GRCm39) |
critical splice donor site |
probably null |
|
R5347:Hc
|
UTSW |
2 |
34,927,636 (GRCm39) |
missense |
probably benign |
0.04 |
R5356:Hc
|
UTSW |
2 |
34,885,007 (GRCm39) |
missense |
probably benign |
0.00 |
R5379:Hc
|
UTSW |
2 |
34,881,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5403:Hc
|
UTSW |
2 |
34,947,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R5418:Hc
|
UTSW |
2 |
34,898,195 (GRCm39) |
critical splice donor site |
probably null |
|
R5450:Hc
|
UTSW |
2 |
34,903,050 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5494:Hc
|
UTSW |
2 |
34,893,551 (GRCm39) |
splice site |
probably null |
|
R5713:Hc
|
UTSW |
2 |
34,903,543 (GRCm39) |
missense |
probably damaging |
0.99 |
R5898:Hc
|
UTSW |
2 |
34,887,449 (GRCm39) |
missense |
probably benign |
0.06 |
R5925:Hc
|
UTSW |
2 |
34,920,462 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5942:Hc
|
UTSW |
2 |
34,918,137 (GRCm39) |
nonsense |
probably null |
|
R5991:Hc
|
UTSW |
2 |
34,896,117 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6036:Hc
|
UTSW |
2 |
34,929,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6036:Hc
|
UTSW |
2 |
34,929,696 (GRCm39) |
missense |
probably benign |
0.00 |
R6115:Hc
|
UTSW |
2 |
34,903,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R6234:Hc
|
UTSW |
2 |
34,918,058 (GRCm39) |
missense |
probably benign |
|
R6264:Hc
|
UTSW |
2 |
34,896,285 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6313:Hc
|
UTSW |
2 |
34,879,851 (GRCm39) |
splice site |
probably null |
|
R6525:Hc
|
UTSW |
2 |
34,881,236 (GRCm39) |
missense |
probably benign |
0.06 |
R6577:Hc
|
UTSW |
2 |
34,922,138 (GRCm39) |
missense |
probably benign |
0.00 |
R6601:Hc
|
UTSW |
2 |
34,935,906 (GRCm39) |
missense |
probably benign |
0.03 |
R6916:Hc
|
UTSW |
2 |
34,900,044 (GRCm39) |
nonsense |
probably null |
|
R7108:Hc
|
UTSW |
2 |
34,929,706 (GRCm39) |
missense |
probably benign |
0.03 |
R7143:Hc
|
UTSW |
2 |
34,940,450 (GRCm39) |
missense |
probably benign |
0.00 |
R7388:Hc
|
UTSW |
2 |
34,874,859 (GRCm39) |
splice site |
probably null |
|
R7468:Hc
|
UTSW |
2 |
34,918,063 (GRCm39) |
missense |
probably benign |
0.00 |
R7504:Hc
|
UTSW |
2 |
34,951,331 (GRCm39) |
missense |
not run |
|
R7521:Hc
|
UTSW |
2 |
34,935,344 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7582:Hc
|
UTSW |
2 |
34,881,278 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7596:Hc
|
UTSW |
2 |
34,890,859 (GRCm39) |
missense |
probably damaging |
0.96 |
R7599:Hc
|
UTSW |
2 |
34,940,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R7692:Hc
|
UTSW |
2 |
34,914,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R7853:Hc
|
UTSW |
2 |
34,900,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:Hc
|
UTSW |
2 |
34,887,411 (GRCm39) |
nonsense |
probably null |
|
R8329:Hc
|
UTSW |
2 |
34,902,910 (GRCm39) |
splice site |
probably null |
|
R8375:Hc
|
UTSW |
2 |
34,873,731 (GRCm39) |
missense |
probably benign |
0.32 |
R8477:Hc
|
UTSW |
2 |
34,879,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Hc
|
UTSW |
2 |
34,909,535 (GRCm39) |
missense |
probably benign |
0.06 |
R8888:Hc
|
UTSW |
2 |
34,890,861 (GRCm39) |
missense |
probably benign |
0.00 |
R8895:Hc
|
UTSW |
2 |
34,890,861 (GRCm39) |
missense |
probably benign |
0.00 |
R8968:Hc
|
UTSW |
2 |
34,922,317 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8969:Hc
|
UTSW |
2 |
34,909,475 (GRCm39) |
critical splice donor site |
probably null |
|
R9146:Hc
|
UTSW |
2 |
34,924,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R9218:Hc
|
UTSW |
2 |
34,922,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9340:Hc
|
UTSW |
2 |
34,876,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R9396:Hc
|
UTSW |
2 |
34,927,615 (GRCm39) |
nonsense |
probably null |
|
R9569:Hc
|
UTSW |
2 |
34,926,359 (GRCm39) |
missense |
probably benign |
0.00 |
R9576:Hc
|
UTSW |
2 |
34,873,767 (GRCm39) |
missense |
probably benign |
0.01 |
R9706:Hc
|
UTSW |
2 |
34,914,196 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Hc
|
UTSW |
2 |
34,873,723 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Hc
|
UTSW |
2 |
34,919,482 (GRCm39) |
missense |
probably benign |
0.02 |
Z1088:Hc
|
UTSW |
2 |
34,898,261 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1176:Hc
|
UTSW |
2 |
34,896,285 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Hc
|
UTSW |
2 |
34,903,622 (GRCm39) |
missense |
probably damaging |
1.00 |
|