Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts3 |
T |
C |
5: 90,009,256 (GRCm39) |
S136G |
probably benign |
Het |
Apba3 |
T |
A |
10: 81,108,180 (GRCm39) |
N445K |
probably damaging |
Het |
Aqp6 |
A |
G |
15: 99,501,652 (GRCm39) |
K237E |
possibly damaging |
Het |
Arhgap23 |
A |
G |
11: 97,391,169 (GRCm39) |
T1229A |
probably benign |
Het |
Bpifb1 |
T |
C |
2: 154,056,071 (GRCm39) |
I379T |
probably damaging |
Het |
Bpnt2 |
G |
A |
4: 4,778,207 (GRCm39) |
T177I |
probably damaging |
Het |
Ccdc169 |
A |
G |
3: 55,047,530 (GRCm39) |
D7G |
probably damaging |
Het |
Cyp2f2 |
T |
A |
7: 26,830,784 (GRCm39) |
|
probably null |
Het |
Daam2 |
T |
A |
17: 49,787,755 (GRCm39) |
K453* |
probably null |
Het |
Dennd4c |
T |
C |
4: 86,729,849 (GRCm39) |
L817P |
probably damaging |
Het |
Efcab6 |
T |
A |
15: 83,755,189 (GRCm39) |
R1376W |
probably damaging |
Het |
Esrra |
G |
T |
19: 6,891,214 (GRCm39) |
A182E |
possibly damaging |
Het |
Fam234b |
T |
A |
6: 135,203,874 (GRCm39) |
V392E |
probably damaging |
Het |
Fanca |
A |
G |
8: 123,997,999 (GRCm39) |
V1229A |
probably benign |
Het |
Fdps |
G |
T |
3: 89,006,693 (GRCm39) |
Q66K |
probably benign |
Het |
Fer1l6 |
T |
A |
15: 58,499,438 (GRCm39) |
D1269E |
probably benign |
Het |
Foxred1 |
G |
A |
9: 35,116,932 (GRCm39) |
R353W |
probably damaging |
Het |
Gabrg2 |
C |
T |
11: 41,858,451 (GRCm39) |
V226I |
possibly damaging |
Het |
Gcnt2 |
C |
A |
13: 41,014,343 (GRCm39) |
C171* |
probably null |
Het |
Glyat |
C |
A |
19: 12,617,172 (GRCm39) |
A8E |
probably damaging |
Het |
Golgb1 |
C |
A |
16: 36,695,758 (GRCm39) |
R86S |
unknown |
Het |
Hdac1 |
G |
T |
4: 129,411,259 (GRCm39) |
S421* |
probably null |
Het |
Hmcn2 |
G |
T |
2: 31,246,298 (GRCm39) |
A756S |
possibly damaging |
Het |
Igkv8-26 |
A |
G |
6: 70,170,571 (GRCm39) |
N54S |
probably benign |
Het |
Itgae |
T |
A |
11: 73,012,786 (GRCm39) |
V706E |
possibly damaging |
Het |
Itgax |
G |
A |
7: 127,747,262 (GRCm39) |
V992M |
probably damaging |
Het |
Klk10 |
A |
G |
7: 43,433,851 (GRCm39) |
D221G |
probably benign |
Het |
Klkb1 |
T |
C |
8: 45,731,150 (GRCm39) |
I205V |
probably benign |
Het |
Kpna2 |
T |
C |
11: 106,889,583 (GRCm39) |
N8S |
probably null |
Het |
L3mbtl1 |
A |
C |
2: 162,806,434 (GRCm39) |
T442P |
possibly damaging |
Het |
Lrp1b |
C |
T |
2: 40,551,561 (GRCm39) |
C4181Y |
|
Het |
Mcat |
T |
C |
15: 83,431,872 (GRCm39) |
Y332C |
probably damaging |
Het |
Mecom |
T |
C |
3: 30,010,534 (GRCm39) |
D648G |
probably damaging |
Het |
Mesp2 |
A |
T |
7: 79,460,717 (GRCm39) |
D14V |
probably damaging |
Het |
Mlh3 |
A |
T |
12: 85,314,973 (GRCm39) |
Y404* |
probably null |
Het |
Mterf3 |
A |
T |
13: 67,065,212 (GRCm39) |
F230I |
probably damaging |
Het |
Nrxn3 |
T |
C |
12: 89,478,832 (GRCm39) |
V602A |
probably benign |
Het |
Or4a74 |
T |
A |
2: 89,439,571 (GRCm39) |
I292F |
possibly damaging |
Het |
Plekhg6 |
A |
G |
6: 125,351,623 (GRCm39) |
F209L |
probably damaging |
Het |
Pmp22 |
C |
A |
11: 63,049,174 (GRCm39) |
A139D |
probably damaging |
Het |
Polr2e |
T |
C |
10: 79,874,404 (GRCm39) |
D34G |
possibly damaging |
Het |
Ppard |
T |
A |
17: 28,516,091 (GRCm39) |
L105H |
probably damaging |
Het |
Ptpn14 |
T |
A |
1: 189,582,942 (GRCm39) |
D596E |
probably benign |
Het |
Ptprz1 |
C |
T |
6: 23,002,518 (GRCm39) |
A1536V |
not run |
Het |
Qng1 |
T |
A |
13: 58,529,649 (GRCm39) |
H321L |
probably damaging |
Het |
Rabgap1 |
TGGGG |
TGGG |
2: 37,392,908 (GRCm39) |
|
probably null |
Het |
Retreg1 |
T |
A |
15: 25,971,727 (GRCm39) |
D222E |
probably benign |
Het |
Rmnd1 |
T |
C |
10: 4,363,404 (GRCm39) |
K282R |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Sall3 |
C |
T |
18: 81,015,267 (GRCm39) |
R887H |
possibly damaging |
Het |
Samd3 |
A |
G |
10: 26,139,711 (GRCm39) |
D281G |
probably benign |
Het |
Scube1 |
T |
A |
15: 83,497,653 (GRCm39) |
D766V |
probably damaging |
Het |
Sec24b |
TGC |
TGCAGC |
3: 129,834,460 (GRCm39) |
|
probably benign |
Het |
Slc2a2 |
A |
G |
3: 28,752,166 (GRCm39) |
M1V |
probably null |
Het |
Slc39a2 |
A |
T |
14: 52,132,488 (GRCm39) |
T144S |
probably benign |
Het |
Slc5a9 |
T |
C |
4: 111,734,937 (GRCm39) |
H619R |
probably benign |
Het |
Slco4a1 |
T |
C |
2: 180,113,048 (GRCm39) |
F427L |
probably benign |
Het |
Snapc3 |
C |
A |
4: 83,336,073 (GRCm39) |
Y28* |
probably null |
Het |
St3gal6 |
C |
T |
16: 58,293,800 (GRCm39) |
R243H |
probably benign |
Het |
Stat2 |
T |
A |
10: 128,113,066 (GRCm39) |
N119K |
possibly damaging |
Het |
Syne2 |
G |
C |
12: 76,013,145 (GRCm39) |
V2779L |
probably benign |
Het |
Tacc1 |
T |
A |
8: 25,691,301 (GRCm39) |
M1L |
probably damaging |
Het |
Tbc1d32 |
A |
T |
10: 56,027,929 (GRCm39) |
F724L |
possibly damaging |
Het |
Ttc23l |
A |
G |
15: 10,533,766 (GRCm39) |
I259T |
possibly damaging |
Het |
Ucn2 |
T |
C |
9: 108,815,292 (GRCm39) |
I18T |
probably benign |
Het |
Wdr35 |
G |
C |
12: 9,074,886 (GRCm39) |
A1000P |
probably benign |
Het |
Wnk1 |
C |
A |
6: 119,906,789 (GRCm39) |
C244F |
possibly damaging |
Het |
Zeb2 |
T |
G |
2: 44,884,625 (GRCm39) |
D1022A |
probably damaging |
Het |
Zfp26 |
A |
T |
9: 20,349,129 (GRCm39) |
H478Q |
probably damaging |
Het |
Zfp410 |
A |
G |
12: 84,378,630 (GRCm39) |
K265R |
probably benign |
Het |
Zfp575 |
T |
C |
7: 24,286,093 (GRCm39) |
D21G |
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 |
R0197:Hc
|
UTSW |
2 |
34,874,762 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|