Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca9 |
T |
A |
11: 110,011,522 (GRCm39) |
T1174S |
|
Het |
Aoc2 |
C |
T |
11: 101,216,262 (GRCm39) |
P115L |
possibly damaging |
Het |
Arhgef19 |
C |
T |
4: 140,973,738 (GRCm39) |
P75L |
probably benign |
Het |
Atad3a |
A |
G |
4: 155,838,052 (GRCm39) |
V240A |
possibly damaging |
Het |
AW551984 |
A |
T |
9: 39,508,973 (GRCm39) |
L317* |
probably null |
Het |
Bdkrb1 |
T |
C |
12: 105,570,700 (GRCm39) |
S89P |
probably damaging |
Het |
Bpifb4 |
T |
A |
2: 153,790,607 (GRCm39) |
L166* |
probably null |
Het |
Ccdc27 |
A |
G |
4: 154,124,014 (GRCm39) |
V173A |
unknown |
Het |
Ccl8 |
T |
C |
11: 82,006,877 (GRCm39) |
V30A |
probably benign |
Het |
Cdc16 |
C |
T |
8: 13,831,501 (GRCm39) |
A578V |
probably benign |
Het |
Cnksr1 |
T |
C |
4: 133,959,365 (GRCm39) |
Y423C |
probably damaging |
Het |
Cyp3a44 |
T |
C |
5: 145,727,519 (GRCm39) |
D270G |
probably damaging |
Het |
Ep300 |
A |
G |
15: 81,532,730 (GRCm39) |
E1656G |
unknown |
Het |
Eppk1 |
A |
G |
15: 75,992,472 (GRCm39) |
F1470L |
probably benign |
Het |
Fbxw16 |
T |
A |
9: 109,270,135 (GRCm39) |
D202V |
probably damaging |
Het |
Fndc3a |
G |
A |
14: 72,811,840 (GRCm39) |
T330I |
probably benign |
Het |
Gm36864 |
A |
T |
7: 43,887,028 (GRCm39) |
Q307L |
probably benign |
Het |
Gm37240 |
T |
C |
3: 84,426,946 (GRCm39) |
E38G |
probably damaging |
Het |
Gm6871 |
A |
T |
7: 41,195,262 (GRCm39) |
C492S |
probably damaging |
Het |
Gnaq |
T |
C |
19: 16,355,638 (GRCm39) |
Y285H |
probably benign |
Het |
Il21r |
G |
A |
7: 125,231,472 (GRCm39) |
S300N |
probably damaging |
Het |
Itm2b |
G |
A |
14: 73,605,856 (GRCm39) |
|
probably benign |
Het |
Kat6a |
T |
C |
8: 23,425,754 (GRCm39) |
S1100P |
probably damaging |
Het |
Kcnj2 |
T |
C |
11: 110,963,415 (GRCm39) |
I269T |
probably damaging |
Het |
Kmt2c |
G |
A |
5: 25,488,208 (GRCm39) |
A4635V |
probably damaging |
Het |
Kng2 |
A |
T |
16: 22,847,546 (GRCm39) |
D38E |
probably damaging |
Het |
Lgr5 |
A |
C |
10: 115,314,454 (GRCm39) |
L161R |
probably damaging |
Het |
Lrig2 |
A |
T |
3: 104,368,914 (GRCm39) |
I923N |
probably benign |
Het |
Mrgprh |
T |
C |
17: 13,096,200 (GRCm39) |
S147P |
probably damaging |
Het |
Mthfd1 |
C |
T |
12: 76,350,754 (GRCm39) |
T712M |
probably benign |
Het |
Nsmaf |
A |
T |
4: 6,418,523 (GRCm39) |
S427R |
probably damaging |
Het |
Or8g53 |
G |
T |
9: 39,684,038 (GRCm39) |
D19E |
probably benign |
Het |
Pdcd11 |
G |
T |
19: 47,101,658 (GRCm39) |
G948C |
probably damaging |
Het |
Pdzd2 |
A |
G |
15: 12,375,612 (GRCm39) |
Y1508H |
probably damaging |
Het |
Prmt5 |
G |
T |
14: 54,753,564 (GRCm39) |
A105E |
probably benign |
Het |
Prr23a3 |
T |
C |
9: 98,747,213 (GRCm39) |
S56P |
probably damaging |
Het |
Slc44a2 |
A |
G |
9: 21,265,077 (GRCm39) |
E705G |
probably damaging |
Het |
Sostdc1 |
A |
T |
12: 36,364,431 (GRCm39) |
N47Y |
probably benign |
Het |
Speg |
T |
C |
1: 75,405,882 (GRCm39) |
Y3029H |
probably damaging |
Het |
Srd5a1 |
G |
A |
13: 69,748,413 (GRCm39) |
R129* |
probably null |
Het |
Srrm4 |
A |
G |
5: 116,605,586 (GRCm39) |
S224P |
unknown |
Het |
Syne2 |
A |
G |
12: 75,999,618 (GRCm39) |
E2337G |
possibly damaging |
Het |
Tmem150c |
C |
A |
5: 100,240,958 (GRCm39) |
V32L |
probably benign |
Het |
Topaz1 |
T |
C |
9: 122,619,192 (GRCm39) |
I1263T |
possibly damaging |
Het |
Ttc39d |
C |
T |
17: 80,523,349 (GRCm39) |
R3W |
probably benign |
Het |
Xylt1 |
T |
C |
7: 117,250,038 (GRCm39) |
|
probably null |
Het |
Zfp933 |
A |
T |
4: 147,911,021 (GRCm39) |
C192S |
probably damaging |
Het |
Zswim8 |
G |
A |
14: 20,761,119 (GRCm39) |
G129D |
probably damaging |
Het |
|
Other mutations in Htt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00230:Htt
|
APN |
5 |
34,956,752 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00233:Htt
|
APN |
5 |
35,053,370 (GRCm39) |
splice site |
probably null |
|
IGL00559:Htt
|
APN |
5 |
35,006,448 (GRCm39) |
splice site |
probably benign |
|
IGL00765:Htt
|
APN |
5 |
35,034,769 (GRCm39) |
splice site |
probably benign |
|
IGL00950:Htt
|
APN |
5 |
35,048,785 (GRCm39) |
missense |
probably benign |
|
IGL00953:Htt
|
APN |
5 |
34,976,021 (GRCm39) |
missense |
probably benign |
0.04 |
IGL00957:Htt
|
APN |
5 |
34,964,068 (GRCm39) |
missense |
probably benign |
|
IGL01314:Htt
|
APN |
5 |
35,036,200 (GRCm39) |
missense |
probably benign |
|
IGL01412:Htt
|
APN |
5 |
35,055,916 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01510:Htt
|
APN |
5 |
35,064,856 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01617:Htt
|
APN |
5 |
35,034,099 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01893:Htt
|
APN |
5 |
35,034,174 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01914:Htt
|
APN |
5 |
34,987,053 (GRCm39) |
missense |
probably benign |
|
IGL01994:Htt
|
APN |
5 |
34,989,948 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02102:Htt
|
APN |
5 |
35,048,825 (GRCm39) |
splice site |
probably benign |
|
IGL02381:Htt
|
APN |
5 |
34,987,104 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02529:Htt
|
APN |
5 |
34,976,387 (GRCm39) |
splice site |
probably benign |
|
IGL02678:Htt
|
APN |
5 |
35,057,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02707:Htt
|
APN |
5 |
34,987,225 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02731:Htt
|
APN |
5 |
34,961,137 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02931:Htt
|
APN |
5 |
35,034,097 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03167:Htt
|
APN |
5 |
34,976,330 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03343:Htt
|
APN |
5 |
34,983,385 (GRCm39) |
missense |
probably benign |
|
IGL03344:Htt
|
APN |
5 |
35,037,172 (GRCm39) |
missense |
probably benign |
0.39 |
IGL03344:Htt
|
APN |
5 |
35,064,810 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03366:Htt
|
APN |
5 |
35,064,924 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03410:Htt
|
APN |
5 |
34,956,789 (GRCm39) |
missense |
probably damaging |
0.99 |
Chalk
|
UTSW |
5 |
35,064,430 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02796:Htt
|
UTSW |
5 |
35,034,826 (GRCm39) |
missense |
probably benign |
0.43 |
PIT4377001:Htt
|
UTSW |
5 |
35,033,309 (GRCm39) |
missense |
probably benign |
0.10 |
R0013:Htt
|
UTSW |
5 |
34,977,448 (GRCm39) |
missense |
probably benign |
0.25 |
R0049:Htt
|
UTSW |
5 |
35,066,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R0049:Htt
|
UTSW |
5 |
35,066,006 (GRCm39) |
missense |
probably damaging |
0.97 |
R0056:Htt
|
UTSW |
5 |
34,983,422 (GRCm39) |
splice site |
probably benign |
|
R0207:Htt
|
UTSW |
5 |
35,054,252 (GRCm39) |
missense |
probably benign |
0.11 |
R0329:Htt
|
UTSW |
5 |
34,974,478 (GRCm39) |
splice site |
probably benign |
|
R0494:Htt
|
UTSW |
5 |
34,979,188 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0548:Htt
|
UTSW |
5 |
35,028,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Htt
|
UTSW |
5 |
35,003,347 (GRCm39) |
missense |
probably benign |
0.08 |
R0799:Htt
|
UTSW |
5 |
34,975,097 (GRCm39) |
missense |
probably benign |
0.00 |
R0947:Htt
|
UTSW |
5 |
35,056,268 (GRCm39) |
missense |
probably damaging |
1.00 |
R1053:Htt
|
UTSW |
5 |
35,008,561 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1147:Htt
|
UTSW |
5 |
35,008,596 (GRCm39) |
missense |
probably damaging |
0.98 |
R1147:Htt
|
UTSW |
5 |
35,008,596 (GRCm39) |
missense |
probably damaging |
0.98 |
R1478:Htt
|
UTSW |
5 |
34,961,171 (GRCm39) |
missense |
probably damaging |
0.99 |
R1573:Htt
|
UTSW |
5 |
35,021,718 (GRCm39) |
splice site |
probably benign |
|
R1677:Htt
|
UTSW |
5 |
34,985,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Htt
|
UTSW |
5 |
35,064,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R1816:Htt
|
UTSW |
5 |
34,961,084 (GRCm39) |
missense |
probably benign |
0.01 |
R1833:Htt
|
UTSW |
5 |
35,063,092 (GRCm39) |
splice site |
probably benign |
|
R1837:Htt
|
UTSW |
5 |
34,976,367 (GRCm39) |
missense |
probably benign |
0.00 |
R1846:Htt
|
UTSW |
5 |
35,006,288 (GRCm39) |
missense |
probably damaging |
0.98 |
R1875:Htt
|
UTSW |
5 |
34,951,456 (GRCm39) |
missense |
probably benign |
0.05 |
R1899:Htt
|
UTSW |
5 |
35,064,429 (GRCm39) |
missense |
probably benign |
0.01 |
R2013:Htt
|
UTSW |
5 |
35,010,215 (GRCm39) |
missense |
probably damaging |
0.99 |
R2062:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2064:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2067:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2068:Htt
|
UTSW |
5 |
34,983,326 (GRCm39) |
missense |
probably benign |
0.00 |
R2131:Htt
|
UTSW |
5 |
35,034,453 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2162:Htt
|
UTSW |
5 |
34,979,062 (GRCm39) |
missense |
probably benign |
0.44 |
R2169:Htt
|
UTSW |
5 |
35,034,819 (GRCm39) |
missense |
probably benign |
0.08 |
R2345:Htt
|
UTSW |
5 |
34,983,348 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2433:Htt
|
UTSW |
5 |
35,064,885 (GRCm39) |
missense |
possibly damaging |
0.65 |
R3027:Htt
|
UTSW |
5 |
34,977,439 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3123:Htt
|
UTSW |
5 |
34,961,875 (GRCm39) |
missense |
probably benign |
|
R3125:Htt
|
UTSW |
5 |
34,961,875 (GRCm39) |
missense |
probably benign |
|
R3717:Htt
|
UTSW |
5 |
34,968,866 (GRCm39) |
splice site |
probably benign |
|
R3758:Htt
|
UTSW |
5 |
35,053,314 (GRCm39) |
missense |
probably damaging |
0.97 |
R3805:Htt
|
UTSW |
5 |
35,034,548 (GRCm39) |
splice site |
probably null |
|
R3833:Htt
|
UTSW |
5 |
34,979,062 (GRCm39) |
missense |
probably benign |
0.44 |
R4066:Htt
|
UTSW |
5 |
35,036,191 (GRCm39) |
missense |
probably benign |
|
R4272:Htt
|
UTSW |
5 |
35,006,413 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4625:Htt
|
UTSW |
5 |
34,987,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R4634:Htt
|
UTSW |
5 |
35,033,292 (GRCm39) |
missense |
probably benign |
0.06 |
R4655:Htt
|
UTSW |
5 |
35,063,476 (GRCm39) |
missense |
probably benign |
0.06 |
R4679:Htt
|
UTSW |
5 |
34,977,424 (GRCm39) |
missense |
probably benign |
|
R4684:Htt
|
UTSW |
5 |
35,010,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R4832:Htt
|
UTSW |
5 |
34,982,184 (GRCm39) |
missense |
probably benign |
0.01 |
R4833:Htt
|
UTSW |
5 |
35,009,569 (GRCm39) |
missense |
probably damaging |
0.98 |
R4973:Htt
|
UTSW |
5 |
34,970,367 (GRCm39) |
missense |
probably damaging |
0.99 |
R5095:Htt
|
UTSW |
5 |
34,981,739 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5132:Htt
|
UTSW |
5 |
35,063,023 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5351:Htt
|
UTSW |
5 |
34,961,177 (GRCm39) |
missense |
probably damaging |
0.99 |
R5361:Htt
|
UTSW |
5 |
35,064,928 (GRCm39) |
missense |
possibly damaging |
0.47 |
R5399:Htt
|
UTSW |
5 |
35,034,495 (GRCm39) |
missense |
probably damaging |
0.98 |
R5462:Htt
|
UTSW |
5 |
35,042,851 (GRCm39) |
nonsense |
probably null |
|
R5552:Htt
|
UTSW |
5 |
34,979,118 (GRCm39) |
missense |
probably benign |
|
R5566:Htt
|
UTSW |
5 |
35,006,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R5595:Htt
|
UTSW |
5 |
35,062,741 (GRCm39) |
missense |
probably damaging |
0.96 |
R5617:Htt
|
UTSW |
5 |
35,028,150 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5835:Htt
|
UTSW |
5 |
34,970,534 (GRCm39) |
missense |
probably benign |
0.16 |
R5891:Htt
|
UTSW |
5 |
35,028,167 (GRCm39) |
missense |
possibly damaging |
0.62 |
R6158:Htt
|
UTSW |
5 |
35,064,430 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6159:Htt
|
UTSW |
5 |
34,962,020 (GRCm39) |
missense |
probably benign |
0.08 |
R6169:Htt
|
UTSW |
5 |
35,064,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Htt
|
UTSW |
5 |
35,003,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R6274:Htt
|
UTSW |
5 |
35,009,431 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6280:Htt
|
UTSW |
5 |
35,028,103 (GRCm39) |
missense |
probably benign |
0.00 |
R6294:Htt
|
UTSW |
5 |
34,979,170 (GRCm39) |
missense |
probably benign |
|
R6331:Htt
|
UTSW |
5 |
35,053,231 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6448:Htt
|
UTSW |
5 |
35,033,336 (GRCm39) |
missense |
probably benign |
0.05 |
R6474:Htt
|
UTSW |
5 |
34,982,239 (GRCm39) |
missense |
probably benign |
0.06 |
R6592:Htt
|
UTSW |
5 |
35,034,388 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6818:Htt
|
UTSW |
5 |
34,940,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R6830:Htt
|
UTSW |
5 |
34,991,670 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6920:Htt
|
UTSW |
5 |
35,034,444 (GRCm39) |
missense |
probably null |
1.00 |
R6962:Htt
|
UTSW |
5 |
35,057,115 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7057:Htt
|
UTSW |
5 |
34,979,067 (GRCm39) |
missense |
probably null |
0.05 |
R7144:Htt
|
UTSW |
5 |
35,003,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R7166:Htt
|
UTSW |
5 |
35,010,238 (GRCm39) |
missense |
probably benign |
0.42 |
R7329:Htt
|
UTSW |
5 |
34,987,099 (GRCm39) |
missense |
probably benign |
0.03 |
R7378:Htt
|
UTSW |
5 |
34,961,143 (GRCm39) |
missense |
probably benign |
0.04 |
R7418:Htt
|
UTSW |
5 |
34,947,697 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7495:Htt
|
UTSW |
5 |
34,968,821 (GRCm39) |
missense |
probably benign |
0.00 |
R7554:Htt
|
UTSW |
5 |
35,022,084 (GRCm39) |
missense |
probably damaging |
0.97 |
R7575:Htt
|
UTSW |
5 |
35,062,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R7763:Htt
|
UTSW |
5 |
35,009,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R7782:Htt
|
UTSW |
5 |
35,040,336 (GRCm39) |
missense |
probably benign |
0.03 |
R7850:Htt
|
UTSW |
5 |
35,009,631 (GRCm39) |
splice site |
probably null |
|
R7870:Htt
|
UTSW |
5 |
35,055,891 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7871:Htt
|
UTSW |
5 |
35,021,993 (GRCm39) |
missense |
probably benign |
0.00 |
R7879:Htt
|
UTSW |
5 |
34,981,252 (GRCm39) |
missense |
probably benign |
|
R7992:Htt
|
UTSW |
5 |
34,987,225 (GRCm39) |
critical splice donor site |
probably null |
|
R8058:Htt
|
UTSW |
5 |
34,977,444 (GRCm39) |
missense |
probably benign |
|
R8168:Htt
|
UTSW |
5 |
35,040,300 (GRCm39) |
missense |
probably benign |
0.00 |
R8188:Htt
|
UTSW |
5 |
34,919,287 (GRCm39) |
missense |
probably benign |
0.03 |
R8262:Htt
|
UTSW |
5 |
35,053,304 (GRCm39) |
missense |
probably benign |
|
R8343:Htt
|
UTSW |
5 |
35,063,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8353:Htt
|
UTSW |
5 |
35,034,499 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8769:Htt
|
UTSW |
5 |
34,977,633 (GRCm39) |
missense |
probably benign |
0.05 |
R8808:Htt
|
UTSW |
5 |
35,046,791 (GRCm39) |
missense |
probably benign |
0.10 |
R8825:Htt
|
UTSW |
5 |
34,983,304 (GRCm39) |
missense |
probably benign |
0.24 |
R8843:Htt
|
UTSW |
5 |
35,046,809 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8856:Htt
|
UTSW |
5 |
35,060,675 (GRCm39) |
missense |
probably benign |
0.44 |
R8882:Htt
|
UTSW |
5 |
34,979,061 (GRCm39) |
missense |
probably benign |
|
R8898:Htt
|
UTSW |
5 |
34,976,376 (GRCm39) |
missense |
probably benign |
0.01 |
R8964:Htt
|
UTSW |
5 |
35,062,720 (GRCm39) |
missense |
probably benign |
0.09 |
R8987:Htt
|
UTSW |
5 |
34,977,368 (GRCm39) |
missense |
probably benign |
0.18 |
R8991:Htt
|
UTSW |
5 |
35,063,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R9005:Htt
|
UTSW |
5 |
34,975,095 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9057:Htt
|
UTSW |
5 |
35,009,454 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9157:Htt
|
UTSW |
5 |
34,987,171 (GRCm39) |
missense |
probably null |
0.89 |
R9205:Htt
|
UTSW |
5 |
34,976,367 (GRCm39) |
missense |
probably benign |
0.00 |
R9223:Htt
|
UTSW |
5 |
35,062,692 (GRCm39) |
missense |
probably benign |
0.01 |
R9243:Htt
|
UTSW |
5 |
35,056,276 (GRCm39) |
splice site |
probably benign |
|
R9329:Htt
|
UTSW |
5 |
34,989,957 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9355:Htt
|
UTSW |
5 |
35,053,247 (GRCm39) |
missense |
probably benign |
|
R9402:Htt
|
UTSW |
5 |
35,006,324 (GRCm39) |
missense |
probably damaging |
1.00 |
R9446:Htt
|
UTSW |
5 |
34,919,272 (GRCm39) |
missense |
probably benign |
|
R9716:Htt
|
UTSW |
5 |
35,012,019 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Htt
|
UTSW |
5 |
35,009,575 (GRCm39) |
missense |
probably null |
0.87 |
|