Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim2 |
A |
G |
5: 36,000,614 (GRCm39) |
|
probably benign |
Het |
Adamts20 |
C |
T |
15: 94,238,968 (GRCm39) |
S750N |
probably damaging |
Het |
Adh6a |
G |
A |
3: 138,036,722 (GRCm39) |
R370H |
possibly damaging |
Het |
Akr1b7 |
A |
G |
6: 34,396,046 (GRCm39) |
N183D |
probably damaging |
Het |
Aktip |
A |
T |
8: 91,856,348 (GRCm39) |
I43N |
probably damaging |
Het |
Ankrd26 |
A |
T |
6: 118,502,883 (GRCm39) |
|
probably benign |
Het |
Ano9 |
G |
A |
7: 140,688,717 (GRCm39) |
T144I |
possibly damaging |
Het |
Anpep |
G |
T |
7: 79,491,571 (GRCm39) |
D143E |
probably benign |
Het |
Aox1 |
C |
A |
1: 58,333,484 (GRCm39) |
Q234K |
probably benign |
Het |
Ap1g1 |
C |
G |
8: 110,559,814 (GRCm39) |
|
probably benign |
Het |
Arhgef4 |
G |
A |
1: 34,849,636 (GRCm39) |
|
probably null |
Het |
Arsj |
A |
G |
3: 126,231,944 (GRCm39) |
Y230C |
possibly damaging |
Het |
Asmt |
C |
T |
X: 169,109,480 (GRCm39) |
|
probably benign |
Het |
Astl |
A |
T |
2: 127,187,405 (GRCm39) |
K72N |
probably damaging |
Het |
Atp2b2 |
G |
A |
6: 113,780,704 (GRCm39) |
|
probably benign |
Het |
Baiap2l1 |
A |
C |
5: 144,261,365 (GRCm39) |
|
probably null |
Het |
C7 |
A |
T |
15: 5,063,821 (GRCm39) |
N193K |
probably damaging |
Het |
Cacna2d4 |
G |
T |
6: 119,247,785 (GRCm39) |
R362L |
probably damaging |
Het |
Cct4 |
T |
A |
11: 22,947,615 (GRCm39) |
D189E |
probably benign |
Het |
Cd300lg |
G |
A |
11: 101,933,938 (GRCm39) |
G62S |
probably benign |
Het |
Cdk14 |
T |
A |
5: 5,060,901 (GRCm39) |
M307L |
probably damaging |
Het |
Cfi |
G |
A |
3: 129,666,768 (GRCm39) |
|
probably null |
Het |
Clec2g |
G |
T |
6: 128,957,273 (GRCm39) |
|
probably null |
Het |
Cntnap2 |
T |
C |
6: 46,965,609 (GRCm39) |
S807P |
probably damaging |
Het |
Col6a3 |
T |
A |
1: 90,755,671 (GRCm39) |
H206L |
probably damaging |
Het |
Ct55 |
A |
G |
X: 52,735,716 (GRCm39) |
E99G |
probably benign |
Het |
Cyp2c23 |
A |
T |
19: 44,009,997 (GRCm39) |
|
probably benign |
Het |
Degs1l |
T |
C |
1: 180,887,252 (GRCm39) |
I279T |
probably damaging |
Het |
Dlec1 |
T |
C |
9: 118,965,767 (GRCm39) |
V1058A |
probably benign |
Het |
Dpp9 |
A |
G |
17: 56,506,038 (GRCm39) |
Y454H |
probably damaging |
Het |
Duox2 |
A |
G |
2: 122,114,378 (GRCm39) |
S1142P |
possibly damaging |
Het |
Fam13a |
C |
T |
6: 58,942,045 (GRCm39) |
|
probably null |
Het |
Filip1l |
A |
G |
16: 57,327,023 (GRCm39) |
R18G |
probably benign |
Het |
Foxa1 |
A |
G |
12: 57,589,527 (GRCm39) |
V231A |
probably damaging |
Het |
Gm4787 |
A |
T |
12: 81,425,303 (GRCm39) |
M285K |
possibly damaging |
Het |
Gm5084 |
T |
A |
13: 60,360,320 (GRCm39) |
|
noncoding transcript |
Het |
Gm6788 |
G |
A |
19: 28,740,586 (GRCm39) |
|
noncoding transcript |
Het |
Gm9922 |
G |
T |
14: 101,966,841 (GRCm39) |
|
probably benign |
Het |
Gtf3c4 |
A |
T |
2: 28,723,988 (GRCm39) |
Y440* |
probably null |
Het |
Helq |
A |
G |
5: 100,921,820 (GRCm39) |
S795P |
probably damaging |
Het |
Helz |
T |
A |
11: 107,489,997 (GRCm39) |
S151T |
possibly damaging |
Het |
Irgm1 |
T |
C |
11: 48,757,440 (GRCm39) |
T124A |
probably benign |
Het |
Itgam |
C |
T |
7: 127,670,109 (GRCm39) |
P134S |
possibly damaging |
Het |
Kdm6a |
T |
C |
X: 18,102,923 (GRCm39) |
Y217H |
probably benign |
Het |
Kif6 |
T |
C |
17: 50,208,812 (GRCm39) |
L744P |
probably benign |
Het |
Kmt2c |
C |
T |
5: 25,489,190 (GRCm39) |
R1203H |
probably damaging |
Het |
Ksr2 |
A |
G |
5: 117,693,535 (GRCm39) |
T328A |
probably damaging |
Het |
Lig1 |
T |
C |
7: 13,034,281 (GRCm39) |
|
probably benign |
Het |
Lpar3 |
G |
A |
3: 145,946,303 (GRCm39) |
|
probably benign |
Het |
Lrrk2 |
T |
C |
15: 91,584,095 (GRCm39) |
F285S |
possibly damaging |
Het |
Marchf7 |
A |
G |
2: 60,062,637 (GRCm39) |
D148G |
probably benign |
Het |
Mcee |
T |
C |
7: 64,050,049 (GRCm39) |
L60S |
probably damaging |
Het |
Mob2 |
A |
G |
7: 141,570,111 (GRCm39) |
I81T |
probably damaging |
Het |
Mphosph8 |
T |
A |
14: 56,909,909 (GRCm39) |
D87E |
probably damaging |
Het |
Msantd5f9 |
A |
G |
4: 73,835,754 (GRCm39) |
F237L |
probably benign |
Het |
Myo1g |
T |
C |
11: 6,462,283 (GRCm39) |
T560A |
probably benign |
Het |
Nagk |
C |
T |
6: 83,774,169 (GRCm39) |
T42I |
probably benign |
Het |
Naip1 |
G |
T |
13: 100,562,747 (GRCm39) |
T806K |
probably benign |
Het |
Ncor2 |
A |
G |
5: 125,195,857 (GRCm39) |
|
probably benign |
Het |
Ocln |
G |
T |
13: 100,647,967 (GRCm39) |
Y401* |
probably null |
Het |
Odad2 |
T |
A |
18: 7,211,630 (GRCm39) |
Y748F |
probably benign |
Het |
Oma1 |
T |
A |
4: 103,182,374 (GRCm39) |
N292K |
probably damaging |
Het |
Or8b55 |
G |
A |
9: 38,727,443 (GRCm39) |
V215I |
probably benign |
Het |
Ovch2 |
T |
A |
7: 107,389,412 (GRCm39) |
|
probably null |
Het |
Pcdhb16 |
T |
C |
18: 37,611,441 (GRCm39) |
F134L |
probably damaging |
Het |
Pipox |
A |
T |
11: 77,772,360 (GRCm39) |
Y337N |
probably benign |
Het |
Polr3b |
A |
G |
10: 84,528,865 (GRCm39) |
D763G |
probably damaging |
Het |
Pygo1 |
T |
A |
9: 72,852,078 (GRCm39) |
N88K |
probably damaging |
Het |
Rab3gap1 |
T |
C |
1: 127,862,251 (GRCm39) |
M674T |
probably damaging |
Het |
Rbm25 |
T |
C |
12: 83,719,501 (GRCm39) |
|
probably benign |
Het |
Rbm26 |
C |
T |
14: 105,354,542 (GRCm39) |
|
probably benign |
Het |
Rbms2 |
G |
A |
10: 127,974,055 (GRCm39) |
T187I |
possibly damaging |
Het |
Rnase11 |
T |
A |
14: 51,287,184 (GRCm39) |
R123S |
probably benign |
Het |
Rngtt |
A |
G |
4: 33,443,614 (GRCm39) |
N485D |
probably benign |
Het |
Rp1l1 |
A |
T |
14: 64,265,415 (GRCm39) |
M334L |
probably benign |
Het |
Rps9 |
T |
A |
7: 3,707,726 (GRCm39) |
L56Q |
probably damaging |
Het |
Saysd1 |
C |
A |
14: 20,133,170 (GRCm39) |
|
probably benign |
Het |
Sema4d |
C |
T |
13: 51,867,727 (GRCm39) |
|
probably null |
Het |
Shisa5 |
A |
T |
9: 108,869,998 (GRCm39) |
D34V |
probably damaging |
Het |
Skil |
A |
G |
3: 31,171,655 (GRCm39) |
D547G |
probably damaging |
Het |
Slc2a5 |
T |
A |
4: 150,227,514 (GRCm39) |
F444L |
probably damaging |
Het |
Slc9b2 |
T |
G |
3: 135,022,892 (GRCm39) |
C10G |
possibly damaging |
Het |
Sorcs2 |
G |
T |
5: 36,386,564 (GRCm39) |
|
probably benign |
Het |
Stk17b |
T |
G |
1: 53,805,140 (GRCm39) |
K140N |
possibly damaging |
Het |
Stradb |
T |
A |
1: 59,033,549 (GRCm39) |
L404Q |
possibly damaging |
Het |
Synj2 |
T |
C |
17: 6,076,826 (GRCm39) |
M432T |
possibly damaging |
Het |
Tanc1 |
G |
T |
2: 59,630,441 (GRCm39) |
R800L |
probably damaging |
Het |
Tenm4 |
A |
G |
7: 96,522,987 (GRCm39) |
M1473V |
probably benign |
Het |
Tesc |
A |
G |
5: 118,199,667 (GRCm39) |
I190V |
probably benign |
Het |
Tex15 |
T |
C |
8: 34,064,262 (GRCm39) |
F1231L |
probably benign |
Het |
Thrsp |
T |
C |
7: 97,066,332 (GRCm39) |
I127V |
probably benign |
Het |
Tlr6 |
A |
T |
5: 65,111,055 (GRCm39) |
C617* |
probably null |
Het |
Trank1 |
A |
T |
9: 111,221,893 (GRCm39) |
I2877F |
probably benign |
Het |
Tut4 |
T |
A |
4: 108,406,552 (GRCm39) |
H1373Q |
probably damaging |
Het |
Ucp1 |
T |
C |
8: 84,024,496 (GRCm39) |
S274P |
probably damaging |
Het |
Ucp2 |
T |
A |
7: 100,147,606 (GRCm39) |
V195E |
probably damaging |
Het |
Vars2 |
T |
C |
17: 35,973,108 (GRCm39) |
T394A |
probably damaging |
Het |
Vmn1r1 |
A |
G |
1: 181,985,371 (GRCm39) |
V98A |
possibly damaging |
Het |
Vmn1r225 |
A |
G |
17: 20,722,918 (GRCm39) |
I120V |
probably benign |
Het |
Vmn2r102 |
A |
T |
17: 19,897,881 (GRCm39) |
M299L |
probably benign |
Het |
Vmn2r25 |
A |
G |
6: 123,802,337 (GRCm39) |
V522A |
probably benign |
Het |
Vmn2r70 |
T |
C |
7: 85,215,130 (GRCm39) |
I135V |
probably benign |
Het |
Vwf |
T |
C |
6: 125,567,138 (GRCm39) |
|
probably benign |
Het |
Zfp446 |
T |
C |
7: 12,713,048 (GRCm39) |
F29L |
probably damaging |
Het |
|
Other mutations in Drosha |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00576:Drosha
|
APN |
15 |
12,883,280 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00736:Drosha
|
APN |
15 |
12,834,045 (GRCm39) |
missense |
unknown |
|
IGL00963:Drosha
|
APN |
15 |
12,926,083 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01010:Drosha
|
APN |
15 |
12,827,375 (GRCm39) |
unclassified |
probably benign |
|
IGL01340:Drosha
|
APN |
15 |
12,834,109 (GRCm39) |
intron |
probably benign |
|
IGL01481:Drosha
|
APN |
15 |
12,842,525 (GRCm39) |
missense |
probably benign |
|
IGL01714:Drosha
|
APN |
15 |
12,878,870 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01721:Drosha
|
APN |
15 |
12,846,198 (GRCm39) |
nonsense |
probably null |
|
IGL01765:Drosha
|
APN |
15 |
12,902,766 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01893:Drosha
|
APN |
15 |
12,866,736 (GRCm39) |
splice site |
probably benign |
|
IGL01944:Drosha
|
APN |
15 |
12,889,805 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02285:Drosha
|
APN |
15 |
12,833,950 (GRCm39) |
missense |
unknown |
|
IGL02970:Drosha
|
APN |
15 |
12,914,042 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02990:Drosha
|
APN |
15 |
12,827,353 (GRCm39) |
unclassified |
probably benign |
|
IGL03019:Drosha
|
APN |
15 |
12,846,185 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03279:Drosha
|
APN |
15 |
12,859,478 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03390:Drosha
|
APN |
15 |
12,885,069 (GRCm39) |
splice site |
probably null |
|
tippicanoe
|
UTSW |
15 |
12,859,551 (GRCm39) |
splice site |
probably null |
|
Tyler
|
UTSW |
15 |
12,861,792 (GRCm39) |
missense |
probably benign |
0.45 |
R0115:Drosha
|
UTSW |
15 |
12,846,216 (GRCm39) |
missense |
probably benign |
0.15 |
R0352:Drosha
|
UTSW |
15 |
12,837,374 (GRCm39) |
missense |
unknown |
|
R0401:Drosha
|
UTSW |
15 |
12,926,117 (GRCm39) |
nonsense |
probably null |
|
R0541:Drosha
|
UTSW |
15 |
12,907,474 (GRCm39) |
missense |
probably benign |
0.09 |
R0784:Drosha
|
UTSW |
15 |
12,867,764 (GRCm39) |
splice site |
probably benign |
|
R0918:Drosha
|
UTSW |
15 |
12,842,619 (GRCm39) |
critical splice donor site |
probably null |
|
R1473:Drosha
|
UTSW |
15 |
12,912,606 (GRCm39) |
missense |
probably benign |
0.04 |
R1503:Drosha
|
UTSW |
15 |
12,848,159 (GRCm39) |
missense |
probably benign |
0.02 |
R1526:Drosha
|
UTSW |
15 |
12,914,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Drosha
|
UTSW |
15 |
12,878,804 (GRCm39) |
missense |
probably benign |
0.14 |
R2004:Drosha
|
UTSW |
15 |
12,915,467 (GRCm39) |
missense |
probably damaging |
0.98 |
R2060:Drosha
|
UTSW |
15 |
12,924,245 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2516:Drosha
|
UTSW |
15 |
12,859,551 (GRCm39) |
splice site |
probably null |
|
R3691:Drosha
|
UTSW |
15 |
12,834,724 (GRCm39) |
missense |
unknown |
|
R3784:Drosha
|
UTSW |
15 |
12,890,615 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3789:Drosha
|
UTSW |
15 |
12,912,623 (GRCm39) |
nonsense |
probably null |
|
R3790:Drosha
|
UTSW |
15 |
12,912,623 (GRCm39) |
nonsense |
probably null |
|
R4020:Drosha
|
UTSW |
15 |
12,837,422 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4817:Drosha
|
UTSW |
15 |
12,914,133 (GRCm39) |
missense |
probably damaging |
0.97 |
R4989:Drosha
|
UTSW |
15 |
12,935,093 (GRCm39) |
missense |
probably benign |
0.05 |
R5080:Drosha
|
UTSW |
15 |
12,842,229 (GRCm39) |
missense |
probably benign |
0.01 |
R5132:Drosha
|
UTSW |
15 |
12,837,377 (GRCm39) |
missense |
unknown |
|
R5215:Drosha
|
UTSW |
15 |
12,885,219 (GRCm39) |
intron |
probably benign |
|
R5386:Drosha
|
UTSW |
15 |
12,842,207 (GRCm39) |
missense |
probably benign |
|
R5457:Drosha
|
UTSW |
15 |
12,926,115 (GRCm39) |
missense |
probably benign |
0.26 |
R5536:Drosha
|
UTSW |
15 |
12,929,797 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5800:Drosha
|
UTSW |
15 |
12,902,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R5800:Drosha
|
UTSW |
15 |
12,865,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R5915:Drosha
|
UTSW |
15 |
12,935,152 (GRCm39) |
missense |
probably damaging |
0.97 |
R5988:Drosha
|
UTSW |
15 |
12,834,582 (GRCm39) |
intron |
probably benign |
|
R6033:Drosha
|
UTSW |
15 |
12,926,085 (GRCm39) |
missense |
probably benign |
0.25 |
R6033:Drosha
|
UTSW |
15 |
12,926,085 (GRCm39) |
missense |
probably benign |
0.25 |
R6063:Drosha
|
UTSW |
15 |
12,834,156 (GRCm39) |
intron |
probably benign |
|
R6391:Drosha
|
UTSW |
15 |
12,889,803 (GRCm39) |
nonsense |
probably null |
|
R6492:Drosha
|
UTSW |
15 |
12,861,792 (GRCm39) |
missense |
probably benign |
0.45 |
R6799:Drosha
|
UTSW |
15 |
12,912,623 (GRCm39) |
nonsense |
probably null |
|
R6870:Drosha
|
UTSW |
15 |
12,907,479 (GRCm39) |
missense |
probably benign |
0.17 |
R6920:Drosha
|
UTSW |
15 |
12,834,396 (GRCm39) |
missense |
unknown |
|
R7101:Drosha
|
UTSW |
15 |
12,865,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7142:Drosha
|
UTSW |
15 |
12,924,232 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7275:Drosha
|
UTSW |
15 |
12,846,169 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7337:Drosha
|
UTSW |
15 |
12,846,285 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7471:Drosha
|
UTSW |
15 |
12,889,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7538:Drosha
|
UTSW |
15 |
12,926,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7559:Drosha
|
UTSW |
15 |
12,842,508 (GRCm39) |
missense |
probably damaging |
0.96 |
R7651:Drosha
|
UTSW |
15 |
12,859,522 (GRCm39) |
missense |
probably benign |
0.30 |
R7652:Drosha
|
UTSW |
15 |
12,859,522 (GRCm39) |
missense |
probably benign |
0.30 |
R7653:Drosha
|
UTSW |
15 |
12,859,522 (GRCm39) |
missense |
probably benign |
0.30 |
R7727:Drosha
|
UTSW |
15 |
12,881,731 (GRCm39) |
missense |
probably damaging |
1.00 |
R7780:Drosha
|
UTSW |
15 |
12,848,172 (GRCm39) |
missense |
probably benign |
0.01 |
R8068:Drosha
|
UTSW |
15 |
12,883,276 (GRCm39) |
nonsense |
probably null |
|
R8283:Drosha
|
UTSW |
15 |
12,890,587 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8523:Drosha
|
UTSW |
15 |
12,834,408 (GRCm39) |
missense |
unknown |
|
R8985:Drosha
|
UTSW |
15 |
12,924,187 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9418:Drosha
|
UTSW |
15 |
12,885,167 (GRCm39) |
missense |
probably benign |
0.02 |
R9501:Drosha
|
UTSW |
15 |
12,928,992 (GRCm39) |
missense |
probably damaging |
1.00 |
R9674:Drosha
|
UTSW |
15 |
12,890,170 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Drosha
|
UTSW |
15 |
12,842,178 (GRCm39) |
missense |
probably benign |
|
|