Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930488N24Rik |
T |
C |
17: 14,326,481 (GRCm39) |
|
noncoding transcript |
Het |
5730455P16Rik |
A |
T |
11: 80,266,346 (GRCm39) |
S132T |
possibly damaging |
Het |
Aadacl3 |
T |
A |
4: 144,184,527 (GRCm39) |
H77L |
probably damaging |
Het |
Actr5 |
T |
A |
2: 158,467,426 (GRCm39) |
V122D |
probably damaging |
Het |
Adamts7 |
A |
G |
9: 90,071,739 (GRCm39) |
D678G |
possibly damaging |
Het |
Alpk1 |
T |
A |
3: 127,464,708 (GRCm39) |
D1190V |
probably benign |
Het |
Apbb1ip |
A |
T |
2: 22,765,265 (GRCm39) |
N649Y |
unknown |
Het |
Atp6v0a1 |
A |
G |
11: 100,933,776 (GRCm39) |
I522V |
probably benign |
Het |
Brd10 |
T |
C |
19: 29,695,809 (GRCm39) |
N1228S |
possibly damaging |
Het |
Cars1 |
T |
C |
7: 143,124,301 (GRCm39) |
D375G |
probably damaging |
Het |
Catspere1 |
A |
T |
1: 177,687,441 (GRCm39) |
|
noncoding transcript |
Het |
Ccdc87 |
A |
G |
19: 4,890,579 (GRCm39) |
D357G |
probably damaging |
Het |
Cd101 |
A |
T |
3: 100,929,471 (GRCm39) |
S8T |
probably benign |
Het |
Cfap65 |
C |
T |
1: 74,966,791 (GRCm39) |
A299T |
probably benign |
Het |
Cic |
T |
C |
7: 24,971,157 (GRCm39) |
V296A |
possibly damaging |
Het |
Col7a1 |
T |
A |
9: 108,797,675 (GRCm39) |
S1686T |
possibly damaging |
Het |
Ctbp2 |
A |
C |
7: 132,615,423 (GRCm39) |
L504R |
probably damaging |
Het |
Cttnbp2nl |
T |
C |
3: 104,918,640 (GRCm39) |
K67E |
probably benign |
Het |
Cyp2c50 |
C |
T |
19: 40,102,024 (GRCm39) |
P480S |
probably damaging |
Het |
Dcdc5 |
A |
C |
2: 106,166,420 (GRCm39) |
|
noncoding transcript |
Het |
Defb2 |
G |
T |
8: 22,333,317 (GRCm39) |
E31* |
probably null |
Het |
Dhrs1 |
T |
A |
14: 55,977,083 (GRCm39) |
N244I |
possibly damaging |
Het |
Dop1b |
A |
G |
16: 93,589,978 (GRCm39) |
I134V |
probably benign |
Het |
Eif1ad11 |
A |
T |
12: 87,994,158 (GRCm39) |
I129F |
unknown |
Het |
Etl4 |
A |
G |
2: 20,811,496 (GRCm39) |
D1193G |
possibly damaging |
Het |
Ezh1 |
A |
C |
11: 101,094,594 (GRCm39) |
S399R |
probably damaging |
Het |
Fam161a |
T |
C |
11: 22,970,076 (GRCm39) |
S26P |
probably damaging |
Het |
Fcgbp |
C |
A |
7: 27,813,383 (GRCm39) |
S2306Y |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,876,512 (GRCm39) |
I2415T |
probably benign |
Het |
Gas2l3 |
A |
G |
10: 89,252,907 (GRCm39) |
L246P |
probably damaging |
Het |
Gdf15 |
C |
T |
8: 71,082,246 (GRCm39) |
V287M |
probably damaging |
Het |
Gm7742 |
T |
C |
17: 21,420,235 (GRCm39) |
|
noncoding transcript |
Het |
Grin2d |
T |
C |
7: 45,507,363 (GRCm39) |
D446G |
probably damaging |
Het |
Hemk1 |
A |
G |
9: 107,205,385 (GRCm39) |
F107L |
probably benign |
Het |
Hmgcr |
C |
T |
13: 96,796,700 (GRCm39) |
G197S |
probably damaging |
Het |
Ift52 |
G |
A |
2: 162,873,108 (GRCm39) |
G207D |
probably benign |
Het |
Iqcf3 |
T |
C |
9: 106,430,788 (GRCm39) |
|
probably benign |
Het |
Kcna1 |
A |
G |
6: 126,619,099 (GRCm39) |
I407T |
probably damaging |
Het |
Kcnrg |
T |
A |
14: 61,845,386 (GRCm39) |
M142K |
probably benign |
Het |
Lhx9 |
C |
A |
1: 138,766,105 (GRCm39) |
V237L |
probably benign |
Het |
Lipo3 |
A |
C |
19: 33,560,497 (GRCm39) |
I56S |
probably damaging |
Het |
Loxhd1 |
C |
G |
18: 77,472,663 (GRCm39) |
P1060R |
probably damaging |
Het |
Map2k4 |
A |
C |
11: 65,587,201 (GRCm39) |
|
probably benign |
Het |
Methig1 |
A |
G |
15: 100,251,416 (GRCm39) |
K109R |
possibly damaging |
Het |
Mmrn1 |
G |
A |
6: 60,950,027 (GRCm39) |
V326I |
probably benign |
Het |
Myo15a |
G |
A |
11: 60,367,741 (GRCm39) |
R167H |
probably damaging |
Het |
Ncoa7 |
G |
A |
10: 30,524,472 (GRCm39) |
T142M |
probably damaging |
Het |
Nfkb2 |
C |
A |
19: 46,296,493 (GRCm39) |
Q254K |
probably damaging |
Het |
Nherf1 |
A |
G |
11: 115,070,918 (GRCm39) |
E290G |
probably benign |
Het |
Nol6 |
G |
T |
4: 41,121,508 (GRCm39) |
P278Q |
probably damaging |
Het |
Nptxr |
T |
A |
15: 79,677,027 (GRCm39) |
D285V |
probably damaging |
Het |
Oosp3 |
T |
C |
19: 11,688,997 (GRCm39) |
W82R |
probably damaging |
Het |
Or6b3 |
A |
T |
1: 92,438,812 (GRCm39) |
*313K |
probably null |
Het |
Or6n1 |
A |
G |
1: 173,916,742 (GRCm39) |
I45M |
possibly damaging |
Het |
Pa2g4 |
G |
T |
10: 128,395,199 (GRCm39) |
T322K |
probably damaging |
Het |
Parp16 |
C |
A |
9: 65,145,175 (GRCm39) |
F291L |
probably damaging |
Het |
Pdzd9 |
A |
T |
7: 120,267,619 (GRCm39) |
D65E |
probably damaging |
Het |
Pgap3 |
A |
G |
11: 98,281,300 (GRCm39) |
W238R |
probably damaging |
Het |
Pgf |
G |
A |
12: 85,218,538 (GRCm39) |
H67Y |
probably benign |
Het |
Pik3cb |
T |
C |
9: 98,955,679 (GRCm39) |
T413A |
probably benign |
Het |
Plcxd2 |
A |
T |
16: 45,800,700 (GRCm39) |
C175S |
probably benign |
Het |
Pou2f1 |
A |
T |
1: 165,719,517 (GRCm39) |
|
probably benign |
Het |
Ppfia1 |
T |
G |
7: 144,052,106 (GRCm39) |
N846T |
probably benign |
Het |
Ppid |
T |
A |
3: 79,502,504 (GRCm39) |
|
probably null |
Het |
Prkcq |
G |
A |
2: 11,231,797 (GRCm39) |
|
probably null |
Het |
Ptgds |
T |
C |
2: 25,359,058 (GRCm39) |
K66E |
probably benign |
Het |
Ptpmt1 |
A |
G |
2: 90,748,283 (GRCm39) |
|
noncoding transcript |
Het |
Rab3il1 |
G |
A |
19: 10,004,034 (GRCm39) |
G51D |
probably benign |
Het |
Rdx |
T |
C |
9: 51,974,891 (GRCm39) |
V9A |
probably damaging |
Het |
Rpl7l1 |
T |
C |
17: 47,089,014 (GRCm39) |
N239S |
probably benign |
Het |
Rrbp1 |
C |
A |
2: 143,806,685 (GRCm39) |
A978S |
possibly damaging |
Het |
Rsf1 |
GCGGCGGCG |
GCGGCGGCGCCGGCGGCG |
7: 97,229,126 (GRCm39) |
|
probably benign |
Het |
Scn3a |
A |
T |
2: 65,291,622 (GRCm39) |
I1708N |
probably damaging |
Het |
Serinc1 |
A |
G |
10: 57,401,466 (GRCm39) |
I109T |
possibly damaging |
Het |
Shroom1 |
G |
A |
11: 53,355,966 (GRCm39) |
V339I |
probably benign |
Het |
Slc30a8 |
T |
A |
15: 52,169,880 (GRCm39) |
C36S |
probably benign |
Het |
Slco1b2 |
A |
G |
6: 141,631,158 (GRCm39) |
I597M |
probably benign |
Het |
Snx27 |
A |
G |
3: 94,427,518 (GRCm39) |
F228S |
probably damaging |
Het |
Spata31f1a |
T |
A |
4: 42,851,815 (GRCm39) |
I114F |
probably damaging |
Het |
Speer4e2 |
G |
T |
5: 15,026,225 (GRCm39) |
T144K |
probably benign |
Het |
Stim1 |
T |
A |
7: 102,064,571 (GRCm39) |
F214I |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,082,664 (GRCm39) |
T1987A |
probably benign |
Het |
Tamm41 |
A |
G |
6: 115,002,378 (GRCm39) |
I18T |
possibly damaging |
Het |
Tmem150b |
T |
A |
7: 4,726,871 (GRCm39) |
D79V |
probably damaging |
Het |
Tmem167 |
T |
A |
13: 90,252,548 (GRCm39) |
I68N |
probably benign |
Het |
Traf3 |
A |
G |
12: 111,227,204 (GRCm39) |
E339G |
possibly damaging |
Het |
Tspan12 |
G |
A |
6: 21,795,660 (GRCm39) |
P177S |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,783,562 (GRCm39) |
I810T |
probably benign |
Het |
Ulk1 |
T |
C |
5: 110,939,996 (GRCm39) |
T407A |
probably benign |
Het |
Uroc1 |
G |
A |
6: 90,334,600 (GRCm39) |
|
probably null |
Het |
Vmn2r-ps69 |
T |
C |
7: 84,959,584 (GRCm39) |
|
noncoding transcript |
Het |
Wdr59 |
T |
C |
8: 112,207,446 (GRCm39) |
N476S |
probably benign |
Het |
Zfp472 |
A |
G |
17: 33,196,416 (GRCm39) |
M164V |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,120,756 (GRCm39) |
N277S |
probably benign |
Het |
Zfp831 |
T |
C |
2: 174,547,097 (GRCm39) |
C1427R |
possibly damaging |
Het |
|
Other mutations in Il17re |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00580:Il17re
|
APN |
6 |
113,446,560 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01568:Il17re
|
APN |
6 |
113,447,013 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01656:Il17re
|
APN |
6 |
113,439,934 (GRCm39) |
splice site |
probably benign |
|
IGL01994:Il17re
|
APN |
6 |
113,445,411 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02261:Il17re
|
APN |
6 |
113,445,472 (GRCm39) |
unclassified |
probably benign |
|
IGL02699:Il17re
|
APN |
6 |
113,445,880 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4382001:Il17re
|
UTSW |
6 |
113,446,038 (GRCm39) |
missense |
probably benign |
0.00 |
R0195:Il17re
|
UTSW |
6 |
113,443,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Il17re
|
UTSW |
6 |
113,446,665 (GRCm39) |
missense |
probably damaging |
0.98 |
R2232:Il17re
|
UTSW |
6 |
113,441,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R2357:Il17re
|
UTSW |
6 |
113,445,431 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2393:Il17re
|
UTSW |
6 |
113,439,314 (GRCm39) |
missense |
possibly damaging |
0.91 |
R2916:Il17re
|
UTSW |
6 |
113,442,989 (GRCm39) |
critical splice donor site |
probably null |
|
R4951:Il17re
|
UTSW |
6 |
113,445,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Il17re
|
UTSW |
6 |
113,446,530 (GRCm39) |
missense |
probably benign |
0.14 |
R5070:Il17re
|
UTSW |
6 |
113,435,971 (GRCm39) |
missense |
probably damaging |
0.97 |
R5166:Il17re
|
UTSW |
6 |
113,439,923 (GRCm39) |
missense |
probably benign |
0.00 |
R5404:Il17re
|
UTSW |
6 |
113,446,063 (GRCm39) |
missense |
probably benign |
0.00 |
R5810:Il17re
|
UTSW |
6 |
113,446,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Il17re
|
UTSW |
6 |
113,447,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R6048:Il17re
|
UTSW |
6 |
113,447,069 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7432:Il17re
|
UTSW |
6 |
113,439,332 (GRCm39) |
missense |
probably benign |
0.07 |
R7548:Il17re
|
UTSW |
6 |
113,443,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R7658:Il17re
|
UTSW |
6 |
113,435,943 (GRCm39) |
missense |
probably benign |
0.23 |
R7716:Il17re
|
UTSW |
6 |
113,439,930 (GRCm39) |
critical splice donor site |
probably null |
|
R7942:Il17re
|
UTSW |
6 |
113,443,111 (GRCm39) |
missense |
probably damaging |
0.99 |
R8051:Il17re
|
UTSW |
6 |
113,436,328 (GRCm39) |
missense |
probably benign |
0.01 |
R8090:Il17re
|
UTSW |
6 |
113,439,250 (GRCm39) |
nonsense |
probably null |
|
R8302:Il17re
|
UTSW |
6 |
113,443,280 (GRCm39) |
nonsense |
probably null |
|
R9299:Il17re
|
UTSW |
6 |
113,440,971 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Il17re
|
UTSW |
6 |
113,441,753 (GRCm39) |
missense |
possibly damaging |
0.47 |
|