Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
T |
3: 137,775,712 (GRCm39) |
T1634S |
probably damaging |
Het |
Adgrl1 |
T |
A |
8: 84,665,693 (GRCm39) |
M1460K |
probably damaging |
Het |
Adig |
T |
A |
2: 158,347,773 (GRCm39) |
L29Q |
unknown |
Het |
Adnp |
T |
G |
2: 168,025,887 (GRCm39) |
K469N |
probably damaging |
Het |
Akap3 |
A |
G |
6: 126,842,200 (GRCm39) |
D273G |
probably benign |
Het |
Albfm1 |
A |
T |
5: 90,727,519 (GRCm39) |
Y379F |
probably damaging |
Het |
Ankrd34b |
T |
C |
13: 92,575,139 (GRCm39) |
Y124H |
possibly damaging |
Het |
Ap2b1 |
T |
G |
11: 83,223,948 (GRCm39) |
F221C |
possibly damaging |
Het |
Atp2c2 |
A |
G |
8: 120,469,160 (GRCm39) |
I358V |
possibly damaging |
Het |
BC051665 |
G |
A |
13: 60,930,536 (GRCm39) |
T272I |
probably benign |
Het |
Cdan1 |
G |
T |
2: 120,560,783 (GRCm39) |
A262E |
probably benign |
Het |
Ces1d |
C |
T |
8: 93,904,763 (GRCm39) |
V326I |
probably benign |
Het |
Chd3 |
T |
C |
11: 69,254,873 (GRCm39) |
R156G |
probably benign |
Het |
Clip1 |
C |
T |
5: 123,751,328 (GRCm39) |
E818K |
|
Het |
Col6a4 |
C |
T |
9: 105,877,519 (GRCm39) |
V2153M |
probably damaging |
Het |
Crlf3 |
T |
C |
11: 79,947,351 (GRCm39) |
N296D |
possibly damaging |
Het |
Cstdc6 |
C |
T |
16: 36,142,193 (GRCm39) |
G61D |
probably benign |
Het |
D130052B06Rik |
A |
G |
11: 33,573,594 (GRCm39) |
I109V |
probably benign |
Het |
Dcaf5 |
G |
T |
12: 80,385,483 (GRCm39) |
T881K |
probably benign |
Het |
Dennd4a |
C |
A |
9: 64,769,238 (GRCm39) |
T408K |
probably damaging |
Het |
Dnaaf9 |
C |
A |
2: 130,648,708 (GRCm39) |
R258L |
unknown |
Het |
Dnah2 |
A |
G |
11: 69,349,972 (GRCm39) |
|
probably null |
Het |
Eif1ad8 |
A |
T |
12: 87,564,006 (GRCm39) |
K114* |
probably null |
Het |
Eif2ak2 |
C |
T |
17: 79,173,760 (GRCm39) |
V273I |
probably benign |
Het |
Elac1 |
C |
T |
18: 73,872,359 (GRCm39) |
G212D |
probably damaging |
Het |
Ercc6l2 |
A |
G |
13: 64,013,798 (GRCm39) |
D623G |
probably damaging |
Het |
Exo1 |
T |
C |
1: 175,716,413 (GRCm39) |
F177L |
probably damaging |
Het |
Fat4 |
A |
G |
3: 38,944,562 (GRCm39) |
T1152A |
probably benign |
Het |
Fbxl12 |
G |
T |
9: 20,529,709 (GRCm39) |
|
probably null |
Het |
Fbxo43 |
T |
C |
15: 36,151,971 (GRCm39) |
Y582C |
probably damaging |
Het |
Fsip2 |
T |
A |
2: 82,812,484 (GRCm39) |
N2934K |
possibly damaging |
Het |
Gna12 |
A |
G |
5: 140,815,847 (GRCm39) |
S69P |
probably damaging |
Het |
Gpatch8 |
C |
A |
11: 102,369,354 (GRCm39) |
G1395C |
probably damaging |
Het |
Gpr137c |
A |
G |
14: 45,516,148 (GRCm39) |
Y294C |
probably damaging |
Het |
Greb1 |
A |
G |
12: 16,724,673 (GRCm39) |
S1834P |
probably damaging |
Het |
Grin2b |
T |
C |
6: 135,757,249 (GRCm39) |
D404G |
probably damaging |
Het |
Hectd2 |
A |
T |
19: 36,574,478 (GRCm39) |
N236I |
probably damaging |
Het |
Hhip |
C |
T |
8: 80,713,641 (GRCm39) |
V562I |
probably benign |
Het |
Hipk2 |
G |
T |
6: 38,692,992 (GRCm39) |
T867N |
probably benign |
Het |
Hmgcl |
T |
C |
4: 135,689,424 (GRCm39) |
V294A |
possibly damaging |
Het |
Hnrnpl |
T |
A |
7: 28,513,400 (GRCm39) |
F158I |
|
Het |
Hspa5 |
T |
C |
2: 34,662,383 (GRCm39) |
V17A |
unknown |
Het |
Hspg2 |
T |
C |
4: 137,235,704 (GRCm39) |
V168A |
probably damaging |
Het |
Idh1 |
A |
G |
1: 65,205,284 (GRCm39) |
F227S |
probably damaging |
Het |
Iigp1c |
A |
G |
18: 60,379,355 (GRCm39) |
S297G |
possibly damaging |
Het |
Immp2l |
T |
C |
12: 41,160,915 (GRCm39) |
V71A |
possibly damaging |
Het |
Iqce |
G |
A |
5: 140,675,713 (GRCm39) |
R193* |
probably null |
Het |
Kcnq5 |
T |
C |
1: 21,472,526 (GRCm39) |
D907G |
probably benign |
Het |
Krt17 |
T |
A |
11: 100,148,613 (GRCm39) |
T306S |
probably benign |
Het |
Lhx3 |
T |
C |
2: 26,093,009 (GRCm39) |
D149G |
probably damaging |
Het |
Lrrc73 |
G |
A |
17: 46,565,488 (GRCm39) |
R73H |
probably damaging |
Het |
Mgat5b |
T |
C |
11: 116,875,809 (GRCm39) |
S678P |
probably benign |
Het |
Mink1 |
T |
C |
11: 70,502,305 (GRCm39) |
|
probably null |
Het |
Mroh5 |
T |
G |
15: 73,663,278 (GRCm39) |
|
probably null |
Het |
Muc5ac |
T |
A |
7: 141,363,254 (GRCm39) |
H2188Q |
unknown |
Het |
Muc5ac |
G |
C |
7: 141,363,424 (GRCm39) |
|
probably benign |
Het |
Musk |
G |
A |
4: 58,344,312 (GRCm39) |
G305D |
probably benign |
Het |
Mx1 |
A |
G |
16: 97,249,496 (GRCm39) |
I347T |
unknown |
Het |
Mybbp1a |
G |
T |
11: 72,334,338 (GRCm39) |
V198F |
probably damaging |
Het |
Mycbp2 |
A |
G |
14: 103,393,733 (GRCm39) |
S2943P |
probably damaging |
Het |
Myo18a |
G |
A |
11: 77,733,059 (GRCm39) |
R1363K |
probably damaging |
Het |
Nav3 |
T |
A |
10: 109,689,185 (GRCm39) |
D364V |
possibly damaging |
Het |
Or13g1 |
T |
C |
7: 85,955,799 (GRCm39) |
H174R |
probably damaging |
Het |
Or14j6 |
T |
C |
17: 38,215,328 (GRCm39) |
L297S |
probably benign |
Het |
Or1e26 |
A |
T |
11: 73,480,561 (GRCm39) |
M1K |
probably null |
Het |
Or1j13 |
T |
A |
2: 36,369,726 (GRCm39) |
N139Y |
possibly damaging |
Het |
Or5k15 |
T |
A |
16: 58,710,252 (GRCm39) |
E110D |
probably damaging |
Het |
Pecr |
T |
C |
1: 72,298,592 (GRCm39) |
D276G |
probably damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Ppp1cb |
A |
T |
5: 32,648,376 (GRCm39) |
T320S |
probably benign |
Het |
Ppp1r9a |
G |
T |
6: 5,159,716 (GRCm39) |
K1084N |
probably damaging |
Het |
Prkg1 |
C |
T |
19: 30,602,090 (GRCm39) |
V389I |
probably damaging |
Het |
Psg25 |
C |
T |
7: 18,266,127 (GRCm39) |
|
probably benign |
Het |
Ptpn6 |
A |
G |
6: 124,698,821 (GRCm39) |
S498P |
possibly damaging |
Het |
Pus3 |
A |
G |
9: 35,477,965 (GRCm39) |
H399R |
probably benign |
Het |
Pus7 |
T |
C |
5: 23,983,450 (GRCm39) |
T6A |
probably benign |
Het |
Rnf169 |
A |
G |
7: 99,574,954 (GRCm39) |
V547A |
probably benign |
Het |
Rsf1 |
GGCGGCGGC |
GGCGGCGGCCGCGGCGGC |
7: 97,229,128 (GRCm39) |
|
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,794,807 (GRCm39) |
D1194N |
probably benign |
Het |
Scn5a |
T |
C |
9: 119,320,610 (GRCm39) |
M1490V |
possibly damaging |
Het |
Sec23b |
A |
G |
2: 144,432,258 (GRCm39) |
D756G |
possibly damaging |
Het |
Selenoo |
T |
A |
15: 88,973,427 (GRCm39) |
M39K |
probably benign |
Het |
Septin8 |
T |
G |
11: 53,427,519 (GRCm39) |
V246G |
possibly damaging |
Het |
Serpina3k |
T |
A |
12: 104,309,367 (GRCm39) |
N270K |
probably damaging |
Het |
Setd5 |
G |
A |
6: 113,098,091 (GRCm39) |
R710H |
probably damaging |
Het |
Sirt4 |
A |
T |
5: 115,621,049 (GRCm39) |
I41N |
possibly damaging |
Het |
Slc26a9 |
T |
A |
1: 131,686,556 (GRCm39) |
Y425* |
probably null |
Het |
Slc4a9 |
A |
G |
18: 36,662,773 (GRCm39) |
E176G |
probably benign |
Het |
Speer1m |
T |
C |
5: 11,970,712 (GRCm39) |
I127T |
|
Het |
Spidr |
A |
T |
16: 15,784,680 (GRCm39) |
W463R |
probably benign |
Het |
Tenm4 |
G |
A |
7: 96,202,703 (GRCm39) |
R106H |
probably benign |
Het |
Tmcc1 |
G |
A |
6: 116,111,198 (GRCm39) |
Q28* |
probably null |
Het |
Tmem52b |
A |
G |
6: 129,493,651 (GRCm39) |
E88G |
probably damaging |
Het |
Trpc7 |
A |
T |
13: 56,974,710 (GRCm39) |
I402K |
probably benign |
Het |
Tshz3 |
T |
C |
7: 36,469,522 (GRCm39) |
Y504H |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,542,549 (GRCm39) |
E33479G |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,711,672 (GRCm39) |
R8290C |
unknown |
Het |
Urb1 |
T |
C |
16: 90,549,003 (GRCm39) |
D2235G |
possibly damaging |
Het |
Usp10 |
T |
C |
8: 120,668,283 (GRCm39) |
F195L |
probably benign |
Het |
Vmn1r31 |
A |
T |
6: 58,449,858 (GRCm39) |
F2L |
|
Het |
Vmn2r109 |
C |
T |
17: 20,761,336 (GRCm39) |
V674M |
probably damaging |
Het |
Vmn2r12 |
G |
A |
5: 109,245,655 (GRCm39) |
P26S |
possibly damaging |
Het |
Vmn2r61 |
T |
A |
7: 41,916,629 (GRCm39) |
M414K |
possibly damaging |
Het |
Yipf3 |
T |
C |
17: 46,562,585 (GRCm39) |
V330A |
probably benign |
Het |
Zic4 |
A |
T |
9: 91,261,450 (GRCm39) |
H235L |
probably benign |
Het |
Zxdc |
T |
A |
6: 90,346,642 (GRCm39) |
W16R |
unknown |
Het |
|
Other mutations in Prdm2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00530:Prdm2
|
APN |
4 |
142,860,329 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00843:Prdm2
|
APN |
4 |
142,860,884 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01419:Prdm2
|
APN |
4 |
142,860,218 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01662:Prdm2
|
APN |
4 |
142,860,138 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01892:Prdm2
|
APN |
4 |
142,860,974 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02104:Prdm2
|
APN |
4 |
142,859,997 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02208:Prdm2
|
APN |
4 |
142,862,313 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02260:Prdm2
|
APN |
4 |
142,861,157 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02479:Prdm2
|
APN |
4 |
142,861,499 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02943:Prdm2
|
APN |
4 |
142,858,542 (GRCm39) |
missense |
probably benign |
|
IGL02972:Prdm2
|
APN |
4 |
142,858,736 (GRCm39) |
missense |
probably benign |
|
IGL03038:Prdm2
|
APN |
4 |
142,860,571 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03399:Prdm2
|
APN |
4 |
142,861,658 (GRCm39) |
missense |
probably benign |
0.07 |
G1patch:Prdm2
|
UTSW |
4 |
142,859,471 (GRCm39) |
missense |
possibly damaging |
0.96 |
PIT4677001:Prdm2
|
UTSW |
4 |
142,861,648 (GRCm39) |
missense |
probably damaging |
1.00 |
R0088:Prdm2
|
UTSW |
4 |
142,861,524 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0153:Prdm2
|
UTSW |
4 |
142,860,338 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0320:Prdm2
|
UTSW |
4 |
142,905,921 (GRCm39) |
missense |
probably damaging |
1.00 |
R0384:Prdm2
|
UTSW |
4 |
142,862,258 (GRCm39) |
missense |
probably benign |
0.01 |
R0400:Prdm2
|
UTSW |
4 |
142,838,240 (GRCm39) |
missense |
probably benign |
|
R0658:Prdm2
|
UTSW |
4 |
142,861,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R0850:Prdm2
|
UTSW |
4 |
142,858,773 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1118:Prdm2
|
UTSW |
4 |
142,858,953 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1355:Prdm2
|
UTSW |
4 |
142,858,533 (GRCm39) |
missense |
probably benign |
0.33 |
R1519:Prdm2
|
UTSW |
4 |
142,862,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1936:Prdm2
|
UTSW |
4 |
142,861,032 (GRCm39) |
missense |
probably benign |
0.00 |
R1987:Prdm2
|
UTSW |
4 |
142,859,079 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2006:Prdm2
|
UTSW |
4 |
142,858,447 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2008:Prdm2
|
UTSW |
4 |
142,861,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2030:Prdm2
|
UTSW |
4 |
142,859,334 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2112:Prdm2
|
UTSW |
4 |
142,858,506 (GRCm39) |
missense |
probably benign |
|
R2221:Prdm2
|
UTSW |
4 |
142,861,469 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2223:Prdm2
|
UTSW |
4 |
142,861,469 (GRCm39) |
missense |
possibly damaging |
0.58 |
R2426:Prdm2
|
UTSW |
4 |
142,838,320 (GRCm39) |
nonsense |
probably null |
|
R2430:Prdm2
|
UTSW |
4 |
142,859,733 (GRCm39) |
missense |
possibly damaging |
0.73 |
R2484:Prdm2
|
UTSW |
4 |
142,861,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R3735:Prdm2
|
UTSW |
4 |
142,860,929 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Prdm2
|
UTSW |
4 |
142,858,385 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4209:Prdm2
|
UTSW |
4 |
142,861,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R4411:Prdm2
|
UTSW |
4 |
142,860,240 (GRCm39) |
missense |
probably benign |
0.18 |
R4647:Prdm2
|
UTSW |
4 |
142,859,525 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4898:Prdm2
|
UTSW |
4 |
142,860,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5032:Prdm2
|
UTSW |
4 |
142,905,937 (GRCm39) |
nonsense |
probably null |
|
R5181:Prdm2
|
UTSW |
4 |
142,861,536 (GRCm39) |
missense |
probably benign |
0.35 |
R5513:Prdm2
|
UTSW |
4 |
142,862,463 (GRCm39) |
small deletion |
probably benign |
|
R5539:Prdm2
|
UTSW |
4 |
142,859,264 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5563:Prdm2
|
UTSW |
4 |
142,861,200 (GRCm39) |
missense |
probably benign |
0.09 |
R5618:Prdm2
|
UTSW |
4 |
142,860,107 (GRCm39) |
missense |
probably benign |
0.00 |
R5900:Prdm2
|
UTSW |
4 |
142,861,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R5990:Prdm2
|
UTSW |
4 |
142,896,683 (GRCm39) |
missense |
probably damaging |
1.00 |
R6148:Prdm2
|
UTSW |
4 |
142,859,477 (GRCm39) |
missense |
probably benign |
0.33 |
R6166:Prdm2
|
UTSW |
4 |
142,861,306 (GRCm39) |
missense |
probably damaging |
0.99 |
R6223:Prdm2
|
UTSW |
4 |
142,868,777 (GRCm39) |
missense |
probably benign |
0.41 |
R6530:Prdm2
|
UTSW |
4 |
142,860,617 (GRCm39) |
missense |
probably benign |
0.05 |
R6631:Prdm2
|
UTSW |
4 |
142,861,454 (GRCm39) |
missense |
probably benign |
0.05 |
R6725:Prdm2
|
UTSW |
4 |
142,859,471 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6847:Prdm2
|
UTSW |
4 |
142,859,520 (GRCm39) |
missense |
probably benign |
0.18 |
R7193:Prdm2
|
UTSW |
4 |
142,907,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:Prdm2
|
UTSW |
4 |
142,859,471 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7417:Prdm2
|
UTSW |
4 |
142,905,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R7748:Prdm2
|
UTSW |
4 |
142,862,459 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7885:Prdm2
|
UTSW |
4 |
142,861,140 (GRCm39) |
missense |
probably benign |
0.41 |
R7936:Prdm2
|
UTSW |
4 |
142,862,434 (GRCm39) |
missense |
probably damaging |
0.99 |
R7976:Prdm2
|
UTSW |
4 |
142,859,812 (GRCm39) |
nonsense |
probably null |
|
R8124:Prdm2
|
UTSW |
4 |
142,861,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R8150:Prdm2
|
UTSW |
4 |
142,859,303 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8156:Prdm2
|
UTSW |
4 |
142,861,338 (GRCm39) |
missense |
probably benign |
0.01 |
R8178:Prdm2
|
UTSW |
4 |
142,859,018 (GRCm39) |
missense |
probably benign |
0.33 |
R8235:Prdm2
|
UTSW |
4 |
142,859,037 (GRCm39) |
nonsense |
probably null |
|
R8404:Prdm2
|
UTSW |
4 |
142,861,584 (GRCm39) |
missense |
probably damaging |
0.98 |
R8498:Prdm2
|
UTSW |
4 |
142,907,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R8502:Prdm2
|
UTSW |
4 |
142,861,584 (GRCm39) |
missense |
probably damaging |
0.98 |
R8688:Prdm2
|
UTSW |
4 |
142,838,310 (GRCm39) |
missense |
probably benign |
|
R8732:Prdm2
|
UTSW |
4 |
142,862,580 (GRCm39) |
missense |
probably benign |
0.00 |
R8796:Prdm2
|
UTSW |
4 |
142,860,017 (GRCm39) |
missense |
probably benign |
0.33 |
R8874:Prdm2
|
UTSW |
4 |
142,859,785 (GRCm39) |
missense |
possibly damaging |
0.70 |
R8887:Prdm2
|
UTSW |
4 |
142,860,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R9119:Prdm2
|
UTSW |
4 |
142,858,449 (GRCm39) |
nonsense |
probably null |
|
R9139:Prdm2
|
UTSW |
4 |
142,858,752 (GRCm39) |
missense |
probably benign |
0.03 |
R9165:Prdm2
|
UTSW |
4 |
142,858,674 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9342:Prdm2
|
UTSW |
4 |
142,861,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R9518:Prdm2
|
UTSW |
4 |
142,860,579 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9546:Prdm2
|
UTSW |
4 |
142,861,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R9547:Prdm2
|
UTSW |
4 |
142,861,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R9680:Prdm2
|
UTSW |
4 |
142,859,079 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9730:Prdm2
|
UTSW |
4 |
142,858,659 (GRCm39) |
missense |
possibly damaging |
0.73 |
X0017:Prdm2
|
UTSW |
4 |
142,861,277 (GRCm39) |
missense |
probably benign |
|
|