Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
C |
T |
14: 32,384,589 (GRCm39) |
V459I |
probably benign |
Het |
4921539E11Rik |
T |
C |
4: 103,088,192 (GRCm39) |
D439G |
probably damaging |
Het |
Adam18 |
T |
C |
8: 25,115,873 (GRCm39) |
N607S |
possibly damaging |
Het |
Adamtsl3 |
A |
T |
7: 82,223,756 (GRCm39) |
N1179I |
possibly damaging |
Het |
Adarb1 |
A |
G |
10: 77,139,129 (GRCm39) |
F552S |
probably damaging |
Het |
Ago1 |
T |
C |
4: 126,347,701 (GRCm39) |
E394G |
probably benign |
Het |
Alb |
G |
A |
5: 90,613,788 (GRCm39) |
C224Y |
probably damaging |
Het |
Alms1 |
T |
A |
6: 85,599,141 (GRCm39) |
H1322Q |
possibly damaging |
Het |
Arhgef18 |
T |
G |
8: 3,501,635 (GRCm39) |
V643G |
probably damaging |
Het |
Asah2 |
T |
C |
19: 31,994,103 (GRCm39) |
Q414R |
probably benign |
Het |
Atpsckmt |
C |
T |
15: 31,606,186 (GRCm39) |
A48V |
probably damaging |
Het |
Bbc3 |
G |
A |
7: 16,046,292 (GRCm39) |
R76H |
possibly damaging |
Het |
Bub1b |
T |
A |
2: 118,471,639 (GRCm39) |
S1000T |
possibly damaging |
Het |
Bud23 |
A |
T |
5: 135,089,982 (GRCm39) |
Y70* |
probably null |
Het |
C1d |
A |
G |
11: 17,212,694 (GRCm39) |
E13G |
probably damaging |
Het |
Camk1 |
T |
A |
6: 113,315,325 (GRCm39) |
I158F |
probably damaging |
Het |
Ccr2 |
A |
C |
9: 123,905,843 (GRCm39) |
D41A |
probably benign |
Het |
Cdh18 |
G |
T |
15: 23,400,683 (GRCm39) |
E348* |
probably null |
Het |
Col6a3 |
A |
G |
1: 90,738,321 (GRCm39) |
L1066P |
possibly damaging |
Het |
Cyp11b1 |
T |
A |
15: 74,711,162 (GRCm39) |
D172V |
probably benign |
Het |
Cyp2j8 |
A |
G |
4: 96,358,785 (GRCm39) |
I378T |
possibly damaging |
Het |
Cys1 |
T |
A |
12: 24,718,647 (GRCm39) |
K69* |
probably null |
Het |
Dip2c |
A |
G |
13: 9,678,048 (GRCm39) |
K1165E |
probably damaging |
Het |
Drd3 |
A |
T |
16: 43,637,496 (GRCm39) |
I232F |
probably benign |
Het |
Dusp7 |
T |
C |
9: 106,250,876 (GRCm39) |
C334R |
probably damaging |
Het |
Eppk1 |
A |
G |
15: 75,995,442 (GRCm39) |
S480P |
not run |
Het |
Erc1 |
G |
T |
6: 119,801,721 (GRCm39) |
P99T |
possibly damaging |
Het |
Fam170b |
C |
T |
14: 32,558,155 (GRCm39) |
P330L |
unknown |
Het |
Fasn |
G |
T |
11: 120,703,513 (GRCm39) |
T1573K |
possibly damaging |
Het |
Fras1 |
A |
T |
5: 96,691,173 (GRCm39) |
T130S |
probably benign |
Het |
Fzd4 |
A |
G |
7: 89,056,918 (GRCm39) |
I322V |
possibly damaging |
Het |
Gbp10 |
G |
A |
5: 105,384,015 (GRCm39) |
|
probably benign |
Het |
Gdpd4 |
A |
T |
7: 97,647,448 (GRCm39) |
H365L |
probably benign |
Het |
Gfy |
A |
G |
7: 44,827,524 (GRCm39) |
S191P |
probably benign |
Het |
Ghr |
A |
T |
15: 3,349,994 (GRCm39) |
S395T |
probably damaging |
Het |
Git2 |
C |
T |
5: 114,904,550 (GRCm39) |
R123H |
probably damaging |
Het |
Htt |
A |
G |
5: 35,062,987 (GRCm39) |
D2873G |
probably damaging |
Het |
Idua |
A |
T |
5: 108,829,565 (GRCm39) |
D476V |
probably damaging |
Het |
Inppl1 |
G |
A |
7: 101,477,689 (GRCm39) |
R683W |
probably damaging |
Het |
Ipp |
T |
C |
4: 116,389,841 (GRCm39) |
S466P |
probably benign |
Het |
Iqgap2 |
A |
G |
13: 95,798,131 (GRCm39) |
V1058A |
probably damaging |
Het |
Jmy |
A |
T |
13: 93,601,103 (GRCm39) |
Y434* |
probably null |
Het |
Kmt2d |
CTGCTGCTG |
CTGCTGCTGATGCTGCTG |
15: 98,747,492 (GRCm39) |
|
probably benign |
Het |
Mogs |
T |
G |
6: 83,092,816 (GRCm39) |
S85R |
probably damaging |
Het |
Mroh2b |
A |
T |
15: 4,964,087 (GRCm39) |
D863V |
probably damaging |
Het |
Mtmr10 |
A |
T |
7: 63,947,213 (GRCm39) |
I43F |
probably damaging |
Het |
Mtr |
T |
C |
13: 12,213,963 (GRCm39) |
D903G |
probably benign |
Het |
Ncor1 |
A |
G |
11: 62,274,082 (GRCm39) |
V186A |
probably benign |
Het |
Notch3 |
C |
T |
17: 32,373,793 (GRCm39) |
D472N |
possibly damaging |
Het |
Or4k44 |
A |
T |
2: 111,368,597 (GRCm39) |
F12L |
probably damaging |
Het |
Or6c68 |
T |
C |
10: 129,157,728 (GRCm39) |
F79L |
probably damaging |
Het |
Or8j3c |
A |
G |
2: 86,253,582 (GRCm39) |
F146S |
probably benign |
Het |
Or9i1 |
T |
C |
19: 13,839,381 (GRCm39) |
S75P |
probably damaging |
Het |
Oxr1 |
T |
G |
15: 41,686,758 (GRCm39) |
L547V |
possibly damaging |
Het |
Pappa2 |
A |
T |
1: 158,642,100 (GRCm39) |
C1319S |
probably damaging |
Het |
Papss1 |
A |
C |
3: 131,348,857 (GRCm39) |
K623N |
probably damaging |
Het |
Parp4 |
T |
C |
14: 56,875,375 (GRCm39) |
F1198S |
probably benign |
Het |
Pcare |
T |
A |
17: 72,057,850 (GRCm39) |
Q609L |
probably damaging |
Het |
Pcnt |
A |
T |
10: 76,225,086 (GRCm39) |
V1806D |
probably benign |
Het |
Pitx2 |
A |
T |
3: 129,009,375 (GRCm39) |
H98L |
probably damaging |
Het |
Polq |
C |
A |
16: 36,911,496 (GRCm39) |
D2410E |
probably benign |
Het |
Preb |
A |
T |
5: 31,115,839 (GRCm39) |
D201E |
probably damaging |
Het |
Rasa3 |
A |
T |
8: 13,645,887 (GRCm39) |
I151N |
possibly damaging |
Het |
Rasgrp2 |
T |
A |
19: 6,454,397 (GRCm39) |
S147T |
probably damaging |
Het |
Rev3l |
A |
G |
10: 39,697,441 (GRCm39) |
D646G |
possibly damaging |
Het |
Sdc1 |
A |
G |
12: 8,840,619 (GRCm39) |
E128G |
probably damaging |
Het |
Slamf7 |
A |
C |
1: 171,466,762 (GRCm39) |
C148G |
probably damaging |
Het |
Slc19a2 |
T |
C |
1: 164,084,691 (GRCm39) |
S194P |
probably damaging |
Het |
Spata31 |
C |
T |
13: 65,070,726 (GRCm39) |
P958L |
unknown |
Het |
Sprr2b |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
CTGAGCCTTGTCCTCCTCCAAAGTGCCCTGAGCCTTGTCCTCCCCCAGTATGCTGTGAGCCTTGTCCTCC |
3: 92,224,826 (GRCm39) |
|
probably benign |
Het |
Stradb |
A |
G |
1: 59,027,739 (GRCm39) |
I90V |
probably benign |
Het |
Tas2r134 |
A |
G |
2: 51,518,166 (GRCm39) |
D215G |
probably damaging |
Het |
Tbc1d4 |
T |
C |
14: 101,685,025 (GRCm39) |
K1209E |
probably damaging |
Het |
Thbs1 |
A |
G |
2: 117,953,409 (GRCm39) |
D942G |
probably damaging |
Het |
Tmem107 |
C |
T |
11: 68,963,633 (GRCm39) |
P139S |
probably benign |
Het |
Tmem216 |
A |
T |
19: 10,529,266 (GRCm39) |
M40K |
probably benign |
Het |
Tpte |
A |
G |
8: 22,845,498 (GRCm39) |
Y516C |
probably damaging |
Het |
Trim54 |
G |
A |
5: 31,291,431 (GRCm39) |
G184D |
possibly damaging |
Het |
Try5 |
A |
T |
6: 41,288,748 (GRCm39) |
L157Q |
probably benign |
Het |
Ubqlnl |
G |
A |
7: 103,797,697 (GRCm39) |
A600V |
probably damaging |
Het |
Uhrf2 |
C |
A |
19: 30,048,768 (GRCm39) |
P258Q |
probably damaging |
Het |
Ush2a |
A |
T |
1: 188,554,885 (GRCm39) |
E3554D |
possibly damaging |
Het |
Usp40 |
A |
C |
1: 87,877,682 (GRCm39) |
L1158W |
probably damaging |
Het |
Vmn1r121 |
T |
A |
7: 20,832,198 (GRCm39) |
R81* |
probably null |
Het |
Vmn1r203 |
C |
A |
13: 22,708,588 (GRCm39) |
T123K |
probably benign |
Het |
Vmn2r101 |
T |
C |
17: 19,831,654 (GRCm39) |
V550A |
probably benign |
Het |
Wdr49 |
A |
T |
3: 75,358,193 (GRCm39) |
M184K |
probably damaging |
Het |
Wipi2 |
A |
G |
5: 142,643,987 (GRCm39) |
N123S |
probably damaging |
Het |
Zbtb14 |
T |
C |
17: 69,694,442 (GRCm39) |
F47L |
probably damaging |
Het |
Zc3h7b |
C |
A |
15: 81,662,086 (GRCm39) |
S385* |
probably null |
Het |
Zhx2 |
T |
A |
15: 57,686,658 (GRCm39) |
F676I |
probably damaging |
Het |
|
Other mutations in Prdm9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01302:Prdm9
|
APN |
17 |
15,773,608 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02322:Prdm9
|
APN |
17 |
15,783,110 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02354:Prdm9
|
APN |
17 |
15,783,109 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02361:Prdm9
|
APN |
17 |
15,783,109 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02724:Prdm9
|
APN |
17 |
15,783,522 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03120:Prdm9
|
APN |
17 |
15,765,193 (GRCm39) |
missense |
probably benign |
|
berlin
|
UTSW |
17 |
15,782,702 (GRCm39) |
missense |
probably damaging |
0.96 |
R0173:Prdm9
|
UTSW |
17 |
15,764,297 (GRCm39) |
missense |
probably benign |
0.00 |
R0173:Prdm9
|
UTSW |
17 |
15,764,275 (GRCm39) |
missense |
probably benign |
0.02 |
R0309:Prdm9
|
UTSW |
17 |
15,777,646 (GRCm39) |
missense |
probably damaging |
0.98 |
R1420:Prdm9
|
UTSW |
17 |
15,764,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R3498:Prdm9
|
UTSW |
17 |
15,783,207 (GRCm39) |
splice site |
probably benign |
|
R3714:Prdm9
|
UTSW |
17 |
15,777,623 (GRCm39) |
nonsense |
probably null |
|
R4118:Prdm9
|
UTSW |
17 |
15,764,275 (GRCm39) |
missense |
probably benign |
0.02 |
R4369:Prdm9
|
UTSW |
17 |
15,764,708 (GRCm39) |
missense |
probably benign |
0.14 |
R4691:Prdm9
|
UTSW |
17 |
15,773,640 (GRCm39) |
missense |
probably benign |
0.03 |
R4742:Prdm9
|
UTSW |
17 |
15,773,783 (GRCm39) |
missense |
probably damaging |
0.99 |
R4910:Prdm9
|
UTSW |
17 |
15,764,585 (GRCm39) |
missense |
probably benign |
0.08 |
R5056:Prdm9
|
UTSW |
17 |
15,782,679 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5130:Prdm9
|
UTSW |
17 |
15,764,729 (GRCm39) |
missense |
probably benign |
0.00 |
R5175:Prdm9
|
UTSW |
17 |
15,777,713 (GRCm39) |
missense |
probably benign |
0.04 |
R5187:Prdm9
|
UTSW |
17 |
15,783,155 (GRCm39) |
missense |
probably damaging |
0.98 |
R5213:Prdm9
|
UTSW |
17 |
15,775,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R5270:Prdm9
|
UTSW |
17 |
15,773,625 (GRCm39) |
missense |
probably benign |
0.16 |
R5635:Prdm9
|
UTSW |
17 |
15,782,702 (GRCm39) |
missense |
probably damaging |
0.96 |
R6753:Prdm9
|
UTSW |
17 |
15,765,218 (GRCm39) |
missense |
probably benign |
0.00 |
R6857:Prdm9
|
UTSW |
17 |
15,764,518 (GRCm39) |
missense |
probably benign |
0.04 |
R7041:Prdm9
|
UTSW |
17 |
15,765,257 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7355:Prdm9
|
UTSW |
17 |
15,765,497 (GRCm39) |
missense |
probably benign |
0.01 |
R7410:Prdm9
|
UTSW |
17 |
15,765,259 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7570:Prdm9
|
UTSW |
17 |
15,775,914 (GRCm39) |
missense |
probably benign |
0.14 |
R7571:Prdm9
|
UTSW |
17 |
15,783,526 (GRCm39) |
missense |
probably damaging |
0.98 |
R7593:Prdm9
|
UTSW |
17 |
15,764,867 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7664:Prdm9
|
UTSW |
17 |
15,775,833 (GRCm39) |
missense |
probably damaging |
0.99 |
R7755:Prdm9
|
UTSW |
17 |
15,765,226 (GRCm39) |
missense |
probably damaging |
1.00 |
R7817:Prdm9
|
UTSW |
17 |
15,779,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R7875:Prdm9
|
UTSW |
17 |
15,773,804 (GRCm39) |
nonsense |
probably null |
|
R8110:Prdm9
|
UTSW |
17 |
15,774,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R8222:Prdm9
|
UTSW |
17 |
15,765,035 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8405:Prdm9
|
UTSW |
17 |
15,764,456 (GRCm39) |
missense |
probably benign |
0.22 |
R8695:Prdm9
|
UTSW |
17 |
15,765,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R8947:Prdm9
|
UTSW |
17 |
15,764,270 (GRCm39) |
missense |
possibly damaging |
0.96 |
X0021:Prdm9
|
UTSW |
17 |
15,773,734 (GRCm39) |
nonsense |
probably null |
|
|