Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akr1c20 |
T |
A |
13: 4,561,275 (GRCm39) |
E126V |
probably benign |
Het |
Alg3 |
A |
T |
16: 20,426,602 (GRCm39) |
L213H |
probably damaging |
Het |
Atp1a4 |
T |
A |
1: 172,059,503 (GRCm39) |
Y863F |
possibly damaging |
Het |
Atp6v0e |
A |
G |
17: 26,914,390 (GRCm39) |
T72A |
probably benign |
Het |
Aup1 |
A |
G |
6: 83,032,123 (GRCm39) |
T97A |
probably benign |
Het |
Bcl6 |
T |
C |
16: 23,791,652 (GRCm39) |
D234G |
probably damaging |
Het |
Cdc42bpa |
T |
C |
1: 179,892,583 (GRCm39) |
L249P |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,705,766 (GRCm39) |
K750E |
possibly damaging |
Het |
Ces1g |
C |
A |
8: 94,043,665 (GRCm39) |
G425C |
possibly damaging |
Het |
Chl1 |
T |
C |
6: 103,683,409 (GRCm39) |
L745P |
probably damaging |
Het |
Csmd2 |
G |
A |
4: 128,343,020 (GRCm39) |
V1471M |
|
Het |
Dnah12 |
G |
A |
14: 26,500,869 (GRCm39) |
|
probably null |
Het |
E4f1 |
G |
A |
17: 24,663,808 (GRCm39) |
Q569* |
probably null |
Het |
Efcab3 |
A |
T |
11: 104,899,787 (GRCm39) |
I4350F |
possibly damaging |
Het |
Fbxw24 |
A |
T |
9: 109,430,328 (GRCm39) |
C439S |
probably benign |
Het |
Ftdc2 |
C |
A |
16: 58,458,140 (GRCm39) |
A54S |
probably benign |
Het |
Gmip |
C |
T |
8: 70,270,452 (GRCm39) |
P721S |
probably benign |
Het |
Grip1 |
A |
G |
10: 119,871,279 (GRCm39) |
I669V |
possibly damaging |
Het |
Gsn |
A |
T |
2: 35,185,061 (GRCm39) |
K339* |
probably null |
Het |
Herc1 |
G |
T |
9: 66,307,056 (GRCm39) |
A959S |
possibly damaging |
Het |
Hic1 |
A |
G |
11: 75,060,056 (GRCm39) |
V97A |
probably benign |
Het |
Il11ra1 |
A |
G |
4: 41,766,189 (GRCm39) |
Y242C |
probably damaging |
Het |
Iqsec3 |
A |
C |
6: 121,450,317 (GRCm39) |
V69G |
unknown |
Het |
Jak3 |
T |
A |
8: 72,138,601 (GRCm39) |
M933K |
probably damaging |
Het |
Kbtbd7 |
G |
A |
14: 79,665,757 (GRCm39) |
V530I |
probably damaging |
Het |
Kif22 |
G |
A |
7: 126,632,150 (GRCm39) |
R345C |
probably benign |
Het |
Klhl7 |
G |
A |
5: 24,343,433 (GRCm39) |
E250K |
probably damaging |
Het |
Klk1b4 |
A |
G |
7: 43,860,531 (GRCm39) |
H183R |
probably damaging |
Het |
Lhfpl4 |
C |
T |
6: 113,153,632 (GRCm39) |
V140I |
probably benign |
Het |
Lhx5 |
T |
A |
5: 120,574,410 (GRCm39) |
M238K |
probably benign |
Het |
Lin28b |
A |
T |
10: 45,345,244 (GRCm39) |
H27Q |
probably benign |
Het |
Mgat4c |
A |
T |
10: 102,214,070 (GRCm39) |
R18* |
probably null |
Het |
Myct1 |
C |
A |
10: 5,554,492 (GRCm39) |
H120N |
probably damaging |
Het |
Nek1 |
A |
T |
8: 61,559,829 (GRCm39) |
D984V |
probably benign |
Het |
Nfu1 |
A |
T |
6: 86,986,863 (GRCm39) |
|
probably benign |
Het |
Nipsnap1 |
A |
T |
11: 4,833,366 (GRCm39) |
|
probably null |
Het |
Nlrp9c |
A |
G |
7: 26,085,046 (GRCm39) |
Y178H |
probably damaging |
Het |
Nrxn3 |
T |
A |
12: 89,477,377 (GRCm39) |
M520K |
probably damaging |
Het |
Oacyl |
A |
G |
18: 65,853,323 (GRCm39) |
D143G |
probably benign |
Het |
Obox5 |
A |
G |
7: 15,492,732 (GRCm39) |
Y229C |
probably damaging |
Het |
Or1j12 |
A |
G |
2: 36,342,702 (GRCm39) |
Y35C |
probably damaging |
Het |
Or1j18 |
G |
A |
2: 36,624,436 (GRCm39) |
M34I |
probably benign |
Het |
Or2a5 |
T |
C |
6: 42,874,024 (GRCm39) |
V213A |
probably damaging |
Het |
Or52n5 |
T |
C |
7: 104,588,405 (GRCm39) |
L224P |
probably damaging |
Het |
Otogl |
C |
T |
10: 107,702,515 (GRCm39) |
A713T |
probably benign |
Het |
Pcdhb17 |
A |
C |
18: 37,619,566 (GRCm39) |
N452T |
probably benign |
Het |
Pi16 |
A |
G |
17: 29,545,313 (GRCm39) |
Y192C |
probably damaging |
Het |
Pla2g5 |
T |
C |
4: 138,531,830 (GRCm39) |
D58G |
probably damaging |
Het |
Plpp4 |
G |
T |
7: 128,981,207 (GRCm39) |
V153F |
unknown |
Het |
Plxna2 |
C |
A |
1: 194,326,876 (GRCm39) |
S270* |
probably null |
Het |
Pole |
T |
A |
5: 110,472,968 (GRCm39) |
|
probably null |
Het |
Ptpn21 |
C |
T |
12: 98,655,171 (GRCm39) |
V599I |
probably damaging |
Het |
Rab26 |
C |
A |
17: 24,749,652 (GRCm39) |
R131L |
probably damaging |
Het |
Raph1 |
A |
T |
1: 60,565,136 (GRCm39) |
V117D |
probably benign |
Het |
Sacs |
T |
C |
14: 61,447,845 (GRCm39) |
V3297A |
probably damaging |
Het |
Serpine1 |
C |
A |
5: 137,095,796 (GRCm39) |
A262S |
probably benign |
Het |
Sgf29 |
A |
G |
7: 126,271,221 (GRCm39) |
D193G |
probably null |
Het |
Sh3rf2 |
G |
A |
18: 42,237,227 (GRCm39) |
|
probably null |
Het |
Sipa1l1 |
T |
C |
12: 82,469,236 (GRCm39) |
V1245A |
possibly damaging |
Het |
Slc22a7 |
A |
G |
17: 46,749,224 (GRCm39) |
L31P |
probably damaging |
Het |
Slc24a5 |
G |
A |
2: 124,930,111 (GRCm39) |
V471I |
probably benign |
Het |
Slc26a7 |
A |
T |
4: 14,533,639 (GRCm39) |
Y395N |
probably damaging |
Het |
Slc38a2 |
T |
C |
15: 96,591,182 (GRCm39) |
M229V |
probably damaging |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Susd1 |
G |
A |
4: 59,411,318 (GRCm39) |
R225* |
probably null |
Het |
Suz12 |
T |
A |
11: 79,884,419 (GRCm39) |
F92I |
probably damaging |
Het |
Tmem114 |
C |
A |
16: 8,242,610 (GRCm39) |
|
probably benign |
Het |
Tmem68 |
A |
G |
4: 3,564,107 (GRCm39) |
V159A |
probably benign |
Het |
Tpra1 |
T |
A |
6: 88,885,276 (GRCm39) |
I76N |
probably damaging |
Het |
Trim45 |
A |
G |
3: 100,839,353 (GRCm39) |
T752A |
unknown |
Het |
Trp63 |
C |
A |
16: 25,639,227 (GRCm39) |
H138Q |
probably damaging |
Het |
Ugt2a2 |
T |
C |
5: 87,608,255 (GRCm39) |
D528G |
possibly damaging |
Het |
Vmn2r39 |
T |
G |
7: 9,017,761 (GRCm39) |
K858N |
possibly damaging |
Het |
Zfp629 |
A |
T |
7: 127,210,484 (GRCm39) |
S442T |
probably damaging |
Het |
|
Other mutations in Prmt7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01080:Prmt7
|
APN |
8 |
106,963,846 (GRCm39) |
splice site |
probably benign |
|
IGL01565:Prmt7
|
APN |
8 |
106,977,041 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02245:Prmt7
|
APN |
8 |
106,963,937 (GRCm39) |
missense |
probably benign |
0.10 |
R0104:Prmt7
|
UTSW |
8 |
106,963,982 (GRCm39) |
missense |
probably damaging |
0.99 |
R0255:Prmt7
|
UTSW |
8 |
106,953,839 (GRCm39) |
splice site |
probably benign |
|
R1432:Prmt7
|
UTSW |
8 |
106,963,916 (GRCm39) |
nonsense |
probably null |
|
R1551:Prmt7
|
UTSW |
8 |
106,964,014 (GRCm39) |
missense |
probably benign |
|
R1848:Prmt7
|
UTSW |
8 |
106,963,640 (GRCm39) |
missense |
probably benign |
|
R2117:Prmt7
|
UTSW |
8 |
106,953,930 (GRCm39) |
missense |
probably damaging |
0.96 |
R3784:Prmt7
|
UTSW |
8 |
106,968,768 (GRCm39) |
missense |
probably benign |
0.01 |
R4599:Prmt7
|
UTSW |
8 |
106,976,961 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4940:Prmt7
|
UTSW |
8 |
106,963,910 (GRCm39) |
missense |
probably benign |
0.01 |
R4983:Prmt7
|
UTSW |
8 |
106,976,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Prmt7
|
UTSW |
8 |
106,974,991 (GRCm39) |
missense |
probably benign |
0.15 |
R6015:Prmt7
|
UTSW |
8 |
106,961,640 (GRCm39) |
intron |
probably benign |
|
R6520:Prmt7
|
UTSW |
8 |
106,961,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R7097:Prmt7
|
UTSW |
8 |
106,961,732 (GRCm39) |
missense |
unknown |
|
R7233:Prmt7
|
UTSW |
8 |
106,946,642 (GRCm39) |
missense |
probably damaging |
0.99 |
R7538:Prmt7
|
UTSW |
8 |
106,964,018 (GRCm39) |
missense |
probably benign |
0.02 |
R7577:Prmt7
|
UTSW |
8 |
106,968,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R7659:Prmt7
|
UTSW |
8 |
106,963,918 (GRCm39) |
missense |
probably benign |
0.00 |
R7858:Prmt7
|
UTSW |
8 |
106,971,320 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8991:Prmt7
|
UTSW |
8 |
106,943,874 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9041:Prmt7
|
UTSW |
8 |
106,963,460 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9188:Prmt7
|
UTSW |
8 |
106,961,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R9338:Prmt7
|
UTSW |
8 |
106,961,665 (GRCm39) |
missense |
unknown |
|
R9406:Prmt7
|
UTSW |
8 |
106,970,435 (GRCm39) |
missense |
probably damaging |
1.00 |
R9517:Prmt7
|
UTSW |
8 |
106,953,930 (GRCm39) |
missense |
probably damaging |
0.96 |
|