Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730596B20Rik |
C |
G |
6: 52,156,254 (GRCm39) |
|
probably benign |
Het |
Abcg3 |
T |
C |
5: 105,125,594 (GRCm39) |
T30A |
probably benign |
Het |
Adra1b |
A |
T |
11: 43,726,194 (GRCm39) |
V241D |
probably damaging |
Het |
Ahctf1 |
A |
T |
1: 179,595,880 (GRCm39) |
N170K |
probably benign |
Het |
Ahr |
A |
G |
12: 35,559,999 (GRCm39) |
L218P |
probably damaging |
Het |
Apol8 |
C |
T |
15: 77,633,959 (GRCm39) |
V206M |
probably damaging |
Het |
Arhgap11a |
T |
A |
2: 113,665,263 (GRCm39) |
|
probably null |
Het |
B3galnt1 |
T |
C |
3: 69,483,108 (GRCm39) |
Y51C |
probably damaging |
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Capn3 |
T |
C |
2: 120,294,646 (GRCm39) |
V98A |
probably benign |
Het |
Casp12 |
T |
C |
9: 5,352,805 (GRCm39) |
L209P |
probably damaging |
Het |
Ccdc96 |
A |
T |
5: 36,643,329 (GRCm39) |
Q445L |
probably damaging |
Het |
Cdc37 |
A |
G |
9: 21,052,260 (GRCm39) |
S301P |
probably damaging |
Het |
Cep89 |
A |
T |
7: 35,131,968 (GRCm39) |
H634L |
probably benign |
Het |
Cert1 |
A |
T |
13: 96,765,575 (GRCm39) |
T447S |
possibly damaging |
Het |
Cfap251 |
A |
G |
5: 123,392,322 (GRCm39) |
|
probably benign |
Het |
Chmp3 |
T |
A |
6: 71,538,008 (GRCm39) |
Y12* |
probably null |
Het |
Clgn |
A |
T |
8: 84,134,829 (GRCm39) |
I156F |
possibly damaging |
Het |
Cmtm1 |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
TCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGGCTGGCTGGTGTCCCGGGTACTGAAGGTCCCTGG |
8: 105,036,334 (GRCm39) |
|
probably null |
Het |
Crb2 |
T |
A |
2: 37,681,603 (GRCm39) |
N815K |
probably benign |
Het |
Crppa |
A |
G |
12: 36,431,902 (GRCm39) |
T44A |
probably benign |
Het |
Csgalnact2 |
A |
C |
6: 118,098,050 (GRCm39) |
L97V |
possibly damaging |
Het |
Ctsh |
T |
A |
9: 89,942,556 (GRCm39) |
M37K |
possibly damaging |
Het |
D630003M21Rik |
T |
C |
2: 158,058,718 (GRCm39) |
E394G |
probably damaging |
Het |
Ddx31 |
T |
G |
2: 28,782,463 (GRCm39) |
L602R |
probably damaging |
Het |
Defb40 |
T |
A |
8: 19,025,050 (GRCm39) |
Y52F |
probably benign |
Het |
Dip2a |
A |
G |
10: 76,126,862 (GRCm39) |
V710A |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,407,419 (GRCm39) |
I150V |
probably benign |
Het |
Eln |
A |
T |
5: 134,766,035 (GRCm39) |
L56Q |
unknown |
Het |
Ezh1 |
T |
C |
11: 101,085,740 (GRCm39) |
N639S |
probably damaging |
Het |
Fzd3 |
A |
G |
14: 65,472,775 (GRCm39) |
F331S |
probably damaging |
Het |
Gbp9 |
T |
C |
5: 105,251,745 (GRCm39) |
T68A |
possibly damaging |
Het |
Gltp |
A |
G |
5: 114,812,161 (GRCm39) |
M104T |
probably benign |
Het |
Gmps |
G |
A |
3: 63,893,048 (GRCm39) |
V118M |
probably damaging |
Het |
Gpsm1 |
T |
C |
2: 26,229,705 (GRCm39) |
L42P |
probably damaging |
Het |
Hsfy2 |
T |
A |
1: 56,675,418 (GRCm39) |
H373L |
probably benign |
Het |
Ica1l |
A |
T |
1: 60,054,953 (GRCm39) |
F93I |
possibly damaging |
Het |
Idh1 |
A |
G |
1: 65,204,277 (GRCm39) |
S278P |
probably damaging |
Het |
Ighmbp2 |
C |
T |
19: 3,317,276 (GRCm39) |
G532D |
possibly damaging |
Het |
Ikbkb |
A |
G |
8: 23,161,742 (GRCm39) |
L382S |
probably benign |
Het |
Il1rap |
T |
A |
16: 26,541,151 (GRCm39) |
M464K |
possibly damaging |
Het |
Ing2 |
G |
A |
8: 48,122,063 (GRCm39) |
R162C |
probably damaging |
Het |
Ints1 |
A |
T |
5: 139,746,522 (GRCm39) |
L1275H |
probably damaging |
Het |
Itga1 |
T |
C |
13: 115,185,837 (GRCm39) |
E55G |
probably damaging |
Het |
Itih4 |
T |
C |
14: 30,623,620 (GRCm39) |
F930L |
probably benign |
Het |
Kcnh8 |
A |
G |
17: 53,263,743 (GRCm39) |
T747A |
probably benign |
Het |
Kit |
A |
G |
5: 75,806,592 (GRCm39) |
E699G |
probably benign |
Het |
Lamc3 |
T |
C |
2: 31,811,775 (GRCm39) |
S921P |
probably benign |
Het |
Lrrc63 |
TGGCGGCGGCGGCGGCGGCGGC |
TGGCGGCGGCGGCGGCGGCGGCGGC |
14: 75,362,661 (GRCm39) |
|
probably benign |
Het |
Map10 |
TCAGTTGTCCAG |
TCAG |
8: 126,397,260 (GRCm39) |
|
probably null |
Het |
Map2k5 |
T |
C |
9: 63,265,300 (GRCm39) |
E76G |
probably damaging |
Het |
Mgat3 |
G |
T |
15: 80,095,973 (GRCm39) |
E267* |
probably null |
Het |
Nhsl3 |
A |
G |
4: 129,116,276 (GRCm39) |
V841A |
probably benign |
Het |
Npepps |
C |
A |
11: 97,139,095 (GRCm39) |
G159V |
probably damaging |
Het |
Nrap |
A |
G |
19: 56,323,720 (GRCm39) |
V1284A |
probably benign |
Het |
Or10a3 |
T |
A |
7: 108,480,610 (GRCm39) |
I68F |
probably damaging |
Het |
Or6c66b |
A |
T |
10: 129,376,562 (GRCm39) |
H52L |
probably benign |
Het |
Oxgr1 |
T |
C |
14: 120,260,281 (GRCm39) |
|
probably null |
Het |
Pcdhb18 |
T |
C |
18: 37,624,308 (GRCm39) |
L546P |
possibly damaging |
Het |
Pcdhga5 |
G |
A |
18: 37,829,633 (GRCm39) |
V694M |
probably damaging |
Het |
Pde9a |
A |
T |
17: 31,679,174 (GRCm39) |
I255F |
possibly damaging |
Het |
Pi4k2a |
G |
A |
19: 42,079,013 (GRCm39) |
G25R |
probably benign |
Het |
Plscr4 |
C |
T |
9: 92,372,843 (GRCm39) |
R322* |
probably null |
Het |
Ppp1r37 |
A |
G |
7: 19,267,989 (GRCm39) |
I302T |
probably damaging |
Het |
Prkar2a |
T |
A |
9: 108,622,744 (GRCm39) |
Y311N |
probably damaging |
Het |
Prkd3 |
A |
T |
17: 79,279,930 (GRCm39) |
D254E |
probably benign |
Het |
Ptpra |
T |
C |
2: 130,346,126 (GRCm39) |
S96P |
probably benign |
Het |
Rnf103 |
A |
G |
6: 71,485,914 (GRCm39) |
T182A |
probably benign |
Het |
Rpusd4 |
A |
G |
9: 35,179,228 (GRCm39) |
S15G |
probably benign |
Het |
Sco1 |
A |
G |
11: 66,949,219 (GRCm39) |
Y229C |
probably damaging |
Het |
Skint5 |
T |
A |
4: 113,417,032 (GRCm39) |
Q1139L |
unknown |
Het |
Slc16a12 |
A |
G |
19: 34,652,579 (GRCm39) |
V189A |
probably damaging |
Het |
Slfn8 |
T |
G |
11: 82,895,081 (GRCm39) |
N575T |
probably damaging |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Stard9 |
T |
C |
2: 120,531,465 (GRCm39) |
L2574P |
probably damaging |
Het |
Syn3 |
A |
T |
10: 85,891,404 (GRCm39) |
|
probably benign |
Het |
Tspo2 |
A |
T |
17: 48,756,985 (GRCm39) |
D32E |
probably damaging |
Het |
Vmn1r72 |
A |
G |
7: 11,403,552 (GRCm39) |
F299L |
probably benign |
Het |
Xbp1 |
G |
A |
11: 5,474,886 (GRCm39) |
M262I |
probably benign |
Het |
Zfp354b |
G |
A |
11: 50,814,632 (GRCm39) |
Q98* |
probably null |
Het |
Zfp582 |
A |
C |
7: 6,357,165 (GRCm39) |
H326P |
probably damaging |
Het |
|
Other mutations in Prmt9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01801:Prmt9
|
APN |
8 |
78,289,069 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02306:Prmt9
|
APN |
8 |
78,287,447 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02971:Prmt9
|
APN |
8 |
78,291,698 (GRCm39) |
missense |
probably benign |
0.00 |
1mM(1):Prmt9
|
UTSW |
8 |
78,282,393 (GRCm39) |
missense |
probably benign |
0.01 |
R0004:Prmt9
|
UTSW |
8 |
78,282,411 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0928:Prmt9
|
UTSW |
8 |
78,307,805 (GRCm39) |
missense |
probably damaging |
1.00 |
R1328:Prmt9
|
UTSW |
8 |
78,299,283 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1777:Prmt9
|
UTSW |
8 |
78,291,737 (GRCm39) |
missense |
probably benign |
0.05 |
R1826:Prmt9
|
UTSW |
8 |
78,282,303 (GRCm39) |
nonsense |
probably null |
|
R1925:Prmt9
|
UTSW |
8 |
78,303,968 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3855:Prmt9
|
UTSW |
8 |
78,294,894 (GRCm39) |
missense |
probably benign |
0.22 |
R3856:Prmt9
|
UTSW |
8 |
78,294,894 (GRCm39) |
missense |
probably benign |
0.22 |
R4089:Prmt9
|
UTSW |
8 |
78,299,174 (GRCm39) |
missense |
probably benign |
0.00 |
R4963:Prmt9
|
UTSW |
8 |
78,282,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R5196:Prmt9
|
UTSW |
8 |
78,291,626 (GRCm39) |
missense |
probably benign |
0.30 |
R5413:Prmt9
|
UTSW |
8 |
78,298,638 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5975:Prmt9
|
UTSW |
8 |
78,287,647 (GRCm39) |
intron |
probably benign |
|
R6271:Prmt9
|
UTSW |
8 |
78,304,092 (GRCm39) |
missense |
probably damaging |
0.96 |
R7023:Prmt9
|
UTSW |
8 |
78,276,086 (GRCm39) |
start gained |
probably benign |
|
R7107:Prmt9
|
UTSW |
8 |
78,294,880 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7159:Prmt9
|
UTSW |
8 |
78,282,393 (GRCm39) |
missense |
probably benign |
0.01 |
R7209:Prmt9
|
UTSW |
8 |
78,291,627 (GRCm39) |
missense |
probably benign |
0.32 |
R7770:Prmt9
|
UTSW |
8 |
78,285,814 (GRCm39) |
splice site |
probably null |
|
R7959:Prmt9
|
UTSW |
8 |
78,287,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R9106:Prmt9
|
UTSW |
8 |
78,276,358 (GRCm39) |
missense |
probably benign |
0.05 |
R9301:Prmt9
|
UTSW |
8 |
78,282,374 (GRCm39) |
nonsense |
probably null |
|
R9368:Prmt9
|
UTSW |
8 |
78,285,663 (GRCm39) |
missense |
probably benign |
0.00 |
R9665:Prmt9
|
UTSW |
8 |
78,307,267 (GRCm39) |
missense |
probably benign |
0.18 |
X0027:Prmt9
|
UTSW |
8 |
78,287,512 (GRCm39) |
missense |
possibly damaging |
0.68 |
|