Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
T |
A |
7: 41,275,990 (GRCm39) |
F564L |
probably damaging |
Het |
Abcc2 |
T |
C |
19: 43,797,126 (GRCm39) |
I499T |
probably damaging |
Het |
Adamts13 |
C |
T |
2: 26,879,336 (GRCm39) |
R630C |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,708,808 (GRCm39) |
F1199I |
probably damaging |
Het |
Agbl5 |
G |
A |
5: 31,048,115 (GRCm39) |
|
probably null |
Het |
Anks1b |
A |
G |
10: 90,516,648 (GRCm39) |
D881G |
possibly damaging |
Het |
Arap2 |
A |
T |
5: 62,855,728 (GRCm39) |
S569R |
possibly damaging |
Het |
Arhgap15 |
T |
C |
2: 43,953,786 (GRCm39) |
S171P |
possibly damaging |
Het |
Arhgef11 |
G |
A |
3: 87,624,482 (GRCm39) |
|
probably null |
Het |
Baz1a |
C |
A |
12: 54,945,550 (GRCm39) |
L1271F |
probably damaging |
Het |
Bdnf |
A |
C |
2: 109,554,275 (GRCm39) |
K216N |
probably benign |
Het |
Bmp7 |
C |
T |
2: 172,711,998 (GRCm39) |
D409N |
probably damaging |
Het |
Bnip5 |
A |
T |
17: 29,127,351 (GRCm39) |
D219E |
probably benign |
Het |
Cacna1c |
T |
A |
6: 118,718,881 (GRCm39) |
I390F |
|
Het |
Chd8 |
A |
G |
14: 52,470,312 (GRCm39) |
S433P |
probably benign |
Het |
Clrn2 |
A |
G |
5: 45,621,251 (GRCm39) |
E215G |
possibly damaging |
Het |
Col19a1 |
T |
G |
1: 24,573,115 (GRCm39) |
D219A |
unknown |
Het |
Col2a1 |
G |
A |
15: 97,878,032 (GRCm39) |
R1036* |
probably null |
Het |
Copg1 |
T |
A |
6: 87,867,257 (GRCm39) |
V110D |
probably benign |
Het |
Cpd |
C |
T |
11: 76,692,605 (GRCm39) |
G744D |
probably damaging |
Het |
Crygs |
G |
A |
16: 22,625,252 (GRCm39) |
P63L |
probably benign |
Het |
Dcn |
A |
G |
10: 97,345,860 (GRCm39) |
D224G |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,540,820 (GRCm39) |
E2518G |
probably benign |
Het |
Efcab6 |
C |
A |
15: 83,873,152 (GRCm39) |
R197L |
probably benign |
Het |
Efr3b |
T |
A |
12: 4,019,588 (GRCm39) |
Y723F |
probably benign |
Het |
Enam |
A |
G |
5: 88,649,523 (GRCm39) |
N344S |
probably damaging |
Het |
Erich4 |
A |
G |
7: 25,315,101 (GRCm39) |
I58T |
possibly damaging |
Het |
Esrp1 |
A |
G |
4: 11,338,809 (GRCm39) |
V665A |
probably benign |
Het |
Etf1 |
G |
A |
18: 35,039,103 (GRCm39) |
T388I |
probably benign |
Het |
Faf1 |
A |
G |
4: 109,652,040 (GRCm39) |
T244A |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,185,844 (GRCm39) |
D1610G |
probably damaging |
Het |
Fcgbpl1 |
C |
T |
7: 27,863,797 (GRCm39) |
T2523M |
possibly damaging |
Het |
Frem1 |
G |
T |
4: 82,932,064 (GRCm39) |
F212L |
probably benign |
Het |
Fuom |
T |
A |
7: 139,681,073 (GRCm39) |
D85V |
probably damaging |
Het |
Gcfc2 |
T |
C |
6: 81,919,993 (GRCm39) |
|
probably null |
Het |
Gpr37 |
C |
T |
6: 25,688,786 (GRCm39) |
A104T |
probably benign |
Het |
Hsp90ab1 |
G |
C |
17: 45,879,974 (GRCm39) |
T514S |
probably benign |
Het |
Ifnl2 |
A |
G |
7: 28,209,094 (GRCm39) |
F74L |
probably benign |
Het |
Ipo11 |
G |
A |
13: 107,028,199 (GRCm39) |
R367* |
probably null |
Het |
Itpr2 |
T |
C |
6: 146,260,838 (GRCm39) |
D963G |
possibly damaging |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Lrch3 |
T |
A |
16: 32,807,125 (GRCm39) |
L466* |
probably null |
Het |
Lrfn5 |
A |
T |
12: 61,887,090 (GRCm39) |
T293S |
probably benign |
Het |
Lrp5 |
A |
G |
19: 3,660,199 (GRCm39) |
I955T |
probably damaging |
Het |
Lrrc4b |
C |
T |
7: 44,111,439 (GRCm39) |
T437M |
probably damaging |
Het |
Man1a |
A |
G |
10: 53,795,283 (GRCm39) |
Y657H |
probably damaging |
Het |
Mapkap1 |
G |
T |
2: 34,325,166 (GRCm39) |
R94L |
probably damaging |
Het |
Mtmr4 |
T |
A |
11: 87,495,383 (GRCm39) |
L480Q |
probably damaging |
Het |
Mycbp2 |
T |
C |
14: 103,389,627 (GRCm39) |
I3504M |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,480,564 (GRCm39) |
C1169S |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,396,802 (GRCm39) |
S1455P |
|
Het |
Niban1 |
A |
G |
1: 151,571,975 (GRCm39) |
T307A |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,818,724 (GRCm39) |
D406G |
probably benign |
Het |
Nrip2 |
A |
G |
6: 128,381,913 (GRCm39) |
I69V |
probably benign |
Het |
Nthl1 |
G |
A |
17: 24,857,598 (GRCm39) |
V266I |
probably benign |
Het |
Or2ag16 |
T |
C |
7: 106,352,589 (GRCm39) |
E2G |
possibly damaging |
Het |
Or5an6 |
G |
T |
19: 12,371,829 (GRCm39) |
L67F |
probably damaging |
Het |
Or5b21 |
A |
G |
19: 12,839,951 (GRCm39) |
T271A |
probably benign |
Het |
Or5g23 |
A |
C |
2: 85,438,832 (GRCm39) |
C141G |
possibly damaging |
Het |
Or5p75-ps1 |
C |
A |
7: 108,107,291 (GRCm39) |
H9Q |
possibly damaging |
Het |
Or8k25 |
A |
G |
2: 86,243,496 (GRCm39) |
V300A |
probably benign |
Het |
Or8s5 |
A |
G |
15: 98,238,192 (GRCm39) |
V226A |
probably benign |
Het |
Pcdhb1 |
A |
C |
18: 37,398,171 (GRCm39) |
S41R |
possibly damaging |
Het |
Pdcd11 |
T |
A |
19: 47,116,436 (GRCm39) |
F1529I |
probably damaging |
Het |
Plcd3 |
C |
A |
11: 102,992,383 (GRCm39) |
|
probably benign |
Het |
Qdpr |
T |
C |
5: 45,596,718 (GRCm39) |
M149V |
probably benign |
Het |
R3hcc1 |
T |
A |
14: 69,943,329 (GRCm39) |
|
probably null |
Het |
Rasgrf2 |
T |
C |
13: 92,041,856 (GRCm39) |
Y392C |
|
Het |
Slc8a3 |
A |
C |
12: 81,361,577 (GRCm39) |
V414G |
probably damaging |
Het |
Slco1a6 |
A |
G |
6: 142,103,003 (GRCm39) |
S54P |
probably benign |
Het |
Sos1 |
C |
A |
17: 80,731,629 (GRCm39) |
V624F |
probably damaging |
Het |
Spdef |
T |
C |
17: 27,936,262 (GRCm39) |
D227G |
probably benign |
Het |
Sptb |
G |
T |
12: 76,671,003 (GRCm39) |
Q447K |
probably damaging |
Het |
Stag3 |
T |
C |
5: 138,289,628 (GRCm39) |
L266P |
probably damaging |
Het |
Sult2b1 |
T |
C |
7: 45,391,862 (GRCm39) |
|
probably benign |
Het |
Taf1a |
A |
G |
1: 183,190,095 (GRCm39) |
T66A |
|
Het |
Tfg |
A |
T |
16: 56,532,972 (GRCm39) |
|
probably null |
Het |
Trim34b |
A |
G |
7: 103,985,604 (GRCm39) |
N413S |
probably benign |
Het |
Txndc15 |
T |
A |
13: 55,869,399 (GRCm39) |
M184K |
probably damaging |
Het |
Umodl1 |
A |
C |
17: 31,201,306 (GRCm39) |
S412R |
probably damaging |
Het |
Zbtb8b |
T |
A |
4: 129,326,683 (GRCm39) |
M161L |
probably benign |
Het |
Zfp597 |
A |
T |
16: 3,684,369 (GRCm39) |
V129E |
probably benign |
Het |
Zfp790 |
T |
C |
7: 29,528,050 (GRCm39) |
I245T |
possibly damaging |
Het |
|
Other mutations in Srsf12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00952:Srsf12
|
APN |
4 |
33,226,103 (GRCm39) |
missense |
possibly damaging |
0.66 |
IGL02245:Srsf12
|
APN |
4 |
33,209,103 (GRCm39) |
unclassified |
probably benign |
|
IGL03197:Srsf12
|
APN |
4 |
33,231,040 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03412:Srsf12
|
APN |
4 |
33,230,929 (GRCm39) |
missense |
probably damaging |
0.99 |
R0173:Srsf12
|
UTSW |
4 |
33,226,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R0704:Srsf12
|
UTSW |
4 |
33,231,069 (GRCm39) |
missense |
probably damaging |
0.99 |
R1618:Srsf12
|
UTSW |
4 |
33,230,974 (GRCm39) |
missense |
probably damaging |
0.99 |
R2130:Srsf12
|
UTSW |
4 |
33,225,764 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R2916:Srsf12
|
UTSW |
4 |
33,231,042 (GRCm39) |
nonsense |
probably null |
|
R2989:Srsf12
|
UTSW |
4 |
33,223,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4350:Srsf12
|
UTSW |
4 |
33,223,612 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4946:Srsf12
|
UTSW |
4 |
33,231,174 (GRCm39) |
missense |
probably damaging |
0.98 |
R5358:Srsf12
|
UTSW |
4 |
33,209,330 (GRCm39) |
missense |
probably damaging |
0.99 |
R5802:Srsf12
|
UTSW |
4 |
33,230,929 (GRCm39) |
missense |
probably damaging |
0.99 |
R6577:Srsf12
|
UTSW |
4 |
33,209,196 (GRCm39) |
unclassified |
probably benign |
|
R7055:Srsf12
|
UTSW |
4 |
33,226,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R8365:Srsf12
|
UTSW |
4 |
33,226,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R8366:Srsf12
|
UTSW |
4 |
33,226,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R8388:Srsf12
|
UTSW |
4 |
33,226,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R8389:Srsf12
|
UTSW |
4 |
33,226,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R8391:Srsf12
|
UTSW |
4 |
33,226,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R8696:Srsf12
|
UTSW |
4 |
33,231,181 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8698:Srsf12
|
UTSW |
4 |
33,231,246 (GRCm39) |
missense |
probably damaging |
0.98 |
R8815:Srsf12
|
UTSW |
4 |
33,226,045 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9653:Srsf12
|
UTSW |
4 |
33,231,249 (GRCm39) |
missense |
possibly damaging |
0.83 |
|