Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1bg |
A |
G |
15: 60,792,629 (GRCm39) |
I106T |
probably benign |
Het |
Aagab |
A |
C |
9: 63,524,795 (GRCm39) |
N35H |
possibly damaging |
Het |
Abcf1 |
A |
C |
17: 36,274,464 (GRCm39) |
N161K |
possibly damaging |
Het |
Adam11 |
T |
A |
11: 102,662,087 (GRCm39) |
H140Q |
probably benign |
Het |
Araf |
G |
T |
X: 20,726,339 (GRCm39) |
R601L |
probably damaging |
Homo |
Arhgef26 |
A |
T |
3: 62,247,213 (GRCm39) |
D99V |
possibly damaging |
Het |
Arhgef28 |
A |
G |
13: 98,121,888 (GRCm39) |
S559P |
probably damaging |
Het |
Capn11 |
A |
G |
17: 45,964,430 (GRCm39) |
|
probably null |
Het |
Ccdc157 |
T |
C |
11: 4,101,912 (GRCm39) |
H3R |
probably damaging |
Het |
Cd101 |
A |
G |
3: 100,927,778 (GRCm39) |
L101P |
probably damaging |
Het |
Clca3a1 |
A |
G |
3: 144,464,993 (GRCm39) |
V80A |
possibly damaging |
Het |
Cnot6 |
T |
A |
11: 49,570,850 (GRCm39) |
I381F |
probably benign |
Het |
Cntn3 |
T |
A |
6: 102,185,092 (GRCm39) |
I675F |
probably benign |
Het |
Cplx2 |
C |
T |
13: 54,527,406 (GRCm39) |
P97S |
probably damaging |
Het |
Crtac1 |
T |
A |
19: 42,312,236 (GRCm39) |
E159V |
possibly damaging |
Het |
Cyp27a1 |
A |
G |
1: 74,776,231 (GRCm39) |
I416V |
probably benign |
Het |
Cyp2d37-ps |
T |
C |
15: 82,574,014 (GRCm39) |
|
noncoding transcript |
Het |
Cyp2d9 |
A |
G |
15: 82,336,728 (GRCm39) |
T26A |
probably benign |
Het |
Cyp2j7 |
T |
A |
4: 96,083,440 (GRCm39) |
R503S |
probably damaging |
Het |
Dclk1 |
A |
T |
3: 55,424,292 (GRCm39) |
|
probably null |
Het |
Dgkq |
A |
T |
5: 108,803,366 (GRCm39) |
C231* |
probably null |
Het |
Dync1i1 |
T |
A |
6: 5,730,679 (GRCm39) |
M38K |
probably benign |
Het |
Eif2ak4 |
C |
T |
2: 118,231,081 (GRCm39) |
|
probably benign |
Het |
Ephx2 |
A |
T |
14: 66,326,961 (GRCm39) |
D411E |
probably benign |
Het |
Ephx2 |
T |
G |
14: 66,349,669 (GRCm39) |
Q34P |
probably benign |
Het |
Fer1l5 |
A |
T |
1: 36,448,517 (GRCm39) |
N1092Y |
probably benign |
Het |
Fetub |
C |
T |
16: 22,751,081 (GRCm39) |
R143C |
probably damaging |
Het |
Fzd4 |
A |
T |
7: 89,057,197 (GRCm39) |
K415* |
probably null |
Het |
Gfi1 |
A |
T |
5: 107,869,397 (GRCm39) |
Y278N |
probably benign |
Het |
Gm11565 |
T |
C |
11: 99,806,070 (GRCm39) |
M154T |
probably benign |
Het |
Gm7247 |
A |
G |
14: 51,759,299 (GRCm39) |
I93V |
possibly damaging |
Het |
Golm1 |
T |
G |
13: 59,792,972 (GRCm39) |
I178L |
probably benign |
Het |
Grip1 |
A |
T |
10: 119,874,219 (GRCm39) |
D302V |
probably damaging |
Het |
Gtf2h1 |
G |
A |
7: 46,456,254 (GRCm39) |
|
probably null |
Het |
Herc2 |
C |
A |
7: 55,806,649 (GRCm39) |
P2372T |
probably damaging |
Het |
Ighv1-59 |
C |
A |
12: 115,298,786 (GRCm39) |
L89F |
probably damaging |
Het |
Ighv7-4 |
G |
A |
12: 114,186,445 (GRCm39) |
A109V |
possibly damaging |
Het |
Kcnk10 |
G |
T |
12: 98,407,031 (GRCm39) |
Q222K |
probably benign |
Het |
Klra6 |
A |
T |
6: 129,995,881 (GRCm39) |
M159K |
probably benign |
Het |
Lzts3 |
T |
C |
2: 130,479,306 (GRCm39) |
T36A |
probably damaging |
Het |
Mgam |
T |
A |
6: 40,724,854 (GRCm39) |
Y443* |
probably null |
Het |
Mmp23 |
T |
A |
4: 155,735,990 (GRCm39) |
M221L |
possibly damaging |
Het |
Mmp7 |
T |
A |
9: 7,695,519 (GRCm39) |
V132E |
probably damaging |
Het |
Npas2 |
C |
A |
1: 39,331,843 (GRCm39) |
T86N |
probably damaging |
Het |
Or1e32 |
T |
A |
11: 73,705,650 (GRCm39) |
H86L |
probably benign |
Het |
Or5al7 |
C |
T |
2: 85,992,628 (GRCm39) |
V222M |
possibly damaging |
Het |
Papola |
A |
T |
12: 105,786,605 (GRCm39) |
E103V |
probably benign |
Het |
Parp9 |
A |
T |
16: 35,767,921 (GRCm39) |
N34Y |
possibly damaging |
Het |
Pcdh7 |
A |
G |
5: 57,877,666 (GRCm39) |
D407G |
probably damaging |
Het |
Pcdhb5 |
T |
G |
18: 37,455,080 (GRCm39) |
Y487D |
probably damaging |
Het |
Pira12 |
C |
G |
7: 3,901,049 (GRCm39) |
|
probably null |
Het |
Pla2g4a |
T |
C |
1: 149,778,181 (GRCm39) |
D5G |
probably damaging |
Het |
Plxnb1 |
T |
C |
9: 108,933,971 (GRCm39) |
L733P |
probably benign |
Het |
Ppfia4 |
T |
C |
1: 134,251,899 (GRCm39) |
D425G |
probably benign |
Het |
Prss2 |
T |
G |
6: 41,498,754 (GRCm39) |
I6S |
unknown |
Het |
Psme3ip1 |
A |
G |
8: 95,302,348 (GRCm39) |
S228P |
probably damaging |
Het |
Qrfprl |
T |
A |
6: 65,433,142 (GRCm39) |
F321I |
probably damaging |
Het |
Qrich2 |
T |
A |
11: 116,344,979 (GRCm39) |
I1693L |
probably benign |
Het |
Rad52 |
T |
C |
6: 119,897,143 (GRCm39) |
V324A |
probably benign |
Het |
Rapgef2 |
A |
T |
3: 78,976,751 (GRCm39) |
Y1352N |
possibly damaging |
Het |
Rsad2 |
T |
G |
12: 26,506,186 (GRCm39) |
Y78S |
probably damaging |
Het |
Scaf1 |
A |
G |
7: 44,656,204 (GRCm39) |
|
probably benign |
Het |
Slc4a10 |
T |
G |
2: 62,073,701 (GRCm39) |
|
probably null |
Het |
Spmap2l |
A |
G |
5: 77,164,183 (GRCm39) |
D62G |
possibly damaging |
Het |
Syt1 |
A |
G |
10: 108,336,597 (GRCm39) |
V357A |
probably benign |
Het |
Tenm2 |
T |
A |
11: 35,937,621 (GRCm39) |
D1685V |
probably damaging |
Het |
Tmc3 |
A |
G |
7: 83,252,543 (GRCm39) |
T315A |
probably benign |
Het |
Tmem266 |
T |
C |
9: 55,344,493 (GRCm39) |
L375P |
probably benign |
Het |
Tsks |
T |
G |
7: 44,603,263 (GRCm39) |
L355R |
probably damaging |
Het |
Uaca |
G |
A |
9: 60,777,326 (GRCm39) |
R571Q |
probably damaging |
Het |
Ube2f |
T |
A |
1: 91,203,041 (GRCm39) |
|
probably null |
Het |
Usp37 |
A |
T |
1: 74,532,087 (GRCm39) |
V102D |
probably damaging |
Het |
Usp44 |
G |
A |
10: 93,683,010 (GRCm39) |
|
probably benign |
Het |
Vmn2r115 |
T |
C |
17: 23,575,983 (GRCm39) |
F527S |
probably benign |
Het |
Zfp101 |
A |
C |
17: 33,600,720 (GRCm39) |
Y345* |
probably null |
Het |
Zfp160 |
C |
A |
17: 21,247,124 (GRCm39) |
A558E |
probably benign |
Het |
Zfp236 |
T |
C |
18: 82,622,372 (GRCm39) |
E1686G |
probably damaging |
Het |
Zfp655 |
T |
A |
5: 145,181,586 (GRCm39) |
D481E |
probably benign |
Het |
Zswim4 |
A |
G |
8: 84,952,774 (GRCm39) |
V396A |
probably benign |
Het |
|
Other mutations in Sfxn5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03404:Sfxn5
|
APN |
6 |
85,276,518 (GRCm39) |
splice site |
probably benign |
|
IGL02991:Sfxn5
|
UTSW |
6 |
85,266,190 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0513:Sfxn5
|
UTSW |
6 |
85,246,955 (GRCm39) |
splice site |
probably benign |
|
R0734:Sfxn5
|
UTSW |
6 |
85,244,847 (GRCm39) |
splice site |
probably benign |
|
R1510:Sfxn5
|
UTSW |
6 |
85,213,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R1776:Sfxn5
|
UTSW |
6 |
85,244,927 (GRCm39) |
splice site |
probably benign |
|
R2483:Sfxn5
|
UTSW |
6 |
85,309,260 (GRCm39) |
critical splice donor site |
probably null |
|
R3732:Sfxn5
|
UTSW |
6 |
85,276,258 (GRCm39) |
intron |
probably benign |
|
R3732:Sfxn5
|
UTSW |
6 |
85,276,258 (GRCm39) |
intron |
probably benign |
|
R3733:Sfxn5
|
UTSW |
6 |
85,276,258 (GRCm39) |
intron |
probably benign |
|
R4199:Sfxn5
|
UTSW |
6 |
85,192,724 (GRCm39) |
missense |
probably benign |
0.44 |
R4212:Sfxn5
|
UTSW |
6 |
85,309,288 (GRCm39) |
nonsense |
probably null |
|
R4850:Sfxn5
|
UTSW |
6 |
85,309,358 (GRCm39) |
unclassified |
probably benign |
|
R5485:Sfxn5
|
UTSW |
6 |
85,309,582 (GRCm39) |
unclassified |
probably benign |
|
R6613:Sfxn5
|
UTSW |
6 |
85,246,890 (GRCm39) |
critical splice donor site |
probably null |
|
R6997:Sfxn5
|
UTSW |
6 |
85,233,414 (GRCm39) |
missense |
probably benign |
0.25 |
R7078:Sfxn5
|
UTSW |
6 |
85,309,366 (GRCm39) |
missense |
unknown |
|
R7154:Sfxn5
|
UTSW |
6 |
85,309,405 (GRCm39) |
missense |
unknown |
|
R7406:Sfxn5
|
UTSW |
6 |
85,244,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Sfxn5
|
UTSW |
6 |
85,244,921 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8810:Sfxn5
|
UTSW |
6 |
85,206,182 (GRCm39) |
missense |
probably benign |
0.44 |
R8960:Sfxn5
|
UTSW |
6 |
85,266,176 (GRCm39) |
missense |
probably damaging |
0.97 |
R9646:Sfxn5
|
UTSW |
6 |
85,266,195 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sfxn5
|
UTSW |
6 |
85,206,232 (GRCm39) |
missense |
probably benign |
0.37 |
|