Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts4 |
G |
A |
1: 171,078,959 (GRCm39) |
S193N |
probably benign |
Het |
Arrdc1 |
C |
A |
2: 24,825,112 (GRCm39) |
V16F |
probably damaging |
Het |
Bhmt1b |
A |
G |
18: 87,775,653 (GRCm39) |
Q392R |
probably benign |
Het |
Bsx |
A |
T |
9: 40,785,517 (GRCm39) |
Q15L |
possibly damaging |
Het |
Casp8ap2 |
A |
G |
4: 32,639,704 (GRCm39) |
T253A |
probably benign |
Het |
Cdkl3 |
T |
C |
11: 51,902,097 (GRCm39) |
L102P |
probably damaging |
Het |
Cgnl1 |
G |
T |
9: 71,632,639 (GRCm39) |
N237K |
probably benign |
Het |
Cldn14 |
T |
A |
16: 93,716,844 (GRCm39) |
M1L |
probably damaging |
Het |
Col1a2 |
C |
T |
6: 4,516,398 (GRCm39) |
R171C |
unknown |
Het |
Col7a1 |
C |
A |
9: 108,802,299 (GRCm39) |
|
probably benign |
Het |
Csgalnact1 |
C |
A |
8: 68,854,144 (GRCm39) |
G219V |
probably damaging |
Het |
Dhrs2 |
G |
A |
14: 55,473,532 (GRCm39) |
V64M |
probably damaging |
Het |
Disp3 |
G |
A |
4: 148,337,158 (GRCm39) |
H886Y |
probably benign |
Het |
Dst |
G |
A |
1: 34,268,332 (GRCm39) |
|
probably null |
Het |
Fnbp4 |
T |
C |
2: 90,581,819 (GRCm39) |
V215A |
probably benign |
Het |
Fzd9 |
A |
G |
5: 135,278,469 (GRCm39) |
L472P |
probably damaging |
Het |
Hpd |
C |
T |
5: 123,319,973 (GRCm39) |
R15Q |
possibly damaging |
Het |
Htra2 |
A |
G |
6: 83,028,592 (GRCm39) |
V412A |
probably damaging |
Het |
Ift80 |
A |
G |
3: 68,805,876 (GRCm39) |
F722S |
probably benign |
Het |
Kcnq2 |
T |
C |
2: 180,723,154 (GRCm39) |
T741A |
probably benign |
Het |
Kl |
A |
C |
5: 150,912,466 (GRCm39) |
E738D |
probably damaging |
Het |
Klra4 |
T |
A |
6: 130,036,506 (GRCm39) |
I178L |
probably damaging |
Het |
Klra9 |
T |
C |
6: 130,168,185 (GRCm39) |
E27G |
probably benign |
Het |
Kntc1 |
T |
C |
5: 123,957,125 (GRCm39) |
Y2145H |
probably benign |
Het |
Mbd5 |
T |
A |
2: 49,147,041 (GRCm39) |
M417K |
probably benign |
Het |
Med31 |
C |
T |
11: 72,102,882 (GRCm39) |
M75I |
probably benign |
Het |
Mpeg1 |
A |
T |
19: 12,438,788 (GRCm39) |
D82V |
probably damaging |
Het |
Msto1 |
A |
G |
3: 88,817,652 (GRCm39) |
Y439H |
probably damaging |
Het |
Or1e17 |
G |
A |
11: 73,831,831 (GRCm39) |
G253E |
probably damaging |
Het |
Or1j15 |
T |
C |
2: 36,458,693 (GRCm39) |
S28P |
possibly damaging |
Het |
Or2av9 |
T |
C |
11: 58,381,365 (GRCm39) |
Y72C |
probably damaging |
Het |
Or5p64 |
T |
A |
7: 107,855,348 (GRCm39) |
|
probably benign |
Het |
Prtg |
G |
A |
9: 72,798,151 (GRCm39) |
V706M |
probably damaging |
Het |
Slc12a5 |
A |
T |
2: 164,824,728 (GRCm39) |
|
probably benign |
Het |
Slc7a3 |
T |
C |
X: 100,126,439 (GRCm39) |
E222G |
probably benign |
Het |
Stox1 |
A |
T |
10: 62,499,826 (GRCm39) |
H911Q |
probably benign |
Het |
Sult3a2 |
A |
T |
10: 33,642,435 (GRCm39) |
N289K |
probably benign |
Het |
Supt20 |
A |
G |
3: 54,622,945 (GRCm39) |
|
probably benign |
Het |
Tchh |
A |
G |
3: 93,351,385 (GRCm39) |
E275G |
unknown |
Het |
Tectb |
A |
T |
19: 55,179,943 (GRCm39) |
N263I |
probably damaging |
Het |
Tsga10 |
C |
T |
1: 37,800,066 (GRCm39) |
R608Q |
possibly damaging |
Het |
Ttyh3 |
A |
G |
5: 140,615,219 (GRCm39) |
Y390H |
probably damaging |
Het |
Utf1 |
C |
A |
7: 139,523,929 (GRCm39) |
S48* |
probably null |
Het |
Zfp358 |
G |
A |
8: 3,546,786 (GRCm39) |
G456D |
probably benign |
Het |
Zup1 |
A |
G |
10: 33,806,150 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Sfxn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00848:Sfxn2
|
APN |
19 |
46,578,596 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01357:Sfxn2
|
APN |
19 |
46,574,212 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02306:Sfxn2
|
APN |
19 |
46,578,987 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02314:Sfxn2
|
APN |
19 |
46,571,026 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1572:Sfxn2
|
UTSW |
19 |
46,570,915 (GRCm39) |
splice site |
probably benign |
|
R2155:Sfxn2
|
UTSW |
19 |
46,579,985 (GRCm39) |
splice site |
probably null |
|
R3547:Sfxn2
|
UTSW |
19 |
46,578,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R3684:Sfxn2
|
UTSW |
19 |
46,579,592 (GRCm39) |
missense |
probably benign |
0.05 |
R4669:Sfxn2
|
UTSW |
19 |
46,574,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R6027:Sfxn2
|
UTSW |
19 |
46,571,291 (GRCm39) |
nonsense |
probably null |
|
R6626:Sfxn2
|
UTSW |
19 |
46,570,967 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6677:Sfxn2
|
UTSW |
19 |
46,570,967 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7764:Sfxn2
|
UTSW |
19 |
46,574,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R8804:Sfxn2
|
UTSW |
19 |
46,574,243 (GRCm39) |
critical splice donor site |
probably benign |
|
R9461:Sfxn2
|
UTSW |
19 |
46,574,192 (GRCm39) |
missense |
probably damaging |
1.00 |
X0027:Sfxn2
|
UTSW |
19 |
46,571,392 (GRCm39) |
missense |
probably damaging |
1.00 |
|