Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
G |
6: 121,616,253 (GRCm39) |
L127R |
probably null |
Het |
Ambp |
T |
C |
4: 63,067,721 (GRCm39) |
E163G |
probably benign |
Het |
Amy1 |
G |
A |
3: 113,349,658 (GRCm39) |
A504V |
probably damaging |
Het |
Angptl3 |
A |
T |
4: 98,921,540 (GRCm39) |
K219N |
probably benign |
Het |
Atp6v1g1 |
A |
G |
4: 63,468,255 (GRCm39) |
N86S |
probably benign |
Het |
Avl9 |
T |
C |
6: 56,713,612 (GRCm39) |
V290A |
probably benign |
Het |
Bad |
A |
G |
19: 6,919,799 (GRCm39) |
R37G |
probably benign |
Het |
Bicra |
T |
C |
7: 15,723,223 (GRCm39) |
D98G |
possibly damaging |
Het |
Cfap251 |
A |
G |
5: 123,392,435 (GRCm39) |
|
probably benign |
Het |
Col4a4 |
G |
A |
1: 82,474,889 (GRCm39) |
T650M |
unknown |
Het |
Cyp11b2 |
T |
C |
15: 74,727,298 (GRCm39) |
R128G |
probably benign |
Het |
Dst |
T |
C |
1: 34,229,303 (GRCm39) |
S1974P |
probably damaging |
Het |
Fabp1 |
T |
C |
6: 71,178,595 (GRCm39) |
L24P |
probably benign |
Het |
Flnb |
T |
C |
14: 7,942,057 (GRCm38) |
V2345A |
probably damaging |
Het |
Gmnc |
G |
T |
16: 26,779,217 (GRCm39) |
H221Q |
probably benign |
Het |
Homer1 |
T |
C |
13: 93,502,929 (GRCm39) |
|
probably benign |
Het |
Kit |
A |
G |
5: 75,806,565 (GRCm39) |
D690G |
probably damaging |
Het |
Lama2 |
C |
T |
10: 26,877,231 (GRCm39) |
E2652K |
probably benign |
Het |
Mc3r |
C |
T |
2: 172,091,588 (GRCm39) |
T270I |
probably benign |
Het |
Mrgpra3 |
A |
C |
7: 47,239,314 (GRCm39) |
L204W |
probably damaging |
Het |
Mroh1 |
C |
T |
15: 76,317,808 (GRCm39) |
T839I |
possibly damaging |
Het |
Naip2 |
T |
A |
13: 100,291,419 (GRCm39) |
H1173L |
probably benign |
Het |
Optc |
T |
C |
1: 133,825,617 (GRCm39) |
D303G |
probably damaging |
Het |
Or2n1d |
A |
G |
17: 38,646,323 (GRCm39) |
I92V |
probably damaging |
Het |
Or5af1 |
A |
T |
11: 58,722,150 (GRCm39) |
M57L |
probably damaging |
Het |
P4ha3 |
C |
T |
7: 99,934,831 (GRCm39) |
A31V |
possibly damaging |
Het |
Plch2 |
A |
G |
4: 155,075,470 (GRCm39) |
|
probably null |
Het |
Plpp2 |
A |
T |
10: 79,363,647 (GRCm39) |
|
probably null |
Het |
Polq |
A |
T |
16: 36,882,699 (GRCm39) |
N1342I |
probably damaging |
Het |
Pter |
T |
A |
2: 13,005,805 (GRCm39) |
L326H |
probably benign |
Het |
Pwwp2a |
C |
T |
11: 43,597,015 (GRCm39) |
Q452* |
probably null |
Het |
Slc8a2 |
T |
G |
7: 15,892,810 (GRCm39) |
V824G |
probably damaging |
Het |
Tmem132e |
A |
G |
11: 82,335,156 (GRCm39) |
Y654C |
probably damaging |
Het |
Trim14 |
C |
T |
4: 46,523,739 (GRCm39) |
V100I |
possibly damaging |
Het |
Tro |
G |
A |
X: 149,429,252 (GRCm39) |
|
probably benign |
Het |
Uspl1 |
T |
A |
5: 149,151,507 (GRCm39) |
|
probably benign |
Het |
Uty |
A |
G |
Y: 1,158,336 (GRCm39) |
I522T |
probably benign |
Het |
Vmn1r120 |
A |
C |
7: 20,787,582 (GRCm39) |
L43W |
probably damaging |
Het |
Vmn2r16 |
A |
T |
5: 109,478,362 (GRCm39) |
D39V |
probably damaging |
Het |
Washc4 |
T |
A |
10: 83,405,866 (GRCm39) |
I454N |
probably benign |
Het |
Wnt16 |
T |
C |
6: 22,298,133 (GRCm39) |
V333A |
probably damaging |
Het |
Ylpm1 |
T |
C |
12: 85,096,644 (GRCm39) |
|
probably null |
Het |
Zfy1 |
A |
T |
Y: 726,357 (GRCm39) |
D469E |
possibly damaging |
Het |
|
Other mutations in Slfn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02141:Slfn2
|
APN |
11 |
82,960,670 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02407:Slfn2
|
APN |
11 |
82,960,402 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03303:Slfn2
|
APN |
11 |
82,960,293 (GRCm39) |
missense |
possibly damaging |
0.82 |
elektra
|
UTSW |
11 |
82,960,426 (GRCm39) |
missense |
probably damaging |
1.00 |
elektra2
|
UTSW |
11 |
82,960,390 (GRCm39) |
missense |
probably benign |
0.05 |
R2270:Slfn2
|
UTSW |
11 |
82,960,761 (GRCm39) |
missense |
probably damaging |
0.99 |
R2392:Slfn2
|
UTSW |
11 |
82,956,154 (GRCm39) |
missense |
possibly damaging |
0.91 |
R3436:Slfn2
|
UTSW |
11 |
82,960,390 (GRCm39) |
missense |
probably benign |
0.05 |
R5849:Slfn2
|
UTSW |
11 |
82,960,402 (GRCm39) |
missense |
probably benign |
0.00 |
R7612:Slfn2
|
UTSW |
11 |
82,961,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R7738:Slfn2
|
UTSW |
11 |
82,960,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R8211:Slfn2
|
UTSW |
11 |
82,960,585 (GRCm39) |
missense |
possibly damaging |
0.50 |
R8465:Slfn2
|
UTSW |
11 |
82,960,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R8986:Slfn2
|
UTSW |
11 |
82,960,427 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8987:Slfn2
|
UTSW |
11 |
82,960,363 (GRCm39) |
missense |
probably damaging |
0.97 |
R9627:Slfn2
|
UTSW |
11 |
82,960,367 (GRCm39) |
missense |
|
|
|