Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf5 |
G |
A |
17: 43,762,048 (GRCm39) |
V1248M |
probably damaging |
Het |
Alb |
T |
C |
5: 90,620,323 (GRCm39) |
S478P |
probably damaging |
Het |
Arhgap17 |
A |
G |
7: 122,886,039 (GRCm39) |
S698P |
probably benign |
Het |
Arhgef5 |
A |
G |
6: 43,250,859 (GRCm39) |
T537A |
possibly damaging |
Het |
Arl6 |
A |
T |
16: 59,439,094 (GRCm39) |
|
probably null |
Het |
Atp13a4 |
A |
T |
16: 29,268,735 (GRCm39) |
W540R |
|
Het |
Birc6 |
A |
T |
17: 74,900,095 (GRCm39) |
D1091V |
probably damaging |
Het |
Bnc1 |
A |
G |
7: 81,623,250 (GRCm39) |
V659A |
probably benign |
Het |
C130074G19Rik |
T |
C |
1: 184,606,571 (GRCm39) |
|
probably null |
Het |
C1ql4 |
T |
A |
15: 98,982,693 (GRCm39) |
H220L |
probably benign |
Het |
Cacna1s |
A |
G |
1: 136,028,363 (GRCm39) |
N1147S |
probably benign |
Het |
Cc2d2a |
T |
C |
5: 43,852,638 (GRCm39) |
|
probably null |
Het |
Ccl1 |
T |
A |
11: 82,070,519 (GRCm39) |
I18L |
probably benign |
Het |
Cfap410 |
C |
T |
10: 77,815,601 (GRCm39) |
T31I |
probably damaging |
Het |
Ecel1 |
A |
T |
1: 87,075,991 (GRCm39) |
Y729N |
probably damaging |
Het |
Epha4 |
T |
A |
1: 77,483,833 (GRCm39) |
I59F |
probably damaging |
Het |
Filip1l |
A |
G |
16: 57,390,074 (GRCm39) |
K221E |
probably damaging |
Het |
Flnc |
A |
G |
6: 29,456,381 (GRCm39) |
E2193G |
possibly damaging |
Het |
Galnt10 |
C |
G |
11: 57,674,549 (GRCm39) |
P513A |
probably damaging |
Het |
Gm5624 |
A |
G |
14: 44,798,190 (GRCm39) |
Y139H |
|
Het |
Golgb1 |
A |
C |
16: 36,735,786 (GRCm39) |
I1719L |
probably benign |
Het |
Hsf1 |
T |
C |
15: 76,382,393 (GRCm39) |
S255P |
probably benign |
Het |
Ighv2-2 |
T |
C |
12: 113,551,914 (GRCm39) |
D108G |
probably damaging |
Het |
Iho1 |
T |
C |
9: 108,282,870 (GRCm39) |
T273A |
probably benign |
Het |
Kbtbd3 |
C |
T |
9: 4,316,878 (GRCm39) |
Q10* |
probably null |
Het |
Kcnh2 |
C |
T |
5: 24,538,034 (GRCm39) |
V110M |
probably benign |
Het |
Magi3 |
A |
C |
3: 103,924,005 (GRCm39) |
L1112W |
probably damaging |
Het |
Malrd1 |
T |
A |
2: 16,132,879 (GRCm39) |
D1933E |
unknown |
Het |
Mki67 |
G |
A |
7: 135,301,453 (GRCm39) |
R1194* |
probably null |
Het |
Nap1l1 |
T |
C |
10: 111,328,769 (GRCm39) |
Y233H |
probably damaging |
Het |
Napsa |
A |
G |
7: 44,234,758 (GRCm39) |
I298V |
probably benign |
Het |
Nkx6-1 |
A |
T |
5: 101,811,465 (GRCm39) |
S212R |
probably damaging |
Het |
Nlrc4 |
A |
T |
17: 74,752,610 (GRCm39) |
I591N |
probably damaging |
Het |
Or5b114-ps1 |
T |
C |
19: 13,352,431 (GRCm39) |
I35T |
possibly damaging |
Het |
Orc2 |
T |
C |
1: 58,506,827 (GRCm39) |
D503G |
possibly damaging |
Het |
Osbp |
T |
A |
19: 11,955,612 (GRCm39) |
S343T |
probably benign |
Het |
Pcdha6 |
T |
G |
18: 37,102,479 (GRCm39) |
D557E |
probably damaging |
Het |
Pdcd11 |
AGAGGAGGAGGAGGAGGAGGAGGAG |
AGAGGAGGAGGAGGAGGAGGAG |
19: 47,101,876 (GRCm39) |
|
probably benign |
Het |
Ppdpf |
A |
G |
2: 180,829,650 (GRCm39) |
Y35C |
probably benign |
Het |
Scube3 |
G |
A |
17: 28,390,200 (GRCm39) |
V955I |
probably benign |
Het |
Slc1a1 |
T |
C |
19: 28,889,161 (GRCm39) |
V478A |
probably benign |
Het |
Slc4a4 |
A |
G |
5: 89,206,137 (GRCm39) |
|
probably null |
Het |
Srrm2 |
T |
C |
17: 24,027,084 (GRCm39) |
L96P |
unknown |
Het |
Strn |
A |
T |
17: 78,977,852 (GRCm39) |
L175Q |
|
Het |
|
Other mutations in Scrn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01410:Scrn2
|
APN |
11 |
96,921,396 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01580:Scrn2
|
APN |
11 |
96,922,956 (GRCm39) |
missense |
probably benign |
|
R1847:Scrn2
|
UTSW |
11 |
96,923,021 (GRCm39) |
missense |
probably benign |
0.22 |
R2509:Scrn2
|
UTSW |
11 |
96,923,992 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2698:Scrn2
|
UTSW |
11 |
96,923,122 (GRCm39) |
unclassified |
probably benign |
|
R4361:Scrn2
|
UTSW |
11 |
96,923,064 (GRCm39) |
missense |
probably null |
1.00 |
R4927:Scrn2
|
UTSW |
11 |
96,924,326 (GRCm39) |
critical splice donor site |
probably null |
|
R5040:Scrn2
|
UTSW |
11 |
96,921,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5367:Scrn2
|
UTSW |
11 |
96,923,953 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5534:Scrn2
|
UTSW |
11 |
96,921,751 (GRCm39) |
missense |
probably benign |
0.00 |
R6145:Scrn2
|
UTSW |
11 |
96,923,679 (GRCm39) |
missense |
probably benign |
0.35 |
R7029:Scrn2
|
UTSW |
11 |
96,921,262 (GRCm39) |
unclassified |
probably benign |
|
R7082:Scrn2
|
UTSW |
11 |
96,923,908 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7165:Scrn2
|
UTSW |
11 |
96,924,634 (GRCm39) |
missense |
probably benign |
|
R7468:Scrn2
|
UTSW |
11 |
96,923,992 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7568:Scrn2
|
UTSW |
11 |
96,921,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R7632:Scrn2
|
UTSW |
11 |
96,923,968 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8239:Scrn2
|
UTSW |
11 |
96,923,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R8398:Scrn2
|
UTSW |
11 |
96,921,730 (GRCm39) |
missense |
probably benign |
0.07 |
R8408:Scrn2
|
UTSW |
11 |
96,921,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R8872:Scrn2
|
UTSW |
11 |
96,922,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R9206:Scrn2
|
UTSW |
11 |
96,922,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R9596:Scrn2
|
UTSW |
11 |
96,923,907 (GRCm39) |
missense |
probably damaging |
0.98 |
R9643:Scrn2
|
UTSW |
11 |
96,921,342 (GRCm39) |
missense |
probably damaging |
0.99 |
R9708:Scrn2
|
UTSW |
11 |
96,922,928 (GRCm39) |
missense |
probably damaging |
1.00 |
|