Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
G |
2: 25,327,733 (GRCm39) |
Y716C |
probably damaging |
Het |
Abcc1 |
A |
G |
16: 14,284,861 (GRCm39) |
I1237V |
probably benign |
Het |
Adam34 |
C |
T |
8: 44,105,565 (GRCm39) |
A27T |
probably benign |
Het |
Aff3 |
T |
C |
1: 38,257,478 (GRCm39) |
S415G |
probably damaging |
Het |
Ak7 |
T |
C |
12: 105,711,532 (GRCm39) |
Y390H |
probably benign |
Het |
Arap2 |
A |
C |
5: 62,826,396 (GRCm39) |
M1056R |
probably damaging |
Het |
Brf1 |
T |
C |
12: 112,923,945 (GRCm39) |
Y676C |
unknown |
Het |
Cachd1 |
T |
A |
4: 100,833,552 (GRCm39) |
H776Q |
possibly damaging |
Het |
Cacng7 |
T |
C |
7: 3,385,183 (GRCm39) |
V28A |
probably damaging |
Het |
Camk2g |
A |
T |
14: 20,792,780 (GRCm39) |
D359E |
probably benign |
Het |
Cd209b |
T |
C |
8: 3,976,638 (GRCm39) |
D16G |
probably benign |
Het |
Ceacam5 |
A |
G |
7: 17,493,410 (GRCm39) |
E811G |
possibly damaging |
Het |
Cecr2 |
T |
A |
6: 120,733,647 (GRCm39) |
S545T |
probably benign |
Het |
Cep55 |
T |
C |
19: 38,048,806 (GRCm39) |
|
probably null |
Het |
Ctif |
C |
A |
18: 75,770,290 (GRCm39) |
V32L |
probably damaging |
Het |
Cwc27 |
G |
A |
13: 104,797,900 (GRCm39) |
A353V |
probably benign |
Het |
Dclk3 |
T |
A |
9: 111,314,064 (GRCm39) |
S713R |
probably damaging |
Het |
Dlec1 |
C |
T |
9: 118,941,214 (GRCm39) |
H255Y |
probably benign |
Het |
Dlgap1 |
A |
G |
17: 70,823,093 (GRCm39) |
H26R |
possibly damaging |
Het |
Dydc1 |
C |
T |
14: 40,800,051 (GRCm39) |
T19I |
possibly damaging |
Het |
Efcab12 |
G |
A |
6: 115,800,474 (GRCm39) |
P183L |
not run |
Het |
Eif1ad19 |
T |
C |
12: 87,740,708 (GRCm39) |
|
probably benign |
Het |
Eri3 |
C |
A |
4: 117,446,343 (GRCm39) |
Q219K |
probably benign |
Het |
Fam135a |
A |
G |
1: 24,083,295 (GRCm39) |
L310P |
probably damaging |
Het |
Fgd5 |
T |
A |
6: 91,965,272 (GRCm39) |
S502T |
possibly damaging |
Het |
Fgf8 |
A |
G |
19: 45,730,106 (GRCm39) |
S57P |
probably benign |
Het |
Gls |
T |
C |
1: 52,259,139 (GRCm39) |
E154G |
probably damaging |
Het |
Gm28042 |
T |
C |
2: 119,870,176 (GRCm39) |
L705P |
probably damaging |
Het |
Golgb1 |
C |
A |
16: 36,736,512 (GRCm39) |
Q1961K |
probably benign |
Het |
Herc3 |
C |
A |
6: 58,833,616 (GRCm39) |
Q168K |
probably benign |
Het |
Il31ra |
C |
A |
13: 112,682,845 (GRCm39) |
C168F |
probably benign |
Het |
Ino80 |
A |
T |
2: 119,257,072 (GRCm39) |
D860E |
probably benign |
Het |
Iqcm |
T |
G |
8: 76,480,044 (GRCm39) |
L334R |
probably benign |
Het |
Lrrk2 |
A |
G |
15: 91,641,204 (GRCm39) |
D1587G |
possibly damaging |
Het |
Map4 |
T |
A |
9: 109,882,201 (GRCm39) |
V355E |
probably benign |
Het |
Mapk13 |
T |
A |
17: 28,995,361 (GRCm39) |
I194N |
probably damaging |
Het |
Mtus2 |
A |
G |
5: 148,013,515 (GRCm39) |
T103A |
probably benign |
Het |
Naglu |
G |
T |
11: 100,961,158 (GRCm39) |
G70W |
probably benign |
Het |
Nlrp4f |
A |
T |
13: 65,343,201 (GRCm39) |
M126K |
possibly damaging |
Het |
Or4c120 |
T |
C |
2: 89,001,714 (GRCm39) |
|
probably benign |
Het |
Or5p61 |
A |
T |
7: 107,758,585 (GRCm39) |
V165E |
probably benign |
Het |
Pdia4 |
T |
C |
6: 47,790,193 (GRCm39) |
T16A |
unknown |
Het |
Pou6f2 |
G |
A |
13: 18,414,298 (GRCm39) |
A159V |
|
Het |
Ripor1 |
A |
G |
8: 106,344,506 (GRCm39) |
T547A |
probably benign |
Het |
Rundc3b |
A |
G |
5: 8,542,506 (GRCm39) |
S389P |
probably damaging |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Supv3l1 |
G |
A |
10: 62,271,328 (GRCm39) |
T403I |
probably damaging |
Het |
Tacstd2 |
G |
A |
6: 67,512,180 (GRCm39) |
R171W |
probably damaging |
Het |
Taok2 |
A |
T |
7: 126,471,552 (GRCm39) |
F542L |
probably damaging |
Het |
Tbc1d31 |
T |
A |
15: 57,801,459 (GRCm39) |
N331K |
possibly damaging |
Het |
Tff2 |
A |
T |
17: 31,361,200 (GRCm39) |
C118S |
probably damaging |
Het |
Tmprss7 |
G |
A |
16: 45,498,317 (GRCm39) |
T354I |
possibly damaging |
Het |
Tmtc3 |
A |
T |
10: 100,313,774 (GRCm39) |
F33I |
probably damaging |
Het |
Tpbpa |
G |
A |
13: 61,088,399 (GRCm39) |
|
probably benign |
Het |
Ube3a |
G |
T |
7: 58,925,653 (GRCm39) |
V165F |
probably benign |
Het |
Vmn2r4 |
T |
G |
3: 64,322,681 (GRCm39) |
T13P |
probably benign |
Het |
Wnt8b |
A |
G |
19: 44,500,121 (GRCm39) |
D236G |
probably benign |
Het |
Ythdf3 |
C |
A |
3: 16,258,451 (GRCm39) |
D210E |
probably benign |
Het |
Zfp110 |
T |
A |
7: 12,583,753 (GRCm39) |
Y800* |
probably null |
Het |
|
Other mutations in Spats2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00093:Spats2
|
APN |
15 |
99,078,474 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL00696:Spats2
|
APN |
15 |
99,108,775 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01524:Spats2
|
APN |
15 |
99,110,127 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02496:Spats2
|
APN |
15 |
99,071,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03031:Spats2
|
APN |
15 |
99,078,569 (GRCm39) |
missense |
probably benign |
0.00 |
R0067:Spats2
|
UTSW |
15 |
99,110,168 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0067:Spats2
|
UTSW |
15 |
99,110,168 (GRCm39) |
missense |
possibly damaging |
0.64 |
R0630:Spats2
|
UTSW |
15 |
99,083,909 (GRCm39) |
splice site |
probably null |
|
R1577:Spats2
|
UTSW |
15 |
99,076,333 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2012:Spats2
|
UTSW |
15 |
99,076,375 (GRCm39) |
missense |
probably damaging |
0.97 |
R2229:Spats2
|
UTSW |
15 |
99,072,334 (GRCm39) |
critical splice donor site |
probably null |
|
R2982:Spats2
|
UTSW |
15 |
99,108,927 (GRCm39) |
missense |
probably benign |
|
R3743:Spats2
|
UTSW |
15 |
99,108,795 (GRCm39) |
missense |
probably benign |
0.09 |
R4679:Spats2
|
UTSW |
15 |
99,078,603 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4857:Spats2
|
UTSW |
15 |
99,072,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Spats2
|
UTSW |
15 |
99,110,157 (GRCm39) |
missense |
probably benign |
0.00 |
R5291:Spats2
|
UTSW |
15 |
99,076,422 (GRCm39) |
missense |
probably benign |
0.16 |
R6879:Spats2
|
UTSW |
15 |
99,071,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R7476:Spats2
|
UTSW |
15 |
99,110,022 (GRCm39) |
missense |
probably benign |
0.00 |
R8084:Spats2
|
UTSW |
15 |
99,064,961 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8239:Spats2
|
UTSW |
15 |
99,106,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Spats2
|
UTSW |
15 |
99,076,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R8979:Spats2
|
UTSW |
15 |
99,110,123 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9013:Spats2
|
UTSW |
15 |
99,097,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R9050:Spats2
|
UTSW |
15 |
99,110,010 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9433:Spats2
|
UTSW |
15 |
99,076,446 (GRCm39) |
nonsense |
probably null |
|
X0062:Spats2
|
UTSW |
15 |
99,076,413 (GRCm39) |
nonsense |
probably null |
|
|