Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn4 |
C |
T |
7: 28,610,995 (GRCm39) |
V248M |
possibly damaging |
Het |
AW209491 |
A |
T |
13: 14,812,328 (GRCm39) |
I394F |
probably benign |
Het |
Cacna1d |
A |
T |
14: 29,796,967 (GRCm39) |
|
probably benign |
Het |
Cacna1i |
A |
T |
15: 80,265,373 (GRCm39) |
I1542F |
probably damaging |
Het |
Cep97 |
A |
T |
16: 55,735,924 (GRCm39) |
N291K |
possibly damaging |
Het |
Clasp2 |
A |
T |
9: 113,689,209 (GRCm39) |
|
probably benign |
Het |
Dennd1c |
T |
C |
17: 57,382,465 (GRCm39) |
Q67R |
probably damaging |
Het |
Eva1c |
A |
T |
16: 90,663,305 (GRCm39) |
D13V |
possibly damaging |
Het |
Fam151b |
T |
C |
13: 92,610,504 (GRCm39) |
K95R |
probably benign |
Het |
Gm13941 |
T |
C |
2: 110,889,761 (GRCm39) |
|
noncoding transcript |
Het |
Gps2 |
C |
T |
11: 69,805,607 (GRCm39) |
Q42* |
probably null |
Het |
Hivep1 |
T |
A |
13: 42,312,132 (GRCm39) |
D1457E |
probably benign |
Het |
L3mbtl1 |
A |
G |
2: 162,790,748 (GRCm39) |
K225E |
probably damaging |
Het |
Limch1 |
A |
G |
5: 67,131,965 (GRCm39) |
S143G |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,369,041 (GRCm39) |
K342E |
possibly damaging |
Het |
Mc5r |
T |
G |
18: 68,472,637 (GRCm39) |
M332R |
probably damaging |
Het |
Mcf2l |
A |
G |
8: 13,063,060 (GRCm39) |
T882A |
probably benign |
Het |
Mtrex |
C |
T |
13: 113,023,396 (GRCm39) |
V727I |
probably benign |
Het |
Myf6 |
A |
T |
10: 107,329,340 (GRCm39) |
|
probably null |
Het |
Plekha5 |
C |
T |
6: 140,470,629 (GRCm39) |
T90I |
probably damaging |
Het |
Ptbp2 |
T |
C |
3: 119,514,290 (GRCm39) |
T478A |
probably benign |
Het |
Rasgrp1 |
C |
A |
2: 117,125,301 (GRCm39) |
R246S |
probably damaging |
Het |
Rflnb |
A |
T |
11: 75,912,987 (GRCm39) |
S134T |
possibly damaging |
Het |
Rnf214 |
A |
G |
9: 45,778,796 (GRCm39) |
|
probably null |
Het |
Satb1 |
T |
C |
17: 52,111,364 (GRCm39) |
T165A |
probably damaging |
Het |
Scamp1 |
T |
C |
13: 94,340,658 (GRCm39) |
Y237C |
probably damaging |
Het |
Skint10 |
A |
T |
4: 112,568,753 (GRCm39) |
F321L |
probably benign |
Het |
Slc8a1 |
A |
G |
17: 81,745,188 (GRCm39) |
V672A |
probably benign |
Het |
Stkld1 |
A |
T |
2: 26,839,352 (GRCm39) |
E339D |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,960,872 (GRCm39) |
T241A |
probably damaging |
Het |
Ticrr |
A |
T |
7: 79,327,158 (GRCm39) |
D622V |
probably damaging |
Het |
Trmt1l |
T |
C |
1: 151,324,131 (GRCm39) |
V326A |
probably benign |
Het |
Ube3c |
A |
G |
5: 29,803,936 (GRCm39) |
T180A |
possibly damaging |
Het |
Unc13a |
A |
C |
8: 72,087,302 (GRCm39) |
F1482V |
probably damaging |
Het |
Unc79 |
A |
G |
12: 103,025,777 (GRCm39) |
E388G |
probably damaging |
Het |
Ush2a |
A |
T |
1: 188,697,043 (GRCm39) |
D5167V |
probably damaging |
Het |
Vmn2r93 |
A |
T |
17: 18,546,672 (GRCm39) |
H848L |
probably benign |
Het |
Zcchc9 |
T |
C |
13: 91,945,368 (GRCm39) |
I72V |
probably benign |
Het |
Zfc3h1 |
G |
T |
10: 115,259,379 (GRCm39) |
L1650F |
possibly damaging |
Het |
Zzz3 |
A |
G |
3: 152,134,040 (GRCm39) |
D366G |
possibly damaging |
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 |
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 |
R7187:Spats2
|
UTSW |
15 |
99,110,054 (GRCm39) |
missense |
probably benign |
0.02 |
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 |
|
|