Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
A |
G |
6: 83,138,336 (GRCm39) |
T127A |
probably damaging |
Het |
Aadacl2 |
C |
T |
3: 59,932,484 (GRCm39) |
T333I |
probably damaging |
Het |
Actl6b |
T |
C |
5: 137,565,313 (GRCm39) |
S366P |
probably damaging |
Het |
Actr10 |
T |
C |
12: 71,001,430 (GRCm39) |
|
probably benign |
Het |
Adgrf5 |
T |
A |
17: 43,750,965 (GRCm39) |
I510N |
probably damaging |
Het |
Adra2a |
A |
G |
19: 54,035,112 (GRCm39) |
Y156C |
probably damaging |
Het |
Angpt4 |
T |
C |
2: 151,767,464 (GRCm39) |
|
probably null |
Het |
Ankdd1a |
T |
A |
9: 65,411,472 (GRCm39) |
|
probably null |
Het |
AW146154 |
C |
A |
7: 41,130,801 (GRCm39) |
G105V |
probably benign |
Het |
Brd3 |
A |
G |
2: 27,340,556 (GRCm39) |
L551P |
probably benign |
Het |
Calb2 |
C |
T |
8: 110,883,610 (GRCm39) |
G38D |
possibly damaging |
Het |
Cand1 |
G |
A |
10: 119,047,933 (GRCm39) |
A519V |
probably benign |
Het |
Cnbd1 |
T |
C |
4: 18,860,517 (GRCm39) |
T410A |
possibly damaging |
Het |
Cndp2 |
A |
T |
18: 84,690,201 (GRCm39) |
M247K |
probably damaging |
Het |
Cog6 |
T |
A |
3: 52,921,237 (GRCm39) |
Q123L |
probably null |
Het |
Crx |
G |
A |
7: 15,602,262 (GRCm39) |
R139C |
probably damaging |
Het |
Ctrc |
A |
G |
4: 141,571,037 (GRCm39) |
Y68H |
probably damaging |
Het |
Ddx4 |
T |
C |
13: 112,757,779 (GRCm39) |
D326G |
probably damaging |
Het |
Depdc1a |
T |
C |
3: 159,232,286 (GRCm39) |
V679A |
probably damaging |
Het |
Dyrk1a |
A |
G |
16: 94,487,440 (GRCm39) |
D512G |
probably damaging |
Het |
Edem1 |
C |
T |
6: 108,831,290 (GRCm39) |
R584C |
possibly damaging |
Het |
Emcn |
A |
G |
3: 137,085,638 (GRCm39) |
T79A |
probably benign |
Het |
Fbrsl1 |
C |
T |
5: 110,526,307 (GRCm39) |
G437R |
probably damaging |
Het |
Fbxo9 |
T |
C |
9: 78,008,938 (GRCm39) |
M12V |
possibly damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,854,914 (GRCm39) |
I1847F |
probably damaging |
Het |
Flii |
A |
G |
11: 60,609,688 (GRCm39) |
S640P |
probably benign |
Het |
Frs2 |
T |
C |
10: 116,913,468 (GRCm39) |
S121G |
probably benign |
Het |
Fsip2 |
A |
T |
2: 82,812,207 (GRCm39) |
N2842I |
possibly damaging |
Het |
Fst |
G |
T |
13: 114,592,241 (GRCm39) |
Q159K |
probably damaging |
Het |
Ggt1 |
T |
C |
10: 75,421,540 (GRCm39) |
|
probably null |
Het |
Gigyf2 |
T |
C |
1: 87,352,860 (GRCm39) |
|
probably benign |
Het |
Gm10439 |
T |
G |
X: 148,419,159 (GRCm39) |
*434E |
probably null |
Het |
Gm9476 |
T |
A |
10: 100,142,996 (GRCm39) |
|
noncoding transcript |
Het |
Gmcl1 |
A |
T |
6: 86,703,127 (GRCm39) |
N102K |
possibly damaging |
Het |
Gml |
T |
C |
15: 74,688,299 (GRCm39) |
N56S |
probably damaging |
Het |
Gpam |
A |
C |
19: 55,079,597 (GRCm39) |
S128R |
probably benign |
Het |
Gucy1b2 |
C |
T |
14: 62,690,779 (GRCm39) |
|
probably null |
Het |
Hhipl2 |
A |
G |
1: 183,214,055 (GRCm39) |
D377G |
probably damaging |
Het |
Hmx3 |
C |
T |
7: 131,146,146 (GRCm39) |
Q285* |
probably null |
Het |
Hspa14 |
A |
G |
2: 3,503,560 (GRCm39) |
V116A |
possibly damaging |
Het |
Ighv5-17 |
T |
C |
12: 113,822,878 (GRCm39) |
D81G |
possibly damaging |
Het |
Ipo5 |
T |
C |
14: 121,163,683 (GRCm39) |
V247A |
probably benign |
Het |
Iqcd |
A |
G |
5: 120,740,440 (GRCm39) |
Q257R |
probably damaging |
Het |
Itpk1 |
T |
C |
12: 102,540,225 (GRCm39) |
N286S |
possibly damaging |
Het |
Knl1 |
T |
A |
2: 118,898,829 (GRCm39) |
C177S |
possibly damaging |
Het |
Knop1 |
T |
C |
7: 118,452,495 (GRCm39) |
K23E |
possibly damaging |
Het |
Ksr2 |
T |
A |
5: 117,846,305 (GRCm39) |
V724E |
probably damaging |
Het |
Lrrc17 |
G |
A |
5: 21,780,156 (GRCm39) |
G377S |
probably damaging |
Het |
Macf1 |
GCCCCC |
GCCCCCC |
4: 123,244,784 (GRCm39) |
|
probably null |
Het |
Morc2b |
T |
A |
17: 33,355,907 (GRCm39) |
T622S |
probably benign |
Het |
Msantd2 |
G |
A |
9: 37,428,555 (GRCm39) |
G185R |
probably damaging |
Het |
Mtmr2 |
A |
G |
9: 13,699,943 (GRCm39) |
Y38C |
probably damaging |
Het |
Mycbpap |
A |
T |
11: 94,398,572 (GRCm39) |
|
probably null |
Het |
Nadsyn1 |
T |
A |
7: 143,362,567 (GRCm39) |
R279W |
probably benign |
Het |
Or1e25 |
T |
A |
11: 73,494,030 (GRCm39) |
V208E |
possibly damaging |
Het |
Or2t48 |
A |
C |
11: 58,420,710 (GRCm39) |
V34G |
probably benign |
Het |
Or56b35 |
T |
A |
7: 104,963,646 (GRCm39) |
F145Y |
probably damaging |
Het |
Or7a38 |
G |
A |
10: 78,753,420 (GRCm39) |
V249I |
possibly damaging |
Het |
Pcdhga4 |
A |
T |
18: 37,819,651 (GRCm39) |
Y400F |
probably damaging |
Het |
Pkd2 |
A |
G |
5: 104,634,515 (GRCm39) |
|
silent |
Het |
Prkar1b |
T |
C |
5: 139,113,544 (GRCm39) |
|
probably null |
Het |
Ric8b |
T |
C |
10: 84,828,076 (GRCm39) |
Y467H |
probably damaging |
Het |
Rin1 |
A |
G |
19: 5,102,652 (GRCm39) |
E387G |
probably damaging |
Het |
Robo2 |
G |
A |
16: 73,695,853 (GRCm39) |
T1430I |
probably benign |
Het |
Slc37a1 |
A |
T |
17: 31,559,236 (GRCm39) |
T439S |
probably damaging |
Het |
Slc6a6 |
T |
C |
6: 91,712,170 (GRCm39) |
F233S |
probably damaging |
Het |
Smyd3 |
A |
T |
1: 179,238,024 (GRCm39) |
D114E |
probably benign |
Het |
Snrnp70 |
GCGGTCCCGGTCCCGGTC |
GCGGTCCCGGTC |
7: 45,026,657 (GRCm39) |
|
probably benign |
Het |
Speer4a1 |
T |
A |
5: 26,241,736 (GRCm39) |
N130I |
probably damaging |
Het |
Spin1 |
A |
G |
13: 51,293,563 (GRCm39) |
Y91C |
probably damaging |
Het |
Tdrd7 |
T |
C |
4: 46,029,757 (GRCm39) |
V1030A |
probably benign |
Het |
Trim30c |
T |
A |
7: 104,037,511 (GRCm39) |
M152L |
possibly damaging |
Het |
Tsga10 |
T |
A |
1: 37,800,598 (GRCm39) |
D542V |
probably damaging |
Het |
Unc93a2 |
A |
T |
17: 7,637,187 (GRCm39) |
C334S |
probably benign |
Het |
Vmn1r175 |
A |
T |
7: 23,508,531 (GRCm39) |
I32N |
possibly damaging |
Het |
Vmn1r81 |
A |
T |
7: 11,994,034 (GRCm39) |
D191E |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,226,973 (GRCm39) |
S812P |
probably damaging |
Het |
Zbtb5 |
C |
A |
4: 44,995,052 (GRCm39) |
V111F |
probably damaging |
Het |
Zdbf2 |
T |
G |
1: 63,343,570 (GRCm39) |
C650G |
possibly damaging |
Het |
Zfp282 |
T |
A |
6: 47,882,261 (GRCm39) |
N649K |
probably benign |
Het |
|
Other mutations in Seh1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02061:Seh1l
|
APN |
18 |
67,920,328 (GRCm39) |
splice site |
probably benign |
|
IGL02166:Seh1l
|
APN |
18 |
67,918,093 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02557:Seh1l
|
APN |
18 |
67,922,483 (GRCm39) |
missense |
probably benign |
0.15 |
IGL03047:Seh1l
|
UTSW |
18 |
67,922,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Seh1l
|
UTSW |
18 |
67,925,086 (GRCm39) |
critical splice donor site |
probably null |
|
R0046:Seh1l
|
UTSW |
18 |
67,925,086 (GRCm39) |
critical splice donor site |
probably null |
|
R1465:Seh1l
|
UTSW |
18 |
67,917,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Seh1l
|
UTSW |
18 |
67,917,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R1618:Seh1l
|
UTSW |
18 |
67,921,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R2112:Seh1l
|
UTSW |
18 |
67,920,249 (GRCm39) |
missense |
probably damaging |
0.98 |
R3433:Seh1l
|
UTSW |
18 |
67,926,222 (GRCm39) |
missense |
probably benign |
0.08 |
R3780:Seh1l
|
UTSW |
18 |
67,908,087 (GRCm39) |
missense |
probably benign |
0.02 |
R4084:Seh1l
|
UTSW |
18 |
67,921,860 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6518:Seh1l
|
UTSW |
18 |
67,922,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R6945:Seh1l
|
UTSW |
18 |
67,922,460 (GRCm39) |
missense |
probably benign |
0.00 |
R7448:Seh1l
|
UTSW |
18 |
67,916,988 (GRCm39) |
missense |
probably damaging |
1.00 |
R7582:Seh1l
|
UTSW |
18 |
67,908,188 (GRCm39) |
nonsense |
probably null |
|
R8383:Seh1l
|
UTSW |
18 |
67,908,126 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8930:Seh1l
|
UTSW |
18 |
67,908,134 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8932:Seh1l
|
UTSW |
18 |
67,908,134 (GRCm39) |
missense |
possibly damaging |
0.88 |
|