Other mutations in this stock |
Total: 120 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017B05Rik |
A |
C |
9: 57,165,635 (GRCm39) |
S246R |
possibly damaging |
Het |
Abca13 |
C |
T |
11: 9,416,411 (GRCm39) |
R4058C |
probably benign |
Het |
Acacb |
A |
T |
5: 114,303,795 (GRCm39) |
R73* |
probably null |
Het |
Adam22 |
C |
T |
5: 8,184,525 (GRCm39) |
C489Y |
probably damaging |
Het |
Agap3 |
A |
T |
5: 24,698,011 (GRCm39) |
K460I |
probably damaging |
Het |
Ak4 |
T |
C |
4: 101,320,833 (GRCm39) |
I214T |
possibly damaging |
Het |
Anpep |
C |
T |
7: 79,488,004 (GRCm39) |
E518K |
probably benign |
Het |
Arrb2 |
T |
A |
11: 70,328,808 (GRCm39) |
H221Q |
probably damaging |
Het |
Atl1 |
T |
G |
12: 70,006,049 (GRCm39) |
F452V |
probably damaging |
Het |
Atp8b5 |
A |
G |
4: 43,357,063 (GRCm39) |
T604A |
probably damaging |
Het |
Bglap3 |
T |
C |
3: 88,276,068 (GRCm39) |
I95V |
probably benign |
Het |
Ccdc88a |
G |
T |
11: 29,411,788 (GRCm39) |
M532I |
probably benign |
Het |
Ccnl1 |
A |
G |
3: 65,854,332 (GRCm39) |
S430P |
possibly damaging |
Het |
Cdhr18 |
C |
T |
14: 13,829,657 (GRCm38) |
S695N |
possibly damaging |
Het |
Cdk5rap2 |
A |
T |
4: 70,321,791 (GRCm39) |
|
probably null |
Het |
Cep126 |
A |
T |
9: 8,120,748 (GRCm39) |
Y92N |
possibly damaging |
Het |
Cfap44 |
A |
C |
16: 44,242,737 (GRCm39) |
T714P |
probably benign |
Het |
Cnga1 |
T |
G |
5: 72,774,068 (GRCm39) |
D90A |
possibly damaging |
Het |
Cnot1 |
T |
C |
8: 96,469,749 (GRCm39) |
I1369V |
possibly damaging |
Het |
Coq3 |
T |
C |
4: 21,910,466 (GRCm39) |
S314P |
probably damaging |
Het |
Crhr1 |
A |
G |
11: 104,060,675 (GRCm39) |
R151G |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 133,806,167 (GRCm39) |
I930V |
probably damaging |
Het |
Ctcf |
T |
A |
8: 106,402,620 (GRCm39) |
|
probably null |
Het |
Dct |
T |
C |
14: 118,271,690 (GRCm39) |
N380S |
probably benign |
Het |
Decr2 |
A |
T |
17: 26,306,387 (GRCm39) |
L83Q |
probably damaging |
Het |
Depdc5 |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
5: 33,067,751 (GRCm39) |
|
probably benign |
Het |
Dgkb |
T |
C |
12: 38,216,776 (GRCm39) |
|
probably null |
Het |
Dnah1 |
T |
C |
14: 31,041,716 (GRCm39) |
D85G |
probably damaging |
Het |
Dnah7a |
T |
C |
1: 53,574,637 (GRCm39) |
D1709G |
probably damaging |
Het |
Dnajc13 |
A |
C |
9: 104,106,136 (GRCm39) |
L346R |
probably damaging |
Het |
Dsc1 |
A |
T |
18: 20,229,045 (GRCm39) |
V415D |
probably damaging |
Het |
Duox2 |
T |
A |
2: 122,125,832 (GRCm39) |
I296F |
probably damaging |
Het |
Ece2 |
T |
A |
16: 20,463,922 (GRCm39) |
L890H |
probably damaging |
Het |
Ecsit |
A |
G |
9: 21,987,815 (GRCm39) |
S75P |
possibly damaging |
Het |
Enpp3 |
A |
G |
10: 24,654,687 (GRCm39) |
C664R |
probably damaging |
Het |
Evpl |
G |
T |
11: 116,117,854 (GRCm39) |
D778E |
probably damaging |
Het |
Eya3 |
T |
A |
4: 132,448,663 (GRCm39) |
|
probably null |
Het |
Fam217b |
A |
T |
2: 178,062,374 (GRCm39) |
I113F |
probably benign |
Het |
Galnt6 |
G |
A |
15: 100,613,999 (GRCm39) |
P101S |
possibly damaging |
Het |
Gm379 |
G |
A |
X: 107,707,870 (GRCm39) |
Q210* |
probably null |
Het |
Grk4 |
A |
T |
5: 34,833,531 (GRCm39) |
|
probably null |
Het |
Gtf3c4 |
A |
G |
2: 28,729,968 (GRCm39) |
V91A |
probably benign |
Het |
Hcfc2 |
G |
T |
10: 82,538,392 (GRCm39) |
G143V |
probably damaging |
Het |
Heatr4 |
A |
C |
12: 84,005,221 (GRCm39) |
H710Q |
probably damaging |
Het |
Htr3a |
A |
T |
9: 48,817,681 (GRCm39) |
D97E |
probably damaging |
Het |
Htr4 |
T |
G |
18: 62,561,193 (GRCm39) |
F151L |
probably benign |
Het |
Il22ra1 |
A |
T |
4: 135,478,219 (GRCm39) |
Q430L |
probably damaging |
Het |
Invs |
T |
A |
4: 48,402,824 (GRCm39) |
|
probably null |
Het |
Ip6k1 |
G |
A |
9: 107,918,195 (GRCm39) |
E77K |
possibly damaging |
Het |
Irs1 |
T |
C |
1: 82,267,182 (GRCm39) |
S345G |
probably damaging |
Het |
Kdm4a |
A |
G |
4: 118,017,596 (GRCm39) |
V490A |
probably benign |
Het |
Kif26a |
C |
T |
12: 112,141,974 (GRCm39) |
R743C |
probably damaging |
Het |
Kif28 |
A |
G |
1: 179,530,088 (GRCm39) |
V691A |
possibly damaging |
Het |
Klhl5 |
T |
A |
5: 65,324,330 (GRCm39) |
L696Q |
probably benign |
Het |
Krtap5-1 |
T |
C |
7: 141,850,084 (GRCm39) |
|
probably benign |
Het |
Lama2 |
A |
C |
10: 27,064,395 (GRCm39) |
D1195E |
probably damaging |
Het |
Lamb1 |
T |
G |
12: 31,379,209 (GRCm39) |
L1722R |
probably damaging |
Het |
Lrp11 |
T |
A |
10: 7,499,544 (GRCm39) |
L245Q |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,876,879 (GRCm39) |
E422G |
probably benign |
Het |
Man2b1 |
T |
A |
8: 85,813,451 (GRCm39) |
D214E |
probably damaging |
Het |
Mlxipl |
A |
T |
5: 135,162,422 (GRCm39) |
D628V |
possibly damaging |
Het |
Msantd5f6 |
T |
A |
4: 73,321,675 (GRCm39) |
Y120F |
probably damaging |
Het |
Myo18b |
G |
A |
5: 112,840,624 (GRCm39) |
R2390C |
probably damaging |
Het |
Mypn |
T |
A |
10: 62,959,176 (GRCm39) |
R1048S |
probably benign |
Het |
Napepld |
A |
G |
5: 21,870,270 (GRCm39) |
S383P |
probably damaging |
Het |
Napsa |
A |
G |
7: 44,231,160 (GRCm39) |
T130A |
probably damaging |
Het |
Nbr1 |
T |
C |
11: 101,465,978 (GRCm39) |
I716T |
probably damaging |
Het |
Nexn |
A |
T |
3: 151,953,818 (GRCm39) |
M212K |
probably damaging |
Het |
Nlrp9b |
T |
A |
7: 19,757,182 (GRCm39) |
S140T |
probably benign |
Het |
Nxpe2 |
T |
C |
9: 48,230,906 (GRCm39) |
T488A |
probably benign |
Het |
Or10g3 |
T |
G |
14: 52,610,174 (GRCm39) |
Q112P |
possibly damaging |
Het |
Or10v1 |
A |
T |
19: 11,873,913 (GRCm39) |
Y176F |
probably benign |
Het |
Or5ac25 |
A |
T |
16: 59,182,526 (GRCm39) |
D18E |
probably benign |
Het |
Or7g12 |
A |
T |
9: 18,900,192 (GRCm39) |
K303* |
probably null |
Het |
Or8k20 |
C |
T |
2: 86,106,190 (GRCm39) |
V214I |
probably benign |
Het |
Pan2 |
T |
G |
10: 128,144,237 (GRCm39) |
L162R |
probably damaging |
Het |
Parp1 |
G |
T |
1: 180,416,235 (GRCm39) |
V545F |
probably damaging |
Het |
Pcdh18 |
A |
G |
3: 49,709,896 (GRCm39) |
V473A |
probably benign |
Het |
Plb1 |
A |
T |
5: 32,448,582 (GRCm39) |
N350I |
probably damaging |
Het |
Polr1a |
A |
G |
6: 71,944,898 (GRCm39) |
K1318R |
probably benign |
Het |
Ppp1r18 |
C |
T |
17: 36,184,738 (GRCm39) |
P130S |
probably damaging |
Het |
Prss48 |
C |
T |
3: 85,905,614 (GRCm39) |
W86* |
probably null |
Het |
Rab3c |
A |
T |
13: 110,220,744 (GRCm39) |
I137N |
probably damaging |
Het |
Rab3gap2 |
G |
C |
1: 184,954,099 (GRCm39) |
R57P |
probably benign |
Het |
Rad54l2 |
A |
C |
9: 106,570,916 (GRCm39) |
|
probably null |
Het |
Ralgapb |
C |
A |
2: 158,337,483 (GRCm39) |
N1147K |
probably benign |
Het |
Rfx7 |
C |
T |
9: 72,524,093 (GRCm39) |
R428C |
probably damaging |
Het |
Robo1 |
A |
G |
16: 72,757,092 (GRCm39) |
Q351R |
probably null |
Het |
Samd4 |
T |
C |
14: 47,311,585 (GRCm39) |
F81S |
probably damaging |
Het |
Shprh |
T |
A |
10: 11,059,541 (GRCm39) |
Y1097* |
probably null |
Het |
Sik3 |
C |
G |
9: 46,132,387 (GRCm39) |
H1276Q |
probably benign |
Het |
Slc24a4 |
T |
A |
12: 102,097,876 (GRCm39) |
D79E |
probably benign |
Het |
Slc7a13 |
A |
T |
4: 19,839,254 (GRCm39) |
I286F |
probably benign |
Het |
Smarca1 |
G |
A |
X: 46,938,840 (GRCm39) |
Q723* |
probably null |
Het |
Spata31d1b |
T |
C |
13: 59,865,882 (GRCm39) |
L1010P |
probably damaging |
Het |
Sult2a1 |
T |
C |
7: 13,569,900 (GRCm39) |
S111G |
possibly damaging |
Het |
Tecpr2 |
C |
T |
12: 110,914,346 (GRCm39) |
T1219M |
probably damaging |
Het |
Tesk1 |
T |
C |
4: 43,446,998 (GRCm39) |
M462T |
probably benign |
Het |
Thoc2l |
T |
A |
5: 104,666,196 (GRCm39) |
S239R |
probably benign |
Het |
Tmem171 |
C |
A |
13: 98,822,924 (GRCm39) |
G292* |
probably null |
Het |
Tmtc2 |
G |
T |
10: 105,025,969 (GRCm39) |
T833N |
probably benign |
Het |
Tnc |
G |
T |
4: 63,918,299 (GRCm39) |
T1204K |
probably benign |
Het |
Tnfaip3 |
T |
C |
10: 18,883,937 (GRCm39) |
K148E |
probably benign |
Het |
Tnrc18 |
G |
A |
5: 142,800,895 (GRCm39) |
S21F |
probably damaging |
Het |
Tns4 |
T |
C |
11: 98,966,401 (GRCm39) |
T425A |
probably damaging |
Het |
Tox |
T |
A |
4: 6,688,948 (GRCm39) |
Y472F |
probably damaging |
Het |
Trak2 |
A |
T |
1: 58,958,014 (GRCm39) |
|
probably null |
Het |
Trim33 |
T |
A |
3: 103,244,760 (GRCm39) |
Y716N |
probably damaging |
Het |
Trrap |
T |
G |
5: 144,752,863 (GRCm39) |
I1813R |
probably damaging |
Het |
Ttc29 |
A |
G |
8: 78,978,361 (GRCm39) |
E137G |
probably benign |
Het |
Ube2j2 |
A |
G |
4: 156,033,483 (GRCm39) |
K19R |
probably benign |
Het |
Ubxn2b |
T |
C |
4: 6,208,889 (GRCm39) |
I206T |
possibly damaging |
Het |
Usp40 |
A |
G |
1: 87,909,778 (GRCm39) |
F559L |
probably benign |
Het |
Utp4 |
T |
A |
8: 107,638,982 (GRCm39) |
|
probably null |
Het |
Vac14 |
A |
G |
8: 111,409,166 (GRCm39) |
N524S |
probably benign |
Het |
Vps13c |
T |
C |
9: 67,801,334 (GRCm39) |
S605P |
probably damaging |
Het |
Vwa5b2 |
G |
T |
16: 20,423,582 (GRCm39) |
S1165I |
possibly damaging |
Het |
Zdhhc19 |
C |
T |
16: 32,317,231 (GRCm39) |
R28* |
probably null |
Het |
Zfp106 |
T |
C |
2: 120,357,329 (GRCm39) |
I1189V |
probably benign |
Het |
Zfp189 |
C |
T |
4: 49,529,511 (GRCm39) |
Q205* |
probably null |
Het |
|
Other mutations in Osbpl5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01560:Osbpl5
|
APN |
7 |
143,269,430 (GRCm39) |
nonsense |
probably null |
|
IGL01996:Osbpl5
|
APN |
7 |
143,261,081 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02135:Osbpl5
|
APN |
7 |
143,258,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02331:Osbpl5
|
APN |
7 |
143,263,532 (GRCm39) |
missense |
probably benign |
0.22 |
IGL02993:Osbpl5
|
APN |
7 |
143,253,071 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0240:Osbpl5
|
UTSW |
7 |
143,295,406 (GRCm39) |
splice site |
probably null |
|
R0601:Osbpl5
|
UTSW |
7 |
143,263,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R0609:Osbpl5
|
UTSW |
7 |
143,248,558 (GRCm39) |
missense |
probably damaging |
0.99 |
R0659:Osbpl5
|
UTSW |
7 |
143,258,767 (GRCm39) |
missense |
probably damaging |
0.97 |
R1532:Osbpl5
|
UTSW |
7 |
143,248,817 (GRCm39) |
missense |
probably benign |
|
R1579:Osbpl5
|
UTSW |
7 |
143,262,939 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1595:Osbpl5
|
UTSW |
7 |
143,256,955 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1666:Osbpl5
|
UTSW |
7 |
143,262,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R1668:Osbpl5
|
UTSW |
7 |
143,262,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Osbpl5
|
UTSW |
7 |
143,248,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R1868:Osbpl5
|
UTSW |
7 |
143,269,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Osbpl5
|
UTSW |
7 |
143,256,918 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1902:Osbpl5
|
UTSW |
7 |
143,256,918 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1911:Osbpl5
|
UTSW |
7 |
143,243,662 (GRCm39) |
missense |
probably benign |
0.00 |
R1982:Osbpl5
|
UTSW |
7 |
143,295,408 (GRCm39) |
critical splice donor site |
probably null |
|
R2014:Osbpl5
|
UTSW |
7 |
143,295,429 (GRCm39) |
missense |
probably damaging |
0.98 |
R2076:Osbpl5
|
UTSW |
7 |
143,262,881 (GRCm39) |
missense |
probably damaging |
1.00 |
R2192:Osbpl5
|
UTSW |
7 |
143,247,596 (GRCm39) |
nonsense |
probably null |
|
R2256:Osbpl5
|
UTSW |
7 |
143,262,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R4271:Osbpl5
|
UTSW |
7 |
143,249,339 (GRCm39) |
nonsense |
probably null |
|
R4418:Osbpl5
|
UTSW |
7 |
143,263,552 (GRCm39) |
nonsense |
probably null |
|
R4450:Osbpl5
|
UTSW |
7 |
143,248,643 (GRCm39) |
missense |
probably benign |
0.00 |
R4573:Osbpl5
|
UTSW |
7 |
143,248,053 (GRCm39) |
missense |
probably benign |
0.00 |
R5325:Osbpl5
|
UTSW |
7 |
143,245,665 (GRCm39) |
missense |
probably damaging |
0.99 |
R5439:Osbpl5
|
UTSW |
7 |
143,295,433 (GRCm39) |
missense |
possibly damaging |
0.83 |
R5617:Osbpl5
|
UTSW |
7 |
143,246,684 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5775:Osbpl5
|
UTSW |
7 |
143,258,266 (GRCm39) |
missense |
probably benign |
0.00 |
R5935:Osbpl5
|
UTSW |
7 |
143,310,695 (GRCm39) |
start gained |
probably benign |
|
R6906:Osbpl5
|
UTSW |
7 |
143,248,065 (GRCm39) |
missense |
probably damaging |
0.99 |
R7076:Osbpl5
|
UTSW |
7 |
143,263,577 (GRCm39) |
missense |
probably benign |
0.12 |
R7117:Osbpl5
|
UTSW |
7 |
143,263,520 (GRCm39) |
missense |
probably benign |
0.01 |
R7292:Osbpl5
|
UTSW |
7 |
143,255,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7555:Osbpl5
|
UTSW |
7 |
143,248,670 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7594:Osbpl5
|
UTSW |
7 |
143,247,534 (GRCm39) |
missense |
probably benign |
0.02 |
R8028:Osbpl5
|
UTSW |
7 |
143,269,472 (GRCm39) |
missense |
probably benign |
0.00 |
R8061:Osbpl5
|
UTSW |
7 |
143,256,461 (GRCm39) |
missense |
probably benign |
0.03 |
R8314:Osbpl5
|
UTSW |
7 |
143,248,833 (GRCm39) |
missense |
probably benign |
0.05 |
R8482:Osbpl5
|
UTSW |
7 |
143,258,731 (GRCm39) |
missense |
probably benign |
0.12 |
R9202:Osbpl5
|
UTSW |
7 |
143,254,498 (GRCm39) |
missense |
probably benign |
0.45 |
R9430:Osbpl5
|
UTSW |
7 |
143,263,526 (GRCm39) |
missense |
probably benign |
0.01 |
R9687:Osbpl5
|
UTSW |
7 |
143,247,598 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9735:Osbpl5
|
UTSW |
7 |
143,248,673 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9749:Osbpl5
|
UTSW |
7 |
143,249,308 (GRCm39) |
missense |
probably benign |
0.14 |
YA93:Osbpl5
|
UTSW |
7 |
143,247,607 (GRCm39) |
missense |
probably benign |
0.01 |
|