Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130023H24Rik |
A |
G |
7: 127,835,897 (GRCm39) |
L232P |
possibly damaging |
Het |
Acaa1a |
T |
C |
9: 119,178,104 (GRCm39) |
V312A |
probably damaging |
Het |
Bmp2 |
A |
G |
2: 133,403,604 (GRCm39) |
D385G |
probably damaging |
Het |
C1qtnf9 |
T |
C |
14: 61,017,241 (GRCm39) |
V257A |
probably damaging |
Het |
Cd3d |
G |
A |
9: 44,896,991 (GRCm39) |
V122I |
probably damaging |
Het |
Cdc37 |
T |
C |
9: 21,053,519 (GRCm39) |
E199G |
probably damaging |
Het |
Crb2 |
T |
A |
2: 37,677,696 (GRCm39) |
D326E |
probably benign |
Het |
Cyp2c29 |
A |
C |
19: 39,318,781 (GRCm39) |
K420N |
possibly damaging |
Het |
Cyp2g1 |
A |
C |
7: 26,520,184 (GRCm39) |
D472A |
probably damaging |
Het |
Dab2 |
A |
C |
15: 6,451,732 (GRCm39) |
H116P |
probably damaging |
Het |
Dnah7b |
G |
C |
1: 46,275,969 (GRCm39) |
E2619Q |
probably benign |
Het |
Dsg4 |
A |
T |
18: 20,584,909 (GRCm39) |
M208L |
probably benign |
Het |
Eif4enif1 |
T |
G |
11: 3,184,040 (GRCm39) |
V521G |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,403,196 (GRCm39) |
M55T |
probably damaging |
Het |
Grhpr |
A |
G |
4: 44,985,362 (GRCm39) |
S101G |
probably damaging |
Het |
Kif15 |
T |
A |
9: 122,840,679 (GRCm39) |
D33E |
possibly damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Lama4 |
A |
G |
10: 38,936,158 (GRCm39) |
Q611R |
possibly damaging |
Het |
Lrrc47 |
T |
A |
4: 154,104,909 (GRCm39) |
*123R |
probably null |
Het |
Map4k3 |
A |
C |
17: 80,988,344 (GRCm39) |
V36G |
probably damaging |
Het |
Mme |
T |
A |
3: 63,276,344 (GRCm39) |
I707N |
probably damaging |
Het |
Muc2 |
A |
G |
7: 141,305,194 (GRCm39) |
E166G |
unknown |
Het |
Mucl1 |
T |
A |
15: 103,783,844 (GRCm39) |
T108S |
possibly damaging |
Het |
Myo1h |
A |
T |
5: 114,497,805 (GRCm39) |
D53V |
possibly damaging |
Het |
Naa15 |
T |
A |
3: 51,380,205 (GRCm39) |
L811Q |
possibly damaging |
Het |
Nalcn |
T |
C |
14: 123,525,267 (GRCm39) |
T1487A |
probably benign |
Het |
Nme8 |
A |
T |
13: 19,878,498 (GRCm39) |
L87H |
probably damaging |
Het |
Nr2e1 |
A |
G |
10: 42,444,374 (GRCm39) |
V245A |
probably damaging |
Het |
Nt5c2 |
A |
T |
19: 46,881,974 (GRCm39) |
F291Y |
possibly damaging |
Het |
Ooep |
T |
C |
9: 78,285,683 (GRCm39) |
N43S |
possibly damaging |
Het |
Or10ak13 |
T |
C |
4: 118,639,183 (GRCm39) |
M200V |
probably benign |
Het |
Or4e1 |
T |
C |
14: 52,700,932 (GRCm39) |
D178G |
possibly damaging |
Het |
Or52i2 |
A |
T |
7: 102,319,937 (GRCm39) |
Q270L |
probably benign |
Het |
Or52n2c |
A |
T |
7: 104,574,717 (GRCm39) |
C85S |
probably benign |
Het |
Ovch2 |
A |
T |
7: 107,395,772 (GRCm39) |
I82N |
probably damaging |
Het |
Palb2 |
A |
T |
7: 121,713,622 (GRCm39) |
M524K |
possibly damaging |
Het |
Patj |
T |
C |
4: 98,329,317 (GRCm39) |
S524P |
probably benign |
Het |
Patl1 |
T |
A |
19: 11,907,318 (GRCm39) |
Y401N |
possibly damaging |
Het |
Pcdhb20 |
A |
T |
18: 37,637,770 (GRCm39) |
T99S |
probably benign |
Het |
Plcb4 |
G |
A |
2: 135,774,182 (GRCm39) |
A155T |
probably benign |
Het |
Rpap3 |
A |
G |
15: 97,576,993 (GRCm39) |
V585A |
possibly damaging |
Het |
Spen |
T |
A |
4: 141,221,693 (GRCm39) |
T302S |
unknown |
Het |
Tenm4 |
G |
A |
7: 96,202,703 (GRCm39) |
R106H |
probably benign |
Het |
Ube2o |
T |
C |
11: 116,432,686 (GRCm39) |
E760G |
probably benign |
Het |
Uimc1 |
T |
A |
13: 55,223,267 (GRCm39) |
|
probably null |
Het |
Usp16 |
C |
T |
16: 87,277,817 (GRCm39) |
A689V |
probably damaging |
Het |
Vmn2r60 |
G |
A |
7: 41,791,666 (GRCm39) |
A530T |
probably benign |
Het |
Vps8 |
T |
A |
16: 21,393,772 (GRCm39) |
M1185K |
probably damaging |
Het |
Vwa8 |
T |
C |
14: 79,149,645 (GRCm39) |
S136P |
probably damaging |
Het |
Ythdc2 |
A |
G |
18: 44,967,529 (GRCm39) |
N175S |
probably benign |
Het |
Zfp160 |
A |
T |
17: 21,246,794 (GRCm39) |
H448L |
probably damaging |
Het |
Zfp90 |
T |
A |
8: 107,151,641 (GRCm39) |
C451* |
probably null |
Het |
Zfp945 |
A |
G |
17: 23,071,264 (GRCm39) |
C212R |
probably damaging |
Het |
|
Other mutations in Sorbs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00160:Sorbs1
|
APN |
19 |
40,306,473 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00776:Sorbs1
|
APN |
19 |
40,332,795 (GRCm39) |
splice site |
probably null |
|
IGL00788:Sorbs1
|
APN |
19 |
40,325,487 (GRCm39) |
splice site |
probably benign |
|
IGL00943:Sorbs1
|
APN |
19 |
40,283,484 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01525:Sorbs1
|
APN |
19 |
40,338,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01530:Sorbs1
|
APN |
19 |
40,365,091 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01951:Sorbs1
|
APN |
19 |
40,306,460 (GRCm39) |
splice site |
probably benign |
|
IGL02159:Sorbs1
|
APN |
19 |
40,316,040 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02252:Sorbs1
|
APN |
19 |
40,302,841 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02613:Sorbs1
|
APN |
19 |
40,315,991 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02643:Sorbs1
|
APN |
19 |
40,353,577 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL02668:Sorbs1
|
APN |
19 |
40,303,125 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02738:Sorbs1
|
APN |
19 |
40,365,348 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02965:Sorbs1
|
APN |
19 |
40,365,187 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03083:Sorbs1
|
APN |
19 |
40,302,820 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03173:Sorbs1
|
APN |
19 |
40,351,706 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03286:Sorbs1
|
APN |
19 |
40,332,858 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03292:Sorbs1
|
APN |
19 |
40,362,009 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0016:Sorbs1
|
UTSW |
19 |
40,303,182 (GRCm39) |
splice site |
probably benign |
|
R0016:Sorbs1
|
UTSW |
19 |
40,303,182 (GRCm39) |
splice site |
probably benign |
|
R0306:Sorbs1
|
UTSW |
19 |
40,332,855 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0526:Sorbs1
|
UTSW |
19 |
40,338,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R0551:Sorbs1
|
UTSW |
19 |
40,300,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R0688:Sorbs1
|
UTSW |
19 |
40,351,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Sorbs1
|
UTSW |
19 |
40,371,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Sorbs1
|
UTSW |
19 |
40,371,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1185:Sorbs1
|
UTSW |
19 |
40,371,050 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Sorbs1
|
UTSW |
19 |
40,381,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R2066:Sorbs1
|
UTSW |
19 |
40,353,472 (GRCm39) |
splice site |
probably null |
|
R2148:Sorbs1
|
UTSW |
19 |
40,365,268 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2214:Sorbs1
|
UTSW |
19 |
40,285,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R2410:Sorbs1
|
UTSW |
19 |
40,361,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R2940:Sorbs1
|
UTSW |
19 |
40,362,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R3847:Sorbs1
|
UTSW |
19 |
40,302,887 (GRCm39) |
missense |
probably damaging |
0.97 |
R4405:Sorbs1
|
UTSW |
19 |
40,384,189 (GRCm39) |
missense |
probably benign |
0.03 |
R4544:Sorbs1
|
UTSW |
19 |
40,300,294 (GRCm39) |
missense |
probably damaging |
0.99 |
R4618:Sorbs1
|
UTSW |
19 |
40,361,962 (GRCm39) |
missense |
probably damaging |
0.99 |
R4731:Sorbs1
|
UTSW |
19 |
40,303,133 (GRCm39) |
missense |
probably benign |
0.29 |
R4732:Sorbs1
|
UTSW |
19 |
40,303,133 (GRCm39) |
missense |
probably benign |
0.29 |
R4733:Sorbs1
|
UTSW |
19 |
40,303,133 (GRCm39) |
missense |
probably benign |
0.29 |
R4860:Sorbs1
|
UTSW |
19 |
40,325,449 (GRCm39) |
missense |
probably benign |
0.44 |
R4860:Sorbs1
|
UTSW |
19 |
40,325,449 (GRCm39) |
missense |
probably benign |
0.44 |
R4907:Sorbs1
|
UTSW |
19 |
40,328,491 (GRCm39) |
nonsense |
probably null |
|
R4912:Sorbs1
|
UTSW |
19 |
40,300,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R5229:Sorbs1
|
UTSW |
19 |
40,329,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Sorbs1
|
UTSW |
19 |
40,310,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R5416:Sorbs1
|
UTSW |
19 |
40,365,433 (GRCm39) |
missense |
probably benign |
0.06 |
R5706:Sorbs1
|
UTSW |
19 |
40,365,325 (GRCm39) |
missense |
probably benign |
|
R5871:Sorbs1
|
UTSW |
19 |
40,387,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R5936:Sorbs1
|
UTSW |
19 |
40,313,216 (GRCm39) |
missense |
probably damaging |
0.96 |
R6073:Sorbs1
|
UTSW |
19 |
40,303,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324:Sorbs1
|
UTSW |
19 |
40,310,263 (GRCm39) |
missense |
probably damaging |
0.99 |
R6343:Sorbs1
|
UTSW |
19 |
40,365,426 (GRCm39) |
critical splice donor site |
probably null |
|
R6561:Sorbs1
|
UTSW |
19 |
40,314,496 (GRCm39) |
missense |
probably benign |
|
R6646:Sorbs1
|
UTSW |
19 |
40,313,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R6768:Sorbs1
|
UTSW |
19 |
40,315,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R6850:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R6878:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R6879:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R6880:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R6908:Sorbs1
|
UTSW |
19 |
40,340,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Sorbs1
|
UTSW |
19 |
40,316,060 (GRCm39) |
nonsense |
probably null |
|
R7041:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7110:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7122:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7170:Sorbs1
|
UTSW |
19 |
40,314,573 (GRCm39) |
nonsense |
probably null |
|
R7180:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7185:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7187:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7254:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7255:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7401:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7595:Sorbs1
|
UTSW |
19 |
40,303,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R7819:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R7876:Sorbs1
|
UTSW |
19 |
40,285,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R7894:Sorbs1
|
UTSW |
19 |
40,316,020 (GRCm39) |
missense |
probably benign |
0.02 |
R7986:Sorbs1
|
UTSW |
19 |
40,353,449 (GRCm39) |
missense |
probably damaging |
0.99 |
R8031:Sorbs1
|
UTSW |
19 |
40,314,933 (GRCm39) |
missense |
probably benign |
0.17 |
R8082:Sorbs1
|
UTSW |
19 |
40,353,527 (GRCm39) |
missense |
probably benign |
0.08 |
R8282:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8283:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8446:Sorbs1
|
UTSW |
19 |
40,314,602 (GRCm39) |
missense |
probably benign |
|
R8526:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8527:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8528:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8539:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8540:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8542:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8543:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8544:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8545:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8684:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8699:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8702:Sorbs1
|
UTSW |
19 |
40,365,244 (GRCm39) |
missense |
probably benign |
|
R8752:Sorbs1
|
UTSW |
19 |
40,349,872 (GRCm39) |
critical splice donor site |
probably null |
|
R8937:Sorbs1
|
UTSW |
19 |
40,362,006 (GRCm39) |
missense |
probably benign |
0.02 |
R8956:Sorbs1
|
UTSW |
19 |
40,351,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R8960:Sorbs1
|
UTSW |
19 |
40,387,048 (GRCm39) |
missense |
probably damaging |
0.98 |
R9175:Sorbs1
|
UTSW |
19 |
40,315,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R9208:Sorbs1
|
UTSW |
19 |
40,353,462 (GRCm39) |
start gained |
probably benign |
|
R9211:Sorbs1
|
UTSW |
19 |
40,332,798 (GRCm39) |
critical splice donor site |
probably null |
|
R9371:Sorbs1
|
UTSW |
19 |
40,315,324 (GRCm39) |
missense |
probably damaging |
0.98 |
R9374:Sorbs1
|
UTSW |
19 |
40,361,923 (GRCm39) |
nonsense |
probably null |
|
R9377:Sorbs1
|
UTSW |
19 |
40,387,048 (GRCm39) |
missense |
probably damaging |
0.98 |
R9551:Sorbs1
|
UTSW |
19 |
40,361,923 (GRCm39) |
nonsense |
probably null |
|
R9552:Sorbs1
|
UTSW |
19 |
40,361,923 (GRCm39) |
nonsense |
probably null |
|
R9686:Sorbs1
|
UTSW |
19 |
40,381,954 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Sorbs1
|
UTSW |
19 |
40,315,339 (GRCm39) |
missense |
probably damaging |
0.98 |
|