Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aanat |
A |
T |
11: 116,486,472 (GRCm39) |
I4F |
probably benign |
Het |
Adamts17 |
T |
G |
7: 66,499,626 (GRCm39) |
|
probably benign |
Het |
Adcy1 |
A |
T |
11: 7,117,156 (GRCm39) |
M1008L |
probably damaging |
Het |
Atp2a3 |
C |
A |
11: 72,866,165 (GRCm39) |
H262N |
probably benign |
Het |
Atrnl1 |
T |
G |
19: 57,638,873 (GRCm39) |
|
probably benign |
Het |
Brd3 |
T |
A |
2: 27,344,362 (GRCm39) |
E456V |
probably damaging |
Het |
Ccna1 |
T |
A |
3: 54,961,807 (GRCm39) |
T38S |
probably damaging |
Het |
Chadl |
T |
A |
15: 81,580,059 (GRCm39) |
I59F |
probably benign |
Het |
Chmp3 |
T |
C |
6: 71,529,417 (GRCm39) |
M27T |
possibly damaging |
Het |
Clcn1 |
C |
T |
6: 42,275,763 (GRCm39) |
T295I |
probably damaging |
Het |
Col6a6 |
A |
G |
9: 105,604,369 (GRCm39) |
|
probably null |
Het |
Dennd2a |
T |
A |
6: 39,447,290 (GRCm39) |
H776L |
probably benign |
Het |
Dimt1 |
G |
A |
13: 107,085,219 (GRCm39) |
R55K |
probably benign |
Het |
Dlg5 |
T |
A |
14: 24,196,319 (GRCm39) |
D1626V |
probably damaging |
Het |
Dock10 |
T |
A |
1: 80,551,840 (GRCm39) |
Y665F |
probably damaging |
Het |
Hectd4 |
T |
C |
5: 121,487,465 (GRCm39) |
S3487P |
possibly damaging |
Het |
Hivep1 |
T |
C |
13: 42,310,787 (GRCm39) |
V1009A |
possibly damaging |
Het |
Ifna12 |
A |
T |
4: 88,521,091 (GRCm39) |
V152E |
probably damaging |
Het |
Igf2r |
A |
T |
17: 12,930,974 (GRCm39) |
C903S |
possibly damaging |
Het |
Ipo9 |
T |
C |
1: 135,313,672 (GRCm39) |
D1002G |
possibly damaging |
Het |
Isyna1 |
T |
C |
8: 71,048,904 (GRCm39) |
S328P |
probably damaging |
Het |
Itprid2 |
T |
C |
2: 79,472,303 (GRCm39) |
|
probably benign |
Het |
Lamc1 |
G |
A |
1: 153,122,788 (GRCm39) |
T764I |
possibly damaging |
Het |
Lta4h |
T |
C |
10: 93,308,831 (GRCm39) |
V377A |
probably benign |
Het |
Lyz2 |
C |
T |
10: 117,118,090 (GRCm39) |
V20I |
probably benign |
Het |
Myo3a |
A |
T |
2: 22,328,418 (GRCm39) |
L329F |
probably benign |
Het |
Nlgn2 |
T |
C |
11: 69,716,628 (GRCm39) |
T638A |
probably benign |
Het |
Oasl2 |
A |
G |
5: 115,035,753 (GRCm39) |
T10A |
probably damaging |
Het |
Or14j8 |
A |
T |
17: 38,263,864 (GRCm39) |
F17Y |
probably damaging |
Het |
Or5k1 |
T |
A |
16: 58,617,713 (GRCm39) |
R165S |
probably damaging |
Het |
Pde10a |
A |
T |
17: 9,172,604 (GRCm39) |
N296I |
probably damaging |
Het |
Plb1 |
A |
G |
5: 32,519,912 (GRCm39) |
I1385M |
probably benign |
Het |
Pld1 |
T |
C |
3: 28,141,378 (GRCm39) |
V647A |
probably damaging |
Het |
Pnp |
T |
C |
14: 51,185,303 (GRCm39) |
|
probably benign |
Het |
Ppl |
A |
T |
16: 4,905,327 (GRCm39) |
I1656K |
probably damaging |
Het |
Rimbp3 |
G |
T |
16: 17,027,472 (GRCm39) |
E299* |
probably null |
Het |
Sbsn |
C |
A |
7: 30,452,683 (GRCm39) |
A566D |
probably damaging |
Het |
Sh3rf1 |
T |
A |
8: 61,816,225 (GRCm39) |
M494K |
probably damaging |
Het |
Slc2a2 |
T |
A |
3: 28,772,885 (GRCm39) |
V226E |
probably damaging |
Het |
Smarca2 |
T |
A |
19: 26,617,986 (GRCm39) |
I339N |
possibly damaging |
Het |
Tenm2 |
G |
T |
11: 36,097,912 (GRCm39) |
S445R |
possibly damaging |
Het |
Tlcd5 |
C |
A |
9: 43,022,783 (GRCm39) |
K190N |
probably benign |
Het |
Tnip2 |
A |
T |
5: 34,671,075 (GRCm39) |
L56Q |
probably damaging |
Het |
Trpv1 |
C |
T |
11: 73,141,612 (GRCm39) |
S485F |
probably damaging |
Het |
Vmn2r23 |
T |
C |
6: 123,681,437 (GRCm39) |
M115T |
probably benign |
Het |
Zbtb38 |
G |
A |
9: 96,568,672 (GRCm39) |
T804I |
probably damaging |
Het |
Zfhx3 |
T |
C |
8: 109,520,167 (GRCm39) |
S430P |
possibly damaging |
Het |
|
Other mutations in Cabin1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01434:Cabin1
|
APN |
10 |
75,561,420 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01457:Cabin1
|
APN |
10 |
75,578,263 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02217:Cabin1
|
APN |
10 |
75,535,881 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02737:Cabin1
|
APN |
10 |
75,549,419 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02792:Cabin1
|
APN |
10 |
75,582,573 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03047:Cabin1
|
APN |
10 |
75,535,934 (GRCm39) |
splice site |
probably benign |
|
IGL03106:Cabin1
|
APN |
10 |
75,569,462 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03276:Cabin1
|
APN |
10 |
75,568,247 (GRCm39) |
missense |
probably damaging |
1.00 |
bison
|
UTSW |
10 |
75,520,157 (GRCm39) |
missense |
probably damaging |
1.00 |
range
|
UTSW |
10 |
75,494,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R0335:Cabin1
|
UTSW |
10 |
75,492,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R0557:Cabin1
|
UTSW |
10 |
75,562,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R0578:Cabin1
|
UTSW |
10 |
75,549,444 (GRCm39) |
missense |
probably damaging |
0.96 |
R0588:Cabin1
|
UTSW |
10 |
75,581,171 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1115:Cabin1
|
UTSW |
10 |
75,553,511 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1120:Cabin1
|
UTSW |
10 |
75,561,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Cabin1
|
UTSW |
10 |
75,492,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Cabin1
|
UTSW |
10 |
75,530,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R1794:Cabin1
|
UTSW |
10 |
75,561,579 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1844:Cabin1
|
UTSW |
10 |
75,579,184 (GRCm39) |
splice site |
probably null |
|
R1959:Cabin1
|
UTSW |
10 |
75,570,924 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2008:Cabin1
|
UTSW |
10 |
75,570,810 (GRCm39) |
splice site |
probably null |
|
R2279:Cabin1
|
UTSW |
10 |
75,589,295 (GRCm39) |
missense |
probably benign |
|
R3150:Cabin1
|
UTSW |
10 |
75,492,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R3929:Cabin1
|
UTSW |
10 |
75,587,452 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3945:Cabin1
|
UTSW |
10 |
75,581,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R3946:Cabin1
|
UTSW |
10 |
75,581,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R4206:Cabin1
|
UTSW |
10 |
75,590,675 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4812:Cabin1
|
UTSW |
10 |
75,482,428 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4944:Cabin1
|
UTSW |
10 |
75,575,255 (GRCm39) |
missense |
probably damaging |
0.99 |
R4944:Cabin1
|
UTSW |
10 |
75,557,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5078:Cabin1
|
UTSW |
10 |
75,557,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R5082:Cabin1
|
UTSW |
10 |
75,574,164 (GRCm39) |
missense |
probably damaging |
0.99 |
R5319:Cabin1
|
UTSW |
10 |
75,561,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R5481:Cabin1
|
UTSW |
10 |
75,570,900 (GRCm39) |
missense |
probably benign |
0.29 |
R5504:Cabin1
|
UTSW |
10 |
75,488,843 (GRCm39) |
missense |
probably benign |
0.00 |
R5710:Cabin1
|
UTSW |
10 |
75,482,852 (GRCm39) |
missense |
probably benign |
0.00 |
R5908:Cabin1
|
UTSW |
10 |
75,557,366 (GRCm39) |
missense |
probably damaging |
1.00 |
R5975:Cabin1
|
UTSW |
10 |
75,493,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R5982:Cabin1
|
UTSW |
10 |
75,561,394 (GRCm39) |
missense |
probably benign |
0.00 |
R6038:Cabin1
|
UTSW |
10 |
75,575,200 (GRCm39) |
missense |
probably benign |
0.02 |
R6038:Cabin1
|
UTSW |
10 |
75,575,200 (GRCm39) |
missense |
probably benign |
0.02 |
R6114:Cabin1
|
UTSW |
10 |
75,583,805 (GRCm39) |
missense |
probably benign |
0.00 |
R6285:Cabin1
|
UTSW |
10 |
75,520,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R6341:Cabin1
|
UTSW |
10 |
75,494,573 (GRCm39) |
missense |
probably damaging |
0.98 |
R6361:Cabin1
|
UTSW |
10 |
75,562,699 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6395:Cabin1
|
UTSW |
10 |
75,582,576 (GRCm39) |
missense |
probably benign |
0.10 |
R6422:Cabin1
|
UTSW |
10 |
75,492,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R6575:Cabin1
|
UTSW |
10 |
75,561,535 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6763:Cabin1
|
UTSW |
10 |
75,582,564 (GRCm39) |
missense |
probably damaging |
0.99 |
R6845:Cabin1
|
UTSW |
10 |
75,557,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R6936:Cabin1
|
UTSW |
10 |
75,551,592 (GRCm39) |
splice site |
probably null |
|
R7050:Cabin1
|
UTSW |
10 |
75,549,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R7055:Cabin1
|
UTSW |
10 |
75,579,117 (GRCm39) |
missense |
probably benign |
0.04 |
R7101:Cabin1
|
UTSW |
10 |
75,587,401 (GRCm39) |
missense |
probably benign |
|
R7138:Cabin1
|
UTSW |
10 |
75,581,187 (GRCm39) |
missense |
probably damaging |
0.98 |
R7173:Cabin1
|
UTSW |
10 |
75,582,396 (GRCm39) |
missense |
probably benign |
0.00 |
R7265:Cabin1
|
UTSW |
10 |
75,557,257 (GRCm39) |
missense |
|
|
R7284:Cabin1
|
UTSW |
10 |
75,530,668 (GRCm39) |
missense |
|
|
R7472:Cabin1
|
UTSW |
10 |
75,494,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7571:Cabin1
|
UTSW |
10 |
75,482,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R7617:Cabin1
|
UTSW |
10 |
75,568,277 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7739:Cabin1
|
UTSW |
10 |
75,494,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R7997:Cabin1
|
UTSW |
10 |
75,569,609 (GRCm39) |
missense |
probably benign |
0.01 |
R8347:Cabin1
|
UTSW |
10 |
75,578,201 (GRCm39) |
missense |
probably damaging |
0.98 |
R8544:Cabin1
|
UTSW |
10 |
75,585,890 (GRCm39) |
missense |
probably benign |
0.17 |
R8546:Cabin1
|
UTSW |
10 |
75,578,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R8692:Cabin1
|
UTSW |
10 |
75,587,410 (GRCm39) |
missense |
probably benign |
0.28 |
R8839:Cabin1
|
UTSW |
10 |
75,492,650 (GRCm39) |
missense |
probably benign |
0.00 |
R9010:Cabin1
|
UTSW |
10 |
75,570,892 (GRCm39) |
nonsense |
probably null |
|
R9108:Cabin1
|
UTSW |
10 |
75,492,973 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9204:Cabin1
|
UTSW |
10 |
75,530,550 (GRCm39) |
missense |
probably benign |
0.01 |
R9259:Cabin1
|
UTSW |
10 |
75,582,576 (GRCm39) |
missense |
probably benign |
|
R9312:Cabin1
|
UTSW |
10 |
75,561,569 (GRCm39) |
missense |
probably benign |
0.07 |
R9421:Cabin1
|
UTSW |
10 |
75,493,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R9439:Cabin1
|
UTSW |
10 |
75,581,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R9578:Cabin1
|
UTSW |
10 |
75,590,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R9645:Cabin1
|
UTSW |
10 |
75,494,543 (GRCm39) |
missense |
probably benign |
0.36 |
R9649:Cabin1
|
UTSW |
10 |
75,575,239 (GRCm39) |
missense |
probably damaging |
0.98 |
R9711:Cabin1
|
UTSW |
10 |
75,579,090 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Cabin1
|
UTSW |
10 |
75,483,957 (GRCm39) |
missense |
probably benign |
0.03 |
|