Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acly |
C |
A |
11: 100,370,081 (GRCm39) |
V994F |
probably damaging |
Het |
Arfgap3 |
T |
C |
15: 83,214,741 (GRCm39) |
T182A |
probably benign |
Het |
Bcl2l14 |
T |
C |
6: 134,409,102 (GRCm39) |
|
probably benign |
Het |
Ccr7 |
A |
T |
11: 99,036,103 (GRCm39) |
I273K |
possibly damaging |
Het |
Cd40 |
A |
G |
2: 164,912,681 (GRCm39) |
M211V |
possibly damaging |
Het |
Coro2b |
T |
G |
9: 62,338,609 (GRCm39) |
E208A |
probably damaging |
Het |
Dennd5a |
A |
C |
7: 109,517,968 (GRCm39) |
M556R |
probably damaging |
Het |
Efcab2 |
A |
T |
1: 178,265,062 (GRCm39) |
|
probably benign |
Het |
Fastkd2 |
T |
C |
1: 63,787,114 (GRCm39) |
|
probably benign |
Het |
Fbxw8 |
A |
C |
5: 118,215,636 (GRCm39) |
|
probably benign |
Het |
Fhip1a |
T |
C |
3: 85,629,802 (GRCm39) |
E263G |
probably benign |
Het |
Frem1 |
T |
C |
4: 82,939,007 (GRCm39) |
D25G |
probably benign |
Het |
Gtf3c3 |
C |
T |
1: 54,456,937 (GRCm39) |
A488T |
probably damaging |
Het |
Ift52 |
A |
G |
2: 162,871,702 (GRCm39) |
K178R |
probably benign |
Het |
Kit |
T |
C |
5: 75,810,192 (GRCm39) |
|
probably benign |
Het |
Map1a |
T |
C |
2: 121,137,859 (GRCm39) |
|
probably null |
Het |
Mxra7 |
G |
T |
11: 116,701,696 (GRCm39) |
|
probably benign |
Het |
Myt1 |
C |
A |
2: 181,453,024 (GRCm39) |
S7* |
probably null |
Het |
Nphs1 |
C |
T |
7: 30,180,803 (GRCm39) |
|
probably benign |
Het |
Or10h28 |
C |
T |
17: 33,487,940 (GRCm39) |
R81* |
probably null |
Het |
Or1l8 |
C |
A |
2: 36,817,514 (GRCm39) |
G204V |
possibly damaging |
Het |
Osgin2 |
A |
T |
4: 15,998,085 (GRCm39) |
D512E |
possibly damaging |
Het |
Pde4b |
T |
A |
4: 102,399,352 (GRCm39) |
|
probably benign |
Het |
Rasef |
G |
T |
4: 73,666,841 (GRCm39) |
T146K |
possibly damaging |
Het |
Ren1 |
T |
A |
1: 133,284,256 (GRCm39) |
V207D |
probably damaging |
Het |
S100a8 |
A |
G |
3: 90,577,180 (GRCm39) |
D59G |
probably damaging |
Het |
Sdcbp |
G |
A |
4: 6,377,143 (GRCm39) |
|
probably null |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Slamf7 |
A |
T |
1: 171,466,751 (GRCm39) |
D151E |
probably benign |
Het |
Slco1b2 |
A |
G |
6: 141,628,980 (GRCm39) |
M561V |
probably benign |
Het |
Sned1 |
G |
A |
1: 93,209,376 (GRCm39) |
V830M |
possibly damaging |
Het |
Stard9 |
T |
C |
2: 120,523,331 (GRCm39) |
I662T |
probably benign |
Het |
Vwf |
T |
A |
6: 125,632,028 (GRCm39) |
V20D |
unknown |
Het |
Znhit6 |
G |
T |
3: 145,300,440 (GRCm39) |
|
probably null |
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 |
IGL02649:Cabin1
|
APN |
10 |
75,573,252 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|