Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
C |
T |
7: 45,629,449 (GRCm39) |
V1293M |
probably damaging |
Het |
Agt |
A |
G |
8: 125,290,537 (GRCm39) |
W257R |
possibly damaging |
Het |
Arhgef11 |
T |
A |
3: 87,620,406 (GRCm39) |
N457K |
probably benign |
Het |
Bcl3 |
G |
T |
7: 19,554,082 (GRCm39) |
H95Q |
probably benign |
Het |
C1d |
T |
A |
11: 17,213,662 (GRCm39) |
N64K |
probably damaging |
Het |
Casc3 |
C |
T |
11: 98,713,607 (GRCm39) |
R280C |
probably damaging |
Het |
Cd300c2 |
C |
T |
11: 114,891,466 (GRCm39) |
S136N |
probably benign |
Het |
Cdh8 |
A |
G |
8: 99,757,672 (GRCm39) |
V642A |
possibly damaging |
Het |
Cep290 |
A |
T |
10: 100,331,706 (GRCm39) |
I180F |
possibly damaging |
Het |
Copz2 |
A |
G |
11: 96,744,887 (GRCm39) |
E86G |
probably damaging |
Het |
Cplane1 |
A |
G |
15: 8,230,635 (GRCm39) |
I971V |
probably benign |
Het |
Csf3r |
A |
T |
4: 125,923,712 (GRCm39) |
D74V |
possibly damaging |
Het |
Cyp11b1 |
T |
G |
15: 74,710,789 (GRCm39) |
E257A |
possibly damaging |
Het |
Dlg2 |
A |
G |
7: 92,024,875 (GRCm39) |
Q580R |
probably damaging |
Het |
Dnai2 |
A |
T |
11: 114,645,275 (GRCm39) |
K570M |
unknown |
Het |
Dock8 |
A |
G |
19: 25,133,281 (GRCm39) |
K1143E |
probably benign |
Het |
Dxo |
T |
C |
17: 35,058,099 (GRCm39) |
S394P |
probably benign |
Het |
Etl4 |
A |
G |
2: 20,810,977 (GRCm39) |
D1388G |
probably benign |
Het |
F13a1 |
C |
A |
13: 37,209,692 (GRCm39) |
R91L |
probably damaging |
Het |
Fam50b |
C |
T |
13: 34,930,856 (GRCm39) |
R111* |
probably null |
Het |
Fat2 |
T |
G |
11: 55,202,535 (GRCm39) |
N180H |
probably damaging |
Het |
Fitm2 |
A |
T |
2: 163,311,768 (GRCm39) |
H148Q |
probably benign |
Het |
Fjx1 |
A |
T |
2: 102,281,156 (GRCm39) |
S260T |
possibly damaging |
Het |
Fos |
T |
C |
12: 85,522,466 (GRCm39) |
L165P |
probably damaging |
Het |
Gm39115 |
C |
A |
7: 141,689,710 (GRCm39) |
C21F |
unknown |
Het |
Gucy1a1 |
C |
T |
3: 82,005,000 (GRCm39) |
C595Y |
probably damaging |
Het |
Hectd4 |
G |
T |
5: 121,467,172 (GRCm39) |
W2478L |
possibly damaging |
Het |
I830077J02Rik |
T |
A |
3: 105,836,060 (GRCm39) |
K9N |
probably damaging |
Het |
Ift70a1 |
T |
C |
2: 75,811,519 (GRCm39) |
D188G |
probably benign |
Het |
Ireb2 |
T |
C |
9: 54,811,265 (GRCm39) |
F723L |
possibly damaging |
Het |
Itpr1 |
G |
A |
6: 108,496,309 (GRCm39) |
V2580I |
probably damaging |
Het |
Kcnu1 |
G |
A |
8: 26,382,092 (GRCm39) |
G481R |
probably damaging |
Het |
Kdm3b |
G |
T |
18: 34,926,129 (GRCm39) |
A90S |
probably benign |
Het |
Klra8 |
A |
G |
6: 130,105,056 (GRCm39) |
V23A |
probably damaging |
Het |
Lig4 |
A |
G |
8: 10,023,777 (GRCm39) |
M1T |
probably null |
Het |
Lpin3 |
C |
T |
2: 160,737,273 (GRCm39) |
P107S |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 41,265,867 (GRCm39) |
K1100* |
probably null |
Het |
Obscn |
G |
A |
11: 58,929,700 (GRCm39) |
H5172Y |
probably damaging |
Het |
Or10a3m |
T |
A |
7: 108,313,418 (GRCm39) |
M286K |
possibly damaging |
Het |
Or4p20 |
A |
G |
2: 88,253,745 (GRCm39) |
I208T |
probably benign |
Het |
Or5ae1 |
C |
T |
7: 84,565,787 (GRCm39) |
H267Y |
probably benign |
Het |
Or6z1 |
T |
A |
7: 6,504,734 (GRCm39) |
T170S |
probably damaging |
Het |
Or8c14-ps1 |
A |
T |
9: 38,101,498 (GRCm39) |
H159L |
possibly damaging |
Het |
Orc3 |
A |
G |
4: 34,593,173 (GRCm39) |
L298P |
probably damaging |
Het |
Otub1 |
A |
G |
19: 7,177,360 (GRCm39) |
F96L |
probably damaging |
Het |
Pcnx3 |
A |
G |
19: 5,736,670 (GRCm39) |
S156P |
probably benign |
Het |
Pde3b |
A |
G |
7: 114,126,129 (GRCm39) |
M788V |
probably damaging |
Het |
Pias4 |
A |
G |
10: 80,992,844 (GRCm39) |
|
probably null |
Het |
Polg |
A |
G |
7: 79,114,743 (GRCm39) |
C73R |
probably benign |
Het |
Ptbp2 |
T |
C |
3: 119,541,467 (GRCm39) |
Y190C |
probably damaging |
Het |
Rab33b |
T |
A |
3: 51,401,050 (GRCm39) |
F175I |
probably damaging |
Het |
Rfx1 |
A |
G |
8: 84,806,515 (GRCm39) |
T108A |
probably benign |
Het |
Ribc2 |
A |
G |
15: 85,019,461 (GRCm39) |
D81G |
probably benign |
Het |
Rnf213 |
T |
G |
11: 119,340,149 (GRCm39) |
M3460R |
|
Het |
Rsf1 |
T |
A |
7: 97,266,103 (GRCm39) |
S86T |
|
Het |
Rxfp2 |
C |
A |
5: 149,973,068 (GRCm39) |
T181N |
possibly damaging |
Het |
Samm50 |
G |
A |
15: 84,094,702 (GRCm39) |
E365K |
possibly damaging |
Het |
Shld2 |
A |
C |
14: 33,989,942 (GRCm39) |
N321K |
probably benign |
Het |
Slc22a18 |
T |
C |
7: 143,051,123 (GRCm39) |
V334A |
probably damaging |
Het |
Slc23a3 |
A |
T |
1: 75,110,085 (GRCm39) |
C97S |
probably benign |
Het |
Smchd1 |
T |
A |
17: 71,714,244 (GRCm39) |
H873L |
probably benign |
Het |
Snrpa1 |
G |
A |
7: 65,720,381 (GRCm39) |
G195R |
probably benign |
Het |
Sphkap |
T |
A |
1: 83,255,953 (GRCm39) |
I599F |
probably benign |
Het |
Stox1 |
A |
G |
10: 62,501,543 (GRCm39) |
V339A |
probably damaging |
Het |
Tlx1 |
A |
G |
19: 45,142,036 (GRCm39) |
E220G |
probably damaging |
Het |
Tmem71 |
C |
A |
15: 66,413,421 (GRCm39) |
|
probably null |
Het |
Tmprss3 |
T |
C |
17: 31,413,976 (GRCm39) |
D56G |
possibly damaging |
Het |
Trabd |
A |
G |
15: 88,970,107 (GRCm39) |
R368G |
probably benign |
Het |
Trf |
A |
G |
9: 103,094,675 (GRCm39) |
I461T |
probably damaging |
Het |
Trpm3 |
A |
G |
19: 22,676,226 (GRCm39) |
T133A |
possibly damaging |
Het |
Trpv3 |
G |
A |
11: 73,186,209 (GRCm39) |
V667I |
possibly damaging |
Het |
Vps13b |
T |
A |
15: 35,455,246 (GRCm39) |
N718K |
probably benign |
Het |
Zdbf2 |
T |
C |
1: 63,345,166 (GRCm39) |
S1182P |
possibly damaging |
Het |
Zfp13 |
T |
C |
17: 23,795,866 (GRCm39) |
D235G |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,227,987 (GRCm39) |
E1874G |
probably damaging |
Het |
Zfp503 |
T |
C |
14: 22,036,277 (GRCm39) |
K213R |
probably benign |
Het |
Zkscan2 |
A |
G |
7: 123,084,651 (GRCm39) |
V491A |
probably damaging |
Het |
|
Other mutations in Cracdl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01376:Cracdl
|
APN |
1 |
37,667,425 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01413:Cracdl
|
APN |
1 |
37,651,387 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01812:Cracdl
|
APN |
1 |
37,664,446 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02183:Cracdl
|
APN |
1 |
37,664,459 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02498:Cracdl
|
APN |
1 |
37,662,926 (GRCm39) |
missense |
probably benign |
|
IGL02713:Cracdl
|
APN |
1 |
37,663,218 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02736:Cracdl
|
APN |
1 |
37,676,954 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4449:Cracdl
|
UTSW |
1 |
37,664,117 (GRCm39) |
nonsense |
probably null |
|
FR4449:Cracdl
|
UTSW |
1 |
37,664,116 (GRCm39) |
missense |
probably benign |
0.40 |
FR4548:Cracdl
|
UTSW |
1 |
37,664,183 (GRCm39) |
missense |
probably damaging |
0.96 |
FR4548:Cracdl
|
UTSW |
1 |
37,664,116 (GRCm39) |
missense |
probably benign |
0.40 |
FR4548:Cracdl
|
UTSW |
1 |
37,664,117 (GRCm39) |
nonsense |
probably null |
|
FR4737:Cracdl
|
UTSW |
1 |
37,664,117 (GRCm39) |
nonsense |
probably null |
|
FR4737:Cracdl
|
UTSW |
1 |
37,664,116 (GRCm39) |
missense |
probably benign |
0.40 |
FR4976:Cracdl
|
UTSW |
1 |
37,664,183 (GRCm39) |
missense |
probably damaging |
0.96 |
FR4976:Cracdl
|
UTSW |
1 |
37,664,116 (GRCm39) |
missense |
probably benign |
0.40 |
FR4976:Cracdl
|
UTSW |
1 |
37,664,117 (GRCm39) |
nonsense |
probably null |
|
R0022:Cracdl
|
UTSW |
1 |
37,667,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Cracdl
|
UTSW |
1 |
37,667,326 (GRCm39) |
missense |
probably damaging |
1.00 |
R0055:Cracdl
|
UTSW |
1 |
37,663,337 (GRCm39) |
missense |
probably benign |
0.18 |
R0153:Cracdl
|
UTSW |
1 |
37,663,720 (GRCm39) |
missense |
probably benign |
|
R0523:Cracdl
|
UTSW |
1 |
37,683,710 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R0699:Cracdl
|
UTSW |
1 |
37,651,411 (GRCm39) |
missense |
possibly damaging |
0.85 |
R0928:Cracdl
|
UTSW |
1 |
37,663,663 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1457:Cracdl
|
UTSW |
1 |
37,665,093 (GRCm39) |
nonsense |
probably null |
|
R1759:Cracdl
|
UTSW |
1 |
37,664,791 (GRCm39) |
missense |
probably benign |
0.00 |
R1888:Cracdl
|
UTSW |
1 |
37,663,364 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1888:Cracdl
|
UTSW |
1 |
37,663,364 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2289:Cracdl
|
UTSW |
1 |
37,651,342 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2421:Cracdl
|
UTSW |
1 |
37,652,556 (GRCm39) |
missense |
probably benign |
0.33 |
R2422:Cracdl
|
UTSW |
1 |
37,652,556 (GRCm39) |
missense |
probably benign |
0.33 |
R2509:Cracdl
|
UTSW |
1 |
37,664,381 (GRCm39) |
missense |
probably benign |
|
R2510:Cracdl
|
UTSW |
1 |
37,664,381 (GRCm39) |
missense |
probably benign |
|
R2511:Cracdl
|
UTSW |
1 |
37,664,381 (GRCm39) |
missense |
probably benign |
|
R3893:Cracdl
|
UTSW |
1 |
37,670,539 (GRCm39) |
missense |
probably benign |
0.00 |
R4351:Cracdl
|
UTSW |
1 |
37,663,993 (GRCm39) |
missense |
probably benign |
|
R4454:Cracdl
|
UTSW |
1 |
37,663,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Cracdl
|
UTSW |
1 |
37,670,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R4798:Cracdl
|
UTSW |
1 |
37,664,046 (GRCm39) |
missense |
probably benign |
0.12 |
R5599:Cracdl
|
UTSW |
1 |
37,652,424 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5920:Cracdl
|
UTSW |
1 |
37,677,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R6051:Cracdl
|
UTSW |
1 |
37,663,306 (GRCm39) |
missense |
probably damaging |
0.98 |
R6106:Cracdl
|
UTSW |
1 |
37,652,493 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6794:Cracdl
|
UTSW |
1 |
37,676,936 (GRCm39) |
splice site |
probably null |
|
R6828:Cracdl
|
UTSW |
1 |
37,663,898 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6930:Cracdl
|
UTSW |
1 |
37,664,026 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7044:Cracdl
|
UTSW |
1 |
37,651,361 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7069:Cracdl
|
UTSW |
1 |
37,670,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R7149:Cracdl
|
UTSW |
1 |
37,651,352 (GRCm39) |
nonsense |
probably null |
|
R7296:Cracdl
|
UTSW |
1 |
37,653,699 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7698:Cracdl
|
UTSW |
1 |
37,664,452 (GRCm39) |
missense |
probably benign |
0.12 |
R7714:Cracdl
|
UTSW |
1 |
37,663,858 (GRCm39) |
missense |
probably benign |
0.33 |
R8071:Cracdl
|
UTSW |
1 |
37,663,010 (GRCm39) |
nonsense |
probably null |
|
R8205:Cracdl
|
UTSW |
1 |
37,664,047 (GRCm39) |
missense |
probably benign |
0.06 |
R8720:Cracdl
|
UTSW |
1 |
37,652,522 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8917:Cracdl
|
UTSW |
1 |
37,676,993 (GRCm39) |
missense |
probably damaging |
0.99 |
R9056:Cracdl
|
UTSW |
1 |
37,663,553 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9158:Cracdl
|
UTSW |
1 |
37,670,442 (GRCm39) |
missense |
probably damaging |
0.99 |
R9290:Cracdl
|
UTSW |
1 |
37,663,634 (GRCm39) |
missense |
probably damaging |
0.97 |
R9483:Cracdl
|
UTSW |
1 |
37,670,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R9641:Cracdl
|
UTSW |
1 |
37,663,592 (GRCm39) |
missense |
possibly damaging |
0.85 |
X0025:Cracdl
|
UTSW |
1 |
37,664,026 (GRCm39) |
missense |
probably benign |
0.33 |
|