Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510039O18Rik |
T |
A |
4: 148,029,440 (GRCm39) |
F470Y |
probably damaging |
Het |
Adra1a |
T |
C |
14: 66,875,250 (GRCm39) |
L75P |
probably damaging |
Het |
Agap1 |
T |
C |
1: 89,762,188 (GRCm39) |
S560P |
probably damaging |
Het |
Ahcyl |
T |
C |
16: 45,974,970 (GRCm39) |
T136A |
probably benign |
Het |
Arrdc4 |
T |
A |
7: 68,391,623 (GRCm39) |
I215L |
probably damaging |
Het |
Atad3a |
C |
T |
4: 155,840,610 (GRCm39) |
A97T |
probably damaging |
Het |
Bcas3 |
A |
T |
11: 85,386,713 (GRCm39) |
T383S |
probably benign |
Het |
C2cd5 |
G |
A |
6: 142,995,951 (GRCm39) |
R379* |
probably null |
Het |
Cacna1e |
G |
T |
1: 154,274,549 (GRCm39) |
H2138N |
probably benign |
Het |
Card14 |
A |
T |
11: 119,216,328 (GRCm39) |
D303V |
possibly damaging |
Het |
Ccdc202 |
T |
C |
14: 96,119,252 (GRCm39) |
V3A |
probably benign |
Het |
Cfhr1 |
T |
C |
1: 139,475,478 (GRCm39) |
Y331C |
unknown |
Het |
Chp1 |
G |
A |
2: 119,415,146 (GRCm39) |
D183N |
probably benign |
Het |
Cntn2 |
T |
C |
1: 132,443,882 (GRCm39) |
T966A |
probably benign |
Het |
Cpne9 |
T |
G |
6: 113,266,965 (GRCm39) |
C133G |
probably damaging |
Het |
Cul7 |
C |
T |
17: 46,963,747 (GRCm39) |
Q275* |
probably null |
Het |
Cyp11b1 |
T |
C |
15: 74,710,897 (GRCm39) |
D221G |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 49,979,685 (GRCm39) |
F107I |
probably benign |
Het |
Dnhd1 |
A |
G |
7: 105,363,170 (GRCm39) |
I3911V |
probably benign |
Het |
Eif1ad16 |
A |
G |
12: 87,985,259 (GRCm39) |
Y95H |
probably damaging |
Het |
Eloa |
T |
C |
4: 135,736,595 (GRCm39) |
H551R |
probably benign |
Het |
Fam171b |
T |
A |
2: 83,709,732 (GRCm39) |
V468D |
probably benign |
Het |
Fat2 |
A |
G |
11: 55,200,666 (GRCm39) |
W803R |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,163,201 (GRCm39) |
D2G |
probably benign |
Het |
Fbxo8 |
A |
G |
8: 57,041,120 (GRCm39) |
T179A |
probably benign |
Het |
Gdap1 |
A |
G |
1: 17,231,623 (GRCm39) |
T323A |
probably damaging |
Het |
Gm136 |
T |
C |
4: 34,743,875 (GRCm39) |
N323S |
probably null |
Het |
Gm6899 |
A |
T |
11: 26,543,819 (GRCm39) |
T129S |
unknown |
Het |
Gnb3 |
A |
T |
6: 124,814,183 (GRCm39) |
C166S |
possibly damaging |
Het |
Gpr61 |
A |
G |
3: 108,057,966 (GRCm39) |
F232L |
probably damaging |
Het |
Gpx8 |
T |
C |
13: 113,179,711 (GRCm39) |
M197V |
probably benign |
Het |
Gse1 |
G |
T |
8: 121,295,217 (GRCm39) |
R446L |
unknown |
Het |
Itch |
A |
T |
2: 155,054,987 (GRCm39) |
T764S |
probably benign |
Het |
Itch |
A |
G |
2: 155,051,922 (GRCm39) |
K614E |
probably damaging |
Het |
Itpkb |
T |
G |
1: 180,241,544 (GRCm39) |
M738R |
probably damaging |
Het |
Jph1 |
T |
A |
1: 17,074,192 (GRCm39) |
K609* |
probably null |
Het |
Kcns1 |
G |
A |
2: 164,010,241 (GRCm39) |
R173C |
probably damaging |
Het |
Larp4b |
C |
T |
13: 9,186,834 (GRCm39) |
S54L |
probably damaging |
Het |
Lonrf1 |
G |
T |
8: 36,715,918 (GRCm39) |
S239* |
probably null |
Het |
Lyst |
T |
G |
13: 13,857,808 (GRCm39) |
|
probably null |
Het |
Mccc1 |
T |
A |
3: 36,015,132 (GRCm39) |
R663* |
probably null |
Het |
Mcm3 |
A |
G |
1: 20,876,997 (GRCm39) |
V646A |
probably benign |
Het |
Mdn1 |
T |
C |
4: 32,739,912 (GRCm39) |
L3722P |
probably damaging |
Het |
Mmp27 |
T |
G |
9: 7,579,002 (GRCm39) |
D392E |
probably damaging |
Het |
Ms4a14 |
A |
G |
19: 11,279,906 (GRCm39) |
I884T |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,574,439 (GRCm39) |
T963I |
probably benign |
Het |
Muc6 |
G |
C |
7: 141,217,659 (GRCm39) |
P2338R |
probably damaging |
Het |
Mucl3 |
C |
A |
17: 35,948,969 (GRCm39) |
S210I |
possibly damaging |
Het |
Nbeal1 |
G |
C |
1: 60,276,310 (GRCm39) |
V684L |
probably benign |
Het |
Ndrg2 |
C |
T |
14: 52,147,812 (GRCm39) |
A102T |
possibly damaging |
Het |
Nhsl3 |
T |
C |
4: 129,117,566 (GRCm39) |
N411S |
probably benign |
Het |
Nos1 |
A |
G |
5: 118,035,792 (GRCm39) |
D431G |
probably damaging |
Het |
Oog4 |
CAA |
CA |
4: 143,164,022 (GRCm39) |
|
probably null |
Het |
Otog |
T |
C |
7: 45,901,480 (GRCm39) |
L393P |
probably damaging |
Het |
Plcl1 |
A |
G |
1: 55,736,627 (GRCm39) |
N656S |
probably damaging |
Het |
Pole3 |
C |
A |
4: 62,443,060 (GRCm39) |
V27F |
probably damaging |
Het |
Prrt4 |
T |
A |
6: 29,177,140 (GRCm39) |
I210F |
probably damaging |
Het |
Ptpn18 |
G |
A |
1: 34,512,445 (GRCm39) |
D417N |
possibly damaging |
Het |
Rbpms |
A |
T |
8: 34,354,387 (GRCm39) |
S53T |
possibly damaging |
Het |
Rgs7 |
C |
A |
1: 174,949,296 (GRCm39) |
V203L |
probably benign |
Het |
Riok1 |
A |
T |
13: 38,229,263 (GRCm39) |
D150V |
probably damaging |
Het |
Rrp1b |
T |
C |
17: 32,274,900 (GRCm39) |
L335P |
probably benign |
Het |
Rsph6a |
T |
G |
7: 18,801,962 (GRCm39) |
I592S |
possibly damaging |
Het |
Skor1 |
C |
T |
9: 63,052,661 (GRCm39) |
G436D |
probably damaging |
Het |
Slc17a8 |
T |
C |
10: 89,433,319 (GRCm39) |
T51A |
possibly damaging |
Het |
Slc22a8 |
T |
C |
19: 8,585,248 (GRCm39) |
S266P |
probably damaging |
Het |
Socs2 |
A |
G |
10: 95,250,845 (GRCm39) |
|
probably benign |
Het |
Tas2r106 |
A |
G |
6: 131,655,668 (GRCm39) |
I61T |
possibly damaging |
Het |
Tfap2a |
T |
C |
13: 40,882,051 (GRCm39) |
N77D |
probably damaging |
Het |
Tmem236 |
T |
A |
2: 14,197,076 (GRCm39) |
L88Q |
probably damaging |
Het |
Ttc41 |
A |
G |
10: 86,595,088 (GRCm39) |
E954G |
probably damaging |
Het |
Vmn1r34 |
G |
T |
6: 66,613,994 (GRCm39) |
S248* |
probably null |
Het |
Wipf1 |
T |
C |
2: 73,262,789 (GRCm39) |
R483G |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,476,946 (GRCm39) |
N3187S |
probably benign |
Het |
Zfp202 |
C |
A |
9: 40,121,829 (GRCm39) |
P309T |
probably benign |
Het |
Zfp39 |
T |
C |
11: 58,781,469 (GRCm39) |
H431R |
probably damaging |
Het |
Zfp658 |
T |
A |
7: 43,224,102 (GRCm39) |
H792Q |
probably benign |
Het |
|
Other mutations in Cspg4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01723:Cspg4b
|
APN |
13 |
113,504,091 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL03023:Cspg4b
|
APN |
13 |
113,488,275 (GRCm39) |
missense |
probably benign |
0.03 |
cumpleanos
|
UTSW |
13 |
113,504,870 (GRCm39) |
missense |
possibly damaging |
0.87 |
Sorpresa
|
UTSW |
13 |
113,454,725 (GRCm39) |
missense |
probably damaging |
1.00 |
P0018:Cspg4b
|
UTSW |
13 |
113,504,040 (GRCm39) |
missense |
possibly damaging |
0.60 |
R0003:Cspg4b
|
UTSW |
13 |
113,505,310 (GRCm39) |
missense |
probably benign |
0.00 |
R0016:Cspg4b
|
UTSW |
13 |
113,502,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Cspg4b
|
UTSW |
13 |
113,502,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R0053:Cspg4b
|
UTSW |
13 |
113,505,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0053:Cspg4b
|
UTSW |
13 |
113,505,023 (GRCm39) |
missense |
probably benign |
0.00 |
R0158:Cspg4b
|
UTSW |
13 |
113,505,687 (GRCm39) |
nonsense |
probably null |
|
R0281:Cspg4b
|
UTSW |
13 |
113,505,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R1212:Cspg4b
|
UTSW |
13 |
113,505,951 (GRCm39) |
intron |
probably benign |
|
R1300:Cspg4b
|
UTSW |
13 |
113,502,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Cspg4b
|
UTSW |
13 |
113,505,026 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1509:Cspg4b
|
UTSW |
13 |
113,504,790 (GRCm39) |
missense |
probably damaging |
0.99 |
R1738:Cspg4b
|
UTSW |
13 |
113,504,034 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1758:Cspg4b
|
UTSW |
13 |
113,505,266 (GRCm39) |
missense |
possibly damaging |
0.78 |
R1828:Cspg4b
|
UTSW |
13 |
113,505,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R2061:Cspg4b
|
UTSW |
13 |
113,454,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R2570:Cspg4b
|
UTSW |
13 |
113,455,121 (GRCm39) |
missense |
probably benign |
0.34 |
R2884:Cspg4b
|
UTSW |
13 |
113,457,216 (GRCm39) |
missense |
probably damaging |
1.00 |
R2884:Cspg4b
|
UTSW |
13 |
113,505,725 (GRCm39) |
missense |
probably benign |
0.00 |
R3004:Cspg4b
|
UTSW |
13 |
113,502,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R3150:Cspg4b
|
UTSW |
13 |
113,488,294 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Cspg4b
|
UTSW |
13 |
113,454,743 (GRCm39) |
missense |
probably benign |
0.12 |
R3864:Cspg4b
|
UTSW |
13 |
113,459,485 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3971:Cspg4b
|
UTSW |
13 |
113,453,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R4004:Cspg4b
|
UTSW |
13 |
113,454,914 (GRCm39) |
missense |
probably benign |
0.00 |
R4271:Cspg4b
|
UTSW |
13 |
113,478,904 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4382:Cspg4b
|
UTSW |
13 |
113,459,288 (GRCm39) |
missense |
probably benign |
0.10 |
R4484:Cspg4b
|
UTSW |
13 |
113,455,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R4570:Cspg4b
|
UTSW |
13 |
113,454,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Cspg4b
|
UTSW |
13 |
113,455,783 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4622:Cspg4b
|
UTSW |
13 |
113,456,615 (GRCm39) |
missense |
probably benign |
0.00 |
R4676:Cspg4b
|
UTSW |
13 |
113,505,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R4676:Cspg4b
|
UTSW |
13 |
113,505,341 (GRCm39) |
missense |
probably damaging |
0.98 |
R4677:Cspg4b
|
UTSW |
13 |
113,516,020 (GRCm39) |
missense |
unknown |
|
R4775:Cspg4b
|
UTSW |
13 |
113,454,229 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4779:Cspg4b
|
UTSW |
13 |
113,504,870 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4780:Cspg4b
|
UTSW |
13 |
113,454,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Cspg4b
|
UTSW |
13 |
113,504,696 (GRCm39) |
missense |
probably benign |
0.05 |
R4841:Cspg4b
|
UTSW |
13 |
113,502,724 (GRCm39) |
missense |
probably benign |
0.00 |
R4879:Cspg4b
|
UTSW |
13 |
113,456,321 (GRCm39) |
missense |
probably benign |
0.03 |
R4930:Cspg4b
|
UTSW |
13 |
113,464,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Cspg4b
|
UTSW |
13 |
113,504,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R4987:Cspg4b
|
UTSW |
13 |
113,454,635 (GRCm39) |
missense |
probably benign |
0.07 |
R5065:Cspg4b
|
UTSW |
13 |
113,457,453 (GRCm39) |
missense |
probably benign |
0.01 |
R5216:Cspg4b
|
UTSW |
13 |
113,478,947 (GRCm39) |
missense |
probably benign |
0.20 |
R5236:Cspg4b
|
UTSW |
13 |
113,502,754 (GRCm39) |
missense |
probably benign |
0.14 |
R5247:Cspg4b
|
UTSW |
13 |
113,455,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Cspg4b
|
UTSW |
13 |
113,456,305 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5337:Cspg4b
|
UTSW |
13 |
113,455,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R5342:Cspg4b
|
UTSW |
13 |
113,502,803 (GRCm39) |
critical splice donor site |
probably null |
|
R5426:Cspg4b
|
UTSW |
13 |
113,505,587 (GRCm39) |
missense |
probably benign |
0.01 |
R5472:Cspg4b
|
UTSW |
13 |
113,455,703 (GRCm39) |
missense |
probably benign |
0.12 |
R5526:Cspg4b
|
UTSW |
13 |
113,504,427 (GRCm39) |
missense |
probably benign |
0.22 |
R5543:Cspg4b
|
UTSW |
13 |
113,457,407 (GRCm39) |
missense |
probably damaging |
0.96 |
R5589:Cspg4b
|
UTSW |
13 |
113,454,484 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5623:Cspg4b
|
UTSW |
13 |
113,483,168 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5668:Cspg4b
|
UTSW |
13 |
113,453,701 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5793:Cspg4b
|
UTSW |
13 |
113,457,556 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5824:Cspg4b
|
UTSW |
13 |
113,505,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R6038:Cspg4b
|
UTSW |
13 |
113,455,153 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6038:Cspg4b
|
UTSW |
13 |
113,455,153 (GRCm39) |
missense |
possibly damaging |
0.49 |
R6053:Cspg4b
|
UTSW |
13 |
113,457,260 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6125:Cspg4b
|
UTSW |
13 |
113,454,217 (GRCm39) |
missense |
probably benign |
0.00 |
R6129:Cspg4b
|
UTSW |
13 |
113,505,340 (GRCm39) |
nonsense |
probably null |
|
R6290:Cspg4b
|
UTSW |
13 |
113,456,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R6291:Cspg4b
|
UTSW |
13 |
113,456,981 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6302:Cspg4b
|
UTSW |
13 |
113,504,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R6317:Cspg4b
|
UTSW |
13 |
113,504,802 (GRCm39) |
missense |
probably benign |
0.09 |
R6395:Cspg4b
|
UTSW |
13 |
113,506,003 (GRCm39) |
missense |
probably damaging |
1.00 |
R6673:Cspg4b
|
UTSW |
13 |
113,504,366 (GRCm39) |
nonsense |
probably null |
|
R6783:Cspg4b
|
UTSW |
13 |
113,456,743 (GRCm39) |
nonsense |
probably null |
|
R6800:Cspg4b
|
UTSW |
13 |
113,504,686 (GRCm39) |
missense |
probably benign |
0.02 |
R6857:Cspg4b
|
UTSW |
13 |
113,456,492 (GRCm39) |
missense |
probably damaging |
0.97 |
R6889:Cspg4b
|
UTSW |
13 |
113,454,912 (GRCm39) |
missense |
probably damaging |
0.99 |
R6934:Cspg4b
|
UTSW |
13 |
113,505,800 (GRCm39) |
missense |
probably benign |
|
R7019:Cspg4b
|
UTSW |
13 |
113,488,284 (GRCm39) |
missense |
probably benign |
0.01 |
R7100:Cspg4b
|
UTSW |
13 |
113,455,501 (GRCm39) |
missense |
|
|
R7115:Cspg4b
|
UTSW |
13 |
113,457,310 (GRCm39) |
missense |
|
|
R7152:Cspg4b
|
UTSW |
13 |
113,455,384 (GRCm39) |
missense |
|
|
R7195:Cspg4b
|
UTSW |
13 |
113,504,463 (GRCm39) |
missense |
|
|
R7213:Cspg4b
|
UTSW |
13 |
113,454,475 (GRCm39) |
missense |
|
|
R7250:Cspg4b
|
UTSW |
13 |
113,455,349 (GRCm39) |
missense |
|
|
R7341:Cspg4b
|
UTSW |
13 |
113,454,706 (GRCm39) |
missense |
|
|
R7358:Cspg4b
|
UTSW |
13 |
113,456,501 (GRCm39) |
missense |
|
|
R7359:Cspg4b
|
UTSW |
13 |
113,478,964 (GRCm39) |
missense |
|
|
R7396:Cspg4b
|
UTSW |
13 |
113,455,524 (GRCm39) |
missense |
|
|
R7632:Cspg4b
|
UTSW |
13 |
113,457,420 (GRCm39) |
missense |
|
|
R7713:Cspg4b
|
UTSW |
13 |
113,483,075 (GRCm39) |
missense |
|
|
R7892:Cspg4b
|
UTSW |
13 |
113,456,140 (GRCm39) |
missense |
|
|
R7975:Cspg4b
|
UTSW |
13 |
113,455,841 (GRCm39) |
missense |
|
|
R8017:Cspg4b
|
UTSW |
13 |
113,456,157 (GRCm39) |
missense |
|
|
R8019:Cspg4b
|
UTSW |
13 |
113,456,157 (GRCm39) |
missense |
|
|
R8034:Cspg4b
|
UTSW |
13 |
113,479,045 (GRCm39) |
missense |
|
|
R8101:Cspg4b
|
UTSW |
13 |
113,457,425 (GRCm39) |
missense |
|
|
R8104:Cspg4b
|
UTSW |
13 |
113,456,263 (GRCm39) |
missense |
|
|
R8122:Cspg4b
|
UTSW |
13 |
113,455,442 (GRCm39) |
missense |
|
|
R8126:Cspg4b
|
UTSW |
13 |
113,504,697 (GRCm39) |
missense |
|
|
R8272:Cspg4b
|
UTSW |
13 |
113,504,889 (GRCm39) |
missense |
|
|
R8679:Cspg4b
|
UTSW |
13 |
113,488,163 (GRCm39) |
missense |
|
|
R8973:Cspg4b
|
UTSW |
13 |
113,456,293 (GRCm39) |
missense |
|
|
R9123:Cspg4b
|
UTSW |
13 |
113,505,374 (GRCm39) |
missense |
|
|
R9125:Cspg4b
|
UTSW |
13 |
113,505,374 (GRCm39) |
missense |
|
|
R9182:Cspg4b
|
UTSW |
13 |
113,457,358 (GRCm39) |
missense |
|
|
R9233:Cspg4b
|
UTSW |
13 |
113,502,754 (GRCm39) |
missense |
|
|
R9264:Cspg4b
|
UTSW |
13 |
113,456,014 (GRCm39) |
missense |
|
|
R9306:Cspg4b
|
UTSW |
13 |
113,506,010 (GRCm39) |
missense |
unknown |
|
R9327:Cspg4b
|
UTSW |
13 |
113,453,710 (GRCm39) |
missense |
|
|
R9411:Cspg4b
|
UTSW |
13 |
113,504,767 (GRCm39) |
missense |
|
|
R9516:Cspg4b
|
UTSW |
13 |
113,455,649 (GRCm39) |
missense |
|
|
R9562:Cspg4b
|
UTSW |
13 |
113,504,574 (GRCm39) |
missense |
|
|
R9605:Cspg4b
|
UTSW |
13 |
113,456,503 (GRCm39) |
missense |
|
|
|