Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930438A08Rik |
T |
C |
11: 58,179,242 (GRCm39) |
|
probably null |
Het |
Abca2 |
A |
G |
2: 25,332,088 (GRCm39) |
D1400G |
probably benign |
Het |
Actl11 |
A |
T |
9: 107,806,069 (GRCm39) |
K131* |
probably null |
Het |
Adam39 |
A |
T |
8: 41,277,812 (GRCm39) |
R68* |
probably null |
Het |
Akap7 |
A |
T |
10: 25,147,405 (GRCm39) |
N108K |
probably damaging |
Het |
Arhgef10l |
C |
A |
4: 140,338,721 (GRCm39) |
A14S |
probably benign |
Het |
Ccdc141 |
T |
G |
2: 76,879,927 (GRCm39) |
N632T |
probably benign |
Het |
Ccm2 |
T |
C |
11: 6,546,302 (GRCm39) |
S435P |
probably damaging |
Het |
Cd36 |
A |
G |
5: 18,019,187 (GRCm39) |
L178P |
probably damaging |
Het |
Cd7 |
T |
C |
11: 120,929,075 (GRCm39) |
I59V |
probably benign |
Het |
Cds2 |
T |
A |
2: 132,135,204 (GRCm39) |
S32T |
probably benign |
Het |
Cep19 |
A |
G |
16: 31,925,904 (GRCm39) |
D104G |
probably damaging |
Het |
Col1a2 |
C |
T |
6: 4,510,753 (GRCm39) |
P68S |
unknown |
Het |
Col20a1 |
A |
G |
2: 180,649,024 (GRCm39) |
H1011R |
probably damaging |
Het |
D7Ertd443e |
A |
G |
7: 133,896,851 (GRCm39) |
V513A |
probably damaging |
Het |
Egfr |
C |
T |
11: 16,818,162 (GRCm39) |
P228L |
probably damaging |
Het |
Fam243 |
C |
T |
16: 92,118,037 (GRCm39) |
V84M |
probably damaging |
Het |
Fam78b |
A |
G |
1: 166,906,131 (GRCm39) |
R97G |
probably damaging |
Het |
Flt1 |
C |
T |
5: 147,540,386 (GRCm39) |
V768M |
probably damaging |
Het |
Gdap1l1 |
A |
T |
2: 163,288,050 (GRCm39) |
N96Y |
probably damaging |
Het |
Gm7168 |
T |
A |
17: 14,169,622 (GRCm39) |
Y330N |
probably benign |
Het |
Hnrnpul1 |
T |
C |
7: 25,424,203 (GRCm39) |
N683S |
unknown |
Het |
Ice2 |
C |
T |
9: 69,335,782 (GRCm39) |
P922S |
possibly damaging |
Het |
Iglv2 |
A |
G |
16: 19,079,260 (GRCm39) |
V81A |
not run |
Het |
Irs1 |
A |
G |
1: 82,265,177 (GRCm39) |
I1013T |
probably benign |
Het |
Itih4 |
T |
C |
14: 30,621,432 (GRCm39) |
S832P |
probably damaging |
Het |
Klhl1 |
A |
T |
14: 96,517,513 (GRCm39) |
Y388N |
probably benign |
Het |
Lrrc37a |
G |
A |
11: 103,348,601 (GRCm39) |
S2698L |
unknown |
Het |
Map4k4 |
T |
C |
1: 40,058,829 (GRCm39) |
Y1008H |
possibly damaging |
Het |
Mdn1 |
G |
T |
4: 32,701,823 (GRCm39) |
G1519W |
probably damaging |
Het |
Mga |
T |
A |
2: 119,747,809 (GRCm39) |
D653E |
probably damaging |
Het |
Npas1 |
T |
C |
7: 16,208,733 (GRCm39) |
E48G |
probably damaging |
Het |
Nup188 |
G |
A |
2: 30,231,842 (GRCm39) |
|
probably null |
Het |
Or1p1b |
G |
T |
11: 74,130,394 (GRCm39) |
M1I |
probably null |
Het |
Or3a4 |
T |
A |
11: 73,945,223 (GRCm39) |
M121L |
probably damaging |
Het |
Or4c110 |
G |
A |
2: 88,832,075 (GRCm39) |
L186F |
|
Het |
Or51a39 |
A |
G |
7: 102,362,873 (GRCm39) |
V249A |
possibly damaging |
Het |
Or55b4 |
A |
T |
7: 102,133,574 (GRCm39) |
V251D |
probably damaging |
Het |
Or7h8 |
A |
G |
9: 20,123,840 (GRCm39) |
N65S |
probably damaging |
Het |
Oxct1 |
T |
C |
15: 4,158,383 (GRCm39) |
V439A |
probably damaging |
Het |
Pcdhb22 |
G |
T |
18: 37,652,341 (GRCm39) |
G13W |
probably damaging |
Het |
Pex11g |
A |
G |
8: 3,509,237 (GRCm39) |
V230A |
probably benign |
Het |
Pop1 |
C |
T |
15: 34,510,525 (GRCm39) |
S439L |
probably damaging |
Het |
Ptpn9 |
T |
A |
9: 56,929,533 (GRCm39) |
H83Q |
probably benign |
Het |
Qrfp |
C |
T |
2: 31,698,704 (GRCm39) |
R76H |
probably benign |
Het |
Slc30a3 |
A |
G |
5: 31,246,139 (GRCm39) |
V197A |
probably benign |
Het |
Slc8a3 |
T |
C |
12: 81,361,047 (GRCm39) |
N591D |
possibly damaging |
Het |
Sp4 |
G |
T |
12: 118,263,807 (GRCm39) |
Q80K |
possibly damaging |
Het |
Spock1 |
C |
T |
13: 58,055,316 (GRCm39) |
G29D |
possibly damaging |
Het |
Sprr1a |
G |
T |
3: 92,391,674 (GRCm39) |
P109Q |
probably damaging |
Het |
Suz12 |
T |
A |
11: 79,904,309 (GRCm39) |
F239L |
probably damaging |
Het |
Tbx3 |
A |
G |
5: 119,813,648 (GRCm39) |
Y248C |
probably damaging |
Het |
Trabd2b |
T |
C |
4: 114,266,637 (GRCm39) |
L217P |
probably damaging |
Het |
Ubxn11 |
A |
C |
4: 133,853,726 (GRCm39) |
I398L |
possibly damaging |
Het |
Vmn1r173 |
T |
A |
7: 23,401,884 (GRCm39) |
S40T |
probably damaging |
Het |
Vmn2r2 |
T |
C |
3: 64,023,900 (GRCm39) |
S894G |
probably benign |
Het |
Vmn2r65 |
A |
G |
7: 84,592,347 (GRCm39) |
|
probably null |
Het |
Vps13c |
G |
A |
9: 67,853,107 (GRCm39) |
G2400D |
possibly damaging |
Het |
Vps8 |
T |
C |
16: 21,275,032 (GRCm39) |
Y197H |
probably damaging |
Het |
Wdr91 |
T |
C |
6: 34,866,209 (GRCm39) |
N486D |
possibly damaging |
Het |
Wwp1 |
A |
G |
4: 19,627,908 (GRCm39) |
I695T |
possibly damaging |
Het |
Zc3hc1 |
T |
C |
6: 30,382,547 (GRCm39) |
D133G |
probably benign |
Het |
Zcchc14 |
T |
C |
8: 122,335,200 (GRCm39) |
I307V |
unknown |
Het |
Zfp933 |
G |
A |
4: 147,910,636 (GRCm39) |
T320I |
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 |
|
|
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 |
|
|
R7689:Cspg4b
|
UTSW |
13 |
113,515,948 (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 |
|
|
|