Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A630089N07Rik |
C |
T |
16: 97,867,651 (GRCm39) |
A104T |
probably damaging |
Het |
Abhd18 |
T |
A |
3: 40,884,627 (GRCm39) |
L222Q |
probably damaging |
Het |
Adam30 |
C |
T |
3: 98,070,348 (GRCm39) |
T727M |
possibly damaging |
Het |
Adh6b |
A |
T |
3: 138,058,729 (GRCm39) |
Q137L |
probably damaging |
Het |
Alpl |
C |
T |
4: 137,475,127 (GRCm39) |
V269I |
probably benign |
Het |
Ang2 |
C |
T |
14: 51,432,996 (GRCm39) |
G129S |
probably benign |
Het |
Atp6v0a1 |
A |
T |
11: 100,920,015 (GRCm39) |
H216L |
possibly damaging |
Het |
BC030500 |
C |
T |
8: 59,366,049 (GRCm39) |
T61I |
unknown |
Het |
Brpf1 |
T |
G |
6: 113,293,491 (GRCm39) |
L520R |
probably damaging |
Het |
Btbd10 |
A |
G |
7: 112,927,626 (GRCm39) |
I243T |
possibly damaging |
Het |
Bub1 |
C |
A |
2: 127,646,139 (GRCm39) |
C947F |
probably damaging |
Het |
C4b |
T |
C |
17: 34,953,459 (GRCm39) |
E1008G |
probably damaging |
Het |
Ccdc40 |
A |
G |
11: 119,155,323 (GRCm39) |
T1188A |
probably benign |
Het |
Cdcp3 |
A |
G |
7: 130,875,485 (GRCm39) |
T1770A |
unknown |
Het |
Cnn1 |
G |
T |
9: 22,010,557 (GRCm39) |
|
probably benign |
Het |
Colgalt2 |
T |
C |
1: 152,360,662 (GRCm39) |
M233T |
probably damaging |
Het |
Cox15 |
A |
T |
19: 43,735,181 (GRCm39) |
C195* |
probably null |
Het |
Cped1 |
A |
T |
6: 22,059,941 (GRCm39) |
R202S |
possibly damaging |
Het |
Dact2 |
A |
T |
17: 14,417,146 (GRCm39) |
C351* |
probably null |
Het |
Dbnl |
A |
G |
11: 5,738,582 (GRCm39) |
N8S |
probably benign |
Het |
Depdc1a |
T |
A |
3: 159,228,356 (GRCm39) |
N369K |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,415,005 (GRCm39) |
L243Q |
probably damaging |
Het |
Dscaml1 |
T |
A |
9: 45,341,759 (GRCm39) |
Y57N |
probably benign |
Het |
Eif2b3 |
A |
G |
4: 116,927,944 (GRCm39) |
T388A |
probably benign |
Het |
Eif4h |
A |
C |
5: 134,654,393 (GRCm39) |
|
probably null |
Het |
Elf1 |
C |
T |
14: 79,810,667 (GRCm39) |
Q288* |
probably null |
Het |
Fbxl5 |
A |
T |
5: 43,908,362 (GRCm39) |
|
probably benign |
Het |
Fgl2 |
C |
T |
5: 21,580,677 (GRCm39) |
R340* |
probably null |
Het |
Fut4 |
T |
C |
9: 14,662,082 (GRCm39) |
D404G |
probably damaging |
Het |
Glmn |
G |
A |
5: 107,718,152 (GRCm39) |
P255L |
probably benign |
Het |
Gm14322 |
C |
T |
2: 177,411,481 (GRCm39) |
T97I |
probably benign |
Het |
Gm44511 |
C |
A |
6: 128,797,997 (GRCm39) |
C32F |
probably damaging |
Het |
Gm5478 |
A |
G |
15: 101,553,871 (GRCm39) |
F247S |
probably damaging |
Het |
Golgb1 |
T |
A |
16: 36,739,563 (GRCm39) |
M2675K |
probably damaging |
Het |
Hectd1 |
T |
C |
12: 51,849,000 (GRCm39) |
D368G |
possibly damaging |
Het |
Hnrnpul2 |
A |
G |
19: 8,798,064 (GRCm39) |
N140S |
probably benign |
Het |
Htr4 |
A |
T |
18: 62,561,209 (GRCm39) |
I157L |
probably damaging |
Het |
Igf2bp3 |
G |
T |
6: 49,086,009 (GRCm39) |
|
probably benign |
Het |
Kcnma1 |
T |
G |
14: 23,436,332 (GRCm39) |
M790L |
probably benign |
Het |
Kcnv1 |
G |
A |
15: 44,977,999 (GRCm39) |
S13L |
unknown |
Het |
Kctd20 |
C |
T |
17: 29,184,025 (GRCm39) |
R312* |
probably null |
Het |
Kdm3b |
T |
A |
18: 34,960,435 (GRCm39) |
I1340N |
probably damaging |
Het |
Kdm6b |
A |
G |
11: 69,292,919 (GRCm39) |
F1286L |
unknown |
Het |
Knl1 |
T |
A |
2: 118,899,524 (GRCm39) |
F408L |
probably benign |
Het |
Lypd5 |
G |
T |
7: 24,053,101 (GRCm39) |
G253W |
probably damaging |
Het |
Mea1 |
A |
G |
17: 46,992,614 (GRCm39) |
T21A |
probably benign |
Het |
Metrnl |
A |
G |
11: 121,606,842 (GRCm39) |
E299G |
possibly damaging |
Het |
Mindy4 |
T |
A |
6: 55,256,055 (GRCm39) |
|
probably benign |
Het |
Muc5ac |
C |
T |
7: 141,363,481 (GRCm39) |
|
probably benign |
Het |
Nbn |
G |
A |
4: 15,963,911 (GRCm39) |
S104N |
probably damaging |
Het |
Nxpe2 |
A |
T |
9: 48,238,073 (GRCm39) |
F61I |
probably benign |
Het |
Or6c1b |
T |
C |
10: 129,273,334 (GRCm39) |
Y218H |
probably benign |
Het |
Or6c70 |
T |
A |
10: 129,710,092 (GRCm39) |
D178V |
probably damaging |
Het |
Pgr |
C |
A |
9: 8,901,544 (GRCm39) |
P359Q |
probably damaging |
Het |
Pi4k2b |
G |
A |
5: 52,908,031 (GRCm39) |
V157I |
probably benign |
Het |
Piezo2 |
C |
T |
18: 63,242,956 (GRCm39) |
S621N |
probably benign |
Het |
Plekhm1 |
A |
C |
11: 103,258,444 (GRCm39) |
F1031L |
probably damaging |
Het |
Pltp |
A |
G |
2: 164,696,301 (GRCm39) |
S124P |
probably damaging |
Het |
Polr3gl |
T |
A |
3: 96,487,154 (GRCm39) |
E177V |
probably benign |
Het |
Pstk |
G |
T |
7: 130,973,024 (GRCm39) |
R41L |
possibly damaging |
Het |
Ptprk |
C |
A |
10: 28,442,541 (GRCm39) |
|
probably benign |
Het |
Rasgrp1 |
T |
C |
2: 117,119,158 (GRCm39) |
E493G |
probably benign |
Het |
Rtn3 |
A |
G |
19: 7,434,726 (GRCm39) |
L422P |
probably benign |
Het |
Rusc2 |
C |
T |
4: 43,401,351 (GRCm39) |
|
probably benign |
Het |
Sbno2 |
A |
G |
10: 79,911,090 (GRCm39) |
F6S |
probably benign |
Het |
Sh2d4a |
A |
G |
8: 68,798,695 (GRCm39) |
Y348C |
probably damaging |
Het |
Sh3rf3 |
A |
G |
10: 58,939,992 (GRCm39) |
|
probably null |
Het |
Sipa1l2 |
T |
C |
8: 126,177,125 (GRCm39) |
E1163G |
probably benign |
Het |
Strip1 |
G |
C |
3: 107,521,964 (GRCm39) |
A738G |
probably damaging |
Het |
Tdrkh |
C |
T |
3: 94,333,299 (GRCm39) |
R255C |
probably benign |
Het |
Tex11 |
C |
T |
X: 100,059,191 (GRCm39) |
V190I |
possibly damaging |
Het |
Tln1 |
A |
T |
4: 43,555,911 (GRCm39) |
M101K |
possibly damaging |
Het |
Trav6-2 |
A |
C |
14: 52,905,028 (GRCm39) |
|
probably benign |
Het |
Tspan11 |
A |
T |
6: 127,900,674 (GRCm39) |
I82F |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,779,320 (GRCm39) |
K1233E |
unknown |
Het |
U2af2 |
T |
A |
7: 5,070,432 (GRCm39) |
|
probably benign |
Het |
Usp29 |
A |
T |
7: 6,965,917 (GRCm39) |
S587C |
probably damaging |
Het |
Vmn1r235 |
A |
T |
17: 21,482,056 (GRCm39) |
Q127L |
probably damaging |
Het |
Vmn1r65 |
C |
A |
7: 6,011,503 (GRCm39) |
A244S |
probably damaging |
Het |
Vmn2r18 |
A |
G |
5: 151,508,462 (GRCm39) |
S221P |
probably damaging |
Het |
Zfp229 |
T |
C |
17: 21,964,828 (GRCm39) |
S353P |
probably damaging |
Het |
Zpld2 |
T |
C |
4: 133,930,150 (GRCm39) |
K52E |
probably benign |
Het |
|
Other mutations in Pcdhb20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01071:Pcdhb20
|
APN |
18 |
37,637,738 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01373:Pcdhb20
|
APN |
18 |
37,639,621 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01556:Pcdhb20
|
APN |
18 |
37,637,852 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01621:Pcdhb20
|
APN |
18 |
37,637,860 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL01768:Pcdhb20
|
APN |
18 |
37,639,768 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01859:Pcdhb20
|
APN |
18 |
37,637,616 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02492:Pcdhb20
|
APN |
18 |
37,639,453 (GRCm39) |
missense |
probably benign |
0.43 |
IGL03057:Pcdhb20
|
APN |
18 |
37,637,851 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL02991:Pcdhb20
|
UTSW |
18 |
37,639,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R0799:Pcdhb20
|
UTSW |
18 |
37,638,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Pcdhb20
|
UTSW |
18 |
37,637,750 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Pcdhb20
|
UTSW |
18 |
37,637,750 (GRCm39) |
missense |
probably damaging |
0.99 |
R2012:Pcdhb20
|
UTSW |
18 |
37,638,127 (GRCm39) |
missense |
probably damaging |
0.99 |
R2079:Pcdhb20
|
UTSW |
18 |
37,638,224 (GRCm39) |
missense |
probably benign |
0.07 |
R2350:Pcdhb20
|
UTSW |
18 |
37,637,563 (GRCm39) |
missense |
probably benign |
0.01 |
R2363:Pcdhb20
|
UTSW |
18 |
37,638,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R2364:Pcdhb20
|
UTSW |
18 |
37,638,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R2870:Pcdhb20
|
UTSW |
18 |
37,638,833 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2870:Pcdhb20
|
UTSW |
18 |
37,638,833 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4060:Pcdhb20
|
UTSW |
18 |
37,639,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R4609:Pcdhb20
|
UTSW |
18 |
37,638,849 (GRCm39) |
missense |
probably benign |
0.02 |
R4750:Pcdhb20
|
UTSW |
18 |
37,639,184 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4897:Pcdhb20
|
UTSW |
18 |
37,639,298 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4970:Pcdhb20
|
UTSW |
18 |
37,639,824 (GRCm39) |
missense |
probably benign |
0.00 |
R5098:Pcdhb20
|
UTSW |
18 |
37,637,858 (GRCm39) |
missense |
probably damaging |
1.00 |
R5616:Pcdhb20
|
UTSW |
18 |
37,637,585 (GRCm39) |
missense |
probably damaging |
0.97 |
R5890:Pcdhb20
|
UTSW |
18 |
37,638,286 (GRCm39) |
missense |
probably benign |
0.00 |
R6225:Pcdhb20
|
UTSW |
18 |
37,638,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R6248:Pcdhb20
|
UTSW |
18 |
37,639,285 (GRCm39) |
missense |
probably damaging |
0.99 |
R6419:Pcdhb20
|
UTSW |
18 |
37,638,608 (GRCm39) |
missense |
probably damaging |
1.00 |
R6814:Pcdhb20
|
UTSW |
18 |
37,639,218 (GRCm39) |
missense |
probably benign |
0.22 |
R6821:Pcdhb20
|
UTSW |
18 |
37,639,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R6824:Pcdhb20
|
UTSW |
18 |
37,638,752 (GRCm39) |
missense |
probably benign |
0.06 |
R6872:Pcdhb20
|
UTSW |
18 |
37,639,218 (GRCm39) |
missense |
probably benign |
0.22 |
R7040:Pcdhb20
|
UTSW |
18 |
37,637,770 (GRCm39) |
missense |
probably benign |
0.00 |
R7145:Pcdhb20
|
UTSW |
18 |
37,638,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R7165:Pcdhb20
|
UTSW |
18 |
37,638,123 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Pcdhb20
|
UTSW |
18 |
37,638,439 (GRCm39) |
missense |
probably benign |
0.24 |
R7265:Pcdhb20
|
UTSW |
18 |
37,638,616 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7372:Pcdhb20
|
UTSW |
18 |
37,639,840 (GRCm39) |
missense |
probably benign |
0.00 |
R7402:Pcdhb20
|
UTSW |
18 |
37,638,005 (GRCm39) |
missense |
probably benign |
0.05 |
R7718:Pcdhb20
|
UTSW |
18 |
37,638,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R7794:Pcdhb20
|
UTSW |
18 |
37,637,485 (GRCm39) |
missense |
probably benign |
0.00 |
R7842:Pcdhb20
|
UTSW |
18 |
37,638,112 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8084:Pcdhb20
|
UTSW |
18 |
37,639,226 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8133:Pcdhb20
|
UTSW |
18 |
37,639,663 (GRCm39) |
nonsense |
probably null |
|
R8422:Pcdhb20
|
UTSW |
18 |
37,637,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R8477:Pcdhb20
|
UTSW |
18 |
37,638,307 (GRCm39) |
missense |
probably benign |
0.12 |
R8733:Pcdhb20
|
UTSW |
18 |
37,638,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R8951:Pcdhb20
|
UTSW |
18 |
37,639,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R9196:Pcdhb20
|
UTSW |
18 |
37,638,024 (GRCm39) |
missense |
probably benign |
0.00 |
R9384:Pcdhb20
|
UTSW |
18 |
37,638,024 (GRCm39) |
missense |
probably benign |
0.00 |
R9388:Pcdhb20
|
UTSW |
18 |
37,638,853 (GRCm39) |
missense |
probably benign |
0.02 |
R9462:Pcdhb20
|
UTSW |
18 |
37,639,799 (GRCm39) |
missense |
probably benign |
0.30 |
R9667:Pcdhb20
|
UTSW |
18 |
37,637,839 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Pcdhb20
|
UTSW |
18 |
37,637,641 (GRCm39) |
missense |
possibly damaging |
0.95 |
|