Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930523C07Rik |
T |
C |
1: 159,902,978 (GRCm39) |
S83P |
possibly damaging |
Het |
Actr10 |
A |
T |
12: 70,999,733 (GRCm39) |
E176D |
probably benign |
Het |
Adcy3 |
G |
A |
12: 4,258,662 (GRCm39) |
|
probably null |
Het |
AI429214 |
T |
A |
8: 37,461,278 (GRCm39) |
I142N |
probably damaging |
Het |
Alox12 |
A |
G |
11: 70,143,936 (GRCm39) |
L148S |
probably damaging |
Het |
Ank3 |
A |
G |
10: 69,809,680 (GRCm39) |
I1147V |
probably benign |
Het |
Apoc2 |
C |
T |
7: 19,407,493 (GRCm39) |
V12I |
probably benign |
Het |
Arap3 |
T |
C |
18: 38,124,407 (GRCm39) |
S311G |
probably benign |
Het |
Arih2 |
G |
T |
9: 108,488,841 (GRCm39) |
H292Q |
probably damaging |
Het |
Cdc14a |
A |
T |
3: 116,101,843 (GRCm39) |
D312E |
probably benign |
Het |
Cdh12 |
T |
G |
15: 21,237,800 (GRCm39) |
W12G |
possibly damaging |
Het |
Cisd2 |
A |
T |
3: 135,114,616 (GRCm39) |
N118K |
probably damaging |
Het |
Cntnap5b |
A |
G |
1: 99,999,827 (GRCm39) |
Q195R |
probably benign |
Het |
Cyp2r1 |
A |
G |
7: 114,161,966 (GRCm39) |
|
probably null |
Het |
Cyp4f37 |
A |
G |
17: 32,848,864 (GRCm39) |
D244G |
possibly damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dido1 |
T |
A |
2: 180,302,048 (GRCm39) |
H1952L |
probably damaging |
Het |
Dnah10 |
T |
A |
5: 124,871,283 (GRCm39) |
|
probably null |
Het |
Dnal4 |
T |
A |
15: 79,646,714 (GRCm39) |
M56L |
probably damaging |
Het |
Emilin2 |
A |
G |
17: 71,581,112 (GRCm39) |
V538A |
probably benign |
Het |
Eps8l2 |
A |
G |
7: 140,922,015 (GRCm39) |
D31G |
probably damaging |
Het |
Erp44 |
A |
T |
4: 48,219,479 (GRCm39) |
L112* |
probably null |
Het |
Etl4 |
C |
T |
2: 20,813,900 (GRCm39) |
T1907I |
possibly damaging |
Het |
Exoc3 |
A |
G |
13: 74,330,400 (GRCm39) |
F510L |
probably benign |
Het |
Fam114a2 |
G |
T |
11: 57,383,942 (GRCm39) |
T324K |
possibly damaging |
Het |
Fer1l4 |
G |
A |
2: 155,888,091 (GRCm39) |
R465C |
probably damaging |
Het |
Frmd4b |
A |
C |
6: 97,436,173 (GRCm39) |
S2R |
probably benign |
Het |
Fscn1 |
A |
T |
5: 142,946,778 (GRCm39) |
D192V |
possibly damaging |
Het |
Gm3486 |
T |
A |
14: 41,206,472 (GRCm39) |
*200C |
probably null |
Het |
Gusb |
A |
T |
5: 130,029,366 (GRCm39) |
H138Q |
probably benign |
Het |
Hdac9 |
A |
T |
12: 34,578,293 (GRCm39) |
M4K |
possibly damaging |
Het |
Hhipl1 |
G |
T |
12: 108,284,964 (GRCm39) |
R439L |
probably benign |
Het |
Hoxd9 |
A |
G |
2: 74,528,980 (GRCm39) |
E194G |
probably benign |
Het |
Itgb1 |
A |
G |
8: 129,448,902 (GRCm39) |
S503G |
possibly damaging |
Het |
Kcnt2 |
T |
A |
1: 140,437,216 (GRCm39) |
C500S |
probably damaging |
Het |
Kdm7a |
G |
A |
6: 39,123,983 (GRCm39) |
S727L |
possibly damaging |
Het |
Klhdc4 |
A |
G |
8: 122,540,507 (GRCm39) |
F92L |
probably damaging |
Het |
Klrb1a |
A |
G |
6: 128,596,137 (GRCm39) |
V62A |
probably damaging |
Het |
Krit1 |
A |
G |
5: 3,863,032 (GRCm39) |
|
probably null |
Het |
Krt40 |
A |
G |
11: 99,432,566 (GRCm39) |
I150T |
possibly damaging |
Het |
Larp4b |
A |
G |
13: 9,208,738 (GRCm39) |
T464A |
probably benign |
Het |
Lrrc52 |
T |
G |
1: 167,293,964 (GRCm39) |
D107A |
probably damaging |
Het |
Mapkap1 |
G |
T |
2: 34,408,692 (GRCm39) |
V35F |
probably damaging |
Het |
Mccc1 |
A |
G |
3: 36,044,313 (GRCm39) |
V171A |
probably damaging |
Het |
Metap1d |
A |
T |
2: 71,346,104 (GRCm39) |
R222* |
probably null |
Het |
Mrgpre |
G |
A |
7: 143,334,603 (GRCm39) |
A300V |
probably benign |
Het |
Mterf1b |
C |
A |
5: 4,246,606 (GRCm39) |
N82K |
probably benign |
Het |
Myh9 |
C |
T |
15: 77,669,422 (GRCm39) |
W533* |
probably null |
Het |
Myom2 |
A |
G |
8: 15,148,472 (GRCm39) |
|
probably null |
Het |
Ncor1 |
G |
A |
11: 62,257,808 (GRCm39) |
P329S |
probably damaging |
Het |
Nr2f1 |
T |
C |
13: 78,344,611 (GRCm39) |
|
probably benign |
Het |
Or10x1 |
T |
G |
1: 174,197,236 (GRCm39) |
V251G |
probably benign |
Het |
Or11a4 |
T |
A |
17: 37,536,451 (GRCm39) |
L145* |
probably null |
Het |
Or2a57 |
C |
T |
6: 43,212,838 (GRCm39) |
Q99* |
probably null |
Het |
Or2w6 |
A |
T |
13: 21,843,244 (GRCm39) |
I83N |
possibly damaging |
Het |
Or52p2 |
T |
C |
7: 102,237,237 (GRCm39) |
T238A |
probably benign |
Het |
Or6c210 |
A |
G |
10: 129,496,532 (GRCm39) |
I286V |
probably benign |
Het |
Or6z1 |
A |
T |
7: 6,504,675 (GRCm39) |
C183* |
probably null |
Het |
Pcdha11 |
T |
C |
18: 37,138,950 (GRCm39) |
L193P |
probably benign |
Het |
Pde1a |
T |
C |
2: 79,708,545 (GRCm39) |
H291R |
probably damaging |
Het |
Pfkm |
G |
A |
15: 98,024,260 (GRCm39) |
V423M |
probably damaging |
Het |
Pira1 |
C |
A |
7: 3,739,337 (GRCm39) |
E510D |
probably benign |
Het |
Pkd2l1 |
G |
T |
19: 44,146,108 (GRCm39) |
Q149K |
probably benign |
Het |
Pkhd1l1 |
T |
A |
15: 44,392,955 (GRCm39) |
N1763K |
probably benign |
Het |
Pla2g4a |
G |
A |
1: 149,748,338 (GRCm39) |
T282I |
probably damaging |
Het |
Prpf39 |
A |
C |
12: 65,089,528 (GRCm39) |
N89H |
probably damaging |
Het |
Rad54l2 |
A |
G |
9: 106,587,537 (GRCm39) |
F743L |
probably damaging |
Het |
Raver2 |
A |
G |
4: 100,991,320 (GRCm39) |
|
probably null |
Het |
Ric8b |
T |
C |
10: 84,783,709 (GRCm39) |
L189P |
probably damaging |
Het |
Sccpdh |
T |
C |
1: 179,495,957 (GRCm39) |
F13L |
probably benign |
Het |
Scd2 |
T |
C |
19: 44,291,448 (GRCm39) |
F296L |
probably damaging |
Het |
Scg2 |
G |
T |
1: 79,414,023 (GRCm39) |
D233E |
probably benign |
Het |
Sema5b |
C |
A |
16: 35,448,377 (GRCm39) |
|
probably null |
Het |
Skint5 |
A |
T |
4: 113,636,286 (GRCm39) |
V644E |
unknown |
Het |
Slc44a5 |
G |
T |
3: 153,969,678 (GRCm39) |
V612F |
possibly damaging |
Het |
Snd1 |
C |
T |
6: 28,520,234 (GRCm39) |
R107* |
probably null |
Het |
Sun5 |
G |
T |
2: 153,702,589 (GRCm39) |
T189K |
probably damaging |
Het |
Tap1 |
A |
T |
17: 34,412,151 (GRCm39) |
E452V |
probably damaging |
Het |
Tcam1 |
A |
G |
11: 106,173,652 (GRCm39) |
N32S |
probably benign |
Het |
Tep1 |
T |
C |
14: 51,067,715 (GRCm39) |
E2167G |
probably damaging |
Het |
Tm9sf1 |
C |
T |
14: 55,873,827 (GRCm39) |
R557H |
probably damaging |
Het |
Tmem175 |
T |
C |
5: 108,793,821 (GRCm39) |
V317A |
probably damaging |
Het |
Tsga13 |
A |
G |
6: 30,874,139 (GRCm39) |
V231A |
probably benign |
Het |
Tspan12 |
A |
G |
6: 21,799,970 (GRCm39) |
S126P |
probably damaging |
Het |
Uvrag |
G |
T |
7: 98,637,398 (GRCm39) |
D143E |
probably damaging |
Het |
Vmn1r230 |
T |
A |
17: 21,067,036 (GRCm39) |
M75K |
possibly damaging |
Het |
Vmn2r120 |
A |
T |
17: 57,852,287 (GRCm39) |
F10I |
probably benign |
Het |
Vmn2r57 |
T |
C |
7: 41,049,284 (GRCm39) |
T822A |
probably benign |
Het |
Vmn2r67 |
T |
C |
7: 84,799,768 (GRCm39) |
Y490C |
probably damaging |
Het |
Zc3h7b |
T |
A |
15: 81,667,386 (GRCm39) |
W644R |
probably damaging |
Het |
Zeb1 |
A |
G |
18: 5,766,962 (GRCm39) |
D491G |
probably damaging |
Het |
Zfp709 |
TCGACG |
TCG |
8: 72,644,552 (GRCm39) |
|
probably benign |
Het |
Zfp831 |
A |
T |
2: 174,486,308 (GRCm39) |
T328S |
possibly damaging |
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 |
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 |
R8727:Pcdhb20
|
UTSW |
18 |
37,638,437 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|