Other mutations in this stock |
Total: 70 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam7 |
A |
T |
14: 68,750,094 (GRCm39) |
V442E |
possibly damaging |
Het |
Adgrv1 |
A |
T |
13: 81,721,433 (GRCm39) |
V715D |
probably damaging |
Het |
Aldh1l1 |
A |
C |
6: 90,546,894 (GRCm39) |
D399A |
probably benign |
Het |
Ankrd23 |
T |
C |
1: 36,570,808 (GRCm39) |
N274S |
probably damaging |
Het |
Aopep |
A |
T |
13: 63,304,407 (GRCm39) |
H473L |
possibly damaging |
Het |
Arid5b |
C |
T |
10: 67,934,417 (GRCm39) |
G495E |
probably benign |
Het |
Arpc4 |
A |
T |
6: 113,362,565 (GRCm39) |
M149L |
probably benign |
Het |
Bdp1 |
T |
C |
13: 100,191,759 (GRCm39) |
T1407A |
possibly damaging |
Het |
Calml3 |
A |
T |
13: 3,854,121 (GRCm39) |
I28N |
probably damaging |
Het |
Cdhr3 |
A |
G |
12: 33,110,319 (GRCm39) |
S322P |
probably damaging |
Het |
Cilk1 |
G |
C |
9: 78,074,902 (GRCm39) |
V586L |
probably benign |
Het |
Cntn5 |
A |
G |
9: 9,704,934 (GRCm39) |
S622P |
probably benign |
Het |
Col22a1 |
A |
G |
15: 71,824,166 (GRCm39) |
|
probably null |
Het |
Csf2rb2 |
A |
T |
15: 78,177,041 (GRCm39) |
I143N |
probably benign |
Het |
Cwh43 |
T |
C |
5: 73,572,377 (GRCm39) |
L205P |
probably damaging |
Het |
Dennd5b |
T |
C |
6: 148,970,064 (GRCm39) |
T52A |
probably benign |
Het |
Dhx40 |
A |
G |
11: 86,666,502 (GRCm39) |
I597T |
possibly damaging |
Het |
Dnajc21 |
A |
G |
15: 10,460,133 (GRCm39) |
L268P |
probably damaging |
Het |
Dzip1 |
A |
T |
14: 119,120,805 (GRCm39) |
D717E |
probably benign |
Het |
Elmo3 |
A |
G |
8: 106,034,876 (GRCm39) |
N389D |
probably damaging |
Het |
Evi2a |
T |
C |
11: 79,418,768 (GRCm39) |
E14G |
unknown |
Het |
Fam149a |
T |
A |
8: 45,834,554 (GRCm39) |
R82W |
probably damaging |
Het |
Farp1 |
A |
T |
14: 121,513,665 (GRCm39) |
E820V |
probably benign |
Het |
Fgd5 |
T |
A |
6: 91,965,440 (GRCm39) |
S400T |
possibly damaging |
Het |
Flnc |
G |
A |
6: 29,456,443 (GRCm39) |
V2214I |
possibly damaging |
Het |
Galnt4 |
C |
A |
10: 98,944,975 (GRCm39) |
N233K |
possibly damaging |
Het |
Gbp5 |
A |
G |
3: 142,208,841 (GRCm39) |
Y128C |
probably damaging |
Het |
Gm4871 |
G |
A |
5: 144,969,420 (GRCm39) |
T33I |
probably benign |
Het |
Gm5592 |
T |
C |
7: 40,936,118 (GRCm39) |
S207P |
probably benign |
Het |
Gtf2ird1 |
A |
T |
5: 134,445,985 (GRCm39) |
C15* |
probably null |
Het |
Ido2 |
T |
A |
8: 25,037,242 (GRCm39) |
I155F |
probably damaging |
Het |
Ifi27l2b |
A |
T |
12: 103,423,268 (GRCm39) |
|
probably null |
Het |
Il15ra |
C |
T |
2: 11,728,404 (GRCm39) |
T49I |
probably damaging |
Het |
Itpr3 |
T |
A |
17: 27,337,571 (GRCm39) |
C2460* |
probably null |
Het |
Kcnj11 |
T |
C |
7: 45,749,179 (GRCm39) |
N48S |
probably damaging |
Het |
Lmo7 |
A |
C |
14: 102,136,012 (GRCm39) |
N695T |
possibly damaging |
Het |
Mmp15 |
C |
A |
8: 96,094,776 (GRCm39) |
H217N |
probably damaging |
Het |
Mtcl2 |
C |
T |
2: 156,869,504 (GRCm39) |
A1044T |
probably benign |
Het |
Muc21 |
A |
T |
17: 35,929,798 (GRCm39) |
S1463T |
unknown |
Het |
Mug1 |
C |
A |
6: 121,838,179 (GRCm39) |
H470N |
possibly damaging |
Het |
Myo5c |
A |
T |
9: 75,186,627 (GRCm39) |
D991V |
probably damaging |
Het |
Nfkbid |
T |
A |
7: 30,126,603 (GRCm39) |
N396K |
probably damaging |
Het |
Oas1c |
A |
G |
5: 120,939,107 (GRCm39) |
F361L |
probably benign |
Het |
Or10aa1 |
A |
G |
1: 173,869,650 (GRCm39) |
I45V |
probably benign |
Het |
Or1e1b-ps1 |
A |
T |
11: 73,845,948 (GRCm39) |
Y144F |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 108,919,691 (GRCm39) |
K606E |
probably benign |
Het |
Pkp2 |
C |
A |
16: 16,043,272 (GRCm39) |
L111I |
probably benign |
Het |
Pogz |
A |
G |
3: 94,782,544 (GRCm39) |
Y635C |
probably damaging |
Het |
Prdx2 |
A |
G |
8: 85,698,303 (GRCm39) |
T165A |
probably benign |
Het |
Ptprd |
G |
A |
4: 75,916,841 (GRCm39) |
T770I |
probably damaging |
Het |
Rapgef6 |
A |
G |
11: 54,585,225 (GRCm39) |
Y1541C |
probably damaging |
Het |
Rilpl1 |
A |
T |
5: 124,634,200 (GRCm39) |
|
probably null |
Het |
Rimbp3 |
T |
A |
16: 17,030,568 (GRCm39) |
Y1331N |
probably benign |
Het |
Sav1 |
T |
C |
12: 70,030,995 (GRCm39) |
R176G |
probably damaging |
Het |
Sirt5 |
A |
G |
13: 43,536,623 (GRCm39) |
H219R |
probably benign |
Het |
Skint5 |
T |
G |
4: 113,403,715 (GRCm39) |
D1169A |
unknown |
Het |
Slfn9 |
G |
T |
11: 82,873,467 (GRCm39) |
Q479K |
possibly damaging |
Het |
Spata31f1e |
A |
T |
4: 42,793,546 (GRCm39) |
H195Q |
possibly damaging |
Het |
Susd4 |
T |
C |
1: 182,722,767 (GRCm39) |
I483T |
possibly damaging |
Het |
Tmem156 |
C |
T |
5: 65,232,912 (GRCm39) |
V217I |
possibly damaging |
Het |
Tmem79 |
A |
G |
3: 88,239,949 (GRCm39) |
Y254H |
probably benign |
Het |
Tmprss2 |
T |
A |
16: 97,377,429 (GRCm39) |
K223* |
probably null |
Het |
Trav3-1 |
T |
C |
14: 52,818,581 (GRCm39) |
V85A |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,716,100 (GRCm39) |
|
probably null |
Het |
Vmn2r22 |
T |
C |
6: 123,614,559 (GRCm39) |
I344V |
not run |
Het |
Vps13c |
A |
T |
9: 67,847,765 (GRCm39) |
M2176L |
probably benign |
Het |
Wdfy3 |
A |
T |
5: 101,996,223 (GRCm39) |
V3213D |
probably damaging |
Het |
Zbtb21 |
G |
A |
16: 97,752,654 (GRCm39) |
T543M |
possibly damaging |
Het |
Zc3hav1 |
A |
T |
6: 38,309,691 (GRCm39) |
V377D |
probably benign |
Het |
Zswim3 |
T |
C |
2: 164,661,699 (GRCm39) |
C60R |
probably damaging |
Het |
|
Other mutations in Ptcd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00767:Ptcd3
|
APN |
6 |
71,880,432 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00903:Ptcd3
|
APN |
6 |
71,884,828 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01545:Ptcd3
|
APN |
6 |
71,865,561 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01924:Ptcd3
|
APN |
6 |
71,875,411 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02675:Ptcd3
|
APN |
6 |
71,860,426 (GRCm39) |
critical splice donor site |
probably null |
|
R0732:Ptcd3
|
UTSW |
6 |
71,858,155 (GRCm39) |
unclassified |
probably benign |
|
R1374:Ptcd3
|
UTSW |
6 |
71,885,637 (GRCm39) |
nonsense |
probably null |
|
R1393:Ptcd3
|
UTSW |
6 |
71,866,605 (GRCm39) |
missense |
probably benign |
0.00 |
R1498:Ptcd3
|
UTSW |
6 |
71,870,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R1646:Ptcd3
|
UTSW |
6 |
71,875,379 (GRCm39) |
missense |
probably benign |
0.26 |
R1712:Ptcd3
|
UTSW |
6 |
71,885,637 (GRCm39) |
nonsense |
probably null |
|
R2022:Ptcd3
|
UTSW |
6 |
71,862,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R2248:Ptcd3
|
UTSW |
6 |
71,871,269 (GRCm39) |
critical splice donor site |
probably null |
|
R2406:Ptcd3
|
UTSW |
6 |
71,865,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R3418:Ptcd3
|
UTSW |
6 |
71,860,470 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3419:Ptcd3
|
UTSW |
6 |
71,860,470 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4677:Ptcd3
|
UTSW |
6 |
71,870,498 (GRCm39) |
missense |
probably benign |
0.17 |
R4741:Ptcd3
|
UTSW |
6 |
71,879,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R4752:Ptcd3
|
UTSW |
6 |
71,878,296 (GRCm39) |
missense |
probably damaging |
0.99 |
R5441:Ptcd3
|
UTSW |
6 |
71,858,505 (GRCm39) |
missense |
possibly damaging |
0.62 |
R5583:Ptcd3
|
UTSW |
6 |
71,879,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R5681:Ptcd3
|
UTSW |
6 |
71,884,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R6028:Ptcd3
|
UTSW |
6 |
71,875,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R6324:Ptcd3
|
UTSW |
6 |
71,862,311 (GRCm39) |
missense |
probably benign |
0.00 |
R6537:Ptcd3
|
UTSW |
6 |
71,874,094 (GRCm39) |
splice site |
probably null |
|
R6600:Ptcd3
|
UTSW |
6 |
71,860,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R6783:Ptcd3
|
UTSW |
6 |
71,885,627 (GRCm39) |
missense |
probably benign |
0.00 |
R6810:Ptcd3
|
UTSW |
6 |
71,862,516 (GRCm39) |
missense |
probably damaging |
0.99 |
R6860:Ptcd3
|
UTSW |
6 |
71,874,094 (GRCm39) |
splice site |
probably null |
|
R6993:Ptcd3
|
UTSW |
6 |
71,862,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R7578:Ptcd3
|
UTSW |
6 |
71,885,691 (GRCm39) |
missense |
probably benign |
|
R7851:Ptcd3
|
UTSW |
6 |
71,879,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R7888:Ptcd3
|
UTSW |
6 |
71,860,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R7889:Ptcd3
|
UTSW |
6 |
71,865,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R7919:Ptcd3
|
UTSW |
6 |
71,880,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R8162:Ptcd3
|
UTSW |
6 |
71,884,798 (GRCm39) |
missense |
probably benign |
0.02 |
R8351:Ptcd3
|
UTSW |
6 |
71,885,625 (GRCm39) |
missense |
probably benign |
0.00 |
R8451:Ptcd3
|
UTSW |
6 |
71,885,625 (GRCm39) |
missense |
probably benign |
0.00 |
R8701:Ptcd3
|
UTSW |
6 |
71,862,495 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8826:Ptcd3
|
UTSW |
6 |
71,885,645 (GRCm39) |
missense |
probably benign |
0.01 |
R8926:Ptcd3
|
UTSW |
6 |
71,869,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R8969:Ptcd3
|
UTSW |
6 |
71,880,431 (GRCm39) |
missense |
probably benign |
0.44 |
R9031:Ptcd3
|
UTSW |
6 |
71,880,458 (GRCm39) |
nonsense |
probably null |
|
R9046:Ptcd3
|
UTSW |
6 |
71,870,364 (GRCm39) |
critical splice donor site |
probably null |
|
R9384:Ptcd3
|
UTSW |
6 |
71,874,110 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9668:Ptcd3
|
UTSW |
6 |
71,871,275 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9771:Ptcd3
|
UTSW |
6 |
71,872,903 (GRCm39) |
nonsense |
probably null |
|
X0024:Ptcd3
|
UTSW |
6 |
71,878,258 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Ptcd3
|
UTSW |
6 |
71,884,790 (GRCm39) |
missense |
probably benign |
0.00 |
|