Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy2 |
C |
T |
13: 68,878,436 (GRCm39) |
G401S |
probably damaging |
Het |
Akap8l |
C |
T |
17: 32,551,457 (GRCm39) |
R511H |
probably damaging |
Het |
Bmp2 |
T |
C |
2: 133,402,847 (GRCm39) |
F133L |
probably damaging |
Het |
C1qtnf3 |
A |
G |
15: 10,978,670 (GRCm39) |
E290G |
probably damaging |
Het |
Ccdc180 |
C |
A |
4: 45,914,589 (GRCm39) |
D701E |
probably benign |
Het |
Chmp7 |
C |
T |
14: 69,956,899 (GRCm39) |
M336I |
probably benign |
Het |
Csmd3 |
A |
T |
15: 47,539,213 (GRCm39) |
I1508N |
probably damaging |
Het |
Dgkh |
T |
C |
14: 78,862,329 (GRCm39) |
R80G |
probably damaging |
Het |
Dock1 |
T |
A |
7: 134,449,902 (GRCm39) |
V805D |
possibly damaging |
Het |
Eef2 |
C |
CN |
10: 81,014,603 (GRCm39) |
|
probably null |
Het |
Ercc6l2 |
T |
A |
13: 64,016,934 (GRCm39) |
V679D |
possibly damaging |
Het |
Esp6 |
T |
C |
17: 40,876,284 (GRCm39) |
Y111H |
probably benign |
Het |
Focad |
T |
C |
4: 88,244,417 (GRCm39) |
F799S |
unknown |
Het |
Foxred1 |
C |
A |
9: 35,116,333 (GRCm39) |
M438I |
probably benign |
Het |
Galnt11 |
T |
G |
5: 25,463,943 (GRCm39) |
V405G |
probably damaging |
Het |
Gm4847 |
A |
G |
1: 166,457,935 (GRCm39) |
Y473H |
probably damaging |
Het |
Gpbp1l1 |
C |
T |
4: 116,450,115 (GRCm39) |
T461M |
probably damaging |
Het |
Hnrnpu |
A |
T |
1: 178,158,790 (GRCm39) |
|
probably benign |
Het |
Kmt2d |
A |
T |
15: 98,755,646 (GRCm39) |
|
probably benign |
Het |
Matr3 |
A |
G |
18: 35,705,948 (GRCm39) |
H291R |
probably damaging |
Het |
Mfsd14b |
C |
T |
13: 65,243,506 (GRCm39) |
S46N |
probably benign |
Het |
Mtch1 |
C |
T |
17: 29,552,744 (GRCm39) |
|
probably null |
Het |
Muc6 |
G |
T |
7: 141,218,685 (GRCm39) |
T1996N |
possibly damaging |
Het |
Mylk |
T |
C |
16: 34,820,688 (GRCm39) |
I1880T |
probably damaging |
Het |
N4bp2 |
T |
C |
5: 65,965,815 (GRCm39) |
L1288P |
probably damaging |
Het |
Ncf2 |
A |
T |
1: 152,706,123 (GRCm39) |
H245L |
probably damaging |
Het |
Nmd3 |
T |
A |
3: 69,654,049 (GRCm39) |
|
probably benign |
Het |
Npdc1 |
G |
T |
2: 25,297,727 (GRCm39) |
A127S |
probably benign |
Het |
Nudt3 |
C |
A |
17: 27,842,080 (GRCm39) |
R27L |
probably benign |
Het |
Nwd1 |
C |
T |
8: 73,424,397 (GRCm39) |
|
probably benign |
Het |
Pex7 |
T |
A |
10: 19,764,434 (GRCm39) |
I170F |
probably benign |
Het |
Pkhd1 |
G |
A |
1: 20,593,053 (GRCm39) |
P1687S |
possibly damaging |
Het |
Plekhj1 |
A |
T |
10: 80,633,654 (GRCm39) |
|
probably null |
Het |
Prss21 |
T |
A |
17: 24,091,968 (GRCm39) |
L312H |
probably damaging |
Het |
Samsn1 |
T |
C |
16: 75,670,408 (GRCm39) |
I232V |
probably null |
Het |
Sec63 |
A |
T |
10: 42,682,542 (GRCm39) |
D411V |
probably damaging |
Het |
Slc44a4 |
C |
T |
17: 35,146,998 (GRCm39) |
H343Y |
probably damaging |
Het |
Sucla2 |
C |
T |
14: 73,798,074 (GRCm39) |
|
probably benign |
Het |
Tedc2 |
T |
A |
17: 24,435,291 (GRCm39) |
E366V |
probably damaging |
Het |
Tedc2 |
C |
A |
17: 24,435,292 (GRCm39) |
E366* |
probably null |
Het |
Tent2 |
C |
T |
13: 93,312,205 (GRCm39) |
|
probably null |
Het |
Tmtc3 |
A |
G |
10: 100,307,905 (GRCm39) |
|
probably benign |
Het |
Trafd1 |
C |
T |
5: 121,511,387 (GRCm39) |
R477H |
possibly damaging |
Het |
Uhrf2 |
T |
A |
19: 30,033,626 (GRCm39) |
|
probably benign |
Het |
Vmn2r68 |
T |
A |
7: 84,871,549 (GRCm39) |
D578V |
possibly damaging |
Het |
Wdcp |
G |
A |
12: 4,901,655 (GRCm39) |
V504I |
possibly damaging |
Het |
Wdr93 |
T |
C |
7: 79,423,196 (GRCm39) |
Y487H |
probably damaging |
Het |
Zfp457 |
T |
C |
13: 67,441,846 (GRCm39) |
H147R |
probably damaging |
Het |
|
Other mutations in Phyhipl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Phyhipl
|
APN |
10 |
70,406,660 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03374:Phyhipl
|
APN |
10 |
70,401,109 (GRCm39) |
missense |
possibly damaging |
0.47 |
PIT4366001:Phyhipl
|
UTSW |
10 |
70,404,788 (GRCm39) |
missense |
probably benign |
|
R0512:Phyhipl
|
UTSW |
10 |
70,404,748 (GRCm39) |
missense |
probably damaging |
0.99 |
R0688:Phyhipl
|
UTSW |
10 |
70,395,085 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Phyhipl
|
UTSW |
10 |
70,406,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Phyhipl
|
UTSW |
10 |
70,406,798 (GRCm39) |
missense |
probably damaging |
1.00 |
R1802:Phyhipl
|
UTSW |
10 |
70,434,855 (GRCm39) |
missense |
probably benign |
|
R1978:Phyhipl
|
UTSW |
10 |
70,395,591 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4077:Phyhipl
|
UTSW |
10 |
70,404,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R4960:Phyhipl
|
UTSW |
10 |
70,404,815 (GRCm39) |
missense |
probably benign |
0.40 |
R4976:Phyhipl
|
UTSW |
10 |
70,404,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5119:Phyhipl
|
UTSW |
10 |
70,404,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R5739:Phyhipl
|
UTSW |
10 |
70,395,399 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6303:Phyhipl
|
UTSW |
10 |
70,395,387 (GRCm39) |
splice site |
probably null |
|
R6304:Phyhipl
|
UTSW |
10 |
70,395,387 (GRCm39) |
splice site |
probably null |
|
R6649:Phyhipl
|
UTSW |
10 |
70,404,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R9150:Phyhipl
|
UTSW |
10 |
70,404,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9237:Phyhipl
|
UTSW |
10 |
70,406,720 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9293:Phyhipl
|
UTSW |
10 |
70,401,116 (GRCm39) |
missense |
probably damaging |
0.97 |
R9461:Phyhipl
|
UTSW |
10 |
70,395,243 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9595:Phyhipl
|
UTSW |
10 |
70,395,512 (GRCm39) |
nonsense |
probably null |
|
X0022:Phyhipl
|
UTSW |
10 |
70,404,791 (GRCm39) |
missense |
probably damaging |
0.99 |
|