Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932438H23Rik |
T |
G |
16: 91,055,612 (GRCm38) |
Y212S |
probably damaging |
Het |
Angpt1 |
T |
C |
15: 42,512,399 (GRCm38) |
N154D |
probably damaging |
Het |
Angpt2 |
G |
A |
8: 18,741,119 (GRCm38) |
R54* |
probably null |
Het |
Ankrd27 |
T |
A |
7: 35,601,626 (GRCm38) |
L117* |
probably null |
Het |
Arhgap21 |
C |
T |
2: 20,854,180 (GRCm38) |
M1234I |
probably benign |
Het |
Arhgef33 |
A |
G |
17: 80,367,335 (GRCm38) |
E387G |
probably damaging |
Het |
Atp13a4 |
T |
A |
16: 29,454,769 (GRCm38) |
K444* |
probably null |
Het |
Atp6v1a |
G |
A |
16: 44,101,862 (GRCm38) |
R338C |
probably damaging |
Het |
Canx |
T |
C |
11: 50,311,647 (GRCm38) |
D44G |
possibly damaging |
Het |
Ccdc141 |
T |
A |
2: 77,132,244 (GRCm38) |
M119L |
probably benign |
Het |
Ckmt1 |
A |
C |
2: 121,362,691 (GRCm38) |
Q299P |
possibly damaging |
Het |
Dhx16 |
T |
C |
17: 35,885,920 (GRCm38) |
S601P |
probably damaging |
Het |
Dna2 |
A |
C |
10: 62,950,894 (GRCm38) |
R140S |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,782,409 (GRCm38) |
T670A |
probably benign |
Het |
Eif1ad10 |
T |
G |
12: 88,249,685 (GRCm38) |
E139A |
unknown |
Het |
Eogt |
A |
G |
6: 97,143,998 (GRCm38) |
S85P |
possibly damaging |
Het |
Fbf1 |
A |
T |
11: 116,165,881 (GRCm38) |
M1K |
probably null |
Het |
Fbxl12 |
C |
A |
9: 20,638,864 (GRCm38) |
R165L |
possibly damaging |
Het |
Flnb |
G |
A |
14: 7,950,394 (GRCm38) |
V2571I |
probably damaging |
Het |
Gm43518 |
A |
G |
5: 123,938,259 (GRCm38) |
E123G |
unknown |
Het |
Gpatch2 |
A |
G |
1: 187,304,355 (GRCm38) |
N374S |
probably benign |
Het |
Hey1 |
G |
C |
3: 8,664,776 (GRCm38) |
A207G |
probably benign |
Het |
Hoxa11 |
T |
C |
6: 52,245,802 (GRCm38) |
|
probably benign |
Het |
Hydin |
G |
A |
8: 110,582,018 (GRCm38) |
V3979I |
probably benign |
Het |
Ighe |
C |
T |
12: 113,271,793 (GRCm38) |
W277* |
probably null |
Het |
Kmt2c |
G |
T |
5: 25,314,122 (GRCm38) |
T2330K |
probably benign |
Het |
Krt6a |
T |
A |
15: 101,692,735 (GRCm38) |
K261M |
probably damaging |
Het |
Lats2 |
A |
C |
14: 57,722,705 (GRCm38) |
S161A |
probably benign |
Het |
Med13l |
T |
A |
5: 118,754,321 (GRCm38) |
D1936E |
probably benign |
Het |
Mipol1 |
T |
C |
12: 57,306,088 (GRCm38) |
V71A |
possibly damaging |
Het |
Mphosph8 |
A |
T |
14: 56,676,546 (GRCm38) |
K415* |
probably null |
Het |
Npepps |
A |
G |
11: 97,244,426 (GRCm38) |
|
probably null |
Het |
Ntn4 |
A |
T |
10: 93,741,104 (GRCm38) |
N545Y |
possibly damaging |
Het |
Or11g1 |
A |
C |
14: 50,413,675 (GRCm38) |
M44L |
probably benign |
Het |
Or1n1b |
A |
G |
2: 36,890,354 (GRCm38) |
S165P |
probably damaging |
Het |
Or2m12 |
T |
C |
16: 19,286,701 (GRCm38) |
D14G |
probably benign |
Het |
Or9i2 |
A |
T |
19: 13,838,402 (GRCm38) |
M257K |
possibly damaging |
Het |
Osbpl2 |
T |
A |
2: 180,155,343 (GRCm38) |
V358E |
possibly damaging |
Het |
Pdcd11 |
C |
A |
19: 47,119,806 (GRCm38) |
P1204Q |
probably damaging |
Het |
Ppm1g |
G |
T |
5: 31,204,528 (GRCm38) |
R373S |
probably damaging |
Het |
Rnf130 |
A |
G |
11: 50,087,437 (GRCm38) |
D275G |
probably damaging |
Het |
Rps18-ps5 |
A |
G |
13: 28,257,711 (GRCm38) |
I26V |
probably benign |
Het |
Setd5 |
T |
C |
6: 113,121,087 (GRCm38) |
S696P |
probably damaging |
Het |
Sgip1 |
A |
G |
4: 102,915,071 (GRCm38) |
Q219R |
probably benign |
Het |
Slc1a2 |
T |
C |
2: 102,736,085 (GRCm38) |
|
probably null |
Het |
Slc22a12 |
T |
C |
19: 6,542,437 (GRCm38) |
T106A |
probably benign |
Het |
Slc22a14 |
A |
G |
9: 119,180,585 (GRCm38) |
L148P |
probably damaging |
Het |
Slc2a9 |
A |
T |
5: 38,382,078 (GRCm38) |
F375I |
probably damaging |
Het |
Sorbs3 |
A |
T |
14: 70,202,947 (GRCm38) |
D117E |
probably benign |
Het |
Spata31d1e |
A |
G |
13: 59,743,598 (GRCm38) |
L136P |
probably benign |
Het |
Sphkap |
G |
A |
1: 83,276,500 (GRCm38) |
T1176I |
probably damaging |
Het |
Supt16 |
A |
T |
14: 52,181,589 (GRCm38) |
V193D |
probably damaging |
Het |
Sytl3 |
A |
G |
17: 6,728,291 (GRCm38) |
T362A |
probably damaging |
Het |
Tctn1 |
T |
A |
5: 122,246,611 (GRCm38) |
Q410L |
probably benign |
Het |
Trbc2 |
T |
C |
6: 41,547,777 (GRCm38) |
Y133H |
|
Het |
Ttc28 |
G |
A |
5: 111,233,341 (GRCm38) |
D1240N |
probably benign |
Het |
Vmn2r120 |
A |
G |
17: 57,525,843 (GRCm38) |
V112A |
probably benign |
Het |
Zfp354b |
A |
T |
11: 50,923,470 (GRCm38) |
S209R |
probably benign |
Het |
Zfp362 |
T |
C |
4: 128,774,606 (GRCm38) |
H391R |
probably damaging |
Het |
|
Other mutations in Pnliprp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00786:Pnliprp2
|
APN |
19 |
58,760,497 (GRCm38) |
missense |
probably benign |
|
IGL02739:Pnliprp2
|
APN |
19 |
58,760,509 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02881:Pnliprp2
|
APN |
19 |
58,771,446 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03411:Pnliprp2
|
APN |
19 |
58,760,415 (GRCm38) |
missense |
probably benign |
|
R0140:Pnliprp2
|
UTSW |
19 |
58,766,363 (GRCm38) |
missense |
probably benign |
0.00 |
R0558:Pnliprp2
|
UTSW |
19 |
58,774,087 (GRCm38) |
missense |
probably benign |
0.00 |
R1873:Pnliprp2
|
UTSW |
19 |
58,763,389 (GRCm38) |
missense |
probably benign |
0.00 |
R1874:Pnliprp2
|
UTSW |
19 |
58,763,389 (GRCm38) |
missense |
probably benign |
0.00 |
R1875:Pnliprp2
|
UTSW |
19 |
58,763,389 (GRCm38) |
missense |
probably benign |
0.00 |
R2382:Pnliprp2
|
UTSW |
19 |
58,768,630 (GRCm38) |
missense |
probably benign |
0.00 |
R3893:Pnliprp2
|
UTSW |
19 |
58,766,273 (GRCm38) |
missense |
probably benign |
0.19 |
R3915:Pnliprp2
|
UTSW |
19 |
58,760,362 (GRCm38) |
missense |
probably damaging |
1.00 |
R4620:Pnliprp2
|
UTSW |
19 |
58,762,286 (GRCm38) |
missense |
possibly damaging |
0.67 |
R4893:Pnliprp2
|
UTSW |
19 |
58,771,421 (GRCm38) |
missense |
probably benign |
0.08 |
R4957:Pnliprp2
|
UTSW |
19 |
58,775,145 (GRCm38) |
missense |
possibly damaging |
0.72 |
R4959:Pnliprp2
|
UTSW |
19 |
58,766,318 (GRCm38) |
missense |
probably benign |
0.16 |
R4973:Pnliprp2
|
UTSW |
19 |
58,766,318 (GRCm38) |
missense |
probably benign |
0.16 |
R5346:Pnliprp2
|
UTSW |
19 |
58,759,800 (GRCm38) |
missense |
probably benign |
|
R6049:Pnliprp2
|
UTSW |
19 |
58,760,452 (GRCm38) |
missense |
possibly damaging |
0.77 |
R6228:Pnliprp2
|
UTSW |
19 |
58,763,442 (GRCm38) |
critical splice donor site |
probably null |
|
R6394:Pnliprp2
|
UTSW |
19 |
58,761,598 (GRCm38) |
missense |
probably benign |
|
R6829:Pnliprp2
|
UTSW |
19 |
58,759,873 (GRCm38) |
missense |
probably benign |
|
R7235:Pnliprp2
|
UTSW |
19 |
58,775,227 (GRCm38) |
missense |
probably benign |
0.03 |
R7534:Pnliprp2
|
UTSW |
19 |
58,775,142 (GRCm38) |
missense |
probably benign |
|
R7834:Pnliprp2
|
UTSW |
19 |
58,774,159 (GRCm38) |
missense |
probably benign |
0.25 |
R8015:Pnliprp2
|
UTSW |
19 |
58,766,282 (GRCm38) |
missense |
probably damaging |
0.99 |
R9000:Pnliprp2
|
UTSW |
19 |
58,774,123 (GRCm38) |
missense |
probably benign |
0.00 |
R9560:Pnliprp2
|
UTSW |
19 |
58,774,091 (GRCm38) |
missense |
possibly damaging |
0.94 |
X0058:Pnliprp2
|
UTSW |
19 |
58,774,142 (GRCm38) |
missense |
possibly damaging |
0.59 |
Z1088:Pnliprp2
|
UTSW |
19 |
58,762,325 (GRCm38) |
missense |
probably damaging |
1.00 |
|