Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acan |
T |
C |
7: 78,761,065 (GRCm39) |
W1926R |
probably damaging |
Het |
Arhgef25 |
T |
C |
10: 127,023,063 (GRCm39) |
T106A |
probably benign |
Het |
Baz1b |
G |
A |
5: 135,239,629 (GRCm39) |
R243Q |
probably damaging |
Het |
Cdhr3 |
A |
G |
12: 33,099,068 (GRCm39) |
Y508H |
probably benign |
Het |
Cyp2d9 |
T |
A |
15: 82,336,680 (GRCm39) |
W10R |
probably damaging |
Het |
Dmxl1 |
A |
G |
18: 50,013,858 (GRCm39) |
T1549A |
possibly damaging |
Het |
Dnah8 |
A |
T |
17: 31,070,705 (GRCm39) |
R4464W |
probably damaging |
Het |
Dpp4 |
G |
A |
2: 62,217,477 (GRCm39) |
T40M |
possibly damaging |
Het |
Dync1h1 |
A |
G |
12: 110,607,654 (GRCm39) |
H2723R |
possibly damaging |
Het |
E2f3 |
C |
T |
13: 30,095,289 (GRCm39) |
S333N |
probably damaging |
Het |
Fam120a |
G |
T |
13: 49,121,069 (GRCm39) |
A79E |
probably damaging |
Het |
Fat3 |
A |
G |
9: 15,877,399 (GRCm39) |
S3405P |
probably benign |
Het |
Gaa |
T |
C |
11: 119,174,531 (GRCm39) |
S793P |
possibly damaging |
Het |
Galc |
A |
C |
12: 98,193,540 (GRCm39) |
F350V |
probably damaging |
Het |
Garre1 |
A |
G |
7: 33,955,916 (GRCm39) |
V391A |
possibly damaging |
Het |
Gm136 |
A |
G |
4: 34,746,541 (GRCm39) |
C157R |
probably damaging |
Het |
Gm3327 |
A |
C |
14: 44,363,720 (GRCm39) |
N108T |
unknown |
Het |
H2-M10.2 |
A |
G |
17: 36,596,771 (GRCm39) |
Y102H |
possibly damaging |
Het |
Hmcn1 |
A |
T |
1: 150,490,972 (GRCm39) |
D4192E |
probably benign |
Het |
Hpse2 |
A |
C |
19: 43,001,482 (GRCm39) |
|
probably null |
Het |
Idh3a |
T |
C |
9: 54,510,633 (GRCm39) |
V362A |
probably benign |
Het |
Kdm7a |
A |
T |
6: 39,147,697 (GRCm39) |
|
probably null |
Het |
Krt6b |
A |
G |
15: 101,588,216 (GRCm39) |
V148A |
probably damaging |
Het |
Lrba |
G |
A |
3: 86,439,394 (GRCm39) |
R1977H |
probably damaging |
Het |
Magi2 |
A |
T |
5: 19,883,750 (GRCm39) |
Y134F |
probably benign |
Het |
Mamdc4 |
T |
C |
2: 25,455,914 (GRCm39) |
Y801C |
probably damaging |
Het |
Maml1 |
T |
C |
11: 50,149,371 (GRCm39) |
T790A |
probably benign |
Het |
Map3k19 |
A |
G |
1: 127,750,823 (GRCm39) |
Y843H |
probably damaging |
Het |
Mdfic |
A |
T |
6: 15,741,041 (GRCm39) |
H45L |
possibly damaging |
Het |
Mlx |
C |
T |
11: 100,979,080 (GRCm39) |
T87I |
probably benign |
Het |
Mms22l |
T |
A |
4: 24,521,269 (GRCm39) |
I382K |
probably benign |
Het |
Mtf1 |
A |
G |
4: 124,732,697 (GRCm39) |
N585S |
probably benign |
Het |
Mylk2 |
C |
T |
2: 152,755,588 (GRCm39) |
P251S |
probably damaging |
Het |
Myorg |
A |
G |
4: 41,499,165 (GRCm39) |
V155A |
probably benign |
Het |
Nox4 |
A |
T |
7: 86,955,958 (GRCm39) |
T157S |
probably benign |
Het |
Oas2 |
A |
T |
5: 120,886,682 (GRCm39) |
H161Q |
probably benign |
Het |
Obscn |
A |
T |
11: 58,994,268 (GRCm39) |
V1563E |
probably damaging |
Het |
Or2n1b |
T |
C |
17: 38,460,322 (GRCm39) |
V281A |
possibly damaging |
Het |
Or55b3 |
T |
C |
7: 102,126,354 (GRCm39) |
K241R |
probably damaging |
Het |
Or6c203 |
A |
C |
10: 129,009,966 (GRCm39) |
F308C |
probably benign |
Het |
Pcdhb11 |
T |
A |
18: 37,555,375 (GRCm39) |
I235N |
probably benign |
Het |
Ptges |
C |
T |
2: 30,782,722 (GRCm39) |
G110D |
possibly damaging |
Het |
Rsph4a |
A |
T |
10: 33,784,094 (GRCm39) |
I239L |
possibly damaging |
Het |
Setx |
A |
G |
2: 29,034,813 (GRCm39) |
I433V |
probably benign |
Het |
Smyd4 |
T |
C |
11: 75,281,927 (GRCm39) |
S467P |
probably benign |
Het |
Snai2 |
A |
T |
16: 14,523,866 (GRCm39) |
H10L |
possibly damaging |
Het |
Snw1 |
T |
C |
12: 87,497,589 (GRCm39) |
I467V |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,883,420 (GRCm39) |
C301S |
probably damaging |
Het |
Tax1bp1 |
T |
A |
6: 52,735,342 (GRCm39) |
|
probably null |
Het |
Tmem70 |
C |
A |
1: 16,735,575 (GRCm39) |
P15Q |
probably benign |
Het |
Tmem87a |
T |
C |
2: 120,224,859 (GRCm39) |
E134G |
probably damaging |
Het |
Ubr4 |
C |
T |
4: 139,200,516 (GRCm39) |
|
probably benign |
Het |
Ugt2b37 |
C |
T |
5: 87,402,569 (GRCm39) |
V21M |
probably damaging |
Het |
Ugt2b38 |
T |
A |
5: 87,569,551 (GRCm39) |
I259F |
probably damaging |
Het |
Zfp804a |
T |
A |
2: 82,066,188 (GRCm39) |
L53Q |
probably damaging |
Het |
|
Other mutations in Pcsk5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Pcsk5
|
APN |
19 |
17,488,785 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL00423:Pcsk5
|
APN |
19 |
17,619,923 (GRCm39) |
missense |
probably benign |
0.23 |
IGL01315:Pcsk5
|
APN |
19 |
17,429,322 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01372:Pcsk5
|
APN |
19 |
17,595,108 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01738:Pcsk5
|
APN |
19 |
17,411,144 (GRCm39) |
splice site |
probably benign |
|
IGL01874:Pcsk5
|
APN |
19 |
17,573,041 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02070:Pcsk5
|
APN |
19 |
17,416,406 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02311:Pcsk5
|
APN |
19 |
17,410,784 (GRCm39) |
nonsense |
probably null |
|
IGL02436:Pcsk5
|
APN |
19 |
17,542,072 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02498:Pcsk5
|
APN |
19 |
17,488,920 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02504:Pcsk5
|
APN |
19 |
17,455,236 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02664:Pcsk5
|
APN |
19 |
17,434,134 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02735:Pcsk5
|
APN |
19 |
17,652,832 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02941:Pcsk5
|
APN |
19 |
17,424,865 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4377001:Pcsk5
|
UTSW |
19 |
17,416,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R0007:Pcsk5
|
UTSW |
19 |
17,632,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0007:Pcsk5
|
UTSW |
19 |
17,632,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:Pcsk5
|
UTSW |
19 |
17,542,179 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0032:Pcsk5
|
UTSW |
19 |
17,542,179 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0373:Pcsk5
|
UTSW |
19 |
17,632,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Pcsk5
|
UTSW |
19 |
17,692,133 (GRCm39) |
missense |
probably benign |
0.06 |
R0843:Pcsk5
|
UTSW |
19 |
17,632,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R1014:Pcsk5
|
UTSW |
19 |
17,542,194 (GRCm39) |
missense |
probably damaging |
1.00 |
R1221:Pcsk5
|
UTSW |
19 |
17,814,512 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1435:Pcsk5
|
UTSW |
19 |
17,541,246 (GRCm39) |
nonsense |
probably null |
|
R1471:Pcsk5
|
UTSW |
19 |
17,545,688 (GRCm39) |
missense |
probably damaging |
1.00 |
R1564:Pcsk5
|
UTSW |
19 |
17,632,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R1597:Pcsk5
|
UTSW |
19 |
17,413,964 (GRCm39) |
missense |
probably benign |
0.00 |
R1614:Pcsk5
|
UTSW |
19 |
17,492,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1661:Pcsk5
|
UTSW |
19 |
17,424,938 (GRCm39) |
missense |
probably damaging |
0.98 |
R1671:Pcsk5
|
UTSW |
19 |
17,432,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R1703:Pcsk5
|
UTSW |
19 |
17,729,458 (GRCm39) |
missense |
probably benign |
0.15 |
R1793:Pcsk5
|
UTSW |
19 |
17,432,114 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1855:Pcsk5
|
UTSW |
19 |
17,492,556 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1909:Pcsk5
|
UTSW |
19 |
17,410,825 (GRCm39) |
missense |
probably benign |
0.00 |
R1959:Pcsk5
|
UTSW |
19 |
17,410,782 (GRCm39) |
missense |
unknown |
|
R2006:Pcsk5
|
UTSW |
19 |
17,455,280 (GRCm39) |
missense |
probably benign |
0.32 |
R2045:Pcsk5
|
UTSW |
19 |
17,558,508 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2061:Pcsk5
|
UTSW |
19 |
17,432,236 (GRCm39) |
missense |
probably benign |
0.03 |
R2110:Pcsk5
|
UTSW |
19 |
17,450,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R2402:Pcsk5
|
UTSW |
19 |
17,452,198 (GRCm39) |
nonsense |
probably null |
|
R4115:Pcsk5
|
UTSW |
19 |
17,410,783 (GRCm39) |
missense |
unknown |
|
R4504:Pcsk5
|
UTSW |
19 |
17,429,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R4616:Pcsk5
|
UTSW |
19 |
17,538,114 (GRCm39) |
missense |
probably benign |
0.00 |
R4683:Pcsk5
|
UTSW |
19 |
17,450,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R4717:Pcsk5
|
UTSW |
19 |
17,502,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R4761:Pcsk5
|
UTSW |
19 |
17,814,512 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4789:Pcsk5
|
UTSW |
19 |
17,410,963 (GRCm39) |
missense |
probably benign |
0.09 |
R4880:Pcsk5
|
UTSW |
19 |
17,425,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Pcsk5
|
UTSW |
19 |
17,492,499 (GRCm39) |
critical splice donor site |
probably null |
|
R5114:Pcsk5
|
UTSW |
19 |
17,652,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R5116:Pcsk5
|
UTSW |
19 |
17,440,798 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5193:Pcsk5
|
UTSW |
19 |
17,542,174 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5279:Pcsk5
|
UTSW |
19 |
17,573,022 (GRCm39) |
splice site |
probably null |
|
R5334:Pcsk5
|
UTSW |
19 |
17,439,215 (GRCm39) |
missense |
probably benign |
0.00 |
R5369:Pcsk5
|
UTSW |
19 |
17,558,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R5451:Pcsk5
|
UTSW |
19 |
17,440,720 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5547:Pcsk5
|
UTSW |
19 |
17,729,488 (GRCm39) |
missense |
probably benign |
0.08 |
R5630:Pcsk5
|
UTSW |
19 |
17,553,195 (GRCm39) |
missense |
probably benign |
0.04 |
R5805:Pcsk5
|
UTSW |
19 |
17,434,193 (GRCm39) |
missense |
probably benign |
0.01 |
R6063:Pcsk5
|
UTSW |
19 |
17,432,045 (GRCm39) |
critical splice donor site |
probably null |
|
R6130:Pcsk5
|
UTSW |
19 |
17,488,920 (GRCm39) |
missense |
probably damaging |
0.99 |
R6153:Pcsk5
|
UTSW |
19 |
17,488,856 (GRCm39) |
missense |
probably damaging |
0.98 |
R6163:Pcsk5
|
UTSW |
19 |
17,450,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Pcsk5
|
UTSW |
19 |
17,814,317 (GRCm39) |
critical splice donor site |
probably null |
|
R6228:Pcsk5
|
UTSW |
19 |
17,558,631 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6426:Pcsk5
|
UTSW |
19 |
17,595,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Pcsk5
|
UTSW |
19 |
17,488,744 (GRCm39) |
missense |
probably benign |
0.00 |
R6648:Pcsk5
|
UTSW |
19 |
17,553,185 (GRCm39) |
missense |
probably damaging |
0.99 |
R6789:Pcsk5
|
UTSW |
19 |
17,434,150 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6807:Pcsk5
|
UTSW |
19 |
17,549,986 (GRCm39) |
splice site |
probably null |
|
R6837:Pcsk5
|
UTSW |
19 |
17,416,448 (GRCm39) |
missense |
probably benign |
0.01 |
R6998:Pcsk5
|
UTSW |
19 |
17,450,476 (GRCm39) |
missense |
probably benign |
0.20 |
R7051:Pcsk5
|
UTSW |
19 |
17,411,095 (GRCm39) |
missense |
probably benign |
0.00 |
R7164:Pcsk5
|
UTSW |
19 |
17,429,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R7173:Pcsk5
|
UTSW |
19 |
17,455,241 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7348:Pcsk5
|
UTSW |
19 |
17,434,182 (GRCm39) |
nonsense |
probably null |
|
R7360:Pcsk5
|
UTSW |
19 |
17,492,577 (GRCm39) |
missense |
probably benign |
0.00 |
R7407:Pcsk5
|
UTSW |
19 |
17,652,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R7447:Pcsk5
|
UTSW |
19 |
17,487,600 (GRCm39) |
missense |
probably benign |
0.31 |
R7521:Pcsk5
|
UTSW |
19 |
17,432,196 (GRCm39) |
missense |
probably benign |
0.29 |
R7525:Pcsk5
|
UTSW |
19 |
17,619,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Pcsk5
|
UTSW |
19 |
17,814,336 (GRCm39) |
missense |
probably benign |
0.01 |
R7566:Pcsk5
|
UTSW |
19 |
17,549,821 (GRCm39) |
missense |
probably benign |
|
R7631:Pcsk5
|
UTSW |
19 |
17,542,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R7654:Pcsk5
|
UTSW |
19 |
17,434,168 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7677:Pcsk5
|
UTSW |
19 |
17,558,593 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7711:Pcsk5
|
UTSW |
19 |
17,416,444 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7903:Pcsk5
|
UTSW |
19 |
17,549,847 (GRCm39) |
missense |
probably damaging |
0.98 |
R7938:Pcsk5
|
UTSW |
19 |
17,443,549 (GRCm39) |
critical splice acceptor site |
probably null |
|
R8025:Pcsk5
|
UTSW |
19 |
17,538,415 (GRCm39) |
intron |
probably benign |
|
R8032:Pcsk5
|
UTSW |
19 |
17,692,151 (GRCm39) |
missense |
probably damaging |
0.98 |
R8064:Pcsk5
|
UTSW |
19 |
17,692,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R8115:Pcsk5
|
UTSW |
19 |
17,487,530 (GRCm39) |
critical splice donor site |
probably null |
|
R8193:Pcsk5
|
UTSW |
19 |
17,563,415 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8408:Pcsk5
|
UTSW |
19 |
17,410,809 (GRCm39) |
missense |
probably benign |
0.00 |
R8466:Pcsk5
|
UTSW |
19 |
17,549,864 (GRCm39) |
nonsense |
probably null |
|
R8739:Pcsk5
|
UTSW |
19 |
17,432,138 (GRCm39) |
missense |
probably benign |
0.00 |
R8753:Pcsk5
|
UTSW |
19 |
17,446,408 (GRCm39) |
missense |
probably benign |
0.00 |
R8797:Pcsk5
|
UTSW |
19 |
17,443,472 (GRCm39) |
missense |
probably benign |
0.00 |
R8944:Pcsk5
|
UTSW |
19 |
17,452,275 (GRCm39) |
missense |
probably damaging |
0.96 |
R9041:Pcsk5
|
UTSW |
19 |
17,538,132 (GRCm39) |
nonsense |
probably null |
|
R9135:Pcsk5
|
UTSW |
19 |
17,563,472 (GRCm39) |
missense |
|
|
R9288:Pcsk5
|
UTSW |
19 |
17,814,345 (GRCm39) |
missense |
probably benign |
0.10 |
R9406:Pcsk5
|
UTSW |
19 |
17,771,097 (GRCm39) |
missense |
probably benign |
0.14 |
R9581:Pcsk5
|
UTSW |
19 |
17,432,196 (GRCm39) |
missense |
probably benign |
|
R9592:Pcsk5
|
UTSW |
19 |
17,652,899 (GRCm39) |
nonsense |
probably null |
|
R9659:Pcsk5
|
UTSW |
19 |
17,455,245 (GRCm39) |
missense |
probably benign |
0.00 |
R9788:Pcsk5
|
UTSW |
19 |
17,455,245 (GRCm39) |
missense |
probably benign |
0.00 |
X0023:Pcsk5
|
UTSW |
19 |
17,452,236 (GRCm39) |
missense |
possibly damaging |
0.66 |
X0063:Pcsk5
|
UTSW |
19 |
17,424,968 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Pcsk5
|
UTSW |
19 |
17,440,738 (GRCm39) |
missense |
probably damaging |
1.00 |
|