Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5031439G07Rik |
C |
T |
15: 84,833,848 (GRCm39) |
V403I |
possibly damaging |
Het |
Actn1 |
G |
A |
12: 80,224,033 (GRCm39) |
R475C |
possibly damaging |
Het |
Adam11 |
T |
C |
11: 102,662,757 (GRCm39) |
L191P |
possibly damaging |
Het |
Adam21 |
G |
T |
12: 81,606,008 (GRCm39) |
Q585K |
probably benign |
Het |
Akap3 |
T |
C |
6: 126,841,729 (GRCm39) |
V116A |
probably benign |
Het |
Alpk1 |
A |
T |
3: 127,478,024 (GRCm39) |
Y74* |
probably null |
Het |
Alx4 |
G |
T |
2: 93,473,202 (GRCm39) |
G67C |
possibly damaging |
Het |
Ankrd17 |
A |
T |
5: 90,407,976 (GRCm39) |
C1414S |
possibly damaging |
Het |
Ankrd44 |
T |
C |
1: 54,805,550 (GRCm39) |
D170G |
probably damaging |
Het |
Arpc2 |
T |
A |
1: 74,303,531 (GRCm39) |
M266K |
probably damaging |
Het |
Atp12a |
A |
T |
14: 56,621,837 (GRCm39) |
N794I |
probably damaging |
Het |
Cabin1 |
A |
G |
10: 75,582,396 (GRCm39) |
L340P |
probably benign |
Het |
Ccer1 |
A |
T |
10: 97,529,217 (GRCm39) |
|
probably benign |
Het |
Cfap73 |
A |
T |
5: 120,772,279 (GRCm39) |
Y8N |
probably damaging |
Het |
Cfhr4 |
C |
A |
1: 139,659,415 (GRCm39) |
E705* |
probably null |
Het |
Cln3 |
T |
C |
7: 126,178,589 (GRCm39) |
T173A |
probably damaging |
Het |
Cxcl3 |
A |
T |
5: 90,934,008 (GRCm39) |
|
probably benign |
Het |
Cyp2c66 |
G |
C |
19: 39,159,401 (GRCm39) |
C284S |
probably benign |
Het |
Dnajc22 |
T |
C |
15: 98,999,187 (GRCm39) |
V124A |
probably benign |
Het |
Dync1h1 |
C |
G |
12: 110,568,173 (GRCm39) |
D45E |
probably benign |
Het |
Elmod3 |
A |
T |
6: 72,554,235 (GRCm39) |
|
probably null |
Het |
Enpp3 |
A |
C |
10: 24,649,945 (GRCm39) |
V827G |
probably damaging |
Het |
Esyt2 |
T |
C |
12: 116,327,154 (GRCm39) |
I574T |
probably benign |
Het |
Ext2 |
A |
T |
2: 93,643,957 (GRCm39) |
I108N |
probably damaging |
Het |
Fam186a |
T |
C |
15: 99,843,531 (GRCm39) |
I904M |
unknown |
Het |
Fmnl2 |
T |
C |
2: 53,004,202 (GRCm39) |
I638T |
unknown |
Het |
Fndc3c1 |
G |
C |
X: 105,478,679 (GRCm39) |
L724V |
possibly damaging |
Het |
Fras1 |
G |
T |
5: 96,925,937 (GRCm39) |
A3714S |
probably damaging |
Het |
Fsd1 |
C |
A |
17: 56,303,696 (GRCm39) |
R479S |
possibly damaging |
Het |
Gaa |
C |
T |
11: 119,169,817 (GRCm39) |
L624F |
probably damaging |
Het |
Galnt2 |
G |
A |
8: 125,032,292 (GRCm39) |
V86I |
probably benign |
Het |
Gdap1l1 |
T |
G |
2: 163,280,608 (GRCm39) |
V48G |
probably damaging |
Het |
Gm10549 |
A |
G |
18: 33,597,462 (GRCm39) |
T83A |
unknown |
Het |
Gm11437 |
T |
G |
11: 84,055,374 (GRCm39) |
T81P |
probably benign |
Het |
Gm16253 |
T |
C |
3: 96,487,979 (GRCm39) |
|
probably null |
Het |
Gprc6a |
A |
T |
10: 51,504,595 (GRCm39) |
M83K |
probably benign |
Het |
Grik5 |
T |
C |
7: 24,767,587 (GRCm39) |
D31G |
probably damaging |
Het |
Hcrtr2 |
A |
G |
9: 76,167,013 (GRCm39) |
L108P |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,853,575 (GRCm39) |
L3689Q |
probably damaging |
Het |
Igf2bp1 |
T |
C |
11: 95,859,290 (GRCm39) |
M407V |
probably benign |
Het |
Irgq |
A |
T |
7: 24,233,185 (GRCm39) |
E342V |
probably damaging |
Het |
Itih2 |
A |
T |
2: 10,109,974 (GRCm39) |
I593N |
probably damaging |
Het |
Ivd |
G |
T |
2: 118,701,870 (GRCm39) |
G101C |
probably damaging |
Het |
Jakmip1 |
G |
A |
5: 37,248,708 (GRCm39) |
G123S |
probably damaging |
Het |
Kif14 |
T |
A |
1: 136,406,908 (GRCm39) |
I580N |
probably damaging |
Het |
Kmt2e |
A |
T |
5: 23,669,855 (GRCm39) |
Y114F |
probably damaging |
Het |
Ly6g5b |
C |
A |
17: 35,333,680 (GRCm39) |
C99F |
probably damaging |
Het |
Map3k20 |
C |
T |
2: 72,271,758 (GRCm39) |
P629S |
probably benign |
Het |
Mpl |
A |
G |
4: 118,305,741 (GRCm39) |
|
probably null |
Het |
Muc4 |
T |
C |
16: 32,582,862 (GRCm39) |
F476L |
probably damaging |
Het |
Mup18 |
T |
C |
4: 61,590,199 (GRCm39) |
T110A |
probably benign |
Het |
Nlrp9a |
A |
G |
7: 26,257,603 (GRCm39) |
D407G |
probably benign |
Het |
Nmur1 |
G |
A |
1: 86,314,190 (GRCm39) |
R359C |
probably benign |
Het |
Or5ac24 |
T |
C |
16: 59,165,510 (GRCm39) |
T185A |
probably benign |
Het |
Or5p64 |
C |
T |
7: 107,854,955 (GRCm39) |
C130Y |
possibly damaging |
Het |
Panx3 |
A |
T |
9: 37,572,596 (GRCm39) |
M318K |
probably damaging |
Het |
Pcnx1 |
T |
C |
12: 81,999,777 (GRCm39) |
|
probably null |
Het |
Psme3ip1 |
A |
T |
8: 95,315,486 (GRCm39) |
F15L |
probably damaging |
Het |
Rere |
G |
A |
4: 150,553,195 (GRCm39) |
R129H |
probably damaging |
Het |
Rpgrip1 |
A |
G |
14: 52,349,633 (GRCm39) |
Y7C |
possibly damaging |
Het |
Serpina6 |
T |
C |
12: 103,613,253 (GRCm39) |
N349S |
possibly damaging |
Het |
Slc10a1 |
T |
G |
12: 81,002,750 (GRCm39) |
E296A |
probably damaging |
Het |
Slc2a9 |
A |
T |
5: 38,610,214 (GRCm39) |
|
probably null |
Het |
Sptan1 |
T |
A |
2: 29,873,221 (GRCm39) |
M138K |
probably benign |
Het |
Tbl3 |
T |
C |
17: 24,924,233 (GRCm39) |
T175A |
probably benign |
Het |
Tbrg4 |
T |
C |
11: 6,570,810 (GRCm39) |
T221A |
possibly damaging |
Het |
Tenm2 |
T |
C |
11: 35,932,378 (GRCm39) |
T1739A |
probably damaging |
Het |
Tmed5 |
T |
C |
5: 108,280,187 (GRCm39) |
D35G |
probably benign |
Het |
Tnfsf15 |
A |
T |
4: 63,647,889 (GRCm39) |
S250R |
probably damaging |
Het |
Tnpo2 |
G |
T |
8: 85,781,707 (GRCm39) |
V830F |
probably benign |
Het |
Ttbk2 |
G |
T |
2: 120,570,592 (GRCm39) |
S1187Y |
probably damaging |
Het |
Ttn |
G |
A |
2: 76,625,029 (GRCm39) |
T15183M |
possibly damaging |
Het |
Tubgcp3 |
T |
C |
8: 12,689,259 (GRCm39) |
|
probably null |
Het |
Vmn1r38 |
T |
C |
6: 66,753,278 (GRCm39) |
I279M |
possibly damaging |
Het |
Vmn1r49 |
A |
T |
6: 90,049,250 (GRCm39) |
Y251N |
possibly damaging |
Het |
Vmn1r66 |
C |
T |
7: 10,008,482 (GRCm39) |
V184I |
probably benign |
Het |
Vmn2r26 |
T |
A |
6: 124,038,255 (GRCm39) |
M610K |
probably benign |
Het |
Xrn2 |
C |
T |
2: 146,884,013 (GRCm39) |
P591S |
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 |
|
R2496:Pcsk5
|
UTSW |
19 |
17,443,522 (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 |
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 |
|