Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6330409D20Rik |
T |
C |
2: 32,630,559 (GRCm39) |
|
probably benign |
Het |
Ago4 |
T |
C |
4: 126,410,729 (GRCm39) |
I221V |
probably benign |
Het |
Ankfy1 |
C |
T |
11: 72,645,233 (GRCm39) |
Q771* |
probably null |
Het |
Ankrd50 |
T |
C |
3: 38,509,536 (GRCm39) |
T944A |
probably damaging |
Het |
Armh4 |
T |
C |
14: 50,008,040 (GRCm39) |
T478A |
probably damaging |
Het |
AU040320 |
A |
C |
4: 126,747,073 (GRCm39) |
|
probably null |
Het |
Axdnd1 |
A |
G |
1: 156,208,344 (GRCm39) |
|
probably null |
Het |
Cdadc1 |
A |
T |
14: 59,823,981 (GRCm39) |
D170E |
probably damaging |
Het |
Cep164 |
C |
A |
9: 45,721,123 (GRCm39) |
R93L |
probably damaging |
Het |
Cep250 |
T |
C |
2: 155,827,294 (GRCm39) |
|
probably null |
Het |
Cfdp1 |
G |
A |
8: 112,495,361 (GRCm39) |
R286* |
probably null |
Het |
Chrdl2 |
A |
G |
7: 99,682,871 (GRCm39) |
I377V |
possibly damaging |
Het |
Cntrob |
A |
T |
11: 69,198,880 (GRCm39) |
S623T |
probably benign |
Het |
Col6a5 |
C |
T |
9: 105,808,412 (GRCm39) |
G879S |
unknown |
Het |
Cyp2c38 |
T |
A |
19: 39,426,756 (GRCm39) |
I182F |
probably benign |
Het |
Dennd4a |
T |
C |
9: 64,804,618 (GRCm39) |
V1319A |
probably damaging |
Het |
Dysf |
T |
G |
6: 84,016,549 (GRCm39) |
V70G |
probably damaging |
Het |
Edn3 |
A |
G |
2: 174,603,398 (GRCm39) |
T49A |
possibly damaging |
Het |
Elac1 |
C |
G |
18: 73,872,316 (GRCm39) |
L226F |
probably damaging |
Het |
Eps8l3 |
A |
G |
3: 107,798,268 (GRCm39) |
D445G |
probably benign |
Het |
Fgf11 |
G |
T |
11: 69,692,279 (GRCm39) |
T58K |
probably benign |
Het |
Fyb2 |
A |
G |
4: 104,802,652 (GRCm39) |
R185G |
probably benign |
Het |
Gal3st2c |
G |
A |
1: 93,936,766 (GRCm39) |
R237H |
probably damaging |
Het |
Galnt15 |
G |
T |
14: 31,771,822 (GRCm39) |
R289L |
probably damaging |
Het |
Garin4 |
T |
A |
1: 190,896,631 (GRCm39) |
K4M |
possibly damaging |
Het |
Gdf5 |
T |
A |
2: 155,784,001 (GRCm39) |
D317V |
probably damaging |
Het |
Gm7808 |
A |
G |
9: 19,839,410 (GRCm39) |
|
probably benign |
Het |
Hcn3 |
T |
C |
3: 89,055,570 (GRCm39) |
E559G |
probably benign |
Het |
Hdlbp |
A |
T |
1: 93,349,959 (GRCm39) |
|
probably benign |
Het |
Hhip |
T |
C |
8: 80,701,675 (GRCm39) |
T620A |
probably benign |
Het |
Hs3st3a1 |
T |
C |
11: 64,411,268 (GRCm39) |
S269P |
probably damaging |
Het |
Il17ra |
A |
T |
6: 120,454,355 (GRCm39) |
|
probably null |
Het |
Kif2a |
T |
C |
13: 107,113,503 (GRCm39) |
N417S |
possibly damaging |
Het |
Klhl41 |
T |
A |
2: 69,504,963 (GRCm39) |
|
probably benign |
Het |
L3mbtl4 |
G |
T |
17: 68,766,800 (GRCm39) |
C169F |
probably damaging |
Het |
Lap3 |
T |
C |
5: 45,669,252 (GRCm39) |
F467S |
probably damaging |
Het |
Lpar6 |
A |
T |
14: 73,476,579 (GRCm39) |
Y180F |
probably benign |
Het |
Lrig3 |
T |
C |
10: 125,838,262 (GRCm39) |
|
probably benign |
Het |
Ltbp2 |
A |
T |
12: 84,877,432 (GRCm39) |
S378T |
probably damaging |
Het |
Ltf |
T |
C |
9: 110,851,913 (GRCm39) |
F117L |
possibly damaging |
Het |
Med16 |
T |
C |
10: 79,734,765 (GRCm39) |
E533G |
probably damaging |
Het |
Meltf |
T |
C |
16: 31,700,787 (GRCm39) |
|
probably null |
Het |
Mphosph10 |
C |
T |
7: 64,030,776 (GRCm39) |
E488K |
possibly damaging |
Het |
Mroh1 |
A |
G |
15: 76,317,585 (GRCm39) |
T812A |
probably benign |
Het |
Mto1 |
T |
C |
9: 78,368,799 (GRCm39) |
|
probably benign |
Het |
Ndst1 |
A |
T |
18: 60,845,793 (GRCm39) |
|
probably null |
Het |
Ndst4 |
T |
A |
3: 125,491,544 (GRCm39) |
|
probably null |
Het |
Nhlh1 |
A |
T |
1: 171,881,608 (GRCm39) |
I86N |
probably damaging |
Het |
Nme9 |
A |
C |
9: 99,341,827 (GRCm39) |
D59A |
probably damaging |
Het |
Nox4 |
A |
T |
7: 87,010,004 (GRCm39) |
R402* |
probably null |
Het |
Npr1 |
T |
C |
3: 90,369,495 (GRCm39) |
D410G |
probably damaging |
Het |
Nrip1 |
T |
A |
16: 76,088,927 (GRCm39) |
T877S |
probably benign |
Het |
Nsd2 |
A |
G |
5: 34,003,513 (GRCm39) |
N221S |
probably benign |
Het |
Ophn1 |
A |
T |
X: 97,769,665 (GRCm39) |
Y181* |
probably null |
Het |
Or13a28 |
A |
T |
7: 140,218,505 (GRCm39) |
D297V |
probably damaging |
Het |
Or1e17 |
C |
A |
11: 73,831,486 (GRCm39) |
P138Q |
possibly damaging |
Het |
Or4c123 |
T |
C |
2: 89,127,014 (GRCm39) |
N200S |
probably damaging |
Het |
Or51ac3 |
A |
T |
7: 103,213,814 (GRCm39) |
L224* |
probably null |
Het |
Or51f5 |
A |
T |
7: 102,424,538 (GRCm39) |
H269L |
probably benign |
Het |
Or5b109 |
T |
A |
19: 13,212,277 (GRCm39) |
I221K |
possibly damaging |
Het |
Or8c10 |
A |
T |
9: 38,279,360 (GRCm39) |
I173L |
probably benign |
Het |
Parp1 |
A |
G |
1: 180,424,904 (GRCm39) |
K819R |
probably damaging |
Het |
Parp9 |
T |
C |
16: 35,792,591 (GRCm39) |
S829P |
probably benign |
Het |
Pde6c |
T |
A |
19: 38,150,388 (GRCm39) |
F511Y |
probably damaging |
Het |
Per3 |
G |
T |
4: 151,125,883 (GRCm39) |
H145Q |
probably damaging |
Het |
Pglyrp1 |
C |
T |
7: 18,624,151 (GRCm39) |
R145W |
probably damaging |
Het |
Piezo1 |
T |
C |
8: 123,209,384 (GRCm39) |
|
probably benign |
Het |
Plb1 |
T |
C |
5: 32,444,191 (GRCm39) |
I312T |
probably benign |
Het |
Plin3 |
T |
A |
17: 56,586,824 (GRCm39) |
T408S |
possibly damaging |
Het |
Polr2a |
A |
T |
11: 69,634,772 (GRCm39) |
I636N |
probably damaging |
Het |
Pramel51 |
A |
C |
12: 88,144,030 (GRCm39) |
L261R |
probably benign |
Het |
Prb1b |
A |
T |
6: 132,291,661 (GRCm39) |
L11Q |
unknown |
Het |
Prex2 |
G |
T |
1: 11,232,590 (GRCm39) |
E886* |
probably null |
Het |
Proca1 |
A |
T |
11: 78,095,847 (GRCm39) |
I73F |
probably damaging |
Het |
Ptpn6 |
A |
G |
6: 124,705,896 (GRCm39) |
S83P |
probably benign |
Het |
Rtp1 |
G |
T |
16: 23,248,049 (GRCm39) |
V41L |
probably benign |
Het |
Scn4a |
A |
G |
11: 106,218,359 (GRCm39) |
I1035T |
probably damaging |
Het |
Sell |
A |
T |
1: 163,892,907 (GRCm39) |
Y41F |
probably damaging |
Het |
Serping1 |
C |
T |
2: 84,601,793 (GRCm39) |
V226M |
probably damaging |
Het |
Sf3b1 |
A |
T |
1: 55,037,347 (GRCm39) |
D856E |
possibly damaging |
Het |
Sfmbt1 |
T |
A |
14: 30,524,524 (GRCm39) |
Y503N |
probably damaging |
Het |
Slc16a1 |
T |
A |
3: 104,560,880 (GRCm39) |
V395D |
probably damaging |
Het |
Slc22a7 |
A |
T |
17: 46,749,157 (GRCm39) |
D53E |
probably benign |
Het |
Slc35b3 |
A |
G |
13: 39,144,587 (GRCm39) |
|
probably null |
Het |
Slc6a1 |
T |
C |
6: 114,288,815 (GRCm39) |
M274T |
possibly damaging |
Het |
Slco1a5 |
A |
G |
6: 142,187,789 (GRCm39) |
S517P |
probably benign |
Het |
Smo |
A |
G |
6: 29,736,055 (GRCm39) |
R16G |
unknown |
Het |
Srebf1 |
A |
G |
11: 60,094,312 (GRCm39) |
L601P |
probably damaging |
Het |
Sspo |
A |
G |
6: 48,436,284 (GRCm39) |
I1086M |
probably benign |
Het |
Tas2r106 |
A |
T |
6: 131,655,373 (GRCm39) |
N159K |
probably damaging |
Het |
Thsd1 |
G |
A |
8: 22,742,334 (GRCm39) |
|
probably benign |
Het |
Tmeff1 |
T |
C |
4: 48,658,938 (GRCm39) |
|
probably benign |
Het |
Tmem140 |
G |
A |
6: 34,849,838 (GRCm39) |
C118Y |
possibly damaging |
Het |
Tmem168 |
A |
G |
6: 13,583,070 (GRCm39) |
C220R |
probably benign |
Het |
Tox2 |
A |
T |
2: 163,118,087 (GRCm39) |
N129Y |
probably damaging |
Het |
Trappc12 |
C |
T |
12: 28,796,984 (GRCm39) |
E183K |
probably damaging |
Het |
Unc50 |
A |
G |
1: 37,477,880 (GRCm39) |
Y254C |
probably damaging |
Het |
Unk |
T |
G |
11: 115,949,907 (GRCm39) |
D691E |
probably benign |
Het |
Uox |
T |
A |
3: 146,316,134 (GRCm39) |
V23D |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,853,176 (GRCm39) |
C2313R |
probably benign |
Het |
Zfp804b |
T |
A |
5: 6,819,283 (GRCm39) |
H1260L |
probably damaging |
Het |
Zfyve26 |
A |
G |
12: 79,311,125 (GRCm39) |
L147P |
probably damaging |
Het |
Zmynd10 |
A |
T |
9: 107,427,236 (GRCm39) |
Q288L |
probably benign |
Het |
Zzef1 |
T |
A |
11: 72,739,540 (GRCm39) |
D662E |
probably damaging |
Het |
|
Other mutations in Fstl5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01632:Fstl5
|
APN |
3 |
76,615,135 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01658:Fstl5
|
APN |
3 |
76,389,562 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01917:Fstl5
|
APN |
3 |
76,615,153 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02073:Fstl5
|
APN |
3 |
76,566,959 (GRCm39) |
splice site |
probably benign |
|
IGL02329:Fstl5
|
APN |
3 |
76,496,302 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02651:Fstl5
|
APN |
3 |
76,500,841 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02967:Fstl5
|
APN |
3 |
76,229,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03004:Fstl5
|
APN |
3 |
76,555,738 (GRCm39) |
splice site |
probably benign |
|
IGL03107:Fstl5
|
APN |
3 |
76,443,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03113:Fstl5
|
APN |
3 |
76,337,099 (GRCm39) |
nonsense |
probably null |
|
P0038:Fstl5
|
UTSW |
3 |
76,052,369 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Fstl5
|
UTSW |
3 |
76,567,006 (GRCm39) |
missense |
probably damaging |
0.99 |
R0015:Fstl5
|
UTSW |
3 |
76,229,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R0015:Fstl5
|
UTSW |
3 |
76,229,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R0032:Fstl5
|
UTSW |
3 |
76,555,742 (GRCm39) |
splice site |
probably benign |
|
R0032:Fstl5
|
UTSW |
3 |
76,555,742 (GRCm39) |
splice site |
probably benign |
|
R0078:Fstl5
|
UTSW |
3 |
76,566,952 (GRCm39) |
splice site |
probably benign |
|
R0137:Fstl5
|
UTSW |
3 |
76,614,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R0183:Fstl5
|
UTSW |
3 |
76,229,579 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0330:Fstl5
|
UTSW |
3 |
76,615,060 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0427:Fstl5
|
UTSW |
3 |
76,615,034 (GRCm39) |
nonsense |
probably null |
|
R0687:Fstl5
|
UTSW |
3 |
76,615,119 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1642:Fstl5
|
UTSW |
3 |
76,317,929 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1765:Fstl5
|
UTSW |
3 |
76,500,783 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1996:Fstl5
|
UTSW |
3 |
76,615,141 (GRCm39) |
missense |
probably benign |
0.19 |
R2157:Fstl5
|
UTSW |
3 |
76,615,372 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2228:Fstl5
|
UTSW |
3 |
76,389,659 (GRCm39) |
missense |
probably damaging |
1.00 |
R2851:Fstl5
|
UTSW |
3 |
76,337,045 (GRCm39) |
splice site |
probably benign |
|
R4021:Fstl5
|
UTSW |
3 |
76,536,282 (GRCm39) |
missense |
probably benign |
0.00 |
R4086:Fstl5
|
UTSW |
3 |
76,555,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Fstl5
|
UTSW |
3 |
76,500,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R4829:Fstl5
|
UTSW |
3 |
76,229,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Fstl5
|
UTSW |
3 |
76,496,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R4955:Fstl5
|
UTSW |
3 |
76,131,183 (GRCm39) |
critical splice donor site |
probably null |
|
R4977:Fstl5
|
UTSW |
3 |
76,317,801 (GRCm39) |
nonsense |
probably null |
|
R5166:Fstl5
|
UTSW |
3 |
76,536,267 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5232:Fstl5
|
UTSW |
3 |
76,052,284 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5313:Fstl5
|
UTSW |
3 |
76,500,812 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5584:Fstl5
|
UTSW |
3 |
76,229,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R5647:Fstl5
|
UTSW |
3 |
76,496,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R5842:Fstl5
|
UTSW |
3 |
76,229,590 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5978:Fstl5
|
UTSW |
3 |
76,052,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R6007:Fstl5
|
UTSW |
3 |
76,317,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R6064:Fstl5
|
UTSW |
3 |
76,229,605 (GRCm39) |
missense |
probably benign |
0.13 |
R6327:Fstl5
|
UTSW |
3 |
76,615,108 (GRCm39) |
missense |
probably benign |
0.31 |
R6386:Fstl5
|
UTSW |
3 |
76,229,373 (GRCm39) |
missense |
probably benign |
0.13 |
R6523:Fstl5
|
UTSW |
3 |
76,443,641 (GRCm39) |
missense |
probably benign |
0.00 |
R6852:Fstl5
|
UTSW |
3 |
76,615,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R6861:Fstl5
|
UTSW |
3 |
76,229,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R6866:Fstl5
|
UTSW |
3 |
76,229,532 (GRCm39) |
missense |
probably damaging |
0.99 |
R7100:Fstl5
|
UTSW |
3 |
76,443,600 (GRCm39) |
missense |
probably benign |
0.11 |
R7341:Fstl5
|
UTSW |
3 |
76,389,704 (GRCm39) |
splice site |
probably null |
|
R7495:Fstl5
|
UTSW |
3 |
76,615,099 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7558:Fstl5
|
UTSW |
3 |
76,337,092 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7731:Fstl5
|
UTSW |
3 |
76,569,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R7787:Fstl5
|
UTSW |
3 |
76,337,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R7852:Fstl5
|
UTSW |
3 |
76,615,275 (GRCm39) |
missense |
probably benign |
0.00 |
R7874:Fstl5
|
UTSW |
3 |
76,569,093 (GRCm39) |
missense |
probably benign |
0.10 |
R7881:Fstl5
|
UTSW |
3 |
76,443,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Fstl5
|
UTSW |
3 |
76,337,097 (GRCm39) |
missense |
probably damaging |
0.98 |
R8039:Fstl5
|
UTSW |
3 |
76,555,725 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8050:Fstl5
|
UTSW |
3 |
76,614,810 (GRCm39) |
missense |
probably benign |
0.00 |
R8844:Fstl5
|
UTSW |
3 |
76,337,154 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8929:Fstl5
|
UTSW |
3 |
76,615,138 (GRCm39) |
missense |
probably damaging |
0.98 |
R9012:Fstl5
|
UTSW |
3 |
76,567,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Fstl5
|
UTSW |
3 |
76,615,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R9221:Fstl5
|
UTSW |
3 |
76,569,114 (GRCm39) |
missense |
probably damaging |
0.98 |
R9373:Fstl5
|
UTSW |
3 |
76,555,669 (GRCm39) |
nonsense |
probably null |
|
R9427:Fstl5
|
UTSW |
3 |
76,229,583 (GRCm39) |
missense |
|
|
R9490:Fstl5
|
UTSW |
3 |
76,615,060 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9603:Fstl5
|
UTSW |
3 |
76,496,260 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Fstl5
|
UTSW |
3 |
76,615,289 (GRCm39) |
missense |
probably damaging |
1.00 |
|