Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acads |
A |
T |
5: 115,250,331 (GRCm39) |
F198I |
probably damaging |
Het |
Acy1 |
A |
G |
9: 106,314,826 (GRCm39) |
|
probably null |
Het |
Adk |
A |
G |
14: 21,126,376 (GRCm39) |
M1V |
probably null |
Het |
Ahi1 |
A |
G |
10: 20,839,590 (GRCm39) |
D167G |
probably benign |
Het |
Ankrd16 |
T |
C |
2: 11,791,054 (GRCm39) |
V290A |
possibly damaging |
Het |
Arhgef5 |
T |
A |
6: 43,251,351 (GRCm39) |
S701T |
possibly damaging |
Het |
Atp13a5 |
C |
A |
16: 29,100,769 (GRCm39) |
M673I |
probably damaging |
Het |
BC005624 |
T |
C |
2: 30,868,940 (GRCm39) |
D78G |
possibly damaging |
Het |
Bcat2 |
C |
T |
7: 45,238,745 (GRCm39) |
H347Y |
probably damaging |
Het |
Bpifb4 |
A |
G |
2: 153,784,547 (GRCm39) |
Y85C |
possibly damaging |
Het |
Cdc42 |
T |
A |
4: 137,049,932 (GRCm39) |
|
probably null |
Het |
Cep170 |
G |
A |
1: 176,589,003 (GRCm39) |
L541F |
possibly damaging |
Het |
Cfap97d2 |
CA |
CAA |
8: 13,784,865 (GRCm39) |
|
probably null |
Het |
Cgrrf1 |
T |
A |
14: 47,091,179 (GRCm39) |
N234K |
probably benign |
Het |
Ctrc |
C |
T |
4: 141,568,879 (GRCm39) |
C108Y |
probably damaging |
Het |
Cyp2u1 |
C |
T |
3: 131,091,945 (GRCm39) |
V192M |
possibly damaging |
Het |
Dhx38 |
A |
T |
8: 110,279,307 (GRCm39) |
L1013Q |
probably damaging |
Het |
Dnah1 |
T |
A |
14: 31,009,733 (GRCm39) |
N1945I |
probably damaging |
Het |
Dnah10 |
C |
G |
5: 124,898,514 (GRCm39) |
N3765K |
possibly damaging |
Het |
Dnah17 |
C |
A |
11: 117,950,905 (GRCm39) |
R2906L |
possibly damaging |
Het |
Dnajc10 |
C |
T |
2: 80,161,680 (GRCm39) |
T306I |
probably benign |
Het |
Efemp2 |
T |
A |
19: 5,530,273 (GRCm39) |
C287S |
probably damaging |
Het |
Efna1 |
T |
C |
3: 89,180,091 (GRCm39) |
R143G |
probably benign |
Het |
Emilin1 |
A |
C |
5: 31,074,421 (GRCm39) |
N221H |
probably damaging |
Het |
Fam184b |
T |
A |
5: 45,690,243 (GRCm39) |
|
probably null |
Het |
Fchsd2 |
T |
A |
7: 100,926,621 (GRCm39) |
C570* |
probably null |
Het |
Gm4787 |
A |
T |
12: 81,425,974 (GRCm39) |
D61E |
probably benign |
Het |
Gm7356 |
C |
T |
17: 14,221,925 (GRCm39) |
G35R |
probably damaging |
Het |
Gm8220 |
A |
G |
14: 44,525,645 (GRCm39) |
T20A |
probably damaging |
Het |
Hivep2 |
C |
T |
10: 14,004,245 (GRCm39) |
T281M |
probably damaging |
Het |
Ighv2-9-1 |
A |
G |
12: 113,733,692 (GRCm39) |
V43A |
probably damaging |
Het |
Klhl33 |
A |
T |
14: 51,129,373 (GRCm39) |
C619S |
probably benign |
Het |
Kmt2a |
A |
T |
9: 44,740,558 (GRCm39) |
|
probably benign |
Het |
Lax1 |
A |
G |
1: 133,607,896 (GRCm39) |
C282R |
probably benign |
Het |
Lrrd1 |
A |
G |
5: 3,901,395 (GRCm39) |
K567E |
probably benign |
Het |
Luzp1 |
C |
T |
4: 136,268,124 (GRCm39) |
R116* |
probably null |
Het |
Lypd3 |
G |
C |
7: 24,337,858 (GRCm39) |
G75R |
probably damaging |
Het |
Macrod2 |
A |
T |
2: 140,261,833 (GRCm39) |
N38I |
probably damaging |
Het |
Map3k14 |
A |
T |
11: 103,132,958 (GRCm39) |
I80N |
probably damaging |
Het |
Mcm9 |
A |
G |
10: 53,496,299 (GRCm39) |
S368P |
probably benign |
Het |
Mfge8 |
T |
C |
7: 78,793,049 (GRCm39) |
D139G |
probably benign |
Het |
Mmp19 |
A |
T |
10: 128,627,523 (GRCm39) |
I54F |
probably benign |
Het |
Myo15a |
G |
T |
11: 60,390,320 (GRCm39) |
W2114L |
probably damaging |
Het |
Myo1a |
G |
T |
10: 127,546,327 (GRCm39) |
V277L |
probably benign |
Het |
Myoc |
A |
G |
1: 162,466,915 (GRCm39) |
D28G |
probably damaging |
Het |
Myrf |
G |
T |
19: 10,196,924 (GRCm39) |
N487K |
probably damaging |
Het |
Omd |
T |
A |
13: 49,743,710 (GRCm39) |
F253L |
probably damaging |
Het |
Or2ag19 |
G |
T |
7: 106,444,009 (GRCm39) |
G64* |
probably null |
Het |
Or5t5 |
C |
G |
2: 86,616,499 (GRCm39) |
L142V |
probably damaging |
Het |
Or6n1 |
G |
A |
1: 173,917,316 (GRCm39) |
A237T |
probably damaging |
Het |
Papss1 |
T |
G |
3: 131,305,732 (GRCm39) |
I238S |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,632,675 (GRCm39) |
F580Y |
probably benign |
Het |
Polk |
T |
A |
13: 96,653,189 (GRCm39) |
K70N |
probably damaging |
Het |
Ppig |
T |
A |
2: 69,562,755 (GRCm39) |
D31E |
probably benign |
Het |
Ppp6r1 |
G |
T |
7: 4,636,291 (GRCm39) |
S766R |
possibly damaging |
Het |
Rab11fip5 |
T |
C |
6: 85,318,540 (GRCm39) |
D783G |
probably benign |
Het |
Reln |
T |
C |
5: 22,190,855 (GRCm39) |
I1511V |
probably benign |
Het |
Rnh1 |
T |
C |
7: 140,743,096 (GRCm39) |
N268S |
probably damaging |
Het |
Rpia |
A |
G |
6: 70,750,424 (GRCm39) |
V236A |
probably benign |
Het |
Rpl10a |
G |
T |
17: 28,548,424 (GRCm39) |
V80L |
probably benign |
Het |
Sap130 |
T |
G |
18: 31,799,407 (GRCm39) |
S295A |
possibly damaging |
Het |
Sgms1 |
C |
T |
19: 32,120,193 (GRCm39) |
V238I |
probably benign |
Het |
Sh3tc1 |
A |
G |
5: 35,864,778 (GRCm39) |
S470P |
probably benign |
Het |
Slc25a32 |
A |
G |
15: 38,960,984 (GRCm39) |
V233A |
possibly damaging |
Het |
Slc2a2 |
T |
C |
3: 28,771,668 (GRCm39) |
S158P |
probably benign |
Het |
Slc6a2 |
A |
G |
8: 93,722,653 (GRCm39) |
Y550C |
probably benign |
Het |
Slc7a9 |
C |
A |
7: 35,151,936 (GRCm39) |
T77K |
probably benign |
Het |
Snd1 |
A |
T |
6: 28,626,100 (GRCm39) |
D385V |
probably benign |
Het |
Ssh3 |
A |
T |
19: 4,314,448 (GRCm39) |
F369I |
probably damaging |
Het |
Syk |
A |
G |
13: 52,766,495 (GRCm39) |
|
probably null |
Het |
Tbc1d16 |
A |
G |
11: 119,099,742 (GRCm39) |
S211P |
probably damaging |
Het |
Ttc3 |
A |
G |
16: 94,244,312 (GRCm39) |
T1439A |
probably benign |
Het |
Usp18 |
A |
G |
6: 121,229,473 (GRCm39) |
M31V |
probably benign |
Het |
Vav1 |
G |
T |
17: 57,609,330 (GRCm39) |
E415D |
possibly damaging |
Het |
Vps13a |
A |
T |
19: 16,655,439 (GRCm39) |
V1863D |
probably benign |
Het |
Xdh |
T |
A |
17: 74,229,557 (GRCm39) |
I299F |
probably damaging |
Het |
Zc3h14 |
A |
G |
12: 98,737,336 (GRCm39) |
|
probably benign |
Het |
Zfp345 |
G |
A |
2: 150,315,331 (GRCm39) |
H69Y |
probably damaging |
Het |
Zfp652 |
G |
T |
11: 95,654,667 (GRCm39) |
V357L |
probably benign |
Het |
Zfp712 |
A |
T |
13: 67,188,891 (GRCm39) |
Y545* |
probably null |
Het |
Zgrf1 |
T |
C |
3: 127,353,281 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Epg5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01680:Epg5
|
APN |
18 |
78,055,956 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01778:Epg5
|
APN |
18 |
78,062,489 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01936:Epg5
|
APN |
18 |
78,028,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02189:Epg5
|
APN |
18 |
78,056,085 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02323:Epg5
|
APN |
18 |
78,056,047 (GRCm39) |
nonsense |
probably null |
|
IGL02567:Epg5
|
APN |
18 |
78,076,288 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02805:Epg5
|
APN |
18 |
78,073,406 (GRCm39) |
splice site |
probably benign |
|
IGL03282:Epg5
|
APN |
18 |
78,029,641 (GRCm39) |
missense |
probably benign |
0.25 |
stitch
|
UTSW |
18 |
77,991,514 (GRCm39) |
nonsense |
probably null |
|
R0011:Epg5
|
UTSW |
18 |
77,991,698 (GRCm39) |
missense |
probably benign |
|
R0172:Epg5
|
UTSW |
18 |
78,070,574 (GRCm39) |
missense |
probably benign |
0.00 |
R0335:Epg5
|
UTSW |
18 |
78,029,687 (GRCm39) |
missense |
probably benign |
0.25 |
R0380:Epg5
|
UTSW |
18 |
78,004,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:Epg5
|
UTSW |
18 |
78,066,486 (GRCm39) |
splice site |
probably benign |
|
R0443:Epg5
|
UTSW |
18 |
77,999,118 (GRCm39) |
splice site |
probably benign |
|
R0445:Epg5
|
UTSW |
18 |
78,057,399 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0448:Epg5
|
UTSW |
18 |
78,066,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R0892:Epg5
|
UTSW |
18 |
78,011,843 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1081:Epg5
|
UTSW |
18 |
78,002,748 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1183:Epg5
|
UTSW |
18 |
78,003,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R1374:Epg5
|
UTSW |
18 |
78,024,541 (GRCm39) |
missense |
probably benign |
|
R1428:Epg5
|
UTSW |
18 |
78,005,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R1727:Epg5
|
UTSW |
18 |
78,059,030 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1780:Epg5
|
UTSW |
18 |
78,067,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R1801:Epg5
|
UTSW |
18 |
78,026,705 (GRCm39) |
missense |
possibly damaging |
0.63 |
R1864:Epg5
|
UTSW |
18 |
78,018,246 (GRCm39) |
missense |
probably damaging |
0.99 |
R1908:Epg5
|
UTSW |
18 |
78,002,247 (GRCm39) |
missense |
probably benign |
0.26 |
R1909:Epg5
|
UTSW |
18 |
78,002,247 (GRCm39) |
missense |
probably benign |
0.26 |
R1916:Epg5
|
UTSW |
18 |
78,008,236 (GRCm39) |
missense |
probably benign |
0.00 |
R1986:Epg5
|
UTSW |
18 |
78,025,521 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2048:Epg5
|
UTSW |
18 |
78,067,202 (GRCm39) |
missense |
probably damaging |
0.98 |
R2080:Epg5
|
UTSW |
18 |
77,991,960 (GRCm39) |
missense |
probably benign |
0.01 |
R2106:Epg5
|
UTSW |
18 |
78,034,578 (GRCm39) |
nonsense |
probably null |
|
R2144:Epg5
|
UTSW |
18 |
77,997,412 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2151:Epg5
|
UTSW |
18 |
78,070,517 (GRCm39) |
missense |
probably benign |
|
R2217:Epg5
|
UTSW |
18 |
77,992,287 (GRCm39) |
missense |
probably benign |
|
R2424:Epg5
|
UTSW |
18 |
78,011,828 (GRCm39) |
missense |
probably benign |
0.05 |
R2909:Epg5
|
UTSW |
18 |
78,026,691 (GRCm39) |
missense |
probably damaging |
1.00 |
R3725:Epg5
|
UTSW |
18 |
78,060,894 (GRCm39) |
missense |
probably benign |
0.00 |
R3899:Epg5
|
UTSW |
18 |
78,000,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R4019:Epg5
|
UTSW |
18 |
78,073,665 (GRCm39) |
missense |
probably damaging |
0.98 |
R4260:Epg5
|
UTSW |
18 |
78,058,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R4260:Epg5
|
UTSW |
18 |
78,002,336 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4448:Epg5
|
UTSW |
18 |
78,005,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R4475:Epg5
|
UTSW |
18 |
77,991,723 (GRCm39) |
missense |
probably benign |
|
R4612:Epg5
|
UTSW |
18 |
78,025,629 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4666:Epg5
|
UTSW |
18 |
78,056,079 (GRCm39) |
missense |
probably benign |
0.45 |
R4767:Epg5
|
UTSW |
18 |
78,066,498 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4779:Epg5
|
UTSW |
18 |
78,034,580 (GRCm39) |
missense |
probably benign |
0.01 |
R4791:Epg5
|
UTSW |
18 |
77,992,211 (GRCm39) |
nonsense |
probably null |
|
R4797:Epg5
|
UTSW |
18 |
78,073,614 (GRCm39) |
missense |
probably benign |
0.00 |
R4812:Epg5
|
UTSW |
18 |
78,022,399 (GRCm39) |
missense |
probably benign |
0.01 |
R4899:Epg5
|
UTSW |
18 |
78,028,272 (GRCm39) |
missense |
probably damaging |
1.00 |
R5000:Epg5
|
UTSW |
18 |
77,997,376 (GRCm39) |
missense |
probably benign |
|
R5031:Epg5
|
UTSW |
18 |
78,072,163 (GRCm39) |
missense |
probably benign |
0.00 |
R5050:Epg5
|
UTSW |
18 |
78,019,156 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5114:Epg5
|
UTSW |
18 |
78,038,828 (GRCm39) |
missense |
probably benign |
|
R5144:Epg5
|
UTSW |
18 |
78,058,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R5209:Epg5
|
UTSW |
18 |
77,994,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R5213:Epg5
|
UTSW |
18 |
78,058,049 (GRCm39) |
missense |
probably benign |
0.01 |
R5270:Epg5
|
UTSW |
18 |
78,026,778 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5324:Epg5
|
UTSW |
18 |
78,005,660 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5443:Epg5
|
UTSW |
18 |
78,070,712 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5503:Epg5
|
UTSW |
18 |
77,994,422 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5593:Epg5
|
UTSW |
18 |
78,000,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R5718:Epg5
|
UTSW |
18 |
78,029,618 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Epg5
|
UTSW |
18 |
78,004,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R5828:Epg5
|
UTSW |
18 |
78,064,066 (GRCm39) |
missense |
probably damaging |
0.99 |
R5847:Epg5
|
UTSW |
18 |
78,073,270 (GRCm39) |
missense |
probably benign |
0.06 |
R5858:Epg5
|
UTSW |
18 |
77,991,514 (GRCm39) |
nonsense |
probably null |
|
R5914:Epg5
|
UTSW |
18 |
78,002,847 (GRCm39) |
critical splice donor site |
probably null |
|
R6124:Epg5
|
UTSW |
18 |
78,073,260 (GRCm39) |
missense |
probably benign |
|
R6228:Epg5
|
UTSW |
18 |
77,991,677 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6252:Epg5
|
UTSW |
18 |
78,028,382 (GRCm39) |
missense |
probably damaging |
1.00 |
R6269:Epg5
|
UTSW |
18 |
77,991,585 (GRCm39) |
missense |
probably benign |
|
R6312:Epg5
|
UTSW |
18 |
78,022,426 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6320:Epg5
|
UTSW |
18 |
78,005,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R6328:Epg5
|
UTSW |
18 |
78,072,179 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6430:Epg5
|
UTSW |
18 |
78,019,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6458:Epg5
|
UTSW |
18 |
77,991,469 (GRCm39) |
missense |
probably benign |
0.03 |
R6852:Epg5
|
UTSW |
18 |
78,056,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R6915:Epg5
|
UTSW |
18 |
78,022,380 (GRCm39) |
missense |
probably benign |
0.00 |
R6930:Epg5
|
UTSW |
18 |
78,057,378 (GRCm39) |
missense |
probably damaging |
0.99 |
R7127:Epg5
|
UTSW |
18 |
78,072,140 (GRCm39) |
missense |
probably damaging |
1.00 |
R7207:Epg5
|
UTSW |
18 |
77,992,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R7225:Epg5
|
UTSW |
18 |
78,055,917 (GRCm39) |
missense |
probably benign |
0.45 |
R7358:Epg5
|
UTSW |
18 |
78,002,252 (GRCm39) |
missense |
possibly damaging |
0.78 |
R7414:Epg5
|
UTSW |
18 |
78,026,747 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7437:Epg5
|
UTSW |
18 |
78,066,493 (GRCm39) |
missense |
probably benign |
0.01 |
R7535:Epg5
|
UTSW |
18 |
78,076,141 (GRCm39) |
missense |
probably benign |
0.18 |
R7586:Epg5
|
UTSW |
18 |
78,073,275 (GRCm39) |
missense |
probably benign |
|
R7651:Epg5
|
UTSW |
18 |
78,024,615 (GRCm39) |
nonsense |
probably null |
|
R7715:Epg5
|
UTSW |
18 |
78,011,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R7753:Epg5
|
UTSW |
18 |
77,991,560 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7981:Epg5
|
UTSW |
18 |
78,052,929 (GRCm39) |
critical splice donor site |
probably null |
|
R8114:Epg5
|
UTSW |
18 |
78,073,365 (GRCm39) |
missense |
probably benign |
0.41 |
R8124:Epg5
|
UTSW |
18 |
78,008,211 (GRCm39) |
missense |
probably benign |
0.05 |
R8307:Epg5
|
UTSW |
18 |
78,065,894 (GRCm39) |
missense |
probably damaging |
1.00 |
R8458:Epg5
|
UTSW |
18 |
77,991,946 (GRCm39) |
missense |
probably benign |
0.00 |
R8751:Epg5
|
UTSW |
18 |
78,008,225 (GRCm39) |
missense |
probably benign |
0.28 |
R8751:Epg5
|
UTSW |
18 |
78,008,224 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8751:Epg5
|
UTSW |
18 |
78,008,223 (GRCm39) |
missense |
probably benign |
0.07 |
R8888:Epg5
|
UTSW |
18 |
78,056,086 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8971:Epg5
|
UTSW |
18 |
78,022,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R9045:Epg5
|
UTSW |
18 |
77,992,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R9291:Epg5
|
UTSW |
18 |
78,056,065 (GRCm39) |
nonsense |
probably null |
|
R9327:Epg5
|
UTSW |
18 |
77,991,435 (GRCm39) |
missense |
probably benign |
0.00 |
R9365:Epg5
|
UTSW |
18 |
77,997,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R9742:Epg5
|
UTSW |
18 |
78,024,170 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Epg5
|
UTSW |
18 |
78,011,872 (GRCm39) |
missense |
probably damaging |
0.99 |
X0060:Epg5
|
UTSW |
18 |
78,005,700 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1088:Epg5
|
UTSW |
18 |
78,002,354 (GRCm39) |
missense |
probably benign |
0.00 |
|