Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4833420G17Rik |
T |
A |
13: 119,622,386 (GRCm39) |
V618E |
possibly damaging |
Het |
Abca6 |
T |
C |
11: 110,103,036 (GRCm39) |
R852G |
probably benign |
Het |
Akap12 |
G |
A |
10: 4,306,685 (GRCm39) |
R1165H |
probably benign |
Het |
Asxl1 |
T |
C |
2: 153,243,826 (GRCm39) |
S1459P |
probably damaging |
Het |
Bahcc1 |
C |
T |
11: 120,176,225 (GRCm39) |
R1957C |
probably damaging |
Het |
Bcar1 |
A |
G |
8: 112,442,030 (GRCm39) |
V270A |
probably damaging |
Het |
Camsap3 |
C |
T |
8: 3,654,708 (GRCm39) |
R782C |
probably damaging |
Het |
Capn15 |
C |
A |
17: 26,183,837 (GRCm39) |
A215S |
probably benign |
Het |
Casz1 |
T |
C |
4: 149,017,415 (GRCm39) |
F235L |
probably damaging |
Het |
Ccdc57 |
A |
T |
11: 120,794,134 (GRCm39) |
|
probably benign |
Het |
Cdh23 |
A |
G |
10: 60,159,349 (GRCm39) |
V2142A |
probably damaging |
Het |
Cdx1 |
A |
G |
18: 61,152,970 (GRCm39) |
V212A |
probably benign |
Het |
Cep104 |
T |
C |
4: 154,074,296 (GRCm39) |
L516P |
possibly damaging |
Het |
Cep95 |
C |
T |
11: 106,705,464 (GRCm39) |
T483I |
probably damaging |
Het |
Cfap100 |
T |
C |
6: 90,389,329 (GRCm39) |
|
probably benign |
Het |
Chia1 |
T |
A |
3: 106,035,875 (GRCm39) |
N238K |
probably benign |
Het |
Cntrl |
T |
C |
2: 35,052,873 (GRCm39) |
M1126T |
probably benign |
Het |
Col28a1 |
A |
G |
6: 8,176,333 (GRCm39) |
F8S |
probably benign |
Het |
Cpeb3 |
C |
T |
19: 37,031,665 (GRCm39) |
R579Q |
probably damaging |
Het |
Dbh |
A |
G |
2: 27,058,234 (GRCm39) |
D134G |
probably damaging |
Het |
Diaph3 |
A |
C |
14: 86,893,921 (GRCm39) |
N29K |
probably damaging |
Het |
Dnajc2 |
A |
G |
5: 21,986,317 (GRCm39) |
|
probably null |
Het |
Ephb1 |
C |
T |
9: 101,806,577 (GRCm39) |
C819Y |
probably damaging |
Het |
Erlin1 |
T |
C |
19: 44,047,504 (GRCm39) |
Y139C |
probably damaging |
Het |
Fezf2 |
A |
T |
14: 12,343,988 (GRCm38) |
V301E |
probably damaging |
Het |
Fnbp4 |
T |
C |
2: 90,609,537 (GRCm39) |
|
probably benign |
Het |
Gal3st4 |
T |
A |
5: 138,263,672 (GRCm39) |
K442N |
probably benign |
Het |
Gas6 |
T |
C |
8: 13,527,152 (GRCm39) |
T199A |
probably benign |
Het |
Gm10644 |
G |
A |
8: 84,660,479 (GRCm39) |
|
probably benign |
Het |
Gpr88 |
G |
T |
3: 116,046,073 (GRCm39) |
S79R |
possibly damaging |
Het |
Grm4 |
A |
T |
17: 27,653,686 (GRCm39) |
C755S |
probably damaging |
Het |
Hdgfl2 |
A |
G |
17: 56,403,978 (GRCm39) |
D278G |
probably damaging |
Het |
Heatr5a |
G |
T |
12: 51,952,250 (GRCm39) |
A1130E |
probably damaging |
Het |
Heatr9 |
T |
G |
11: 83,409,035 (GRCm39) |
I171L |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,460,357 (GRCm39) |
T2209A |
probably benign |
Het |
Hsh2d |
A |
G |
8: 72,947,365 (GRCm39) |
T21A |
probably damaging |
Het |
Ing1 |
T |
A |
8: 11,611,577 (GRCm39) |
V63E |
probably damaging |
Het |
Irf4 |
A |
T |
13: 30,945,445 (GRCm39) |
Q397L |
probably benign |
Het |
Itgae |
T |
A |
11: 73,009,469 (GRCm39) |
|
probably benign |
Het |
Jrkl |
A |
T |
9: 13,245,609 (GRCm39) |
D17E |
possibly damaging |
Het |
Kcnh6 |
T |
A |
11: 105,908,270 (GRCm39) |
Y295* |
probably null |
Het |
Klf5 |
T |
C |
14: 99,539,357 (GRCm39) |
S177P |
probably benign |
Het |
Lats1 |
T |
A |
10: 7,586,221 (GRCm39) |
|
probably benign |
Het |
Lilrb4a |
A |
G |
10: 51,368,045 (GRCm39) |
I53M |
probably benign |
Het |
Lrrc2 |
T |
A |
9: 110,810,007 (GRCm39) |
Y348N |
probably damaging |
Het |
Man1c1 |
G |
C |
4: 134,430,749 (GRCm39) |
P11R |
probably damaging |
Het |
Med25 |
A |
G |
7: 44,534,046 (GRCm39) |
S245P |
probably benign |
Het |
Mlh3 |
T |
C |
12: 85,308,442 (GRCm39) |
Y1115C |
probably benign |
Het |
Mslnl |
G |
A |
17: 25,961,908 (GRCm39) |
V128M |
probably damaging |
Het |
Myh10 |
T |
C |
11: 68,681,034 (GRCm39) |
L1025P |
probably damaging |
Het |
Myof |
T |
A |
19: 37,966,141 (GRCm39) |
N393I |
probably damaging |
Het |
Naip6 |
T |
A |
13: 100,435,936 (GRCm39) |
E862D |
probably benign |
Het |
Ncald |
C |
T |
15: 37,397,324 (GRCm39) |
A119T |
probably benign |
Het |
Nipbl |
T |
C |
15: 8,373,114 (GRCm39) |
E1044G |
possibly damaging |
Het |
Nyap2 |
T |
C |
1: 81,169,602 (GRCm39) |
S120P |
probably damaging |
Het |
Oas1a |
A |
T |
5: 121,043,876 (GRCm39) |
N85K |
possibly damaging |
Het |
Or8b12i |
T |
C |
9: 20,082,324 (GRCm39) |
Y181C |
probably benign |
Het |
Pappa2 |
A |
T |
1: 158,578,133 (GRCm39) |
D1721E |
probably damaging |
Het |
Pcid2 |
A |
T |
8: 13,144,141 (GRCm39) |
|
probably null |
Het |
Pou2f2 |
C |
T |
7: 24,799,581 (GRCm39) |
A92T |
possibly damaging |
Het |
Ppp1r16a |
T |
C |
15: 76,577,268 (GRCm39) |
L212P |
probably damaging |
Het |
Ptbp3 |
A |
T |
4: 59,517,635 (GRCm39) |
L84Q |
probably damaging |
Het |
Ptgr2 |
A |
T |
12: 84,349,096 (GRCm39) |
Q145L |
probably benign |
Het |
Pudp |
T |
C |
18: 50,701,278 (GRCm39) |
N152D |
probably benign |
Het |
Rabggta |
A |
T |
14: 55,958,646 (GRCm39) |
F62L |
possibly damaging |
Het |
Rasal3 |
G |
A |
17: 32,615,324 (GRCm39) |
Q505* |
probably null |
Het |
Rbm20 |
T |
A |
19: 53,852,518 (GRCm39) |
L1166Q |
probably damaging |
Het |
Rictor |
T |
G |
15: 6,789,053 (GRCm39) |
I223R |
probably damaging |
Het |
Ripor1 |
A |
T |
8: 106,343,518 (GRCm39) |
E270D |
probably damaging |
Het |
Rorc |
T |
C |
3: 94,298,480 (GRCm39) |
C322R |
probably damaging |
Het |
Rpgrip1l |
T |
C |
8: 91,959,552 (GRCm39) |
D1116G |
probably benign |
Het |
Rsph4a |
A |
T |
10: 33,789,068 (GRCm39) |
N638Y |
probably damaging |
Het |
Scn9a |
A |
G |
2: 66,396,594 (GRCm39) |
F100L |
probably damaging |
Het |
Siglece |
A |
G |
7: 43,307,219 (GRCm39) |
V256A |
probably benign |
Het |
Slc23a2 |
A |
T |
2: 131,898,686 (GRCm39) |
L617Q |
probably damaging |
Het |
Snx9 |
T |
C |
17: 5,978,531 (GRCm39) |
I567T |
possibly damaging |
Het |
Sptan1 |
C |
G |
2: 29,901,048 (GRCm39) |
Q1425E |
probably benign |
Het |
Srd5a3 |
G |
A |
5: 76,295,552 (GRCm39) |
V81I |
probably benign |
Het |
Sugp2 |
T |
A |
8: 70,706,310 (GRCm39) |
I790K |
probably damaging |
Het |
Syde2 |
T |
G |
3: 145,720,071 (GRCm39) |
Y764* |
probably null |
Het |
Tbl1xr1 |
T |
C |
3: 22,245,074 (GRCm39) |
|
probably benign |
Het |
Tmem130 |
A |
G |
5: 144,674,666 (GRCm39) |
F353S |
probably damaging |
Het |
Tmem131 |
T |
A |
1: 36,835,347 (GRCm39) |
K1591N |
probably damaging |
Het |
Trim43c |
T |
A |
9: 88,722,670 (GRCm39) |
D105E |
probably benign |
Het |
Urb2 |
C |
A |
8: 124,756,537 (GRCm39) |
T748K |
possibly damaging |
Het |
Vmn2r18 |
T |
C |
5: 151,499,286 (GRCm39) |
N393D |
probably benign |
Het |
Zfp292 |
G |
A |
4: 34,805,100 (GRCm39) |
S2648F |
possibly damaging |
Het |
|
Other mutations in Eps8l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01420:Eps8l2
|
APN |
7 |
140,937,576 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01444:Eps8l2
|
APN |
7 |
140,941,288 (GRCm39) |
splice site |
probably benign |
|
IGL01467:Eps8l2
|
APN |
7 |
140,941,514 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01803:Eps8l2
|
APN |
7 |
140,938,143 (GRCm39) |
missense |
probably benign |
|
IGL02598:Eps8l2
|
APN |
7 |
140,934,849 (GRCm39) |
splice site |
probably benign |
|
IGL02823:Eps8l2
|
APN |
7 |
140,921,988 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03061:Eps8l2
|
APN |
7 |
140,937,148 (GRCm39) |
unclassified |
probably benign |
|
IGL03112:Eps8l2
|
APN |
7 |
140,941,649 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03251:Eps8l2
|
APN |
7 |
140,922,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Eps8l2
|
UTSW |
7 |
140,922,884 (GRCm39) |
missense |
probably benign |
0.08 |
R0133:Eps8l2
|
UTSW |
7 |
140,942,120 (GRCm39) |
missense |
unknown |
|
R0361:Eps8l2
|
UTSW |
7 |
140,936,112 (GRCm39) |
missense |
probably benign |
0.05 |
R0409:Eps8l2
|
UTSW |
7 |
140,922,893 (GRCm39) |
missense |
probably damaging |
1.00 |
R0611:Eps8l2
|
UTSW |
7 |
140,935,646 (GRCm39) |
missense |
probably damaging |
1.00 |
R1487:Eps8l2
|
UTSW |
7 |
140,941,531 (GRCm39) |
missense |
probably benign |
|
R1679:Eps8l2
|
UTSW |
7 |
140,940,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R1915:Eps8l2
|
UTSW |
7 |
140,941,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R1918:Eps8l2
|
UTSW |
7 |
140,941,637 (GRCm39) |
missense |
probably damaging |
0.99 |
R2098:Eps8l2
|
UTSW |
7 |
140,935,705 (GRCm39) |
splice site |
probably null |
|
R2170:Eps8l2
|
UTSW |
7 |
140,921,984 (GRCm39) |
missense |
probably benign |
0.02 |
R3429:Eps8l2
|
UTSW |
7 |
140,937,832 (GRCm39) |
critical splice donor site |
probably null |
|
R3734:Eps8l2
|
UTSW |
7 |
140,937,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R4296:Eps8l2
|
UTSW |
7 |
140,938,175 (GRCm39) |
nonsense |
probably null |
|
R4701:Eps8l2
|
UTSW |
7 |
140,937,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4758:Eps8l2
|
UTSW |
7 |
140,940,286 (GRCm39) |
missense |
probably damaging |
0.98 |
R5564:Eps8l2
|
UTSW |
7 |
140,936,534 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5567:Eps8l2
|
UTSW |
7 |
140,934,920 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5570:Eps8l2
|
UTSW |
7 |
140,934,920 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5735:Eps8l2
|
UTSW |
7 |
140,940,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R5893:Eps8l2
|
UTSW |
7 |
140,937,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R5905:Eps8l2
|
UTSW |
7 |
140,937,746 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5927:Eps8l2
|
UTSW |
7 |
140,936,259 (GRCm39) |
missense |
probably benign |
|
R6028:Eps8l2
|
UTSW |
7 |
140,937,746 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6248:Eps8l2
|
UTSW |
7 |
140,922,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R6631:Eps8l2
|
UTSW |
7 |
140,936,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R7152:Eps8l2
|
UTSW |
7 |
140,935,678 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7231:Eps8l2
|
UTSW |
7 |
140,940,305 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Eps8l2
|
UTSW |
7 |
140,922,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R9021:Eps8l2
|
UTSW |
7 |
140,936,117 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1177:Eps8l2
|
UTSW |
7 |
140,922,008 (GRCm39) |
missense |
probably benign |
0.02 |
|