Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933409G03Rik |
G |
A |
2: 68,432,137 (GRCm39) |
E74K |
unknown |
Het |
Adam10 |
A |
T |
9: 70,647,399 (GRCm39) |
H176L |
probably benign |
Het |
Anapc5 |
C |
T |
5: 122,926,476 (GRCm39) |
E621K |
probably damaging |
Het |
Asf1a |
T |
A |
10: 53,482,266 (GRCm39) |
L26Q |
probably damaging |
Het |
Atxn1l |
A |
G |
8: 110,458,264 (GRCm39) |
L666P |
probably damaging |
Het |
Cep290 |
G |
A |
10: 100,373,515 (GRCm39) |
R1265H |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,441,888 (GRCm39) |
|
probably null |
Het |
Ctse |
T |
A |
1: 131,600,251 (GRCm39) |
Y333* |
probably null |
Het |
Diras2 |
C |
T |
13: 52,661,786 (GRCm39) |
V174M |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,070,209 (GRCm39) |
V1532D |
possibly damaging |
Het |
Dnai7 |
A |
T |
6: 145,123,157 (GRCm39) |
W570R |
probably damaging |
Het |
Ercc6 |
G |
A |
14: 32,238,916 (GRCm39) |
M1I |
probably null |
Het |
Fbxl4 |
A |
G |
4: 22,386,017 (GRCm39) |
E208G |
probably damaging |
Het |
Fstl4 |
G |
T |
11: 52,959,374 (GRCm39) |
M138I |
probably benign |
Het |
Galnt17 |
T |
A |
5: 130,929,466 (GRCm39) |
Q447L |
probably benign |
Het |
H2-Q7 |
T |
A |
17: 35,658,916 (GRCm39) |
C122* |
probably null |
Het |
Herpud1 |
C |
T |
8: 95,116,041 (GRCm39) |
L69F |
probably damaging |
Het |
Hnrnpa3 |
A |
G |
2: 75,495,584 (GRCm39) |
Y365C |
probably benign |
Het |
Kif13a |
A |
G |
13: 46,986,212 (GRCm39) |
Y38H |
probably damaging |
Het |
Klk1b21 |
A |
G |
7: 43,755,100 (GRCm39) |
I132V |
probably benign |
Het |
Lamb2 |
T |
C |
9: 108,365,001 (GRCm39) |
S1252P |
possibly damaging |
Het |
Lct |
T |
A |
1: 128,214,414 (GRCm39) |
D1786V |
probably damaging |
Het |
Lrig2 |
T |
A |
3: 104,368,873 (GRCm39) |
M572L |
probably benign |
Het |
Lrp1 |
C |
T |
10: 127,408,813 (GRCm39) |
V1710I |
possibly damaging |
Het |
Mmp12 |
C |
A |
9: 7,353,000 (GRCm39) |
S250R |
probably benign |
Het |
Mycbp2 |
T |
C |
14: 103,479,615 (GRCm39) |
D1226G |
probably damaging |
Het |
Myocd |
A |
G |
11: 65,069,575 (GRCm39) |
I755T |
possibly damaging |
Het |
Nup210l |
T |
C |
3: 90,081,677 (GRCm39) |
L1003P |
probably damaging |
Het |
Or11h23 |
G |
A |
14: 50,948,324 (GRCm39) |
C179Y |
probably damaging |
Het |
Or1af1 |
T |
C |
2: 37,109,777 (GRCm39) |
I92T |
possibly damaging |
Het |
Or52e8b |
A |
T |
7: 104,674,184 (GRCm39) |
M1K |
probably null |
Het |
Palmd |
T |
A |
3: 116,717,481 (GRCm39) |
M339L |
probably benign |
Het |
Phtf1 |
T |
A |
3: 103,898,491 (GRCm39) |
N307K |
probably benign |
Het |
Ppp2r3c |
T |
C |
12: 55,335,411 (GRCm39) |
I243V |
probably benign |
Het |
Ptafr |
A |
G |
4: 132,306,646 (GRCm39) |
E12G |
probably damaging |
Het |
Rpgrip1 |
T |
A |
14: 52,378,042 (GRCm39) |
N463K |
probably benign |
Het |
Sgcb |
T |
C |
5: 73,801,748 (GRCm39) |
N39S |
probably damaging |
Het |
Skint5 |
A |
G |
4: 113,799,700 (GRCm39) |
|
probably null |
Het |
Slc45a2 |
C |
T |
15: 11,027,871 (GRCm39) |
T480I |
probably damaging |
Het |
Slfn8 |
C |
A |
11: 82,895,042 (GRCm39) |
S588I |
probably damaging |
Het |
Tcea2 |
A |
G |
2: 181,322,227 (GRCm39) |
I10V |
probably damaging |
Het |
Tlr3 |
C |
T |
8: 45,851,851 (GRCm39) |
D349N |
possibly damaging |
Het |
Top2a |
C |
T |
11: 98,913,202 (GRCm39) |
V77I |
probably benign |
Het |
Vps51 |
T |
G |
19: 6,121,063 (GRCm39) |
E283D |
probably benign |
Het |
Vrk1 |
A |
G |
12: 106,018,024 (GRCm39) |
K98E |
possibly damaging |
Het |
Zcchc2 |
C |
T |
1: 105,958,322 (GRCm39) |
T931I |
possibly damaging |
Het |
Zfc3h1 |
T |
A |
10: 115,246,598 (GRCm39) |
L895H |
probably damaging |
Het |
Zfp101 |
T |
C |
17: 33,601,318 (GRCm39) |
E108G |
probably benign |
Het |
Zfp609 |
A |
G |
9: 65,610,137 (GRCm39) |
V942A |
probably benign |
Het |
|
Other mutations in Ino80 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01402:Ino80
|
APN |
2 |
119,287,199 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01404:Ino80
|
APN |
2 |
119,287,199 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01985:Ino80
|
APN |
2 |
119,263,802 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02039:Ino80
|
APN |
2 |
119,210,554 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02187:Ino80
|
APN |
2 |
119,275,938 (GRCm39) |
splice site |
probably benign |
|
IGL02726:Ino80
|
APN |
2 |
119,272,964 (GRCm39) |
missense |
probably damaging |
1.00 |
Chosen
|
UTSW |
2 |
119,212,750 (GRCm39) |
splice site |
probably null |
|
PIT4677001:Ino80
|
UTSW |
2 |
119,208,026 (GRCm39) |
missense |
probably benign |
|
R0004:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0004:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0057:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0114:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0115:Ino80
|
UTSW |
2 |
119,261,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R0138:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0189:Ino80
|
UTSW |
2 |
119,210,160 (GRCm39) |
missense |
probably benign |
0.36 |
R0363:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0364:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0365:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0481:Ino80
|
UTSW |
2 |
119,261,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Ino80
|
UTSW |
2 |
119,212,464 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0580:Ino80
|
UTSW |
2 |
119,213,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0610:Ino80
|
UTSW |
2 |
119,213,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R0675:Ino80
|
UTSW |
2 |
119,213,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R1275:Ino80
|
UTSW |
2 |
119,257,536 (GRCm39) |
missense |
probably benign |
0.12 |
R1470:Ino80
|
UTSW |
2 |
119,210,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Ino80
|
UTSW |
2 |
119,210,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R1506:Ino80
|
UTSW |
2 |
119,255,746 (GRCm39) |
nonsense |
probably null |
|
R1510:Ino80
|
UTSW |
2 |
119,280,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R1570:Ino80
|
UTSW |
2 |
119,277,509 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1613:Ino80
|
UTSW |
2 |
119,223,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1673:Ino80
|
UTSW |
2 |
119,212,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R1773:Ino80
|
UTSW |
2 |
119,248,890 (GRCm39) |
missense |
probably benign |
0.18 |
R1795:Ino80
|
UTSW |
2 |
119,237,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Ino80
|
UTSW |
2 |
119,257,151 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2105:Ino80
|
UTSW |
2 |
119,262,410 (GRCm39) |
missense |
probably null |
1.00 |
R2113:Ino80
|
UTSW |
2 |
119,284,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R3618:Ino80
|
UTSW |
2 |
119,277,353 (GRCm39) |
missense |
probably null |
0.81 |
R4572:Ino80
|
UTSW |
2 |
119,232,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Ino80
|
UTSW |
2 |
119,261,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R4919:Ino80
|
UTSW |
2 |
119,273,073 (GRCm39) |
missense |
probably damaging |
1.00 |
R5113:Ino80
|
UTSW |
2 |
119,262,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R5138:Ino80
|
UTSW |
2 |
119,213,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R5458:Ino80
|
UTSW |
2 |
119,242,910 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5502:Ino80
|
UTSW |
2 |
119,232,877 (GRCm39) |
missense |
probably damaging |
1.00 |
R5531:Ino80
|
UTSW |
2 |
119,276,056 (GRCm39) |
missense |
probably benign |
|
R5740:Ino80
|
UTSW |
2 |
119,261,510 (GRCm39) |
missense |
probably damaging |
1.00 |
R5892:Ino80
|
UTSW |
2 |
119,270,028 (GRCm39) |
intron |
probably benign |
|
R5914:Ino80
|
UTSW |
2 |
119,288,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R6000:Ino80
|
UTSW |
2 |
119,204,989 (GRCm39) |
missense |
probably benign |
0.04 |
R6263:Ino80
|
UTSW |
2 |
119,213,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R6505:Ino80
|
UTSW |
2 |
119,281,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R6942:Ino80
|
UTSW |
2 |
119,213,983 (GRCm39) |
missense |
probably damaging |
0.99 |
R7052:Ino80
|
UTSW |
2 |
119,257,068 (GRCm39) |
critical splice donor site |
probably null |
|
R7100:Ino80
|
UTSW |
2 |
119,204,994 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7163:Ino80
|
UTSW |
2 |
119,223,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R7187:Ino80
|
UTSW |
2 |
119,257,072 (GRCm39) |
missense |
probably benign |
0.00 |
R7202:Ino80
|
UTSW |
2 |
119,204,918 (GRCm39) |
missense |
probably benign |
0.00 |
R7218:Ino80
|
UTSW |
2 |
119,288,608 (GRCm39) |
missense |
probably benign |
|
R7389:Ino80
|
UTSW |
2 |
119,273,010 (GRCm39) |
missense |
probably benign |
0.00 |
R7419:Ino80
|
UTSW |
2 |
119,210,495 (GRCm39) |
missense |
probably benign |
0.00 |
R7437:Ino80
|
UTSW |
2 |
119,273,067 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7607:Ino80
|
UTSW |
2 |
119,212,750 (GRCm39) |
splice site |
probably null |
|
R7702:Ino80
|
UTSW |
2 |
119,273,054 (GRCm39) |
missense |
probably benign |
0.01 |
R7975:Ino80
|
UTSW |
2 |
119,286,948 (GRCm39) |
splice site |
probably null |
|
R7978:Ino80
|
UTSW |
2 |
119,269,874 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8376:Ino80
|
UTSW |
2 |
119,272,968 (GRCm39) |
missense |
probably benign |
0.14 |
R8469:Ino80
|
UTSW |
2 |
119,210,074 (GRCm39) |
missense |
probably benign |
|
R8720:Ino80
|
UTSW |
2 |
119,232,868 (GRCm39) |
missense |
probably damaging |
1.00 |
R8751:Ino80
|
UTSW |
2 |
119,237,389 (GRCm39) |
missense |
probably benign |
|
R8958:Ino80
|
UTSW |
2 |
119,213,862 (GRCm39) |
missense |
probably damaging |
1.00 |
R8992:Ino80
|
UTSW |
2 |
119,210,059 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9319:Ino80
|
UTSW |
2 |
119,205,005 (GRCm39) |
missense |
probably benign |
0.13 |
R9346:Ino80
|
UTSW |
2 |
119,257,439 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9370:Ino80
|
UTSW |
2 |
119,232,848 (GRCm39) |
missense |
probably damaging |
1.00 |
R9621:Ino80
|
UTSW |
2 |
119,280,496 (GRCm39) |
missense |
probably damaging |
0.98 |
R9641:Ino80
|
UTSW |
2 |
119,275,965 (GRCm39) |
missense |
probably benign |
0.08 |
R9650:Ino80
|
UTSW |
2 |
119,277,464 (GRCm39) |
missense |
probably damaging |
1.00 |
|