Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr10 |
T |
A |
12: 71,001,430 (GRCm39) |
|
probably null |
Het |
Ankhd1 |
T |
C |
18: 36,780,756 (GRCm39) |
V1936A |
probably benign |
Het |
Ap3m1 |
C |
A |
14: 21,095,588 (GRCm39) |
E81* |
probably null |
Het |
Camkk1 |
T |
C |
11: 72,919,995 (GRCm39) |
|
probably benign |
Het |
Cdc45 |
C |
T |
16: 18,617,479 (GRCm39) |
M200I |
probably benign |
Het |
Cmc1 |
A |
G |
9: 117,894,376 (GRCm39) |
Y33H |
probably damaging |
Het |
Cntnap5b |
A |
T |
1: 99,999,794 (GRCm39) |
D184V |
probably damaging |
Het |
F5 |
A |
T |
1: 164,021,644 (GRCm39) |
D1373V |
probably damaging |
Het |
Fam169a |
T |
C |
13: 97,247,796 (GRCm39) |
|
probably benign |
Het |
Fem1c |
G |
A |
18: 46,639,019 (GRCm39) |
R328W |
probably damaging |
Het |
Gba2 |
T |
C |
4: 43,568,919 (GRCm39) |
R579G |
probably benign |
Het |
Gm42641 |
G |
A |
9: 108,887,698 (GRCm39) |
Q98* |
probably null |
Het |
Hsd17b7 |
A |
G |
1: 169,792,058 (GRCm39) |
F117L |
possibly damaging |
Het |
Map1a |
T |
C |
2: 121,130,585 (GRCm39) |
I467T |
probably damaging |
Het |
Map2k4 |
T |
A |
11: 65,581,567 (GRCm39) |
I382F |
possibly damaging |
Het |
Myh1 |
T |
G |
11: 67,097,088 (GRCm39) |
|
probably benign |
Het |
Nr1h4 |
C |
T |
10: 89,309,701 (GRCm39) |
A339T |
probably damaging |
Het |
Opn4 |
T |
A |
14: 34,315,014 (GRCm39) |
T420S |
probably benign |
Het |
Or5h22 |
A |
C |
16: 58,895,155 (GRCm39) |
M96R |
probably benign |
Het |
Or6n1 |
A |
G |
1: 173,916,756 (GRCm39) |
Y50C |
probably benign |
Het |
Rnf123 |
G |
A |
9: 107,945,501 (GRCm39) |
R390* |
probably null |
Het |
Slc17a3 |
T |
A |
13: 24,026,434 (GRCm39) |
M1K |
probably null |
Het |
T |
T |
A |
17: 8,654,190 (GRCm39) |
I125N |
probably damaging |
Het |
Tns2 |
T |
A |
15: 102,020,263 (GRCm39) |
S710T |
probably benign |
Het |
Trav3-1 |
T |
A |
14: 52,818,551 (GRCm39) |
V75E |
probably benign |
Het |
U2surp |
A |
G |
9: 95,354,143 (GRCm39) |
Y832H |
possibly damaging |
Het |
Zng1 |
T |
A |
19: 24,935,269 (GRCm39) |
E78D |
probably damaging |
Het |
|
Other mutations in Itsn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01109:Itsn1
|
APN |
16 |
91,603,089 (GRCm39) |
unclassified |
probably benign |
|
IGL01799:Itsn1
|
APN |
16 |
91,645,770 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02328:Itsn1
|
APN |
16 |
91,612,295 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02333:Itsn1
|
APN |
16 |
91,617,564 (GRCm39) |
intron |
probably benign |
|
IGL02503:Itsn1
|
APN |
16 |
91,686,092 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02666:Itsn1
|
APN |
16 |
91,617,606 (GRCm39) |
intron |
probably benign |
|
IGL03007:Itsn1
|
APN |
16 |
91,581,050 (GRCm39) |
splice site |
probably benign |
|
IGL03223:Itsn1
|
APN |
16 |
91,702,194 (GRCm39) |
missense |
probably benign |
0.00 |
raphael
|
UTSW |
16 |
91,617,684 (GRCm39) |
intron |
probably benign |
|
Sector
|
UTSW |
16 |
91,705,375 (GRCm39) |
critical splice donor site |
probably null |
|
Weevil
|
UTSW |
16 |
91,615,440 (GRCm39) |
intron |
probably benign |
|
R0234:Itsn1
|
UTSW |
16 |
91,625,168 (GRCm39) |
nonsense |
probably null |
|
R0234:Itsn1
|
UTSW |
16 |
91,625,168 (GRCm39) |
nonsense |
probably null |
|
R0255:Itsn1
|
UTSW |
16 |
91,602,978 (GRCm39) |
unclassified |
probably benign |
|
R0432:Itsn1
|
UTSW |
16 |
91,612,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0455:Itsn1
|
UTSW |
16 |
91,665,036 (GRCm39) |
intron |
probably benign |
|
R0471:Itsn1
|
UTSW |
16 |
91,696,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R0558:Itsn1
|
UTSW |
16 |
91,696,511 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0563:Itsn1
|
UTSW |
16 |
91,617,684 (GRCm39) |
intron |
probably benign |
|
R1657:Itsn1
|
UTSW |
16 |
91,706,111 (GRCm39) |
missense |
probably damaging |
1.00 |
R1671:Itsn1
|
UTSW |
16 |
91,609,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R1742:Itsn1
|
UTSW |
16 |
91,613,847 (GRCm39) |
critical splice donor site |
probably null |
|
R1859:Itsn1
|
UTSW |
16 |
91,686,042 (GRCm39) |
intron |
probably benign |
|
R1898:Itsn1
|
UTSW |
16 |
91,696,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R2016:Itsn1
|
UTSW |
16 |
91,702,389 (GRCm39) |
critical splice donor site |
probably null |
|
R2221:Itsn1
|
UTSW |
16 |
91,650,656 (GRCm39) |
intron |
probably benign |
|
R2244:Itsn1
|
UTSW |
16 |
91,650,659 (GRCm39) |
missense |
probably null |
|
R3160:Itsn1
|
UTSW |
16 |
91,649,932 (GRCm39) |
nonsense |
probably null |
|
R3162:Itsn1
|
UTSW |
16 |
91,649,932 (GRCm39) |
nonsense |
probably null |
|
R3814:Itsn1
|
UTSW |
16 |
91,649,809 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4162:Itsn1
|
UTSW |
16 |
91,649,790 (GRCm39) |
missense |
probably benign |
0.00 |
R4254:Itsn1
|
UTSW |
16 |
91,615,440 (GRCm39) |
intron |
probably benign |
|
R4319:Itsn1
|
UTSW |
16 |
91,615,440 (GRCm39) |
intron |
probably benign |
|
R4321:Itsn1
|
UTSW |
16 |
91,615,440 (GRCm39) |
intron |
probably benign |
|
R4323:Itsn1
|
UTSW |
16 |
91,615,440 (GRCm39) |
intron |
probably benign |
|
R4326:Itsn1
|
UTSW |
16 |
91,650,743 (GRCm39) |
intron |
probably benign |
|
R4515:Itsn1
|
UTSW |
16 |
91,696,537 (GRCm39) |
missense |
probably damaging |
0.99 |
R4584:Itsn1
|
UTSW |
16 |
91,617,471 (GRCm39) |
intron |
probably benign |
|
R4600:Itsn1
|
UTSW |
16 |
91,696,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R4649:Itsn1
|
UTSW |
16 |
91,638,476 (GRCm39) |
missense |
probably damaging |
1.00 |
R4834:Itsn1
|
UTSW |
16 |
91,703,677 (GRCm39) |
nonsense |
probably null |
|
R4868:Itsn1
|
UTSW |
16 |
91,582,205 (GRCm39) |
missense |
probably damaging |
0.98 |
R5036:Itsn1
|
UTSW |
16 |
91,579,123 (GRCm39) |
splice site |
probably benign |
|
R5122:Itsn1
|
UTSW |
16 |
91,690,732 (GRCm39) |
intron |
probably benign |
|
R5161:Itsn1
|
UTSW |
16 |
91,705,726 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5437:Itsn1
|
UTSW |
16 |
91,615,479 (GRCm39) |
intron |
probably benign |
|
R5538:Itsn1
|
UTSW |
16 |
91,580,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R5683:Itsn1
|
UTSW |
16 |
91,702,268 (GRCm39) |
missense |
probably benign |
0.00 |
R5697:Itsn1
|
UTSW |
16 |
91,598,477 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5749:Itsn1
|
UTSW |
16 |
91,703,743 (GRCm39) |
missense |
probably damaging |
0.99 |
R6083:Itsn1
|
UTSW |
16 |
91,649,899 (GRCm39) |
missense |
probably benign |
0.01 |
R6148:Itsn1
|
UTSW |
16 |
91,613,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R6291:Itsn1
|
UTSW |
16 |
91,664,984 (GRCm39) |
intron |
probably benign |
|
R6524:Itsn1
|
UTSW |
16 |
91,708,883 (GRCm39) |
missense |
probably damaging |
0.96 |
R7175:Itsn1
|
UTSW |
16 |
91,664,938 (GRCm39) |
missense |
unknown |
|
R7261:Itsn1
|
UTSW |
16 |
91,702,194 (GRCm39) |
missense |
probably benign |
0.00 |
R7320:Itsn1
|
UTSW |
16 |
91,636,587 (GRCm39) |
missense |
unknown |
|
R7366:Itsn1
|
UTSW |
16 |
91,705,338 (GRCm39) |
missense |
unknown |
|
R7462:Itsn1
|
UTSW |
16 |
91,650,073 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7665:Itsn1
|
UTSW |
16 |
91,638,491 (GRCm39) |
missense |
unknown |
|
R7720:Itsn1
|
UTSW |
16 |
91,664,971 (GRCm39) |
missense |
unknown |
|
R7856:Itsn1
|
UTSW |
16 |
91,705,375 (GRCm39) |
critical splice donor site |
probably null |
|
R7864:Itsn1
|
UTSW |
16 |
91,598,454 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7896:Itsn1
|
UTSW |
16 |
91,615,446 (GRCm39) |
missense |
unknown |
|
R7897:Itsn1
|
UTSW |
16 |
91,615,446 (GRCm39) |
missense |
unknown |
|
R7980:Itsn1
|
UTSW |
16 |
91,702,182 (GRCm39) |
missense |
unknown |
|
R7998:Itsn1
|
UTSW |
16 |
91,647,824 (GRCm39) |
missense |
unknown |
|
R8075:Itsn1
|
UTSW |
16 |
91,686,097 (GRCm39) |
missense |
unknown |
|
R8144:Itsn1
|
UTSW |
16 |
91,708,893 (GRCm39) |
missense |
unknown |
|
R8160:Itsn1
|
UTSW |
16 |
91,615,446 (GRCm39) |
missense |
unknown |
|
R8161:Itsn1
|
UTSW |
16 |
91,615,446 (GRCm39) |
missense |
unknown |
|
R8176:Itsn1
|
UTSW |
16 |
91,645,597 (GRCm39) |
splice site |
probably null |
|
R8215:Itsn1
|
UTSW |
16 |
91,608,996 (GRCm39) |
missense |
probably damaging |
0.99 |
R8385:Itsn1
|
UTSW |
16 |
91,690,699 (GRCm39) |
missense |
unknown |
|
R8725:Itsn1
|
UTSW |
16 |
91,636,721 (GRCm39) |
missense |
unknown |
|
R9012:Itsn1
|
UTSW |
16 |
91,645,849 (GRCm39) |
missense |
unknown |
|
R9039:Itsn1
|
UTSW |
16 |
91,703,658 (GRCm39) |
missense |
unknown |
|
R9092:Itsn1
|
UTSW |
16 |
91,609,002 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9134:Itsn1
|
UTSW |
16 |
91,666,514 (GRCm39) |
missense |
unknown |
|
R9401:Itsn1
|
UTSW |
16 |
91,612,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R9449:Itsn1
|
UTSW |
16 |
91,625,264 (GRCm39) |
makesense |
probably null |
|
R9568:Itsn1
|
UTSW |
16 |
91,649,782 (GRCm39) |
missense |
probably benign |
|
R9616:Itsn1
|
UTSW |
16 |
91,650,055 (GRCm39) |
missense |
probably benign |
0.11 |
|