Other mutations in this stock |
Total: 20 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy2 |
T |
A |
13: 68,805,512 (GRCm39) |
I819F |
possibly damaging |
Het |
Carm1 |
T |
A |
9: 21,490,789 (GRCm39) |
M219K |
probably damaging |
Het |
Casd1 |
T |
C |
6: 4,641,859 (GRCm39) |
I712T |
probably benign |
Het |
Dido1 |
A |
G |
2: 180,326,917 (GRCm39) |
V402A |
possibly damaging |
Het |
Frem3 |
T |
C |
8: 81,417,402 (GRCm39) |
S2036P |
probably damaging |
Het |
Galnt3 |
T |
C |
2: 65,921,567 (GRCm39) |
Y488C |
probably damaging |
Het |
Mcmbp |
A |
C |
7: 128,325,865 (GRCm39) |
M71R |
probably damaging |
Het |
Nid1 |
T |
G |
13: 13,650,831 (GRCm39) |
L456R |
probably damaging |
Het |
Obscn |
T |
C |
11: 58,984,274 (GRCm39) |
D1752G |
probably damaging |
Het |
Or4f47 |
A |
G |
2: 111,972,952 (GRCm39) |
I221V |
probably benign |
Het |
Osbpl3 |
T |
A |
6: 50,285,407 (GRCm39) |
D647V |
probably damaging |
Het |
Rbpms2 |
ACTGCTGCTGCTGCTGC |
ACTGCTGCTGCTGCTGCTGC |
9: 65,558,948 (GRCm39) |
|
probably benign |
Het |
Shank1 |
G |
T |
7: 44,006,462 (GRCm39) |
G2060W |
probably damaging |
Het |
Skint5 |
A |
G |
4: 113,512,881 (GRCm39) |
S884P |
unknown |
Het |
Slit2 |
G |
A |
5: 48,374,832 (GRCm39) |
S370N |
probably benign |
Het |
Sorcs3 |
G |
A |
19: 48,682,440 (GRCm39) |
|
probably null |
Het |
Strip2 |
G |
T |
6: 29,929,828 (GRCm39) |
R305L |
probably damaging |
Het |
Trim30d |
T |
C |
7: 104,132,610 (GRCm39) |
R226G |
probably benign |
Het |
Vmn1r173 |
T |
G |
7: 23,402,323 (GRCm39) |
V186G |
possibly damaging |
Het |
Zfp719 |
A |
G |
7: 43,239,867 (GRCm39) |
D485G |
possibly damaging |
Het |
|
Other mutations in Ints8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01390:Ints8
|
APN |
4 |
11,218,679 (GRCm39) |
splice site |
probably benign |
|
IGL01925:Ints8
|
APN |
4 |
11,235,617 (GRCm39) |
splice site |
probably benign |
|
IGL02195:Ints8
|
APN |
4 |
11,221,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02215:Ints8
|
APN |
4 |
11,209,244 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02429:Ints8
|
APN |
4 |
11,231,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02484:Ints8
|
APN |
4 |
11,208,834 (GRCm39) |
nonsense |
probably null |
|
IGL02558:Ints8
|
APN |
4 |
11,218,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02725:Ints8
|
APN |
4 |
11,239,406 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02742:Ints8
|
APN |
4 |
11,241,627 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02831:Ints8
|
APN |
4 |
11,245,896 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03140:Ints8
|
APN |
4 |
11,235,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03171:Ints8
|
APN |
4 |
11,231,702 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03335:Ints8
|
APN |
4 |
11,216,460 (GRCm39) |
missense |
probably damaging |
1.00 |
G1Funyon:Ints8
|
UTSW |
4 |
11,246,120 (GRCm39) |
missense |
probably damaging |
1.00 |
P0026:Ints8
|
UTSW |
4 |
11,225,788 (GRCm39) |
nonsense |
probably null |
|
R0054:Ints8
|
UTSW |
4 |
11,204,595 (GRCm39) |
utr 3 prime |
probably benign |
|
R0063:Ints8
|
UTSW |
4 |
11,252,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Ints8
|
UTSW |
4 |
11,252,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Ints8
|
UTSW |
4 |
11,218,637 (GRCm39) |
missense |
probably benign |
0.03 |
R0299:Ints8
|
UTSW |
4 |
11,246,097 (GRCm39) |
missense |
probably benign |
0.04 |
R0499:Ints8
|
UTSW |
4 |
11,246,097 (GRCm39) |
missense |
probably benign |
0.04 |
R0540:Ints8
|
UTSW |
4 |
11,252,926 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0657:Ints8
|
UTSW |
4 |
11,246,097 (GRCm39) |
missense |
probably benign |
0.04 |
R1232:Ints8
|
UTSW |
4 |
11,234,587 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1296:Ints8
|
UTSW |
4 |
11,221,204 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1503:Ints8
|
UTSW |
4 |
11,245,842 (GRCm39) |
missense |
probably damaging |
0.97 |
R1587:Ints8
|
UTSW |
4 |
11,245,722 (GRCm39) |
critical splice donor site |
probably null |
|
R1701:Ints8
|
UTSW |
4 |
11,231,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Ints8
|
UTSW |
4 |
11,241,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R1757:Ints8
|
UTSW |
4 |
11,254,109 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R1777:Ints8
|
UTSW |
4 |
11,225,600 (GRCm39) |
critical splice donor site |
probably null |
|
R1867:Ints8
|
UTSW |
4 |
11,241,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R1868:Ints8
|
UTSW |
4 |
11,241,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R1952:Ints8
|
UTSW |
4 |
11,221,150 (GRCm39) |
missense |
probably benign |
0.21 |
R2084:Ints8
|
UTSW |
4 |
11,230,377 (GRCm39) |
missense |
probably benign |
0.31 |
R2108:Ints8
|
UTSW |
4 |
11,235,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R2202:Ints8
|
UTSW |
4 |
11,225,712 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2203:Ints8
|
UTSW |
4 |
11,225,712 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2205:Ints8
|
UTSW |
4 |
11,225,712 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2439:Ints8
|
UTSW |
4 |
11,225,725 (GRCm39) |
missense |
probably benign |
0.29 |
R2504:Ints8
|
UTSW |
4 |
11,241,642 (GRCm39) |
missense |
probably benign |
0.03 |
R3824:Ints8
|
UTSW |
4 |
11,225,621 (GRCm39) |
nonsense |
probably null |
|
R4664:Ints8
|
UTSW |
4 |
11,227,152 (GRCm39) |
missense |
probably benign |
0.04 |
R4703:Ints8
|
UTSW |
4 |
11,223,785 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4895:Ints8
|
UTSW |
4 |
11,230,367 (GRCm39) |
nonsense |
probably null |
|
R5206:Ints8
|
UTSW |
4 |
11,216,477 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5262:Ints8
|
UTSW |
4 |
11,211,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5505:Ints8
|
UTSW |
4 |
11,221,143 (GRCm39) |
missense |
probably benign |
0.18 |
R5513:Ints8
|
UTSW |
4 |
11,248,303 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5750:Ints8
|
UTSW |
4 |
11,241,654 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5892:Ints8
|
UTSW |
4 |
11,223,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6007:Ints8
|
UTSW |
4 |
11,208,845 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6229:Ints8
|
UTSW |
4 |
11,252,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6466:Ints8
|
UTSW |
4 |
11,252,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R6709:Ints8
|
UTSW |
4 |
11,221,117 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6986:Ints8
|
UTSW |
4 |
11,204,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R6998:Ints8
|
UTSW |
4 |
11,204,537 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7074:Ints8
|
UTSW |
4 |
11,204,574 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7221:Ints8
|
UTSW |
4 |
11,225,613 (GRCm39) |
missense |
probably benign |
0.01 |
R7772:Ints8
|
UTSW |
4 |
11,227,190 (GRCm39) |
missense |
probably damaging |
0.97 |
R7872:Ints8
|
UTSW |
4 |
11,254,062 (GRCm39) |
missense |
probably benign |
0.00 |
R7953:Ints8
|
UTSW |
4 |
11,227,128 (GRCm39) |
missense |
probably benign |
|
R8184:Ints8
|
UTSW |
4 |
11,204,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R8301:Ints8
|
UTSW |
4 |
11,246,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Ints8
|
UTSW |
4 |
11,208,824 (GRCm39) |
critical splice donor site |
probably null |
|
R8868:Ints8
|
UTSW |
4 |
11,230,488 (GRCm39) |
missense |
probably benign |
|
R9245:Ints8
|
UTSW |
4 |
11,213,811 (GRCm39) |
critical splice acceptor site |
probably null |
|
|