Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933412E24Rik |
A |
T |
15: 59,888,215 (GRCm39) |
L75Q |
possibly damaging |
Het |
Cep290 |
T |
C |
10: 100,348,263 (GRCm39) |
|
probably null |
Het |
Col11a2 |
A |
G |
17: 34,264,748 (GRCm39) |
T268A |
probably benign |
Het |
Crnkl1 |
T |
A |
2: 145,774,247 (GRCm39) |
D72V |
possibly damaging |
Het |
Csn2 |
C |
T |
5: 87,845,935 (GRCm39) |
M1I |
probably null |
Het |
Dhcr24 |
T |
C |
4: 106,431,075 (GRCm39) |
F255L |
probably benign |
Het |
Epn2 |
A |
G |
11: 61,437,348 (GRCm39) |
Y75H |
probably damaging |
Het |
Galnt3 |
A |
T |
2: 65,915,671 (GRCm39) |
H563Q |
probably damaging |
Het |
Galnt9 |
T |
C |
5: 110,762,074 (GRCm39) |
V37A |
probably damaging |
Het |
Glb1l3 |
A |
C |
9: 26,740,343 (GRCm39) |
M329R |
probably damaging |
Het |
Gorab |
A |
T |
1: 163,224,635 (GRCm39) |
D55E |
possibly damaging |
Het |
Herc2 |
G |
A |
7: 55,806,159 (GRCm39) |
R2318Q |
probably damaging |
Het |
Hspa2 |
T |
C |
12: 76,452,542 (GRCm39) |
V412A |
probably damaging |
Het |
Hspb8 |
A |
G |
5: 116,547,403 (GRCm39) |
V193A |
probably benign |
Het |
Ly75 |
A |
G |
2: 60,183,339 (GRCm39) |
L481P |
probably damaging |
Het |
Lyzl1 |
T |
C |
18: 4,169,140 (GRCm39) |
L48P |
probably damaging |
Het |
Mettl27 |
C |
T |
5: 134,969,463 (GRCm39) |
Q212* |
probably null |
Het |
Mmachc |
T |
A |
4: 116,563,215 (GRCm39) |
T47S |
probably damaging |
Het |
Ncam2 |
C |
T |
16: 81,287,211 (GRCm39) |
S375L |
probably benign |
Het |
Ogfrl1 |
T |
C |
1: 23,418,045 (GRCm39) |
|
probably benign |
Het |
Parp9 |
T |
C |
16: 35,780,417 (GRCm39) |
L461P |
probably damaging |
Het |
Pcsk7 |
A |
G |
9: 45,839,305 (GRCm39) |
|
probably null |
Het |
Plekhh1 |
C |
A |
12: 79,101,957 (GRCm39) |
H342Q |
probably benign |
Het |
Prdm13 |
T |
G |
4: 21,685,774 (GRCm39) |
|
probably benign |
Het |
Prkaa2 |
T |
C |
4: 104,908,444 (GRCm39) |
N144D |
probably damaging |
Het |
Ptpn12 |
A |
T |
5: 21,207,508 (GRCm39) |
Y283* |
probably null |
Het |
Rab12 |
T |
C |
17: 66,807,396 (GRCm39) |
Y111C |
possibly damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,842,486 (GRCm39) |
N61S |
probably damaging |
Het |
Rims1 |
T |
C |
1: 22,514,793 (GRCm39) |
S537G |
probably damaging |
Het |
Skint5 |
G |
T |
4: 113,743,011 (GRCm39) |
T352K |
unknown |
Het |
Slc12a5 |
A |
G |
2: 164,834,250 (GRCm39) |
E757G |
probably benign |
Het |
Sycp2 |
C |
A |
2: 178,022,720 (GRCm39) |
M470I |
possibly damaging |
Het |
Szt2 |
T |
C |
4: 118,222,149 (GRCm39) |
|
probably benign |
Het |
Tbc1d1 |
A |
G |
5: 64,473,771 (GRCm39) |
T765A |
probably damaging |
Het |
Tgfbr2 |
T |
C |
9: 116,004,105 (GRCm39) |
M1V |
probably null |
Het |
Tnfrsf11a |
A |
G |
1: 105,755,464 (GRCm39) |
|
probably null |
Het |
Trim43b |
A |
G |
9: 88,973,400 (GRCm39) |
L111P |
probably damaging |
Het |
Ttbk2 |
A |
T |
2: 120,576,276 (GRCm39) |
S900R |
probably benign |
Het |
Unc79 |
G |
A |
12: 103,041,208 (GRCm39) |
C747Y |
possibly damaging |
Het |
Vmn1r218 |
T |
C |
13: 23,320,971 (GRCm39) |
V26A |
possibly damaging |
Het |
Vmn2r115 |
A |
T |
17: 23,564,077 (GRCm39) |
Y83F |
probably benign |
Het |
Zfp536 |
A |
T |
7: 37,268,975 (GRCm39) |
L147Q |
probably damaging |
Het |
Zfp931 |
T |
A |
2: 177,709,777 (GRCm39) |
Q203L |
possibly damaging |
Het |
Zswim2 |
G |
A |
2: 83,746,338 (GRCm39) |
H367Y |
probably damaging |
Het |
|
Other mutations in Sash1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00987:Sash1
|
APN |
10 |
8,627,177 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01535:Sash1
|
APN |
10 |
8,617,341 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01537:Sash1
|
APN |
10 |
8,605,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01788:Sash1
|
APN |
10 |
8,609,410 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01933:Sash1
|
APN |
10 |
8,626,897 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02126:Sash1
|
APN |
10 |
8,615,229 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02285:Sash1
|
APN |
10 |
8,616,098 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02400:Sash1
|
APN |
10 |
8,609,411 (GRCm39) |
nonsense |
probably null |
|
IGL02504:Sash1
|
APN |
10 |
8,605,676 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02630:Sash1
|
APN |
10 |
8,620,299 (GRCm39) |
missense |
probably benign |
0.06 |
boyscout
|
UTSW |
10 |
8,618,186 (GRCm39) |
splice site |
probably null |
|
cubscout
|
UTSW |
10 |
8,605,477 (GRCm39) |
missense |
probably benign |
0.01 |
R0592:Sash1
|
UTSW |
10 |
8,605,546 (GRCm39) |
missense |
probably benign |
0.00 |
R0647:Sash1
|
UTSW |
10 |
8,605,316 (GRCm39) |
missense |
probably damaging |
0.99 |
R0656:Sash1
|
UTSW |
10 |
8,626,901 (GRCm39) |
critical splice donor site |
probably null |
|
R0830:Sash1
|
UTSW |
10 |
8,605,673 (GRCm39) |
missense |
probably benign |
0.01 |
R0919:Sash1
|
UTSW |
10 |
8,605,843 (GRCm39) |
missense |
probably benign |
0.01 |
R1470:Sash1
|
UTSW |
10 |
8,665,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Sash1
|
UTSW |
10 |
8,665,357 (GRCm39) |
missense |
probably damaging |
1.00 |
R1606:Sash1
|
UTSW |
10 |
8,605,721 (GRCm39) |
missense |
probably benign |
0.00 |
R1707:Sash1
|
UTSW |
10 |
8,606,141 (GRCm39) |
missense |
probably benign |
0.00 |
R1922:Sash1
|
UTSW |
10 |
8,603,672 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1940:Sash1
|
UTSW |
10 |
8,605,696 (GRCm39) |
missense |
probably benign |
|
R1964:Sash1
|
UTSW |
10 |
8,605,477 (GRCm39) |
missense |
probably benign |
0.01 |
R2013:Sash1
|
UTSW |
10 |
8,605,177 (GRCm39) |
missense |
probably benign |
0.03 |
R2014:Sash1
|
UTSW |
10 |
8,605,177 (GRCm39) |
missense |
probably benign |
0.03 |
R2015:Sash1
|
UTSW |
10 |
8,605,177 (GRCm39) |
missense |
probably benign |
0.03 |
R2074:Sash1
|
UTSW |
10 |
8,632,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R2252:Sash1
|
UTSW |
10 |
8,605,741 (GRCm39) |
missense |
probably benign |
0.01 |
R2253:Sash1
|
UTSW |
10 |
8,605,741 (GRCm39) |
missense |
probably benign |
0.01 |
R2260:Sash1
|
UTSW |
10 |
8,662,142 (GRCm39) |
nonsense |
probably null |
|
R3085:Sash1
|
UTSW |
10 |
8,618,186 (GRCm39) |
splice site |
probably null |
|
R4024:Sash1
|
UTSW |
10 |
8,605,681 (GRCm39) |
missense |
probably benign |
0.00 |
R4290:Sash1
|
UTSW |
10 |
8,606,006 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4292:Sash1
|
UTSW |
10 |
8,606,006 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4295:Sash1
|
UTSW |
10 |
8,606,006 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4301:Sash1
|
UTSW |
10 |
8,627,234 (GRCm39) |
missense |
probably benign |
0.00 |
R4657:Sash1
|
UTSW |
10 |
8,601,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R4669:Sash1
|
UTSW |
10 |
8,606,149 (GRCm39) |
missense |
probably benign |
0.00 |
R4719:Sash1
|
UTSW |
10 |
8,605,477 (GRCm39) |
missense |
probably benign |
0.01 |
R4745:Sash1
|
UTSW |
10 |
8,605,672 (GRCm39) |
missense |
probably benign |
|
R5197:Sash1
|
UTSW |
10 |
8,615,989 (GRCm39) |
missense |
probably damaging |
1.00 |
R5217:Sash1
|
UTSW |
10 |
8,656,368 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5420:Sash1
|
UTSW |
10 |
8,621,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R5591:Sash1
|
UTSW |
10 |
8,601,482 (GRCm39) |
missense |
probably benign |
0.36 |
R6505:Sash1
|
UTSW |
10 |
8,605,291 (GRCm39) |
missense |
probably benign |
0.21 |
R6679:Sash1
|
UTSW |
10 |
8,615,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6761:Sash1
|
UTSW |
10 |
8,620,286 (GRCm39) |
missense |
probably damaging |
0.99 |
R6885:Sash1
|
UTSW |
10 |
8,659,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Sash1
|
UTSW |
10 |
8,605,612 (GRCm39) |
missense |
probably benign |
0.00 |
R7034:Sash1
|
UTSW |
10 |
8,605,847 (GRCm39) |
nonsense |
probably null |
|
R7036:Sash1
|
UTSW |
10 |
8,605,847 (GRCm39) |
nonsense |
probably null |
|
R7088:Sash1
|
UTSW |
10 |
8,605,481 (GRCm39) |
nonsense |
probably null |
|
R7289:Sash1
|
UTSW |
10 |
8,605,960 (GRCm39) |
missense |
probably damaging |
0.99 |
R7464:Sash1
|
UTSW |
10 |
8,632,509 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7661:Sash1
|
UTSW |
10 |
8,605,155 (GRCm39) |
missense |
probably benign |
0.01 |
R7752:Sash1
|
UTSW |
10 |
8,656,328 (GRCm39) |
nonsense |
probably null |
|
R7856:Sash1
|
UTSW |
10 |
8,605,472 (GRCm39) |
missense |
probably benign |
0.00 |
R7901:Sash1
|
UTSW |
10 |
8,656,328 (GRCm39) |
nonsense |
probably null |
|
R8152:Sash1
|
UTSW |
10 |
8,626,805 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8218:Sash1
|
UTSW |
10 |
8,627,000 (GRCm39) |
missense |
probably damaging |
0.99 |
R8317:Sash1
|
UTSW |
10 |
8,605,150 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8358:Sash1
|
UTSW |
10 |
8,605,745 (GRCm39) |
missense |
probably benign |
|
R8503:Sash1
|
UTSW |
10 |
8,656,277 (GRCm39) |
splice site |
probably benign |
|
R8696:Sash1
|
UTSW |
10 |
8,609,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Sash1
|
UTSW |
10 |
8,605,595 (GRCm39) |
missense |
probably damaging |
0.99 |
R8710:Sash1
|
UTSW |
10 |
8,656,285 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8822:Sash1
|
UTSW |
10 |
8,761,615 (GRCm39) |
start gained |
probably benign |
|
R8826:Sash1
|
UTSW |
10 |
8,637,869 (GRCm39) |
start codon destroyed |
probably null |
|
R8891:Sash1
|
UTSW |
10 |
8,603,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R8968:Sash1
|
UTSW |
10 |
8,606,179 (GRCm39) |
missense |
probably benign |
0.00 |
R8984:Sash1
|
UTSW |
10 |
8,626,808 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9194:Sash1
|
UTSW |
10 |
8,615,969 (GRCm39) |
missense |
probably damaging |
0.99 |
R9248:Sash1
|
UTSW |
10 |
8,617,296 (GRCm39) |
missense |
probably damaging |
1.00 |
R9405:Sash1
|
UTSW |
10 |
8,637,994 (GRCm39) |
start gained |
probably benign |
|
R9408:Sash1
|
UTSW |
10 |
8,637,994 (GRCm39) |
start gained |
probably benign |
|
R9489:Sash1
|
UTSW |
10 |
8,605,169 (GRCm39) |
missense |
probably benign |
0.05 |
R9576:Sash1
|
UTSW |
10 |
8,620,299 (GRCm39) |
missense |
probably benign |
0.06 |
R9632:Sash1
|
UTSW |
10 |
8,615,969 (GRCm39) |
missense |
probably damaging |
1.00 |
|