Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adprhl1 |
T |
A |
8: 13,271,929 (GRCm39) |
R1610W |
probably damaging |
Het |
Aig1 |
A |
T |
10: 13,744,417 (GRCm39) |
M29K |
probably damaging |
Het |
Alms1 |
A |
T |
6: 85,618,362 (GRCm39) |
I2334F |
probably benign |
Het |
Ano6 |
A |
G |
15: 95,839,190 (GRCm39) |
Y423C |
probably damaging |
Het |
Arap3 |
T |
C |
18: 38,122,232 (GRCm39) |
M619V |
probably benign |
Het |
Armh4 |
T |
A |
14: 50,010,670 (GRCm39) |
T346S |
probably benign |
Het |
Asb13 |
T |
A |
13: 3,699,413 (GRCm39) |
F204L |
probably damaging |
Het |
Btaf1 |
T |
C |
19: 36,926,565 (GRCm39) |
V79A |
probably benign |
Het |
Casp8ap2 |
A |
G |
4: 32,645,909 (GRCm39) |
T1661A |
probably benign |
Het |
Ccna1 |
G |
T |
3: 54,958,010 (GRCm39) |
T165K |
possibly damaging |
Het |
Cdc42ep1 |
T |
A |
15: 78,731,973 (GRCm39) |
S139R |
possibly damaging |
Het |
Chil3 |
A |
C |
3: 106,057,464 (GRCm39) |
Y233* |
probably null |
Het |
Clec1a |
T |
C |
6: 129,409,150 (GRCm39) |
S159G |
probably benign |
Het |
Cltc |
A |
T |
11: 86,627,967 (GRCm39) |
N60K |
probably benign |
Het |
Dlgap4 |
T |
A |
2: 156,591,054 (GRCm39) |
Y747N |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,266,163 (GRCm39) |
N2244S |
probably benign |
Het |
Ephb3 |
A |
G |
16: 21,040,434 (GRCm39) |
T811A |
probably damaging |
Het |
Fbxo21 |
T |
C |
5: 118,146,212 (GRCm39) |
Y612H |
possibly damaging |
Het |
Gale |
T |
C |
4: 135,692,982 (GRCm39) |
L75P |
probably damaging |
Het |
Golgb1 |
T |
C |
16: 36,734,466 (GRCm39) |
S1279P |
probably benign |
Het |
Hdgfl3 |
T |
C |
7: 81,583,706 (GRCm39) |
Y22C |
possibly damaging |
Het |
Hmx3 |
T |
G |
7: 131,146,111 (GRCm39) |
I273S |
probably damaging |
Het |
Hpse2 |
T |
C |
19: 43,373,248 (GRCm39) |
N127S |
probably benign |
Het |
Hsf2bp |
C |
T |
17: 32,226,743 (GRCm39) |
R204H |
probably damaging |
Het |
Ifit1bl1 |
T |
A |
19: 34,571,224 (GRCm39) |
H411L |
probably benign |
Het |
Krtap27-1 |
T |
C |
16: 88,468,340 (GRCm39) |
N68S |
probably benign |
Het |
Ltbp1 |
T |
G |
17: 75,697,546 (GRCm39) |
*1713G |
probably null |
Het |
Lypd6b |
A |
G |
2: 49,833,612 (GRCm39) |
E84G |
probably damaging |
Het |
Meiosin |
T |
A |
7: 18,834,011 (GRCm39) |
K508N |
unknown |
Het |
Mrgprx2 |
T |
C |
7: 48,132,753 (GRCm39) |
T22A |
probably benign |
Het |
Mrto4 |
T |
C |
4: 139,077,000 (GRCm39) |
Y39C |
probably benign |
Het |
Mtmr4 |
T |
C |
11: 87,495,254 (GRCm39) |
V437A |
probably damaging |
Het |
Mylk4 |
T |
C |
13: 32,911,096 (GRCm39) |
T221A |
probably benign |
Het |
Neb |
T |
C |
2: 52,161,360 (GRCm39) |
D2144G |
probably damaging |
Het |
Nup210 |
T |
G |
6: 91,050,179 (GRCm39) |
D430A |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,984,235 (GRCm39) |
E1740V |
probably damaging |
Het |
Or8i2 |
A |
G |
2: 86,852,657 (GRCm39) |
V77A |
probably benign |
Het |
Panx1 |
A |
G |
9: 14,919,125 (GRCm39) |
C245R |
probably damaging |
Het |
Pcdha6 |
C |
A |
18: 37,101,965 (GRCm39) |
T386N |
possibly damaging |
Het |
Pcsk1 |
G |
A |
13: 75,280,211 (GRCm39) |
A679T |
probably benign |
Het |
Pdzph1 |
T |
C |
17: 59,239,455 (GRCm39) |
T958A |
probably damaging |
Het |
Pkd2l2 |
T |
A |
18: 34,560,481 (GRCm39) |
Y363N |
possibly damaging |
Het |
Plekha5 |
T |
A |
6: 140,526,201 (GRCm39) |
H946Q |
possibly damaging |
Het |
Rhbg |
A |
G |
3: 88,155,007 (GRCm39) |
L168P |
probably benign |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rtn2 |
T |
A |
7: 19,020,987 (GRCm39) |
S153R |
probably benign |
Het |
Serpinb1a |
C |
A |
13: 33,034,239 (GRCm39) |
A51S |
probably benign |
Het |
Serpinb6e |
T |
A |
13: 34,016,588 (GRCm39) |
T382S |
probably damaging |
Het |
Sgip1 |
T |
G |
4: 102,772,298 (GRCm39) |
M229R |
probably benign |
Het |
Slc1a5 |
C |
A |
7: 16,523,807 (GRCm39) |
R271S |
possibly damaging |
Het |
Slc23a3 |
A |
G |
1: 75,106,040 (GRCm39) |
|
probably null |
Het |
Slc7a6 |
C |
T |
8: 106,906,239 (GRCm39) |
P157L |
possibly damaging |
Het |
Spsb1 |
T |
C |
4: 149,990,903 (GRCm39) |
I222V |
probably benign |
Het |
Syne2 |
A |
T |
12: 75,951,079 (GRCm39) |
E410V |
probably damaging |
Het |
Trappc3 |
T |
C |
4: 126,168,999 (GRCm39) |
I163T |
probably damaging |
Het |
Ttc6 |
T |
G |
12: 57,707,229 (GRCm39) |
L712R |
possibly damaging |
Het |
Ttn |
G |
T |
2: 76,715,309 (GRCm39) |
Q7928K |
unknown |
Het |
Tuft1 |
G |
A |
3: 94,539,909 (GRCm39) |
P159S |
probably benign |
Het |
Vmn2r108 |
T |
C |
17: 20,691,890 (GRCm39) |
H211R |
probably damaging |
Het |
Wapl |
T |
C |
14: 34,399,105 (GRCm39) |
I58T |
probably benign |
Het |
Zfp78 |
C |
T |
7: 6,381,589 (GRCm39) |
T213I |
possibly damaging |
Het |
Zmat4 |
T |
A |
8: 24,238,436 (GRCm39) |
I6N |
possibly damaging |
Het |
Zp3r |
G |
T |
1: 130,524,560 (GRCm39) |
P226Q |
probably damaging |
Het |
|
Other mutations in Treh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00493:Treh
|
APN |
9 |
44,595,197 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00984:Treh
|
APN |
9 |
44,594,264 (GRCm39) |
unclassified |
probably benign |
|
IGL02111:Treh
|
APN |
9 |
44,594,258 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02493:Treh
|
APN |
9 |
44,594,246 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03242:Treh
|
APN |
9 |
44,596,634 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03392:Treh
|
APN |
9 |
44,597,228 (GRCm39) |
missense |
probably damaging |
0.96 |
delight
|
UTSW |
9 |
44,592,823 (GRCm39) |
missense |
probably damaging |
1.00 |
trixie
|
UTSW |
9 |
44,594,910 (GRCm39) |
missense |
probably benign |
0.27 |
R0041:Treh
|
UTSW |
9 |
44,594,910 (GRCm39) |
missense |
probably benign |
0.27 |
R1391:Treh
|
UTSW |
9 |
44,596,602 (GRCm39) |
missense |
probably benign |
0.02 |
R2099:Treh
|
UTSW |
9 |
44,595,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R2142:Treh
|
UTSW |
9 |
44,592,438 (GRCm39) |
missense |
probably damaging |
1.00 |
R3936:Treh
|
UTSW |
9 |
44,595,840 (GRCm39) |
missense |
probably benign |
0.02 |
R4577:Treh
|
UTSW |
9 |
44,597,208 (GRCm39) |
missense |
probably benign |
0.11 |
R4715:Treh
|
UTSW |
9 |
44,594,615 (GRCm39) |
missense |
probably benign |
0.44 |
R4735:Treh
|
UTSW |
9 |
44,592,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Treh
|
UTSW |
9 |
44,593,945 (GRCm39) |
missense |
probably damaging |
0.99 |
R5028:Treh
|
UTSW |
9 |
44,594,186 (GRCm39) |
missense |
probably null |
0.96 |
R5214:Treh
|
UTSW |
9 |
44,594,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R5645:Treh
|
UTSW |
9 |
44,593,975 (GRCm39) |
missense |
probably damaging |
0.99 |
R7311:Treh
|
UTSW |
9 |
44,597,245 (GRCm39) |
missense |
probably benign |
|
R7892:Treh
|
UTSW |
9 |
44,596,015 (GRCm39) |
missense |
probably damaging |
1.00 |
R7945:Treh
|
UTSW |
9 |
44,592,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R8338:Treh
|
UTSW |
9 |
44,595,808 (GRCm39) |
missense |
probably benign |
0.27 |
R8818:Treh
|
UTSW |
9 |
44,592,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R8884:Treh
|
UTSW |
9 |
44,595,800 (GRCm39) |
unclassified |
probably benign |
|
R9041:Treh
|
UTSW |
9 |
44,596,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R9311:Treh
|
UTSW |
9 |
44,592,655 (GRCm39) |
missense |
probably benign |
0.39 |
R9489:Treh
|
UTSW |
9 |
44,592,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R9605:Treh
|
UTSW |
9 |
44,592,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R9701:Treh
|
UTSW |
9 |
44,594,648 (GRCm39) |
missense |
probably damaging |
1.00 |
|