Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730071L15Rik |
A |
T |
11: 6,150,161 (GRCm39) |
|
probably benign |
Het |
Abca13 |
A |
T |
11: 9,283,310 (GRCm39) |
N3244I |
probably benign |
Het |
Adgrf5 |
A |
G |
17: 43,748,562 (GRCm39) |
T219A |
probably damaging |
Het |
Adgrg5 |
A |
T |
8: 95,660,649 (GRCm39) |
N92I |
probably damaging |
Het |
Agt |
A |
C |
8: 125,283,694 (GRCm39) |
V475G |
probably damaging |
Het |
Akap6 |
A |
G |
12: 52,934,061 (GRCm39) |
K518E |
possibly damaging |
Het |
Apoh |
T |
G |
11: 108,295,697 (GRCm39) |
D133E |
probably benign |
Het |
Axdnd1 |
T |
A |
1: 156,220,319 (GRCm39) |
M234L |
possibly damaging |
Het |
Cacna1d |
A |
G |
14: 29,804,468 (GRCm39) |
I1335T |
probably damaging |
Het |
Cdh15 |
G |
A |
8: 123,588,763 (GRCm39) |
R279Q |
probably damaging |
Het |
Cfap206 |
T |
A |
4: 34,711,566 (GRCm39) |
K444* |
probably null |
Het |
Clasp2 |
A |
G |
9: 113,707,832 (GRCm39) |
I614M |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,940,275 (GRCm39) |
D1218E |
possibly damaging |
Het |
Cplane1 |
T |
C |
15: 8,230,753 (GRCm39) |
V1010A |
possibly damaging |
Het |
Csmd3 |
CCTTTGCGCTT |
CCTT |
15: 47,604,632 (GRCm39) |
|
probably null |
Het |
D130043K22Rik |
C |
T |
13: 25,067,874 (GRCm39) |
T870M |
probably damaging |
Het |
Dagla |
C |
A |
19: 10,225,516 (GRCm39) |
A883S |
probably benign |
Het |
Dhx30 |
A |
G |
9: 109,926,263 (GRCm39) |
V87A |
probably damaging |
Het |
Ecm2 |
T |
A |
13: 49,683,605 (GRCm39) |
S528T |
possibly damaging |
Het |
Eeig2 |
T |
A |
3: 108,886,164 (GRCm39) |
N356I |
probably benign |
Het |
Egfem1 |
A |
T |
3: 29,637,080 (GRCm39) |
N172I |
probably damaging |
Het |
Fam13a |
T |
G |
6: 58,912,594 (GRCm39) |
R686S |
probably damaging |
Het |
Fam243 |
A |
G |
16: 92,118,207 (GRCm39) |
L27P |
probably damaging |
Het |
Fmo1 |
T |
A |
1: 162,663,828 (GRCm39) |
I234L |
probably benign |
Het |
Foxj2 |
C |
T |
6: 122,805,331 (GRCm39) |
R68W |
probably damaging |
Het |
Foxo6 |
A |
T |
4: 120,125,961 (GRCm39) |
M278K |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,820,775 (GRCm39) |
S5503G |
probably benign |
Het |
Gdf5 |
C |
G |
2: 155,784,010 (GRCm39) |
R100G |
probably benign |
Het |
Il1b |
A |
T |
2: 129,209,242 (GRCm39) |
D129E |
probably damaging |
Het |
Klhl29 |
A |
G |
12: 5,141,350 (GRCm39) |
S545P |
probably damaging |
Het |
Krt87 |
G |
T |
15: 101,385,708 (GRCm39) |
R296S |
possibly damaging |
Het |
Llgl1 |
T |
G |
11: 60,599,638 (GRCm39) |
S509R |
probably damaging |
Het |
Lmod1 |
A |
T |
1: 135,291,702 (GRCm39) |
K186* |
probably null |
Het |
Lrpprc |
C |
T |
17: 85,034,077 (GRCm39) |
A973T |
probably damaging |
Het |
Marco |
T |
C |
1: 120,422,514 (GRCm39) |
H49R |
possibly damaging |
Het |
Mylk4 |
T |
C |
13: 32,906,001 (GRCm39) |
N394S |
probably null |
Het |
Myo5a |
A |
G |
9: 75,030,322 (GRCm39) |
Y147C |
probably damaging |
Het |
Myo5a |
T |
C |
9: 75,059,179 (GRCm39) |
V469A |
probably damaging |
Het |
Myot |
A |
G |
18: 44,470,283 (GRCm39) |
T87A |
probably benign |
Het |
Nav2 |
A |
G |
7: 49,247,312 (GRCm39) |
H2154R |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,999,112 (GRCm38) |
E1037G |
possibly damaging |
Het |
Or1j13 |
T |
C |
2: 36,369,986 (GRCm39) |
D52G |
probably damaging |
Het |
Or52e4 |
A |
G |
7: 104,705,878 (GRCm39) |
T142A |
probably benign |
Het |
Or5k17 |
A |
G |
16: 58,746,286 (GRCm39) |
V216A |
probably benign |
Het |
Pitrm1 |
G |
T |
13: 6,625,128 (GRCm39) |
V869F |
probably benign |
Het |
Plekhm3 |
CCTGCTGCTGCTGCTGCTGCTGCTGC |
CCTGCTGCTGCTGCTGCTGCTGC |
1: 64,976,940 (GRCm39) |
|
probably benign |
Het |
Prdx1 |
T |
G |
4: 116,550,997 (GRCm39) |
I156S |
probably benign |
Het |
Rbks |
T |
A |
5: 31,823,096 (GRCm39) |
T107S |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,506,219 (GRCm39) |
R3468W |
probably damaging |
Het |
Scn1a |
C |
T |
2: 66,103,813 (GRCm39) |
D1805N |
probably damaging |
Het |
Sirpa |
T |
C |
2: 129,457,568 (GRCm39) |
V214A |
probably benign |
Het |
Slc35c1 |
T |
C |
2: 92,289,225 (GRCm39) |
N94D |
probably benign |
Het |
Sorbs2 |
A |
T |
8: 46,248,407 (GRCm39) |
K553* |
probably null |
Het |
Tectb |
C |
G |
19: 55,169,431 (GRCm39) |
|
probably benign |
Het |
Thg1l |
A |
G |
11: 45,842,392 (GRCm39) |
V142A |
probably benign |
Het |
Tiparp |
T |
A |
3: 65,460,551 (GRCm39) |
Y513* |
probably null |
Het |
Tmc6 |
A |
G |
11: 117,663,646 (GRCm39) |
V522A |
probably benign |
Het |
Trim39 |
T |
A |
17: 36,580,056 (GRCm39) |
|
probably benign |
Het |
Trrap |
G |
A |
5: 144,780,179 (GRCm39) |
|
probably null |
Het |
Tulp3 |
C |
T |
6: 128,304,601 (GRCm39) |
V218I |
probably benign |
Het |
Vmn1r38 |
T |
A |
6: 66,753,955 (GRCm39) |
I54F |
probably benign |
Het |
Vmn2r23 |
T |
A |
6: 123,719,147 (GRCm39) |
Y833* |
probably null |
Het |
Zfp810 |
A |
T |
9: 22,190,534 (GRCm39) |
S125T |
probably benign |
Het |
|
Other mutations in Dtx1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02733:Dtx1
|
APN |
5 |
120,819,500 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03104:Dtx1
|
APN |
5 |
120,833,030 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03139:Dtx1
|
APN |
5 |
120,832,955 (GRCm39) |
missense |
probably damaging |
0.96 |
R0094:Dtx1
|
UTSW |
5 |
120,820,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R0173:Dtx1
|
UTSW |
5 |
120,820,818 (GRCm39) |
unclassified |
probably benign |
|
R0268:Dtx1
|
UTSW |
5 |
120,819,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R0375:Dtx1
|
UTSW |
5 |
120,819,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R0452:Dtx1
|
UTSW |
5 |
120,833,057 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1109:Dtx1
|
UTSW |
5 |
120,848,484 (GRCm39) |
start gained |
probably benign |
|
R1456:Dtx1
|
UTSW |
5 |
120,848,569 (GRCm39) |
utr 5 prime |
probably benign |
|
R1541:Dtx1
|
UTSW |
5 |
120,848,411 (GRCm39) |
start gained |
probably benign |
|
R1554:Dtx1
|
UTSW |
5 |
120,821,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R2042:Dtx1
|
UTSW |
5 |
120,832,541 (GRCm39) |
missense |
probably benign |
0.24 |
R3946:Dtx1
|
UTSW |
5 |
120,819,351 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4697:Dtx1
|
UTSW |
5 |
120,832,473 (GRCm39) |
critical splice donor site |
probably null |
|
R6150:Dtx1
|
UTSW |
5 |
120,819,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R6564:Dtx1
|
UTSW |
5 |
120,833,082 (GRCm39) |
missense |
probably benign |
0.13 |
R6980:Dtx1
|
UTSW |
5 |
120,819,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7000:Dtx1
|
UTSW |
5 |
120,833,148 (GRCm39) |
missense |
probably damaging |
0.98 |
R7399:Dtx1
|
UTSW |
5 |
120,820,458 (GRCm39) |
missense |
possibly damaging |
0.60 |
R9117:Dtx1
|
UTSW |
5 |
120,848,356 (GRCm39) |
missense |
probably benign |
|
Z1176:Dtx1
|
UTSW |
5 |
120,821,360 (GRCm39) |
missense |
probably benign |
|
Z1177:Dtx1
|
UTSW |
5 |
120,819,416 (GRCm39) |
missense |
probably damaging |
1.00 |
|