Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
T |
C |
14: 32,382,912 (GRCm39) |
T1018A |
possibly damaging |
Het |
Aak1 |
T |
A |
6: 86,827,044 (GRCm39) |
F4I |
probably damaging |
Het |
Adamts8 |
G |
T |
9: 30,862,684 (GRCm39) |
E296D |
probably benign |
Het |
Ankrd35 |
T |
A |
3: 96,586,471 (GRCm39) |
|
probably null |
Het |
Arhgap20 |
G |
A |
9: 51,738,135 (GRCm39) |
|
probably null |
Het |
Bhmt |
T |
A |
13: 93,762,007 (GRCm39) |
|
probably benign |
Het |
Cacna1b |
C |
A |
2: 24,567,923 (GRCm39) |
R1055L |
probably benign |
Het |
Cdk5r1 |
A |
G |
11: 80,369,035 (GRCm39) |
Y234C |
probably damaging |
Het |
Cdx2 |
G |
T |
5: 147,243,539 (GRCm39) |
A85D |
possibly damaging |
Het |
Cenpe |
G |
A |
3: 134,949,479 (GRCm39) |
G88D |
probably damaging |
Het |
Cfap300 |
A |
T |
9: 8,026,071 (GRCm39) |
L167Q |
probably damaging |
Het |
Dennd5a |
A |
C |
7: 109,526,032 (GRCm39) |
|
probably null |
Het |
Erich6 |
G |
A |
3: 58,526,229 (GRCm39) |
A591V |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,221,424 (GRCm39) |
I944V |
probably damaging |
Het |
Fbln5 |
A |
G |
12: 101,723,618 (GRCm39) |
V374A |
probably damaging |
Het |
Fmn1 |
G |
A |
2: 113,467,080 (GRCm39) |
S1327N |
probably benign |
Het |
Fnip2 |
A |
T |
3: 79,369,442 (GRCm39) |
V1081E |
probably damaging |
Het |
Gpaa1 |
A |
C |
15: 76,216,667 (GRCm39) |
|
probably benign |
Het |
Grina |
T |
A |
15: 76,133,529 (GRCm39) |
L334Q |
probably damaging |
Het |
Gulp1 |
T |
A |
1: 44,747,829 (GRCm39) |
Y27* |
probably null |
Het |
Kdm3b |
A |
T |
18: 34,928,797 (GRCm39) |
I183F |
probably benign |
Het |
Loxhd1 |
A |
T |
18: 77,460,025 (GRCm39) |
I758F |
probably damaging |
Het |
Msi2 |
T |
C |
11: 88,237,914 (GRCm39) |
H346R |
probably benign |
Het |
Naip6 |
T |
A |
13: 100,452,657 (GRCm39) |
I135F |
probably benign |
Het |
Npr3 |
T |
G |
15: 11,848,599 (GRCm39) |
E202A |
probably benign |
Het |
Nsun4 |
A |
T |
4: 115,891,248 (GRCm39) |
L377Q |
probably damaging |
Het |
Oog2 |
A |
C |
4: 143,921,411 (GRCm39) |
H107P |
probably damaging |
Het |
Or14c40 |
C |
A |
7: 86,313,602 (GRCm39) |
T244N |
probably damaging |
Het |
Otof |
A |
G |
5: 30,539,762 (GRCm39) |
L1032P |
probably damaging |
Het |
Pcdh9 |
T |
A |
14: 94,124,956 (GRCm39) |
R405* |
probably null |
Het |
Pcdhb19 |
T |
A |
18: 37,632,243 (GRCm39) |
N679K |
probably benign |
Het |
Pigr |
G |
A |
1: 130,769,554 (GRCm39) |
D122N |
probably benign |
Het |
Prol1 |
A |
T |
5: 88,476,530 (GRCm39) |
I307F |
unknown |
Het |
Pycr1 |
T |
C |
11: 120,532,949 (GRCm39) |
I104V |
probably benign |
Het |
Ralgapa1 |
C |
T |
12: 55,687,429 (GRCm39) |
R2019Q |
probably damaging |
Het |
Rb1cc1 |
T |
C |
1: 6,335,887 (GRCm39) |
|
probably benign |
Het |
Skint11 |
C |
A |
4: 114,101,856 (GRCm39) |
Q99K |
probably benign |
Het |
Skint3 |
A |
G |
4: 112,112,832 (GRCm39) |
I147M |
possibly damaging |
Het |
Slc22a14 |
T |
G |
9: 119,007,498 (GRCm39) |
M304L |
probably benign |
Het |
Slc22a14 |
T |
C |
9: 119,008,934 (GRCm39) |
N178S |
possibly damaging |
Het |
Slc2a1 |
T |
G |
4: 118,990,313 (GRCm39) |
I179S |
probably damaging |
Het |
Slco2b1 |
G |
T |
7: 99,309,333 (GRCm39) |
T666N |
probably benign |
Het |
Smap1 |
T |
C |
1: 23,887,506 (GRCm39) |
M258V |
probably benign |
Het |
Smr3a |
A |
T |
5: 88,156,013 (GRCm39) |
|
probably benign |
Het |
Stt3b |
T |
A |
9: 115,083,969 (GRCm39) |
E402D |
probably damaging |
Het |
Sync |
T |
C |
4: 129,200,535 (GRCm39) |
|
probably benign |
Het |
Tbx20 |
T |
A |
9: 24,681,040 (GRCm39) |
I151F |
probably damaging |
Het |
Tomm22 |
C |
A |
15: 79,555,206 (GRCm39) |
|
probably benign |
Het |
Trank1 |
C |
A |
9: 111,202,592 (GRCm39) |
Y1652* |
probably null |
Het |
Trim34a |
T |
A |
7: 103,910,223 (GRCm39) |
C342S |
probably benign |
Het |
Txnl4a |
T |
A |
18: 80,265,471 (GRCm39) |
M112K |
probably benign |
Het |
Zfp146 |
A |
G |
7: 29,861,865 (GRCm39) |
V59A |
possibly damaging |
Het |
|
Other mutations in Gm5174 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
Laco
|
UTSW |
10 |
86,491,972 (GRCm39) |
unclassified |
noncoding transcript |
|
R1083:Gm5174
|
UTSW |
10 |
86,491,972 (GRCm39) |
unclassified |
noncoding transcript |
|
R1199:Gm5174
|
UTSW |
10 |
86,493,189 (GRCm39) |
unclassified |
noncoding transcript |
|
R1296:Gm5174
|
UTSW |
10 |
86,492,866 (GRCm39) |
unclassified |
noncoding transcript |
|
R1715:Gm5174
|
UTSW |
10 |
86,492,776 (GRCm39) |
unclassified |
noncoding transcript |
|
R1957:Gm5174
|
UTSW |
10 |
86,492,617 (GRCm39) |
unclassified |
noncoding transcript |
|
R2221:Gm5174
|
UTSW |
10 |
86,492,372 (GRCm39) |
unclassified |
noncoding transcript |
|
R2223:Gm5174
|
UTSW |
10 |
86,492,372 (GRCm39) |
unclassified |
noncoding transcript |
|
R3104:Gm5174
|
UTSW |
10 |
86,492,519 (GRCm39) |
unclassified |
noncoding transcript |
|
R4165:Gm5174
|
UTSW |
10 |
86,492,797 (GRCm39) |
unclassified |
noncoding transcript |
|
R4243:Gm5174
|
UTSW |
10 |
86,492,144 (GRCm39) |
unclassified |
noncoding transcript |
|
R4244:Gm5174
|
UTSW |
10 |
86,492,144 (GRCm39) |
unclassified |
noncoding transcript |
|
R5024:Gm5174
|
UTSW |
10 |
86,492,451 (GRCm39) |
unclassified |
noncoding transcript |
|
R5292:Gm5174
|
UTSW |
10 |
86,492,562 (GRCm39) |
unclassified |
noncoding transcript |
|
R5586:Gm5174
|
UTSW |
10 |
86,492,409 (GRCm39) |
unclassified |
noncoding transcript |
|
R5864:Gm5174
|
UTSW |
10 |
86,493,045 (GRCm39) |
unclassified |
noncoding transcript |
|
|