Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abr |
T |
C |
11: 76,399,898 (GRCm39) |
D33G |
probably damaging |
Het |
Adgre1 |
T |
A |
17: 57,748,359 (GRCm39) |
S520T |
probably damaging |
Het |
Afg2a |
C |
T |
3: 37,486,178 (GRCm39) |
T300I |
probably benign |
Het |
Ankrd40 |
A |
G |
11: 94,230,433 (GRCm39) |
|
probably null |
Het |
Aph1b |
A |
T |
9: 66,686,616 (GRCm39) |
I177K |
possibly damaging |
Het |
Armc3 |
A |
T |
2: 19,300,204 (GRCm39) |
N579I |
probably damaging |
Het |
Atxn7l1 |
T |
C |
12: 33,376,099 (GRCm39) |
V131A |
probably benign |
Het |
C130073F10Rik |
A |
G |
4: 101,747,992 (GRCm39) |
Y61H |
probably damaging |
Het |
C1s2 |
A |
T |
6: 124,608,071 (GRCm39) |
L214Q |
probably damaging |
Het |
Caprin2 |
A |
T |
6: 148,760,176 (GRCm39) |
S425T |
possibly damaging |
Het |
Cdc42ep4 |
G |
A |
11: 113,619,522 (GRCm39) |
R290C |
probably damaging |
Het |
Cenpf |
T |
C |
1: 189,404,825 (GRCm39) |
T352A |
probably benign |
Het |
Col6a4 |
A |
T |
9: 105,943,990 (GRCm39) |
F1161L |
probably damaging |
Het |
Dctn2 |
T |
C |
10: 127,113,809 (GRCm39) |
|
probably null |
Het |
Ddx24 |
T |
C |
12: 103,391,817 (GRCm39) |
|
probably benign |
Het |
Dsg1c |
C |
A |
18: 20,412,752 (GRCm39) |
A591D |
possibly damaging |
Het |
Efnb3 |
T |
C |
11: 69,446,798 (GRCm39) |
D304G |
probably damaging |
Het |
Erbb3 |
T |
C |
10: 128,422,094 (GRCm39) |
Y50C |
probably benign |
Het |
Eya3 |
T |
G |
4: 132,422,113 (GRCm39) |
D275E |
probably benign |
Het |
Fam81a |
G |
T |
9: 70,000,929 (GRCm39) |
Q272K |
probably benign |
Het |
Foxf1 |
T |
C |
8: 121,811,919 (GRCm39) |
V261A |
probably damaging |
Het |
Gnb4 |
C |
T |
3: 32,645,356 (GRCm39) |
V112I |
probably benign |
Het |
Gtf2h2 |
A |
T |
13: 100,625,433 (GRCm39) |
L61Q |
probably damaging |
Het |
Hey2 |
T |
A |
10: 30,710,382 (GRCm39) |
I124F |
probably benign |
Het |
Hoxb3 |
A |
T |
11: 96,236,789 (GRCm39) |
Y289F |
probably damaging |
Het |
Kctd3 |
C |
T |
1: 188,713,538 (GRCm39) |
R399Q |
probably damaging |
Het |
Kif26b |
C |
G |
1: 178,743,218 (GRCm39) |
P1105A |
probably benign |
Het |
Klhl30 |
C |
T |
1: 91,285,585 (GRCm39) |
T369M |
probably damaging |
Het |
Lipo2 |
C |
T |
19: 33,708,339 (GRCm39) |
G225D |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,274,327 (GRCm39) |
K6350E |
probably damaging |
Het |
Myh13 |
A |
C |
11: 67,232,058 (GRCm39) |
N446T |
probably damaging |
Het |
Nos1ap |
T |
C |
1: 170,146,150 (GRCm39) |
D468G |
probably damaging |
Het |
Or10j2 |
C |
T |
1: 173,098,242 (GRCm39) |
P167S |
possibly damaging |
Het |
Or11h7 |
G |
A |
14: 50,891,419 (GRCm39) |
G242R |
possibly damaging |
Het |
Or4a77 |
C |
A |
2: 89,487,459 (GRCm39) |
E109* |
probably null |
Het |
Pde3a |
T |
C |
6: 141,195,725 (GRCm39) |
L137P |
probably damaging |
Het |
Ppm1f |
G |
A |
16: 16,733,172 (GRCm39) |
R233Q |
probably benign |
Het |
Rtf2 |
C |
A |
2: 172,308,216 (GRCm39) |
A205E |
possibly damaging |
Het |
Sh2d5 |
T |
C |
4: 137,985,629 (GRCm39) |
F359S |
probably benign |
Het |
Siglec1 |
G |
A |
2: 130,916,188 (GRCm39) |
T1254M |
probably benign |
Het |
Slc39a11 |
G |
A |
11: 113,354,905 (GRCm39) |
P108L |
probably benign |
Het |
Slc6a5 |
G |
A |
7: 49,567,113 (GRCm39) |
|
probably null |
Het |
Snph |
C |
T |
2: 151,435,642 (GRCm39) |
V360M |
probably damaging |
Het |
Snx29 |
A |
G |
16: 11,223,651 (GRCm39) |
|
probably null |
Het |
Sos1 |
A |
G |
17: 80,759,408 (GRCm39) |
|
probably null |
Het |
St8sia6 |
T |
A |
2: 13,662,093 (GRCm39) |
N246I |
probably damaging |
Het |
Thy1 |
T |
A |
9: 43,958,030 (GRCm39) |
F53I |
probably damaging |
Het |
Tle3 |
T |
A |
9: 61,317,387 (GRCm39) |
Y421* |
probably null |
Het |
Ttc21b |
C |
T |
2: 66,056,355 (GRCm39) |
R677Q |
probably benign |
Het |
Vmn2r107 |
A |
T |
17: 20,595,252 (GRCm39) |
I602F |
probably benign |
Het |
Wdr17 |
C |
A |
8: 55,096,226 (GRCm39) |
G1016C |
probably benign |
Het |
Wdr62 |
T |
C |
7: 29,953,486 (GRCm39) |
E182G |
possibly damaging |
Het |
Zfp597 |
A |
G |
16: 3,684,228 (GRCm39) |
I176T |
probably benign |
Het |
|
Other mutations in Gm9637 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02304:Gm9637
|
APN |
14 |
19,402,545 (GRCm38) |
exon |
noncoding transcript |
|
IGL02449:Gm9637
|
APN |
14 |
19,402,436 (GRCm38) |
exon |
noncoding transcript |
|
IGL02492:Gm9637
|
APN |
14 |
19,402,182 (GRCm38) |
exon |
noncoding transcript |
|
IGL03060:Gm9637
|
APN |
14 |
19,402,173 (GRCm38) |
exon |
noncoding transcript |
|
R0062:Gm9637
|
UTSW |
14 |
19,402,570 (GRCm38) |
exon |
noncoding transcript |
|
R1122:Gm9637
|
UTSW |
14 |
19,401,879 (GRCm38) |
exon |
noncoding transcript |
|
R1762:Gm9637
|
UTSW |
14 |
19,402,408 (GRCm38) |
exon |
noncoding transcript |
|
R1812:Gm9637
|
UTSW |
14 |
19,402,395 (GRCm38) |
exon |
noncoding transcript |
|
R2880:Gm9637
|
UTSW |
14 |
19,401,978 (GRCm38) |
exon |
noncoding transcript |
|
R3685:Gm9637
|
UTSW |
14 |
19,401,950 (GRCm38) |
exon |
noncoding transcript |
|
R3810:Gm9637
|
UTSW |
14 |
19,402,398 (GRCm38) |
exon |
noncoding transcript |
|
R3812:Gm9637
|
UTSW |
14 |
19,402,398 (GRCm38) |
exon |
noncoding transcript |
|
R5415:Gm9637
|
UTSW |
14 |
19,402,143 (GRCm38) |
exon |
noncoding transcript |
|
R8245:Gm9637
|
UTSW |
14 |
19,402,598 (GRCm38) |
missense |
noncoding transcript |
|
Z1088:Gm9637
|
UTSW |
14 |
19,401,731 (GRCm38) |
exon |
noncoding transcript |
|
|