Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afap1l2 |
G |
A |
19: 56,902,682 (GRCm39) |
Q720* |
probably null |
Het |
Amph |
A |
G |
13: 19,278,984 (GRCm39) |
E153G |
probably damaging |
Het |
Atad2 |
T |
C |
15: 57,985,842 (GRCm39) |
|
probably benign |
Het |
Atosa |
A |
G |
9: 74,917,450 (GRCm39) |
D683G |
probably damaging |
Het |
Cep152 |
C |
T |
2: 125,461,907 (GRCm39) |
|
probably benign |
Het |
Cntn2 |
C |
T |
1: 132,456,678 (GRCm39) |
V123I |
probably benign |
Het |
Dhrs2 |
C |
A |
14: 55,474,775 (GRCm39) |
Q137K |
probably benign |
Het |
Fam124a |
A |
G |
14: 62,843,353 (GRCm39) |
Y287C |
probably benign |
Het |
Flg2 |
C |
T |
3: 93,110,920 (GRCm39) |
R983W |
unknown |
Het |
Helz2 |
A |
G |
2: 180,871,015 (GRCm39) |
|
probably null |
Het |
Iars1 |
G |
A |
13: 49,843,923 (GRCm39) |
|
probably null |
Het |
Igll1 |
A |
T |
16: 16,680,291 (GRCm39) |
|
probably null |
Het |
Iqch |
A |
G |
9: 63,432,196 (GRCm39) |
Y361H |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 40,527,765 (GRCm39) |
H105Q |
probably benign |
Het |
Mapk6 |
A |
G |
9: 75,305,084 (GRCm39) |
M111T |
probably damaging |
Het |
Mrtfa |
G |
A |
15: 80,929,523 (GRCm39) |
R27W |
probably damaging |
Het |
Mt1 |
T |
A |
8: 94,906,522 (GRCm39) |
|
probably benign |
Het |
Myh7b |
A |
T |
2: 155,474,671 (GRCm39) |
D1768V |
probably damaging |
Het |
Myo6 |
A |
T |
9: 80,168,159 (GRCm39) |
Q441L |
probably benign |
Het |
Nt5c3b |
A |
T |
11: 100,327,045 (GRCm39) |
Y84N |
probably damaging |
Het |
Ntmt2 |
T |
C |
1: 163,544,692 (GRCm39) |
D97G |
probably damaging |
Het |
Or1e29 |
A |
G |
11: 73,667,289 (GRCm39) |
F288S |
probably damaging |
Het |
Paxx |
A |
G |
2: 25,350,196 (GRCm39) |
L137P |
probably damaging |
Het |
Ptprz1 |
T |
C |
6: 22,972,834 (GRCm39) |
V248A |
probably damaging |
Het |
Rif1 |
T |
A |
2: 52,002,149 (GRCm39) |
C1868S |
probably damaging |
Het |
Sec23a |
A |
T |
12: 59,032,891 (GRCm39) |
C403S |
probably benign |
Het |
Skint4 |
G |
A |
4: 111,975,432 (GRCm39) |
V131I |
probably benign |
Het |
Sugp2 |
T |
C |
8: 70,695,837 (GRCm39) |
V270A |
possibly damaging |
Het |
Tmed9 |
A |
G |
13: 55,743,321 (GRCm39) |
D151G |
possibly damaging |
Het |
Tubgcp4 |
A |
G |
2: 121,007,071 (GRCm39) |
|
probably benign |
Het |
Uaca |
A |
G |
9: 60,777,148 (GRCm39) |
R512G |
probably damaging |
Het |
Unc80 |
A |
G |
1: 66,676,169 (GRCm39) |
Y1999C |
possibly damaging |
Het |
Vwf |
T |
A |
6: 125,640,523 (GRCm39) |
C2320S |
probably damaging |
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 |
|
R0062:Gm9637
|
UTSW |
14 |
19,402,570 (GRCm38) |
exon |
noncoding transcript |
|
R0621:Gm9637
|
UTSW |
14 |
19,402,011 (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 |
|
|