Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ano4 |
C |
T |
10: 88,948,661 (GRCm39) |
E150K |
probably damaging |
Het |
Blnk |
T |
C |
19: 40,950,899 (GRCm39) |
Y84C |
probably damaging |
Het |
Brinp3 |
G |
A |
1: 146,777,740 (GRCm39) |
R729H |
probably damaging |
Het |
Bsn |
C |
T |
9: 107,990,266 (GRCm39) |
A1829T |
possibly damaging |
Het |
Cd300c |
A |
T |
11: 114,850,616 (GRCm39) |
N62K |
probably benign |
Het |
Chd3 |
T |
C |
11: 69,242,946 (GRCm39) |
D1425G |
probably damaging |
Het |
Ewsr1 |
C |
A |
11: 5,028,523 (GRCm39) |
|
probably benign |
Het |
Gm4076 |
G |
A |
13: 85,275,357 (GRCm39) |
|
noncoding transcript |
Het |
Greb1l |
A |
T |
18: 10,547,288 (GRCm39) |
N1502I |
possibly damaging |
Het |
H13 |
A |
G |
2: 152,537,481 (GRCm39) |
M309V |
probably damaging |
Het |
Lmf2 |
A |
G |
15: 89,235,856 (GRCm39) |
S683P |
possibly damaging |
Het |
Lrit1 |
T |
A |
14: 36,779,394 (GRCm39) |
L109Q |
probably damaging |
Het |
Maml2 |
A |
T |
9: 13,531,893 (GRCm39) |
|
probably null |
Het |
Map3k14 |
C |
A |
11: 103,111,858 (GRCm39) |
R941L |
probably damaging |
Het |
Megf6 |
A |
G |
4: 154,337,006 (GRCm39) |
K262E |
probably damaging |
Het |
Mtnr1b |
T |
G |
9: 15,774,102 (GRCm39) |
Y319S |
probably damaging |
Het |
Myh8 |
A |
G |
11: 67,188,090 (GRCm39) |
K954R |
probably damaging |
Het |
Myof |
T |
C |
19: 37,911,473 (GRCm39) |
D1486G |
probably benign |
Het |
Nbea |
A |
G |
3: 55,554,779 (GRCm39) |
V2623A |
probably benign |
Het |
Pak1 |
T |
A |
7: 97,554,018 (GRCm39) |
Y463N |
probably damaging |
Het |
Pex5l |
T |
A |
3: 33,047,152 (GRCm39) |
|
probably null |
Het |
Rasa4 |
T |
C |
5: 136,120,625 (GRCm39) |
V87A |
probably damaging |
Het |
Rnf112 |
G |
A |
11: 61,341,293 (GRCm39) |
H431Y |
possibly damaging |
Het |
Slc25a30 |
A |
G |
14: 76,007,651 (GRCm39) |
V118A |
probably benign |
Het |
Slc4a7 |
T |
A |
14: 14,773,277 (GRCm38) |
I872K |
probably damaging |
Het |
Slc5a11 |
GGTGC |
G |
7: 122,838,595 (GRCm39) |
|
probably null |
Het |
Sycp1 |
T |
C |
3: 102,726,214 (GRCm39) |
E970G |
probably damaging |
Het |
Tex15 |
T |
A |
8: 34,064,935 (GRCm39) |
L1455* |
probably null |
Het |
Tgfb2 |
T |
A |
1: 186,436,752 (GRCm39) |
T74S |
probably damaging |
Het |
Vmn2r65 |
A |
T |
7: 84,613,094 (GRCm39) |
C42S |
probably damaging |
Het |
Zbtb12 |
T |
A |
17: 35,114,455 (GRCm39) |
I80N |
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 |
|
IGL03060:Gm9637
|
APN |
14 |
19,402,173 (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 |
|
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 |
|
|