Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahnak |
A |
G |
19: 8,986,387 (GRCm39) |
E2557G |
possibly damaging |
Het |
Arid1a |
A |
G |
4: 133,414,075 (GRCm39) |
S1248P |
unknown |
Het |
C2cd3 |
T |
C |
7: 100,081,205 (GRCm39) |
L1327S |
probably damaging |
Het |
Ccnh |
T |
C |
13: 85,354,243 (GRCm39) |
|
probably benign |
Het |
Eprs1 |
T |
C |
1: 185,105,205 (GRCm39) |
F160S |
probably damaging |
Het |
F9 |
A |
G |
X: 59,064,345 (GRCm39) |
I190V |
probably benign |
Het |
Fam185a |
C |
A |
5: 21,660,804 (GRCm39) |
A273D |
probably damaging |
Het |
Fhod1 |
G |
A |
8: 106,058,270 (GRCm39) |
|
probably benign |
Het |
Gpat4 |
G |
A |
8: 23,670,171 (GRCm39) |
P286L |
probably damaging |
Het |
Hipk2 |
T |
C |
6: 38,720,029 (GRCm39) |
D534G |
probably damaging |
Het |
Ints6l |
T |
C |
X: 55,526,731 (GRCm39) |
L220S |
probably damaging |
Het |
Kat7 |
T |
C |
11: 95,182,357 (GRCm39) |
T250A |
probably benign |
Het |
Kif23 |
G |
A |
9: 61,832,274 (GRCm39) |
S623L |
probably benign |
Het |
Krt32 |
A |
G |
11: 99,978,947 (GRCm39) |
C36R |
probably benign |
Het |
Megf10 |
G |
A |
18: 57,410,177 (GRCm39) |
G653S |
probably damaging |
Het |
Mpp3 |
G |
T |
11: 101,914,193 (GRCm39) |
S134* |
probably null |
Het |
Msh6 |
G |
T |
17: 88,293,609 (GRCm39) |
R788L |
probably damaging |
Het |
Mxi1 |
C |
A |
19: 53,360,160 (GRCm39) |
A294E |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,359,883 (GRCm39) |
E451G |
probably benign |
Het |
Naip5 |
T |
C |
13: 100,359,902 (GRCm39) |
I445V |
probably benign |
Het |
Nlrp1b |
T |
C |
11: 71,047,126 (GRCm39) |
|
probably benign |
Het |
Npy1r |
T |
C |
8: 67,157,502 (GRCm39) |
F271L |
possibly damaging |
Het |
Nup160 |
G |
T |
2: 90,552,420 (GRCm39) |
C1132F |
probably benign |
Het |
Or13p3 |
C |
T |
4: 118,567,351 (GRCm39) |
T249I |
probably damaging |
Het |
Or1o2 |
T |
A |
17: 37,543,121 (GRCm39) |
I47F |
probably damaging |
Het |
Pcdhga5 |
A |
G |
18: 37,828,167 (GRCm39) |
E205G |
possibly damaging |
Het |
Pdgfc |
A |
G |
3: 81,048,858 (GRCm39) |
T89A |
probably damaging |
Het |
Pecr |
A |
G |
1: 72,298,530 (GRCm39) |
F297L |
probably benign |
Het |
Pgr15l |
G |
T |
X: 96,120,747 (GRCm39) |
R181M |
probably damaging |
Het |
Pomgnt1 |
G |
A |
4: 116,011,325 (GRCm39) |
R230H |
probably damaging |
Het |
Ppm1d |
T |
C |
11: 85,227,993 (GRCm39) |
I303T |
probably damaging |
Het |
Ptprc |
T |
G |
1: 137,992,511 (GRCm39) |
Q1205H |
probably damaging |
Het |
Rnf112 |
A |
T |
11: 61,341,011 (GRCm39) |
|
probably benign |
Het |
Slc25a13 |
T |
A |
6: 6,109,288 (GRCm39) |
Q358L |
probably damaging |
Het |
Slc25a19 |
A |
G |
11: 115,506,285 (GRCm39) |
Y303H |
probably damaging |
Het |
Sympk |
T |
C |
7: 18,769,880 (GRCm39) |
F186L |
probably damaging |
Het |
Tek |
A |
G |
4: 94,692,549 (GRCm39) |
D219G |
probably benign |
Het |
Tmem59l |
A |
G |
8: 70,939,951 (GRCm39) |
L6S |
unknown |
Het |
Tnik |
T |
C |
3: 28,692,568 (GRCm39) |
Y820H |
probably damaging |
Het |
Tnrc6c |
C |
T |
11: 117,614,355 (GRCm39) |
R838W |
probably damaging |
Het |
Vmn2r29 |
C |
G |
7: 7,243,011 (GRCm39) |
D500H |
probably damaging |
Het |
|
Other mutations in Dcdc5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0017:Dcdc5
|
UTSW |
2 |
106,187,541 (GRCm39) |
splice site |
noncoding transcript |
|
R0017:Dcdc5
|
UTSW |
2 |
106,187,541 (GRCm39) |
splice site |
noncoding transcript |
|
R0544:Dcdc5
|
UTSW |
2 |
106,181,909 (GRCm39) |
exon |
noncoding transcript |
|
R0563:Dcdc5
|
UTSW |
2 |
106,180,035 (GRCm39) |
exon |
noncoding transcript |
|
R1456:Dcdc5
|
UTSW |
2 |
106,181,910 (GRCm39) |
exon |
noncoding transcript |
|
R1476:Dcdc5
|
UTSW |
2 |
106,188,977 (GRCm39) |
exon |
noncoding transcript |
|
R1521:Dcdc5
|
UTSW |
2 |
106,182,014 (GRCm39) |
critical splice donor site |
noncoding transcript |
|
R1555:Dcdc5
|
UTSW |
2 |
106,214,480 (GRCm39) |
exon |
noncoding transcript |
|
R2280:Dcdc5
|
UTSW |
2 |
106,202,867 (GRCm39) |
critical splice donor site |
noncoding transcript |
|
R2304:Dcdc5
|
UTSW |
2 |
106,166,488 (GRCm39) |
critical splice donor site |
noncoding transcript |
|
R4820:Dcdc5
|
UTSW |
2 |
106,166,420 (GRCm39) |
exon |
noncoding transcript |
|
R4874:Dcdc5
|
UTSW |
2 |
106,198,451 (GRCm39) |
exon |
noncoding transcript |
|
R4910:Dcdc5
|
UTSW |
2 |
106,195,895 (GRCm39) |
exon |
noncoding transcript |
|
R5285:Dcdc5
|
UTSW |
2 |
106,198,500 (GRCm39) |
exon |
noncoding transcript |
|
R5583:Dcdc5
|
UTSW |
2 |
106,195,778 (GRCm39) |
exon |
noncoding transcript |
|
R5634:Dcdc5
|
UTSW |
2 |
106,234,325 (GRCm39) |
exon |
noncoding transcript |
|
R6313:Dcdc5
|
UTSW |
2 |
106,198,516 (GRCm39) |
critical splice donor site |
noncoding transcript |
|
|