Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
G |
A |
8: 60,969,147 (GRCm39) |
|
probably null |
Het |
Adamtsl1 |
A |
G |
4: 86,260,729 (GRCm39) |
N988S |
possibly damaging |
Het |
Aph1b |
A |
T |
9: 66,697,878 (GRCm39) |
|
probably null |
Het |
B4galnt3 |
C |
A |
6: 120,184,167 (GRCm39) |
R880L |
probably damaging |
Het |
Bcam |
T |
C |
7: 19,503,247 (GRCm39) |
|
probably benign |
Het |
Cr2 |
A |
T |
1: 194,858,878 (GRCm39) |
I14N |
possibly damaging |
Het |
Dcdc5 |
T |
C |
2: 106,198,451 (GRCm39) |
|
noncoding transcript |
Het |
Dll1 |
A |
T |
17: 15,590,501 (GRCm39) |
M405K |
probably benign |
Het |
Dync1h1 |
C |
A |
12: 110,624,560 (GRCm39) |
T3700N |
probably damaging |
Het |
Ern2 |
T |
C |
7: 121,775,810 (GRCm39) |
D428G |
probably benign |
Het |
Esp36 |
A |
T |
17: 38,727,987 (GRCm39) |
M98K |
unknown |
Het |
Foxd2 |
G |
T |
4: 114,764,768 (GRCm39) |
H417Q |
possibly damaging |
Het |
Glrb |
T |
C |
3: 80,758,349 (GRCm39) |
N304D |
possibly damaging |
Het |
Haus3 |
A |
G |
5: 34,324,972 (GRCm39) |
V229A |
probably benign |
Het |
Hpgd |
A |
T |
8: 56,770,838 (GRCm39) |
I159F |
possibly damaging |
Het |
Ighv1-22 |
T |
A |
12: 114,710,036 (GRCm39) |
I70F |
probably benign |
Het |
Il16 |
A |
T |
7: 83,310,153 (GRCm39) |
F584L |
possibly damaging |
Het |
Lamc2 |
T |
C |
1: 153,030,141 (GRCm39) |
D167G |
probably null |
Het |
Megf10 |
G |
A |
18: 57,426,930 (GRCm39) |
V1083I |
probably benign |
Het |
Mertk |
T |
C |
2: 128,592,079 (GRCm39) |
S268P |
probably damaging |
Het |
Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
Mki67 |
T |
C |
7: 135,310,500 (GRCm39) |
D132G |
probably damaging |
Het |
Nbas |
A |
G |
12: 13,371,756 (GRCm39) |
N419D |
probably damaging |
Het |
Negr1 |
T |
C |
3: 156,565,082 (GRCm39) |
L56S |
probably damaging |
Het |
Nup214 |
A |
G |
2: 31,870,596 (GRCm39) |
|
probably null |
Het |
Opn5 |
C |
G |
17: 42,891,610 (GRCm39) |
A276P |
probably damaging |
Het |
Or10j5 |
A |
G |
1: 172,785,166 (GRCm39) |
E268G |
probably benign |
Het |
Or2d3 |
C |
T |
7: 106,490,642 (GRCm39) |
V225I |
probably benign |
Het |
Or5t9 |
T |
A |
2: 86,659,598 (GRCm39) |
H167Q |
probably damaging |
Het |
Papln |
G |
T |
12: 83,823,917 (GRCm39) |
V499L |
probably benign |
Het |
Pgap1 |
A |
T |
1: 54,569,296 (GRCm39) |
W357R |
probably damaging |
Het |
Pibf1 |
T |
C |
14: 99,377,992 (GRCm39) |
Y373H |
probably damaging |
Het |
Pitpnm1 |
T |
C |
19: 4,162,252 (GRCm39) |
|
probably null |
Het |
Prcd |
T |
A |
11: 116,550,597 (GRCm39) |
W3R |
probably null |
Het |
Prkaa1 |
A |
G |
15: 5,203,838 (GRCm39) |
N249S |
probably benign |
Het |
Reg3b |
T |
A |
6: 78,349,809 (GRCm39) |
N116K |
possibly damaging |
Het |
Rpusd2 |
T |
C |
2: 118,865,360 (GRCm39) |
L19P |
probably benign |
Het |
Rufy1 |
T |
C |
11: 50,297,277 (GRCm39) |
T392A |
possibly damaging |
Het |
Sall3 |
T |
C |
18: 81,017,188 (GRCm39) |
K247E |
probably benign |
Het |
Shank1 |
C |
T |
7: 43,965,497 (GRCm39) |
T191M |
unknown |
Het |
Slit1 |
C |
T |
19: 41,717,493 (GRCm39) |
|
probably null |
Het |
Sorl1 |
A |
T |
9: 41,975,048 (GRCm39) |
V520E |
probably damaging |
Het |
Vmn2r115 |
T |
A |
17: 23,578,825 (GRCm39) |
F766Y |
probably damaging |
Het |
Zfp644 |
A |
G |
5: 106,783,279 (GRCm39) |
S1032P |
probably damaging |
Het |
|
Other mutations in Wdr87-ps |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Wdr87-ps
|
APN |
7 |
29,237,047 (GRCm39) |
exon |
noncoding transcript |
|
IGL00505:Wdr87-ps
|
APN |
7 |
29,233,608 (GRCm39) |
exon |
noncoding transcript |
|
IGL00557:Wdr87-ps
|
APN |
7 |
29,235,227 (GRCm39) |
exon |
noncoding transcript |
|
IGL00569:Wdr87-ps
|
APN |
7 |
29,233,565 (GRCm39) |
exon |
noncoding transcript |
|
IGL00966:Wdr87-ps
|
APN |
7 |
29,236,888 (GRCm39) |
exon |
noncoding transcript |
|
IGL01668:Wdr87-ps
|
APN |
7 |
29,236,855 (GRCm39) |
exon |
noncoding transcript |
|
K7371:Wdr87-ps
|
UTSW |
7 |
29,230,417 (GRCm39) |
exon |
noncoding transcript |
|
P0037:Wdr87-ps
|
UTSW |
7 |
29,233,039 (GRCm39) |
exon |
noncoding transcript |
|
R0179:Wdr87-ps
|
UTSW |
7 |
29,235,365 (GRCm39) |
exon |
noncoding transcript |
|
R0357:Wdr87-ps
|
UTSW |
7 |
29,235,007 (GRCm39) |
exon |
noncoding transcript |
|
R0358:Wdr87-ps
|
UTSW |
7 |
29,231,636 (GRCm39) |
exon |
noncoding transcript |
|
R0412:Wdr87-ps
|
UTSW |
7 |
29,229,995 (GRCm39) |
exon |
noncoding transcript |
|
R0530:Wdr87-ps
|
UTSW |
7 |
29,229,545 (GRCm39) |
exon |
noncoding transcript |
|
R0600:Wdr87-ps
|
UTSW |
7 |
29,232,690 (GRCm39) |
exon |
noncoding transcript |
|
R0675:Wdr87-ps
|
UTSW |
7 |
29,231,942 (GRCm39) |
exon |
noncoding transcript |
|
R1118:Wdr87-ps
|
UTSW |
7 |
29,233,669 (GRCm39) |
exon |
noncoding transcript |
|
R1395:Wdr87-ps
|
UTSW |
7 |
29,230,812 (GRCm39) |
exon |
noncoding transcript |
|
R1444:Wdr87-ps
|
UTSW |
7 |
29,229,380 (GRCm39) |
exon |
noncoding transcript |
|
R1476:Wdr87-ps
|
UTSW |
7 |
29,234,315 (GRCm39) |
exon |
noncoding transcript |
|
R1534:Wdr87-ps
|
UTSW |
7 |
29,229,854 (GRCm39) |
exon |
noncoding transcript |
|
R1535:Wdr87-ps
|
UTSW |
7 |
29,229,004 (GRCm39) |
exon |
noncoding transcript |
|
R2023:Wdr87-ps
|
UTSW |
7 |
29,230,959 (GRCm39) |
exon |
noncoding transcript |
|
R2127:Wdr87-ps
|
UTSW |
7 |
29,236,565 (GRCm39) |
exon |
noncoding transcript |
|
R2141:Wdr87-ps
|
UTSW |
7 |
29,230,935 (GRCm39) |
exon |
noncoding transcript |
|
R2198:Wdr87-ps
|
UTSW |
7 |
29,226,697 (GRCm39) |
exon |
noncoding transcript |
|
R2201:Wdr87-ps
|
UTSW |
7 |
29,235,950 (GRCm39) |
exon |
noncoding transcript |
|
R2262:Wdr87-ps
|
UTSW |
7 |
29,231,987 (GRCm39) |
exon |
noncoding transcript |
|
R2263:Wdr87-ps
|
UTSW |
7 |
29,231,987 (GRCm39) |
exon |
noncoding transcript |
|
R5064:Wdr87-ps
|
UTSW |
7 |
29,235,080 (GRCm39) |
exon |
noncoding transcript |
|
R5130:Wdr87-ps
|
UTSW |
7 |
29,228,699 (GRCm39) |
exon |
noncoding transcript |
|
R5366:Wdr87-ps
|
UTSW |
7 |
29,232,964 (GRCm39) |
exon |
noncoding transcript |
|
|