Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A930003A15Rik |
T |
C |
16: 19,702,518 (GRCm39) |
|
noncoding transcript |
Het |
Angpt4 |
A |
G |
2: 151,785,342 (GRCm39) |
M453V |
probably benign |
Het |
Atr |
T |
A |
9: 95,779,783 (GRCm39) |
D1380E |
probably benign |
Het |
Carmil1 |
A |
T |
13: 24,278,438 (GRCm39) |
M177K |
probably damaging |
Het |
Cenpk |
T |
A |
13: 104,379,280 (GRCm39) |
I203N |
probably damaging |
Het |
Cerk |
A |
T |
15: 86,027,014 (GRCm39) |
N165K |
probably benign |
Het |
Col27a1 |
G |
A |
4: 63,242,869 (GRCm39) |
|
probably benign |
Het |
Crb2 |
A |
T |
2: 37,681,428 (GRCm39) |
D757V |
probably benign |
Het |
Csnk1a1 |
A |
G |
18: 61,701,376 (GRCm39) |
D91G |
probably damaging |
Het |
Dnajc6 |
G |
T |
4: 101,474,057 (GRCm39) |
W486L |
probably damaging |
Het |
Elmod1 |
C |
T |
9: 53,841,507 (GRCm39) |
|
probably benign |
Het |
Ercc3 |
G |
T |
18: 32,381,360 (GRCm39) |
R392L |
possibly damaging |
Het |
Fam135b |
C |
T |
15: 71,335,410 (GRCm39) |
V595I |
probably benign |
Het |
Fem1al |
T |
A |
11: 29,774,360 (GRCm39) |
I366F |
probably damaging |
Het |
Fermt1 |
A |
T |
2: 132,775,059 (GRCm39) |
S256T |
probably damaging |
Het |
Fstl5 |
G |
T |
3: 76,443,618 (GRCm39) |
C321F |
probably damaging |
Het |
Gpatch1 |
T |
G |
7: 35,002,742 (GRCm39) |
N256T |
probably benign |
Het |
Gpd2 |
T |
A |
2: 57,245,581 (GRCm39) |
S425R |
probably damaging |
Het |
Igkv4-57-1 |
T |
G |
6: 69,521,574 (GRCm39) |
M43L |
probably benign |
Het |
Itgae |
A |
G |
11: 73,004,427 (GRCm39) |
Q238R |
probably damaging |
Het |
Lats1 |
T |
A |
10: 7,588,510 (GRCm39) |
D1042E |
probably benign |
Het |
Lcn8 |
G |
A |
2: 25,545,377 (GRCm39) |
G156D |
probably damaging |
Het |
Loxl4 |
A |
C |
19: 42,593,718 (GRCm39) |
V224G |
probably benign |
Het |
Lrp2 |
T |
A |
2: 69,285,177 (GRCm39) |
D3827V |
probably damaging |
Het |
Neb |
C |
A |
2: 52,073,837 (GRCm39) |
R231S |
probably benign |
Het |
Or2g1 |
G |
A |
17: 38,106,679 (GRCm39) |
V115I |
probably benign |
Het |
Or5b105 |
A |
T |
19: 13,080,401 (GRCm39) |
M89K |
probably benign |
Het |
Or6c211 |
A |
G |
10: 129,505,809 (GRCm39) |
M193T |
probably benign |
Het |
Or8g54 |
T |
G |
9: 39,707,475 (GRCm39) |
M268R |
probably benign |
Het |
Pappa |
T |
G |
4: 65,122,940 (GRCm39) |
S758R |
probably damaging |
Het |
Pced1a |
G |
A |
2: 130,264,755 (GRCm39) |
T61I |
possibly damaging |
Het |
Pik3cg |
T |
C |
12: 32,250,594 (GRCm39) |
D731G |
probably damaging |
Het |
Plxnb1 |
G |
A |
9: 108,934,054 (GRCm39) |
D761N |
probably benign |
Het |
Pmp22 |
T |
C |
11: 63,049,135 (GRCm39) |
V126A |
probably benign |
Het |
Ppp6r2 |
G |
T |
15: 89,152,748 (GRCm39) |
R296S |
probably damaging |
Het |
Prkcq |
A |
C |
2: 11,265,597 (GRCm39) |
H438P |
probably damaging |
Het |
Ryr1 |
T |
A |
7: 28,774,624 (GRCm39) |
Y2339F |
probably damaging |
Het |
Scaper |
T |
C |
9: 55,765,686 (GRCm39) |
|
probably benign |
Het |
Scp2 |
T |
A |
4: 107,955,312 (GRCm39) |
I144F |
probably benign |
Het |
Secisbp2 |
T |
C |
13: 51,806,793 (GRCm39) |
|
probably null |
Het |
Sema5a |
T |
A |
15: 32,669,554 (GRCm39) |
Y693N |
probably damaging |
Het |
Sin3b |
T |
A |
8: 73,480,213 (GRCm39) |
I905K |
probably damaging |
Het |
Slc13a3 |
T |
A |
2: 165,279,227 (GRCm39) |
M195L |
probably benign |
Het |
Strada |
A |
G |
11: 106,054,863 (GRCm39) |
|
probably benign |
Het |
Stx18 |
G |
A |
5: 38,293,655 (GRCm39) |
V294M |
probably damaging |
Het |
Tbpl2 |
A |
T |
2: 23,983,845 (GRCm39) |
N197K |
probably benign |
Het |
Tdrd9 |
A |
T |
12: 112,009,274 (GRCm39) |
H1060L |
probably damaging |
Het |
Tm4sf5 |
G |
A |
11: 70,396,223 (GRCm39) |
V23M |
possibly damaging |
Het |
Tmem54 |
C |
A |
4: 129,004,705 (GRCm39) |
L187I |
probably damaging |
Het |
Tmprss5 |
A |
G |
9: 49,024,528 (GRCm39) |
H281R |
possibly damaging |
Het |
Trim30c |
A |
G |
7: 104,031,820 (GRCm39) |
Y332H |
possibly damaging |
Het |
Uba6 |
T |
A |
5: 86,275,633 (GRCm39) |
|
probably benign |
Het |
Unc80 |
C |
A |
1: 66,670,613 (GRCm39) |
P1912Q |
probably damaging |
Het |
|
Other mutations in Or6d13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01063:Or6d13
|
APN |
6 |
116,517,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02671:Or6d13
|
APN |
6 |
116,518,104 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0041:Or6d13
|
UTSW |
6 |
116,518,295 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0426:Or6d13
|
UTSW |
6 |
116,517,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R0627:Or6d13
|
UTSW |
6 |
116,517,949 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0829:Or6d13
|
UTSW |
6 |
116,518,226 (GRCm39) |
missense |
probably benign |
0.01 |
R2111:Or6d13
|
UTSW |
6 |
116,517,611 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2112:Or6d13
|
UTSW |
6 |
116,517,611 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2120:Or6d13
|
UTSW |
6 |
116,517,416 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
R3161:Or6d13
|
UTSW |
6 |
116,517,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R3700:Or6d13
|
UTSW |
6 |
116,517,489 (GRCm39) |
missense |
probably benign |
0.10 |
R4710:Or6d13
|
UTSW |
6 |
116,517,611 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5244:Or6d13
|
UTSW |
6 |
116,518,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R5859:Or6d13
|
UTSW |
6 |
116,517,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R6273:Or6d13
|
UTSW |
6 |
116,518,277 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6505:Or6d13
|
UTSW |
6 |
116,517,561 (GRCm39) |
missense |
probably benign |
0.01 |
R7350:Or6d13
|
UTSW |
6 |
116,517,495 (GRCm39) |
missense |
probably benign |
0.28 |
R7380:Or6d13
|
UTSW |
6 |
116,517,894 (GRCm39) |
missense |
probably benign |
0.03 |
R7474:Or6d13
|
UTSW |
6 |
116,517,999 (GRCm39) |
missense |
probably damaging |
0.99 |
R8054:Or6d13
|
UTSW |
6 |
116,517,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R8476:Or6d13
|
UTSW |
6 |
116,517,507 (GRCm39) |
missense |
probably benign |
|
R8862:Or6d13
|
UTSW |
6 |
116,518,186 (GRCm39) |
missense |
probably benign |
0.03 |
R9082:Or6d13
|
UTSW |
6 |
116,517,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R9100:Or6d13
|
UTSW |
6 |
116,517,990 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9124:Or6d13
|
UTSW |
6 |
116,517,416 (GRCm39) |
start codon destroyed |
probably null |
0.04 |
R9151:Or6d13
|
UTSW |
6 |
116,517,990 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9321:Or6d13
|
UTSW |
6 |
116,518,370 (GRCm39) |
missense |
probably benign |
|
R9404:Or6d13
|
UTSW |
6 |
116,517,708 (GRCm39) |
missense |
probably damaging |
1.00 |
|