Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,618,345 (GRCm39) |
I213V |
probably null |
Het |
Abcc4 |
A |
T |
14: 118,763,755 (GRCm39) |
C952S |
probably benign |
Het |
Adhfe1 |
T |
C |
1: 9,620,816 (GRCm39) |
|
probably benign |
Het |
Apob |
T |
A |
12: 8,060,080 (GRCm39) |
L2854* |
probably null |
Het |
Arhgap5 |
T |
A |
12: 52,565,109 (GRCm39) |
N693K |
probably benign |
Het |
Arid5b |
A |
G |
10: 67,933,649 (GRCm39) |
V508A |
probably damaging |
Het |
Atl1 |
A |
G |
12: 70,000,214 (GRCm39) |
E288G |
probably damaging |
Het |
Bank1 |
A |
G |
3: 135,806,270 (GRCm39) |
S455P |
possibly damaging |
Het |
Ces1c |
A |
T |
8: 93,857,392 (GRCm39) |
L63Q |
probably damaging |
Het |
Crmp1 |
A |
T |
5: 37,426,036 (GRCm39) |
|
probably null |
Het |
Csnka2ip |
T |
C |
16: 64,298,780 (GRCm39) |
D528G |
unknown |
Het |
Dkk2 |
T |
C |
3: 131,880,760 (GRCm39) |
L135P |
probably damaging |
Het |
Drc3 |
A |
G |
11: 60,278,129 (GRCm39) |
N381S |
probably benign |
Het |
Dsg4 |
T |
C |
18: 20,591,578 (GRCm39) |
V439A |
possibly damaging |
Het |
Dysf |
C |
T |
6: 84,114,340 (GRCm39) |
P1240S |
probably damaging |
Het |
Esyt1 |
A |
T |
10: 128,361,520 (GRCm39) |
V58E |
probably damaging |
Het |
Exo1 |
G |
T |
1: 175,721,338 (GRCm39) |
A326S |
probably damaging |
Het |
Fam20b |
A |
G |
1: 156,518,135 (GRCm39) |
S220P |
probably damaging |
Het |
Fmo6 |
G |
A |
1: 162,745,817 (GRCm39) |
T402I |
probably benign |
Het |
Galnt10 |
A |
T |
11: 57,656,410 (GRCm39) |
D198V |
probably benign |
Het |
Gsap |
A |
T |
5: 21,483,108 (GRCm39) |
E604D |
probably benign |
Het |
Il20rb |
A |
G |
9: 100,343,481 (GRCm39) |
Y258H |
probably benign |
Het |
Impg1 |
A |
T |
9: 80,285,776 (GRCm39) |
S409R |
probably damaging |
Het |
Jak3 |
G |
T |
8: 72,131,425 (GRCm39) |
V97F |
possibly damaging |
Het |
Lbhd1 |
T |
C |
19: 8,861,523 (GRCm39) |
S52P |
probably damaging |
Het |
Lman2l |
A |
G |
1: 36,482,599 (GRCm39) |
|
probably benign |
Het |
Lnpep |
C |
A |
17: 17,788,625 (GRCm39) |
M493I |
probably benign |
Het |
Mpp4 |
T |
C |
1: 59,188,774 (GRCm39) |
D132G |
probably damaging |
Het |
Nlrp1a |
G |
A |
11: 71,014,378 (GRCm39) |
R291W |
probably benign |
Het |
Or1e23 |
G |
T |
11: 73,407,247 (GRCm39) |
Y259* |
probably null |
Het |
Or4a79 |
T |
A |
2: 89,551,730 (GRCm39) |
I242F |
probably benign |
Het |
Or4b13 |
C |
T |
2: 90,082,441 (GRCm39) |
R297Q |
possibly damaging |
Het |
Or4f15 |
G |
A |
2: 111,814,308 (GRCm39) |
A37V |
probably benign |
Het |
Or4n4b |
T |
A |
14: 50,536,656 (GRCm39) |
I37F |
probably damaging |
Het |
Orc5 |
A |
G |
5: 22,738,787 (GRCm39) |
V158A |
probably benign |
Het |
Pate8 |
C |
A |
9: 36,493,854 (GRCm39) |
W26C |
unknown |
Het |
Pcdhga3 |
A |
G |
18: 37,808,674 (GRCm39) |
N376D |
probably damaging |
Het |
Ptprr |
T |
A |
10: 116,072,659 (GRCm39) |
I207N |
probably damaging |
Het |
Recql5 |
A |
G |
11: 115,785,402 (GRCm39) |
V698A |
probably benign |
Het |
Rnf212 |
A |
T |
5: 108,877,826 (GRCm39) |
M222K |
probably benign |
Het |
Rsph6a |
A |
G |
7: 18,788,820 (GRCm39) |
S51G |
probably benign |
Het |
Smap2 |
T |
C |
4: 120,839,365 (GRCm39) |
K121E |
probably damaging |
Het |
Syt11 |
A |
T |
3: 88,655,296 (GRCm39) |
V335D |
possibly damaging |
Het |
Terb1 |
A |
T |
8: 105,215,222 (GRCm39) |
C251* |
probably null |
Het |
Tmprss11d |
C |
A |
5: 86,474,432 (GRCm39) |
R37L |
probably damaging |
Het |
Ttbk2 |
T |
C |
2: 120,576,265 (GRCm39) |
N904S |
possibly damaging |
Het |
Vmn1r119 |
T |
A |
7: 20,745,714 (GRCm39) |
I223F |
probably damaging |
Het |
Vmn1r66 |
T |
C |
7: 10,008,683 (GRCm39) |
R117G |
possibly damaging |
Het |
Zfp106 |
T |
C |
2: 120,362,113 (GRCm39) |
D1025G |
probably damaging |
Het |
|
Other mutations in Dact2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01867:Dact2
|
APN |
17 |
14,415,932 (GRCm39) |
missense |
probably damaging |
0.98 |
R0597:Dact2
|
UTSW |
17 |
14,417,303 (GRCm39) |
missense |
probably benign |
|
R1657:Dact2
|
UTSW |
17 |
14,418,252 (GRCm39) |
missense |
probably benign |
0.03 |
R1717:Dact2
|
UTSW |
17 |
14,418,175 (GRCm39) |
missense |
probably benign |
0.11 |
R1734:Dact2
|
UTSW |
17 |
14,416,901 (GRCm39) |
missense |
probably benign |
0.00 |
R1883:Dact2
|
UTSW |
17 |
14,418,085 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2238:Dact2
|
UTSW |
17 |
14,417,312 (GRCm39) |
missense |
probably damaging |
0.99 |
R2878:Dact2
|
UTSW |
17 |
14,416,176 (GRCm39) |
missense |
probably damaging |
1.00 |
R4290:Dact2
|
UTSW |
17 |
14,416,833 (GRCm39) |
missense |
probably benign |
0.00 |
R4291:Dact2
|
UTSW |
17 |
14,416,833 (GRCm39) |
missense |
probably benign |
0.00 |
R4902:Dact2
|
UTSW |
17 |
14,416,991 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5029:Dact2
|
UTSW |
17 |
14,416,114 (GRCm39) |
missense |
probably benign |
0.00 |
R5084:Dact2
|
UTSW |
17 |
14,418,214 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5436:Dact2
|
UTSW |
17 |
14,416,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R5837:Dact2
|
UTSW |
17 |
14,416,515 (GRCm39) |
missense |
probably damaging |
1.00 |
R5847:Dact2
|
UTSW |
17 |
14,419,450 (GRCm39) |
missense |
probably damaging |
0.97 |
R6048:Dact2
|
UTSW |
17 |
14,417,567 (GRCm39) |
missense |
probably damaging |
1.00 |
R6377:Dact2
|
UTSW |
17 |
14,419,450 (GRCm39) |
missense |
probably damaging |
0.97 |
R7268:Dact2
|
UTSW |
17 |
14,416,797 (GRCm39) |
missense |
probably benign |
0.01 |
R7425:Dact2
|
UTSW |
17 |
14,416,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Dact2
|
UTSW |
17 |
14,417,146 (GRCm39) |
nonsense |
probably null |
|
R8727:Dact2
|
UTSW |
17 |
14,417,146 (GRCm39) |
nonsense |
probably null |
|
|