Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad12 |
T |
C |
5: 121,742,358 (GRCm39) |
I417V |
probably benign |
Het |
Adad1 |
T |
C |
3: 37,119,399 (GRCm39) |
V160A |
possibly damaging |
Het |
Adcy7 |
A |
G |
8: 89,051,487 (GRCm39) |
E869G |
probably damaging |
Het |
Birc6 |
G |
A |
17: 74,977,242 (GRCm39) |
A4352T |
probably damaging |
Het |
Brd2 |
T |
A |
17: 34,334,205 (GRCm39) |
T286S |
probably damaging |
Het |
Bsn |
G |
T |
9: 107,988,123 (GRCm39) |
|
probably benign |
Het |
Cables1 |
A |
G |
18: 12,057,884 (GRCm39) |
T335A |
probably benign |
Het |
Cacna1d |
A |
T |
14: 30,072,682 (GRCm39) |
S98T |
possibly damaging |
Het |
Ccdc181 |
A |
G |
1: 164,105,810 (GRCm39) |
Y15C |
probably damaging |
Het |
Dlgap4 |
T |
G |
2: 156,587,839 (GRCm39) |
V39G |
probably damaging |
Het |
Epb41l3 |
G |
A |
17: 69,569,268 (GRCm39) |
R504H |
probably benign |
Het |
Fbxo7 |
T |
C |
10: 85,857,954 (GRCm39) |
L23P |
probably damaging |
Het |
Gm42791 |
A |
C |
5: 148,887,178 (GRCm39) |
|
probably benign |
Het |
Gprc5b |
A |
T |
7: 118,582,910 (GRCm39) |
F320I |
possibly damaging |
Het |
Gtf3c1 |
G |
A |
7: 125,262,580 (GRCm39) |
T1093M |
possibly damaging |
Het |
Hddc3 |
G |
T |
7: 79,993,543 (GRCm39) |
R83L |
probably damaging |
Het |
Iars2 |
T |
C |
1: 185,055,318 (GRCm39) |
|
probably benign |
Het |
Ift25 |
T |
A |
4: 107,136,998 (GRCm39) |
I132N |
probably damaging |
Het |
Igfn1 |
T |
C |
1: 135,895,599 (GRCm39) |
K1656E |
probably benign |
Het |
Itk |
A |
C |
11: 46,228,926 (GRCm39) |
|
probably null |
Het |
Klra6 |
G |
A |
6: 129,995,932 (GRCm39) |
T142I |
probably benign |
Het |
Knop1 |
C |
T |
7: 118,454,993 (GRCm39) |
A3T |
probably damaging |
Het |
Lamc3 |
A |
G |
2: 31,808,608 (GRCm39) |
H788R |
probably damaging |
Het |
Lrif1 |
A |
G |
3: 106,639,859 (GRCm39) |
R315G |
probably damaging |
Het |
Mfap3l |
A |
G |
8: 61,109,903 (GRCm39) |
D93G |
probably benign |
Het |
Ngef |
T |
C |
1: 87,473,552 (GRCm39) |
S77G |
probably benign |
Het |
Or9s13 |
T |
C |
1: 92,548,084 (GRCm39) |
V152A |
probably benign |
Het |
Pclo |
T |
C |
5: 14,729,761 (GRCm39) |
|
probably benign |
Het |
Pkhd1l1 |
C |
T |
15: 44,378,368 (GRCm39) |
Q1041* |
probably null |
Het |
Ppl |
G |
A |
16: 4,906,987 (GRCm39) |
R1103* |
probably null |
Het |
Ppp4r3b |
T |
A |
11: 29,161,667 (GRCm39) |
D680E |
probably benign |
Het |
Rasgrf2 |
T |
G |
13: 92,267,941 (GRCm39) |
K21T |
possibly damaging |
Het |
Rev1 |
T |
A |
1: 38,094,407 (GRCm39) |
K1004* |
probably null |
Het |
Rgs9 |
T |
G |
11: 109,130,277 (GRCm39) |
|
probably null |
Het |
Rnf31 |
T |
C |
14: 55,829,693 (GRCm39) |
L86P |
probably damaging |
Het |
Rps13 |
A |
G |
7: 115,933,155 (GRCm39) |
Y18H |
probably damaging |
Het |
Rxfp2 |
T |
C |
5: 149,958,909 (GRCm39) |
F33S |
probably damaging |
Het |
Sfmbt1 |
G |
A |
14: 30,538,777 (GRCm39) |
V799M |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,532,428 (GRCm39) |
V2895D |
probably benign |
Het |
Syn3 |
T |
C |
10: 86,187,428 (GRCm39) |
N232S |
possibly damaging |
Het |
Taok3 |
T |
A |
5: 117,404,140 (GRCm39) |
Y772N |
probably damaging |
Het |
Tspan4 |
A |
G |
7: 141,062,483 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
A |
2: 76,684,530 (GRCm39) |
|
probably benign |
Het |
Vwa3b |
T |
A |
1: 37,084,120 (GRCm39) |
W98R |
probably damaging |
Het |
Vwa5b2 |
A |
T |
16: 20,415,058 (GRCm39) |
D360V |
probably damaging |
Het |
Wdr73 |
A |
T |
7: 80,541,557 (GRCm39) |
D328E |
probably benign |
Het |
Xpo5 |
A |
G |
17: 46,545,406 (GRCm39) |
N824S |
probably benign |
Het |
Zbtb2 |
C |
T |
10: 4,318,566 (GRCm39) |
G487S |
possibly damaging |
Het |
|
Other mutations in Nt5dc3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00476:Nt5dc3
|
APN |
10 |
86,669,838 (GRCm39) |
splice site |
probably null |
|
IGL00767:Nt5dc3
|
APN |
10 |
86,656,137 (GRCm39) |
splice site |
probably benign |
|
IGL01318:Nt5dc3
|
APN |
10 |
86,661,089 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL01369:Nt5dc3
|
APN |
10 |
86,656,139 (GRCm39) |
splice site |
probably benign |
|
IGL01376:Nt5dc3
|
APN |
10 |
86,670,028 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01568:Nt5dc3
|
APN |
10 |
86,669,802 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02286:Nt5dc3
|
APN |
10 |
86,656,644 (GRCm39) |
splice site |
probably benign |
|
IGL02692:Nt5dc3
|
APN |
10 |
86,640,642 (GRCm39) |
splice site |
probably null |
|
R0372:Nt5dc3
|
UTSW |
10 |
86,661,155 (GRCm39) |
missense |
possibly damaging |
0.82 |
R0714:Nt5dc3
|
UTSW |
10 |
86,648,238 (GRCm39) |
missense |
probably damaging |
1.00 |
R1755:Nt5dc3
|
UTSW |
10 |
86,660,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R1888:Nt5dc3
|
UTSW |
10 |
86,669,926 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1888:Nt5dc3
|
UTSW |
10 |
86,669,926 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3973:Nt5dc3
|
UTSW |
10 |
86,660,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R4097:Nt5dc3
|
UTSW |
10 |
86,669,820 (GRCm39) |
missense |
probably benign |
0.01 |
R4871:Nt5dc3
|
UTSW |
10 |
86,652,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5482:Nt5dc3
|
UTSW |
10 |
86,647,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R5530:Nt5dc3
|
UTSW |
10 |
86,656,857 (GRCm39) |
missense |
probably damaging |
0.99 |
R5861:Nt5dc3
|
UTSW |
10 |
86,651,738 (GRCm39) |
missense |
probably damaging |
1.00 |
R6260:Nt5dc3
|
UTSW |
10 |
86,647,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R8251:Nt5dc3
|
UTSW |
10 |
86,656,091 (GRCm39) |
missense |
probably damaging |
0.98 |
R8734:Nt5dc3
|
UTSW |
10 |
86,669,863 (GRCm39) |
missense |
possibly damaging |
0.94 |
|