Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc9 |
G |
A |
6: 142,536,102 (GRCm39) |
A1544V |
possibly damaging |
Het |
Akap6 |
A |
G |
12: 52,933,341 (GRCm39) |
T278A |
probably benign |
Het |
Arfgef1 |
T |
A |
1: 10,233,977 (GRCm39) |
I1106F |
probably benign |
Het |
Armc7 |
T |
C |
11: 115,367,038 (GRCm39) |
L61S |
probably damaging |
Het |
Atp1a3 |
G |
A |
7: 24,700,027 (GRCm39) |
T111M |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,095,565 (GRCm39) |
K1103* |
probably null |
Het |
Cacna2d4 |
T |
A |
6: 119,322,023 (GRCm39) |
S962R |
probably benign |
Het |
Camsap2 |
T |
C |
1: 136,204,936 (GRCm39) |
T526A |
|
Het |
Casq2 |
A |
T |
3: 102,052,622 (GRCm39) |
D378V |
unknown |
Het |
Chst8 |
C |
T |
7: 34,374,646 (GRCm39) |
D398N |
possibly damaging |
Het |
Cmya5 |
C |
T |
13: 93,226,604 (GRCm39) |
G2828D |
probably damaging |
Het |
Cntnap2 |
T |
A |
6: 45,969,009 (GRCm39) |
N250K |
probably damaging |
Het |
Cpne5 |
T |
C |
17: 29,380,520 (GRCm39) |
N401D |
probably damaging |
Het |
Cse1l |
A |
G |
2: 166,757,119 (GRCm39) |
N7S |
probably damaging |
Het |
Cyp4f39 |
G |
A |
17: 32,705,920 (GRCm39) |
G337D |
probably damaging |
Het |
Dera |
C |
T |
6: 137,814,135 (GRCm39) |
R308C |
probably benign |
Het |
Drd5 |
T |
A |
5: 38,478,174 (GRCm39) |
I389N |
possibly damaging |
Het |
F830016B08Rik |
A |
G |
18: 60,433,237 (GRCm39) |
T107A |
probably damaging |
Het |
Fbxw22 |
C |
A |
9: 109,212,986 (GRCm39) |
L320F |
probably damaging |
Het |
Fndc3b |
G |
T |
3: 27,552,941 (GRCm39) |
T352K |
probably damaging |
Het |
Gm36864 |
T |
A |
7: 43,886,275 (GRCm39) |
I169K |
unknown |
Het |
Hdac4 |
A |
T |
1: 91,889,277 (GRCm39) |
D749E |
probably damaging |
Het |
Herc1 |
C |
T |
9: 66,304,594 (GRCm39) |
A805V |
possibly damaging |
Het |
Hrh1 |
A |
G |
6: 114,457,453 (GRCm39) |
K245E |
probably benign |
Het |
Khdc1a |
A |
G |
1: 21,421,204 (GRCm39) |
T130A |
probably benign |
Het |
Lrp5 |
C |
G |
19: 3,641,712 (GRCm39) |
A1417P |
probably benign |
Het |
Macf1 |
T |
C |
4: 123,365,002 (GRCm39) |
Q3253R |
possibly damaging |
Het |
Mdn1 |
T |
A |
4: 32,684,723 (GRCm39) |
L811* |
probably null |
Het |
Mettl8 |
T |
C |
2: 70,812,383 (GRCm39) |
D84G |
possibly damaging |
Het |
Miga1 |
T |
G |
3: 151,993,186 (GRCm39) |
T412P |
probably benign |
Het |
Mtor |
G |
T |
4: 148,632,092 (GRCm39) |
R2322L |
possibly damaging |
Het |
Muc16 |
T |
C |
9: 18,567,147 (GRCm39) |
N1791D |
unknown |
Het |
Myo9b |
C |
G |
8: 71,743,075 (GRCm39) |
S45R |
possibly damaging |
Het |
Nup50l |
A |
T |
6: 96,142,156 (GRCm39) |
L296Q |
possibly damaging |
Het |
Olfm4 |
T |
C |
14: 80,243,747 (GRCm39) |
F105S |
probably damaging |
Het |
Or5af2 |
A |
T |
11: 58,708,370 (GRCm39) |
I179F |
possibly damaging |
Het |
Osbpl1a |
T |
C |
18: 13,015,277 (GRCm39) |
I384V |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,030,435 (GRCm39) |
L1131P |
|
Het |
Pex6 |
T |
A |
17: 47,035,322 (GRCm39) |
V827E |
probably damaging |
Het |
Plek |
A |
C |
11: 16,940,119 (GRCm39) |
S197A |
probably benign |
Het |
Pmpca |
T |
C |
2: 26,282,598 (GRCm39) |
Y269H |
probably benign |
Het |
Pop1 |
T |
C |
15: 34,512,881 (GRCm39) |
I493T |
probably benign |
Het |
Rap1gap2 |
T |
C |
11: 74,283,954 (GRCm39) |
N615D |
probably benign |
Het |
Rtp3 |
T |
C |
9: 110,815,198 (GRCm39) |
Y389C |
unknown |
Het |
Rusf1 |
T |
A |
7: 127,875,676 (GRCm39) |
D253V |
possibly damaging |
Het |
Sardh |
T |
C |
2: 27,120,513 (GRCm39) |
Q423R |
probably benign |
Het |
Slc11a1 |
T |
C |
1: 74,422,688 (GRCm39) |
|
probably null |
Het |
Slc5a4b |
T |
C |
10: 75,896,239 (GRCm39) |
D572G |
probably damaging |
Het |
Slco1a8 |
T |
G |
6: 141,949,234 (GRCm39) |
|
probably null |
Het |
Slfn14 |
A |
G |
11: 83,170,048 (GRCm39) |
V532A |
probably benign |
Het |
Spmip10 |
T |
C |
18: 56,725,450 (GRCm39) |
W37R |
probably benign |
Het |
Stxbp1 |
T |
C |
2: 32,701,120 (GRCm39) |
Y264C |
possibly damaging |
Het |
Syce1l |
T |
C |
8: 114,381,750 (GRCm39) |
I230T |
unknown |
Het |
Taf5l |
T |
C |
8: 124,730,173 (GRCm39) |
Y172C |
|
Het |
Trpc4 |
A |
T |
3: 54,102,248 (GRCm39) |
K49* |
probably null |
Het |
Ttc13 |
A |
G |
8: 125,415,284 (GRCm39) |
V285A |
probably benign |
Het |
Ttc17 |
A |
T |
2: 94,204,890 (GRCm39) |
L344Q |
probably damaging |
Het |
Unc79 |
A |
G |
12: 103,135,972 (GRCm39) |
H2469R |
probably benign |
Het |
Xkr7 |
A |
G |
2: 152,896,393 (GRCm39) |
I416V |
probably benign |
Het |
Zeb2 |
C |
A |
2: 44,987,180 (GRCm39) |
D35Y |
unknown |
Het |
Zfp28 |
A |
G |
7: 6,397,917 (GRCm39) |
H784R |
probably benign |
Het |
Zfp644 |
A |
C |
5: 106,783,909 (GRCm39) |
S848R |
probably benign |
Het |
Zfp809 |
G |
A |
9: 22,150,384 (GRCm39) |
E294K |
possibly damaging |
Het |
Zfp820 |
A |
G |
17: 22,038,861 (GRCm39) |
Y156H |
probably benign |
Het |
|
Other mutations in 5730455P16Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00516:5730455P16Rik
|
APN |
11 |
80,267,638 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL03096:5730455P16Rik
|
APN |
11 |
80,265,005 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4431001:5730455P16Rik
|
UTSW |
11 |
80,254,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R0383:5730455P16Rik
|
UTSW |
11 |
80,254,767 (GRCm39) |
nonsense |
probably null |
|
R0635:5730455P16Rik
|
UTSW |
11 |
80,264,891 (GRCm39) |
splice site |
probably benign |
|
R1376:5730455P16Rik
|
UTSW |
11 |
80,254,735 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1376:5730455P16Rik
|
UTSW |
11 |
80,254,735 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1598:5730455P16Rik
|
UTSW |
11 |
80,254,838 (GRCm39) |
nonsense |
probably null |
|
R1953:5730455P16Rik
|
UTSW |
11 |
80,268,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R3236:5730455P16Rik
|
UTSW |
11 |
80,258,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R4056:5730455P16Rik
|
UTSW |
11 |
80,266,329 (GRCm39) |
splice site |
probably benign |
|
R4612:5730455P16Rik
|
UTSW |
11 |
80,268,806 (GRCm39) |
start codon destroyed |
probably null |
0.90 |
R4777:5730455P16Rik
|
UTSW |
11 |
80,265,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R4820:5730455P16Rik
|
UTSW |
11 |
80,266,346 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4847:5730455P16Rik
|
UTSW |
11 |
80,264,940 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:5730455P16Rik
|
UTSW |
11 |
80,268,778 (GRCm39) |
start codon destroyed |
probably null |
|
R7125:5730455P16Rik
|
UTSW |
11 |
80,255,751 (GRCm39) |
missense |
probably damaging |
0.97 |
R8049:5730455P16Rik
|
UTSW |
11 |
80,268,798 (GRCm39) |
missense |
possibly damaging |
0.86 |
|