Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc10 |
A |
G |
17: 46,626,304 (GRCm39) |
|
probably null |
Het |
Actrt3 |
T |
C |
3: 30,652,356 (GRCm39) |
K246R |
probably benign |
Het |
Adam23 |
T |
A |
1: 63,584,621 (GRCm39) |
V343D |
probably damaging |
Het |
Ak2 |
T |
C |
4: 128,893,005 (GRCm39) |
S55P |
probably damaging |
Het |
Ank2 |
G |
A |
3: 126,739,777 (GRCm39) |
Q2036* |
probably null |
Het |
Ano10 |
A |
G |
9: 122,104,597 (GRCm39) |
I40T |
probably benign |
Het |
Aoc2 |
T |
A |
11: 101,217,005 (GRCm39) |
C363S |
possibly damaging |
Het |
Aplp2 |
A |
T |
9: 31,069,077 (GRCm39) |
V584E |
possibly damaging |
Het |
Arhgap32 |
A |
T |
9: 32,168,263 (GRCm39) |
T749S |
probably benign |
Het |
Atm |
A |
T |
9: 53,424,427 (GRCm39) |
F625I |
probably damaging |
Het |
Atr |
T |
C |
9: 95,824,766 (GRCm39) |
L2387P |
probably damaging |
Het |
Barhl1 |
C |
T |
2: 28,799,803 (GRCm39) |
G274D |
probably damaging |
Het |
Bcl2a1a |
A |
T |
9: 88,839,345 (GRCm39) |
D81V |
probably damaging |
Het |
Ccdc63 |
T |
G |
5: 122,251,267 (GRCm39) |
D381A |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,610,578 (GRCm39) |
|
probably null |
Het |
Crat |
C |
T |
2: 30,294,577 (GRCm39) |
R497Q |
probably benign |
Het |
Cyp4b1 |
T |
A |
4: 115,485,884 (GRCm39) |
D351V |
probably damaging |
Het |
D130043K22Rik |
A |
G |
13: 25,056,353 (GRCm39) |
S562G |
probably damaging |
Het |
Dgkb |
T |
A |
12: 38,189,391 (GRCm39) |
|
probably null |
Het |
Dmbt1 |
C |
T |
7: 130,690,481 (GRCm39) |
Q905* |
probably null |
Het |
Dnajc21 |
A |
C |
15: 10,462,381 (GRCm39) |
Y81* |
probably null |
Het |
Dnali1 |
T |
C |
4: 124,959,331 (GRCm39) |
T21A |
probably benign |
Het |
Dpp8 |
A |
T |
9: 64,986,064 (GRCm39) |
L851F |
probably damaging |
Het |
Dpt |
T |
C |
1: 164,646,477 (GRCm39) |
Y149H |
probably benign |
Het |
Ep300 |
T |
C |
15: 81,512,627 (GRCm39) |
V983A |
unknown |
Het |
Faf1 |
C |
T |
4: 109,783,154 (GRCm39) |
R549C |
probably damaging |
Het |
Gcm1 |
A |
G |
9: 77,971,749 (GRCm39) |
N230S |
possibly damaging |
Het |
Gm10803 |
T |
A |
2: 93,394,513 (GRCm39) |
I95N |
probably damaging |
Het |
Hectd4 |
T |
A |
5: 121,456,798 (GRCm39) |
I721N |
possibly damaging |
Het |
Hsp90ab1 |
T |
C |
17: 45,881,197 (GRCm39) |
H315R |
probably damaging |
Het |
Igkv10-95 |
T |
A |
6: 68,657,740 (GRCm39) |
S85R |
possibly damaging |
Het |
Katnip |
G |
T |
7: 125,469,838 (GRCm39) |
V1436L |
probably damaging |
Het |
Kcnq5 |
T |
C |
1: 21,472,545 (GRCm39) |
T901A |
probably benign |
Het |
Kremen1 |
C |
T |
11: 5,144,964 (GRCm39) |
V471M |
possibly damaging |
Het |
Lama2 |
C |
A |
10: 26,980,257 (GRCm39) |
D1853Y |
possibly damaging |
Het |
Lrif1 |
A |
G |
3: 106,639,217 (GRCm39) |
T76A |
probably benign |
Het |
Lrrtm2 |
T |
A |
18: 35,345,818 (GRCm39) |
I495F |
possibly damaging |
Het |
Ltbr |
G |
T |
6: 125,284,204 (GRCm39) |
Q413K |
probably benign |
Het |
Myrfl |
T |
A |
10: 116,664,902 (GRCm39) |
Y376F |
probably damaging |
Het |
Nup50l |
A |
C |
6: 96,142,373 (GRCm39) |
L224V |
probably benign |
Het |
Nup98 |
G |
T |
7: 101,825,596 (GRCm39) |
N414K |
probably benign |
Het |
Nynrin |
A |
G |
14: 56,109,041 (GRCm39) |
T1383A |
probably damaging |
Het |
Or4c15 |
G |
A |
2: 88,760,149 (GRCm39) |
P170L |
probably damaging |
Het |
Or5j1 |
A |
T |
2: 86,879,478 (GRCm39) |
I34N |
probably benign |
Het |
Or6c208 |
T |
A |
10: 129,223,901 (GRCm39) |
I133N |
probably damaging |
Het |
Or7g27 |
C |
A |
9: 19,250,569 (GRCm39) |
T271K |
possibly damaging |
Het |
Or8b1d |
G |
T |
9: 38,558,191 (GRCm39) |
P210T |
possibly damaging |
Het |
Pcdhb5 |
T |
A |
18: 37,455,425 (GRCm39) |
S602T |
possibly damaging |
Het |
Sall3 |
A |
G |
18: 81,017,745 (GRCm39) |
F61S |
probably benign |
Het |
Scube1 |
G |
T |
15: 83,606,088 (GRCm39) |
C61* |
probably null |
Het |
Sec31b |
T |
C |
19: 44,519,995 (GRCm39) |
|
probably null |
Het |
Sec31b |
T |
C |
19: 44,531,762 (GRCm39) |
D49G |
probably damaging |
Het |
Skic2 |
A |
G |
17: 35,060,651 (GRCm39) |
I822T |
possibly damaging |
Het |
Slc19a3 |
C |
T |
1: 83,000,469 (GRCm39) |
V183M |
possibly damaging |
Het |
Slc41a2 |
T |
C |
10: 83,152,653 (GRCm39) |
|
probably benign |
Het |
Sphk2 |
C |
A |
7: 45,361,931 (GRCm39) |
V169L |
probably damaging |
Het |
Synpo |
C |
A |
18: 60,729,349 (GRCm39) |
R951L |
probably damaging |
Het |
Tbc1d9b |
G |
A |
11: 50,061,543 (GRCm39) |
C1017Y |
probably damaging |
Het |
Tmtc4 |
C |
A |
14: 123,215,563 (GRCm39) |
V28F |
probably benign |
Het |
Tprkb |
A |
G |
6: 85,905,809 (GRCm39) |
I165V |
probably benign |
Het |
Ttc23l |
T |
A |
15: 10,533,794 (GRCm39) |
I250F |
probably damaging |
Het |
Tut4 |
T |
C |
4: 108,336,543 (GRCm39) |
V89A |
probably benign |
Het |
Ubr3 |
G |
A |
2: 69,821,847 (GRCm39) |
V1370I |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,460,306 (GRCm39) |
|
probably null |
Het |
Usp9y |
T |
C |
Y: 1,384,451 (GRCm39) |
Y689C |
probably damaging |
Het |
Vmn1r56 |
A |
T |
7: 5,198,895 (GRCm39) |
Y241N |
probably damaging |
Het |
Vmn2r6 |
T |
C |
3: 64,472,683 (GRCm39) |
T13A |
probably benign |
Het |
Vmn2r92 |
T |
A |
17: 18,387,028 (GRCm39) |
N122K |
probably benign |
Het |
Vps9d1 |
A |
G |
8: 123,977,456 (GRCm39) |
F131S |
probably damaging |
Het |
Vwa8 |
A |
C |
14: 79,219,674 (GRCm39) |
|
probably null |
Het |
Wfdc16 |
A |
T |
2: 164,480,547 (GRCm39) |
|
probably null |
Het |
Zbtb41 |
T |
A |
1: 139,351,795 (GRCm39) |
Y303N |
probably benign |
Het |
Zbtb5 |
T |
C |
4: 44,993,678 (GRCm39) |
T569A |
probably benign |
Het |
Zfp111 |
A |
G |
7: 23,898,025 (GRCm39) |
S530P |
possibly damaging |
Het |
|
Other mutations in Ms4a20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02142:Ms4a20
|
APN |
19 |
11,087,695 (GRCm39) |
nonsense |
probably null |
|
IGL02182:Ms4a20
|
APN |
19 |
11,074,436 (GRCm39) |
splice site |
probably benign |
|
IGL03156:Ms4a20
|
APN |
19 |
11,083,114 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0189:Ms4a20
|
UTSW |
19 |
11,074,311 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0218:Ms4a20
|
UTSW |
19 |
11,093,801 (GRCm39) |
nonsense |
probably null |
|
R0464:Ms4a20
|
UTSW |
19 |
11,089,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R0617:Ms4a20
|
UTSW |
19 |
11,089,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R1171:Ms4a20
|
UTSW |
19 |
11,089,741 (GRCm39) |
missense |
probably damaging |
0.97 |
R2341:Ms4a20
|
UTSW |
19 |
11,083,157 (GRCm39) |
missense |
probably benign |
|
R5099:Ms4a20
|
UTSW |
19 |
11,089,825 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5330:Ms4a20
|
UTSW |
19 |
11,069,222 (GRCm39) |
unclassified |
probably benign |
|
R5331:Ms4a20
|
UTSW |
19 |
11,069,222 (GRCm39) |
unclassified |
probably benign |
|
R5341:Ms4a20
|
UTSW |
19 |
11,087,745 (GRCm39) |
intron |
probably benign |
|
R6109:Ms4a20
|
UTSW |
19 |
11,079,276 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6177:Ms4a20
|
UTSW |
19 |
11,083,114 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6970:Ms4a20
|
UTSW |
19 |
11,089,678 (GRCm39) |
critical splice donor site |
probably null |
|
R7038:Ms4a20
|
UTSW |
19 |
11,087,675 (GRCm39) |
missense |
probably benign |
|
R7752:Ms4a20
|
UTSW |
19 |
11,079,224 (GRCm39) |
missense |
probably benign |
0.02 |
R7854:Ms4a20
|
UTSW |
19 |
11,089,741 (GRCm39) |
missense |
probably benign |
0.01 |
R8261:Ms4a20
|
UTSW |
19 |
11,087,707 (GRCm39) |
missense |
probably damaging |
0.97 |
R8723:Ms4a20
|
UTSW |
19 |
11,083,055 (GRCm39) |
missense |
probably damaging |
0.99 |
R9027:Ms4a20
|
UTSW |
19 |
11,083,055 (GRCm39) |
missense |
probably damaging |
0.99 |
R9264:Ms4a20
|
UTSW |
19 |
11,093,830 (GRCm39) |
start codon destroyed |
probably benign |
0.14 |
X0019:Ms4a20
|
UTSW |
19 |
11,083,156 (GRCm39) |
missense |
probably benign |
0.00 |
|