Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
G |
6: 121,615,375 (GRCm39) |
D83G |
probably benign |
Het |
Ablim1 |
T |
C |
19: 57,143,681 (GRCm39) |
T80A |
probably damaging |
Het |
Adam6b |
C |
A |
12: 113,454,200 (GRCm39) |
P339H |
possibly damaging |
Het |
Adgrb2 |
A |
T |
4: 129,915,995 (GRCm39) |
H1505L |
possibly damaging |
Het |
Ankrd46 |
G |
A |
15: 36,486,175 (GRCm39) |
T26I |
probably benign |
Het |
Bmpr1b |
T |
C |
3: 141,562,176 (GRCm39) |
N337S |
probably damaging |
Het |
Ccdc47 |
C |
T |
11: 106,101,176 (GRCm39) |
R162Q |
probably benign |
Het |
Cct5 |
A |
G |
15: 31,594,448 (GRCm39) |
|
probably benign |
Het |
Cdca2 |
T |
C |
14: 67,914,920 (GRCm39) |
K780E |
possibly damaging |
Het |
Cds1 |
T |
C |
5: 101,946,361 (GRCm39) |
S187P |
probably damaging |
Het |
Ces3a |
G |
A |
8: 105,784,188 (GRCm39) |
E416K |
probably damaging |
Het |
Chd8 |
T |
A |
14: 52,439,571 (GRCm39) |
|
probably benign |
Het |
Chuk |
A |
T |
19: 44,067,394 (GRCm39) |
V587E |
probably damaging |
Het |
Clec16a |
G |
A |
16: 10,549,543 (GRCm39) |
C872Y |
probably damaging |
Het |
Commd10 |
T |
C |
18: 47,093,497 (GRCm39) |
V19A |
probably damaging |
Het |
Ctsa |
A |
G |
2: 164,676,229 (GRCm39) |
|
probably benign |
Het |
Dnah6 |
T |
A |
6: 73,051,573 (GRCm39) |
I3074F |
probably damaging |
Het |
Dydc1 |
T |
C |
14: 40,804,320 (GRCm39) |
|
probably null |
Het |
Ear-ps2 |
G |
A |
14: 44,284,517 (GRCm39) |
|
noncoding transcript |
Het |
Elp1 |
T |
C |
4: 56,800,001 (GRCm39) |
T42A |
probably benign |
Het |
Enpp3 |
T |
A |
10: 24,684,058 (GRCm39) |
N227I |
probably damaging |
Het |
Fam131c |
A |
T |
4: 141,110,141 (GRCm39) |
T180S |
probably benign |
Het |
Fam193a |
C |
A |
5: 34,622,915 (GRCm39) |
|
probably null |
Het |
Fbxo41 |
T |
C |
6: 85,456,888 (GRCm39) |
E427G |
probably benign |
Het |
Gabrr2 |
A |
G |
4: 33,082,583 (GRCm39) |
K236E |
possibly damaging |
Het |
Gm10152 |
A |
T |
7: 144,317,283 (GRCm39) |
|
noncoding transcript |
Het |
Gm18025 |
C |
T |
12: 34,340,574 (GRCm39) |
C173Y |
probably benign |
Het |
Gm5414 |
C |
A |
15: 101,533,099 (GRCm39) |
V443F |
probably damaging |
Het |
Gm7334 |
T |
C |
17: 51,006,160 (GRCm39) |
S149P |
possibly damaging |
Het |
Gpaa1 |
T |
A |
15: 76,216,511 (GRCm39) |
|
probably benign |
Het |
Grik2 |
G |
A |
10: 49,008,867 (GRCm39) |
T740M |
probably damaging |
Het |
Gvin3 |
T |
C |
7: 106,197,958 (GRCm39) |
|
noncoding transcript |
Het |
Hdac5 |
T |
C |
11: 102,088,180 (GRCm39) |
Y930C |
probably damaging |
Het |
Hepacam2 |
T |
C |
6: 3,483,377 (GRCm39) |
T211A |
probably benign |
Het |
Herc4 |
G |
T |
10: 63,143,578 (GRCm39) |
E703* |
probably null |
Het |
Hras |
T |
C |
7: 140,772,853 (GRCm39) |
M1V |
probably null |
Het |
Il23r |
T |
G |
6: 67,400,479 (GRCm39) |
Q617P |
probably damaging |
Het |
Insc |
T |
A |
7: 114,444,273 (GRCm39) |
M420K |
probably damaging |
Het |
Ints10 |
A |
T |
8: 69,273,472 (GRCm39) |
|
probably null |
Het |
Kank1 |
A |
G |
19: 25,388,693 (GRCm39) |
T789A |
probably damaging |
Het |
Kat6a |
T |
A |
8: 23,430,000 (GRCm39) |
L1785Q |
unknown |
Het |
Kcnj12 |
A |
G |
11: 60,961,012 (GRCm39) |
K437E |
probably benign |
Het |
Knl1 |
T |
A |
2: 118,900,736 (GRCm39) |
D812E |
possibly damaging |
Het |
Luc7l |
C |
A |
17: 26,494,707 (GRCm39) |
C104* |
probably null |
Het |
Lurap1 |
G |
A |
4: 116,001,601 (GRCm39) |
L31F |
probably damaging |
Het |
Mia2 |
A |
G |
12: 59,142,598 (GRCm39) |
S5G |
probably benign |
Het |
Mon1b |
C |
T |
8: 114,362,899 (GRCm39) |
T49I |
probably null |
Het |
Mrgprb3 |
T |
C |
7: 48,292,682 (GRCm39) |
T290A |
possibly damaging |
Het |
Mxd3 |
T |
C |
13: 55,477,071 (GRCm39) |
|
probably benign |
Het |
Negr1 |
A |
T |
3: 156,774,913 (GRCm39) |
K210* |
probably null |
Het |
Nek7 |
A |
T |
1: 138,426,312 (GRCm39) |
|
probably null |
Het |
Nktr |
T |
C |
9: 121,581,834 (GRCm39) |
|
probably benign |
Het |
Nrxn2 |
A |
G |
19: 6,540,111 (GRCm39) |
T796A |
probably damaging |
Het |
Nwd2 |
C |
A |
5: 63,963,859 (GRCm39) |
L1148I |
probably benign |
Het |
Or5d46 |
T |
C |
2: 88,170,332 (GRCm39) |
L141P |
probably damaging |
Het |
Osmr |
G |
C |
15: 6,872,362 (GRCm39) |
T244S |
probably damaging |
Het |
Ovol3 |
T |
C |
7: 29,932,904 (GRCm39) |
D177G |
possibly damaging |
Het |
Pcdha4 |
G |
A |
18: 37,087,755 (GRCm39) |
R646H |
probably benign |
Het |
Pdilt |
T |
C |
7: 119,114,147 (GRCm39) |
E117G |
possibly damaging |
Het |
Pecr |
A |
G |
1: 72,314,005 (GRCm39) |
|
probably benign |
Het |
Per3 |
G |
T |
4: 151,125,759 (GRCm39) |
L187I |
probably damaging |
Het |
Plcl2 |
G |
A |
17: 50,816,876 (GRCm39) |
A81T |
probably benign |
Het |
Polr2a |
T |
C |
11: 69,638,101 (GRCm39) |
N123D |
probably benign |
Het |
Prex2 |
T |
A |
1: 11,210,235 (GRCm39) |
D558E |
possibly damaging |
Het |
Psma5 |
T |
G |
3: 108,175,386 (GRCm39) |
V146G |
possibly damaging |
Het |
Rgs11 |
A |
T |
17: 26,421,947 (GRCm39) |
M1L |
probably benign |
Het |
Rgsl1 |
T |
C |
1: 153,678,038 (GRCm39) |
N130S |
probably benign |
Het |
Rhbg |
T |
A |
3: 88,152,775 (GRCm39) |
T313S |
probably benign |
Het |
Ripply2 |
T |
A |
9: 86,897,691 (GRCm39) |
|
probably benign |
Het |
Scap |
T |
C |
9: 110,210,701 (GRCm39) |
V1011A |
probably benign |
Het |
Scara5 |
CG |
C |
14: 65,997,111 (GRCm39) |
|
probably null |
Het |
Scarf1 |
G |
A |
11: 75,406,406 (GRCm39) |
G230D |
probably damaging |
Het |
Slc17a8 |
A |
G |
10: 89,425,356 (GRCm39) |
|
probably null |
Het |
Slc22a14 |
A |
T |
9: 119,059,662 (GRCm39) |
L153Q |
probably damaging |
Het |
Slc22a27 |
A |
G |
19: 7,856,820 (GRCm39) |
I406T |
probably benign |
Het |
Slc30a6 |
A |
G |
17: 74,730,190 (GRCm39) |
D355G |
probably benign |
Het |
Socs7 |
A |
G |
11: 97,268,852 (GRCm39) |
D382G |
possibly damaging |
Het |
Sphkap |
A |
G |
1: 83,254,503 (GRCm39) |
V1082A |
probably benign |
Het |
Stox2 |
G |
A |
8: 47,866,662 (GRCm39) |
|
probably benign |
Het |
Tacc2 |
T |
C |
7: 130,335,258 (GRCm39) |
S524P |
probably damaging |
Het |
Tbc1d9b |
C |
T |
11: 50,037,140 (GRCm39) |
A263V |
probably benign |
Het |
Tekt5 |
C |
T |
16: 10,179,193 (GRCm39) |
M391I |
probably benign |
Het |
Tfap2b |
A |
T |
1: 19,296,722 (GRCm39) |
M222L |
probably benign |
Het |
Themis2 |
T |
C |
4: 132,510,244 (GRCm39) |
D652G |
possibly damaging |
Het |
Tmem185b |
A |
G |
1: 119,455,322 (GRCm39) |
|
probably benign |
Het |
Trpv4 |
A |
G |
5: 114,773,604 (GRCm39) |
Y253H |
probably damaging |
Het |
Trpv5 |
G |
A |
6: 41,637,266 (GRCm39) |
R358C |
probably benign |
Het |
Ush2a |
G |
A |
1: 188,460,578 (GRCm39) |
G2613E |
probably benign |
Het |
Usp25 |
C |
A |
16: 76,847,446 (GRCm39) |
Q185K |
probably damaging |
Het |
Xkr5 |
G |
A |
8: 18,983,484 (GRCm39) |
|
probably benign |
Het |
Zfp541 |
C |
T |
7: 15,829,683 (GRCm39) |
P1331S |
probably 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 |
|
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 |
|
R7584:Ms4a20
|
UTSW |
19 |
11,087,725 (GRCm39) |
missense |
possibly damaging |
0.94 |
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 |
|