Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca4 |
T |
C |
3: 121,963,575 (GRCm39) |
S2060P |
probably benign |
Het |
Abcg4 |
A |
G |
9: 44,189,014 (GRCm39) |
F426S |
probably benign |
Het |
Actn1 |
C |
T |
12: 80,222,929 (GRCm39) |
|
probably null |
Het |
Adgrd1 |
T |
A |
5: 129,208,648 (GRCm39) |
H251Q |
probably benign |
Het |
Adgrg3 |
C |
T |
8: 95,766,483 (GRCm39) |
P385S |
probably damaging |
Het |
Ampd2 |
G |
T |
3: 107,987,660 (GRCm39) |
|
probably benign |
Het |
Arhgap42 |
A |
G |
9: 9,155,360 (GRCm39) |
S86P |
probably damaging |
Het |
Art5 |
C |
T |
7: 101,747,123 (GRCm39) |
E121K |
probably null |
Het |
Atad5 |
G |
A |
11: 79,985,023 (GRCm39) |
E37K |
probably benign |
Het |
Atp13a5 |
A |
G |
16: 29,053,315 (GRCm39) |
V1084A |
probably benign |
Het |
Cfap44 |
T |
C |
16: 44,241,507 (GRCm39) |
I626T |
probably benign |
Het |
Col16a1 |
T |
A |
4: 129,945,440 (GRCm39) |
|
probably null |
Het |
Defa22 |
T |
G |
8: 21,653,130 (GRCm39) |
C81G |
possibly damaging |
Het |
Dnm2 |
A |
G |
9: 21,411,649 (GRCm39) |
Y622C |
probably damaging |
Het |
Efna5 |
T |
A |
17: 62,914,340 (GRCm39) |
L201F |
unknown |
Het |
Elac1 |
T |
C |
18: 73,871,991 (GRCm39) |
R335G |
probably benign |
Het |
Enpp5 |
T |
C |
17: 44,396,468 (GRCm39) |
V460A |
probably benign |
Het |
Esr2 |
A |
G |
12: 76,169,969 (GRCm39) |
V453A |
probably benign |
Het |
Fam210b |
T |
A |
2: 172,194,497 (GRCm39) |
|
probably benign |
Het |
Fcgr1 |
T |
C |
3: 96,191,893 (GRCm39) |
Y305C |
probably benign |
Het |
Fcrlb |
A |
G |
1: 170,736,248 (GRCm39) |
V176A |
probably damaging |
Het |
Gabrq |
T |
A |
X: 71,879,783 (GRCm39) |
V256E |
possibly damaging |
Het |
Gba1 |
T |
C |
3: 89,113,148 (GRCm39) |
L193P |
probably damaging |
Het |
Gm10717 |
C |
T |
9: 3,025,616 (GRCm39) |
S67L |
probably benign |
Het |
Helq |
A |
G |
5: 100,930,960 (GRCm39) |
F597L |
probably benign |
Het |
Hrh1 |
A |
T |
6: 114,457,204 (GRCm39) |
I162L |
probably damaging |
Het |
Jph1 |
A |
T |
1: 17,161,884 (GRCm39) |
F259L |
probably damaging |
Het |
Kdm2b |
C |
T |
5: 123,085,898 (GRCm39) |
E238K |
probably damaging |
Het |
Kdm4c |
T |
A |
4: 74,225,253 (GRCm39) |
|
probably null |
Het |
Kif13a |
T |
C |
13: 46,925,011 (GRCm39) |
T308A |
probably benign |
Het |
Lars1 |
C |
T |
18: 42,360,345 (GRCm39) |
V704M |
probably benign |
Het |
Lcmt2 |
A |
G |
2: 120,969,394 (GRCm39) |
L343P |
possibly damaging |
Het |
Lhfpl1 |
A |
G |
X: 144,123,733 (GRCm39) |
F125L |
probably benign |
Het |
Lmbrd2 |
C |
A |
15: 9,186,772 (GRCm39) |
D582E |
probably damaging |
Het |
Lrrn2 |
T |
A |
1: 132,866,983 (GRCm39) |
S683T |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,365,842 (GRCm39) |
D1408G |
probably benign |
Het |
Magi3 |
T |
C |
3: 103,923,219 (GRCm39) |
K1166R |
probably benign |
Het |
Marchf5 |
T |
C |
19: 37,197,892 (GRCm39) |
|
probably benign |
Het |
Naa25 |
A |
G |
5: 121,564,825 (GRCm39) |
Q555R |
possibly damaging |
Het |
Npat |
A |
G |
9: 53,481,207 (GRCm39) |
T1005A |
probably benign |
Het |
Nt5c3 |
G |
A |
6: 56,863,670 (GRCm39) |
A108V |
probably damaging |
Het |
Ocrl |
T |
A |
X: 47,024,995 (GRCm39) |
M322K |
probably damaging |
Het |
Odad2 |
C |
A |
18: 7,214,601 (GRCm39) |
W733C |
probably damaging |
Het |
Or8g2 |
A |
G |
9: 39,821,935 (GRCm39) |
T279A |
possibly damaging |
Het |
Psg23 |
A |
T |
7: 18,344,345 (GRCm39) |
V370E |
probably benign |
Het |
Rassf2 |
A |
T |
2: 131,838,353 (GRCm39) |
M311K |
possibly damaging |
Het |
Rhobtb3 |
A |
G |
13: 76,025,614 (GRCm39) |
Y501H |
probably damaging |
Het |
Rpl4 |
A |
G |
9: 64,083,488 (GRCm39) |
D179G |
possibly damaging |
Het |
Scn2a |
T |
A |
2: 65,546,182 (GRCm39) |
I915N |
probably damaging |
Het |
Scn3a |
T |
A |
2: 65,356,965 (GRCm39) |
T160S |
possibly damaging |
Het |
Slx4ip |
T |
G |
2: 136,909,942 (GRCm39) |
N242K |
possibly damaging |
Het |
Spidr |
T |
A |
16: 15,865,945 (GRCm39) |
Q288L |
probably benign |
Het |
Sun1 |
A |
T |
5: 139,216,918 (GRCm39) |
H255L |
possibly damaging |
Het |
Tacc1 |
C |
T |
8: 25,665,233 (GRCm39) |
G51S |
probably damaging |
Het |
Tet2 |
T |
A |
3: 133,185,900 (GRCm39) |
N1179I |
possibly damaging |
Het |
Tgfbrap1 |
T |
C |
1: 43,101,752 (GRCm39) |
Y349C |
probably damaging |
Het |
Tnrc6a |
T |
C |
7: 122,751,414 (GRCm39) |
|
probably benign |
Het |
Trim32 |
T |
C |
4: 65,532,736 (GRCm39) |
L431P |
probably damaging |
Het |
Vmn1r35 |
A |
G |
6: 66,656,334 (GRCm39) |
L112S |
probably damaging |
Het |
Vmn2r100 |
A |
C |
17: 19,742,583 (GRCm39) |
H319P |
probably damaging |
Het |
Wdr20rt |
A |
G |
12: 65,274,039 (GRCm39) |
T328A |
probably benign |
Het |
Zbtb17 |
T |
C |
4: 141,192,293 (GRCm39) |
Y413H |
probably benign |
Het |
|
Other mutations in Ms4a20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
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 |
|
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 |
|