Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apol7b |
T |
A |
15: 77,307,430 (GRCm39) |
Q355L |
probably benign |
Het |
Asb14 |
A |
T |
14: 26,633,945 (GRCm39) |
Q383H |
probably benign |
Het |
Ash1l |
T |
G |
3: 88,977,553 (GRCm39) |
M2661R |
probably damaging |
Het |
Cacna1e |
G |
T |
1: 154,577,313 (GRCm39) |
|
probably null |
Het |
Ccdc40 |
G |
T |
11: 119,150,870 (GRCm39) |
|
probably null |
Het |
Cd27 |
T |
A |
6: 125,210,188 (GRCm39) |
|
probably null |
Het |
Ces3b |
T |
C |
8: 105,817,385 (GRCm39) |
L371S |
possibly damaging |
Het |
Clec4a2 |
T |
A |
6: 123,117,711 (GRCm39) |
Y210N |
probably damaging |
Het |
Cpeb2 |
A |
T |
5: 43,394,681 (GRCm39) |
H553L |
|
Het |
Cpne8 |
T |
C |
15: 90,503,881 (GRCm39) |
I95V |
probably benign |
Het |
D630039A03Rik |
T |
C |
4: 57,910,525 (GRCm39) |
T96A |
probably benign |
Het |
Dand5 |
C |
A |
8: 85,543,147 (GRCm39) |
G110C |
probably damaging |
Het |
Erich3 |
C |
T |
3: 154,470,210 (GRCm39) |
T1554M |
unknown |
Het |
Evi5l |
T |
C |
8: 4,241,300 (GRCm39) |
S278P |
probably damaging |
Het |
Farp2 |
C |
A |
1: 93,548,325 (GRCm39) |
H1003Q |
probably damaging |
Het |
G530012D18Rik |
C |
G |
1: 85,504,935 (GRCm39) |
D113E |
unknown |
Het |
Gm13741 |
A |
C |
2: 87,486,446 (GRCm39) |
M273R |
possibly damaging |
Het |
Gm28363 |
T |
A |
1: 117,626,641 (GRCm39) |
D26E |
unknown |
Het |
Gm8674 |
A |
T |
13: 50,054,407 (GRCm39) |
D700E |
noncoding transcript |
Het |
Gtf3c4 |
G |
A |
2: 28,724,593 (GRCm39) |
Q380* |
probably null |
Het |
Idh2 |
GGTCCCAG |
GG |
7: 79,748,077 (GRCm39) |
|
probably benign |
Het |
Il1a |
A |
T |
2: 129,148,477 (GRCm39) |
S78T |
possibly damaging |
Het |
Kdm2b |
A |
T |
5: 123,072,856 (GRCm39) |
Y341N |
probably damaging |
Het |
Mcc |
T |
C |
18: 44,582,508 (GRCm39) |
|
probably null |
Het |
Met |
A |
G |
6: 17,547,061 (GRCm39) |
D898G |
probably damaging |
Het |
Mogs |
T |
C |
6: 83,092,863 (GRCm39) |
V101A |
probably damaging |
Het |
Mrgpra4 |
A |
T |
7: 47,631,221 (GRCm39) |
Y127N |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,569,197 (GRCm39) |
T148S |
unknown |
Het |
Nutm1 |
G |
A |
2: 112,078,817 (GRCm39) |
L1033F |
probably benign |
Het |
Ocstamp |
G |
T |
2: 165,239,787 (GRCm39) |
A133D |
probably damaging |
Het |
Or1ab2 |
T |
G |
8: 72,864,253 (GRCm39) |
V281G |
noncoding transcript |
Het |
Or5p63 |
T |
C |
7: 107,810,995 (GRCm39) |
H247R |
probably damaging |
Het |
Or8g17 |
T |
A |
9: 38,930,249 (GRCm39) |
D196V |
probably benign |
Het |
Or9s18 |
G |
A |
13: 65,300,734 (GRCm39) |
R232Q |
probably damaging |
Het |
Phf12 |
C |
A |
11: 77,915,651 (GRCm39) |
P46Q |
probably damaging |
Het |
Prf1 |
A |
G |
10: 61,138,749 (GRCm39) |
T236A |
probably damaging |
Het |
Ptcd3 |
A |
G |
6: 71,884,798 (GRCm39) |
V47A |
probably benign |
Het |
Rapgef1 |
A |
T |
2: 29,626,011 (GRCm39) |
N1071Y |
probably damaging |
Het |
Rftn1 |
G |
T |
17: 50,354,408 (GRCm39) |
A318D |
probably damaging |
Het |
Rnf26rt |
C |
A |
6: 76,473,558 (GRCm39) |
A353S |
probably benign |
Het |
Tango6 |
C |
T |
8: 107,409,882 (GRCm39) |
P33L |
possibly damaging |
Het |
Tasor2 |
G |
T |
13: 3,649,691 (GRCm39) |
T36N |
probably damaging |
Het |
Tbc1d2b |
C |
T |
9: 90,089,937 (GRCm39) |
R864H |
probably damaging |
Het |
Tent2 |
A |
G |
13: 93,304,432 (GRCm39) |
|
probably null |
Het |
Trav10n |
A |
T |
14: 53,359,929 (GRCm39) |
I69L |
probably benign |
Het |
Tsks |
A |
G |
7: 44,603,296 (GRCm39) |
Q366R |
probably damaging |
Het |
Vcan |
G |
T |
13: 89,853,106 (GRCm39) |
S618* |
probably null |
Het |
Vwf |
T |
A |
6: 125,622,799 (GRCm39) |
|
probably null |
Het |
Zfp827 |
T |
A |
8: 79,787,206 (GRCm39) |
L124* |
probably null |
Het |
|
Other mutations in Ms4a18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0556:Ms4a18
|
UTSW |
19 |
10,991,065 (GRCm39) |
missense |
probably damaging |
0.98 |
R1987:Ms4a18
|
UTSW |
19 |
10,991,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R2031:Ms4a18
|
UTSW |
19 |
10,991,014 (GRCm39) |
missense |
probably benign |
0.06 |
R2137:Ms4a18
|
UTSW |
19 |
10,974,695 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2138:Ms4a18
|
UTSW |
19 |
10,974,695 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2139:Ms4a18
|
UTSW |
19 |
10,974,695 (GRCm39) |
missense |
possibly damaging |
0.86 |
R2192:Ms4a18
|
UTSW |
19 |
10,991,029 (GRCm39) |
missense |
probably benign |
0.09 |
R2211:Ms4a18
|
UTSW |
19 |
10,974,669 (GRCm39) |
missense |
probably benign |
0.33 |
R3739:Ms4a18
|
UTSW |
19 |
10,988,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R5586:Ms4a18
|
UTSW |
19 |
10,991,038 (GRCm39) |
missense |
probably benign |
0.00 |
R6102:Ms4a18
|
UTSW |
19 |
10,990,887 (GRCm39) |
missense |
probably benign |
|
R7091:Ms4a18
|
UTSW |
19 |
10,986,092 (GRCm39) |
missense |
probably damaging |
0.98 |
R7316:Ms4a18
|
UTSW |
19 |
10,979,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R8854:Ms4a18
|
UTSW |
19 |
10,990,887 (GRCm39) |
missense |
probably benign |
|
R9098:Ms4a18
|
UTSW |
19 |
10,990,741 (GRCm39) |
missense |
|
|
R9157:Ms4a18
|
UTSW |
19 |
10,988,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R9313:Ms4a18
|
UTSW |
19 |
10,988,804 (GRCm39) |
missense |
probably damaging |
0.98 |
R9583:Ms4a18
|
UTSW |
19 |
10,974,714 (GRCm39) |
missense |
probably benign |
|
|