Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm5 |
A |
T |
7: 119,137,511 (GRCm39) |
I402F |
probably damaging |
Het |
Acvr2b |
T |
C |
9: 119,261,570 (GRCm39) |
Y388H |
probably damaging |
Het |
Adh1 |
G |
A |
3: 137,988,512 (GRCm39) |
D162N |
possibly damaging |
Het |
C6 |
G |
T |
15: 4,822,236 (GRCm39) |
R585I |
probably damaging |
Het |
Ccdc169 |
T |
A |
3: 55,070,732 (GRCm39) |
|
probably null |
Het |
Cdh13 |
T |
A |
8: 119,401,916 (GRCm39) |
M106K |
probably damaging |
Het |
Cep78 |
C |
T |
19: 15,938,359 (GRCm39) |
E530K |
probably damaging |
Het |
Cyfip1 |
T |
A |
7: 55,546,487 (GRCm39) |
L533Q |
probably damaging |
Het |
Etl4 |
T |
C |
2: 20,811,460 (GRCm39) |
V1181A |
probably benign |
Het |
Galnt7 |
T |
G |
8: 57,984,769 (GRCm39) |
|
probably benign |
Het |
Gm11595 |
G |
A |
11: 99,663,498 (GRCm39) |
R61C |
unknown |
Het |
Gucy1a1 |
T |
A |
3: 82,016,560 (GRCm39) |
I143F |
possibly damaging |
Het |
Hmcn1 |
T |
C |
1: 150,613,050 (GRCm39) |
N1410D |
possibly damaging |
Het |
Ltbp2 |
G |
A |
12: 84,856,020 (GRCm39) |
T741I |
probably benign |
Het |
Mfsd4b2 |
A |
G |
10: 39,798,193 (GRCm39) |
|
probably benign |
Het |
Mrgprb5 |
T |
G |
7: 47,818,172 (GRCm39) |
I188L |
probably benign |
Het |
Naip6 |
T |
A |
13: 100,436,862 (GRCm39) |
S554C |
probably damaging |
Het |
Nav2 |
A |
G |
7: 49,220,957 (GRCm39) |
N1715D |
probably damaging |
Het |
Nav3 |
A |
T |
10: 109,605,119 (GRCm39) |
S985T |
possibly damaging |
Het |
Nme7 |
A |
G |
1: 164,155,866 (GRCm39) |
Q22R |
probably benign |
Het |
Or52i2 |
T |
C |
7: 102,319,927 (GRCm39) |
W267R |
probably damaging |
Het |
Otulinl |
C |
T |
15: 27,658,151 (GRCm39) |
D290N |
probably damaging |
Het |
Pabir1 |
A |
G |
19: 24,453,948 (GRCm39) |
V258A |
probably benign |
Het |
Ppp1r9a |
A |
G |
6: 5,115,322 (GRCm39) |
E815G |
probably damaging |
Het |
Ppp2r2c |
T |
A |
5: 37,083,744 (GRCm39) |
I95N |
probably damaging |
Het |
Ppp4r4 |
G |
A |
12: 103,569,225 (GRCm39) |
E717K |
possibly damaging |
Het |
Prdm2 |
A |
G |
4: 142,860,138 (GRCm39) |
S1051P |
possibly damaging |
Het |
Rnf214 |
T |
C |
9: 45,811,084 (GRCm39) |
D193G |
probably damaging |
Het |
Sirpb1b |
G |
T |
3: 15,608,244 (GRCm39) |
T167K |
probably damaging |
Het |
Slc16a3 |
C |
A |
11: 120,847,532 (GRCm39) |
S240* |
probably null |
Het |
Snx14 |
T |
A |
9: 88,267,891 (GRCm39) |
|
probably benign |
Het |
Sorbs2 |
A |
G |
8: 46,256,866 (GRCm39) |
|
probably benign |
Het |
Stk-ps2 |
A |
T |
1: 46,068,522 (GRCm39) |
|
noncoding transcript |
Het |
Taar7b |
A |
T |
10: 23,875,874 (GRCm39) |
D13V |
probably benign |
Het |
Trp53bp1 |
T |
C |
2: 121,066,506 (GRCm39) |
E740G |
probably damaging |
Het |
Unc79 |
C |
T |
12: 103,115,279 (GRCm39) |
A2054V |
possibly damaging |
Het |
Zfp106 |
A |
G |
2: 120,354,034 (GRCm39) |
V211A |
probably benign |
Het |
Zfp112 |
A |
G |
7: 23,825,379 (GRCm39) |
H449R |
probably benign |
Het |
|
Other mutations in Mdc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01473:Mdc1
|
APN |
17 |
36,158,912 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01931:Mdc1
|
APN |
17 |
36,159,123 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02542:Mdc1
|
APN |
17 |
36,164,048 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02823:Mdc1
|
APN |
17 |
36,163,815 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03411:Mdc1
|
APN |
17 |
36,164,018 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02799:Mdc1
|
UTSW |
17 |
36,157,083 (GRCm39) |
missense |
possibly damaging |
0.86 |
PIT4362001:Mdc1
|
UTSW |
17 |
36,155,361 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0054:Mdc1
|
UTSW |
17 |
36,159,925 (GRCm39) |
missense |
probably benign |
0.00 |
R0129:Mdc1
|
UTSW |
17 |
36,165,337 (GRCm39) |
missense |
probably benign |
0.04 |
R0131:Mdc1
|
UTSW |
17 |
36,163,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R0131:Mdc1
|
UTSW |
17 |
36,163,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R0132:Mdc1
|
UTSW |
17 |
36,163,473 (GRCm39) |
missense |
probably damaging |
0.99 |
R1406:Mdc1
|
UTSW |
17 |
36,164,424 (GRCm39) |
missense |
probably benign |
0.10 |
R1406:Mdc1
|
UTSW |
17 |
36,164,424 (GRCm39) |
missense |
probably benign |
0.10 |
R1597:Mdc1
|
UTSW |
17 |
36,156,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Mdc1
|
UTSW |
17 |
36,158,718 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1888:Mdc1
|
UTSW |
17 |
36,165,117 (GRCm39) |
missense |
probably benign |
0.03 |
R1888:Mdc1
|
UTSW |
17 |
36,165,117 (GRCm39) |
missense |
probably benign |
0.03 |
R1912:Mdc1
|
UTSW |
17 |
36,161,703 (GRCm39) |
missense |
probably benign |
0.19 |
R1912:Mdc1
|
UTSW |
17 |
36,155,430 (GRCm39) |
missense |
probably benign |
0.00 |
R1977:Mdc1
|
UTSW |
17 |
36,161,822 (GRCm39) |
missense |
probably benign |
0.01 |
R2121:Mdc1
|
UTSW |
17 |
36,158,835 (GRCm39) |
missense |
probably benign |
0.03 |
R2122:Mdc1
|
UTSW |
17 |
36,158,835 (GRCm39) |
missense |
probably benign |
0.03 |
R2357:Mdc1
|
UTSW |
17 |
36,158,337 (GRCm39) |
missense |
probably benign |
0.00 |
R2842:Mdc1
|
UTSW |
17 |
36,159,686 (GRCm39) |
missense |
probably benign |
0.01 |
R2851:Mdc1
|
UTSW |
17 |
36,159,902 (GRCm39) |
missense |
probably benign |
0.04 |
R2852:Mdc1
|
UTSW |
17 |
36,159,902 (GRCm39) |
missense |
probably benign |
0.04 |
R2964:Mdc1
|
UTSW |
17 |
36,164,529 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2996:Mdc1
|
UTSW |
17 |
36,158,785 (GRCm39) |
unclassified |
probably benign |
|
R3752:Mdc1
|
UTSW |
17 |
36,156,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4234:Mdc1
|
UTSW |
17 |
36,159,716 (GRCm39) |
missense |
probably benign |
0.00 |
R4641:Mdc1
|
UTSW |
17 |
36,168,361 (GRCm39) |
missense |
probably benign |
0.09 |
R4706:Mdc1
|
UTSW |
17 |
36,163,671 (GRCm39) |
missense |
probably damaging |
0.99 |
R4809:Mdc1
|
UTSW |
17 |
36,159,993 (GRCm39) |
critical splice donor site |
probably null |
|
R4833:Mdc1
|
UTSW |
17 |
36,161,286 (GRCm39) |
missense |
probably benign |
0.20 |
R5032:Mdc1
|
UTSW |
17 |
36,161,481 (GRCm39) |
missense |
probably benign |
0.00 |
R5047:Mdc1
|
UTSW |
17 |
36,158,736 (GRCm39) |
missense |
probably benign |
0.00 |
R5086:Mdc1
|
UTSW |
17 |
36,159,522 (GRCm39) |
missense |
probably benign |
0.00 |
R5172:Mdc1
|
UTSW |
17 |
36,163,982 (GRCm39) |
missense |
probably benign |
0.00 |
R5254:Mdc1
|
UTSW |
17 |
36,158,814 (GRCm39) |
missense |
probably benign |
0.00 |
R5473:Mdc1
|
UTSW |
17 |
36,158,952 (GRCm39) |
missense |
probably benign |
0.01 |
R5550:Mdc1
|
UTSW |
17 |
36,156,776 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5561:Mdc1
|
UTSW |
17 |
36,159,438 (GRCm39) |
missense |
probably benign |
0.00 |
R5888:Mdc1
|
UTSW |
17 |
36,158,712 (GRCm39) |
missense |
probably benign |
0.01 |
R6020:Mdc1
|
UTSW |
17 |
36,168,464 (GRCm39) |
missense |
probably benign |
0.01 |
R6020:Mdc1
|
UTSW |
17 |
36,159,525 (GRCm39) |
missense |
probably benign |
0.04 |
R6219:Mdc1
|
UTSW |
17 |
36,161,566 (GRCm39) |
missense |
probably benign |
0.10 |
R7053:Mdc1
|
UTSW |
17 |
36,157,218 (GRCm39) |
missense |
probably benign |
0.00 |
R7073:Mdc1
|
UTSW |
17 |
36,164,960 (GRCm39) |
missense |
probably benign |
0.18 |
R7077:Mdc1
|
UTSW |
17 |
36,156,839 (GRCm39) |
missense |
probably damaging |
0.97 |
R7424:Mdc1
|
UTSW |
17 |
36,164,201 (GRCm39) |
missense |
probably benign |
0.04 |
R7443:Mdc1
|
UTSW |
17 |
36,161,712 (GRCm39) |
missense |
probably damaging |
0.98 |
R7467:Mdc1
|
UTSW |
17 |
36,155,448 (GRCm39) |
missense |
probably benign |
0.29 |
R7549:Mdc1
|
UTSW |
17 |
36,159,749 (GRCm39) |
missense |
probably null |
0.04 |
R7655:Mdc1
|
UTSW |
17 |
36,161,773 (GRCm39) |
missense |
probably benign |
0.01 |
R7656:Mdc1
|
UTSW |
17 |
36,161,773 (GRCm39) |
missense |
probably benign |
0.01 |
R7960:Mdc1
|
UTSW |
17 |
36,161,570 (GRCm39) |
nonsense |
probably null |
|
R8350:Mdc1
|
UTSW |
17 |
36,159,191 (GRCm39) |
missense |
probably benign |
0.00 |
R8450:Mdc1
|
UTSW |
17 |
36,159,191 (GRCm39) |
missense |
probably benign |
0.00 |
R8688:Mdc1
|
UTSW |
17 |
36,161,383 (GRCm39) |
missense |
probably benign |
0.10 |
R8726:Mdc1
|
UTSW |
17 |
36,158,475 (GRCm39) |
missense |
probably benign |
0.04 |
R8919:Mdc1
|
UTSW |
17 |
36,158,843 (GRCm39) |
missense |
probably benign |
0.00 |
R8961:Mdc1
|
UTSW |
17 |
36,159,407 (GRCm39) |
missense |
probably benign |
0.10 |
R9324:Mdc1
|
UTSW |
17 |
36,164,258 (GRCm39) |
missense |
probably benign |
0.10 |
R9363:Mdc1
|
UTSW |
17 |
36,162,019 (GRCm39) |
missense |
probably benign |
0.00 |
R9385:Mdc1
|
UTSW |
17 |
36,161,396 (GRCm39) |
missense |
probably benign |
0.00 |
RF025:Mdc1
|
UTSW |
17 |
36,165,299 (GRCm39) |
critical splice acceptor site |
probably benign |
|
X0022:Mdc1
|
UTSW |
17 |
36,161,829 (GRCm39) |
missense |
probably benign |
0.01 |
|