Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5930422O12Rik |
C |
T |
8: 33,919,201 (GRCm39) |
S7L |
unknown |
Het |
Aggf1 |
T |
C |
13: 95,488,125 (GRCm39) |
K674R |
possibly damaging |
Het |
Ampd1 |
T |
C |
3: 102,997,389 (GRCm39) |
F264L |
probably damaging |
Het |
Ankle1 |
A |
T |
8: 71,860,387 (GRCm39) |
S302C |
probably damaging |
Het |
Ankrd17 |
G |
A |
5: 90,514,310 (GRCm39) |
|
probably benign |
Het |
Arhgap18 |
T |
A |
10: 26,725,917 (GRCm39) |
N47K |
possibly damaging |
Het |
Atp5pb |
T |
C |
3: 105,851,083 (GRCm39) |
N205D |
probably benign |
Het |
Atp8b3 |
C |
T |
10: 80,355,858 (GRCm39) |
E1285K |
probably benign |
Het |
Atp8b3 |
C |
A |
10: 80,365,552 (GRCm39) |
V401L |
probably damaging |
Het |
Cacna1a |
G |
A |
8: 85,356,544 (GRCm39) |
R1929Q |
possibly damaging |
Het |
Cadm2 |
C |
T |
16: 66,679,767 (GRCm39) |
S22N |
possibly damaging |
Het |
Ccdc177 |
C |
T |
12: 80,805,927 (GRCm39) |
V116M |
probably damaging |
Het |
Cdhr18 |
A |
G |
14: 13,828,486 (GRCm38) |
V758A |
|
Het |
Cdkl2 |
A |
T |
5: 92,181,084 (GRCm39) |
I185N |
probably damaging |
Het |
Cfhr2 |
T |
A |
1: 139,738,716 (GRCm39) |
I282L |
probably benign |
Het |
Clns1a |
T |
A |
7: 97,361,824 (GRCm39) |
|
probably null |
Het |
Commd2 |
A |
T |
3: 57,554,107 (GRCm39) |
I198N |
probably damaging |
Het |
Creb3l2 |
C |
T |
6: 37,313,200 (GRCm39) |
V365I |
possibly damaging |
Het |
Dcaf6 |
A |
T |
1: 165,251,886 (GRCm39) |
N79K |
possibly damaging |
Het |
Dlg5 |
T |
C |
14: 24,196,263 (GRCm39) |
N1622D |
possibly damaging |
Het |
Dock7 |
C |
T |
4: 98,834,969 (GRCm39) |
R1802H |
probably damaging |
Het |
Dpy19l2 |
T |
C |
9: 24,495,789 (GRCm39) |
K643R |
probably benign |
Het |
Dscam |
G |
A |
16: 96,620,986 (GRCm39) |
T574M |
probably benign |
Het |
Fam209 |
A |
G |
2: 172,315,969 (GRCm39) |
T115A |
probably damaging |
Het |
Fastkd5 |
C |
T |
2: 130,456,337 (GRCm39) |
C751Y |
probably damaging |
Het |
Fat3 |
C |
A |
9: 16,289,123 (GRCm39) |
L133F |
probably damaging |
Het |
Fcsk |
A |
T |
8: 111,616,971 (GRCm39) |
I393N |
probably damaging |
Het |
Frmd6 |
T |
C |
12: 70,944,170 (GRCm39) |
V516A |
possibly damaging |
Het |
Fry |
G |
A |
5: 150,318,634 (GRCm39) |
D955N |
possibly damaging |
Het |
Gm7298 |
T |
C |
6: 121,751,993 (GRCm39) |
|
probably null |
Het |
Golga7b |
T |
A |
19: 42,256,899 (GRCm39) |
*168R |
probably null |
Het |
Golim4 |
T |
A |
3: 75,800,309 (GRCm39) |
Q395L |
probably benign |
Het |
Gxylt2 |
T |
A |
6: 100,781,537 (GRCm39) |
L404* |
probably null |
Het |
H1f4 |
A |
G |
13: 23,806,422 (GRCm39) |
V20A |
probably benign |
Het |
Irf8 |
C |
T |
8: 121,466,581 (GRCm39) |
R9W |
probably damaging |
Het |
Itga4 |
T |
C |
2: 79,148,470 (GRCm39) |
V788A |
possibly damaging |
Het |
Kifap3 |
G |
A |
1: 163,621,649 (GRCm39) |
R99H |
probably damaging |
Het |
Kiss1r |
T |
C |
10: 79,754,688 (GRCm39) |
S61P |
probably damaging |
Het |
Krtap6-1 |
A |
T |
16: 88,828,606 (GRCm39) |
M1L |
unknown |
Het |
Large2 |
A |
T |
2: 92,197,367 (GRCm39) |
M411K |
probably damaging |
Het |
Lcor |
A |
G |
19: 41,574,191 (GRCm39) |
D982G |
probably benign |
Het |
Lingo1 |
A |
G |
9: 56,527,467 (GRCm39) |
V374A |
probably benign |
Het |
Lrch1 |
A |
G |
14: 75,022,962 (GRCm39) |
V637A |
probably damaging |
Het |
Lyar |
T |
C |
5: 38,382,024 (GRCm39) |
V2A |
probably damaging |
Het |
Nell1 |
C |
T |
7: 50,098,592 (GRCm39) |
S298L |
unknown |
Het |
Ogfod3 |
T |
A |
11: 121,086,031 (GRCm39) |
I188F |
probably damaging |
Het |
Opa3 |
C |
A |
7: 18,978,961 (GRCm39) |
A142E |
possibly damaging |
Het |
Or5b123 |
T |
A |
19: 13,596,769 (GRCm39) |
M81K |
possibly damaging |
Het |
Or5k1 |
T |
C |
16: 58,617,538 (GRCm39) |
T224A |
probably benign |
Het |
Pald1 |
T |
C |
10: 61,159,125 (GRCm39) |
R769G |
probably benign |
Het |
Pappa2 |
T |
A |
1: 158,784,753 (GRCm39) |
T86S |
unknown |
Het |
Papss1 |
T |
C |
3: 131,307,811 (GRCm39) |
Y266H |
probably damaging |
Het |
Pcdhga7 |
C |
A |
18: 37,849,994 (GRCm39) |
A667D |
probably damaging |
Het |
Pcsk5 |
T |
A |
19: 17,411,095 (GRCm39) |
T1766S |
probably benign |
Het |
Pds5b |
T |
A |
5: 150,717,747 (GRCm39) |
N1129K |
possibly damaging |
Het |
Pop7 |
T |
C |
5: 137,499,952 (GRCm39) |
N127S |
probably damaging |
Het |
Ppfibp2 |
A |
G |
7: 107,316,925 (GRCm39) |
E300G |
probably damaging |
Het |
Ppp4r3b |
A |
G |
11: 29,132,507 (GRCm39) |
K87E |
probably damaging |
Het |
Psmd3 |
T |
A |
11: 98,573,659 (GRCm39) |
M35K |
possibly damaging |
Het |
Pus7 |
A |
G |
5: 23,980,677 (GRCm39) |
V191A |
probably damaging |
Het |
Rptor |
C |
T |
11: 119,765,012 (GRCm39) |
|
probably benign |
Het |
Sacs |
A |
G |
14: 61,446,377 (GRCm39) |
M2808V |
probably benign |
Het |
Scube3 |
G |
A |
17: 28,386,573 (GRCm39) |
V831I |
probably benign |
Het |
Sin3a |
A |
T |
9: 57,011,218 (GRCm39) |
N492Y |
probably damaging |
Het |
Slc12a3 |
A |
G |
8: 95,092,572 (GRCm39) |
T998A |
probably damaging |
Het |
Slc4a1 |
T |
C |
11: 102,247,084 (GRCm39) |
N501S |
probably benign |
Het |
Sltm |
G |
A |
9: 70,466,348 (GRCm39) |
G94R |
probably damaging |
Het |
Smc4 |
T |
A |
3: 68,934,835 (GRCm39) |
W650R |
probably damaging |
Het |
Smg7 |
A |
G |
1: 152,724,601 (GRCm39) |
S527P |
probably damaging |
Het |
Tcf20 |
T |
C |
15: 82,740,279 (GRCm39) |
N391D |
probably damaging |
Het |
Tiam2 |
G |
A |
17: 3,498,758 (GRCm39) |
V845M |
probably damaging |
Het |
Tln2 |
A |
G |
9: 67,253,699 (GRCm39) |
F793L |
probably benign |
Het |
Uckl1 |
T |
C |
2: 181,216,037 (GRCm39) |
I193V |
probably damaging |
Het |
Ugt1a5 |
A |
G |
1: 88,094,077 (GRCm39) |
M102V |
probably benign |
Het |
Usp38 |
G |
A |
8: 81,727,750 (GRCm39) |
P328S |
possibly damaging |
Het |
Vmn1r189 |
A |
G |
13: 22,286,285 (GRCm39) |
V184A |
possibly damaging |
Het |
Vps13d |
C |
A |
4: 144,889,914 (GRCm39) |
A597S |
probably benign |
Het |
Wdr47 |
T |
A |
3: 108,525,840 (GRCm39) |
L121Q |
probably damaging |
Het |
Wiz |
A |
G |
17: 32,580,507 (GRCm39) |
S315P |
probably damaging |
Het |
Zc3h13 |
T |
C |
14: 75,568,597 (GRCm39) |
S1297P |
probably damaging |
Het |
Zfp27 |
AATCCGCTTGTGCA |
AA |
7: 29,594,446 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Ighmbp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00423:Ighmbp2
|
APN |
19 |
3,318,704 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01160:Ighmbp2
|
APN |
19 |
3,326,750 (GRCm39) |
splice site |
probably benign |
|
IGL01358:Ighmbp2
|
APN |
19 |
3,318,817 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01478:Ighmbp2
|
APN |
19 |
3,324,531 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01509:Ighmbp2
|
APN |
19 |
3,318,711 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01557:Ighmbp2
|
APN |
19 |
3,331,472 (GRCm39) |
missense |
probably benign |
0.13 |
IGL01635:Ighmbp2
|
APN |
19 |
3,317,265 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01712:Ighmbp2
|
APN |
19 |
3,323,038 (GRCm39) |
splice site |
probably benign |
|
IGL01949:Ighmbp2
|
APN |
19 |
3,315,538 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03106:Ighmbp2
|
APN |
19 |
3,323,022 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL03212:Ighmbp2
|
APN |
19 |
3,329,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R0038:Ighmbp2
|
UTSW |
19 |
3,312,097 (GRCm39) |
missense |
probably damaging |
0.96 |
R0455:Ighmbp2
|
UTSW |
19 |
3,315,072 (GRCm39) |
missense |
probably benign |
0.34 |
R1661:Ighmbp2
|
UTSW |
19 |
3,317,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R1756:Ighmbp2
|
UTSW |
19 |
3,318,669 (GRCm39) |
missense |
probably damaging |
0.99 |
R1851:Ighmbp2
|
UTSW |
19 |
3,312,075 (GRCm39) |
missense |
probably benign |
0.12 |
R2055:Ighmbp2
|
UTSW |
19 |
3,315,095 (GRCm39) |
missense |
probably benign |
0.00 |
R2194:Ighmbp2
|
UTSW |
19 |
3,315,116 (GRCm39) |
missense |
probably benign |
0.00 |
R3838:Ighmbp2
|
UTSW |
19 |
3,321,658 (GRCm39) |
missense |
probably benign |
0.01 |
R4409:Ighmbp2
|
UTSW |
19 |
3,321,536 (GRCm39) |
missense |
probably benign |
|
R4583:Ighmbp2
|
UTSW |
19 |
3,315,324 (GRCm39) |
missense |
probably benign |
0.01 |
R4806:Ighmbp2
|
UTSW |
19 |
3,311,589 (GRCm39) |
missense |
probably damaging |
1.00 |
R5091:Ighmbp2
|
UTSW |
19 |
3,315,084 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5274:Ighmbp2
|
UTSW |
19 |
3,315,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R5319:Ighmbp2
|
UTSW |
19 |
3,321,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R5500:Ighmbp2
|
UTSW |
19 |
3,318,687 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5574:Ighmbp2
|
UTSW |
19 |
3,321,536 (GRCm39) |
missense |
probably benign |
|
R5698:Ighmbp2
|
UTSW |
19 |
3,324,538 (GRCm39) |
missense |
probably damaging |
1.00 |
R5722:Ighmbp2
|
UTSW |
19 |
3,329,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R5864:Ighmbp2
|
UTSW |
19 |
3,311,467 (GRCm39) |
missense |
probably benign |
0.00 |
R5980:Ighmbp2
|
UTSW |
19 |
3,315,295 (GRCm39) |
missense |
probably benign |
|
R6194:Ighmbp2
|
UTSW |
19 |
3,312,003 (GRCm39) |
missense |
possibly damaging |
0.90 |
R6939:Ighmbp2
|
UTSW |
19 |
3,326,907 (GRCm39) |
missense |
probably damaging |
0.97 |
R7147:Ighmbp2
|
UTSW |
19 |
3,321,676 (GRCm39) |
missense |
probably benign |
0.05 |
R7257:Ighmbp2
|
UTSW |
19 |
3,316,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R7274:Ighmbp2
|
UTSW |
19 |
3,314,951 (GRCm39) |
missense |
probably benign |
|
R7567:Ighmbp2
|
UTSW |
19 |
3,322,981 (GRCm39) |
missense |
probably benign |
0.01 |
R7737:Ighmbp2
|
UTSW |
19 |
3,324,467 (GRCm39) |
missense |
unknown |
|
R7819:Ighmbp2
|
UTSW |
19 |
3,317,276 (GRCm39) |
missense |
possibly damaging |
0.46 |
R7877:Ighmbp2
|
UTSW |
19 |
3,311,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R8175:Ighmbp2
|
UTSW |
19 |
3,316,365 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8417:Ighmbp2
|
UTSW |
19 |
3,311,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R8951:Ighmbp2
|
UTSW |
19 |
3,318,726 (GRCm39) |
nonsense |
probably null |
|
R9171:Ighmbp2
|
UTSW |
19 |
3,315,641 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9409:Ighmbp2
|
UTSW |
19 |
3,318,832 (GRCm39) |
missense |
possibly damaging |
0.47 |
R9567:Ighmbp2
|
UTSW |
19 |
3,332,785 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R9663:Ighmbp2
|
UTSW |
19 |
3,315,325 (GRCm39) |
missense |
probably benign |
0.27 |
R9752:Ighmbp2
|
UTSW |
19 |
3,324,360 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Ighmbp2
|
UTSW |
19 |
3,321,665 (GRCm39) |
nonsense |
probably null |
|
Z1177:Ighmbp2
|
UTSW |
19 |
3,317,242 (GRCm39) |
missense |
probably null |
1.00 |
Z1177:Ighmbp2
|
UTSW |
19 |
3,315,635 (GRCm39) |
missense |
probably damaging |
1.00 |
|