Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA986860 |
C |
T |
1: 130,668,908 (GRCm39) |
Q92* |
probably null |
Het |
Accsl |
T |
C |
2: 93,694,748 (GRCm39) |
|
probably null |
Het |
Ahnak2 |
T |
C |
12: 112,745,365 (GRCm39) |
|
probably benign |
Het |
Alcam |
T |
C |
16: 52,130,212 (GRCm39) |
D46G |
probably benign |
Het |
Asap2 |
T |
C |
12: 21,218,247 (GRCm39) |
S57P |
probably damaging |
Het |
Atg14 |
A |
T |
14: 47,784,752 (GRCm39) |
V314D |
possibly damaging |
Het |
C230029F24Rik |
C |
T |
1: 49,377,307 (GRCm39) |
|
noncoding transcript |
Het |
Calcr |
A |
T |
6: 3,707,592 (GRCm39) |
I236N |
probably benign |
Het |
Cass4 |
G |
A |
2: 172,258,107 (GRCm39) |
G35E |
probably damaging |
Het |
Chmp6 |
T |
C |
11: 119,807,517 (GRCm39) |
I120T |
probably benign |
Het |
Col13a1 |
A |
G |
10: 61,684,919 (GRCm39) |
|
probably benign |
Het |
Cstdc4 |
T |
A |
16: 36,004,631 (GRCm39) |
M1K |
probably null |
Het |
Ddhd2 |
T |
A |
8: 26,238,629 (GRCm39) |
L328F |
probably damaging |
Het |
Defa40 |
T |
A |
8: 21,740,359 (GRCm39) |
|
probably null |
Het |
Dnmt3l |
A |
G |
10: 77,887,860 (GRCm39) |
D123G |
possibly damaging |
Het |
Eea1 |
T |
A |
10: 95,838,810 (GRCm39) |
V287E |
possibly damaging |
Het |
Efcc1 |
A |
G |
6: 87,708,164 (GRCm39) |
N97S |
probably benign |
Het |
Exd1 |
A |
G |
2: 119,369,262 (GRCm39) |
S118P |
probably benign |
Het |
Ext2 |
G |
T |
2: 93,642,317 (GRCm39) |
T184K |
probably benign |
Het |
Fam186a |
G |
A |
15: 99,864,705 (GRCm39) |
Q42* |
probably null |
Het |
Gbp2 |
A |
T |
3: 142,337,843 (GRCm39) |
I320L |
probably benign |
Het |
Gramd2a |
G |
A |
9: 59,615,299 (GRCm39) |
G13R |
probably benign |
Het |
H2-Q5 |
T |
C |
17: 35,613,115 (GRCm39) |
M5T |
unknown |
Het |
Jak3 |
C |
T |
8: 72,131,344 (GRCm39) |
L70F |
probably damaging |
Het |
Lhpp |
G |
A |
7: 132,307,364 (GRCm39) |
V254M |
probably damaging |
Het |
Lig1 |
T |
A |
7: 13,030,184 (GRCm39) |
V387E |
possibly damaging |
Het |
Lipo3 |
T |
C |
19: 33,755,093 (GRCm39) |
|
probably benign |
Het |
Lrrc8b |
C |
T |
5: 105,629,208 (GRCm39) |
S518L |
probably benign |
Het |
Narf |
T |
C |
11: 121,135,480 (GRCm39) |
Y111H |
probably damaging |
Het |
Ncf4 |
A |
G |
15: 78,135,177 (GRCm39) |
K78R |
probably benign |
Het |
Nrap |
A |
T |
19: 56,330,601 (GRCm39) |
C1118* |
probably null |
Het |
Nubp2 |
A |
G |
17: 25,104,772 (GRCm39) |
V23A |
probably damaging |
Het |
Or4l1 |
A |
T |
14: 50,166,497 (GRCm39) |
F168Y |
probably damaging |
Het |
Or6c219 |
A |
T |
10: 129,781,780 (GRCm39) |
D50E |
possibly damaging |
Het |
Or8g55 |
T |
C |
9: 39,785,392 (GRCm39) |
S274P |
possibly damaging |
Het |
Pdzd7 |
G |
A |
19: 45,025,428 (GRCm39) |
P356S |
probably benign |
Het |
Rttn |
T |
C |
18: 89,056,070 (GRCm39) |
V984A |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,516,925 (GRCm39) |
S3334P |
probably damaging |
Het |
Senp7 |
G |
A |
16: 55,959,468 (GRCm39) |
|
probably null |
Het |
Slc25a3 |
A |
C |
10: 90,957,903 (GRCm39) |
Y50D |
probably benign |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Slc38a2 |
A |
T |
15: 96,592,970 (GRCm39) |
S163T |
probably benign |
Het |
Sp110 |
A |
C |
1: 85,505,050 (GRCm39) |
F434C |
probably benign |
Het |
Stam2 |
A |
T |
2: 52,610,922 (GRCm39) |
C4* |
probably null |
Het |
Taf1a |
A |
G |
1: 183,177,272 (GRCm39) |
D50G |
possibly damaging |
Het |
Taf6l |
A |
T |
19: 8,759,995 (GRCm39) |
Y106N |
possibly damaging |
Het |
Taf7l2 |
T |
C |
10: 115,948,674 (GRCm39) |
E284G |
probably damaging |
Het |
Tex10 |
A |
G |
4: 48,433,295 (GRCm39) |
V829A |
possibly damaging |
Het |
Tgfbr3 |
T |
C |
5: 107,257,474 (GRCm39) |
|
probably benign |
Het |
Tnfsf10 |
G |
T |
3: 27,389,742 (GRCm39) |
V268F |
probably damaging |
Het |
Trrap |
A |
G |
5: 144,767,755 (GRCm39) |
T2571A |
probably benign |
Het |
|
Other mutations in Tbx20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Tbx20
|
APN |
9 |
24,670,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00572:Tbx20
|
APN |
9 |
24,636,984 (GRCm39) |
missense |
probably benign |
|
IGL01016:Tbx20
|
APN |
9 |
24,661,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01317:Tbx20
|
APN |
9 |
24,681,051 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02643:Tbx20
|
APN |
9 |
24,685,009 (GRCm39) |
unclassified |
probably benign |
|
IGL02690:Tbx20
|
APN |
9 |
24,685,033 (GRCm39) |
missense |
probably benign |
0.27 |
BB006:Tbx20
|
UTSW |
9 |
24,637,059 (GRCm39) |
missense |
possibly damaging |
0.86 |
BB016:Tbx20
|
UTSW |
9 |
24,637,059 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0853:Tbx20
|
UTSW |
9 |
24,636,908 (GRCm39) |
missense |
probably benign |
0.05 |
R0855:Tbx20
|
UTSW |
9 |
24,636,908 (GRCm39) |
missense |
probably benign |
0.05 |
R0856:Tbx20
|
UTSW |
9 |
24,636,908 (GRCm39) |
missense |
probably benign |
0.05 |
R1781:Tbx20
|
UTSW |
9 |
24,636,795 (GRCm39) |
missense |
probably benign |
0.00 |
R1840:Tbx20
|
UTSW |
9 |
24,636,972 (GRCm39) |
missense |
probably benign |
0.22 |
R1981:Tbx20
|
UTSW |
9 |
24,682,209 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2063:Tbx20
|
UTSW |
9 |
24,681,067 (GRCm39) |
nonsense |
probably null |
|
R2357:Tbx20
|
UTSW |
9 |
24,681,072 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4166:Tbx20
|
UTSW |
9 |
24,681,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Tbx20
|
UTSW |
9 |
24,637,010 (GRCm39) |
missense |
probably benign |
0.34 |
R4904:Tbx20
|
UTSW |
9 |
24,670,129 (GRCm39) |
missense |
probably damaging |
0.98 |
R5436:Tbx20
|
UTSW |
9 |
24,681,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Tbx20
|
UTSW |
9 |
24,670,155 (GRCm39) |
missense |
probably damaging |
1.00 |
R6914:Tbx20
|
UTSW |
9 |
24,636,779 (GRCm39) |
missense |
probably benign |
0.19 |
R6962:Tbx20
|
UTSW |
9 |
24,681,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R7556:Tbx20
|
UTSW |
9 |
24,661,573 (GRCm39) |
splice site |
probably null |
|
R7731:Tbx20
|
UTSW |
9 |
24,681,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R7741:Tbx20
|
UTSW |
9 |
24,651,581 (GRCm39) |
splice site |
probably null |
|
R7832:Tbx20
|
UTSW |
9 |
24,685,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R7929:Tbx20
|
UTSW |
9 |
24,637,059 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7982:Tbx20
|
UTSW |
9 |
24,685,220 (GRCm39) |
unclassified |
probably benign |
|
R8110:Tbx20
|
UTSW |
9 |
24,636,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R8974:Tbx20
|
UTSW |
9 |
24,681,082 (GRCm39) |
missense |
probably damaging |
1.00 |
R9058:Tbx20
|
UTSW |
9 |
24,681,019 (GRCm39) |
missense |
probably damaging |
1.00 |
|