Other mutations in this stock |
Total: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actr8 |
T |
A |
14: 29,715,030 (GRCm39) |
M615K |
possibly damaging |
Het |
Acvr1c |
A |
T |
2: 58,205,886 (GRCm39) |
C25S |
probably damaging |
Het |
Adk |
A |
T |
14: 21,473,616 (GRCm39) |
E291V |
probably benign |
Het |
Ahnak |
C |
A |
19: 8,986,711 (GRCm39) |
|
probably benign |
Het |
Alg11 |
A |
G |
8: 22,552,044 (GRCm39) |
T63A |
probably benign |
Het |
Alox12 |
A |
T |
11: 70,142,413 (GRCm39) |
S272T |
probably benign |
Het |
Armc10 |
T |
A |
5: 21,865,581 (GRCm39) |
S195T |
probably damaging |
Het |
AW209491 |
C |
T |
13: 14,812,365 (GRCm39) |
A406V |
probably benign |
Het |
Baat |
G |
A |
4: 49,502,871 (GRCm39) |
P84S |
probably damaging |
Het |
BB014433 |
G |
A |
8: 15,091,854 (GRCm39) |
T333I |
probably damaging |
Het |
BC035947 |
G |
A |
1: 78,475,843 (GRCm39) |
R230* |
probably null |
Het |
Ccdc88b |
T |
C |
19: 6,833,348 (GRCm39) |
E233G |
probably damaging |
Het |
Cep295 |
A |
G |
9: 15,252,770 (GRCm39) |
F353L |
probably damaging |
Het |
Chd8 |
T |
C |
14: 52,455,395 (GRCm39) |
M1031V |
probably damaging |
Het |
Col17a1 |
C |
G |
19: 47,642,659 (GRCm39) |
G885R |
probably damaging |
Het |
Cyp11a1 |
A |
C |
9: 57,928,117 (GRCm39) |
I214L |
probably benign |
Het |
Cyp3a44 |
A |
T |
5: 145,731,728 (GRCm39) |
S139R |
probably damaging |
Het |
Ddhd2 |
G |
A |
8: 26,238,589 (GRCm39) |
R64C |
probably damaging |
Het |
Dll3 |
A |
G |
7: 27,993,537 (GRCm39) |
W561R |
probably damaging |
Het |
Dnajc3 |
T |
C |
14: 119,195,376 (GRCm39) |
V97A |
possibly damaging |
Het |
Drosha |
C |
T |
15: 12,834,582 (GRCm39) |
|
probably benign |
Het |
E2f8 |
T |
C |
7: 48,524,743 (GRCm39) |
D302G |
probably damaging |
Het |
Ecd |
C |
G |
14: 20,374,629 (GRCm39) |
D504H |
probably damaging |
Het |
Eif1ad15 |
T |
A |
12: 88,288,202 (GRCm39) |
N17I |
unknown |
Het |
Eif4g2 |
C |
A |
7: 110,676,437 (GRCm39) |
V331L |
probably benign |
Het |
Fam124a |
T |
C |
14: 62,824,986 (GRCm39) |
I160T |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,482,493 (GRCm39) |
T3051A |
probably benign |
Het |
Gm10271 |
A |
T |
10: 116,808,497 (GRCm39) |
F6L |
probably damaging |
Het |
Gm572 |
A |
G |
4: 148,752,964 (GRCm39) |
E281G |
possibly damaging |
Het |
Gm9944 |
T |
C |
4: 144,179,775 (GRCm39) |
|
probably benign |
Het |
Gstm5 |
A |
C |
3: 107,803,270 (GRCm39) |
M1L |
probably benign |
Het |
Havcr1 |
A |
G |
11: 46,646,964 (GRCm39) |
T133A |
probably damaging |
Het |
Hey1 |
T |
G |
3: 8,731,379 (GRCm39) |
S68R |
probably damaging |
Het |
Hsf2bp |
C |
T |
17: 32,230,149 (GRCm39) |
|
probably null |
Het |
Id2 |
T |
C |
12: 25,145,723 (GRCm39) |
N96S |
probably benign |
Het |
Ifi206 |
A |
C |
1: 173,308,906 (GRCm39) |
S363R |
possibly damaging |
Het |
Il21r |
T |
C |
7: 125,231,460 (GRCm39) |
F296S |
probably damaging |
Het |
Irgm2 |
A |
G |
11: 58,111,013 (GRCm39) |
T247A |
probably benign |
Het |
Irx5 |
T |
A |
8: 93,087,299 (GRCm39) |
Y410* |
probably null |
Het |
Kmt2c |
A |
G |
5: 25,516,118 (GRCm39) |
I2575T |
probably benign |
Het |
Lmbrd2 |
T |
A |
15: 9,182,493 (GRCm39) |
|
probably null |
Het |
Lrig1 |
A |
C |
6: 94,605,023 (GRCm39) |
S191A |
probably damaging |
Het |
Lrrc37 |
T |
C |
11: 103,506,722 (GRCm39) |
|
probably benign |
Het |
Lypd6b |
T |
A |
2: 49,836,178 (GRCm39) |
C120S |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,202,812 (GRCm39) |
|
probably null |
Het |
Myh6 |
G |
T |
14: 55,202,851 (GRCm39) |
R23S |
probably damaging |
Het |
Nat8f6 |
C |
T |
6: 85,786,040 (GRCm39) |
M36I |
probably benign |
Het |
Nol8 |
T |
A |
13: 49,826,090 (GRCm39) |
M970K |
possibly damaging |
Het |
Nrxn2 |
T |
C |
19: 6,542,901 (GRCm39) |
F1042L |
possibly damaging |
Het |
Nup160 |
T |
C |
2: 90,519,553 (GRCm39) |
W277R |
probably damaging |
Het |
Ogfr |
A |
T |
2: 180,236,026 (GRCm39) |
T204S |
probably damaging |
Het |
Or10j5 |
T |
A |
1: 172,784,723 (GRCm39) |
Y120* |
probably null |
Het |
Or1ak2 |
A |
G |
2: 36,827,236 (GRCm39) |
Y35C |
probably damaging |
Het |
Or1p1 |
T |
C |
11: 74,179,679 (GRCm39) |
V69A |
probably benign |
Het |
Or2n1d |
T |
C |
17: 38,646,911 (GRCm39) |
F288L |
probably damaging |
Het |
Or52n2b |
A |
T |
7: 104,566,125 (GRCm39) |
V126E |
probably damaging |
Het |
Or8c20 |
T |
C |
9: 38,261,045 (GRCm39) |
V222A |
probably benign |
Het |
Pcdh15 |
A |
G |
10: 74,215,189 (GRCm39) |
I648V |
probably benign |
Het |
Pced1b |
T |
A |
15: 97,282,228 (GRCm39) |
V89E |
probably damaging |
Het |
Phax |
G |
T |
18: 56,708,564 (GRCm39) |
A43S |
probably benign |
Het |
Phf20 |
A |
G |
2: 156,149,250 (GRCm39) |
E976G |
probably damaging |
Het |
Plin4 |
T |
C |
17: 56,416,567 (GRCm39) |
T8A |
probably benign |
Het |
Plxna1 |
G |
A |
6: 89,334,522 (GRCm39) |
Q36* |
probably null |
Het |
Pold1 |
T |
C |
7: 44,190,004 (GRCm39) |
Y394C |
probably damaging |
Het |
Ppp1r26 |
T |
A |
2: 28,342,566 (GRCm39) |
V732E |
probably benign |
Het |
Pramel5 |
A |
T |
4: 143,999,716 (GRCm39) |
C124S |
possibly damaging |
Het |
Prorp |
T |
A |
12: 55,424,002 (GRCm39) |
M441K |
probably damaging |
Het |
Prr14l |
C |
A |
5: 32,988,195 (GRCm39) |
L433F |
probably damaging |
Het |
Ptpn14 |
A |
G |
1: 189,582,584 (GRCm39) |
Y477C |
probably damaging |
Het |
Rcl1 |
T |
A |
19: 29,099,167 (GRCm39) |
I154N |
probably damaging |
Het |
Rfpl4 |
T |
C |
7: 5,118,501 (GRCm39) |
Y23C |
probably damaging |
Het |
Rims1 |
T |
C |
1: 22,635,544 (GRCm39) |
K146E |
probably damaging |
Het |
Rims2 |
A |
T |
15: 39,155,577 (GRCm39) |
K126M |
probably damaging |
Het |
Rpusd4 |
T |
A |
9: 35,183,816 (GRCm39) |
|
probably null |
Het |
Scn7a |
C |
T |
2: 66,556,558 (GRCm39) |
W342* |
probably null |
Het |
Sh3pxd2a |
A |
G |
19: 47,353,077 (GRCm39) |
V128A |
probably benign |
Het |
Slc15a5 |
T |
C |
6: 138,020,529 (GRCm39) |
H268R |
probably benign |
Het |
Slc22a3 |
T |
C |
17: 12,652,782 (GRCm39) |
I321V |
possibly damaging |
Het |
Slc7a6os |
A |
G |
8: 106,928,965 (GRCm39) |
S231P |
probably benign |
Het |
Smad5 |
T |
C |
13: 56,883,798 (GRCm39) |
S395P |
probably damaging |
Het |
Sorbs3 |
G |
A |
14: 70,440,752 (GRCm39) |
T20I |
probably benign |
Het |
Spata9 |
A |
G |
13: 76,116,236 (GRCm39) |
I42V |
probably benign |
Het |
Srl |
C |
T |
16: 4,340,892 (GRCm39) |
C9Y |
unknown |
Het |
Sugp2 |
T |
C |
8: 70,695,875 (GRCm39) |
F283L |
probably benign |
Het |
Syne2 |
T |
C |
12: 75,976,191 (GRCm39) |
|
probably null |
Het |
Taar6 |
A |
G |
10: 23,861,154 (GRCm39) |
Y131H |
probably damaging |
Het |
Tango2 |
T |
C |
16: 18,120,554 (GRCm39) |
T137A |
probably damaging |
Het |
Tas2r106 |
T |
A |
6: 131,655,606 (GRCm39) |
I82L |
probably benign |
Het |
Tbc1d32 |
T |
C |
10: 55,964,433 (GRCm39) |
E922G |
probably damaging |
Het |
Tgfb2 |
G |
T |
1: 186,436,778 (GRCm39) |
P65Q |
probably benign |
Het |
Tjp2 |
T |
G |
19: 24,091,464 (GRCm39) |
I566L |
probably benign |
Het |
Tnrc6a |
T |
A |
7: 122,781,603 (GRCm39) |
N1424K |
probably damaging |
Het |
Trim7 |
A |
T |
11: 48,728,513 (GRCm39) |
M54L |
probably benign |
Het |
Trpm1 |
T |
A |
7: 63,876,553 (GRCm39) |
S535R |
probably benign |
Het |
Tsc2 |
T |
A |
17: 24,839,740 (GRCm39) |
N417I |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,800,132 (GRCm39) |
R359G |
probably benign |
Het |
Vim |
A |
G |
2: 13,587,296 (GRCm39) |
T458A |
probably benign |
Het |
Vps11 |
A |
T |
9: 44,265,221 (GRCm39) |
S612R |
probably benign |
Het |
Wdfy3 |
A |
G |
5: 102,032,004 (GRCm39) |
S2273P |
probably benign |
Het |
Wwox |
G |
T |
8: 115,433,081 (GRCm39) |
R249L |
probably benign |
Het |
Zbtb4 |
G |
T |
11: 69,669,790 (GRCm39) |
G838C |
probably damaging |
Het |
Zkscan3 |
A |
T |
13: 21,580,461 (GRCm39) |
C76S |
probably damaging |
Het |
Znrf3 |
C |
T |
11: 5,231,776 (GRCm39) |
C483Y |
probably damaging |
Het |
Zscan2 |
A |
G |
7: 80,525,947 (GRCm39) |
K556R |
possibly damaging |
Het |
|
Other mutations in Bcr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Bcr
|
APN |
10 |
74,992,903 (GRCm39) |
unclassified |
probably benign |
|
IGL00662:Bcr
|
APN |
10 |
75,003,932 (GRCm39) |
splice site |
probably benign |
|
IGL01359:Bcr
|
APN |
10 |
74,995,611 (GRCm39) |
unclassified |
probably benign |
|
IGL01737:Bcr
|
APN |
10 |
74,990,783 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01908:Bcr
|
APN |
10 |
74,897,705 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01954:Bcr
|
APN |
10 |
75,011,173 (GRCm39) |
splice site |
probably null |
|
IGL02169:Bcr
|
APN |
10 |
74,995,714 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02379:Bcr
|
APN |
10 |
74,992,980 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02380:Bcr
|
APN |
10 |
75,011,131 (GRCm39) |
missense |
probably benign |
|
IGL02385:Bcr
|
APN |
10 |
74,981,235 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02657:Bcr
|
APN |
10 |
74,990,796 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02682:Bcr
|
APN |
10 |
75,001,878 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02959:Bcr
|
APN |
10 |
74,996,222 (GRCm39) |
missense |
probably benign |
0.44 |
accrual
|
UTSW |
10 |
74,897,338 (GRCm39) |
missense |
possibly damaging |
0.77 |
Appreciation
|
UTSW |
10 |
74,896,957 (GRCm39) |
nonsense |
probably null |
|
R0329:Bcr
|
UTSW |
10 |
75,017,466 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0330:Bcr
|
UTSW |
10 |
75,017,466 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0376:Bcr
|
UTSW |
10 |
74,981,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R0685:Bcr
|
UTSW |
10 |
74,967,475 (GRCm39) |
missense |
probably damaging |
1.00 |
R0828:Bcr
|
UTSW |
10 |
74,993,039 (GRCm39) |
unclassified |
probably benign |
|
R0892:Bcr
|
UTSW |
10 |
74,960,895 (GRCm39) |
missense |
probably benign |
0.00 |
R1143:Bcr
|
UTSW |
10 |
74,897,197 (GRCm39) |
missense |
probably benign |
0.00 |
R1416:Bcr
|
UTSW |
10 |
74,897,338 (GRCm39) |
missense |
possibly damaging |
0.77 |
R1479:Bcr
|
UTSW |
10 |
74,896,957 (GRCm39) |
nonsense |
probably null |
|
R1611:Bcr
|
UTSW |
10 |
74,961,034 (GRCm39) |
splice site |
probably null |
|
R1636:Bcr
|
UTSW |
10 |
74,966,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R1837:Bcr
|
UTSW |
10 |
75,003,932 (GRCm39) |
splice site |
probably benign |
|
R2341:Bcr
|
UTSW |
10 |
74,966,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2343:Bcr
|
UTSW |
10 |
74,981,254 (GRCm39) |
missense |
probably benign |
0.03 |
R3753:Bcr
|
UTSW |
10 |
74,971,772 (GRCm39) |
missense |
probably benign |
0.05 |
R4273:Bcr
|
UTSW |
10 |
74,960,943 (GRCm39) |
missense |
probably damaging |
0.97 |
R4624:Bcr
|
UTSW |
10 |
74,989,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R4723:Bcr
|
UTSW |
10 |
75,011,161 (GRCm39) |
missense |
probably benign |
0.45 |
R5013:Bcr
|
UTSW |
10 |
74,960,898 (GRCm39) |
missense |
probably benign |
0.00 |
R5359:Bcr
|
UTSW |
10 |
75,001,917 (GRCm39) |
missense |
probably damaging |
0.99 |
R5458:Bcr
|
UTSW |
10 |
74,990,792 (GRCm39) |
missense |
probably benign |
|
R5982:Bcr
|
UTSW |
10 |
75,012,248 (GRCm39) |
missense |
probably benign |
0.08 |
R6220:Bcr
|
UTSW |
10 |
74,898,124 (GRCm39) |
missense |
probably benign |
|
R6827:Bcr
|
UTSW |
10 |
74,966,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R6886:Bcr
|
UTSW |
10 |
74,989,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R6990:Bcr
|
UTSW |
10 |
74,966,868 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7003:Bcr
|
UTSW |
10 |
74,897,393 (GRCm39) |
missense |
probably benign |
0.08 |
R7424:Bcr
|
UTSW |
10 |
74,992,932 (GRCm39) |
missense |
probably benign |
|
R7443:Bcr
|
UTSW |
10 |
74,978,968 (GRCm39) |
critical splice donor site |
probably null |
|
R7488:Bcr
|
UTSW |
10 |
74,996,162 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8232:Bcr
|
UTSW |
10 |
75,001,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R8360:Bcr
|
UTSW |
10 |
74,981,271 (GRCm39) |
missense |
probably damaging |
0.96 |
R8992:Bcr
|
UTSW |
10 |
74,967,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R9362:Bcr
|
UTSW |
10 |
74,993,023 (GRCm39) |
missense |
probably benign |
0.19 |
R9487:Bcr
|
UTSW |
10 |
74,967,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Bcr
|
UTSW |
10 |
74,990,745 (GRCm39) |
nonsense |
probably null |
|
R9610:Bcr
|
UTSW |
10 |
74,990,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R9611:Bcr
|
UTSW |
10 |
74,990,745 (GRCm39) |
nonsense |
probably null |
|
R9611:Bcr
|
UTSW |
10 |
74,990,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Bcr
|
UTSW |
10 |
74,966,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R9662:Bcr
|
UTSW |
10 |
75,011,152 (GRCm39) |
missense |
probably benign |
0.00 |
|