Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
C |
A |
15: 94,333,695 (GRCm38) |
R871L |
possibly damaging |
Het |
Adcy5 |
G |
A |
16: 35,268,993 (GRCm38) |
C520Y |
probably damaging |
Het |
AI661453 |
G |
A |
17: 47,468,117 (GRCm38) |
|
probably benign |
Het |
Cnot10 |
T |
A |
9: 114,631,881 (GRCm38) |
K74* |
probably null |
Het |
Ctc1 |
C |
T |
11: 69,022,871 (GRCm38) |
P200S |
probably damaging |
Het |
Dact1 |
T |
C |
12: 71,317,185 (GRCm38) |
Y210H |
probably damaging |
Het |
Dbn1 |
T |
C |
13: 55,475,381 (GRCm38) |
T430A |
probably benign |
Het |
Dmd |
A |
C |
X: 83,722,018 (GRCm38) |
T657P |
probably benign |
Het |
Efnb2 |
C |
T |
8: 8,620,832 (GRCm38) |
R256H |
possibly damaging |
Het |
Eif4a1 |
T |
C |
11: 69,669,244 (GRCm38) |
I116M |
possibly damaging |
Het |
F730035P03Rik |
A |
T |
7: 99,780,268 (GRCm38) |
|
noncoding transcript |
Het |
Fbn1 |
C |
T |
2: 125,397,781 (GRCm38) |
V329I |
probably benign |
Het |
Gpr20 |
G |
A |
15: 73,696,276 (GRCm38) |
T88I |
probably benign |
Het |
Herc1 |
T |
G |
9: 66,479,453 (GRCm38) |
V3783G |
probably benign |
Het |
Khdc1a |
A |
G |
1: 21,350,393 (GRCm38) |
D79G |
possibly damaging |
Het |
Klk1b16 |
A |
T |
7: 44,141,427 (GRCm38) |
I218F |
probably damaging |
Het |
Malrd1 |
C |
T |
2: 16,150,783 (GRCm38) |
T2001I |
unknown |
Het |
Mia3 |
A |
G |
1: 183,330,878 (GRCm38) |
S556P |
probably damaging |
Het |
Myo3a |
T |
A |
2: 22,577,842 (GRCm38) |
D369E |
probably benign |
Het |
Nelfa |
T |
C |
5: 33,901,279 (GRCm38) |
D279G |
possibly damaging |
Het |
Ntrk3 |
A |
T |
7: 78,250,769 (GRCm38) |
C607* |
probably null |
Het |
Olfr53 |
T |
C |
7: 140,652,828 (GRCm38) |
V283A |
possibly damaging |
Het |
Pclo |
A |
T |
5: 14,775,366 (GRCm38) |
Q1371L |
probably damaging |
Het |
Pdzd2 |
A |
T |
15: 12,375,975 (GRCm38) |
V1358E |
probably benign |
Het |
Pgr |
T |
C |
9: 8,903,749 (GRCm38) |
|
probably null |
Het |
Prag1 |
A |
G |
8: 36,103,655 (GRCm38) |
D464G |
probably damaging |
Het |
Prickle4 |
A |
G |
17: 47,690,531 (GRCm38) |
|
probably benign |
Het |
Prim2 |
A |
G |
1: 33,512,111 (GRCm38) |
Y309H |
probably damaging |
Het |
Prkaa1 |
A |
G |
15: 5,177,161 (GRCm38) |
Q464R |
possibly damaging |
Het |
Rab36 |
G |
A |
10: 75,044,496 (GRCm38) |
V63I |
probably damaging |
Het |
Rint1 |
T |
A |
5: 23,794,447 (GRCm38) |
I78K |
possibly damaging |
Het |
Rnf130 |
T |
A |
11: 50,071,378 (GRCm38) |
F217Y |
probably benign |
Het |
Smad7 |
T |
C |
18: 75,394,163 (GRCm38) |
V360A |
probably damaging |
Het |
Sp110 |
A |
C |
1: 85,577,329 (GRCm38) |
F434C |
probably benign |
Het |
Stag1 |
A |
G |
9: 100,956,606 (GRCm38) |
|
probably benign |
Het |
Tlr12 |
T |
A |
4: 128,616,195 (GRCm38) |
D754V |
probably benign |
Het |
Tmf1 |
G |
A |
6: 97,178,896 (GRCm38) |
P43L |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 64,980,856 (GRCm38) |
N873S |
probably benign |
Het |
Tsn |
C |
T |
1: 118,311,069 (GRCm38) |
|
probably benign |
Het |
Ubn1 |
A |
G |
16: 5,064,425 (GRCm38) |
K250R |
probably damaging |
Het |
Vmn1r25 |
A |
T |
6: 57,978,827 (GRCm38) |
V159D |
probably damaging |
Het |
Vmn2r89 |
T |
C |
14: 51,452,094 (GRCm38) |
L18P |
probably damaging |
Het |
Vps8 |
T |
G |
16: 21,504,466 (GRCm38) |
N689K |
probably damaging |
Het |
Ythdc1 |
G |
T |
5: 86,835,820 (GRCm38) |
|
probably benign |
Het |
Ythdc1 |
T |
A |
5: 86,815,654 (GRCm38) |
D30E |
possibly damaging |
Het |
Zfp407 |
G |
A |
18: 84,562,731 (GRCm38) |
Q86* |
probably null |
Het |
Zfp521 |
C |
T |
18: 13,846,544 (GRCm38) |
E271K |
probably benign |
Het |
|
Other mutations in Bptf |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00553:Bptf
|
APN |
11 |
107,055,279 (GRCm38) |
missense |
possibly damaging |
0.88 |
IGL00664:Bptf
|
APN |
11 |
107,077,665 (GRCm38) |
missense |
possibly damaging |
0.78 |
IGL00705:Bptf
|
APN |
11 |
107,095,708 (GRCm38) |
splice site |
probably benign |
|
IGL00796:Bptf
|
APN |
11 |
107,054,550 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00834:Bptf
|
APN |
11 |
107,073,928 (GRCm38) |
missense |
possibly damaging |
0.59 |
IGL01155:Bptf
|
APN |
11 |
107,080,727 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01314:Bptf
|
APN |
11 |
107,054,853 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01371:Bptf
|
APN |
11 |
107,055,907 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01567:Bptf
|
APN |
11 |
107,058,774 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01794:Bptf
|
APN |
11 |
107,053,221 (GRCm38) |
critical splice donor site |
probably null |
|
IGL02108:Bptf
|
APN |
11 |
107,074,988 (GRCm38) |
missense |
probably benign |
0.45 |
IGL02367:Bptf
|
APN |
11 |
107,073,352 (GRCm38) |
missense |
probably benign |
|
IGL02437:Bptf
|
APN |
11 |
107,074,695 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02589:Bptf
|
APN |
11 |
107,111,531 (GRCm38) |
missense |
possibly damaging |
0.92 |
IGL02897:Bptf
|
APN |
11 |
107,047,121 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02935:Bptf
|
APN |
11 |
107,080,799 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02954:Bptf
|
APN |
11 |
107,054,749 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL02982:Bptf
|
APN |
11 |
107,076,674 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03109:Bptf
|
APN |
11 |
107,061,701 (GRCm38) |
missense |
possibly damaging |
0.53 |
IGL03265:Bptf
|
APN |
11 |
107,054,628 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03403:Bptf
|
APN |
11 |
107,099,733 (GRCm38) |
missense |
possibly damaging |
0.51 |
Anodyne
|
UTSW |
11 |
107,043,631 (GRCm38) |
critical splice donor site |
probably null |
|
Arroyo
|
UTSW |
11 |
107,042,690 (GRCm38) |
missense |
probably benign |
0.32 |
mojado
|
UTSW |
11 |
107,044,640 (GRCm38) |
missense |
probably benign |
0.03 |
IGL03097:Bptf
|
UTSW |
11 |
107,077,680 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4486001:Bptf
|
UTSW |
11 |
107,054,788 (GRCm38) |
missense |
probably damaging |
0.98 |
R0066:Bptf
|
UTSW |
11 |
107,062,136 (GRCm38) |
missense |
possibly damaging |
0.90 |
R0157:Bptf
|
UTSW |
11 |
107,074,658 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0320:Bptf
|
UTSW |
11 |
107,072,819 (GRCm38) |
missense |
probably damaging |
1.00 |
R0328:Bptf
|
UTSW |
11 |
107,047,127 (GRCm38) |
missense |
probably damaging |
1.00 |
R0402:Bptf
|
UTSW |
11 |
107,074,114 (GRCm38) |
missense |
probably damaging |
1.00 |
R0482:Bptf
|
UTSW |
11 |
107,081,262 (GRCm38) |
missense |
probably benign |
0.13 |
R0574:Bptf
|
UTSW |
11 |
107,076,527 (GRCm38) |
missense |
probably damaging |
1.00 |
R0598:Bptf
|
UTSW |
11 |
107,072,965 (GRCm38) |
missense |
probably damaging |
0.99 |
R0599:Bptf
|
UTSW |
11 |
107,068,382 (GRCm38) |
missense |
probably damaging |
1.00 |
R0601:Bptf
|
UTSW |
11 |
107,061,692 (GRCm38) |
missense |
probably benign |
0.04 |
R0744:Bptf
|
UTSW |
11 |
107,110,812 (GRCm38) |
critical splice donor site |
probably null |
|
R0836:Bptf
|
UTSW |
11 |
107,110,812 (GRCm38) |
critical splice donor site |
probably null |
|
R0885:Bptf
|
UTSW |
11 |
107,043,791 (GRCm38) |
missense |
probably damaging |
1.00 |
R1070:Bptf
|
UTSW |
11 |
107,055,055 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1252:Bptf
|
UTSW |
11 |
107,073,251 (GRCm38) |
missense |
probably benign |
0.00 |
R1370:Bptf
|
UTSW |
11 |
107,047,094 (GRCm38) |
missense |
probably damaging |
0.99 |
R1428:Bptf
|
UTSW |
11 |
107,073,047 (GRCm38) |
missense |
probably damaging |
0.99 |
R1467:Bptf
|
UTSW |
11 |
107,055,055 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1467:Bptf
|
UTSW |
11 |
107,055,055 (GRCm38) |
missense |
possibly damaging |
0.92 |
R1742:Bptf
|
UTSW |
11 |
107,110,951 (GRCm38) |
missense |
probably damaging |
1.00 |
R1816:Bptf
|
UTSW |
11 |
107,060,579 (GRCm38) |
missense |
probably damaging |
1.00 |
R1858:Bptf
|
UTSW |
11 |
107,073,301 (GRCm38) |
missense |
probably benign |
0.00 |
R1989:Bptf
|
UTSW |
11 |
107,074,826 (GRCm38) |
missense |
probably damaging |
1.00 |
R2253:Bptf
|
UTSW |
11 |
107,111,322 (GRCm38) |
missense |
probably damaging |
1.00 |
R2392:Bptf
|
UTSW |
11 |
107,072,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R2431:Bptf
|
UTSW |
11 |
107,047,240 (GRCm38) |
missense |
possibly damaging |
0.48 |
R3022:Bptf
|
UTSW |
11 |
107,111,637 (GRCm38) |
critical splice acceptor site |
probably null |
|
R3161:Bptf
|
UTSW |
11 |
107,074,476 (GRCm38) |
missense |
probably damaging |
1.00 |
R3686:Bptf
|
UTSW |
11 |
107,074,198 (GRCm38) |
missense |
probably benign |
0.25 |
R3687:Bptf
|
UTSW |
11 |
107,074,198 (GRCm38) |
missense |
probably benign |
0.25 |
R3688:Bptf
|
UTSW |
11 |
107,074,198 (GRCm38) |
missense |
probably benign |
0.25 |
R3787:Bptf
|
UTSW |
11 |
107,073,827 (GRCm38) |
missense |
probably damaging |
1.00 |
R3834:Bptf
|
UTSW |
11 |
107,073,857 (GRCm38) |
missense |
probably benign |
0.05 |
R3885:Bptf
|
UTSW |
11 |
107,074,513 (GRCm38) |
missense |
probably damaging |
0.97 |
R4090:Bptf
|
UTSW |
11 |
107,081,523 (GRCm38) |
missense |
probably damaging |
0.99 |
R4437:Bptf
|
UTSW |
11 |
107,074,474 (GRCm38) |
missense |
possibly damaging |
0.59 |
R4514:Bptf
|
UTSW |
11 |
107,077,692 (GRCm38) |
missense |
probably damaging |
1.00 |
R4565:Bptf
|
UTSW |
11 |
107,073,010 (GRCm38) |
missense |
probably damaging |
1.00 |
R4715:Bptf
|
UTSW |
11 |
107,047,181 (GRCm38) |
missense |
probably damaging |
1.00 |
R4748:Bptf
|
UTSW |
11 |
107,095,880 (GRCm38) |
missense |
probably damaging |
0.96 |
R4764:Bptf
|
UTSW |
11 |
107,043,694 (GRCm38) |
missense |
probably damaging |
1.00 |
R4885:Bptf
|
UTSW |
11 |
107,074,648 (GRCm38) |
missense |
probably benign |
0.39 |
R4901:Bptf
|
UTSW |
11 |
107,110,860 (GRCm38) |
nonsense |
probably null |
|
R4995:Bptf
|
UTSW |
11 |
107,054,565 (GRCm38) |
missense |
probably damaging |
0.98 |
R5057:Bptf
|
UTSW |
11 |
107,082,528 (GRCm38) |
missense |
probably damaging |
0.98 |
R5120:Bptf
|
UTSW |
11 |
107,073,385 (GRCm38) |
missense |
probably damaging |
0.99 |
R5320:Bptf
|
UTSW |
11 |
107,081,367 (GRCm38) |
nonsense |
probably null |
|
R5329:Bptf
|
UTSW |
11 |
107,073,295 (GRCm38) |
missense |
probably benign |
0.06 |
R5418:Bptf
|
UTSW |
11 |
107,111,294 (GRCm38) |
missense |
probably damaging |
1.00 |
R5461:Bptf
|
UTSW |
11 |
107,061,764 (GRCm38) |
missense |
probably damaging |
1.00 |
R5664:Bptf
|
UTSW |
11 |
107,073,699 (GRCm38) |
missense |
probably benign |
0.01 |
R5718:Bptf
|
UTSW |
11 |
107,111,434 (GRCm38) |
missense |
probably damaging |
1.00 |
R5774:Bptf
|
UTSW |
11 |
107,111,137 (GRCm38) |
missense |
probably damaging |
1.00 |
R5851:Bptf
|
UTSW |
11 |
107,110,862 (GRCm38) |
missense |
probably damaging |
1.00 |
R5930:Bptf
|
UTSW |
11 |
107,073,196 (GRCm38) |
missense |
probably damaging |
1.00 |
R5949:Bptf
|
UTSW |
11 |
107,111,089 (GRCm38) |
missense |
probably damaging |
0.99 |
R5975:Bptf
|
UTSW |
11 |
107,035,864 (GRCm38) |
utr 3 prime |
probably benign |
|
R6027:Bptf
|
UTSW |
11 |
107,074,945 (GRCm38) |
missense |
probably damaging |
1.00 |
R6128:Bptf
|
UTSW |
11 |
107,074,690 (GRCm38) |
missense |
possibly damaging |
0.87 |
R6337:Bptf
|
UTSW |
11 |
107,058,779 (GRCm38) |
missense |
possibly damaging |
0.89 |
R6407:Bptf
|
UTSW |
11 |
107,111,126 (GRCm38) |
missense |
probably damaging |
1.00 |
R6470:Bptf
|
UTSW |
11 |
107,072,767 (GRCm38) |
missense |
probably damaging |
1.00 |
R6487:Bptf
|
UTSW |
11 |
107,077,726 (GRCm38) |
missense |
probably damaging |
0.99 |
R6501:Bptf
|
UTSW |
11 |
107,077,683 (GRCm38) |
missense |
probably null |
1.00 |
R6755:Bptf
|
UTSW |
11 |
107,047,256 (GRCm38) |
missense |
probably benign |
0.27 |
R6861:Bptf
|
UTSW |
11 |
107,062,565 (GRCm38) |
missense |
probably damaging |
1.00 |
R6866:Bptf
|
UTSW |
11 |
107,073,580 (GRCm38) |
missense |
probably damaging |
1.00 |
R6879:Bptf
|
UTSW |
11 |
107,042,690 (GRCm38) |
missense |
probably benign |
0.32 |
R6927:Bptf
|
UTSW |
11 |
107,054,595 (GRCm38) |
missense |
probably damaging |
1.00 |
R6944:Bptf
|
UTSW |
11 |
107,080,823 (GRCm38) |
missense |
probably damaging |
1.00 |
R7082:Bptf
|
UTSW |
11 |
107,086,747 (GRCm38) |
missense |
probably benign |
0.00 |
R7136:Bptf
|
UTSW |
11 |
107,099,715 (GRCm38) |
missense |
probably damaging |
1.00 |
R7162:Bptf
|
UTSW |
11 |
107,043,631 (GRCm38) |
critical splice donor site |
probably null |
|
R7171:Bptf
|
UTSW |
11 |
107,131,407 (GRCm38) |
missense |
unknown |
|
R7193:Bptf
|
UTSW |
11 |
107,054,809 (GRCm38) |
nonsense |
probably null |
|
R7210:Bptf
|
UTSW |
11 |
107,054,464 (GRCm38) |
nonsense |
probably null |
|
R7221:Bptf
|
UTSW |
11 |
107,054,832 (GRCm38) |
missense |
probably damaging |
1.00 |
R7316:Bptf
|
UTSW |
11 |
107,110,914 (GRCm38) |
nonsense |
probably null |
|
R7316:Bptf
|
UTSW |
11 |
107,073,109 (GRCm38) |
missense |
probably damaging |
1.00 |
R7422:Bptf
|
UTSW |
11 |
107,060,558 (GRCm38) |
missense |
probably damaging |
1.00 |
R7454:Bptf
|
UTSW |
11 |
107,044,640 (GRCm38) |
missense |
probably benign |
0.03 |
R7657:Bptf
|
UTSW |
11 |
107,074,729 (GRCm38) |
missense |
probably damaging |
1.00 |
R7718:Bptf
|
UTSW |
11 |
107,081,456 (GRCm38) |
missense |
possibly damaging |
0.65 |
R7827:Bptf
|
UTSW |
11 |
107,047,187 (GRCm38) |
missense |
probably benign |
0.01 |
R7844:Bptf
|
UTSW |
11 |
107,074,061 (GRCm38) |
missense |
probably damaging |
0.97 |
R7992:Bptf
|
UTSW |
11 |
107,110,883 (GRCm38) |
missense |
probably benign |
0.00 |
R8001:Bptf
|
UTSW |
11 |
107,047,340 (GRCm38) |
nonsense |
probably null |
|
R8037:Bptf
|
UTSW |
11 |
107,055,950 (GRCm38) |
missense |
probably damaging |
1.00 |
R8122:Bptf
|
UTSW |
11 |
107,036,591 (GRCm38) |
critical splice acceptor site |
probably null |
|
R8235:Bptf
|
UTSW |
11 |
107,076,632 (GRCm38) |
missense |
probably benign |
0.04 |
R8308:Bptf
|
UTSW |
11 |
107,052,989 (GRCm38) |
missense |
probably damaging |
0.99 |
R8409:Bptf
|
UTSW |
11 |
107,062,669 (GRCm38) |
missense |
probably damaging |
1.00 |
R8464:Bptf
|
UTSW |
11 |
107,131,342 (GRCm38) |
missense |
probably benign |
0.01 |
R8477:Bptf
|
UTSW |
11 |
107,052,853 (GRCm38) |
missense |
probably damaging |
0.98 |
R8482:Bptf
|
UTSW |
11 |
107,043,698 (GRCm38) |
missense |
probably benign |
0.19 |
R8515:Bptf
|
UTSW |
11 |
107,055,238 (GRCm38) |
missense |
possibly damaging |
0.85 |
R8519:Bptf
|
UTSW |
11 |
107,061,764 (GRCm38) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
107,073,314 (GRCm38) |
missense |
probably damaging |
1.00 |
R8708:Bptf
|
UTSW |
11 |
107,073,313 (GRCm38) |
missense |
probably damaging |
0.99 |
R8722:Bptf
|
UTSW |
11 |
107,131,469 (GRCm38) |
missense |
unknown |
|
R8732:Bptf
|
UTSW |
11 |
107,040,380 (GRCm38) |
missense |
probably damaging |
1.00 |
R8783:Bptf
|
UTSW |
11 |
107,131,531 (GRCm38) |
missense |
unknown |
|
R8828:Bptf
|
UTSW |
11 |
107,055,010 (GRCm38) |
missense |
probably damaging |
0.98 |
R9004:Bptf
|
UTSW |
11 |
107,054,887 (GRCm38) |
missense |
probably damaging |
1.00 |
R9010:Bptf
|
UTSW |
11 |
107,073,750 (GRCm38) |
missense |
probably damaging |
1.00 |
R9035:Bptf
|
UTSW |
11 |
107,073,016 (GRCm38) |
missense |
probably damaging |
1.00 |
R9083:Bptf
|
UTSW |
11 |
107,068,350 (GRCm38) |
missense |
probably damaging |
1.00 |
R9211:Bptf
|
UTSW |
11 |
107,055,298 (GRCm38) |
missense |
probably damaging |
1.00 |
R9345:Bptf
|
UTSW |
11 |
107,080,762 (GRCm38) |
missense |
possibly damaging |
0.77 |
R9393:Bptf
|
UTSW |
11 |
107,074,308 (GRCm38) |
missense |
probably benign |
0.00 |
R9451:Bptf
|
UTSW |
11 |
107,044,585 (GRCm38) |
missense |
probably damaging |
1.00 |
R9561:Bptf
|
UTSW |
11 |
107,074,128 (GRCm38) |
nonsense |
probably null |
|
R9632:Bptf
|
UTSW |
11 |
107,061,719 (GRCm38) |
missense |
probably damaging |
1.00 |
R9648:Bptf
|
UTSW |
11 |
107,052,894 (GRCm38) |
missense |
probably damaging |
0.99 |
R9650:Bptf
|
UTSW |
11 |
107,044,586 (GRCm38) |
missense |
probably benign |
0.15 |
R9658:Bptf
|
UTSW |
11 |
107,111,344 (GRCm38) |
missense |
probably damaging |
1.00 |
R9775:Bptf
|
UTSW |
11 |
107,043,676 (GRCm38) |
missense |
probably benign |
0.04 |
R9776:Bptf
|
UTSW |
11 |
107,078,570 (GRCm38) |
missense |
probably damaging |
1.00 |
Z1088:Bptf
|
UTSW |
11 |
107,074,582 (GRCm38) |
missense |
probably benign |
0.00 |
Z1176:Bptf
|
UTSW |
11 |
107,058,684 (GRCm38) |
missense |
probably damaging |
1.00 |
|