Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adpgk |
T |
C |
9: 59,217,566 (GRCm39) |
V193A |
possibly damaging |
Het |
Ahnak |
A |
C |
19: 8,991,290 (GRCm39) |
E4191D |
probably benign |
Het |
BC024139 |
T |
A |
15: 76,004,542 (GRCm39) |
|
probably benign |
Het |
Bst1 |
T |
G |
5: 43,997,834 (GRCm39) |
|
probably null |
Het |
Cacna1c |
C |
T |
6: 118,589,586 (GRCm39) |
R1446H |
probably damaging |
Het |
Carf |
A |
G |
1: 60,186,998 (GRCm39) |
K499E |
probably benign |
Het |
Casq2 |
A |
G |
3: 102,024,199 (GRCm39) |
E147G |
probably damaging |
Het |
Cd8a |
T |
A |
6: 71,350,712 (GRCm39) |
V59D |
probably damaging |
Het |
Chrm5 |
T |
C |
2: 112,310,214 (GRCm39) |
T301A |
probably benign |
Het |
Cog5 |
G |
A |
12: 31,920,056 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
T |
C |
15: 48,156,170 (GRCm39) |
|
probably null |
Het |
Dop1a |
T |
C |
9: 86,367,609 (GRCm39) |
S31P |
probably damaging |
Het |
Eif1ad9 |
A |
T |
12: 88,296,438 (GRCm39) |
I139F |
unknown |
Het |
Epb41 |
T |
C |
4: 131,727,502 (GRCm39) |
|
probably benign |
Het |
Fhod3 |
C |
T |
18: 25,118,293 (GRCm39) |
A210V |
probably damaging |
Het |
Gdpgp1 |
T |
C |
7: 79,888,250 (GRCm39) |
F94L |
probably benign |
Het |
Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
Htr3b |
T |
C |
9: 48,847,390 (GRCm39) |
K375R |
possibly damaging |
Het |
Inhbe |
G |
A |
10: 127,187,186 (GRCm39) |
R77W |
probably damaging |
Het |
Itgb8 |
T |
C |
12: 119,166,231 (GRCm39) |
E100G |
probably damaging |
Het |
Jakmip1 |
T |
C |
5: 37,248,472 (GRCm39) |
V44A |
possibly damaging |
Het |
Lrp12 |
A |
G |
15: 39,741,827 (GRCm39) |
V315A |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 40,567,506 (GRCm39) |
T305S |
unknown |
Het |
Map3k2 |
A |
G |
18: 32,350,211 (GRCm39) |
T354A |
probably benign |
Het |
Mmp16 |
T |
C |
4: 17,987,726 (GRCm39) |
|
probably null |
Het |
Mphosph10 |
T |
C |
7: 64,038,607 (GRCm39) |
|
probably benign |
Het |
Or10a48 |
A |
G |
7: 108,424,385 (GRCm39) |
S274P |
probably damaging |
Het |
Or10ak7 |
A |
T |
4: 118,791,614 (GRCm39) |
C144S |
probably damaging |
Het |
Or4c52 |
T |
A |
2: 89,845,598 (GRCm39) |
I108N |
possibly damaging |
Het |
Or4k47 |
T |
C |
2: 111,452,086 (GRCm39) |
E111G |
probably damaging |
Het |
Or5p52 |
G |
A |
7: 107,502,130 (GRCm39) |
V69I |
possibly damaging |
Het |
Slc43a3 |
C |
A |
2: 84,768,140 (GRCm39) |
F37L |
probably benign |
Het |
Slf2 |
G |
T |
19: 44,919,855 (GRCm39) |
A36S |
probably damaging |
Het |
Sorcs1 |
T |
C |
19: 50,132,598 (GRCm39) |
|
probably benign |
Het |
Thsd7b |
A |
C |
1: 130,117,672 (GRCm39) |
|
probably null |
Het |
Tnfrsf18 |
A |
C |
4: 156,112,739 (GRCm39) |
I142L |
probably benign |
Het |
Ttn |
A |
G |
2: 76,632,855 (GRCm39) |
|
probably benign |
Het |
Tufm |
T |
A |
7: 126,088,614 (GRCm39) |
|
probably null |
Het |
Vmn2r69 |
A |
T |
7: 85,059,058 (GRCm39) |
|
probably benign |
Het |
Zfp385c |
T |
C |
11: 100,520,709 (GRCm39) |
|
probably benign |
Het |
Zfp964 |
T |
A |
8: 70,116,503 (GRCm39) |
C368S |
unknown |
Het |
Zswim8 |
G |
A |
14: 20,771,736 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Bpifb9a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00833:Bpifb9a
|
APN |
2 |
154,106,195 (GRCm39) |
nonsense |
probably null |
|
IGL00899:Bpifb9a
|
APN |
2 |
154,106,647 (GRCm39) |
splice site |
probably null |
|
IGL01998:Bpifb9a
|
APN |
2 |
154,110,120 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02158:Bpifb9a
|
APN |
2 |
154,108,733 (GRCm39) |
splice site |
probably benign |
|
IGL02331:Bpifb9a
|
APN |
2 |
154,104,307 (GRCm39) |
missense |
possibly damaging |
0.45 |
R0066:Bpifb9a
|
UTSW |
2 |
154,108,761 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0480:Bpifb9a
|
UTSW |
2 |
154,106,608 (GRCm39) |
missense |
probably benign |
0.33 |
R0545:Bpifb9a
|
UTSW |
2 |
154,103,870 (GRCm39) |
nonsense |
probably null |
|
R0904:Bpifb9a
|
UTSW |
2 |
154,106,145 (GRCm39) |
splice site |
probably benign |
|
R1028:Bpifb9a
|
UTSW |
2 |
154,104,327 (GRCm39) |
missense |
possibly damaging |
0.45 |
R1465:Bpifb9a
|
UTSW |
2 |
154,112,941 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1465:Bpifb9a
|
UTSW |
2 |
154,112,941 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1902:Bpifb9a
|
UTSW |
2 |
154,103,911 (GRCm39) |
missense |
probably benign |
0.00 |
R2015:Bpifb9a
|
UTSW |
2 |
154,110,120 (GRCm39) |
critical splice donor site |
probably null |
|
R2152:Bpifb9a
|
UTSW |
2 |
154,102,055 (GRCm39) |
missense |
probably benign |
0.28 |
R2206:Bpifb9a
|
UTSW |
2 |
154,106,161 (GRCm39) |
splice site |
probably null |
|
R5410:Bpifb9a
|
UTSW |
2 |
154,112,155 (GRCm39) |
missense |
probably benign |
0.05 |
R5731:Bpifb9a
|
UTSW |
2 |
154,104,163 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5818:Bpifb9a
|
UTSW |
2 |
154,104,215 (GRCm39) |
missense |
probably damaging |
0.98 |
R5865:Bpifb9a
|
UTSW |
2 |
154,108,756 (GRCm39) |
missense |
probably benign |
0.26 |
R6564:Bpifb9a
|
UTSW |
2 |
154,102,098 (GRCm39) |
missense |
probably benign |
0.00 |
R7291:Bpifb9a
|
UTSW |
2 |
154,109,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7294:Bpifb9a
|
UTSW |
2 |
154,109,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7295:Bpifb9a
|
UTSW |
2 |
154,109,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R7453:Bpifb9a
|
UTSW |
2 |
154,106,615 (GRCm39) |
missense |
probably damaging |
0.99 |
R7570:Bpifb9a
|
UTSW |
2 |
154,104,183 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8187:Bpifb9a
|
UTSW |
2 |
154,111,377 (GRCm39) |
missense |
probably benign |
0.00 |
R8245:Bpifb9a
|
UTSW |
2 |
154,104,646 (GRCm39) |
missense |
probably benign |
0.00 |
R8459:Bpifb9a
|
UTSW |
2 |
154,102,153 (GRCm39) |
missense |
probably damaging |
0.98 |
R8481:Bpifb9a
|
UTSW |
2 |
154,111,399 (GRCm39) |
missense |
probably benign |
|
|