Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
T |
A |
1: 71,286,332 (GRCm39) |
T2501S |
probably damaging |
Het |
Abcg3 |
A |
G |
5: 105,125,507 (GRCm39) |
Y59H |
probably benign |
Het |
Acsf2 |
G |
T |
11: 94,464,057 (GRCm39) |
|
probably null |
Het |
Adam25 |
T |
A |
8: 41,206,914 (GRCm39) |
I60K |
probably damaging |
Het |
Agrn |
A |
T |
4: 156,254,261 (GRCm39) |
V1729E |
probably damaging |
Het |
Aldh9a1 |
G |
A |
1: 167,177,895 (GRCm39) |
V31I |
probably benign |
Het |
Aqp5 |
T |
C |
15: 99,489,180 (GRCm39) |
F10L |
possibly damaging |
Het |
Arfgap2 |
T |
A |
2: 91,104,089 (GRCm39) |
|
probably null |
Het |
Asb7 |
T |
C |
7: 66,328,884 (GRCm39) |
H52R |
probably damaging |
Het |
Aspa |
G |
A |
11: 73,204,351 (GRCm39) |
Q206* |
probably null |
Het |
Bpgm |
A |
G |
6: 34,481,223 (GRCm39) |
I207V |
possibly damaging |
Het |
Clec4e |
A |
G |
6: 123,262,533 (GRCm39) |
F128S |
probably benign |
Het |
Crisp3 |
A |
G |
17: 40,545,629 (GRCm39) |
F82L |
probably benign |
Het |
Cry2 |
A |
G |
2: 92,243,350 (GRCm39) |
L497P |
probably damaging |
Het |
Dcxr |
A |
G |
11: 120,617,832 (GRCm39) |
V48A |
probably benign |
Het |
Ddx11 |
A |
T |
17: 66,445,214 (GRCm39) |
T379S |
probably benign |
Het |
Depdc1a |
A |
C |
3: 159,228,276 (GRCm39) |
T343P |
probably damaging |
Het |
Dhx36 |
T |
C |
3: 62,392,389 (GRCm39) |
I546V |
probably damaging |
Het |
Fam114a2 |
A |
G |
11: 57,404,542 (GRCm39) |
V74A |
probably benign |
Het |
Fcgbpl1 |
T |
C |
7: 27,839,656 (GRCm39) |
F490L |
probably benign |
Het |
Flg2 |
A |
T |
3: 93,108,177 (GRCm39) |
R68S |
probably damaging |
Het |
Glb1l3 |
T |
C |
9: 26,764,950 (GRCm39) |
I154V |
possibly damaging |
Het |
Gm45844 |
T |
C |
7: 7,243,185 (GRCm39) |
T22A |
probably benign |
Het |
Gramd2a |
A |
T |
9: 59,617,193 (GRCm39) |
I83F |
probably damaging |
Het |
Hcn4 |
A |
G |
9: 58,767,420 (GRCm39) |
T994A |
unknown |
Het |
Hectd1 |
C |
T |
12: 51,853,150 (GRCm39) |
V124I |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,562,531 (GRCm39) |
D2342E |
probably benign |
Het |
Hyal6 |
A |
T |
6: 24,740,786 (GRCm39) |
H313L |
possibly damaging |
Het |
Ifnab |
T |
A |
4: 88,609,523 (GRCm39) |
|
probably benign |
Het |
Keap1 |
A |
G |
9: 21,148,623 (GRCm39) |
I128T |
probably benign |
Het |
Kit |
T |
C |
5: 75,767,700 (GRCm39) |
S28P |
probably damaging |
Het |
Krtap5-3 |
T |
A |
7: 141,755,942 (GRCm39) |
C260S |
unknown |
Het |
Lepr |
T |
A |
4: 101,609,372 (GRCm39) |
W320R |
probably damaging |
Het |
Lmod3 |
A |
T |
6: 97,225,403 (GRCm39) |
N139K |
probably benign |
Het |
Marchf1 |
C |
G |
8: 66,838,989 (GRCm39) |
S10R |
probably benign |
Het |
Naa35 |
A |
T |
13: 59,765,755 (GRCm39) |
K380* |
probably null |
Het |
Npy1r |
C |
A |
8: 67,157,546 (GRCm39) |
F285L |
probably damaging |
Het |
Nr1h3 |
C |
T |
2: 91,014,739 (GRCm39) |
R427H |
probably damaging |
Het |
Or5p79 |
T |
A |
7: 108,221,269 (GRCm39) |
N83K |
probably benign |
Het |
Pate2 |
A |
G |
9: 35,582,008 (GRCm39) |
|
probably null |
Het |
Pcmt1 |
A |
G |
10: 7,556,369 (GRCm39) |
|
probably null |
Het |
Prg4 |
T |
G |
1: 150,330,786 (GRCm39) |
E629A |
unknown |
Het |
Rin2 |
T |
G |
2: 145,700,419 (GRCm39) |
S199A |
probably benign |
Het |
Ror1 |
T |
A |
4: 100,298,388 (GRCm39) |
L587Q |
probably damaging |
Het |
Rsl1 |
T |
A |
13: 67,324,566 (GRCm39) |
C31S |
possibly damaging |
Het |
Scn4a |
A |
G |
11: 106,239,523 (GRCm39) |
|
probably null |
Het |
Sema3a |
T |
C |
5: 13,615,805 (GRCm39) |
Y410H |
probably damaging |
Het |
Smpd5 |
T |
C |
15: 76,180,539 (GRCm39) |
V447A |
probably benign |
Het |
Tax1bp1 |
A |
T |
6: 52,723,682 (GRCm39) |
D524V |
probably benign |
Het |
Tesc |
A |
T |
5: 118,197,523 (GRCm39) |
Y179F |
probably damaging |
Het |
Tm9sf2 |
T |
C |
14: 122,379,824 (GRCm39) |
S292P |
possibly damaging |
Het |
Unc45b |
A |
G |
11: 82,819,838 (GRCm39) |
D543G |
probably damaging |
Het |
Usp4 |
T |
A |
9: 108,249,879 (GRCm39) |
V469E |
probably damaging |
Het |
Vmn1r10 |
T |
A |
6: 57,090,924 (GRCm39) |
I172N |
possibly damaging |
Het |
Zfyve16 |
A |
G |
13: 92,659,473 (GRCm39) |
L146S |
probably damaging |
Het |
|
Other mutations in Brinp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00327:Brinp2
|
APN |
1 |
158,074,670 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01537:Brinp2
|
APN |
1 |
158,074,379 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02354:Brinp2
|
APN |
1 |
158,074,748 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02361:Brinp2
|
APN |
1 |
158,074,748 (GRCm39) |
missense |
probably damaging |
1.00 |
slowdancing
|
UTSW |
1 |
158,094,030 (GRCm39) |
critical splice donor site |
probably null |
|
R0334:Brinp2
|
UTSW |
1 |
158,123,155 (GRCm39) |
missense |
probably benign |
0.06 |
R0652:Brinp2
|
UTSW |
1 |
158,074,191 (GRCm39) |
missense |
probably damaging |
1.00 |
R1017:Brinp2
|
UTSW |
1 |
158,077,021 (GRCm39) |
missense |
probably damaging |
0.99 |
R1141:Brinp2
|
UTSW |
1 |
158,074,840 (GRCm39) |
missense |
probably damaging |
0.99 |
R1378:Brinp2
|
UTSW |
1 |
158,074,624 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1666:Brinp2
|
UTSW |
1 |
158,074,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R1892:Brinp2
|
UTSW |
1 |
158,082,542 (GRCm39) |
critical splice donor site |
probably null |
|
R1986:Brinp2
|
UTSW |
1 |
158,074,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R3876:Brinp2
|
UTSW |
1 |
158,074,416 (GRCm39) |
missense |
probably damaging |
0.99 |
R3924:Brinp2
|
UTSW |
1 |
158,073,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R4582:Brinp2
|
UTSW |
1 |
158,095,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R5239:Brinp2
|
UTSW |
1 |
158,078,908 (GRCm39) |
missense |
probably benign |
0.00 |
R5537:Brinp2
|
UTSW |
1 |
158,082,583 (GRCm39) |
missense |
probably damaging |
0.97 |
R5582:Brinp2
|
UTSW |
1 |
158,076,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R5762:Brinp2
|
UTSW |
1 |
158,074,156 (GRCm39) |
missense |
probably benign |
|
R5922:Brinp2
|
UTSW |
1 |
158,076,925 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6746:Brinp2
|
UTSW |
1 |
158,094,160 (GRCm39) |
missense |
probably benign |
|
R6999:Brinp2
|
UTSW |
1 |
158,078,875 (GRCm39) |
missense |
probably benign |
0.20 |
R7144:Brinp2
|
UTSW |
1 |
158,122,994 (GRCm39) |
critical splice donor site |
probably null |
|
R7221:Brinp2
|
UTSW |
1 |
158,094,117 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7376:Brinp2
|
UTSW |
1 |
158,078,938 (GRCm39) |
missense |
probably damaging |
0.98 |
R7381:Brinp2
|
UTSW |
1 |
158,073,913 (GRCm39) |
missense |
probably benign |
0.11 |
R7388:Brinp2
|
UTSW |
1 |
158,082,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R7697:Brinp2
|
UTSW |
1 |
158,095,496 (GRCm39) |
missense |
probably benign |
|
R7701:Brinp2
|
UTSW |
1 |
158,094,030 (GRCm39) |
critical splice donor site |
probably null |
|
R7910:Brinp2
|
UTSW |
1 |
158,074,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R7973:Brinp2
|
UTSW |
1 |
158,074,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R7976:Brinp2
|
UTSW |
1 |
158,073,913 (GRCm39) |
missense |
probably benign |
0.03 |
R9343:Brinp2
|
UTSW |
1 |
158,077,090 (GRCm39) |
splice site |
probably benign |
|
R9513:Brinp2
|
UTSW |
1 |
158,074,273 (GRCm39) |
missense |
probably damaging |
1.00 |
X0024:Brinp2
|
UTSW |
1 |
158,095,553 (GRCm39) |
nonsense |
probably null |
|
Z1088:Brinp2
|
UTSW |
1 |
158,074,559 (GRCm39) |
nonsense |
probably null |
|
Z1176:Brinp2
|
UTSW |
1 |
158,074,741 (GRCm39) |
nonsense |
probably null |
|
Z1176:Brinp2
|
UTSW |
1 |
158,074,609 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Brinp2
|
UTSW |
1 |
158,074,352 (GRCm39) |
missense |
possibly damaging |
0.62 |
|