Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900092C05Rik |
T |
G |
7: 12,246,507 (GRCm39) |
M1R |
probably null |
Het |
4933440N22Rik |
C |
A |
6: 117,884,540 (GRCm39) |
|
probably benign |
Het |
5031439G07Rik |
G |
T |
15: 84,837,345 (GRCm39) |
P280T |
probably damaging |
Het |
Abca2 |
C |
T |
2: 25,331,308 (GRCm39) |
S1267L |
probably damaging |
Het |
Acsl3 |
A |
T |
1: 78,684,126 (GRCm39) |
R719S |
probably benign |
Het |
Adam1a |
A |
T |
5: 121,657,839 (GRCm39) |
|
probably null |
Het |
Adamts7 |
T |
C |
9: 90,070,851 (GRCm39) |
|
probably benign |
Het |
Adgrf3 |
G |
A |
5: 30,407,227 (GRCm39) |
|
probably benign |
Het |
Aldh6a1 |
T |
C |
12: 84,488,544 (GRCm39) |
E89G |
possibly damaging |
Het |
Ankrd36 |
A |
G |
11: 5,525,752 (GRCm39) |
Y238C |
probably damaging |
Het |
Ankrd65 |
G |
A |
4: 155,877,362 (GRCm39) |
R291Q |
probably benign |
Het |
Ano2 |
C |
T |
6: 125,773,227 (GRCm39) |
R287W |
probably damaging |
Het |
Ap1ar |
A |
G |
3: 127,606,215 (GRCm39) |
I125T |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,293,197 (GRCm39) |
D705G |
probably damaging |
Het |
Asb18 |
T |
A |
1: 89,924,005 (GRCm39) |
N86I |
probably damaging |
Het |
Bicral |
A |
T |
17: 47,135,519 (GRCm39) |
S564T |
probably benign |
Het |
Bpifa6 |
A |
G |
2: 153,831,192 (GRCm39) |
M253V |
probably benign |
Het |
Braf |
T |
C |
6: 39,642,017 (GRCm39) |
D194G |
probably damaging |
Het |
C7 |
T |
A |
15: 5,041,631 (GRCm39) |
Y425F |
probably damaging |
Het |
Ccdc102a |
T |
C |
8: 95,632,714 (GRCm39) |
K421R |
probably benign |
Het |
Cep89 |
G |
A |
7: 35,120,388 (GRCm39) |
|
probably null |
Het |
Chgb |
A |
T |
2: 132,634,720 (GRCm39) |
M221L |
probably benign |
Het |
Chst14 |
A |
G |
2: 118,758,145 (GRCm39) |
Y313C |
probably damaging |
Het |
Ciita |
G |
A |
16: 10,331,152 (GRCm39) |
|
probably null |
Het |
Clec12b |
A |
T |
6: 129,357,603 (GRCm39) |
I85N |
probably damaging |
Het |
Clec2e |
G |
T |
6: 129,070,459 (GRCm39) |
Y187* |
probably null |
Het |
Crbn |
T |
C |
6: 106,767,804 (GRCm39) |
K229E |
probably benign |
Het |
Ctdspl2 |
A |
T |
2: 121,811,762 (GRCm39) |
Q201L |
probably benign |
Het |
Ctrb1 |
G |
T |
8: 112,416,041 (GRCm39) |
|
probably benign |
Het |
Cyp2c55 |
T |
A |
19: 38,999,525 (GRCm39) |
V77E |
probably damaging |
Het |
Cyp2c69 |
A |
C |
19: 39,837,839 (GRCm39) |
D414E |
probably damaging |
Het |
Ddx47 |
T |
C |
6: 134,988,703 (GRCm39) |
|
probably benign |
Het |
Dlg1 |
A |
G |
16: 31,661,640 (GRCm39) |
|
probably null |
Het |
Dnah5 |
C |
A |
15: 28,230,609 (GRCm39) |
S169* |
probably null |
Het |
Dock4 |
C |
A |
12: 40,805,809 (GRCm39) |
T927K |
probably benign |
Het |
Esrp2 |
T |
G |
8: 106,860,453 (GRCm39) |
D259A |
probably damaging |
Het |
Fam169a |
A |
G |
13: 97,255,038 (GRCm39) |
K418R |
probably benign |
Het |
Fancm |
A |
T |
12: 65,146,067 (GRCm39) |
I597F |
probably damaging |
Het |
Fastkd2 |
G |
T |
1: 63,771,385 (GRCm39) |
|
probably benign |
Het |
Fat1 |
G |
A |
8: 45,463,582 (GRCm39) |
V1375M |
probably damaging |
Het |
Fbxw10 |
A |
T |
11: 62,753,464 (GRCm39) |
D486V |
probably damaging |
Het |
Fech |
C |
T |
18: 64,603,744 (GRCm39) |
|
probably benign |
Het |
Fermt1 |
C |
T |
2: 132,766,942 (GRCm39) |
E342K |
probably benign |
Het |
Foxp1 |
T |
A |
6: 98,955,181 (GRCm39) |
H195L |
possibly damaging |
Het |
Gfra1 |
T |
A |
19: 58,440,407 (GRCm39) |
I138L |
probably benign |
Het |
Gm12185 |
T |
C |
11: 48,806,501 (GRCm39) |
D230G |
possibly damaging |
Het |
Gm14403 |
T |
A |
2: 177,199,024 (GRCm39) |
|
probably benign |
Het |
Gpd2 |
A |
C |
2: 57,245,786 (GRCm39) |
T439P |
probably damaging |
Het |
Gpm6a |
A |
T |
8: 55,490,385 (GRCm39) |
K20N |
probably damaging |
Het |
Hc |
A |
T |
2: 34,873,819 (GRCm39) |
Y158* |
probably null |
Het |
Hectd4 |
A |
T |
5: 121,487,235 (GRCm39) |
D3410V |
possibly damaging |
Het |
Il17b |
G |
A |
18: 61,823,483 (GRCm39) |
|
probably null |
Het |
Irx4 |
G |
T |
13: 73,413,695 (GRCm39) |
R55L |
possibly damaging |
Het |
Itgav |
A |
T |
2: 83,596,245 (GRCm39) |
|
probably benign |
Het |
Lama3 |
T |
C |
18: 12,574,164 (GRCm39) |
V582A |
probably benign |
Het |
Ldhd |
G |
T |
8: 112,353,925 (GRCm39) |
A425E |
possibly damaging |
Het |
Lrp1b |
C |
T |
2: 40,817,841 (GRCm39) |
|
probably null |
Het |
Lrp5 |
T |
C |
19: 3,670,191 (GRCm39) |
T638A |
possibly damaging |
Het |
Lrrk1 |
A |
C |
7: 65,909,722 (GRCm39) |
F1996C |
probably damaging |
Het |
Ly6h |
G |
A |
15: 75,437,986 (GRCm39) |
S21L |
probably benign |
Het |
Mctp1 |
T |
C |
13: 76,973,392 (GRCm39) |
V431A |
probably benign |
Het |
Metap2 |
C |
T |
10: 93,707,345 (GRCm39) |
|
probably null |
Het |
Mfsd2b |
T |
A |
12: 4,920,536 (GRCm39) |
K94* |
probably null |
Het |
Micall2 |
A |
G |
5: 139,705,097 (GRCm39) |
L79P |
probably damaging |
Het |
Mucl2 |
T |
C |
15: 103,927,673 (GRCm39) |
T95A |
possibly damaging |
Het |
Myo15a |
A |
T |
11: 60,396,832 (GRCm39) |
T2634S |
probably damaging |
Het |
Myo5b |
G |
T |
18: 74,873,574 (GRCm39) |
V1467L |
probably damaging |
Het |
Nfic |
G |
T |
10: 81,256,414 (GRCm39) |
D105E |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,873,865 (GRCm39) |
F227Y |
probably benign |
Het |
Nrp2 |
A |
T |
1: 62,777,458 (GRCm39) |
I88F |
probably damaging |
Het |
Nup160 |
A |
T |
2: 90,530,887 (GRCm39) |
H515L |
probably benign |
Het |
Nup205 |
G |
A |
6: 35,202,917 (GRCm39) |
|
probably null |
Het |
Oas1g |
G |
A |
5: 121,020,069 (GRCm39) |
T179I |
probably benign |
Het |
Ogfr |
A |
T |
2: 180,236,543 (GRCm39) |
E376V |
probably damaging |
Het |
Or2l13 |
T |
G |
16: 19,306,378 (GRCm39) |
S263R |
probably benign |
Het |
Or4a69 |
A |
T |
2: 89,312,855 (GRCm39) |
V208D |
possibly damaging |
Het |
Or4c107 |
T |
G |
2: 88,789,387 (GRCm39) |
Y192* |
probably null |
Het |
Or52d1 |
G |
T |
7: 103,755,896 (GRCm39) |
V137F |
possibly damaging |
Het |
Or5p6 |
C |
T |
7: 107,631,595 (GRCm39) |
|
probably null |
Het |
Pard3b |
T |
C |
1: 62,384,188 (GRCm39) |
V851A |
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,611,142 (GRCm39) |
Y34F |
probably damaging |
Het |
Pikfyve |
T |
C |
1: 65,290,825 (GRCm39) |
Y1215H |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,593,565 (GRCm39) |
V1516E |
probably damaging |
Het |
Pla2g4a |
A |
T |
1: 149,763,344 (GRCm39) |
|
probably benign |
Het |
Ptprg |
A |
T |
14: 12,190,767 (GRCm38) |
I818F |
probably benign |
Het |
Ralgapb |
A |
G |
2: 158,304,173 (GRCm39) |
E644G |
possibly damaging |
Het |
Rbm45 |
A |
G |
2: 76,202,459 (GRCm39) |
I127M |
probably damaging |
Het |
Rtp2 |
T |
C |
16: 23,746,220 (GRCm39) |
Y157C |
probably damaging |
Het |
Sema3f |
A |
T |
9: 107,564,771 (GRCm39) |
|
probably benign |
Het |
Sf3b3 |
A |
T |
8: 111,564,006 (GRCm39) |
Y329N |
probably damaging |
Het |
Sfxn1 |
A |
G |
13: 54,239,646 (GRCm39) |
|
probably null |
Het |
Shkbp1 |
A |
T |
7: 27,044,751 (GRCm39) |
C447S |
probably damaging |
Het |
Sipa1l3 |
A |
G |
7: 29,021,685 (GRCm39) |
S689P |
possibly damaging |
Het |
Slc7a8 |
A |
G |
14: 54,970,656 (GRCm39) |
S332P |
probably damaging |
Het |
Slit1 |
C |
A |
19: 41,596,823 (GRCm39) |
C1092F |
probably damaging |
Het |
Slx9 |
A |
G |
10: 77,333,360 (GRCm39) |
|
probably benign |
Het |
Stard9 |
A |
G |
2: 120,533,678 (GRCm39) |
I619V |
possibly damaging |
Het |
Sycp3 |
T |
C |
10: 88,305,454 (GRCm39) |
V185A |
possibly damaging |
Het |
Taar9 |
A |
T |
10: 23,985,382 (GRCm39) |
N17K |
possibly damaging |
Het |
Tbkbp1 |
T |
C |
11: 97,039,814 (GRCm39) |
E102G |
probably damaging |
Het |
Tex44 |
A |
G |
1: 86,354,834 (GRCm39) |
N248D |
probably benign |
Het |
Tmem63b |
C |
G |
17: 45,989,904 (GRCm39) |
R88P |
possibly damaging |
Het |
Tnpo1 |
C |
T |
13: 98,986,665 (GRCm39) |
V781I |
probably benign |
Het |
Tonsl |
C |
T |
15: 76,520,761 (GRCm39) |
|
probably null |
Het |
Ttc6 |
A |
G |
12: 57,721,463 (GRCm39) |
K984R |
possibly damaging |
Het |
Usp34 |
A |
G |
11: 23,391,171 (GRCm39) |
E2263G |
probably damaging |
Het |
Usp8 |
A |
G |
2: 126,596,847 (GRCm39) |
K875E |
probably damaging |
Het |
Vapb |
C |
T |
2: 173,603,905 (GRCm39) |
|
probably benign |
Het |
Vmn1r223 |
A |
G |
13: 23,434,038 (GRCm39) |
I211V |
possibly damaging |
Het |
Vmn2r81 |
G |
A |
10: 79,129,496 (GRCm39) |
V796I |
probably damaging |
Het |
Wdr90 |
A |
T |
17: 26,073,027 (GRCm39) |
V856D |
probably damaging |
Het |
Wnk2 |
T |
A |
13: 49,235,571 (GRCm39) |
T615S |
probably damaging |
Het |
|
Other mutations in Brinp3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00467:Brinp3
|
APN |
1 |
146,777,512 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00503:Brinp3
|
APN |
1 |
146,776,905 (GRCm39) |
missense |
probably benign |
|
IGL01702:Brinp3
|
APN |
1 |
146,627,735 (GRCm39) |
splice site |
probably benign |
|
IGL01728:Brinp3
|
APN |
1 |
146,707,289 (GRCm39) |
splice site |
probably null |
|
IGL01733:Brinp3
|
APN |
1 |
146,390,541 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01937:Brinp3
|
APN |
1 |
146,776,878 (GRCm39) |
missense |
probably benign |
|
IGL02020:Brinp3
|
APN |
1 |
146,777,865 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02082:Brinp3
|
APN |
1 |
146,627,600 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02365:Brinp3
|
APN |
1 |
146,776,860 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02366:Brinp3
|
APN |
1 |
146,577,481 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL02565:Brinp3
|
APN |
1 |
146,777,770 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02999:Brinp3
|
APN |
1 |
146,577,587 (GRCm39) |
splice site |
probably null |
|
IGL03099:Brinp3
|
APN |
1 |
146,777,835 (GRCm39) |
missense |
possibly damaging |
0.91 |
PIT4283001:Brinp3
|
UTSW |
1 |
146,777,161 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4418001:Brinp3
|
UTSW |
1 |
146,777,161 (GRCm39) |
missense |
probably damaging |
0.99 |
R0021:Brinp3
|
UTSW |
1 |
146,777,189 (GRCm39) |
missense |
probably benign |
0.04 |
R0021:Brinp3
|
UTSW |
1 |
146,777,189 (GRCm39) |
missense |
probably benign |
0.04 |
R0266:Brinp3
|
UTSW |
1 |
146,558,418 (GRCm39) |
nonsense |
probably null |
|
R1468:Brinp3
|
UTSW |
1 |
146,777,700 (GRCm39) |
missense |
probably benign |
0.01 |
R1522:Brinp3
|
UTSW |
1 |
146,777,628 (GRCm39) |
missense |
probably damaging |
0.99 |
R1596:Brinp3
|
UTSW |
1 |
146,390,520 (GRCm39) |
missense |
probably benign |
|
R1898:Brinp3
|
UTSW |
1 |
146,776,987 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2036:Brinp3
|
UTSW |
1 |
146,577,579 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2224:Brinp3
|
UTSW |
1 |
146,777,658 (GRCm39) |
nonsense |
probably null |
|
R2272:Brinp3
|
UTSW |
1 |
146,777,142 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2291:Brinp3
|
UTSW |
1 |
146,776,812 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2322:Brinp3
|
UTSW |
1 |
146,577,492 (GRCm39) |
missense |
probably benign |
|
R2880:Brinp3
|
UTSW |
1 |
146,777,740 (GRCm39) |
missense |
probably damaging |
0.98 |
R3918:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3939:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3940:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3941:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R3942:Brinp3
|
UTSW |
1 |
146,627,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R4095:Brinp3
|
UTSW |
1 |
146,777,430 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4783:Brinp3
|
UTSW |
1 |
146,603,378 (GRCm39) |
intron |
probably benign |
|
R5009:Brinp3
|
UTSW |
1 |
146,776,787 (GRCm39) |
missense |
probably benign |
0.25 |
R5034:Brinp3
|
UTSW |
1 |
146,603,458 (GRCm39) |
intron |
probably benign |
|
R5166:Brinp3
|
UTSW |
1 |
146,777,105 (GRCm39) |
missense |
probably damaging |
0.96 |
R5372:Brinp3
|
UTSW |
1 |
146,707,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R5472:Brinp3
|
UTSW |
1 |
146,777,197 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5651:Brinp3
|
UTSW |
1 |
146,577,537 (GRCm39) |
missense |
probably benign |
0.01 |
R5681:Brinp3
|
UTSW |
1 |
146,777,484 (GRCm39) |
missense |
probably benign |
0.12 |
R6351:Brinp3
|
UTSW |
1 |
146,777,323 (GRCm39) |
missense |
probably damaging |
0.96 |
R6470:Brinp3
|
UTSW |
1 |
146,777,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R6499:Brinp3
|
UTSW |
1 |
146,777,431 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7078:Brinp3
|
UTSW |
1 |
146,390,627 (GRCm39) |
nonsense |
probably null |
|
R7223:Brinp3
|
UTSW |
1 |
146,776,812 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7322:Brinp3
|
UTSW |
1 |
146,558,426 (GRCm39) |
nonsense |
probably null |
|
R7347:Brinp3
|
UTSW |
1 |
146,777,824 (GRCm39) |
missense |
probably benign |
0.22 |
R7375:Brinp3
|
UTSW |
1 |
146,777,748 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7412:Brinp3
|
UTSW |
1 |
146,777,748 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7532:Brinp3
|
UTSW |
1 |
146,777,139 (GRCm39) |
missense |
probably damaging |
0.98 |
R7562:Brinp3
|
UTSW |
1 |
146,777,748 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7576:Brinp3
|
UTSW |
1 |
146,777,301 (GRCm39) |
missense |
probably damaging |
0.99 |
R7723:Brinp3
|
UTSW |
1 |
146,577,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R7737:Brinp3
|
UTSW |
1 |
146,558,332 (GRCm39) |
missense |
probably damaging |
0.98 |
R7793:Brinp3
|
UTSW |
1 |
146,622,306 (GRCm39) |
missense |
probably benign |
0.20 |
R8334:Brinp3
|
UTSW |
1 |
146,777,791 (GRCm39) |
missense |
probably damaging |
0.99 |
R8401:Brinp3
|
UTSW |
1 |
146,777,184 (GRCm39) |
missense |
probably benign |
0.17 |
R9205:Brinp3
|
UTSW |
1 |
146,777,827 (GRCm39) |
missense |
possibly damaging |
0.57 |
R9328:Brinp3
|
UTSW |
1 |
146,707,455 (GRCm39) |
missense |
probably damaging |
0.98 |
R9602:Brinp3
|
UTSW |
1 |
146,622,234 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Brinp3
|
UTSW |
1 |
146,777,524 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Brinp3
|
UTSW |
1 |
146,777,814 (GRCm39) |
missense |
probably damaging |
0.99 |
|