Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adh1 |
T |
G |
3: 137,995,596 (GRCm39) |
V333G |
probably damaging |
Het |
Aggf1 |
A |
G |
13: 95,501,383 (GRCm39) |
L333P |
probably damaging |
Het |
Ankmy1 |
A |
G |
1: 92,812,803 (GRCm39) |
V502A |
probably benign |
Het |
Atm |
A |
G |
9: 53,398,112 (GRCm39) |
|
probably null |
Het |
Ccdc180 |
A |
G |
4: 45,949,526 (GRCm39) |
T1594A |
probably damaging |
Het |
Cep290 |
T |
A |
10: 100,373,453 (GRCm39) |
D1244E |
probably benign |
Het |
Ctnna3 |
A |
G |
10: 64,670,385 (GRCm39) |
D638G |
probably damaging |
Het |
Ctsr |
T |
C |
13: 61,308,346 (GRCm39) |
H266R |
possibly damaging |
Het |
D630045J12Rik |
C |
T |
6: 38,172,036 (GRCm39) |
E711K |
probably benign |
Het |
Dnah5 |
T |
C |
15: 28,383,723 (GRCm39) |
S2982P |
probably damaging |
Het |
Dsg1a |
G |
T |
18: 20,464,755 (GRCm39) |
A417S |
probably benign |
Het |
Gdpd1 |
T |
C |
11: 86,950,366 (GRCm39) |
D69G |
probably damaging |
Het |
Gp2 |
C |
T |
7: 119,050,801 (GRCm39) |
R310H |
possibly damaging |
Het |
Ifna2 |
G |
A |
4: 88,601,542 (GRCm39) |
H159Y |
possibly damaging |
Het |
Kptn |
T |
C |
7: 15,859,751 (GRCm39) |
V325A |
probably damaging |
Het |
Marchf7 |
A |
G |
2: 60,062,622 (GRCm39) |
E143G |
probably damaging |
Het |
Mcm4 |
A |
G |
16: 15,454,577 (GRCm39) |
L47P |
probably benign |
Het |
Mcm8 |
T |
C |
2: 132,659,097 (GRCm39) |
F27S |
possibly damaging |
Het |
Nod2 |
T |
A |
8: 89,408,274 (GRCm39) |
V967E |
probably damaging |
Het |
Or10al4 |
T |
G |
17: 38,037,082 (GRCm39) |
C56G |
probably benign |
Het |
Or4x12-ps1 |
A |
G |
2: 89,916,733 (GRCm39) |
V24A |
probably benign |
Het |
Parp10 |
C |
T |
15: 76,125,122 (GRCm39) |
R545Q |
probably benign |
Het |
Ppp2r3d |
T |
C |
9: 101,021,579 (GRCm39) |
E332G |
probably benign |
Het |
Pramel27 |
C |
T |
4: 143,573,103 (GRCm39) |
|
probably benign |
Het |
Ptpdc1 |
A |
G |
13: 48,739,766 (GRCm39) |
V555A |
probably benign |
Het |
Qsox2 |
G |
A |
2: 26,112,300 (GRCm39) |
L81F |
possibly damaging |
Het |
Sbsn |
GAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCA |
GAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCATGGGGTACAGAATGGAGTCAACCAGGCTCAAAAGGAAGCAGAAAAAGTGGCCCA |
7: 30,452,391 (GRCm39) |
|
probably benign |
Het |
Spata31 |
A |
G |
13: 65,069,151 (GRCm39) |
D433G |
probably benign |
Het |
Stpg2 |
T |
C |
3: 138,921,026 (GRCm39) |
I77T |
possibly damaging |
Het |
Sugp2 |
T |
C |
8: 70,710,162 (GRCm39) |
S928P |
probably damaging |
Het |
Syne1 |
A |
G |
10: 5,308,390 (GRCm39) |
S722P |
possibly damaging |
Het |
Szt2 |
A |
T |
4: 118,255,398 (GRCm39) |
S229T |
possibly damaging |
Het |
Tm9sf3 |
A |
G |
19: 41,206,630 (GRCm39) |
L505P |
probably damaging |
Het |
Ttc39d |
G |
A |
17: 80,524,354 (GRCm39) |
A338T |
probably damaging |
Het |
Ubash3b |
A |
G |
9: 40,934,814 (GRCm39) |
F489L |
probably damaging |
Het |
Xpo7 |
A |
T |
14: 70,904,589 (GRCm39) |
Y1015N |
probably benign |
Het |
Zbtb14 |
C |
A |
17: 69,695,302 (GRCm39) |
Y333* |
probably null |
Het |
Zp2 |
T |
C |
7: 119,741,102 (GRCm39) |
T141A |
probably benign |
Het |
|
Other mutations in Nrxn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00490:Nrxn2
|
APN |
19 |
6,523,623 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL01020:Nrxn2
|
APN |
19 |
6,543,473 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01064:Nrxn2
|
APN |
19 |
6,567,083 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01561:Nrxn2
|
APN |
19 |
6,540,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01759:Nrxn2
|
APN |
19 |
6,559,959 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02071:Nrxn2
|
APN |
19 |
6,531,783 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02085:Nrxn2
|
APN |
19 |
6,542,898 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02132:Nrxn2
|
APN |
19 |
6,522,306 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02476:Nrxn2
|
APN |
19 |
6,505,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02605:Nrxn2
|
APN |
19 |
6,500,610 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03123:Nrxn2
|
APN |
19 |
6,531,767 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03288:Nrxn2
|
APN |
19 |
6,540,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R0019:Nrxn2
|
UTSW |
19 |
6,559,987 (GRCm39) |
splice site |
probably benign |
|
R0257:Nrxn2
|
UTSW |
19 |
6,540,728 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0305:Nrxn2
|
UTSW |
19 |
6,569,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R0453:Nrxn2
|
UTSW |
19 |
6,541,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R0512:Nrxn2
|
UTSW |
19 |
6,567,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Nrxn2
|
UTSW |
19 |
6,543,434 (GRCm39) |
missense |
probably damaging |
0.99 |
R0571:Nrxn2
|
UTSW |
19 |
6,523,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R1373:Nrxn2
|
UTSW |
19 |
6,522,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R1434:Nrxn2
|
UTSW |
19 |
6,493,642 (GRCm39) |
splice site |
probably null |
|
R1454:Nrxn2
|
UTSW |
19 |
6,531,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R1671:Nrxn2
|
UTSW |
19 |
6,523,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1692:Nrxn2
|
UTSW |
19 |
6,569,298 (GRCm39) |
missense |
probably damaging |
1.00 |
R1858:Nrxn2
|
UTSW |
19 |
6,538,825 (GRCm39) |
missense |
probably benign |
0.01 |
R1859:Nrxn2
|
UTSW |
19 |
6,538,825 (GRCm39) |
missense |
probably benign |
0.01 |
R2153:Nrxn2
|
UTSW |
19 |
6,554,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R2196:Nrxn2
|
UTSW |
19 |
6,540,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R2209:Nrxn2
|
UTSW |
19 |
6,543,037 (GRCm39) |
missense |
probably benign |
0.01 |
R2278:Nrxn2
|
UTSW |
19 |
6,531,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R2441:Nrxn2
|
UTSW |
19 |
6,478,331 (GRCm39) |
missense |
probably damaging |
1.00 |
R3897:Nrxn2
|
UTSW |
19 |
6,569,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R3943:Nrxn2
|
UTSW |
19 |
6,523,365 (GRCm39) |
missense |
probably damaging |
1.00 |
R4091:Nrxn2
|
UTSW |
19 |
6,523,444 (GRCm39) |
missense |
probably damaging |
1.00 |
R4162:Nrxn2
|
UTSW |
19 |
6,582,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4164:Nrxn2
|
UTSW |
19 |
6,582,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Nrxn2
|
UTSW |
19 |
6,581,429 (GRCm39) |
missense |
probably benign |
0.05 |
R4599:Nrxn2
|
UTSW |
19 |
6,505,282 (GRCm39) |
missense |
probably damaging |
0.98 |
R4735:Nrxn2
|
UTSW |
19 |
6,548,484 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4757:Nrxn2
|
UTSW |
19 |
6,559,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R4890:Nrxn2
|
UTSW |
19 |
6,498,308 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5052:Nrxn2
|
UTSW |
19 |
6,505,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R5311:Nrxn2
|
UTSW |
19 |
6,581,428 (GRCm39) |
missense |
probably benign |
0.05 |
R5330:Nrxn2
|
UTSW |
19 |
6,540,111 (GRCm39) |
missense |
probably damaging |
0.96 |
R5331:Nrxn2
|
UTSW |
19 |
6,540,111 (GRCm39) |
missense |
probably damaging |
0.96 |
R5530:Nrxn2
|
UTSW |
19 |
6,548,397 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5556:Nrxn2
|
UTSW |
19 |
6,540,121 (GRCm39) |
missense |
probably damaging |
1.00 |
R5763:Nrxn2
|
UTSW |
19 |
6,581,369 (GRCm39) |
missense |
probably benign |
0.15 |
R5829:Nrxn2
|
UTSW |
19 |
6,540,879 (GRCm39) |
missense |
probably benign |
0.03 |
R5988:Nrxn2
|
UTSW |
19 |
6,542,901 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6003:Nrxn2
|
UTSW |
19 |
6,548,358 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6032:Nrxn2
|
UTSW |
19 |
6,567,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R6032:Nrxn2
|
UTSW |
19 |
6,567,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R6288:Nrxn2
|
UTSW |
19 |
6,540,591 (GRCm39) |
missense |
probably damaging |
1.00 |
R6334:Nrxn2
|
UTSW |
19 |
6,581,322 (GRCm39) |
splice site |
probably null |
|
R6373:Nrxn2
|
UTSW |
19 |
6,559,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R6397:Nrxn2
|
UTSW |
19 |
6,582,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R6669:Nrxn2
|
UTSW |
19 |
6,531,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R6980:Nrxn2
|
UTSW |
19 |
6,500,609 (GRCm39) |
missense |
probably benign |
0.04 |
R6985:Nrxn2
|
UTSW |
19 |
6,531,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R7184:Nrxn2
|
UTSW |
19 |
6,540,582 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Nrxn2
|
UTSW |
19 |
6,567,112 (GRCm39) |
missense |
probably benign |
0.00 |
R7576:Nrxn2
|
UTSW |
19 |
6,581,540 (GRCm39) |
nonsense |
probably null |
|
R7604:Nrxn2
|
UTSW |
19 |
6,581,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R7631:Nrxn2
|
UTSW |
19 |
6,531,825 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7768:Nrxn2
|
UTSW |
19 |
6,531,409 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7805:Nrxn2
|
UTSW |
19 |
6,581,736 (GRCm39) |
missense |
probably benign |
|
R7896:Nrxn2
|
UTSW |
19 |
6,582,083 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7998:Nrxn2
|
UTSW |
19 |
6,559,905 (GRCm39) |
missense |
probably damaging |
0.98 |
R8383:Nrxn2
|
UTSW |
19 |
6,522,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R8505:Nrxn2
|
UTSW |
19 |
6,540,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R8843:Nrxn2
|
UTSW |
19 |
6,555,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R8881:Nrxn2
|
UTSW |
19 |
6,554,920 (GRCm39) |
missense |
probably benign |
0.07 |
R9086:Nrxn2
|
UTSW |
19 |
6,540,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Nrxn2
|
UTSW |
19 |
6,498,299 (GRCm39) |
missense |
probably benign |
0.02 |
R9420:Nrxn2
|
UTSW |
19 |
6,581,931 (GRCm39) |
missense |
probably benign |
0.40 |
R9445:Nrxn2
|
UTSW |
19 |
6,522,448 (GRCm39) |
missense |
probably damaging |
0.99 |
R9564:Nrxn2
|
UTSW |
19 |
6,559,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R9609:Nrxn2
|
UTSW |
19 |
6,540,203 (GRCm39) |
missense |
probably damaging |
1.00 |
R9708:Nrxn2
|
UTSW |
19 |
6,581,882 (GRCm39) |
missense |
probably benign |
0.00 |
R9794:Nrxn2
|
UTSW |
19 |
6,567,064 (GRCm39) |
missense |
possibly damaging |
0.48 |
X0022:Nrxn2
|
UTSW |
19 |
6,559,947 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Nrxn2
|
UTSW |
19 |
6,548,547 (GRCm39) |
missense |
probably damaging |
0.98 |
|