Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsf2 |
G |
T |
11: 94,453,700 (GRCm39) |
N420K |
probably benign |
Het |
Adam26a |
A |
T |
8: 44,022,229 (GRCm39) |
C420* |
probably null |
Het |
Afap1l1 |
T |
C |
18: 61,874,909 (GRCm39) |
Y424C |
probably damaging |
Het |
Agl |
A |
G |
3: 116,576,246 (GRCm39) |
V553A |
probably benign |
Het |
Akr7a5 |
T |
A |
4: 139,045,434 (GRCm39) |
M325K |
probably damaging |
Het |
Aldh7a1 |
C |
A |
18: 56,692,341 (GRCm39) |
E87* |
probably null |
Het |
Arhgap29 |
A |
G |
3: 121,767,578 (GRCm39) |
K7E |
probably damaging |
Het |
Brca2 |
T |
A |
5: 150,466,114 (GRCm39) |
D1959E |
probably benign |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Chil5 |
G |
T |
3: 105,925,409 (GRCm39) |
Q171K |
probably benign |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Dhrs7c |
A |
T |
11: 67,702,476 (GRCm39) |
I155F |
probably damaging |
Het |
Dip2c |
A |
G |
13: 9,603,300 (GRCm39) |
|
probably null |
Het |
Fam124b |
T |
C |
1: 80,191,056 (GRCm39) |
Y109C |
possibly damaging |
Het |
Gak |
T |
A |
5: 108,739,011 (GRCm39) |
K156M |
probably damaging |
Het |
Gm17535 |
A |
G |
9: 3,035,804 (GRCm39) |
Y224C |
probably null |
Het |
Got1l1 |
C |
G |
8: 27,690,745 (GRCm39) |
|
probably null |
Het |
Grm1 |
T |
C |
10: 10,955,879 (GRCm39) |
D135G |
probably benign |
Het |
Hrh3 |
T |
G |
2: 179,744,547 (GRCm39) |
D131A |
probably damaging |
Het |
Hspg2 |
C |
T |
4: 137,267,411 (GRCm39) |
L2042F |
possibly damaging |
Het |
Itpr1 |
A |
T |
6: 108,366,514 (GRCm39) |
Q979L |
probably null |
Het |
Klb |
G |
C |
5: 65,506,089 (GRCm39) |
R112P |
possibly damaging |
Het |
Lingo2 |
A |
T |
4: 35,709,420 (GRCm39) |
C187S |
possibly damaging |
Het |
Lrp1 |
T |
A |
10: 127,417,760 (GRCm39) |
|
probably null |
Het |
Ltbp4 |
T |
C |
7: 27,028,464 (GRCm39) |
N266S |
unknown |
Het |
Mgam |
G |
A |
6: 40,643,815 (GRCm39) |
S581N |
possibly damaging |
Het |
Mrgpra9 |
T |
A |
7: 46,885,386 (GRCm39) |
I94L |
probably benign |
Het |
Msantd4 |
A |
T |
9: 4,384,023 (GRCm39) |
I115F |
probably benign |
Het |
Or5p59 |
T |
A |
7: 107,702,822 (GRCm39) |
I102N |
probably benign |
Het |
Prl7d1 |
A |
T |
13: 27,893,180 (GRCm39) |
F243I |
possibly damaging |
Het |
Rbm27 |
T |
C |
18: 42,450,746 (GRCm39) |
S509P |
probably damaging |
Het |
Rnf44 |
C |
T |
13: 54,829,821 (GRCm39) |
E306K |
probably damaging |
Het |
Rp1 |
T |
C |
1: 4,416,520 (GRCm39) |
R1531G |
possibly damaging |
Het |
Sf3b4 |
A |
G |
3: 96,080,953 (GRCm39) |
|
probably null |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Sfi1 |
CCTCTC |
CCTCTCTC |
11: 3,127,419 (GRCm39) |
|
probably benign |
Het |
Sp110 |
T |
G |
1: 85,506,800 (GRCm39) |
E421A |
probably benign |
Het |
Stk4 |
C |
T |
2: 163,942,448 (GRCm39) |
T360M |
probably benign |
Het |
Vcan |
T |
A |
13: 89,836,603 (GRCm39) |
E2980D |
probably benign |
Het |
Vwa2 |
C |
T |
19: 56,869,570 (GRCm39) |
P2S |
unknown |
Het |
Wdr77 |
G |
A |
3: 105,874,573 (GRCm39) |
V322I |
possibly damaging |
Het |
Zfp12 |
C |
A |
5: 143,230,535 (GRCm39) |
Y287* |
probably null |
Het |
Zfp937 |
T |
A |
2: 150,080,868 (GRCm39) |
Y299* |
probably null |
Het |
|
Other mutations in Nrxn1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01310:Nrxn1
|
APN |
17 |
90,366,902 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01644:Nrxn1
|
APN |
17 |
90,928,301 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01820:Nrxn1
|
APN |
17 |
90,950,531 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01902:Nrxn1
|
APN |
17 |
91,395,919 (GRCm39) |
splice site |
probably null |
|
IGL02079:Nrxn1
|
APN |
17 |
90,950,511 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02089:Nrxn1
|
APN |
17 |
91,395,829 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02133:Nrxn1
|
APN |
17 |
90,950,671 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02179:Nrxn1
|
APN |
17 |
90,937,511 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02199:Nrxn1
|
APN |
17 |
90,344,686 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02262:Nrxn1
|
APN |
17 |
91,011,636 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02941:Nrxn1
|
APN |
17 |
90,515,811 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4449001:Nrxn1
|
UTSW |
17 |
90,905,007 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4791001:Nrxn1
|
UTSW |
17 |
90,762,931 (GRCm39) |
intron |
probably benign |
|
R0123:Nrxn1
|
UTSW |
17 |
91,302,915 (GRCm39) |
splice site |
probably null |
|
R0212:Nrxn1
|
UTSW |
17 |
90,670,186 (GRCm39) |
unclassified |
probably benign |
|
R0277:Nrxn1
|
UTSW |
17 |
91,008,170 (GRCm39) |
critical splice donor site |
probably null |
|
R0323:Nrxn1
|
UTSW |
17 |
91,008,170 (GRCm39) |
critical splice donor site |
probably null |
|
R0384:Nrxn1
|
UTSW |
17 |
90,515,775 (GRCm39) |
missense |
probably damaging |
1.00 |
R0395:Nrxn1
|
UTSW |
17 |
91,395,742 (GRCm39) |
missense |
possibly damaging |
0.90 |
R0606:Nrxn1
|
UTSW |
17 |
90,872,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R0616:Nrxn1
|
UTSW |
17 |
90,670,285 (GRCm39) |
missense |
probably damaging |
1.00 |
R0624:Nrxn1
|
UTSW |
17 |
91,396,117 (GRCm39) |
missense |
unknown |
|
R0633:Nrxn1
|
UTSW |
17 |
91,011,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R0927:Nrxn1
|
UTSW |
17 |
90,344,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R1035:Nrxn1
|
UTSW |
17 |
90,471,302 (GRCm39) |
missense |
probably damaging |
0.96 |
R1221:Nrxn1
|
UTSW |
17 |
90,950,722 (GRCm39) |
missense |
probably damaging |
0.97 |
R1403:Nrxn1
|
UTSW |
17 |
90,950,481 (GRCm39) |
missense |
probably benign |
0.11 |
R1691:Nrxn1
|
UTSW |
17 |
90,469,717 (GRCm39) |
missense |
probably damaging |
0.98 |
R1703:Nrxn1
|
UTSW |
17 |
90,515,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R1709:Nrxn1
|
UTSW |
17 |
90,344,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Nrxn1
|
UTSW |
17 |
90,469,832 (GRCm39) |
missense |
probably damaging |
1.00 |
R1792:Nrxn1
|
UTSW |
17 |
90,896,252 (GRCm39) |
missense |
probably damaging |
0.96 |
R1980:Nrxn1
|
UTSW |
17 |
91,395,746 (GRCm39) |
missense |
probably benign |
0.01 |
R2116:Nrxn1
|
UTSW |
17 |
91,011,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Nrxn1
|
UTSW |
17 |
91,011,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Nrxn1
|
UTSW |
17 |
90,469,859 (GRCm39) |
missense |
probably damaging |
1.00 |
R3119:Nrxn1
|
UTSW |
17 |
90,904,947 (GRCm39) |
nonsense |
probably null |
|
R3409:Nrxn1
|
UTSW |
17 |
90,515,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R3683:Nrxn1
|
UTSW |
17 |
90,930,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R3885:Nrxn1
|
UTSW |
17 |
90,930,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R3939:Nrxn1
|
UTSW |
17 |
90,515,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R4475:Nrxn1
|
UTSW |
17 |
91,009,410 (GRCm39) |
missense |
probably damaging |
0.98 |
R4640:Nrxn1
|
UTSW |
17 |
90,868,196 (GRCm39) |
missense |
probably damaging |
1.00 |
R4678:Nrxn1
|
UTSW |
17 |
90,930,850 (GRCm39) |
missense |
probably damaging |
1.00 |
R4690:Nrxn1
|
UTSW |
17 |
90,344,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R4790:Nrxn1
|
UTSW |
17 |
90,762,477 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4877:Nrxn1
|
UTSW |
17 |
91,395,605 (GRCm39) |
missense |
probably benign |
0.33 |
R4989:Nrxn1
|
UTSW |
17 |
90,928,274 (GRCm39) |
intron |
probably benign |
|
R5204:Nrxn1
|
UTSW |
17 |
90,469,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5205:Nrxn1
|
UTSW |
17 |
90,471,302 (GRCm39) |
missense |
probably damaging |
0.96 |
R5239:Nrxn1
|
UTSW |
17 |
91,011,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R5250:Nrxn1
|
UTSW |
17 |
90,842,869 (GRCm39) |
intron |
probably benign |
|
R5473:Nrxn1
|
UTSW |
17 |
90,897,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R5629:Nrxn1
|
UTSW |
17 |
90,897,460 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5743:Nrxn1
|
UTSW |
17 |
90,950,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:Nrxn1
|
UTSW |
17 |
91,011,746 (GRCm39) |
nonsense |
probably null |
|
R5961:Nrxn1
|
UTSW |
17 |
90,762,371 (GRCm39) |
missense |
probably damaging |
0.99 |
R5979:Nrxn1
|
UTSW |
17 |
91,395,631 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5992:Nrxn1
|
UTSW |
17 |
90,930,935 (GRCm39) |
missense |
probably benign |
0.01 |
R6024:Nrxn1
|
UTSW |
17 |
90,897,526 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6031:Nrxn1
|
UTSW |
17 |
90,896,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R6031:Nrxn1
|
UTSW |
17 |
90,896,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R6185:Nrxn1
|
UTSW |
17 |
90,344,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Nrxn1
|
UTSW |
17 |
91,395,904 (GRCm39) |
missense |
probably benign |
0.14 |
R6306:Nrxn1
|
UTSW |
17 |
90,872,874 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6621:Nrxn1
|
UTSW |
17 |
90,469,610 (GRCm39) |
missense |
probably damaging |
1.00 |
R6669:Nrxn1
|
UTSW |
17 |
90,366,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R6770:Nrxn1
|
UTSW |
17 |
90,344,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R6798:Nrxn1
|
UTSW |
17 |
90,937,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R6923:Nrxn1
|
UTSW |
17 |
91,395,661 (GRCm39) |
missense |
probably benign |
0.06 |
R7140:Nrxn1
|
UTSW |
17 |
91,396,192 (GRCm39) |
start gained |
probably benign |
|
R7374:Nrxn1
|
UTSW |
17 |
90,896,097 (GRCm39) |
critical splice donor site |
probably null |
|
R7564:Nrxn1
|
UTSW |
17 |
90,670,334 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7570:Nrxn1
|
UTSW |
17 |
90,469,807 (GRCm39) |
missense |
probably benign |
0.35 |
R7800:Nrxn1
|
UTSW |
17 |
91,396,635 (GRCm39) |
unclassified |
probably benign |
|
R7828:Nrxn1
|
UTSW |
17 |
90,366,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R7974:Nrxn1
|
UTSW |
17 |
91,008,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R8001:Nrxn1
|
UTSW |
17 |
91,395,964 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8189:Nrxn1
|
UTSW |
17 |
91,011,637 (GRCm39) |
missense |
probably damaging |
0.96 |
R8258:Nrxn1
|
UTSW |
17 |
90,471,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R8259:Nrxn1
|
UTSW |
17 |
90,471,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R8298:Nrxn1
|
UTSW |
17 |
91,011,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8801:Nrxn1
|
UTSW |
17 |
91,009,393 (GRCm39) |
critical splice donor site |
probably benign |
|
R8814:Nrxn1
|
UTSW |
17 |
90,937,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R8873:Nrxn1
|
UTSW |
17 |
90,872,821 (GRCm39) |
nonsense |
probably null |
|
R8954:Nrxn1
|
UTSW |
17 |
90,897,615 (GRCm39) |
missense |
probably damaging |
1.00 |
R9086:Nrxn1
|
UTSW |
17 |
90,469,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R9110:Nrxn1
|
UTSW |
17 |
90,869,233 (GRCm39) |
nonsense |
probably null |
|
R9498:Nrxn1
|
UTSW |
17 |
90,897,397 (GRCm39) |
missense |
probably damaging |
1.00 |
R9499:Nrxn1
|
UTSW |
17 |
90,937,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R9552:Nrxn1
|
UTSW |
17 |
90,937,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R9780:Nrxn1
|
UTSW |
17 |
90,931,042 (GRCm39) |
missense |
possibly damaging |
0.54 |
RF005:Nrxn1
|
UTSW |
17 |
90,670,304 (GRCm39) |
missense |
probably damaging |
1.00 |
RF024:Nrxn1
|
UTSW |
17 |
90,670,304 (GRCm39) |
missense |
probably damaging |
1.00 |
X0021:Nrxn1
|
UTSW |
17 |
90,897,640 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Nrxn1
|
UTSW |
17 |
90,670,259 (GRCm39) |
missense |
possibly damaging |
0.54 |
Z1088:Nrxn1
|
UTSW |
17 |
90,366,933 (GRCm39) |
missense |
probably damaging |
1.00 |
|