Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
C |
T |
16: 8,400,676 (GRCm39) |
R92C |
probably damaging |
Het |
Adam29 |
C |
A |
8: 56,324,589 (GRCm39) |
V622L |
possibly damaging |
Het |
Bzw2 |
T |
C |
12: 36,157,502 (GRCm39) |
H321R |
probably benign |
Het |
C2cd2 |
C |
T |
16: 97,671,432 (GRCm39) |
R489Q |
probably damaging |
Het |
Cdh23 |
G |
A |
10: 60,359,339 (GRCm39) |
T253I |
possibly damaging |
Het |
Col4a3 |
T |
G |
1: 82,638,608 (GRCm39) |
|
probably null |
Het |
D630039A03Rik |
T |
C |
4: 57,910,309 (GRCm39) |
T168A |
possibly damaging |
Het |
Dnajc19 |
A |
G |
3: 34,132,914 (GRCm39) |
L97P |
possibly damaging |
Het |
Dpep2 |
A |
T |
8: 106,711,776 (GRCm39) |
H550Q |
probably benign |
Het |
Dvl2 |
C |
A |
11: 69,895,626 (GRCm39) |
|
probably null |
Het |
Fam234b |
A |
G |
6: 135,204,149 (GRCm39) |
|
probably null |
Het |
Fxyd5 |
A |
G |
7: 30,739,613 (GRCm39) |
V32A |
possibly damaging |
Het |
Itprid1 |
C |
A |
6: 55,944,710 (GRCm39) |
S477* |
probably null |
Het |
Mak16 |
A |
T |
8: 31,650,557 (GRCm39) |
S251T |
probably benign |
Het |
Med10 |
T |
C |
13: 69,963,747 (GRCm39) |
V116A |
probably benign |
Het |
Mycbp2 |
G |
A |
14: 103,392,343 (GRCm39) |
R50* |
probably null |
Het |
Nckap5 |
G |
A |
1: 125,909,305 (GRCm39) |
P272L |
probably damaging |
Het |
Nf1 |
T |
A |
11: 79,334,947 (GRCm39) |
V933E |
possibly damaging |
Het |
Or51e2 |
A |
C |
7: 102,391,355 (GRCm39) |
V285G |
probably damaging |
Het |
Or5al1 |
C |
A |
2: 85,990,219 (GRCm39) |
R165L |
probably benign |
Het |
Osbpl9 |
T |
C |
4: 108,929,176 (GRCm39) |
Y417C |
probably damaging |
Het |
Otop1 |
G |
A |
5: 38,445,327 (GRCm39) |
A162T |
probably damaging |
Het |
Patl1 |
C |
A |
19: 11,917,054 (GRCm39) |
P634T |
probably damaging |
Het |
Ppl |
A |
T |
16: 4,930,936 (GRCm39) |
S28T |
probably benign |
Het |
Prkar2b |
C |
T |
12: 32,013,016 (GRCm39) |
G367R |
probably damaging |
Het |
Rbl2 |
G |
A |
8: 91,828,826 (GRCm39) |
V576I |
probably damaging |
Het |
Rgl3 |
C |
T |
9: 21,899,559 (GRCm39) |
A53T |
probably benign |
Het |
Rp1 |
T |
A |
1: 4,415,533 (GRCm39) |
I1860F |
possibly damaging |
Het |
Sbno2 |
A |
T |
10: 79,896,475 (GRCm39) |
D877E |
probably damaging |
Het |
Sectm1b |
C |
T |
11: 120,946,761 (GRCm39) |
V45I |
probably damaging |
Het |
Sfmbt2 |
G |
A |
2: 10,582,763 (GRCm39) |
V741I |
probably benign |
Het |
Sugt1 |
T |
A |
14: 79,847,723 (GRCm39) |
L191* |
probably null |
Het |
Tcf21 |
A |
T |
10: 22,693,709 (GRCm39) |
V156E |
possibly damaging |
Het |
Tep1 |
T |
A |
14: 51,071,506 (GRCm39) |
R2046S |
possibly damaging |
Het |
Tmem181a |
T |
C |
17: 6,347,531 (GRCm39) |
F241S |
probably damaging |
Het |
Traf6 |
G |
A |
2: 101,527,138 (GRCm39) |
C296Y |
probably benign |
Het |
Trim40 |
A |
G |
17: 37,200,070 (GRCm39) |
S3P |
probably benign |
Het |
Ttll2 |
A |
T |
17: 7,619,130 (GRCm39) |
Y266N |
probably damaging |
Het |
Vps54 |
A |
G |
11: 21,225,071 (GRCm39) |
N177S |
probably null |
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 |
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 |
PIT4687001:Nrxn2
|
UTSW |
19 |
6,531,338 (GRCm39) |
missense |
probably benign |
0.06 |
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 |
|