Incidental Mutation 'R1464:Nav2'
ID |
200957 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nav2
|
Ensembl Gene |
ENSMUSG00000052512 |
Gene Name |
neuron navigator 2 |
Synonyms |
Rainb1, Unc53H2, 5330421F07Rik, POMFIL2, HELAD1, RAINB2 |
MMRRC Submission |
039518-MU
|
Accession Numbers |
|
Essential gene? |
Possibly essential
(E-score: 0.571)
|
Stock # |
R1464 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
7 |
Chromosomal Location |
48608796-49259838 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to C
at 49011952 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Threonine
at position 61
(I61T)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000139309
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000064395]
[ENSMUST00000183659]
[ENSMUST00000184124]
[ENSMUST00000184945]
|
AlphaFold |
E9Q842 |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000064383
|
SMART Domains |
Protein: ENSMUSP00000066835 Gene: ENSMUSG00000052512
Domain | Start | End | E-Value | Type |
Blast:CH
|
18 |
79 |
2e-35 |
BLAST |
PDB:2YRN|A
|
18 |
80 |
3e-33 |
PDB |
SCOP:d1dxxa1
|
29 |
81 |
4e-15 |
SMART |
low complexity region
|
94 |
102 |
N/A |
INTRINSIC |
low complexity region
|
189 |
202 |
N/A |
INTRINSIC |
low complexity region
|
229 |
240 |
N/A |
INTRINSIC |
low complexity region
|
304 |
316 |
N/A |
INTRINSIC |
coiled coil region
|
378 |
408 |
N/A |
INTRINSIC |
low complexity region
|
472 |
483 |
N/A |
INTRINSIC |
low complexity region
|
505 |
517 |
N/A |
INTRINSIC |
low complexity region
|
532 |
554 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000064395
AA Change: I122T
PolyPhen 2
Score 0.958 (Sensitivity: 0.78; Specificity: 0.95)
|
SMART Domains |
Protein: ENSMUSP00000067448 Gene: ENSMUSG00000052512 AA Change: I122T
Domain | Start | End | E-Value | Type |
CH
|
84 |
187 |
1.58e-13 |
SMART |
low complexity region
|
202 |
210 |
N/A |
INTRINSIC |
low complexity region
|
297 |
310 |
N/A |
INTRINSIC |
low complexity region
|
337 |
348 |
N/A |
INTRINSIC |
low complexity region
|
412 |
424 |
N/A |
INTRINSIC |
coiled coil region
|
486 |
516 |
N/A |
INTRINSIC |
low complexity region
|
580 |
591 |
N/A |
INTRINSIC |
low complexity region
|
613 |
625 |
N/A |
INTRINSIC |
low complexity region
|
640 |
662 |
N/A |
INTRINSIC |
low complexity region
|
846 |
857 |
N/A |
INTRINSIC |
low complexity region
|
920 |
944 |
N/A |
INTRINSIC |
low complexity region
|
947 |
967 |
N/A |
INTRINSIC |
low complexity region
|
990 |
1004 |
N/A |
INTRINSIC |
low complexity region
|
1062 |
1074 |
N/A |
INTRINSIC |
low complexity region
|
1343 |
1360 |
N/A |
INTRINSIC |
low complexity region
|
1368 |
1385 |
N/A |
INTRINSIC |
low complexity region
|
1417 |
1432 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1466 |
N/A |
INTRINSIC |
low complexity region
|
1526 |
1540 |
N/A |
INTRINSIC |
low complexity region
|
1614 |
1628 |
N/A |
INTRINSIC |
coiled coil region
|
1630 |
1717 |
N/A |
INTRINSIC |
low complexity region
|
1789 |
1800 |
N/A |
INTRINSIC |
coiled coil region
|
1841 |
1909 |
N/A |
INTRINSIC |
AAA
|
2093 |
2247 |
1.69e-5 |
SMART |
low complexity region
|
2404 |
2430 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000183659
AA Change: I61T
PolyPhen 2
Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000139309 Gene: ENSMUSG00000052512 AA Change: I61T
Domain | Start | End | E-Value | Type |
low complexity region
|
2 |
11 |
N/A |
INTRINSIC |
CH
|
23 |
126 |
6.19e-16 |
SMART |
low complexity region
|
141 |
149 |
N/A |
INTRINSIC |
low complexity region
|
236 |
249 |
N/A |
INTRINSIC |
low complexity region
|
276 |
287 |
N/A |
INTRINSIC |
low complexity region
|
351 |
363 |
N/A |
INTRINSIC |
coiled coil region
|
425 |
455 |
N/A |
INTRINSIC |
low complexity region
|
519 |
530 |
N/A |
INTRINSIC |
low complexity region
|
552 |
564 |
N/A |
INTRINSIC |
low complexity region
|
579 |
601 |
N/A |
INTRINSIC |
low complexity region
|
785 |
796 |
N/A |
INTRINSIC |
low complexity region
|
859 |
883 |
N/A |
INTRINSIC |
low complexity region
|
886 |
906 |
N/A |
INTRINSIC |
low complexity region
|
929 |
943 |
N/A |
INTRINSIC |
low complexity region
|
1001 |
1013 |
N/A |
INTRINSIC |
low complexity region
|
1282 |
1299 |
N/A |
INTRINSIC |
low complexity region
|
1307 |
1324 |
N/A |
INTRINSIC |
low complexity region
|
1356 |
1371 |
N/A |
INTRINSIC |
low complexity region
|
1393 |
1405 |
N/A |
INTRINSIC |
low complexity region
|
1465 |
1479 |
N/A |
INTRINSIC |
low complexity region
|
1553 |
1567 |
N/A |
INTRINSIC |
coiled coil region
|
1569 |
1656 |
N/A |
INTRINSIC |
low complexity region
|
1728 |
1739 |
N/A |
INTRINSIC |
coiled coil region
|
1780 |
1848 |
N/A |
INTRINSIC |
AAA
|
2032 |
2186 |
1.69e-5 |
SMART |
low complexity region
|
2343 |
2369 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000184124
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000184809
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000184928
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000184945
AA Change: I122T
PolyPhen 2
Score 0.979 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000139045 Gene: ENSMUSG00000052512 AA Change: I122T
Domain | Start | End | E-Value | Type |
CH
|
84 |
187 |
1.58e-13 |
SMART |
low complexity region
|
202 |
210 |
N/A |
INTRINSIC |
low complexity region
|
297 |
310 |
N/A |
INTRINSIC |
low complexity region
|
337 |
348 |
N/A |
INTRINSIC |
low complexity region
|
412 |
424 |
N/A |
INTRINSIC |
coiled coil region
|
486 |
516 |
N/A |
INTRINSIC |
low complexity region
|
580 |
591 |
N/A |
INTRINSIC |
low complexity region
|
613 |
625 |
N/A |
INTRINSIC |
low complexity region
|
640 |
662 |
N/A |
INTRINSIC |
low complexity region
|
846 |
857 |
N/A |
INTRINSIC |
low complexity region
|
920 |
944 |
N/A |
INTRINSIC |
low complexity region
|
947 |
967 |
N/A |
INTRINSIC |
low complexity region
|
990 |
1004 |
N/A |
INTRINSIC |
low complexity region
|
1062 |
1074 |
N/A |
INTRINSIC |
low complexity region
|
1343 |
1360 |
N/A |
INTRINSIC |
low complexity region
|
1368 |
1385 |
N/A |
INTRINSIC |
low complexity region
|
1417 |
1432 |
N/A |
INTRINSIC |
low complexity region
|
1454 |
1466 |
N/A |
INTRINSIC |
low complexity region
|
1526 |
1540 |
N/A |
INTRINSIC |
low complexity region
|
1614 |
1628 |
N/A |
INTRINSIC |
coiled coil region
|
1630 |
1717 |
N/A |
INTRINSIC |
low complexity region
|
1789 |
1800 |
N/A |
INTRINSIC |
coiled coil region
|
1841 |
1909 |
N/A |
INTRINSIC |
AAA
|
2093 |
2247 |
1.69e-5 |
SMART |
low complexity region
|
2404 |
2430 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000184955
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000207743
|
Coding Region Coverage |
- 1x: 97.4%
- 3x: 96.8%
- 10x: 95.0%
- 20x: 91.7%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the neuron navigator gene family, which may play a role in cellular growth and migration. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2011] PHENOTYPE: Homozygous null mice display impaired olfaction and hearing, increased latency in a hot plate test, degeneration of the optic nerve, decreased exploration in new environments, and weight loss. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030469F06Rik |
A |
G |
12: 31,234,914 (GRCm39) |
|
noncoding transcript |
Het |
Abca2 |
T |
G |
2: 25,337,846 (GRCm39) |
|
probably benign |
Het |
Adamts8 |
T |
A |
9: 30,862,673 (GRCm39) |
W86R |
probably benign |
Het |
Adh1 |
A |
G |
3: 137,994,508 (GRCm39) |
|
probably null |
Het |
Adipor2 |
A |
T |
6: 119,338,804 (GRCm39) |
W150R |
probably damaging |
Het |
Aff4 |
T |
A |
11: 53,263,351 (GRCm39) |
S124T |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,982,260 (GRCm39) |
K1181N |
probably damaging |
Het |
Ak2 |
C |
A |
4: 128,896,152 (GRCm39) |
|
probably benign |
Het |
Alkbh5 |
A |
G |
11: 60,429,873 (GRCm39) |
I209V |
probably benign |
Het |
Ankrd11 |
T |
C |
8: 123,619,463 (GRCm39) |
E1442G |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,345,297 (GRCm39) |
D162E |
probably benign |
Het |
Asic3 |
G |
A |
5: 24,618,819 (GRCm39) |
G37E |
probably damaging |
Het |
AU040320 |
A |
T |
4: 126,685,824 (GRCm39) |
K133N |
possibly damaging |
Het |
C1qtnf7 |
A |
G |
5: 43,766,481 (GRCm39) |
S34G |
probably benign |
Het |
Carf |
A |
G |
1: 60,165,065 (GRCm39) |
|
probably benign |
Het |
Ccdc148 |
T |
A |
2: 58,796,374 (GRCm39) |
R463* |
probably null |
Het |
Ccdc148 |
T |
C |
2: 58,824,455 (GRCm39) |
R329G |
probably damaging |
Het |
Ccdc185 |
A |
G |
1: 182,576,263 (GRCm39) |
I142T |
probably benign |
Het |
Cd274 |
T |
C |
19: 29,359,992 (GRCm39) |
|
probably benign |
Het |
Chrna10 |
G |
A |
7: 101,763,454 (GRCm39) |
P114S |
probably damaging |
Het |
Chst10 |
A |
G |
1: 38,904,772 (GRCm39) |
I311T |
probably damaging |
Het |
Cpne9 |
T |
C |
6: 113,271,698 (GRCm39) |
Y353H |
probably damaging |
Het |
Cubn |
G |
T |
2: 13,330,099 (GRCm39) |
A2594E |
possibly damaging |
Het |
Cyp3a13 |
T |
C |
5: 137,903,827 (GRCm39) |
N277S |
possibly damaging |
Het |
Dctn4 |
A |
G |
18: 60,671,478 (GRCm39) |
T117A |
probably damaging |
Het |
Ddah1 |
A |
T |
3: 145,559,029 (GRCm39) |
K96* |
probably null |
Het |
Ddx5 |
A |
C |
11: 106,675,711 (GRCm39) |
D326E |
probably benign |
Het |
Dlg2 |
T |
C |
7: 91,617,406 (GRCm39) |
S323P |
probably damaging |
Het |
Dnaaf1 |
C |
T |
8: 120,306,049 (GRCm39) |
H109Y |
probably damaging |
Het |
Dnah8 |
C |
A |
17: 30,914,147 (GRCm39) |
R1098S |
possibly damaging |
Het |
Dnajc13 |
T |
C |
9: 104,091,366 (GRCm39) |
T642A |
probably benign |
Het |
Dnajc18 |
A |
G |
18: 35,813,900 (GRCm39) |
S290P |
possibly damaging |
Het |
Dscam |
T |
A |
16: 96,602,453 (GRCm39) |
H663L |
possibly damaging |
Het |
Eefsec |
C |
T |
6: 88,353,182 (GRCm39) |
|
probably benign |
Het |
Emc1 |
A |
G |
4: 139,098,248 (GRCm39) |
N740S |
probably damaging |
Het |
Enpp2 |
C |
T |
15: 54,727,208 (GRCm39) |
G541D |
probably damaging |
Het |
Fam234b |
C |
T |
6: 135,205,490 (GRCm39) |
T485I |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,688,989 (GRCm39) |
I773K |
probably benign |
Het |
Fmo4 |
A |
G |
1: 162,621,924 (GRCm39) |
F429S |
possibly damaging |
Het |
Fndc3b |
A |
G |
3: 27,494,334 (GRCm39) |
|
probably benign |
Het |
Frem1 |
T |
C |
4: 82,930,116 (GRCm39) |
S277G |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,163,810 (GRCm39) |
I221V |
probably benign |
Het |
Gnptab |
A |
G |
10: 88,281,616 (GRCm39) |
|
probably benign |
Het |
Gphn |
T |
A |
12: 78,659,738 (GRCm39) |
|
probably benign |
Het |
Helz2 |
T |
C |
2: 180,881,447 (GRCm39) |
E345G |
probably damaging |
Het |
Ifna4 |
G |
T |
4: 88,760,237 (GRCm39) |
R47I |
probably damaging |
Het |
Igsf21 |
C |
A |
4: 139,761,836 (GRCm39) |
A281S |
probably benign |
Het |
Ikzf3 |
T |
A |
11: 98,407,731 (GRCm39) |
I37L |
probably benign |
Het |
Inpp5d |
A |
T |
1: 87,625,827 (GRCm39) |
|
probably benign |
Het |
Jag1 |
T |
C |
2: 136,957,568 (GRCm39) |
E48G |
probably damaging |
Het |
Jarid2 |
G |
T |
13: 45,001,857 (GRCm39) |
V57F |
probably damaging |
Het |
Kcnj4 |
A |
G |
15: 79,369,605 (GRCm39) |
L125P |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,083,891 (GRCm39) |
K713E |
possibly damaging |
Het |
Layn |
T |
A |
9: 50,968,886 (GRCm39) |
S286C |
probably damaging |
Het |
Lepr |
T |
A |
4: 101,592,878 (GRCm39) |
D164E |
probably benign |
Het |
Macroh2a1 |
A |
T |
13: 56,230,949 (GRCm39) |
S310T |
probably damaging |
Het |
Map3k1 |
T |
C |
13: 111,892,405 (GRCm39) |
H950R |
possibly damaging |
Het |
Map4k5 |
C |
A |
12: 69,852,124 (GRCm39) |
V801L |
possibly damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,851,742 (GRCm39) |
S895T |
probably benign |
Het |
Mthfr |
T |
A |
4: 148,138,029 (GRCm39) |
|
probably benign |
Het |
Naca |
T |
A |
10: 127,884,157 (GRCm39) |
M2157K |
probably damaging |
Het |
Nkx2-5 |
C |
A |
17: 27,058,253 (GRCm39) |
A234S |
probably benign |
Het |
Nol8 |
G |
A |
13: 49,830,264 (GRCm39) |
S1116N |
probably benign |
Het |
Nphp3 |
T |
C |
9: 103,909,078 (GRCm39) |
|
probably benign |
Het |
Nppa |
T |
C |
4: 148,085,304 (GRCm39) |
S5P |
probably benign |
Het |
Nup210 |
A |
G |
6: 91,030,551 (GRCm39) |
V123A |
possibly damaging |
Het |
Or13a21 |
G |
T |
7: 139,999,286 (GRCm39) |
N133K |
probably benign |
Het |
Osbpl11 |
A |
G |
16: 33,049,455 (GRCm39) |
K604R |
probably damaging |
Het |
Osbpl1a |
C |
T |
18: 13,047,615 (GRCm39) |
S113N |
probably benign |
Het |
P2rx4 |
C |
A |
5: 122,852,602 (GRCm39) |
P92Q |
probably damaging |
Het |
Pde9a |
A |
T |
17: 31,692,136 (GRCm39) |
Q148L |
probably benign |
Het |
Phf21b |
T |
A |
15: 84,689,160 (GRCm39) |
H122L |
probably damaging |
Het |
Pik3ca |
T |
A |
3: 32,515,990 (GRCm39) |
F977I |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,363,059 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
A |
G |
2: 111,055,748 (GRCm39) |
|
probably null |
Het |
Pp2d1 |
T |
G |
17: 53,823,015 (GRCm39) |
K17T |
possibly damaging |
Het |
Ppp4r2 |
A |
G |
6: 100,843,527 (GRCm39) |
E415G |
probably damaging |
Het |
Pramel19 |
T |
A |
4: 101,798,503 (GRCm39) |
L158Q |
probably damaging |
Het |
Prkg1 |
A |
G |
19: 30,556,270 (GRCm39) |
S559P |
probably damaging |
Het |
Prss45 |
A |
T |
9: 110,670,019 (GRCm39) |
Y276F |
possibly damaging |
Het |
Ptk7 |
G |
T |
17: 46,883,517 (GRCm39) |
N849K |
probably damaging |
Het |
Rnf121 |
A |
G |
7: 101,680,782 (GRCm39) |
I125T |
possibly damaging |
Het |
Rnf17 |
A |
G |
14: 56,699,368 (GRCm39) |
N502S |
probably damaging |
Het |
Sap25 |
T |
A |
5: 137,640,622 (GRCm39) |
Y167* |
probably null |
Het |
Sdk2 |
G |
A |
11: 113,720,906 (GRCm39) |
T1341I |
possibly damaging |
Het |
Sgcb |
A |
G |
5: 73,792,896 (GRCm39) |
V302A |
probably benign |
Het |
Skor1 |
T |
A |
9: 63,047,393 (GRCm39) |
M865L |
possibly damaging |
Het |
Slc25a45 |
T |
C |
19: 5,929,928 (GRCm39) |
|
probably benign |
Het |
Slc2a3 |
A |
G |
6: 122,714,269 (GRCm39) |
|
probably benign |
Het |
Slc35g1 |
C |
A |
19: 38,391,665 (GRCm39) |
L316I |
probably benign |
Het |
Slco1a8 |
C |
T |
6: 141,938,243 (GRCm39) |
W225* |
probably null |
Het |
Spint4 |
T |
A |
2: 164,540,568 (GRCm39) |
L33H |
probably damaging |
Het |
Sptlc3 |
A |
T |
2: 139,389,154 (GRCm39) |
D178V |
probably benign |
Het |
Stoml1 |
A |
G |
9: 58,167,709 (GRCm39) |
|
probably benign |
Het |
Tbc1d2 |
T |
A |
4: 46,606,491 (GRCm39) |
Y818F |
possibly damaging |
Het |
Tbc1d24 |
A |
T |
17: 24,400,197 (GRCm39) |
|
probably null |
Het |
Teddm2 |
C |
T |
1: 153,726,277 (GRCm39) |
W146* |
probably null |
Het |
Ttn |
T |
A |
2: 76,589,338 (GRCm39) |
D12948V |
probably damaging |
Het |
Txndc8 |
T |
C |
4: 58,000,274 (GRCm39) |
T102A |
probably damaging |
Het |
Uxs1 |
G |
A |
1: 43,804,076 (GRCm39) |
Q280* |
probably null |
Het |
Vmn1r167 |
T |
C |
7: 23,204,681 (GRCm39) |
T112A |
possibly damaging |
Het |
Vmn1r195 |
A |
T |
13: 22,463,348 (GRCm39) |
I273L |
probably benign |
Het |
Vmn1r28 |
T |
A |
6: 58,242,217 (GRCm39) |
M20K |
probably benign |
Het |
Vmn1r53 |
G |
A |
6: 90,200,914 (GRCm39) |
L137F |
probably benign |
Het |
Vmn2r105 |
G |
A |
17: 20,449,004 (GRCm39) |
|
probably benign |
Het |
Vps13b |
C |
T |
15: 35,709,630 (GRCm39) |
A1859V |
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,415,019 (GRCm39) |
H347R |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,235,451 (GRCm39) |
P655S |
probably damaging |
Het |
Zan |
T |
G |
5: 137,418,191 (GRCm39) |
D2969A |
unknown |
Het |
Zbtb24 |
A |
G |
10: 41,331,075 (GRCm39) |
H334R |
probably damaging |
Het |
Zfp108 |
A |
G |
7: 23,959,973 (GRCm39) |
D188G |
probably benign |
Het |
Zfp784 |
A |
T |
7: 5,038,800 (GRCm39) |
C253S |
possibly damaging |
Het |
Zfr |
T |
G |
15: 12,146,458 (GRCm39) |
C336W |
probably damaging |
Het |
|
Other mutations in Nav2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01097:Nav2
|
APN |
7 |
49,220,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01150:Nav2
|
APN |
7 |
49,102,269 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01649:Nav2
|
APN |
7 |
49,225,477 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01662:Nav2
|
APN |
7 |
49,220,957 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02297:Nav2
|
APN |
7 |
49,243,977 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02313:Nav2
|
APN |
7 |
49,208,521 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02441:Nav2
|
APN |
7 |
49,102,260 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02472:Nav2
|
APN |
7 |
49,195,789 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02477:Nav2
|
APN |
7 |
49,232,623 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02725:Nav2
|
APN |
7 |
49,214,843 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02944:Nav2
|
APN |
7 |
49,070,004 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02953:Nav2
|
APN |
7 |
49,198,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03105:Nav2
|
APN |
7 |
49,114,627 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03234:Nav2
|
APN |
7 |
49,111,756 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03274:Nav2
|
APN |
7 |
49,011,847 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03294:Nav2
|
APN |
7 |
49,141,205 (GRCm39) |
nonsense |
probably null |
|
R0006:Nav2
|
UTSW |
7 |
49,102,978 (GRCm39) |
missense |
possibly damaging |
0.50 |
R0070:Nav2
|
UTSW |
7 |
49,220,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Nav2
|
UTSW |
7 |
49,185,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R0306:Nav2
|
UTSW |
7 |
49,195,651 (GRCm39) |
missense |
probably benign |
0.01 |
R0346:Nav2
|
UTSW |
7 |
49,254,333 (GRCm39) |
missense |
probably benign |
0.11 |
R0539:Nav2
|
UTSW |
7 |
49,111,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R0669:Nav2
|
UTSW |
7 |
49,058,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R0785:Nav2
|
UTSW |
7 |
49,070,081 (GRCm39) |
missense |
probably benign |
0.06 |
R0970:Nav2
|
UTSW |
7 |
49,233,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1162:Nav2
|
UTSW |
7 |
49,185,788 (GRCm39) |
splice site |
probably benign |
|
R1274:Nav2
|
UTSW |
7 |
49,254,178 (GRCm39) |
nonsense |
probably null |
|
R1463:Nav2
|
UTSW |
7 |
49,185,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Nav2
|
UTSW |
7 |
49,011,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R1536:Nav2
|
UTSW |
7 |
49,195,682 (GRCm39) |
missense |
probably damaging |
1.00 |
R1612:Nav2
|
UTSW |
7 |
49,220,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R1638:Nav2
|
UTSW |
7 |
49,102,213 (GRCm39) |
missense |
probably benign |
|
R1731:Nav2
|
UTSW |
7 |
49,197,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Nav2
|
UTSW |
7 |
49,225,468 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Nav2
|
UTSW |
7 |
49,197,943 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1945:Nav2
|
UTSW |
7 |
49,114,620 (GRCm39) |
missense |
probably damaging |
1.00 |
R1997:Nav2
|
UTSW |
7 |
49,198,219 (GRCm39) |
missense |
probably benign |
0.16 |
R2061:Nav2
|
UTSW |
7 |
49,248,645 (GRCm39) |
splice site |
probably benign |
|
R2117:Nav2
|
UTSW |
7 |
49,114,328 (GRCm39) |
missense |
probably benign |
0.00 |
R2174:Nav2
|
UTSW |
7 |
49,102,411 (GRCm39) |
missense |
probably damaging |
0.99 |
R2182:Nav2
|
UTSW |
7 |
49,247,002 (GRCm39) |
missense |
probably benign |
0.38 |
R2251:Nav2
|
UTSW |
7 |
49,103,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R2283:Nav2
|
UTSW |
7 |
49,141,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R2343:Nav2
|
UTSW |
7 |
49,248,565 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2472:Nav2
|
UTSW |
7 |
49,058,632 (GRCm39) |
missense |
probably benign |
|
R2568:Nav2
|
UTSW |
7 |
49,247,312 (GRCm39) |
missense |
probably damaging |
1.00 |
R2656:Nav2
|
UTSW |
7 |
49,195,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R2964:Nav2
|
UTSW |
7 |
49,206,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R2966:Nav2
|
UTSW |
7 |
49,206,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R3817:Nav2
|
UTSW |
7 |
49,114,310 (GRCm39) |
missense |
probably benign |
0.00 |
R3834:Nav2
|
UTSW |
7 |
49,195,606 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4207:Nav2
|
UTSW |
7 |
49,246,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R4207:Nav2
|
UTSW |
7 |
49,222,046 (GRCm39) |
splice site |
probably null |
|
R4411:Nav2
|
UTSW |
7 |
49,047,857 (GRCm39) |
missense |
probably benign |
0.37 |
R4413:Nav2
|
UTSW |
7 |
49,047,857 (GRCm39) |
missense |
probably benign |
0.37 |
R4440:Nav2
|
UTSW |
7 |
49,225,011 (GRCm39) |
splice site |
probably benign |
|
R4440:Nav2
|
UTSW |
7 |
49,201,785 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4454:Nav2
|
UTSW |
7 |
49,198,292 (GRCm39) |
splice site |
probably null |
|
R4729:Nav2
|
UTSW |
7 |
49,102,567 (GRCm39) |
missense |
probably benign |
0.17 |
R4801:Nav2
|
UTSW |
7 |
49,195,600 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4802:Nav2
|
UTSW |
7 |
49,195,600 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4824:Nav2
|
UTSW |
7 |
49,058,749 (GRCm39) |
intron |
probably benign |
|
R4887:Nav2
|
UTSW |
7 |
49,198,182 (GRCm39) |
nonsense |
probably null |
|
R4908:Nav2
|
UTSW |
7 |
49,254,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R4952:Nav2
|
UTSW |
7 |
48,954,288 (GRCm39) |
intron |
probably benign |
|
R4965:Nav2
|
UTSW |
7 |
49,202,625 (GRCm39) |
nonsense |
probably null |
|
R5169:Nav2
|
UTSW |
7 |
49,198,231 (GRCm39) |
nonsense |
probably null |
|
R5224:Nav2
|
UTSW |
7 |
49,201,473 (GRCm39) |
missense |
probably benign |
0.00 |
R5249:Nav2
|
UTSW |
7 |
49,185,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Nav2
|
UTSW |
7 |
49,197,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5314:Nav2
|
UTSW |
7 |
49,058,440 (GRCm39) |
small deletion |
probably benign |
|
R5320:Nav2
|
UTSW |
7 |
49,141,121 (GRCm39) |
missense |
probably benign |
0.00 |
R5377:Nav2
|
UTSW |
7 |
49,238,908 (GRCm39) |
missense |
probably benign |
0.02 |
R5471:Nav2
|
UTSW |
7 |
49,197,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Nav2
|
UTSW |
7 |
49,206,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5832:Nav2
|
UTSW |
7 |
49,197,817 (GRCm39) |
splice site |
probably null |
|
R5884:Nav2
|
UTSW |
7 |
49,246,917 (GRCm39) |
nonsense |
probably null |
|
R5921:Nav2
|
UTSW |
7 |
48,954,324 (GRCm39) |
intron |
probably benign |
|
R6180:Nav2
|
UTSW |
7 |
49,107,915 (GRCm39) |
missense |
probably benign |
0.39 |
R6208:Nav2
|
UTSW |
7 |
49,213,851 (GRCm39) |
missense |
probably damaging |
0.99 |
R6373:Nav2
|
UTSW |
7 |
49,102,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R6450:Nav2
|
UTSW |
7 |
49,244,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R6522:Nav2
|
UTSW |
7 |
49,247,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R6626:Nav2
|
UTSW |
7 |
49,244,100 (GRCm39) |
missense |
probably damaging |
1.00 |
R6695:Nav2
|
UTSW |
7 |
49,114,652 (GRCm39) |
missense |
probably benign |
0.04 |
R6705:Nav2
|
UTSW |
7 |
49,201,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R6842:Nav2
|
UTSW |
7 |
49,107,917 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6847:Nav2
|
UTSW |
7 |
49,141,204 (GRCm39) |
missense |
probably benign |
0.14 |
R7287:Nav2
|
UTSW |
7 |
49,070,076 (GRCm39) |
missense |
probably benign |
0.01 |
R7312:Nav2
|
UTSW |
7 |
49,111,672 (GRCm39) |
missense |
possibly damaging |
0.55 |
R7315:Nav2
|
UTSW |
7 |
49,198,037 (GRCm39) |
missense |
possibly damaging |
0.61 |
R7337:Nav2
|
UTSW |
7 |
49,201,521 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7366:Nav2
|
UTSW |
7 |
49,203,951 (GRCm39) |
splice site |
probably null |
|
R7451:Nav2
|
UTSW |
7 |
49,202,577 (GRCm39) |
splice site |
probably null |
|
R7545:Nav2
|
UTSW |
7 |
49,232,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R7706:Nav2
|
UTSW |
7 |
49,244,067 (GRCm39) |
missense |
probably benign |
0.35 |
R7730:Nav2
|
UTSW |
7 |
49,222,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R7812:Nav2
|
UTSW |
7 |
49,246,921 (GRCm39) |
missense |
probably benign |
0.13 |
R8097:Nav2
|
UTSW |
7 |
49,237,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R8110:Nav2
|
UTSW |
7 |
49,201,698 (GRCm39) |
nonsense |
probably null |
|
R8119:Nav2
|
UTSW |
7 |
49,103,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R8298:Nav2
|
UTSW |
7 |
49,204,009 (GRCm39) |
critical splice donor site |
probably null |
|
R8306:Nav2
|
UTSW |
7 |
49,195,765 (GRCm39) |
missense |
probably benign |
0.33 |
R8331:Nav2
|
UTSW |
7 |
49,102,371 (GRCm39) |
missense |
probably benign |
|
R8402:Nav2
|
UTSW |
7 |
49,103,185 (GRCm39) |
missense |
probably benign |
0.43 |
R8421:Nav2
|
UTSW |
7 |
49,102,269 (GRCm39) |
missense |
probably benign |
|
R8478:Nav2
|
UTSW |
7 |
49,111,733 (GRCm39) |
missense |
probably damaging |
0.99 |
R8724:Nav2
|
UTSW |
7 |
49,141,184 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8753:Nav2
|
UTSW |
7 |
49,102,320 (GRCm39) |
missense |
probably benign |
|
R8835:Nav2
|
UTSW |
7 |
49,248,551 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8933:Nav2
|
UTSW |
7 |
49,111,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R8957:Nav2
|
UTSW |
7 |
49,220,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R9069:Nav2
|
UTSW |
7 |
49,208,561 (GRCm39) |
missense |
probably damaging |
0.99 |
R9095:Nav2
|
UTSW |
7 |
49,254,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Nav2
|
UTSW |
7 |
49,202,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R9261:Nav2
|
UTSW |
7 |
49,246,904 (GRCm39) |
missense |
probably damaging |
1.00 |
X0023:Nav2
|
UTSW |
7 |
49,197,647 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1177:Nav2
|
UTSW |
7 |
49,243,971 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Nav2
|
UTSW |
7 |
49,102,509 (GRCm39) |
missense |
possibly damaging |
0.47 |
|
Predicted Primers |
PCR Primer
(F):5'- GCTGAATGCCTAGCCAGCACAATG -3'
(R):5'- CCCACAGCCCTGCTGAGTTTTAATG -3'
Sequencing Primer
(F):5'- AATGGTTCTGGCAGCTCC -3'
(R):5'- CCCTGCTGAGTTTTAATGGAAACAG -3'
|
Posted On |
2014-05-23 |