Incidental Mutation 'R2112:Nav1'
ID |
232621 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nav1
|
Ensembl Gene |
ENSMUSG00000009418 |
Gene Name |
neuron navigator 1 |
Synonyms |
9930003A20Rik, unc53H1, steerin-1, POMFIL3, C230080M11Rik |
MMRRC Submission |
040116-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.934)
|
Stock # |
R2112 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
1 |
Chromosomal Location |
135362318-135615843 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to T
at 135376742 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Glutamine
at position 1694
(R1694Q)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000140322
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000040599]
[ENSMUST00000067414]
[ENSMUST00000190298]
|
AlphaFold |
Q8CH77 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000040599
AA Change: R1754Q
PolyPhen 2
Score 0.485 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000043803 Gene: ENSMUSG00000009418 AA Change: R1754Q
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
33 |
N/A |
INTRINSIC |
low complexity region
|
48 |
65 |
N/A |
INTRINSIC |
low complexity region
|
119 |
132 |
N/A |
INTRINSIC |
low complexity region
|
303 |
318 |
N/A |
INTRINSIC |
low complexity region
|
414 |
428 |
N/A |
INTRINSIC |
low complexity region
|
436 |
456 |
N/A |
INTRINSIC |
low complexity region
|
739 |
749 |
N/A |
INTRINSIC |
low complexity region
|
807 |
818 |
N/A |
INTRINSIC |
low complexity region
|
892 |
913 |
N/A |
INTRINSIC |
low complexity region
|
975 |
989 |
N/A |
INTRINSIC |
coiled coil region
|
1070 |
1105 |
N/A |
INTRINSIC |
low complexity region
|
1179 |
1210 |
N/A |
INTRINSIC |
low complexity region
|
1260 |
1281 |
N/A |
INTRINSIC |
low complexity region
|
1296 |
1304 |
N/A |
INTRINSIC |
coiled coil region
|
1328 |
1360 |
N/A |
INTRINSIC |
AAA
|
1548 |
1702 |
3.16e-5 |
SMART |
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000067414
AA Change: R1754Q
PolyPhen 2
Score 0.485 (Sensitivity: 0.88; Specificity: 0.90)
|
SMART Domains |
Protein: ENSMUSP00000067241 Gene: ENSMUSG00000009418 AA Change: R1754Q
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
33 |
N/A |
INTRINSIC |
low complexity region
|
48 |
65 |
N/A |
INTRINSIC |
low complexity region
|
119 |
132 |
N/A |
INTRINSIC |
low complexity region
|
303 |
318 |
N/A |
INTRINSIC |
low complexity region
|
414 |
428 |
N/A |
INTRINSIC |
low complexity region
|
436 |
456 |
N/A |
INTRINSIC |
low complexity region
|
739 |
749 |
N/A |
INTRINSIC |
low complexity region
|
807 |
818 |
N/A |
INTRINSIC |
low complexity region
|
892 |
913 |
N/A |
INTRINSIC |
low complexity region
|
975 |
989 |
N/A |
INTRINSIC |
coiled coil region
|
1070 |
1105 |
N/A |
INTRINSIC |
low complexity region
|
1179 |
1210 |
N/A |
INTRINSIC |
low complexity region
|
1260 |
1281 |
N/A |
INTRINSIC |
low complexity region
|
1296 |
1304 |
N/A |
INTRINSIC |
coiled coil region
|
1328 |
1360 |
N/A |
INTRINSIC |
AAA
|
1548 |
1702 |
3.16e-5 |
SMART |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000187311
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000190298
AA Change: R1694Q
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000140322 Gene: ENSMUSG00000009418 AA Change: R1694Q
Domain | Start | End | E-Value | Type |
low complexity region
|
16 |
33 |
N/A |
INTRINSIC |
low complexity region
|
48 |
65 |
N/A |
INTRINSIC |
low complexity region
|
119 |
132 |
N/A |
INTRINSIC |
low complexity region
|
303 |
318 |
N/A |
INTRINSIC |
low complexity region
|
414 |
428 |
N/A |
INTRINSIC |
low complexity region
|
436 |
456 |
N/A |
INTRINSIC |
low complexity region
|
739 |
749 |
N/A |
INTRINSIC |
low complexity region
|
807 |
818 |
N/A |
INTRINSIC |
low complexity region
|
892 |
913 |
N/A |
INTRINSIC |
low complexity region
|
975 |
989 |
N/A |
INTRINSIC |
coiled coil region
|
1013 |
1048 |
N/A |
INTRINSIC |
low complexity region
|
1122 |
1153 |
N/A |
INTRINSIC |
low complexity region
|
1200 |
1221 |
N/A |
INTRINSIC |
low complexity region
|
1236 |
1244 |
N/A |
INTRINSIC |
coiled coil region
|
1268 |
1300 |
N/A |
INTRINSIC |
AAA
|
1488 |
1642 |
3.16e-5 |
SMART |
|
Meta Mutation Damage Score |
0.1753 |
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.6%
- 10x: 97.3%
- 20x: 95.1%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene belongs to the neuron navigator family and is expressed predominantly in the nervous system. The encoded protein contains coiled-coil domains and a conserved AAA domain characteristic for ATPases associated with a variety of cellular activities. This gene is similar to unc-53, a Caenorhabditis elegans gene involved in axon guidance. The exact function of this gene is not known, but it is thought to play a role in in neuronal development and regeneration. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2009]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 94 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam1b |
A |
G |
5: 121,638,777 (GRCm39) |
|
probably benign |
Het |
Adprhl1 |
A |
G |
8: 13,298,694 (GRCm39) |
Y79H |
probably damaging |
Het |
Ambra1 |
T |
A |
2: 91,706,132 (GRCm39) |
W746R |
probably damaging |
Het |
Ankhd1 |
A |
T |
18: 36,774,679 (GRCm39) |
K1420I |
probably damaging |
Het |
Ap1b1 |
T |
C |
11: 4,965,613 (GRCm39) |
F51L |
probably damaging |
Het |
Arhgap24 |
A |
C |
5: 103,040,366 (GRCm39) |
R434S |
probably damaging |
Het |
Arhgap29 |
T |
C |
3: 121,805,210 (GRCm39) |
L525P |
probably benign |
Het |
Arpc1b |
T |
C |
5: 145,060,579 (GRCm39) |
Y124H |
probably damaging |
Het |
Arr3 |
T |
A |
X: 99,658,247 (GRCm39) |
F269L |
possibly damaging |
Het |
Atp11b |
G |
T |
3: 35,891,677 (GRCm39) |
V830F |
probably damaging |
Het |
Ccdc71l |
T |
A |
12: 32,429,229 (GRCm39) |
F83I |
probably damaging |
Het |
Cdh23 |
G |
T |
10: 60,141,362 (GRCm39) |
F3127L |
probably damaging |
Het |
Cfap251 |
G |
A |
5: 123,392,438 (GRCm39) |
|
probably benign |
Het |
Cldn15 |
T |
A |
5: 136,997,016 (GRCm39) |
M19K |
possibly damaging |
Het |
Cog4 |
A |
G |
8: 111,585,214 (GRCm39) |
Y292C |
possibly damaging |
Het |
Col12a1 |
A |
G |
9: 79,551,181 (GRCm39) |
V2145A |
possibly damaging |
Het |
Col5a3 |
T |
C |
9: 20,721,073 (GRCm39) |
I110V |
unknown |
Het |
Cps1 |
T |
A |
1: 67,216,139 (GRCm39) |
D821E |
probably benign |
Het |
Crnkl1 |
A |
T |
2: 145,772,617 (GRCm39) |
Y153* |
probably null |
Het |
Dock10 |
T |
A |
1: 80,483,359 (GRCm39) |
K2082M |
probably damaging |
Het |
Dock10 |
T |
C |
1: 80,483,360 (GRCm39) |
K2083E |
probably damaging |
Het |
Dst |
T |
C |
1: 34,208,259 (GRCm39) |
S737P |
probably damaging |
Het |
Dthd1 |
T |
C |
5: 63,000,222 (GRCm39) |
S515P |
probably damaging |
Het |
Dthd1 |
T |
C |
5: 62,979,251 (GRCm39) |
Y304H |
probably damaging |
Het |
Etf1 |
A |
T |
18: 35,042,154 (GRCm39) |
|
probably null |
Het |
Fmnl2 |
A |
G |
2: 52,995,549 (GRCm39) |
E424G |
probably damaging |
Het |
Galt |
A |
G |
4: 41,758,245 (GRCm39) |
T337A |
probably benign |
Het |
Gbp4 |
A |
G |
5: 105,283,042 (GRCm39) |
L76P |
possibly damaging |
Het |
Gcfc2 |
C |
A |
6: 81,900,759 (GRCm39) |
D24E |
probably benign |
Het |
Gigyf2 |
A |
G |
1: 87,368,452 (GRCm39) |
H1044R |
probably damaging |
Het |
Glg1 |
T |
C |
8: 111,919,178 (GRCm39) |
D315G |
probably damaging |
Het |
Gm4787 |
C |
T |
12: 81,424,607 (GRCm39) |
C517Y |
probably damaging |
Het |
Gnl3l |
A |
G |
X: 149,780,290 (GRCm39) |
S217P |
probably damaging |
Het |
Gpr37 |
T |
C |
6: 25,669,380 (GRCm39) |
Y488C |
possibly damaging |
Het |
Hap1 |
T |
C |
11: 100,244,825 (GRCm39) |
D240G |
probably benign |
Het |
Hhla1 |
C |
G |
15: 65,808,232 (GRCm39) |
W271S |
probably benign |
Het |
Hmgxb3 |
T |
C |
18: 61,288,458 (GRCm39) |
R470G |
possibly damaging |
Het |
Inpp5a |
A |
G |
7: 139,154,877 (GRCm39) |
D332G |
probably damaging |
Het |
Insr |
A |
G |
8: 3,219,748 (GRCm39) |
S925P |
probably benign |
Het |
Isoc2b |
T |
A |
7: 4,852,474 (GRCm39) |
D171V |
probably damaging |
Het |
Kif20b |
T |
C |
19: 34,909,132 (GRCm39) |
I223T |
probably benign |
Het |
Krt6b |
T |
C |
15: 101,586,999 (GRCm39) |
T258A |
possibly damaging |
Het |
Lipo4 |
G |
A |
19: 33,488,926 (GRCm39) |
P219L |
probably benign |
Het |
Luc7l |
T |
C |
17: 26,474,101 (GRCm39) |
|
probably null |
Het |
Madd |
T |
C |
2: 91,007,321 (GRCm39) |
K264E |
possibly damaging |
Het |
Mcf2l |
A |
T |
8: 13,051,867 (GRCm39) |
K433N |
probably damaging |
Het |
Mob3b |
A |
T |
4: 35,083,795 (GRCm39) |
N131K |
probably damaging |
Het |
Mtus1 |
G |
T |
8: 41,475,608 (GRCm39) |
P819T |
probably damaging |
Het |
Myo15a |
T |
C |
11: 60,384,994 (GRCm39) |
F1699L |
probably damaging |
Het |
Neb |
G |
C |
2: 52,218,776 (GRCm39) |
T78S |
probably damaging |
Het |
Nek2 |
T |
C |
1: 191,559,320 (GRCm39) |
V275A |
probably benign |
Het |
Nfatc1 |
A |
T |
18: 80,678,879 (GRCm39) |
C836* |
probably null |
Het |
Nos1 |
T |
C |
5: 118,074,636 (GRCm39) |
V1060A |
probably benign |
Het |
Notch3 |
T |
A |
17: 32,363,584 (GRCm39) |
I1160F |
probably benign |
Het |
Nox4 |
T |
C |
7: 87,021,216 (GRCm39) |
L476P |
probably damaging |
Het |
Npc1 |
A |
T |
18: 12,346,529 (GRCm39) |
N222K |
possibly damaging |
Het |
Nrn1l |
C |
A |
8: 106,621,378 (GRCm39) |
H109Q |
possibly damaging |
Het |
Or4c11 |
T |
C |
2: 88,695,545 (GRCm39) |
S199P |
possibly damaging |
Het |
Or4k15 |
G |
T |
14: 50,364,080 (GRCm39) |
L15F |
probably damaging |
Het |
Or6d13 |
T |
C |
6: 116,517,611 (GRCm39) |
Y66H |
possibly damaging |
Het |
Or7a41 |
T |
C |
10: 78,871,248 (GRCm39) |
L206P |
probably damaging |
Het |
Or8g27 |
T |
C |
9: 39,129,075 (GRCm39) |
Y141H |
probably benign |
Het |
Or8g33 |
C |
A |
9: 39,337,966 (GRCm39) |
V134L |
probably benign |
Het |
Pcnt |
T |
C |
10: 76,256,360 (GRCm39) |
K627E |
probably damaging |
Het |
Plch1 |
T |
A |
3: 63,630,227 (GRCm39) |
T514S |
probably damaging |
Het |
Ppargc1b |
G |
A |
18: 61,444,321 (GRCm39) |
P297S |
probably benign |
Het |
Ppig |
A |
G |
2: 69,580,451 (GRCm39) |
T662A |
unknown |
Het |
Prdm2 |
A |
C |
4: 142,858,506 (GRCm39) |
S1595A |
probably benign |
Het |
Ptpn5 |
T |
A |
7: 46,732,890 (GRCm39) |
T318S |
probably benign |
Het |
Ralgps2 |
A |
G |
1: 156,660,278 (GRCm39) |
Y265H |
probably damaging |
Het |
Seh1l |
T |
C |
18: 67,920,249 (GRCm39) |
I182T |
probably damaging |
Het |
Slc12a6 |
T |
C |
2: 112,186,830 (GRCm39) |
I943T |
probably damaging |
Het |
Slc5a5 |
A |
T |
8: 71,342,395 (GRCm39) |
|
probably null |
Het |
Sparcl1 |
T |
A |
5: 104,236,289 (GRCm39) |
Q488L |
probably damaging |
Het |
Sphkap |
T |
G |
1: 83,253,602 (GRCm39) |
K1382N |
probably benign |
Het |
Sybu |
T |
C |
15: 44,536,731 (GRCm39) |
S532G |
probably benign |
Het |
Syde2 |
G |
A |
3: 145,704,241 (GRCm39) |
G131S |
possibly damaging |
Het |
Taok1 |
C |
T |
11: 77,462,472 (GRCm39) |
V206I |
probably benign |
Het |
Tas1r2 |
G |
T |
4: 139,382,666 (GRCm39) |
M101I |
probably benign |
Het |
Trpc6 |
C |
T |
9: 8,656,613 (GRCm39) |
T680I |
probably damaging |
Het |
Trub1 |
T |
C |
19: 57,473,646 (GRCm39) |
|
probably null |
Het |
Tspan1 |
G |
T |
4: 116,020,885 (GRCm39) |
|
probably null |
Het |
Ttc28 |
G |
A |
5: 111,424,139 (GRCm39) |
E1438K |
probably damaging |
Het |
Ubr3 |
A |
G |
2: 69,808,136 (GRCm39) |
T1206A |
possibly damaging |
Het |
Ulbp3 |
C |
T |
10: 3,076,459 (GRCm39) |
|
noncoding transcript |
Het |
Usp40 |
A |
G |
1: 87,877,936 (GRCm39) |
I1117T |
probably benign |
Het |
Usp43 |
G |
T |
11: 67,812,536 (GRCm39) |
N113K |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,841,422 (GRCm39) |
D414V |
probably damaging |
Het |
Vmn1r202 |
T |
A |
13: 22,685,904 (GRCm39) |
Y171F |
possibly damaging |
Het |
Zfp142 |
A |
G |
1: 74,612,795 (GRCm39) |
S451P |
probably damaging |
Het |
Zfp516 |
A |
G |
18: 82,975,536 (GRCm39) |
D578G |
probably damaging |
Het |
Zfp90 |
G |
A |
8: 107,152,120 (GRCm39) |
C611Y |
probably damaging |
Het |
Zfp954 |
A |
G |
7: 7,118,609 (GRCm39) |
C312R |
probably damaging |
Het |
Zmym3 |
A |
T |
X: 100,450,993 (GRCm39) |
V1208D |
probably damaging |
Het |
|
Other mutations in Nav1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01061:Nav1
|
APN |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01455:Nav1
|
APN |
1 |
135,397,373 (GRCm39) |
missense |
probably benign |
0.44 |
IGL01650:Nav1
|
APN |
1 |
135,382,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01872:Nav1
|
APN |
1 |
135,381,814 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01967:Nav1
|
APN |
1 |
135,464,983 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02167:Nav1
|
APN |
1 |
135,398,699 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02278:Nav1
|
APN |
1 |
135,391,452 (GRCm39) |
splice site |
probably benign |
|
IGL02343:Nav1
|
APN |
1 |
135,382,490 (GRCm39) |
nonsense |
probably null |
|
IGL02378:Nav1
|
APN |
1 |
135,397,716 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02554:Nav1
|
APN |
1 |
135,512,651 (GRCm39) |
synonymous |
silent |
|
IGL03148:Nav1
|
APN |
1 |
135,397,762 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03286:Nav1
|
APN |
1 |
135,382,274 (GRCm39) |
missense |
probably benign |
|
IGL03372:Nav1
|
APN |
1 |
135,378,641 (GRCm39) |
missense |
probably damaging |
0.99 |
PIT4802001:Nav1
|
UTSW |
1 |
135,380,671 (GRCm39) |
missense |
unknown |
|
R0388:Nav1
|
UTSW |
1 |
135,376,655 (GRCm39) |
splice site |
probably benign |
|
R0390:Nav1
|
UTSW |
1 |
135,377,704 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0395:Nav1
|
UTSW |
1 |
135,460,361 (GRCm39) |
missense |
probably damaging |
0.97 |
R0395:Nav1
|
UTSW |
1 |
135,460,359 (GRCm39) |
nonsense |
probably null |
|
R0416:Nav1
|
UTSW |
1 |
135,398,864 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0463:Nav1
|
UTSW |
1 |
135,379,945 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0538:Nav1
|
UTSW |
1 |
135,392,430 (GRCm39) |
splice site |
probably benign |
|
R0594:Nav1
|
UTSW |
1 |
135,395,381 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0696:Nav1
|
UTSW |
1 |
135,460,352 (GRCm39) |
missense |
probably damaging |
0.99 |
R0699:Nav1
|
UTSW |
1 |
135,380,687 (GRCm39) |
missense |
probably benign |
0.00 |
R0759:Nav1
|
UTSW |
1 |
135,382,998 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1164:Nav1
|
UTSW |
1 |
135,400,148 (GRCm39) |
missense |
probably benign |
|
R1169:Nav1
|
UTSW |
1 |
135,382,943 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Nav1
|
UTSW |
1 |
135,388,163 (GRCm39) |
missense |
probably benign |
0.20 |
R1421:Nav1
|
UTSW |
1 |
135,512,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R1642:Nav1
|
UTSW |
1 |
135,380,010 (GRCm39) |
missense |
probably damaging |
1.00 |
R1705:Nav1
|
UTSW |
1 |
135,512,337 (GRCm39) |
missense |
probably damaging |
1.00 |
R1713:Nav1
|
UTSW |
1 |
135,522,972 (GRCm39) |
intron |
probably benign |
|
R1728:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1729:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1730:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1739:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1740:Nav1
|
UTSW |
1 |
135,386,127 (GRCm39) |
critical splice donor site |
probably null |
|
R1762:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1783:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1784:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1785:Nav1
|
UTSW |
1 |
135,512,465 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1895:Nav1
|
UTSW |
1 |
135,386,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R1896:Nav1
|
UTSW |
1 |
135,388,475 (GRCm39) |
missense |
probably benign |
0.00 |
R1901:Nav1
|
UTSW |
1 |
135,400,148 (GRCm39) |
missense |
probably benign |
0.03 |
R1902:Nav1
|
UTSW |
1 |
135,400,148 (GRCm39) |
missense |
probably benign |
0.03 |
R1925:Nav1
|
UTSW |
1 |
135,534,967 (GRCm39) |
utr 5 prime |
probably benign |
|
R1939:Nav1
|
UTSW |
1 |
135,393,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Nav1
|
UTSW |
1 |
135,460,091 (GRCm39) |
missense |
probably benign |
0.06 |
R2063:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2084:Nav1
|
UTSW |
1 |
135,535,158 (GRCm39) |
unclassified |
probably benign |
|
R2090:Nav1
|
UTSW |
1 |
135,534,903 (GRCm39) |
utr 5 prime |
probably benign |
|
R2107:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2110:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2111:Nav1
|
UTSW |
1 |
135,376,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R2136:Nav1
|
UTSW |
1 |
135,382,174 (GRCm39) |
missense |
probably null |
0.18 |
R2268:Nav1
|
UTSW |
1 |
135,399,974 (GRCm39) |
nonsense |
probably null |
|
R2269:Nav1
|
UTSW |
1 |
135,399,974 (GRCm39) |
nonsense |
probably null |
|
R2847:Nav1
|
UTSW |
1 |
135,378,382 (GRCm39) |
splice site |
probably null |
|
R2869:Nav1
|
UTSW |
1 |
135,388,495 (GRCm39) |
synonymous |
silent |
|
R2871:Nav1
|
UTSW |
1 |
135,388,495 (GRCm39) |
synonymous |
silent |
|
R2872:Nav1
|
UTSW |
1 |
135,388,495 (GRCm39) |
synonymous |
silent |
|
R2904:Nav1
|
UTSW |
1 |
135,512,976 (GRCm39) |
missense |
probably benign |
|
R3690:Nav1
|
UTSW |
1 |
135,395,382 (GRCm39) |
missense |
probably benign |
0.11 |
R3716:Nav1
|
UTSW |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3717:Nav1
|
UTSW |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3718:Nav1
|
UTSW |
1 |
135,378,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R3815:Nav1
|
UTSW |
1 |
135,398,862 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4282:Nav1
|
UTSW |
1 |
135,385,651 (GRCm39) |
intron |
probably benign |
|
R4361:Nav1
|
UTSW |
1 |
135,535,175 (GRCm39) |
unclassified |
probably benign |
|
R4610:Nav1
|
UTSW |
1 |
135,520,186 (GRCm39) |
intron |
probably benign |
|
R4730:Nav1
|
UTSW |
1 |
135,535,049 (GRCm39) |
unclassified |
probably benign |
|
R4784:Nav1
|
UTSW |
1 |
135,386,477 (GRCm39) |
missense |
probably damaging |
1.00 |
R4788:Nav1
|
UTSW |
1 |
135,397,461 (GRCm39) |
missense |
probably benign |
|
R4808:Nav1
|
UTSW |
1 |
135,382,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R4996:Nav1
|
UTSW |
1 |
135,393,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R5284:Nav1
|
UTSW |
1 |
135,377,701 (GRCm39) |
nonsense |
probably null |
|
R5514:Nav1
|
UTSW |
1 |
135,398,299 (GRCm39) |
missense |
probably benign |
0.04 |
R5769:Nav1
|
UTSW |
1 |
135,379,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Nav1
|
UTSW |
1 |
135,460,144 (GRCm39) |
missense |
probably benign |
0.07 |
R5898:Nav1
|
UTSW |
1 |
135,512,884 (GRCm39) |
missense |
probably benign |
|
R6081:Nav1
|
UTSW |
1 |
135,398,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R6344:Nav1
|
UTSW |
1 |
135,378,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R6378:Nav1
|
UTSW |
1 |
135,382,433 (GRCm39) |
missense |
probably damaging |
1.00 |
R7001:Nav1
|
UTSW |
1 |
135,382,349 (GRCm39) |
splice site |
probably null |
|
R7185:Nav1
|
UTSW |
1 |
135,398,746 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7291:Nav1
|
UTSW |
1 |
135,393,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R7361:Nav1
|
UTSW |
1 |
135,380,591 (GRCm39) |
missense |
unknown |
|
R7390:Nav1
|
UTSW |
1 |
135,512,656 (GRCm39) |
missense |
probably benign |
0.01 |
R7464:Nav1
|
UTSW |
1 |
135,512,647 (GRCm39) |
missense |
probably benign |
0.03 |
R7502:Nav1
|
UTSW |
1 |
135,397,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7601:Nav1
|
UTSW |
1 |
135,388,176 (GRCm39) |
missense |
unknown |
|
R7625:Nav1
|
UTSW |
1 |
135,395,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R7639:Nav1
|
UTSW |
1 |
135,398,860 (GRCm39) |
missense |
probably benign |
0.09 |
R7786:Nav1
|
UTSW |
1 |
135,397,733 (GRCm39) |
missense |
probably damaging |
1.00 |
R7808:Nav1
|
UTSW |
1 |
135,379,986 (GRCm39) |
missense |
unknown |
|
R7815:Nav1
|
UTSW |
1 |
135,512,377 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7825:Nav1
|
UTSW |
1 |
135,377,782 (GRCm39) |
missense |
probably damaging |
0.98 |
R8030:Nav1
|
UTSW |
1 |
135,464,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R8370:Nav1
|
UTSW |
1 |
135,398,882 (GRCm39) |
nonsense |
probably null |
|
R8405:Nav1
|
UTSW |
1 |
135,382,508 (GRCm39) |
missense |
unknown |
|
R8720:Nav1
|
UTSW |
1 |
135,388,464 (GRCm39) |
missense |
unknown |
|
R8868:Nav1
|
UTSW |
1 |
135,512,943 (GRCm39) |
missense |
probably benign |
0.05 |
R8973:Nav1
|
UTSW |
1 |
135,512,463 (GRCm39) |
missense |
probably benign |
0.01 |
R9039:Nav1
|
UTSW |
1 |
135,371,487 (GRCm39) |
missense |
unknown |
|
R9261:Nav1
|
UTSW |
1 |
135,388,095 (GRCm39) |
missense |
unknown |
|
R9523:Nav1
|
UTSW |
1 |
135,379,929 (GRCm39) |
missense |
unknown |
|
Z1088:Nav1
|
UTSW |
1 |
135,398,462 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Nav1
|
UTSW |
1 |
135,400,158 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Nav1
|
UTSW |
1 |
135,380,624 (GRCm39) |
missense |
unknown |
|
Z1177:Nav1
|
UTSW |
1 |
135,397,469 (GRCm39) |
missense |
possibly damaging |
0.56 |
|
Predicted Primers |
PCR Primer
(F):5'- ATACAATCCCAGTCCTATGTGG -3'
(R):5'- TTTGCTGGACAGTGGGCAAC -3'
Sequencing Primer
(F):5'- CTTAAGAATAGTGGTTATCAGAGGC -3'
(R):5'- GGCAACCGCAGCTCTCAAAC -3'
|
Posted On |
2014-09-18 |