Incidental Mutation 'R1713:Nav1'
ID |
190730 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nav1
|
Ensembl Gene |
ENSMUSG00000009418 |
Gene Name |
neuron navigator 1 |
Synonyms |
9930003A20Rik, unc53H1, steerin-1, POMFIL3, C230080M11Rik |
MMRRC Submission |
039746-MU
|
Accession Numbers |
|
Essential gene? |
Probably essential
(E-score: 0.934)
|
Stock # |
R1713 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
1 |
Chromosomal Location |
135362318-135615843 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
A to G
at 135522972 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000140322
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000190298]
|
AlphaFold |
Q8CH77 |
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000067468
|
SMART Domains |
Protein: ENSMUSP00000067952 Gene: ENSMUSG00000054412
Domain | Start | End | E-Value | Type |
low complexity region
|
118 |
146 |
N/A |
INTRINSIC |
transmembrane domain
|
164 |
181 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000190298
|
SMART Domains |
Protein: ENSMUSP00000140322 Gene: ENSMUSG00000009418
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 |
0.0898 |
Coding Region Coverage |
- 1x: 99.1%
- 3x: 98.5%
- 10x: 96.7%
- 20x: 93.6%
|
Validation Efficiency |
98% (96/98) |
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: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921539E11Rik |
T |
A |
4: 103,127,964 (GRCm39) |
I54F |
possibly damaging |
Het |
Ackr1 |
A |
T |
1: 173,159,916 (GRCm39) |
H134Q |
probably benign |
Het |
Agtr1b |
A |
T |
3: 20,370,473 (GRCm39) |
F44L |
probably benign |
Het |
Ahnak |
G |
A |
19: 8,989,173 (GRCm39) |
D3486N |
possibly damaging |
Het |
Akap9 |
T |
C |
5: 4,089,345 (GRCm39) |
|
probably null |
Het |
Anks6 |
T |
A |
4: 47,039,726 (GRCm39) |
Q495L |
probably benign |
Het |
Arpp21 |
A |
G |
9: 111,896,237 (GRCm39) |
S684P |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,983,531 (GRCm39) |
E2911G |
probably damaging |
Het |
Avpi1 |
C |
T |
19: 42,113,248 (GRCm39) |
E70K |
probably damaging |
Het |
Btbd17 |
G |
T |
11: 114,686,650 (GRCm39) |
P9T |
probably benign |
Het |
C4b |
A |
G |
17: 34,948,245 (GRCm39) |
|
probably benign |
Het |
Carm1 |
T |
C |
9: 21,497,785 (GRCm39) |
V385A |
probably damaging |
Het |
Casd1 |
A |
G |
6: 4,624,104 (GRCm39) |
D299G |
probably damaging |
Het |
Clca3a1 |
T |
A |
3: 144,730,307 (GRCm39) |
K179N |
probably benign |
Het |
Col1a2 |
T |
C |
6: 4,538,691 (GRCm39) |
S1204P |
unknown |
Het |
Col24a1 |
C |
T |
3: 145,072,624 (GRCm39) |
Q780* |
probably null |
Het |
Cxadr |
C |
A |
16: 78,131,133 (GRCm39) |
N216K |
probably damaging |
Het |
Daam1 |
C |
T |
12: 71,942,656 (GRCm39) |
T40I |
unknown |
Het |
Dab2 |
C |
T |
15: 6,459,182 (GRCm39) |
P365S |
possibly damaging |
Het |
Dnah1 |
A |
T |
14: 31,001,139 (GRCm39) |
I2402N |
probably damaging |
Het |
Dscaml1 |
T |
A |
9: 45,663,988 (GRCm39) |
S1954R |
possibly damaging |
Het |
Dync2h1 |
T |
C |
9: 7,131,891 (GRCm39) |
T1639A |
probably benign |
Het |
Ebf1 |
A |
T |
11: 44,815,393 (GRCm39) |
I336F |
probably damaging |
Het |
Ebna1bp2 |
A |
G |
4: 118,482,881 (GRCm39) |
N290S |
possibly damaging |
Het |
Gabra2 |
A |
G |
5: 71,171,906 (GRCm39) |
I110T |
probably benign |
Het |
Galk2 |
A |
G |
2: 125,773,210 (GRCm39) |
N203S |
probably benign |
Het |
Gria4 |
T |
C |
9: 4,424,448 (GRCm39) |
T806A |
probably benign |
Het |
Impg2 |
A |
G |
16: 56,080,889 (GRCm39) |
T789A |
probably benign |
Het |
Itga6 |
A |
G |
2: 71,617,546 (GRCm39) |
T22A |
probably benign |
Het |
Itgb4 |
T |
A |
11: 115,894,315 (GRCm39) |
I1312N |
probably damaging |
Het |
Kdm4c |
A |
G |
4: 74,216,721 (GRCm39) |
D160G |
probably benign |
Het |
Kdr |
A |
G |
5: 76,129,127 (GRCm39) |
V173A |
probably benign |
Het |
Kif14 |
T |
C |
1: 136,455,202 (GRCm39) |
S1575P |
probably benign |
Het |
Lcp1 |
G |
A |
14: 75,436,884 (GRCm39) |
|
probably null |
Het |
Lipe |
C |
A |
7: 25,084,750 (GRCm39) |
S516I |
probably damaging |
Het |
Lrrc61 |
G |
A |
6: 48,545,708 (GRCm39) |
R177Q |
possibly damaging |
Het |
Macf1 |
A |
G |
4: 123,272,487 (GRCm39) |
I6429T |
probably damaging |
Het |
Map3k4 |
C |
T |
17: 12,468,458 (GRCm39) |
E1012K |
probably benign |
Het |
Map3k5 |
T |
C |
10: 19,986,593 (GRCm39) |
F936L |
possibly damaging |
Het |
Mllt3 |
A |
T |
4: 87,701,901 (GRCm39) |
N497K |
probably damaging |
Het |
Moxd1 |
G |
A |
10: 24,157,394 (GRCm39) |
G342D |
probably damaging |
Het |
Mtdh |
A |
C |
15: 34,114,985 (GRCm39) |
Q202H |
possibly damaging |
Het |
Nop56 |
T |
C |
2: 130,119,886 (GRCm39) |
V109A |
possibly damaging |
Het |
Obscn |
T |
C |
11: 58,970,712 (GRCm39) |
D2540G |
probably damaging |
Het |
Omg |
T |
C |
11: 79,393,679 (GRCm39) |
I60V |
probably benign |
Het |
Or10q12 |
A |
T |
19: 13,746,659 (GRCm39) |
T318S |
probably benign |
Het |
Or12e9 |
A |
T |
2: 87,202,290 (GRCm39) |
Y138F |
probably damaging |
Het |
Osbpl5 |
G |
A |
7: 143,248,110 (GRCm39) |
H652Y |
probably damaging |
Het |
Parvb |
T |
C |
15: 84,182,192 (GRCm39) |
|
probably benign |
Het |
Pcdhb3 |
A |
C |
18: 37,436,375 (GRCm39) |
E780D |
probably benign |
Het |
Pik3c3 |
A |
G |
18: 30,456,639 (GRCm39) |
D723G |
possibly damaging |
Het |
Prkdc |
T |
C |
16: 15,612,958 (GRCm39) |
V3172A |
probably benign |
Het |
Psme4 |
G |
T |
11: 30,756,310 (GRCm39) |
W272L |
probably damaging |
Het |
Rem1 |
G |
A |
2: 152,476,455 (GRCm39) |
V238M |
probably damaging |
Het |
Rhobtb1 |
A |
C |
10: 69,108,601 (GRCm39) |
S434R |
probably benign |
Het |
Rhobtb1 |
G |
C |
10: 69,108,602 (GRCm39) |
S434T |
possibly damaging |
Het |
Rnf8 |
T |
C |
17: 29,853,735 (GRCm39) |
F413S |
probably damaging |
Het |
Rpn2 |
A |
G |
2: 157,156,888 (GRCm39) |
N497S |
probably damaging |
Het |
Rsbn1l |
G |
T |
5: 21,156,488 (GRCm39) |
P99Q |
probably benign |
Het |
Serpinb3b |
A |
T |
1: 107,083,164 (GRCm39) |
M246K |
probably benign |
Het |
Sgsm2 |
T |
C |
11: 74,787,652 (GRCm39) |
E19G |
probably null |
Het |
Shank1 |
A |
G |
7: 43,969,161 (GRCm39) |
H352R |
unknown |
Het |
Slc17a7 |
A |
G |
7: 44,819,728 (GRCm39) |
I177V |
probably benign |
Het |
Slc28a2 |
T |
A |
2: 122,281,494 (GRCm39) |
F228I |
probably damaging |
Het |
Slc35b4 |
C |
T |
6: 34,147,484 (GRCm39) |
V35I |
probably benign |
Het |
Slc38a1 |
T |
C |
15: 96,476,641 (GRCm39) |
I407V |
probably damaging |
Het |
Slc39a13 |
A |
G |
2: 90,893,442 (GRCm39) |
V326A |
probably damaging |
Het |
Slc44a5 |
T |
C |
3: 153,944,743 (GRCm39) |
L120P |
probably damaging |
Het |
Slfn3 |
T |
C |
11: 83,104,140 (GRCm39) |
I214T |
probably damaging |
Het |
Slitrk3 |
A |
C |
3: 72,957,024 (GRCm39) |
S583A |
probably benign |
Het |
Snx14 |
T |
C |
9: 88,297,728 (GRCm39) |
Y180C |
probably damaging |
Het |
Sorl1 |
T |
A |
9: 41,907,538 (GRCm39) |
K1483I |
probably benign |
Het |
Ssrp1 |
C |
A |
2: 84,871,104 (GRCm39) |
H247N |
probably damaging |
Het |
Stk39 |
A |
T |
2: 68,137,460 (GRCm39) |
|
probably benign |
Het |
Syde1 |
C |
T |
10: 78,421,530 (GRCm39) |
G674R |
probably damaging |
Het |
Tent4a |
A |
T |
13: 69,651,170 (GRCm39) |
I565N |
probably benign |
Het |
Themis3 |
G |
A |
17: 66,862,848 (GRCm39) |
S370L |
probably benign |
Het |
Tll1 |
T |
A |
8: 64,554,907 (GRCm39) |
N259Y |
probably damaging |
Het |
Tnip2 |
T |
G |
5: 34,661,175 (GRCm39) |
|
probably benign |
Het |
Top2b |
T |
C |
14: 16,409,823 (GRCm38) |
V830A |
probably benign |
Het |
Trpm8 |
T |
A |
1: 88,292,802 (GRCm39) |
N934K |
probably damaging |
Het |
Ttc14 |
A |
G |
3: 33,857,069 (GRCm39) |
Y179C |
probably damaging |
Het |
Ttn |
T |
G |
2: 76,573,965 (GRCm39) |
I17316L |
possibly damaging |
Het |
Tufm |
T |
C |
7: 126,086,871 (GRCm39) |
V52A |
probably benign |
Het |
Vamp8 |
T |
A |
6: 72,365,270 (GRCm39) |
N20I |
probably benign |
Het |
Vmn1r170 |
A |
T |
7: 23,306,288 (GRCm39) |
H230L |
probably benign |
Het |
Vmn2r50 |
T |
G |
7: 9,771,731 (GRCm39) |
T657P |
probably damaging |
Het |
Xirp2 |
G |
A |
2: 67,342,762 (GRCm39) |
G1668R |
probably benign |
Het |
Zik1 |
C |
A |
7: 10,224,311 (GRCm39) |
R262L |
possibly damaging |
Het |
Zscan25 |
T |
G |
5: 145,220,501 (GRCm39) |
Y99D |
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 |
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 |
R2112: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'- CACTTCCACTGAGGTTGAATTCCCC -3'
(R):5'- TTGGCAAGAGGATTAGAGCCCCTG -3'
Sequencing Primer
(F):5'- tgggaggcagaggcagg -3'
(R):5'- TGGCTCTGCCCATCCAG -3'
|
Posted On |
2014-05-14 |