Incidental Mutation 'R1572:Nin'
ID |
170880 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Nin
|
Ensembl Gene |
ENSMUSG00000021068 |
Gene Name |
ninein |
Synonyms |
3110068G20Rik |
MMRRC Submission |
039611-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1572 (G1)
|
Quality Score |
225 |
Status
|
Validated
|
Chromosome |
12 |
Chromosomal Location |
70058209-70160491 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 70085524 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Valine to Aspartic acid
at position 1569
(V1569D)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000152350
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000021468]
[ENSMUST00000085314]
[ENSMUST00000095666]
[ENSMUST00000169074]
[ENSMUST00000220689]
[ENSMUST00000222237]
[ENSMUST00000222835]
[ENSMUST00000223257]
|
AlphaFold |
Q61043 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000021468
AA Change: V1569D
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000021468 Gene: ENSMUSG00000021068 AA Change: V1569D
Domain | Start | End | E-Value | Type |
internal_repeat_1
|
7 |
67 |
7.83e-8 |
PROSPERO |
low complexity region
|
97 |
108 |
N/A |
INTRINSIC |
low complexity region
|
115 |
132 |
N/A |
INTRINSIC |
internal_repeat_1
|
181 |
242 |
7.83e-8 |
PROSPERO |
low complexity region
|
276 |
289 |
N/A |
INTRINSIC |
low complexity region
|
336 |
353 |
N/A |
INTRINSIC |
coiled coil region
|
358 |
570 |
N/A |
INTRINSIC |
coiled coil region
|
625 |
802 |
N/A |
INTRINSIC |
coiled coil region
|
834 |
926 |
N/A |
INTRINSIC |
coiled coil region
|
957 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1035 |
1044 |
N/A |
INTRINSIC |
low complexity region
|
1047 |
1057 |
N/A |
INTRINSIC |
coiled coil region
|
1069 |
1094 |
N/A |
INTRINSIC |
coiled coil region
|
1178 |
1325 |
N/A |
INTRINSIC |
low complexity region
|
1374 |
1385 |
N/A |
INTRINSIC |
coiled coil region
|
1425 |
1806 |
N/A |
INTRINSIC |
coiled coil region
|
1980 |
2013 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000085314
AA Change: V1569D
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000082422 Gene: ENSMUSG00000021068 AA Change: V1569D
Domain | Start | End | E-Value | Type |
internal_repeat_1
|
7 |
67 |
4.15e-8 |
PROSPERO |
low complexity region
|
97 |
108 |
N/A |
INTRINSIC |
low complexity region
|
115 |
132 |
N/A |
INTRINSIC |
internal_repeat_1
|
181 |
242 |
4.15e-8 |
PROSPERO |
low complexity region
|
276 |
289 |
N/A |
INTRINSIC |
low complexity region
|
336 |
353 |
N/A |
INTRINSIC |
coiled coil region
|
358 |
570 |
N/A |
INTRINSIC |
coiled coil region
|
625 |
802 |
N/A |
INTRINSIC |
coiled coil region
|
834 |
926 |
N/A |
INTRINSIC |
coiled coil region
|
957 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1035 |
1044 |
N/A |
INTRINSIC |
low complexity region
|
1047 |
1057 |
N/A |
INTRINSIC |
coiled coil region
|
1069 |
1094 |
N/A |
INTRINSIC |
coiled coil region
|
1178 |
1325 |
N/A |
INTRINSIC |
low complexity region
|
1374 |
1385 |
N/A |
INTRINSIC |
coiled coil region
|
1425 |
1806 |
N/A |
INTRINSIC |
coiled coil region
|
1971 |
2045 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000095666
AA Change: V1569D
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000093327 Gene: ENSMUSG00000021068 AA Change: V1569D
Domain | Start | End | E-Value | Type |
internal_repeat_1
|
7 |
67 |
7.83e-8 |
PROSPERO |
low complexity region
|
97 |
108 |
N/A |
INTRINSIC |
low complexity region
|
115 |
132 |
N/A |
INTRINSIC |
internal_repeat_1
|
181 |
242 |
7.83e-8 |
PROSPERO |
low complexity region
|
276 |
289 |
N/A |
INTRINSIC |
low complexity region
|
336 |
353 |
N/A |
INTRINSIC |
coiled coil region
|
358 |
570 |
N/A |
INTRINSIC |
coiled coil region
|
625 |
802 |
N/A |
INTRINSIC |
coiled coil region
|
834 |
926 |
N/A |
INTRINSIC |
coiled coil region
|
957 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1035 |
1044 |
N/A |
INTRINSIC |
low complexity region
|
1047 |
1057 |
N/A |
INTRINSIC |
coiled coil region
|
1069 |
1094 |
N/A |
INTRINSIC |
coiled coil region
|
1178 |
1325 |
N/A |
INTRINSIC |
low complexity region
|
1374 |
1385 |
N/A |
INTRINSIC |
coiled coil region
|
1425 |
1806 |
N/A |
INTRINSIC |
coiled coil region
|
1980 |
2013 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000169074
AA Change: V1569D
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000129648 Gene: ENSMUSG00000021068 AA Change: V1569D
Domain | Start | End | E-Value | Type |
internal_repeat_1
|
7 |
67 |
7.83e-8 |
PROSPERO |
low complexity region
|
97 |
108 |
N/A |
INTRINSIC |
low complexity region
|
115 |
132 |
N/A |
INTRINSIC |
internal_repeat_1
|
181 |
242 |
7.83e-8 |
PROSPERO |
low complexity region
|
276 |
289 |
N/A |
INTRINSIC |
low complexity region
|
336 |
353 |
N/A |
INTRINSIC |
coiled coil region
|
358 |
570 |
N/A |
INTRINSIC |
coiled coil region
|
625 |
802 |
N/A |
INTRINSIC |
coiled coil region
|
834 |
926 |
N/A |
INTRINSIC |
coiled coil region
|
957 |
1008 |
N/A |
INTRINSIC |
low complexity region
|
1035 |
1044 |
N/A |
INTRINSIC |
low complexity region
|
1047 |
1057 |
N/A |
INTRINSIC |
coiled coil region
|
1069 |
1094 |
N/A |
INTRINSIC |
coiled coil region
|
1178 |
1325 |
N/A |
INTRINSIC |
low complexity region
|
1374 |
1385 |
N/A |
INTRINSIC |
coiled coil region
|
1425 |
1806 |
N/A |
INTRINSIC |
coiled coil region
|
1980 |
2013 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000220689
AA Change: V862D
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000221486
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000222237
AA Change: V1569D
PolyPhen 2
Score 0.988 (Sensitivity: 0.73; Specificity: 0.96)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000222835
AA Change: V862D
PolyPhen 2
Score 0.787 (Sensitivity: 0.85; Specificity: 0.93)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000223257
AA Change: V1569D
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223469
|
Meta Mutation Damage Score |
0.6467 |
Coding Region Coverage |
- 1x: 98.7%
- 3x: 97.5%
- 10x: 92.9%
- 20x: 80.7%
|
Validation Efficiency |
97% (130/134) |
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes one of the proteins important for centrosomal function. This protein is important for positioning and anchoring the microtubules minus-ends in epithelial cells. Localization of this protein to the centrosome requires three leucine zippers in the central coiled-coil domain. Multiple alternatively spliced transcript variants that encode different isoforms have been reported. [provided by RefSeq, Jul 2008]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 112 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310030G06Rik |
G |
A |
9: 50,651,973 (GRCm39) |
T85M |
probably damaging |
Het |
Actn1 |
A |
G |
12: 80,219,731 (GRCm39) |
|
probably benign |
Het |
Afap1l1 |
A |
T |
18: 61,870,570 (GRCm39) |
S603T |
probably damaging |
Het |
Ahcy |
T |
C |
2: 154,910,851 (GRCm39) |
Y39C |
probably benign |
Het |
Ankmy2 |
T |
C |
12: 36,236,941 (GRCm39) |
|
probably null |
Het |
Anxa13 |
A |
T |
15: 58,220,655 (GRCm39) |
|
noncoding transcript |
Het |
Aoc1 |
T |
C |
6: 48,882,720 (GRCm39) |
S221P |
possibly damaging |
Het |
Arhgef10 |
C |
A |
8: 15,041,211 (GRCm39) |
A770D |
possibly damaging |
Het |
Arhgef19 |
A |
G |
4: 140,982,065 (GRCm39) |
D707G |
probably benign |
Het |
Arhgef3 |
G |
A |
14: 27,123,692 (GRCm39) |
R444H |
probably damaging |
Het |
Asphd1 |
T |
C |
7: 126,548,271 (GRCm39) |
I11V |
probably benign |
Het |
Atp2b1 |
A |
G |
10: 98,830,537 (GRCm39) |
M333V |
probably benign |
Het |
BC051665 |
T |
C |
13: 60,932,841 (GRCm39) |
Y40C |
probably damaging |
Het |
Ccdc87 |
T |
A |
19: 4,890,341 (GRCm39) |
S278T |
probably benign |
Het |
Ccn3 |
T |
A |
15: 54,612,648 (GRCm39) |
M219K |
possibly damaging |
Het |
Cdcp3 |
T |
A |
7: 130,846,560 (GRCm39) |
Y777* |
probably null |
Het |
Chaf1b |
G |
A |
16: 93,698,118 (GRCm39) |
G463D |
possibly damaging |
Het |
Chrna4 |
T |
C |
2: 180,671,100 (GRCm39) |
T219A |
possibly damaging |
Het |
Clcnkb |
T |
G |
4: 141,134,406 (GRCm39) |
T584P |
possibly damaging |
Het |
Clptm1l |
T |
C |
13: 73,755,866 (GRCm39) |
S161P |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,230,777 (GRCm39) |
E1437G |
possibly damaging |
Het |
Col13a1 |
A |
T |
10: 61,702,205 (GRCm39) |
|
probably null |
Het |
Col3a1 |
T |
C |
1: 45,385,128 (GRCm39) |
S82P |
possibly damaging |
Het |
Cpeb3 |
A |
T |
19: 37,116,482 (GRCm39) |
M383K |
probably benign |
Het |
Cr2 |
T |
A |
1: 194,845,622 (GRCm39) |
H111L |
probably damaging |
Het |
Cttnbp2 |
T |
C |
6: 18,375,974 (GRCm39) |
S1522G |
possibly damaging |
Het |
Cul3 |
T |
C |
1: 80,260,506 (GRCm39) |
D281G |
possibly damaging |
Het |
Cyp2c70 |
T |
G |
19: 40,172,426 (GRCm39) |
K72T |
probably benign |
Het |
Cyp39a1 |
A |
T |
17: 43,991,020 (GRCm39) |
I110F |
probably damaging |
Het |
Cyp46a1 |
T |
A |
12: 108,318,198 (GRCm39) |
M203K |
probably null |
Het |
Cyp8b1 |
A |
T |
9: 121,744,024 (GRCm39) |
V436D |
possibly damaging |
Het |
Ddx17 |
T |
C |
15: 79,422,766 (GRCm39) |
D324G |
probably damaging |
Het |
Dop1b |
A |
G |
16: 93,567,041 (GRCm39) |
N1274S |
probably damaging |
Het |
Dscaml1 |
G |
A |
9: 45,632,631 (GRCm39) |
V1166I |
probably benign |
Het |
Dsp |
T |
C |
13: 38,379,714 (GRCm39) |
V1554A |
probably damaging |
Het |
Efr3a |
T |
A |
15: 65,726,641 (GRCm39) |
|
probably null |
Het |
Egfem1 |
A |
T |
3: 29,702,420 (GRCm39) |
N223I |
probably benign |
Het |
Egr2 |
T |
C |
10: 67,375,805 (GRCm39) |
S147P |
probably damaging |
Het |
Elmo3 |
A |
G |
8: 106,034,933 (GRCm39) |
T408A |
probably benign |
Het |
Flnb |
A |
G |
14: 7,883,908 (GRCm38) |
D378G |
probably damaging |
Het |
Foxj2 |
T |
A |
6: 122,810,220 (GRCm39) |
M193K |
probably benign |
Het |
Gm6327 |
A |
G |
16: 12,578,020 (GRCm39) |
|
noncoding transcript |
Het |
Gm7694 |
T |
C |
1: 170,130,335 (GRCm39) |
H21R |
probably benign |
Het |
Gpr107 |
A |
G |
2: 31,057,037 (GRCm39) |
D43G |
probably damaging |
Het |
Grid2 |
T |
A |
6: 64,406,678 (GRCm39) |
Y679* |
probably null |
Het |
Grin2c |
G |
A |
11: 115,146,900 (GRCm39) |
P432S |
possibly damaging |
Het |
H2-M10.1 |
A |
G |
17: 36,636,625 (GRCm39) |
F60L |
possibly damaging |
Het |
Hectd4 |
A |
G |
5: 121,439,941 (GRCm39) |
D1147G |
possibly damaging |
Het |
Idua |
G |
T |
5: 108,828,455 (GRCm39) |
A223S |
probably benign |
Het |
Ifi206 |
T |
C |
1: 173,314,419 (GRCm39) |
Q7R |
probably benign |
Het |
Itgad |
T |
A |
7: 127,802,406 (GRCm39) |
V986E |
probably damaging |
Het |
Itsn2 |
G |
A |
12: 4,700,044 (GRCm39) |
R670H |
probably benign |
Het |
Kdm4a |
T |
C |
4: 117,996,146 (GRCm39) |
E961G |
possibly damaging |
Het |
Klra5 |
T |
A |
6: 129,883,585 (GRCm39) |
I91L |
probably damaging |
Het |
Kntc1 |
A |
G |
5: 123,910,176 (GRCm39) |
T525A |
probably damaging |
Het |
Lct |
A |
G |
1: 128,221,932 (GRCm39) |
F1536L |
probably benign |
Het |
Lmod1 |
T |
A |
1: 135,291,671 (GRCm39) |
D175E |
probably benign |
Het |
Lonrf1 |
A |
C |
8: 36,701,126 (GRCm39) |
D361E |
probably benign |
Het |
Lrrc19 |
T |
C |
4: 94,526,666 (GRCm39) |
Y297C |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,873,431 (GRCm39) |
E1787G |
possibly damaging |
Het |
Mpp2 |
G |
A |
11: 101,951,374 (GRCm39) |
A452V |
probably benign |
Het |
Msh2 |
T |
C |
17: 88,026,080 (GRCm39) |
V686A |
possibly damaging |
Het |
Mthfd1 |
C |
T |
12: 76,317,193 (GRCm39) |
Q15* |
probably null |
Het |
Mtnr1b |
A |
T |
9: 15,774,438 (GRCm39) |
I207N |
probably damaging |
Het |
Nid2 |
A |
G |
14: 19,855,480 (GRCm39) |
T1207A |
probably benign |
Het |
Nrcam |
T |
A |
12: 44,584,147 (GRCm39) |
|
probably benign |
Het |
Nsd1 |
T |
A |
13: 55,394,782 (GRCm39) |
H897Q |
probably damaging |
Het |
Or10g9 |
A |
G |
9: 39,912,490 (GRCm39) |
F11S |
probably benign |
Het |
Or12d2 |
A |
T |
17: 37,624,371 (GRCm39) |
N301K |
probably benign |
Het |
Or2w2 |
T |
A |
13: 21,758,480 (GRCm39) |
I49F |
possibly damaging |
Het |
Or7d10 |
G |
T |
9: 19,832,208 (GRCm39) |
K234N |
probably benign |
Het |
Paip1 |
T |
C |
13: 119,588,320 (GRCm39) |
|
probably benign |
Het |
Pcnx3 |
G |
A |
19: 5,735,375 (GRCm39) |
R484* |
probably null |
Het |
Pdxk |
A |
G |
10: 78,283,814 (GRCm39) |
Y127H |
probably damaging |
Het |
Phf20 |
T |
A |
2: 156,129,754 (GRCm39) |
V442E |
probably benign |
Het |
Phlpp1 |
G |
A |
1: 106,320,519 (GRCm39) |
D1505N |
probably damaging |
Het |
Pkhd1 |
T |
C |
1: 20,417,664 (GRCm39) |
T2496A |
probably benign |
Het |
Pkhd1l1 |
A |
G |
15: 44,406,869 (GRCm39) |
T2369A |
probably benign |
Het |
Plod2 |
T |
A |
9: 92,485,120 (GRCm39) |
|
probably benign |
Het |
Pnpla7 |
T |
A |
2: 24,905,263 (GRCm39) |
M617K |
possibly damaging |
Het |
Ppp1r16a |
C |
T |
15: 76,577,869 (GRCm39) |
Q328* |
probably null |
Het |
Prkch |
T |
A |
12: 73,696,131 (GRCm39) |
|
probably null |
Het |
Prr12 |
G |
A |
7: 44,678,224 (GRCm39) |
H1974Y |
unknown |
Het |
Prr16 |
A |
G |
18: 51,436,042 (GRCm39) |
I174V |
probably benign |
Het |
Prss45 |
A |
T |
9: 110,667,497 (GRCm39) |
T39S |
probably benign |
Het |
Pum1 |
T |
A |
4: 130,445,515 (GRCm39) |
D161E |
probably damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,113 (GRCm39) |
D345G |
probably damaging |
Het |
Ralgapb |
A |
G |
2: 158,288,119 (GRCm39) |
|
probably benign |
Het |
Rasgrp3 |
A |
G |
17: 75,807,729 (GRCm39) |
H262R |
possibly damaging |
Het |
Rnf213 |
T |
A |
11: 119,327,437 (GRCm39) |
I1809N |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 28,761,616 (GRCm39) |
L3177P |
probably damaging |
Het |
Scyl2 |
C |
A |
10: 89,486,818 (GRCm39) |
R230L |
probably damaging |
Het |
Sfxn2 |
T |
C |
19: 46,570,915 (GRCm39) |
|
probably benign |
Het |
Slc18b1 |
T |
C |
10: 23,674,639 (GRCm39) |
|
probably benign |
Het |
Spata31d1d |
T |
C |
13: 59,876,005 (GRCm39) |
H510R |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,872,780 (GRCm39) |
N1109K |
probably damaging |
Het |
Styxl2 |
C |
T |
1: 165,927,024 (GRCm39) |
V863M |
possibly damaging |
Het |
Sult3a2 |
A |
G |
10: 33,657,973 (GRCm39) |
S47P |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,682,028 (GRCm39) |
N2518S |
possibly damaging |
Het |
Tex21 |
G |
T |
12: 76,253,665 (GRCm39) |
P416Q |
probably benign |
Het |
Tex38 |
T |
C |
4: 115,637,503 (GRCm39) |
N100S |
probably benign |
Het |
Thsd4 |
A |
C |
9: 60,301,836 (GRCm39) |
|
probably benign |
Het |
Ticrr |
T |
C |
7: 79,331,572 (GRCm39) |
V723A |
probably damaging |
Het |
Tmprss15 |
A |
G |
16: 78,887,717 (GRCm39) |
V30A |
probably benign |
Het |
Uba3 |
A |
G |
6: 97,162,298 (GRCm39) |
|
probably benign |
Het |
Ubr1 |
T |
C |
2: 120,765,800 (GRCm39) |
|
probably benign |
Het |
Uchl4 |
A |
T |
9: 64,143,013 (GRCm39) |
I165L |
probably benign |
Het |
Vmn2r112 |
A |
T |
17: 22,822,125 (GRCm39) |
T268S |
possibly damaging |
Het |
Wfdc3 |
T |
C |
2: 164,586,114 (GRCm39) |
|
probably benign |
Het |
Zfp282 |
T |
A |
6: 47,869,801 (GRCm39) |
L282Q |
probably damaging |
Het |
Zfp422 |
A |
T |
6: 116,603,745 (GRCm39) |
C85S |
probably damaging |
Het |
Zfp790 |
A |
T |
7: 29,527,564 (GRCm39) |
Q83L |
probably benign |
Het |
|
Other mutations in Nin |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00472:Nin
|
APN |
12 |
70,076,862 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00677:Nin
|
APN |
12 |
70,073,634 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00823:Nin
|
APN |
12 |
70,061,567 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01103:Nin
|
APN |
12 |
70,103,532 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01113:Nin
|
APN |
12 |
70,078,553 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01420:Nin
|
APN |
12 |
70,092,188 (GRCm39) |
missense |
probably benign |
0.08 |
IGL01556:Nin
|
APN |
12 |
70,089,962 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01663:Nin
|
APN |
12 |
70,090,439 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02002:Nin
|
APN |
12 |
70,109,473 (GRCm39) |
nonsense |
probably null |
|
IGL02030:Nin
|
APN |
12 |
70,092,042 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02202:Nin
|
APN |
12 |
70,102,210 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02207:Nin
|
APN |
12 |
70,103,431 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02257:Nin
|
APN |
12 |
70,149,465 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL02394:Nin
|
APN |
12 |
70,090,805 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02531:Nin
|
APN |
12 |
70,067,706 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03028:Nin
|
APN |
12 |
70,082,044 (GRCm39) |
missense |
probably benign |
0.13 |
IGL03155:Nin
|
APN |
12 |
70,078,544 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03197:Nin
|
APN |
12 |
70,073,584 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02835:Nin
|
UTSW |
12 |
70,103,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Nin
|
UTSW |
12 |
70,097,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R0131:Nin
|
UTSW |
12 |
70,097,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R0132:Nin
|
UTSW |
12 |
70,097,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Nin
|
UTSW |
12 |
70,061,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R0211:Nin
|
UTSW |
12 |
70,061,649 (GRCm39) |
missense |
probably damaging |
1.00 |
R0734:Nin
|
UTSW |
12 |
70,076,887 (GRCm39) |
missense |
probably benign |
0.01 |
R0947:Nin
|
UTSW |
12 |
70,107,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1085:Nin
|
UTSW |
12 |
70,067,736 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1367:Nin
|
UTSW |
12 |
70,090,703 (GRCm39) |
missense |
probably damaging |
0.99 |
R1452:Nin
|
UTSW |
12 |
70,064,424 (GRCm39) |
nonsense |
probably null |
|
R1477:Nin
|
UTSW |
12 |
70,090,958 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1518:Nin
|
UTSW |
12 |
70,061,547 (GRCm39) |
missense |
probably benign |
0.27 |
R1566:Nin
|
UTSW |
12 |
70,101,253 (GRCm39) |
missense |
probably damaging |
0.99 |
R1583:Nin
|
UTSW |
12 |
70,078,512 (GRCm39) |
missense |
probably benign |
|
R1584:Nin
|
UTSW |
12 |
70,089,443 (GRCm39) |
missense |
probably benign |
0.03 |
R1699:Nin
|
UTSW |
12 |
70,092,337 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1699:Nin
|
UTSW |
12 |
70,077,712 (GRCm39) |
missense |
probably benign |
0.40 |
R1765:Nin
|
UTSW |
12 |
70,089,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R1794:Nin
|
UTSW |
12 |
70,090,569 (GRCm39) |
nonsense |
probably null |
|
R1952:Nin
|
UTSW |
12 |
70,077,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R2004:Nin
|
UTSW |
12 |
70,072,251 (GRCm39) |
missense |
probably benign |
0.01 |
R2025:Nin
|
UTSW |
12 |
70,076,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R2060:Nin
|
UTSW |
12 |
70,089,192 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2213:Nin
|
UTSW |
12 |
70,092,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R2224:Nin
|
UTSW |
12 |
70,108,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R2247:Nin
|
UTSW |
12 |
70,101,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R2972:Nin
|
UTSW |
12 |
70,109,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R3776:Nin
|
UTSW |
12 |
70,085,456 (GRCm39) |
missense |
possibly damaging |
0.71 |
R3881:Nin
|
UTSW |
12 |
70,089,315 (GRCm39) |
missense |
probably benign |
0.00 |
R3930:Nin
|
UTSW |
12 |
70,125,016 (GRCm39) |
missense |
probably damaging |
1.00 |
R3959:Nin
|
UTSW |
12 |
70,097,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R4229:Nin
|
UTSW |
12 |
70,097,984 (GRCm39) |
missense |
probably damaging |
0.99 |
R4359:Nin
|
UTSW |
12 |
70,061,712 (GRCm39) |
missense |
probably benign |
0.00 |
R4423:Nin
|
UTSW |
12 |
70,089,752 (GRCm39) |
missense |
probably damaging |
1.00 |
R4461:Nin
|
UTSW |
12 |
70,089,359 (GRCm39) |
missense |
probably benign |
0.37 |
R4639:Nin
|
UTSW |
12 |
70,085,375 (GRCm39) |
missense |
probably damaging |
0.97 |
R4791:Nin
|
UTSW |
12 |
70,090,581 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4839:Nin
|
UTSW |
12 |
70,137,325 (GRCm39) |
missense |
possibly damaging |
0.46 |
R4912:Nin
|
UTSW |
12 |
70,090,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R5712:Nin
|
UTSW |
12 |
70,089,543 (GRCm39) |
missense |
probably damaging |
1.00 |
R5726:Nin
|
UTSW |
12 |
70,124,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R5804:Nin
|
UTSW |
12 |
70,092,375 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5874:Nin
|
UTSW |
12 |
70,077,692 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5992:Nin
|
UTSW |
12 |
70,092,298 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6077:Nin
|
UTSW |
12 |
70,066,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6184:Nin
|
UTSW |
12 |
70,090,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R6307:Nin
|
UTSW |
12 |
70,061,631 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6315:Nin
|
UTSW |
12 |
70,092,389 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Nin
|
UTSW |
12 |
70,091,955 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6492:Nin
|
UTSW |
12 |
70,101,308 (GRCm39) |
missense |
probably benign |
0.22 |
R6562:Nin
|
UTSW |
12 |
70,102,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6578:Nin
|
UTSW |
12 |
70,107,968 (GRCm39) |
missense |
probably damaging |
0.99 |
R6613:Nin
|
UTSW |
12 |
70,077,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R7112:Nin
|
UTSW |
12 |
70,149,573 (GRCm39) |
missense |
|
|
R7170:Nin
|
UTSW |
12 |
70,091,013 (GRCm39) |
missense |
|
|
R7324:Nin
|
UTSW |
12 |
70,090,508 (GRCm39) |
missense |
|
|
R7338:Nin
|
UTSW |
12 |
70,090,838 (GRCm39) |
missense |
|
|
R7372:Nin
|
UTSW |
12 |
70,102,803 (GRCm39) |
missense |
|
|
R7431:Nin
|
UTSW |
12 |
70,124,997 (GRCm39) |
missense |
|
|
R7577:Nin
|
UTSW |
12 |
70,109,480 (GRCm39) |
missense |
|
|
R7655:Nin
|
UTSW |
12 |
70,089,542 (GRCm39) |
missense |
|
|
R7656:Nin
|
UTSW |
12 |
70,089,542 (GRCm39) |
missense |
|
|
R7683:Nin
|
UTSW |
12 |
70,124,956 (GRCm39) |
missense |
|
|
R7769:Nin
|
UTSW |
12 |
70,090,004 (GRCm39) |
missense |
|
|
R7981:Nin
|
UTSW |
12 |
70,089,591 (GRCm39) |
missense |
|
|
R8138:Nin
|
UTSW |
12 |
70,089,672 (GRCm39) |
missense |
|
|
R8141:Nin
|
UTSW |
12 |
70,076,795 (GRCm39) |
missense |
|
|
R8754:Nin
|
UTSW |
12 |
70,077,787 (GRCm39) |
intron |
probably benign |
|
R8790:Nin
|
UTSW |
12 |
70,067,793 (GRCm39) |
missense |
|
|
R8899:Nin
|
UTSW |
12 |
70,077,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R8974:Nin
|
UTSW |
12 |
70,124,932 (GRCm39) |
missense |
|
|
R9085:Nin
|
UTSW |
12 |
70,076,786 (GRCm39) |
nonsense |
probably null |
|
R9143:Nin
|
UTSW |
12 |
70,137,349 (GRCm39) |
missense |
|
|
R9380:Nin
|
UTSW |
12 |
70,074,805 (GRCm39) |
missense |
|
|
R9496:Nin
|
UTSW |
12 |
70,102,762 (GRCm39) |
missense |
|
|
R9638:Nin
|
UTSW |
12 |
70,067,618 (GRCm39) |
missense |
|
|
R9709:Nin
|
UTSW |
12 |
70,149,468 (GRCm39) |
missense |
|
|
R9745:Nin
|
UTSW |
12 |
70,089,899 (GRCm39) |
missense |
|
|
R9792:Nin
|
UTSW |
12 |
70,094,009 (GRCm39) |
missense |
|
|
Z1176:Nin
|
UTSW |
12 |
70,095,938 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Nin
|
UTSW |
12 |
70,101,200 (GRCm39) |
missense |
|
|
Z1177:Nin
|
UTSW |
12 |
70,090,869 (GRCm39) |
missense |
|
|
|
Predicted Primers |
PCR Primer
(F):5'- CCTGACCTGCACTTTGTAGTGATCC -3'
(R):5'- ACCCCGTGGTCTGAGATTAACCTG -3'
Sequencing Primer
(F):5'- GCACTTTGTAGTGATCCAGTTC -3'
(R):5'- CTAGACGCAAGGCTGCC -3'
|
Posted On |
2014-04-13 |