Incidental Mutation 'R1938:Otogl'
ID |
213716 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Otogl
|
Ensembl Gene |
ENSMUSG00000091455 |
Gene Name |
otogelin-like |
Synonyms |
Gm6924 |
MMRRC Submission |
039956-MU
|
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
R1938 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
10 |
Chromosomal Location |
107596392-107747995 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 107613436 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Tyrosine to Asparagine
at position 2010
(Y2010N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000129467
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000165341]
|
AlphaFold |
F7A4A7 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000165341
AA Change: Y2010N
PolyPhen 2
Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
|
SMART Domains |
Protein: ENSMUSP00000129467 Gene: ENSMUSG00000091455 AA Change: Y2010N
Domain | Start | End | E-Value | Type |
signal peptide
|
1 |
22 |
N/A |
INTRINSIC |
EGF_like
|
71 |
101 |
3.36e1 |
SMART |
VWD
|
104 |
264 |
4.74e-29 |
SMART |
C8
|
305 |
378 |
6.13e-6 |
SMART |
VWD
|
463 |
625 |
7e-41 |
SMART |
C8
|
668 |
733 |
3.6e-3 |
SMART |
Pfam:TIL
|
736 |
791 |
2.3e-11 |
PFAM |
SCOP:d1coua_
|
833 |
911 |
1e-6 |
SMART |
VWD
|
928 |
1085 |
1.29e-30 |
SMART |
C8
|
1120 |
1194 |
1.81e-26 |
SMART |
Pfam:AbfB
|
1230 |
1350 |
1.2e-10 |
PFAM |
Pfam:TIL
|
1364 |
1418 |
6.1e-8 |
PFAM |
VWD
|
1497 |
1671 |
2.34e-10 |
SMART |
C8
|
1705 |
1775 |
9.56e-17 |
SMART |
Pfam:TIL
|
1778 |
1836 |
1.6e-8 |
PFAM |
low complexity region
|
1870 |
1886 |
N/A |
INTRINSIC |
CT
|
2242 |
2325 |
6.9e-14 |
SMART |
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 96.9%
- 10x: 95.4%
- 20x: 92.8%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene belongs to the otogelin family. This gene is expressed in the inner ear of vertebrates with the highest level of expression seen at the embryonic stage and lowest in adult. Knockdown studies in zebrafish suggest that this gene is essential for normal inner ear function. Mutations in this gene are associated with autosomal recessive deafness. [provided by RefSeq, Dec 2012]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 133 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc8 |
T |
C |
7: 45,824,795 (GRCm39) |
K134R |
possibly damaging |
Het |
Adamts17 |
T |
C |
7: 66,774,820 (GRCm39) |
S980P |
probably damaging |
Het |
Adap2 |
T |
A |
11: 80,061,508 (GRCm39) |
I221K |
probably damaging |
Het |
Adgrv1 |
C |
T |
13: 81,539,876 (GRCm39) |
R5681Q |
probably damaging |
Het |
Adipor1 |
T |
A |
1: 134,350,841 (GRCm39) |
L30Q |
probably benign |
Het |
Agpat5 |
A |
G |
8: 18,928,181 (GRCm39) |
T249A |
probably benign |
Het |
Agxt2 |
G |
T |
15: 10,392,021 (GRCm39) |
G329V |
probably damaging |
Het |
Ankrd28 |
A |
G |
14: 31,427,233 (GRCm39) |
V801A |
possibly damaging |
Het |
Ap1g2 |
A |
G |
14: 55,337,229 (GRCm39) |
V702A |
possibly damaging |
Het |
Arid3a |
A |
G |
10: 79,786,540 (GRCm39) |
Q429R |
probably damaging |
Het |
Arsb |
T |
A |
13: 93,998,658 (GRCm39) |
L322Q |
probably damaging |
Het |
Ash1l |
A |
G |
3: 88,891,729 (GRCm39) |
T1203A |
probably damaging |
Het |
Atad2 |
T |
A |
15: 57,960,101 (GRCm39) |
N1308Y |
possibly damaging |
Het |
Atp10b |
A |
T |
11: 43,121,245 (GRCm39) |
R969S |
probably benign |
Het |
Bmp10 |
T |
C |
6: 87,410,702 (GRCm39) |
I165T |
possibly damaging |
Het |
Ccdc121rt2 |
C |
A |
5: 112,597,667 (GRCm39) |
C71* |
probably null |
Het |
Ccne1 |
A |
G |
7: 37,805,702 (GRCm39) |
|
probably null |
Het |
Cenpe |
A |
G |
3: 134,953,240 (GRCm39) |
N1565D |
probably damaging |
Het |
Chd1 |
A |
T |
17: 15,982,748 (GRCm39) |
E1404D |
probably benign |
Het |
Chd7 |
G |
A |
4: 8,847,200 (GRCm39) |
E1648K |
probably damaging |
Het |
Chodl |
T |
C |
16: 78,738,314 (GRCm39) |
I94T |
possibly damaging |
Het |
Chsy3 |
T |
C |
18: 59,542,584 (GRCm39) |
F574S |
probably damaging |
Het |
Clpb |
A |
T |
7: 101,412,863 (GRCm39) |
I317F |
probably damaging |
Het |
Cnga3 |
T |
A |
1: 37,300,954 (GRCm39) |
V558D |
possibly damaging |
Het |
Col9a1 |
C |
T |
1: 24,261,554 (GRCm39) |
P573S |
probably damaging |
Het |
Crat |
A |
T |
2: 30,303,073 (GRCm39) |
D71E |
probably benign |
Het |
Cspg4 |
A |
G |
9: 56,794,385 (GRCm39) |
T707A |
probably benign |
Het |
Ctsr |
T |
A |
13: 61,310,259 (GRCm39) |
R132S |
probably benign |
Het |
Ctu2 |
T |
C |
8: 123,206,024 (GRCm39) |
L255P |
probably damaging |
Het |
Cyp2c69 |
T |
C |
19: 39,837,810 (GRCm39) |
Y424C |
probably damaging |
Het |
Ddx27 |
A |
T |
2: 166,876,029 (GRCm39) |
K726N |
probably damaging |
Het |
Dennd4a |
A |
G |
9: 64,749,772 (GRCm39) |
Q121R |
probably damaging |
Het |
Dis3 |
A |
G |
14: 99,335,026 (GRCm39) |
F192S |
probably benign |
Het |
Ect2l |
C |
T |
10: 18,020,383 (GRCm39) |
S487N |
probably benign |
Het |
Eml1 |
T |
A |
12: 108,487,655 (GRCm39) |
F524L |
possibly damaging |
Het |
Espl1 |
T |
C |
15: 102,213,477 (GRCm39) |
I601T |
probably benign |
Het |
Fbxo40 |
C |
A |
16: 36,789,713 (GRCm39) |
V466L |
probably damaging |
Het |
Frmpd1 |
C |
T |
4: 45,283,711 (GRCm39) |
T844M |
probably damaging |
Het |
Frs2 |
T |
A |
10: 116,917,011 (GRCm39) |
|
probably benign |
Het |
Fuom |
G |
T |
7: 139,679,521 (GRCm39) |
T133K |
probably benign |
Het |
Garnl3 |
T |
A |
2: 32,895,212 (GRCm39) |
H619L |
probably damaging |
Het |
Gm4861 |
G |
T |
3: 137,257,876 (GRCm39) |
N36K |
unknown |
Het |
Gps2 |
G |
T |
11: 69,806,195 (GRCm39) |
M153I |
probably benign |
Het |
Gtf2ird1 |
A |
G |
5: 134,444,099 (GRCm39) |
V52A |
probably damaging |
Het |
Gtpbp8 |
A |
T |
16: 44,565,785 (GRCm39) |
D137E |
probably benign |
Het |
Haus4 |
A |
G |
14: 54,781,733 (GRCm39) |
C213R |
probably damaging |
Het |
Hdc |
T |
A |
2: 126,448,317 (GRCm39) |
H142L |
possibly damaging |
Het |
Hephl1 |
T |
C |
9: 14,965,283 (GRCm39) |
D1069G |
possibly damaging |
Het |
Herc6 |
T |
A |
6: 57,602,926 (GRCm39) |
V535D |
probably damaging |
Het |
Hipk3 |
A |
T |
2: 104,260,533 (GRCm39) |
H1082Q |
possibly damaging |
Het |
Hps5 |
A |
T |
7: 46,422,691 (GRCm39) |
V513D |
probably damaging |
Het |
Ifna13 |
T |
A |
4: 88,562,412 (GRCm39) |
I71F |
probably damaging |
Het |
Il1rl2 |
T |
C |
1: 40,402,484 (GRCm39) |
I426T |
probably damaging |
Het |
Irf5 |
A |
T |
6: 29,536,738 (GRCm39) |
D483V |
probably benign |
Het |
Jakmip3 |
A |
G |
7: 138,621,867 (GRCm39) |
R256G |
probably damaging |
Het |
Jazf1 |
T |
C |
6: 52,754,600 (GRCm39) |
I159V |
probably damaging |
Het |
Kmo |
A |
G |
1: 175,479,154 (GRCm39) |
D230G |
possibly damaging |
Het |
Lrrc74b |
A |
G |
16: 17,371,058 (GRCm39) |
V213A |
probably benign |
Het |
LTO1 |
A |
G |
7: 144,470,205 (GRCm39) |
S45G |
probably damaging |
Het |
Ly6g5b |
T |
C |
17: 35,333,704 (GRCm39) |
D36G |
possibly damaging |
Het |
Mab21l4 |
T |
C |
1: 93,079,730 (GRCm39) |
*453W |
probably null |
Het |
Macc1 |
T |
G |
12: 119,409,466 (GRCm39) |
L78R |
probably damaging |
Het |
Mettl4 |
A |
T |
17: 95,055,285 (GRCm39) |
D51E |
possibly damaging |
Het |
Mfap1a |
G |
A |
2: 121,332,835 (GRCm39) |
L199F |
possibly damaging |
Het |
Mmp17 |
G |
T |
5: 129,679,190 (GRCm39) |
R363L |
probably damaging |
Het |
Mrc1 |
G |
A |
2: 14,324,052 (GRCm39) |
A1130T |
possibly damaging |
Het |
Mrpl15 |
C |
T |
1: 4,847,805 (GRCm39) |
A165T |
probably damaging |
Het |
Mrpl45 |
G |
A |
11: 97,206,770 (GRCm39) |
|
probably null |
Het |
Ms4a3 |
C |
T |
19: 11,613,204 (GRCm39) |
A85T |
possibly damaging |
Het |
Mttp |
A |
T |
3: 137,830,882 (GRCm39) |
D77E |
probably benign |
Het |
Muc6 |
A |
G |
7: 141,217,011 (GRCm39) |
L2489P |
probably damaging |
Het |
Myl3 |
G |
A |
9: 110,595,802 (GRCm39) |
E100K |
probably damaging |
Het |
Nbea |
T |
A |
3: 55,992,743 (GRCm39) |
N288Y |
probably damaging |
Het |
Ncoa7 |
A |
G |
10: 30,574,166 (GRCm39) |
V181A |
probably benign |
Het |
Oat |
C |
T |
7: 132,159,934 (GRCm39) |
V429M |
probably benign |
Het |
Or2ak6 |
A |
T |
11: 58,593,449 (GRCm39) |
*307C |
probably null |
Het |
Or4x6 |
T |
G |
2: 89,949,427 (GRCm39) |
I172L |
probably damaging |
Het |
Or5d36 |
A |
T |
2: 87,901,300 (GRCm39) |
L142Q |
probably damaging |
Het |
Or5p80 |
T |
C |
7: 108,230,045 (GRCm39) |
I282T |
probably benign |
Het |
Or5w19 |
G |
A |
2: 87,698,805 (GRCm39) |
V157I |
probably benign |
Het |
Or6b13 |
A |
G |
7: 139,782,144 (GRCm39) |
F180L |
probably benign |
Het |
Or6c69b |
T |
A |
10: 129,626,759 (GRCm39) |
K233M |
probably damaging |
Het |
Or8b55 |
A |
G |
9: 38,727,146 (GRCm39) |
T116A |
probably benign |
Het |
Or8s16 |
T |
A |
15: 98,211,261 (GRCm39) |
M57L |
probably damaging |
Het |
Otof |
A |
G |
5: 30,533,713 (GRCm39) |
S1464P |
probably benign |
Het |
Pgap3 |
C |
T |
11: 98,291,040 (GRCm39) |
|
probably null |
Het |
Pgbd5 |
T |
A |
8: 125,100,988 (GRCm39) |
K332* |
probably null |
Het |
Pgs1 |
C |
T |
11: 117,896,553 (GRCm39) |
P410L |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,363,434 (GRCm39) |
S618N |
probably benign |
Het |
Plcb1 |
A |
T |
2: 135,228,222 (GRCm39) |
D1073V |
probably damaging |
Het |
Pola2 |
T |
A |
19: 6,001,208 (GRCm39) |
T309S |
probably benign |
Het |
Polg2 |
T |
A |
11: 106,669,787 (GRCm39) |
H161L |
probably damaging |
Het |
Postn |
T |
A |
3: 54,285,033 (GRCm39) |
|
probably null |
Het |
Ppt1 |
G |
T |
4: 122,739,784 (GRCm39) |
C128F |
probably damaging |
Het |
Ptpn12 |
G |
A |
5: 21,198,261 (GRCm39) |
P678S |
probably damaging |
Het |
Rcan3 |
A |
T |
4: 135,139,812 (GRCm39) |
|
probably null |
Het |
Rgs22 |
T |
C |
15: 36,101,950 (GRCm39) |
N216S |
probably benign |
Het |
Rgs7bp |
T |
A |
13: 105,088,090 (GRCm39) |
D228V |
probably damaging |
Het |
Rhobtb2 |
A |
T |
14: 70,034,062 (GRCm39) |
S388T |
probably benign |
Het |
Rnps1 |
C |
T |
17: 24,639,364 (GRCm39) |
R138C |
unknown |
Het |
Rpl38 |
T |
C |
11: 114,562,602 (GRCm39) |
V36A |
probably benign |
Het |
Rps7 |
G |
T |
12: 28,681,752 (GRCm39) |
H126Q |
possibly damaging |
Het |
Sec24b |
G |
T |
3: 129,785,010 (GRCm39) |
Q999K |
possibly damaging |
Het |
Slc19a3 |
A |
G |
1: 82,997,089 (GRCm39) |
V373A |
possibly damaging |
Het |
Spats2l |
T |
A |
1: 57,924,941 (GRCm39) |
V113E |
probably benign |
Het |
Ss18l1 |
A |
T |
2: 179,705,138 (GRCm39) |
T377S |
unknown |
Het |
Surf1 |
A |
G |
2: 26,805,982 (GRCm39) |
F38L |
probably benign |
Het |
Ticrr |
G |
A |
7: 79,325,142 (GRCm39) |
R556H |
probably damaging |
Het |
Tmem184b |
A |
G |
15: 79,250,014 (GRCm39) |
S254P |
probably damaging |
Het |
Tnfrsf4 |
G |
T |
4: 156,100,692 (GRCm39) |
R237L |
possibly damaging |
Het |
Tnk2 |
C |
A |
16: 32,482,560 (GRCm39) |
|
probably benign |
Het |
Tnks |
A |
T |
8: 35,305,684 (GRCm39) |
D1191E |
probably damaging |
Het |
Tnr |
C |
A |
1: 159,722,607 (GRCm39) |
Y1017* |
probably null |
Het |
Tomm34 |
A |
G |
2: 163,902,926 (GRCm39) |
I128T |
probably benign |
Het |
Trim2 |
G |
A |
3: 84,085,099 (GRCm39) |
S540F |
possibly damaging |
Het |
Trio |
A |
T |
15: 27,732,977 (GRCm39) |
I2968N |
probably damaging |
Het |
Ttc24 |
T |
C |
3: 87,982,181 (GRCm39) |
E17G |
probably benign |
Het |
Ttc41 |
A |
G |
10: 86,612,078 (GRCm39) |
H1117R |
probably benign |
Het |
Ttn |
A |
T |
2: 76,565,752 (GRCm39) |
V28200D |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,592,730 (GRCm39) |
S20801T |
possibly damaging |
Het |
Ube3d |
C |
T |
9: 86,330,840 (GRCm39) |
C114Y |
probably damaging |
Het |
Ugt2b37 |
A |
C |
5: 87,388,716 (GRCm39) |
L499R |
probably damaging |
Het |
Vmn1r81 |
T |
C |
7: 11,994,589 (GRCm39) |
I6M |
possibly damaging |
Het |
Vmn2r97 |
A |
T |
17: 19,149,593 (GRCm39) |
Y327F |
probably benign |
Het |
Vps13b |
T |
C |
15: 35,709,653 (GRCm39) |
S1867P |
probably damaging |
Het |
Wdr11 |
T |
C |
7: 129,208,331 (GRCm39) |
V362A |
probably benign |
Het |
Zan |
T |
A |
5: 137,387,201 (GRCm39) |
M4951L |
unknown |
Het |
Zcwpw1 |
T |
A |
5: 137,809,884 (GRCm39) |
L337Q |
probably damaging |
Het |
Zfp2 |
A |
T |
11: 50,790,809 (GRCm39) |
D411E |
possibly damaging |
Het |
Zfp628 |
C |
T |
7: 4,923,767 (GRCm39) |
T663I |
probably benign |
Het |
Zfpm1 |
T |
A |
8: 123,061,663 (GRCm39) |
|
probably null |
Het |
Zfyve19 |
T |
C |
2: 119,041,693 (GRCm39) |
S87P |
probably benign |
Het |
Zswim9 |
T |
A |
7: 12,994,141 (GRCm39) |
K672* |
probably null |
Het |
|
Other mutations in Otogl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
H8562:Otogl
|
UTSW |
10 |
107,746,817 (GRCm39) |
missense |
probably benign |
0.00 |
R0084:Otogl
|
UTSW |
10 |
107,737,202 (GRCm39) |
missense |
probably damaging |
0.96 |
R0164:Otogl
|
UTSW |
10 |
107,710,391 (GRCm39) |
missense |
probably damaging |
0.97 |
R0164:Otogl
|
UTSW |
10 |
107,710,391 (GRCm39) |
missense |
probably damaging |
0.97 |
R0238:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0238:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0239:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0239:Otogl
|
UTSW |
10 |
107,642,557 (GRCm39) |
missense |
probably damaging |
0.98 |
R0294:Otogl
|
UTSW |
10 |
107,613,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R0360:Otogl
|
UTSW |
10 |
107,606,511 (GRCm39) |
splice site |
probably benign |
|
R0442:Otogl
|
UTSW |
10 |
107,712,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R0488:Otogl
|
UTSW |
10 |
107,639,466 (GRCm39) |
missense |
probably benign |
0.02 |
R0507:Otogl
|
UTSW |
10 |
107,702,601 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0573:Otogl
|
UTSW |
10 |
107,616,849 (GRCm39) |
missense |
probably benign |
0.00 |
R0581:Otogl
|
UTSW |
10 |
107,624,901 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0613:Otogl
|
UTSW |
10 |
107,652,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R0614:Otogl
|
UTSW |
10 |
107,634,216 (GRCm39) |
missense |
probably benign |
0.14 |
R0742:Otogl
|
UTSW |
10 |
107,702,601 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0846:Otogl
|
UTSW |
10 |
107,608,157 (GRCm39) |
missense |
probably benign |
0.40 |
R1146:Otogl
|
UTSW |
10 |
107,722,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1146:Otogl
|
UTSW |
10 |
107,722,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1439:Otogl
|
UTSW |
10 |
107,615,113 (GRCm39) |
missense |
probably benign |
0.02 |
R1457:Otogl
|
UTSW |
10 |
107,714,013 (GRCm39) |
splice site |
probably null |
|
R1526:Otogl
|
UTSW |
10 |
107,705,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R1662:Otogl
|
UTSW |
10 |
107,634,218 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1664:Otogl
|
UTSW |
10 |
107,642,437 (GRCm39) |
missense |
probably benign |
0.00 |
R1667:Otogl
|
UTSW |
10 |
107,649,826 (GRCm39) |
nonsense |
probably null |
|
R1695:Otogl
|
UTSW |
10 |
107,649,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R1731:Otogl
|
UTSW |
10 |
107,652,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1733:Otogl
|
UTSW |
10 |
107,619,573 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1764:Otogl
|
UTSW |
10 |
107,735,322 (GRCm39) |
nonsense |
probably null |
|
R1824:Otogl
|
UTSW |
10 |
107,615,692 (GRCm39) |
missense |
probably benign |
|
R1850:Otogl
|
UTSW |
10 |
107,713,925 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Otogl
|
UTSW |
10 |
107,690,125 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1875:Otogl
|
UTSW |
10 |
107,735,451 (GRCm39) |
missense |
probably damaging |
1.00 |
R1986:Otogl
|
UTSW |
10 |
107,630,051 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2072:Otogl
|
UTSW |
10 |
107,616,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Otogl
|
UTSW |
10 |
107,694,779 (GRCm39) |
missense |
probably benign |
0.06 |
R2219:Otogl
|
UTSW |
10 |
107,692,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R2508:Otogl
|
UTSW |
10 |
107,710,361 (GRCm39) |
missense |
probably damaging |
0.99 |
R2883:Otogl
|
UTSW |
10 |
107,604,842 (GRCm39) |
missense |
probably damaging |
1.00 |
R2931:Otogl
|
UTSW |
10 |
107,655,865 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3620:Otogl
|
UTSW |
10 |
107,710,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R3621:Otogl
|
UTSW |
10 |
107,710,232 (GRCm39) |
missense |
probably damaging |
0.99 |
R3735:Otogl
|
UTSW |
10 |
107,735,390 (GRCm39) |
nonsense |
probably null |
|
R3812:Otogl
|
UTSW |
10 |
107,735,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R3880:Otogl
|
UTSW |
10 |
107,663,565 (GRCm39) |
missense |
probably damaging |
0.96 |
R3958:Otogl
|
UTSW |
10 |
107,657,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R4063:Otogl
|
UTSW |
10 |
107,626,510 (GRCm39) |
missense |
probably benign |
0.02 |
R4064:Otogl
|
UTSW |
10 |
107,626,510 (GRCm39) |
missense |
probably benign |
0.02 |
R4108:Otogl
|
UTSW |
10 |
107,607,105 (GRCm39) |
missense |
probably benign |
0.01 |
R4352:Otogl
|
UTSW |
10 |
107,705,396 (GRCm39) |
missense |
probably damaging |
1.00 |
R4526:Otogl
|
UTSW |
10 |
107,722,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R4614:Otogl
|
UTSW |
10 |
107,727,985 (GRCm39) |
nonsense |
probably null |
|
R4703:Otogl
|
UTSW |
10 |
107,657,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R4741:Otogl
|
UTSW |
10 |
107,615,121 (GRCm39) |
missense |
probably benign |
0.00 |
R4790:Otogl
|
UTSW |
10 |
107,657,894 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4801:Otogl
|
UTSW |
10 |
107,737,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R4802:Otogl
|
UTSW |
10 |
107,737,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R4910:Otogl
|
UTSW |
10 |
107,715,378 (GRCm39) |
missense |
probably benign |
0.05 |
R4913:Otogl
|
UTSW |
10 |
107,712,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R5238:Otogl
|
UTSW |
10 |
107,604,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R5261:Otogl
|
UTSW |
10 |
107,613,453 (GRCm39) |
missense |
probably benign |
0.16 |
R5387:Otogl
|
UTSW |
10 |
107,616,794 (GRCm39) |
missense |
probably benign |
0.03 |
R5395:Otogl
|
UTSW |
10 |
107,652,999 (GRCm39) |
missense |
probably benign |
0.39 |
R5403:Otogl
|
UTSW |
10 |
107,644,617 (GRCm39) |
missense |
probably benign |
0.08 |
R5482:Otogl
|
UTSW |
10 |
107,657,802 (GRCm39) |
missense |
probably damaging |
0.99 |
R5547:Otogl
|
UTSW |
10 |
107,617,909 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5611:Otogl
|
UTSW |
10 |
107,622,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R5642:Otogl
|
UTSW |
10 |
107,722,413 (GRCm39) |
missense |
probably benign |
0.44 |
R5690:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5711:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5731:Otogl
|
UTSW |
10 |
107,717,325 (GRCm39) |
missense |
probably damaging |
0.98 |
R5743:Otogl
|
UTSW |
10 |
107,692,862 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5782:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5820:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R5897:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6004:Otogl
|
UTSW |
10 |
107,715,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R6145:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6146:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6147:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6149:Otogl
|
UTSW |
10 |
107,717,314 (GRCm39) |
missense |
probably benign |
0.36 |
R6226:Otogl
|
UTSW |
10 |
107,607,067 (GRCm39) |
nonsense |
probably null |
|
R6283:Otogl
|
UTSW |
10 |
107,626,361 (GRCm39) |
missense |
probably damaging |
0.98 |
R6414:Otogl
|
UTSW |
10 |
107,617,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R6604:Otogl
|
UTSW |
10 |
107,657,895 (GRCm39) |
splice site |
probably null |
|
R6634:Otogl
|
UTSW |
10 |
107,698,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R6727:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6755:Otogl
|
UTSW |
10 |
107,689,164 (GRCm39) |
nonsense |
probably null |
|
R6795:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6797:Otogl
|
UTSW |
10 |
107,612,978 (GRCm39) |
synonymous |
silent |
|
R6864:Otogl
|
UTSW |
10 |
107,663,667 (GRCm39) |
missense |
probably damaging |
0.96 |
R6924:Otogl
|
UTSW |
10 |
107,644,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Otogl
|
UTSW |
10 |
107,649,911 (GRCm39) |
missense |
probably benign |
0.01 |
R7000:Otogl
|
UTSW |
10 |
107,615,692 (GRCm39) |
missense |
probably benign |
|
R7075:Otogl
|
UTSW |
10 |
107,614,790 (GRCm39) |
missense |
probably benign |
0.16 |
R7122:Otogl
|
UTSW |
10 |
107,702,515 (GRCm39) |
missense |
probably benign |
0.08 |
R7176:Otogl
|
UTSW |
10 |
107,614,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R7184:Otogl
|
UTSW |
10 |
107,599,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Otogl
|
UTSW |
10 |
107,710,394 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7252:Otogl
|
UTSW |
10 |
107,657,804 (GRCm39) |
missense |
probably benign |
0.06 |
R7286:Otogl
|
UTSW |
10 |
107,606,471 (GRCm39) |
missense |
probably benign |
0.00 |
R7373:Otogl
|
UTSW |
10 |
107,737,112 (GRCm39) |
missense |
probably damaging |
1.00 |
R7449:Otogl
|
UTSW |
10 |
107,639,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R7486:Otogl
|
UTSW |
10 |
107,657,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R7493:Otogl
|
UTSW |
10 |
107,722,843 (GRCm39) |
missense |
probably benign |
0.06 |
R7659:Otogl
|
UTSW |
10 |
107,612,981 (GRCm39) |
missense |
probably benign |
0.19 |
R7732:Otogl
|
UTSW |
10 |
107,642,525 (GRCm39) |
missense |
probably benign |
0.01 |
R7754:Otogl
|
UTSW |
10 |
107,705,407 (GRCm39) |
missense |
probably damaging |
0.99 |
R7757:Otogl
|
UTSW |
10 |
107,712,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R7800:Otogl
|
UTSW |
10 |
107,722,376 (GRCm39) |
missense |
probably damaging |
0.99 |
R7864:Otogl
|
UTSW |
10 |
107,705,428 (GRCm39) |
missense |
probably damaging |
1.00 |
R7879:Otogl
|
UTSW |
10 |
107,612,970 (GRCm39) |
missense |
probably benign |
0.00 |
R7941:Otogl
|
UTSW |
10 |
107,642,663 (GRCm39) |
splice site |
probably null |
|
R7956:Otogl
|
UTSW |
10 |
107,713,887 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7988:Otogl
|
UTSW |
10 |
107,731,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R8057:Otogl
|
UTSW |
10 |
107,644,476 (GRCm39) |
missense |
probably benign |
0.00 |
R8058:Otogl
|
UTSW |
10 |
107,598,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R8127:Otogl
|
UTSW |
10 |
107,731,613 (GRCm39) |
missense |
probably damaging |
1.00 |
R8143:Otogl
|
UTSW |
10 |
107,642,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R8310:Otogl
|
UTSW |
10 |
107,613,461 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8319:Otogl
|
UTSW |
10 |
107,689,127 (GRCm39) |
critical splice donor site |
probably null |
|
R8339:Otogl
|
UTSW |
10 |
107,625,397 (GRCm39) |
missense |
probably benign |
0.34 |
R8339:Otogl
|
UTSW |
10 |
107,625,396 (GRCm39) |
missense |
probably damaging |
0.99 |
R8394:Otogl
|
UTSW |
10 |
107,722,326 (GRCm39) |
critical splice donor site |
probably null |
|
R8428:Otogl
|
UTSW |
10 |
107,634,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8444:Otogl
|
UTSW |
10 |
107,692,975 (GRCm39) |
missense |
probably benign |
0.01 |
R8501:Otogl
|
UTSW |
10 |
107,626,421 (GRCm39) |
missense |
probably benign |
|
R8503:Otogl
|
UTSW |
10 |
107,727,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R8680:Otogl
|
UTSW |
10 |
107,747,936 (GRCm39) |
critical splice donor site |
probably null |
|
R9025:Otogl
|
UTSW |
10 |
107,613,432 (GRCm39) |
missense |
probably damaging |
0.99 |
R9090:Otogl
|
UTSW |
10 |
107,652,974 (GRCm39) |
missense |
probably null |
0.99 |
R9223:Otogl
|
UTSW |
10 |
107,690,205 (GRCm39) |
missense |
probably damaging |
0.99 |
R9268:Otogl
|
UTSW |
10 |
107,616,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R9271:Otogl
|
UTSW |
10 |
107,652,974 (GRCm39) |
missense |
probably null |
0.99 |
R9356:Otogl
|
UTSW |
10 |
107,617,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Otogl
|
UTSW |
10 |
107,737,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R9484:Otogl
|
UTSW |
10 |
107,657,894 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9571:Otogl
|
UTSW |
10 |
107,598,364 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9731:Otogl
|
UTSW |
10 |
107,735,328 (GRCm39) |
missense |
probably damaging |
1.00 |
X0065:Otogl
|
UTSW |
10 |
107,731,643 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Otogl
|
UTSW |
10 |
107,702,538 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Otogl
|
UTSW |
10 |
107,614,734 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1176:Otogl
|
UTSW |
10 |
107,613,074 (GRCm39) |
missense |
probably benign |
|
Z1176:Otogl
|
UTSW |
10 |
107,624,893 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Otogl
|
UTSW |
10 |
107,689,258 (GRCm39) |
missense |
possibly damaging |
0.78 |
Z1177:Otogl
|
UTSW |
10 |
107,599,119 (GRCm39) |
nonsense |
probably null |
|
Z1177:Otogl
|
UTSW |
10 |
107,712,764 (GRCm39) |
missense |
probably benign |
0.14 |
|
Predicted Primers |
PCR Primer
(F):5'- AAGGCATGCAGGGTTTCTAGC -3'
(R):5'- GAGCTATGCATTATTTTCCTACGTC -3'
Sequencing Primer
(F):5'- ATGCAGGGTTTCTAGCTCCCAG -3'
(R):5'- ATGCATTATTTTCCTACGTCTCCAC -3'
|
Posted On |
2014-07-14 |