Mutagenetix > Incidental Mutation

Incidental Mutation 'R7449:Otogl'

577576

Institutional Source

Beutler Lab

Gene Symbol

Otogl

Ensembl Gene

ENSMUSG00000091455

Gene Name

otogelin-like

Synonyms

Gm6924

MMRRC Submission

045524-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R7449 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

107760531-107912134 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 107803663 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Cysteine to Arginine at position 1363 (C1363R)

Ref Sequence

ENSEMBL: ENSMUSP00000129467 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000165341]

AlphaFold

F7A4A7

Predicted Effect

probably damaging
Transcript: ENSMUST00000165341
AA Change: C1363R

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000129467
Gene: ENSMUSG00000091455
AA Change: C1363R

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: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.0%

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: 73 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca16	T	A	7: 120,435,908 (GRCm38)	Y306N	possibly damaging	Het
Adgrv1	A	T	13: 81,499,073 (GRCm38)	V3116D	probably damaging	Het
Adssl1	A	T	12: 112,634,151 (GRCm38)	T185S	probably damaging	Het
Ago2	G	A	15: 73,146,499 (GRCm38)	P30L	probably damaging	Het
Atp5j	C	T	16: 84,831,363 (GRCm38)	V44M	probably benign	Het
Atp7b	T	A	8: 22,011,849 (GRCm38)	I833F	probably damaging	Het
Birc6	T	A	17: 74,702,341 (GRCm38)	N4869K	probably benign	Het
Cacna1c	C	T	6: 118,602,349 (GRCm38)	D1796N		Het
Ccng2	C	G	5: 93,273,343 (GRCm38)	S237R	probably benign	Het
Cnga1	A	G	5: 72,605,304 (GRCm38)	I289T	probably benign	Het
Crybg1	C	A	10: 44,004,519 (GRCm38)	E224D	probably benign	Het
Dysf	T	C	6: 84,137,380 (GRCm38)	L1217P	possibly damaging	Het
Ebf2	T	A	14: 67,410,020 (GRCm38)	N339K	probably damaging	Het
Eva1c	T	C	16: 90,876,193 (GRCm38)		probably null	Het
Fam172a	A	G	13: 77,759,442 (GRCm38)	I41V	probably damaging	Het
Fam184a	T	C	10: 53,698,634 (GRCm38)	E293G	probably damaging	Het
Folh1	G	A	7: 86,731,748 (GRCm38)	P506S	probably benign	Het
Ftcd	A	T	10: 76,580,163 (GRCm38)	K210N	probably benign	Het
Gdf6	T	A	4: 9,844,494 (GRCm38)	V6D	possibly damaging	Het
Ghitm	C	A	14: 37,131,581 (GRCm38)	G101C	probably damaging	Het
Gimap5	T	A	6: 48,752,904 (GRCm38)	V136D	probably damaging	Het
Gm9745	T	A	13: 8,943,304 (GRCm38)	H51L	probably damaging	Het
Grm4	C	T	17: 27,435,371 (GRCm38)	G535D	probably damaging	Het
Gse1	T	C	8: 120,229,711 (GRCm38)	S314P	unknown	Het
Hnrnpdl	A	G	5: 100,037,155 (GRCm38)	I279T	probably damaging	Het
Itpr1	T	C	6: 108,389,384 (GRCm38)	S923P	probably damaging	Het
Krt39	C	A	11: 99,518,061 (GRCm38)	C303F	probably benign	Het
Lrrn1	T	C	6: 107,568,521 (GRCm38)	S427P	possibly damaging	Het
Lrrn3	T	A	12: 41,453,488 (GRCm38)	R277W	probably damaging	Het
Ltb4r1	T	C	14: 55,767,918 (GRCm38)	L226P	probably damaging	Het
Map1b	C	T	13: 99,508,140 (GRCm38)	R85Q	probably damaging	Het
Mcoln1	T	C	8: 3,507,285 (GRCm38)	L125P	probably damaging	Het
Nid1	T	G	13: 13,482,051 (GRCm38)	V589G	probably damaging	Het
Nlrp5	T	G	7: 23,417,526 (GRCm38)	F225C	probably benign	Het
Notch3	C	T	17: 32,157,966 (GRCm38)	A322T	probably damaging	Het
Olfr299	A	G	7: 86,465,855 (GRCm38)	H148R	probably benign	Het
Olfr69	G	T	7: 103,767,819 (GRCm38)	Q193K	probably benign	Het
Olfr854	T	A	9: 19,566,866 (GRCm38)	T173S	probably benign	Het
Ovol1	T	A	19: 5,553,597 (GRCm38)	D92V	probably benign	Het
Pigt	T	C	2: 164,502,499 (GRCm38)	L356P	probably damaging	Het
Plekhg3	A	G	12: 76,566,222 (GRCm38)	Q434R	probably damaging	Het
Plekhh1	T	C	12: 79,079,552 (GRCm38)	F1344L	probably benign	Het
Psmd3	T	A	11: 98,695,551 (GRCm38)	L515Q	probably damaging	Het
Pus1	A	G	5: 110,774,586 (GRCm38)	L405P	probably damaging	Het
Qtrt2	T	A	16: 43,881,032 (GRCm38)	H55L	probably benign	Het
Rasgrp1	T	C	2: 117,287,943 (GRCm38)	I522V	probably damaging	Het
Raver2	T	A	4: 101,102,663 (GRCm38)	H113Q	probably damaging	Het
Recql4	T	C	15: 76,705,565 (GRCm38)	D760G	unknown	Het
Rhobtb3	C	T	13: 75,910,741 (GRCm38)	V313M	probably benign	Het
Rhox4d	G	A	X: 37,518,992 (GRCm38)	G191E	unknown	Het
Rictor	C	T	15: 6,772,154 (GRCm38)	S441L	probably benign	Het
Rnf185	T	C	11: 3,426,578 (GRCm38)	Q135R	probably benign	Het
Sema3f	T	C	9: 107,684,036 (GRCm38)	S584G	probably damaging	Het
Sh3pxd2a	T	A	19: 47,267,652 (GRCm38)	T904S	probably benign	Het
Slc4a10	T	C	2: 62,303,946 (GRCm38)	V1002A	probably benign	Het
Taf1b	T	C	12: 24,504,993 (GRCm38)	I55T	probably benign	Het
Tchh	CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC	CTCCGCCGGGAGCAAGAGCTCCGCCGGGAGCAAGAGTTCCGCCGGGAGCAAGAGCTCCGCC	3: 93,446,708 (GRCm38)		probably benign	Het
Tenm4	A	T	7: 96,874,213 (GRCm38)	D1654V	possibly damaging	Het
Tgfb1	G	A	7: 25,704,838 (GRCm38)	V357M	probably damaging	Het
Tnxb	C	T	17: 34,703,361 (GRCm38)	P2383S	possibly damaging	Het
Trpm1	A	T	7: 64,208,975 (GRCm38)	M382L	probably benign	Het
Trrap	A	G	5: 144,851,209 (GRCm38)	Y3516C	probably damaging	Het
Txnrd1	T	A	10: 82,885,233 (GRCm38)	Y494*	probably null	Het
Ubr2	C	T	17: 46,964,788 (GRCm38)	E811K	probably damaging	Het
Ubxn4	T	A	1: 128,244,543 (GRCm38)	F25I	possibly damaging	Het
Vmn2r117	A	G	17: 23,459,895 (GRCm38)	M785T	probably damaging	Het
Vmn2r99	G	A	17: 19,379,145 (GRCm38)	D364N	probably benign	Het
Vps45	C	A	3: 96,047,136 (GRCm38)		probably null	Het
Wdr25	A	C	12: 109,026,441 (GRCm38)	H426P	probably damaging	Het
Wdr83	A	T	8: 85,079,681 (GRCm38)	W136R	probably damaging	Het
Xylt1	A	C	7: 117,592,005 (GRCm38)	I343L	possibly damaging	Het
Znrd1as	A	G	17: 36,964,383 (GRCm38)	D16G	probably damaging	Het
Zscan4b	T	C	7: 10,904,058 (GRCm38)	Q53R	possibly damaging	Het

Other mutations in Otogl

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
H8562:Otogl	UTSW	10	107,910,956 (GRCm38)	missense	probably benign	0.00
R0084:Otogl	UTSW	10	107,901,341 (GRCm38)	missense	probably damaging	0.96
R0164:Otogl	UTSW	10	107,874,530 (GRCm38)	missense	probably damaging	0.97
R0164:Otogl	UTSW	10	107,874,530 (GRCm38)	missense	probably damaging	0.97
R0238:Otogl	UTSW	10	107,806,696 (GRCm38)	missense	probably damaging	0.98
R0238:Otogl	UTSW	10	107,806,696 (GRCm38)	missense	probably damaging	0.98
R0239:Otogl	UTSW	10	107,806,696 (GRCm38)	missense	probably damaging	0.98
R0239:Otogl	UTSW	10	107,806,696 (GRCm38)	missense	probably damaging	0.98
R0294:Otogl	UTSW	10	107,777,228 (GRCm38)	missense	probably damaging	1.00
R0360:Otogl	UTSW	10	107,770,650 (GRCm38)	splice site	probably benign
R0442:Otogl	UTSW	10	107,876,855 (GRCm38)	missense	probably damaging	1.00
R0488:Otogl	UTSW	10	107,803,605 (GRCm38)	missense	probably benign	0.02
R0507:Otogl	UTSW	10	107,866,740 (GRCm38)	missense	possibly damaging	0.51
R0573:Otogl	UTSW	10	107,780,988 (GRCm38)	missense	probably benign	0.00
R0581:Otogl	UTSW	10	107,789,040 (GRCm38)	missense	possibly damaging	0.79
R0613:Otogl	UTSW	10	107,817,070 (GRCm38)	missense	probably damaging	0.99
R0614:Otogl	UTSW	10	107,798,355 (GRCm38)	missense	probably benign	0.14
R0742:Otogl	UTSW	10	107,866,740 (GRCm38)	missense	possibly damaging	0.51
R0846:Otogl	UTSW	10	107,772,296 (GRCm38)	missense	probably benign	0.40
R1146:Otogl	UTSW	10	107,886,513 (GRCm38)	missense	probably damaging	1.00
R1146:Otogl	UTSW	10	107,886,513 (GRCm38)	missense	probably damaging	1.00
R1439:Otogl	UTSW	10	107,779,252 (GRCm38)	missense	probably benign	0.02
R1457:Otogl	UTSW	10	107,878,152 (GRCm38)	splice site	probably null
R1526:Otogl	UTSW	10	107,869,526 (GRCm38)	missense	probably damaging	1.00
R1662:Otogl	UTSW	10	107,798,357 (GRCm38)	missense	possibly damaging	0.84
R1664:Otogl	UTSW	10	107,806,576 (GRCm38)	missense	probably benign	0.00
R1667:Otogl	UTSW	10	107,813,965 (GRCm38)	nonsense	probably null
R1695:Otogl	UTSW	10	107,814,017 (GRCm38)	missense	probably damaging	0.99
R1731:Otogl	UTSW	10	107,817,111 (GRCm38)	missense	probably damaging	1.00
R1733:Otogl	UTSW	10	107,783,712 (GRCm38)	missense	possibly damaging	0.46
R1764:Otogl	UTSW	10	107,899,461 (GRCm38)	nonsense	probably null
R1824:Otogl	UTSW	10	107,779,831 (GRCm38)	missense	probably benign
R1850:Otogl	UTSW	10	107,878,064 (GRCm38)	missense	probably damaging	1.00
R1856:Otogl	UTSW	10	107,854,264 (GRCm38)	missense	possibly damaging	0.92
R1875:Otogl	UTSW	10	107,899,590 (GRCm38)	missense	probably damaging	1.00
R1938:Otogl	UTSW	10	107,777,575 (GRCm38)	missense	probably damaging	0.98
R1986:Otogl	UTSW	10	107,794,190 (GRCm38)	critical splice acceptor site	probably null
R2072:Otogl	UTSW	10	107,781,043 (GRCm38)	missense	probably damaging	1.00
R2117:Otogl	UTSW	10	107,858,918 (GRCm38)	missense	probably benign	0.06
R2219:Otogl	UTSW	10	107,856,977 (GRCm38)	missense	probably damaging	1.00
R2508:Otogl	UTSW	10	107,874,500 (GRCm38)	missense	probably damaging	0.99
R2883:Otogl	UTSW	10	107,768,981 (GRCm38)	missense	probably damaging	1.00
R2931:Otogl	UTSW	10	107,820,004 (GRCm38)	missense	possibly damaging	0.85
R3620:Otogl	UTSW	10	107,874,371 (GRCm38)	missense	probably damaging	0.99
R3621:Otogl	UTSW	10	107,874,371 (GRCm38)	missense	probably damaging	0.99
R3735:Otogl	UTSW	10	107,899,529 (GRCm38)	nonsense	probably null
R3812:Otogl	UTSW	10	107,899,471 (GRCm38)	missense	probably damaging	1.00
R3880:Otogl	UTSW	10	107,827,704 (GRCm38)	missense	probably damaging	0.96
R3958:Otogl	UTSW	10	107,821,925 (GRCm38)	missense	probably damaging	1.00
R4063:Otogl	UTSW	10	107,790,649 (GRCm38)	missense	probably benign	0.02
R4064:Otogl	UTSW	10	107,790,649 (GRCm38)	missense	probably benign	0.02
R4108:Otogl	UTSW	10	107,771,244 (GRCm38)	missense	probably benign	0.01
R4352:Otogl	UTSW	10	107,869,535 (GRCm38)	missense	probably damaging	1.00
R4526:Otogl	UTSW	10	107,886,980 (GRCm38)	missense	probably damaging	1.00
R4614:Otogl	UTSW	10	107,892,124 (GRCm38)	nonsense	probably null
R4703:Otogl	UTSW	10	107,821,924 (GRCm38)	missense	probably damaging	1.00
R4741:Otogl	UTSW	10	107,779,260 (GRCm38)	missense	probably benign	0.00
R4790:Otogl	UTSW	10	107,822,033 (GRCm38)	critical splice acceptor site	probably null
R4801:Otogl	UTSW	10	107,901,336 (GRCm38)	missense	probably damaging	1.00
R4802:Otogl	UTSW	10	107,901,336 (GRCm38)	missense	probably damaging	1.00
R4910:Otogl	UTSW	10	107,879,517 (GRCm38)	missense	probably benign	0.05
R4913:Otogl	UTSW	10	107,876,855 (GRCm38)	missense	probably damaging	0.98
R5238:Otogl	UTSW	10	107,768,973 (GRCm38)	missense	probably damaging	1.00
R5261:Otogl	UTSW	10	107,777,592 (GRCm38)	missense	probably benign	0.16
R5387:Otogl	UTSW	10	107,780,933 (GRCm38)	missense	probably benign	0.03
R5395:Otogl	UTSW	10	107,817,138 (GRCm38)	missense	probably benign	0.39
R5403:Otogl	UTSW	10	107,808,756 (GRCm38)	missense	probably benign	0.08
R5482:Otogl	UTSW	10	107,821,941 (GRCm38)	missense	probably damaging	0.99
R5547:Otogl	UTSW	10	107,782,048 (GRCm38)	missense	possibly damaging	0.55
R5611:Otogl	UTSW	10	107,786,769 (GRCm38)	missense	probably damaging	1.00
R5642:Otogl	UTSW	10	107,886,552 (GRCm38)	missense	probably benign	0.44
R5690:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R5711:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R5731:Otogl	UTSW	10	107,881,464 (GRCm38)	missense	probably damaging	0.98
R5743:Otogl	UTSW	10	107,857,001 (GRCm38)	missense	possibly damaging	0.67
R5782:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R5820:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R5897:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R6004:Otogl	UTSW	10	107,879,529 (GRCm38)	missense	probably damaging	1.00
R6145:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R6146:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R6147:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R6149:Otogl	UTSW	10	107,881,453 (GRCm38)	missense	probably benign	0.36
R6226:Otogl	UTSW	10	107,771,206 (GRCm38)	nonsense	probably null
R6283:Otogl	UTSW	10	107,790,500 (GRCm38)	missense	probably damaging	0.98
R6414:Otogl	UTSW	10	107,782,050 (GRCm38)	missense	probably damaging	1.00
R6604:Otogl	UTSW	10	107,822,034 (GRCm38)	splice site	probably null
R6634:Otogl	UTSW	10	107,862,304 (GRCm38)	missense	probably damaging	1.00
R6727:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R6755:Otogl	UTSW	10	107,853,303 (GRCm38)	nonsense	probably null
R6795:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R6797:Otogl	UTSW	10	107,777,117 (GRCm38)	synonymous	silent
R6864:Otogl	UTSW	10	107,827,806 (GRCm38)	missense	probably damaging	0.96
R6924:Otogl	UTSW	10	107,808,641 (GRCm38)	missense	probably damaging	1.00
R6967:Otogl	UTSW	10	107,814,050 (GRCm38)	missense	probably benign	0.01
R7000:Otogl	UTSW	10	107,779,831 (GRCm38)	missense	probably benign
R7075:Otogl	UTSW	10	107,778,929 (GRCm38)	missense	probably benign	0.16
R7122:Otogl	UTSW	10	107,866,654 (GRCm38)	missense	probably benign	0.08
R7176:Otogl	UTSW	10	107,778,911 (GRCm38)	missense	probably damaging	1.00
R7184:Otogl	UTSW	10	107,763,200 (GRCm38)	missense	probably damaging	1.00
R7199:Otogl	UTSW	10	107,874,533 (GRCm38)	missense	possibly damaging	0.88
R7252:Otogl	UTSW	10	107,821,943 (GRCm38)	missense	probably benign	0.06
R7286:Otogl	UTSW	10	107,770,610 (GRCm38)	missense	probably benign	0.00
R7373:Otogl	UTSW	10	107,901,251 (GRCm38)	missense	probably damaging	1.00
R7486:Otogl	UTSW	10	107,821,988 (GRCm38)	missense	probably damaging	1.00
R7493:Otogl	UTSW	10	107,886,982 (GRCm38)	missense	probably benign	0.06
R7659:Otogl	UTSW	10	107,777,120 (GRCm38)	missense	probably benign	0.19
R7732:Otogl	UTSW	10	107,806,664 (GRCm38)	missense	probably benign	0.01
R7754:Otogl	UTSW	10	107,869,546 (GRCm38)	missense	probably damaging	0.99
R7757:Otogl	UTSW	10	107,876,921 (GRCm38)	missense	probably damaging	1.00
R7800:Otogl	UTSW	10	107,886,515 (GRCm38)	missense	probably damaging	0.99
R7864:Otogl	UTSW	10	107,869,567 (GRCm38)	missense	probably damaging	1.00
R7879:Otogl	UTSW	10	107,777,109 (GRCm38)	missense	probably benign	0.00
R7941:Otogl	UTSW	10	107,806,802 (GRCm38)	splice site	probably null
R7956:Otogl	UTSW	10	107,878,026 (GRCm38)	missense	possibly damaging	0.62
R7988:Otogl	UTSW	10	107,895,776 (GRCm38)	missense	probably damaging	1.00
R8057:Otogl	UTSW	10	107,808,615 (GRCm38)	missense	probably benign	0.00
R8058:Otogl	UTSW	10	107,762,426 (GRCm38)	missense	probably damaging	1.00
R8127:Otogl	UTSW	10	107,895,752 (GRCm38)	missense	probably damaging	1.00
R8143:Otogl	UTSW	10	107,806,666 (GRCm38)	missense	probably damaging	1.00
R8310:Otogl	UTSW	10	107,777,600 (GRCm38)	missense	possibly damaging	0.94
R8319:Otogl	UTSW	10	107,853,266 (GRCm38)	critical splice donor site	probably null
R8339:Otogl	UTSW	10	107,789,536 (GRCm38)	missense	probably benign	0.34
R8339:Otogl	UTSW	10	107,789,535 (GRCm38)	missense	probably damaging	0.99
R8394:Otogl	UTSW	10	107,886,465 (GRCm38)	critical splice donor site	probably null
R8428:Otogl	UTSW	10	107,798,736 (GRCm38)	missense	probably damaging	1.00
R8444:Otogl	UTSW	10	107,857,114 (GRCm38)	missense	probably benign	0.01
R8501:Otogl	UTSW	10	107,790,560 (GRCm38)	missense	probably benign
R8503:Otogl	UTSW	10	107,892,126 (GRCm38)	missense	probably damaging	1.00
R8680:Otogl	UTSW	10	107,912,075 (GRCm38)	critical splice donor site	probably null
R9025:Otogl	UTSW	10	107,777,571 (GRCm38)	missense	probably damaging	0.99
R9090:Otogl	UTSW	10	107,817,113 (GRCm38)	missense	probably null	0.99
R9223:Otogl	UTSW	10	107,854,344 (GRCm38)	missense	probably damaging	0.99
R9268:Otogl	UTSW	10	107,781,056 (GRCm38)	missense	probably damaging	1.00
R9271:Otogl	UTSW	10	107,817,113 (GRCm38)	missense	probably null	0.99
R9356:Otogl	UTSW	10	107,782,029 (GRCm38)	missense	probably damaging	1.00
R9484:Otogl	UTSW	10	107,901,295 (GRCm38)	missense	probably damaging	1.00
R9484:Otogl	UTSW	10	107,822,033 (GRCm38)	critical splice acceptor site	probably null
R9571:Otogl	UTSW	10	107,762,503 (GRCm38)	missense	possibly damaging	0.94
R9731:Otogl	UTSW	10	107,899,467 (GRCm38)	missense	probably damaging	1.00
X0065:Otogl	UTSW	10	107,895,782 (GRCm38)	missense	probably damaging	1.00
X0067:Otogl	UTSW	10	107,866,677 (GRCm38)	missense	probably damaging	1.00
Z1176:Otogl	UTSW	10	107,778,873 (GRCm38)	missense	probably damaging	0.97
Z1176:Otogl	UTSW	10	107,777,213 (GRCm38)	missense	probably benign
Z1176:Otogl	UTSW	10	107,789,032 (GRCm38)	missense	probably benign	0.00
Z1177:Otogl	UTSW	10	107,853,397 (GRCm38)	missense	possibly damaging	0.78
Z1177:Otogl	UTSW	10	107,763,258 (GRCm38)	nonsense	probably null
Z1177:Otogl	UTSW	10	107,876,903 (GRCm38)	missense	probably benign	0.14

Predicted Primers

PCR Primer
(F):5'- CCCATAGGTTAGCATGTGGAAC -3'
(R):5'- TGACACTTTTACCCGGCAG -3'

Sequencing Primer
(F):5'- GCATGTGGAACAAACAGATTTTTGG -3'
(R):5'- GACACTTTTACCCGGCAGTCTTG -3'

Posted On

2019-10-07