Mutagenetix > Incidental Mutation

Incidental Mutation 'R8124:Obox3'

652014

Institutional Source

Beutler Lab

Gene Symbol

Obox3

Ensembl Gene

ENSMUSG00000066772

Gene Name

oocyte specific homeobox 3

Synonyms

Ohx

MMRRC Submission

067553-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.152) question?

Stock #

R8124 (G1)

Quality Score

150.008

Status

Not validated

Chromosome

Chromosomal Location

15359231-15373702 bp(-) (GRCm39)

Type of Mutation

splice site (35745 bp from exon)

DNA Base Change (assembly)

A to T at 15323874 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000083291 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000086122]

AlphaFold

Q3UT54

Predicted Effect

probably null
Transcript: ENSMUST00000086122

SMART Domains

Protein: ENSMUSP00000083291
Gene: ENSMUSG00000066772

Domain	Start	End	E-Value	Type
HOX	94	156	1.84e-16	SMART

Coding Region Coverage

1x: 99.8%
3x: 99.6%
10x: 98.6%
20x: 94.5%

Validation Efficiency

98% (51/52)

Allele List at MGI

Other mutations in this stock

Total: 51 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Agap3	T	A	5: 24,683,128 (GRCm39)	I320N	probably benign	Het
Ahnak	G	A	19: 8,984,487 (GRCm39)	G1924S	probably damaging	Het
Ap2a2	G	A	7: 141,178,757 (GRCm39)	R141H	probably benign	Het
Atf7ip2	T	C	16: 10,026,999 (GRCm39)	V89A	possibly damaging	Het
Clpsl2	G	A	17: 28,769,702 (GRCm39)	G55R	probably damaging	Het
Csnk2a2	G	A	8: 96,182,575 (GRCm39)	P296L		Het
Dab2	T	A	15: 6,458,878 (GRCm39)	C263*	probably null	Het
Dao	AGG	AG	5: 114,153,270 (GRCm39)		probably benign	Het
Ddx60	C	T	8: 62,436,945 (GRCm39)	A965V	probably benign	Het
Dennd5a	A	T	7: 109,497,142 (GRCm39)	I1119N	probably damaging	Het
Dpy30	A	G	17: 74,623,099 (GRCm39)		probably benign	Het
Epg5	G	A	18: 78,008,211 (GRCm39)	A780T	probably benign	Het
Etl4	A	G	2: 20,811,451 (GRCm39)	D1546G	probably benign	Het
Evl	C	T	12: 108,647,783 (GRCm39)	R295*	probably null	Het
F13a1	T	C	13: 37,209,779 (GRCm39)	K62R	probably damaging	Het
Gm2832	T	C	14: 41,000,894 (GRCm39)	M44T		Het
Gm9195	T	C	14: 72,680,063 (GRCm39)	I2249V	probably benign	Het
Hmcn2	T	C	2: 31,290,136 (GRCm39)	V2323A	probably benign	Het
Ice2	T	A	9: 69,307,777 (GRCm39)	N20K	probably damaging	Het
Klf15	T	C	6: 90,443,863 (GRCm39)	F146S	probably damaging	Het
Lgi3	A	G	14: 70,772,178 (GRCm39)	Y241C	probably damaging	Het
Lig4	A	T	8: 10,022,954 (GRCm39)	D275E	probably damaging	Het
Lrit1	T	A	14: 36,784,005 (GRCm39)	S444R	probably benign	Het
Lrrc37	A	G	11: 103,511,257 (GRCm39)	V237A	unknown	Het
Mip	T	C	10: 128,062,070 (GRCm39)	V107A	possibly damaging	Het
Mtrex	A	C	13: 113,063,871 (GRCm39)	D7E	probably benign	Het
Myo15a	G	A	11: 60,398,279 (GRCm39)	V1581M		Het
Nckap1l	A	G	15: 103,382,248 (GRCm39)	D481G	possibly damaging	Het
Or11h4	C	T	14: 50,973,743 (GRCm39)	R292H	probably benign	Het
Or2d3	G	A	7: 106,491,088 (GRCm39)	T76I	possibly damaging	Het
Or5a21	T	A	19: 12,310,834 (GRCm39)	N129Y	probably damaging	Het
Or5p1	C	A	7: 107,916,984 (GRCm39)	N294K	possibly damaging	Het
Or8g27	T	C	9: 39,128,967 (GRCm39)	F105L	probably benign	Het
Pilrb2	T	A	5: 137,869,306 (GRCm39)	E98V	probably damaging	Het
Plekhm1	A	G	11: 103,257,775 (GRCm39)	V1053A	probably benign	Het
Prdm2	A	T	4: 142,861,835 (GRCm39)	V485E	probably damaging	Het
Riox2	G	A	16: 59,306,954 (GRCm39)	E282K	probably benign	Het
Rps6ka2	T	A	17: 7,549,228 (GRCm39)	V379E	possibly damaging	Het
Slc4a7	G	A	14: 14,729,211 (GRCm38)	E20K	possibly damaging	Het
Sned1	G	A	1: 93,210,711 (GRCm39)		probably null	Het
Spata3	C	T	1: 85,952,075 (GRCm39)	R110C	unknown	Het
St6gal1	G	A	16: 23,176,585 (GRCm39)	A393T	probably benign	Het
Tent4a	G	A	13: 69,681,716 (GRCm39)		probably benign	Het
Tmem132d	T	C	5: 127,869,624 (GRCm39)	Q570R	probably damaging	Het
Tmem87a	T	C	2: 120,222,676 (GRCm39)	T168A	probably benign	Het
Trank1	A	G	9: 111,207,995 (GRCm39)	R1747G	probably benign	Het
Txk	C	T	5: 72,860,606 (GRCm39)		probably null	Het
Vcan	T	A	13: 89,852,373 (GRCm39)	L862F	possibly damaging	Het
Wdr64	A	T	1: 175,626,844 (GRCm39)		probably null	Het
Zfp106	G	T	2: 120,354,812 (GRCm39)	Q1343K	probably benign	Het
Zfp719	A	G	7: 43,239,314 (GRCm39)	T301A	probably benign	Het

Other mutations in Obox3

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01943:Obox3	APN	7	15,360,777 (GRCm39)	missense	probably benign	0.00
IGL02601:Obox3	APN	7	15,360,848 (GRCm39)	missense	probably damaging	0.99
IGL02978:Obox3	APN	7	15,360,178 (GRCm39)	missense	probably benign	0.11
IGL03088:Obox3	APN	7	15,360,927 (GRCm39)	splice site	probably benign
IGL03178:Obox3	APN	7	15,361,202 (GRCm39)	missense	probably benign	0.12
IGL03219:Obox3	APN	7	15,359,803 (GRCm39)	missense	probably damaging	0.99
IGL03373:Obox3	APN	7	15,359,715 (GRCm39)	missense	probably benign	0.01
R0119:Obox3	UTSW	7	15,360,252 (GRCm39)	critical splice acceptor site	probably null
R1471:Obox3	UTSW	7	15,360,875 (GRCm39)	missense	probably benign	0.01
R3916:Obox3	UTSW	7	15,361,151 (GRCm39)	missense	probably benign	0.00
R4072:Obox3	UTSW	7	15,359,724 (GRCm39)	missense	possibly damaging	0.92
R4073:Obox3	UTSW	7	15,359,724 (GRCm39)	missense	possibly damaging	0.92
R4075:Obox3	UTSW	7	15,359,724 (GRCm39)	missense	possibly damaging	0.92
R4076:Obox3	UTSW	7	15,359,724 (GRCm39)	missense	possibly damaging	0.92
R4712:Obox3	UTSW	7	15,360,764 (GRCm39)	missense	probably benign	0.04
R4751:Obox3	UTSW	7	15,359,617 (GRCm39)	critical splice donor site	probably null
R4868:Obox3	UTSW	7	15,361,235 (GRCm39)	missense	probably damaging	1.00
R5151:Obox3	UTSW	7	15,360,173 (GRCm39)	missense	probably damaging	1.00
R5290:Obox3	UTSW	7	15,360,774 (GRCm39)	missense	probably benign	0.03
R5399:Obox3	UTSW	7	15,360,213 (GRCm39)	missense	probably benign	0.00
R5882:Obox3	UTSW	7	15,360,893 (GRCm39)	missense	probably benign	0.17
R6147:Obox3	UTSW	7	15,359,926 (GRCm39)	missense	probably damaging	0.99
R6378:Obox3	UTSW	7	15,360,027 (GRCm39)	missense	probably benign	0.00
R7221:Obox3	UTSW	7	15,359,983 (GRCm39)	missense	probably benign	0.01
R7314:Obox3	UTSW	7	15,361,079 (GRCm39)	missense	possibly damaging	0.50
R8711:Obox3	UTSW	7	15,360,148 (GRCm39)	missense	probably benign	0.44
R8825:Obox3	UTSW	7	15,361,226 (GRCm39)	missense	possibly damaging	0.94
Z1176:Obox3	UTSW	7	15,360,149 (GRCm39)	missense	probably benign	0.16

Predicted Primers

PCR Primer
(F):5'- AGAGTCCTCTAGTGACCCCAAC -3'
(R):5'- TCAGTAATGCCAGTGCCTTC -3'

Sequencing Primer
(F):5'- CACGTCCACTGCAATCAAGTCATTC -3'
(R):5'- GGTTCTGGCACTGATGAAAATG -3'

Posted On

2020-09-23