Mutagenetix > Incidental Mutation

Incidental Mutation 'R0560:Ovgp1'

45822

Institutional Source

Beutler Lab

Gene Symbol

Ovgp1

Ensembl Gene

ENSMUSG00000074340

Gene Name

oviductal glycoprotein 1

Synonyms

oviductin, Chit5, OGP, muc9, MOGP, mucin 9

MMRRC Submission

038752-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0560 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

105881118-105894739 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 105893726 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000132424 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000000573] [ENSMUST00000163626]

AlphaFold

Q62010

Predicted Effect

unknown
Transcript: ENSMUST00000000573
AA Change: S500P

SMART Domains

Protein: ENSMUSP00000000573
Gene: ENSMUSG00000074340
AA Change: S500P

Domain	Start	End	E-Value	Type
low complexity region	4	13	N/A	INTRINSIC
Glyco_18	22	360	1.38e-134	SMART
low complexity region	486	515	N/A	INTRINSIC
low complexity region	533	626	N/A	INTRINSIC
low complexity region	637	648	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000092878

Predicted Effect

probably benign
Transcript: ENSMUST00000163626

SMART Domains

Protein: ENSMUSP00000132424
Gene: ENSMUSG00000074340

Domain	Start	End	E-Value	Type
Glyco_18	9	226	8.52e-21	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000167642

Meta Mutation Damage Score

0.0898

Coding Region Coverage

1x: 99.7%
3x: 99.0%
10x: 97.1%
20x: 94.5%

Validation Efficiency

100% (26/26)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a large, carbohydrate-rich, epithelial glycoprotein with numerous O-glycosylation sites located within threonine, serine, and proline-rich tandem repeats. The gene is similar to members of the mucin and the glycosyl hydrolase 18 gene families. Regulation of expression may be estrogen-dependent. Gene expression and protein secretion occur during late follicular development through early cleavage-stage embryonic development. The protein is secreted from non-ciliated oviductal epithelial cells and associates with ovulated oocytes, blastomeres, and spermatozoan acrosomal regions. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for disruptions in this gene show no phenotypic abnormalities. Female reproduction is essentially normal. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 26 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Apob	T	C	12: 8,055,101 (GRCm39)	Y1334H	probably damaging	Het
Arsb	A	G	13: 93,926,706 (GRCm39)	T159A	possibly damaging	Het
Asb18	A	C	1: 89,942,250 (GRCm39)	V17G	probably damaging	Het
Bicd1	A	G	6: 149,413,460 (GRCm39)	K284E	probably benign	Het
Bspry	A	G	4: 62,404,686 (GRCm39)	R161G	probably damaging	Het
Ccdc138	A	G	10: 58,411,539 (GRCm39)	T636A	probably damaging	Het
Cubn	A	T	2: 13,433,491 (GRCm39)	W1140R	probably damaging	Het
Cyp2t4	A	G	7: 26,857,936 (GRCm39)	T479A	probably damaging	Het
Dele1	T	A	18: 38,387,551 (GRCm39)	L230Q	probably damaging	Het
Dtx3l	A	G	16: 35,753,305 (GRCm39)	S434P	probably damaging	Het
Duox2	A	G	2: 122,122,035 (GRCm39)	V611A	probably benign	Het
Epb41l3	T	G	17: 69,581,892 (GRCm39)		probably null	Het
Fam161b	C	T	12: 84,404,492 (GRCm39)	D63N	probably damaging	Het
Gm5422	G	A	10: 31,125,240 (GRCm39)		noncoding transcript	Het
Gpr158	A	T	2: 21,830,085 (GRCm39)	D710V	probably damaging	Het
Krtcap2	T	C	3: 89,156,449 (GRCm39)		probably null	Het
Mtrf1	T	A	14: 79,644,290 (GRCm39)	D199E	probably damaging	Het
Myorg	G	A	4: 41,498,167 (GRCm39)	R488W	probably damaging	Het
Naip6	C	T	13: 100,437,108 (GRCm39)	A472T	probably benign	Het
Ncf2	T	A	1: 152,697,273 (GRCm39)	Y47N	probably damaging	Het
Siglec1	G	T	2: 130,912,266 (GRCm39)	T1692N	probably benign	Het
Slc10a2	T	C	8: 5,139,092 (GRCm39)	N284S	probably benign	Het
Slfn3	T	C	11: 83,103,978 (GRCm39)	F283S	probably damaging	Het
Trank1	T	C	9: 111,220,154 (GRCm39)	F2297S	possibly damaging	Het
Vmn2r69	A	G	7: 85,058,922 (GRCm39)		probably null	Het
Vps13d	T	C	4: 144,780,760 (GRCm39)	E3957G	probably damaging	Het

Other mutations in Ovgp1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00973:Ovgp1	APN	3	105,888,593 (GRCm39)	nonsense	probably null
IGL01152:Ovgp1	APN	3	105,893,488 (GRCm39)	missense	possibly damaging	0.94
IGL01458:Ovgp1	APN	3	105,882,307 (GRCm39)	missense	probably benign	0.01
IGL01646:Ovgp1	APN	3	105,885,665 (GRCm39)	missense	probably damaging	1.00
IGL01768:Ovgp1	APN	3	105,888,667 (GRCm39)	critical splice donor site	probably null
IGL02712:Ovgp1	APN	3	105,893,829 (GRCm39)	unclassified	probably benign
IGL03065:Ovgp1	APN	3	105,893,682 (GRCm39)	missense	probably benign	0.01
IGL03140:Ovgp1	APN	3	105,887,222 (GRCm39)	missense	probably damaging	1.00
IGL03272:Ovgp1	APN	3	105,888,641 (GRCm39)	missense	probably damaging	0.99
PIT4472001:Ovgp1	UTSW	3	105,894,306 (GRCm39)	missense	unknown
R0277:Ovgp1	UTSW	3	105,887,208 (GRCm39)	intron	probably benign
R0718:Ovgp1	UTSW	3	105,882,146 (GRCm39)	splice site	probably benign
R0743:Ovgp1	UTSW	3	105,882,248 (GRCm39)	missense	probably damaging	1.00
R1362:Ovgp1	UTSW	3	105,893,891 (GRCm39)	unclassified	probably benign
R1556:Ovgp1	UTSW	3	105,894,068 (GRCm39)	unclassified	probably benign
R1776:Ovgp1	UTSW	3	105,885,114 (GRCm39)	missense	possibly damaging	0.52
R1831:Ovgp1	UTSW	3	105,892,384 (GRCm39)	missense	probably benign	0.04
R1986:Ovgp1	UTSW	3	105,882,251 (GRCm39)	missense	probably damaging	1.00
R2004:Ovgp1	UTSW	3	105,894,309 (GRCm39)	unclassified	probably benign
R2156:Ovgp1	UTSW	3	105,885,033 (GRCm39)	missense	possibly damaging	0.49
R2254:Ovgp1	UTSW	3	105,894,228 (GRCm39)	unclassified	probably benign
R2860:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R2861:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R3117:Ovgp1	UTSW	3	105,893,768 (GRCm39)	unclassified	probably benign
R3793:Ovgp1	UTSW	3	105,887,487 (GRCm39)	missense	probably benign	0.03
R3835:Ovgp1	UTSW	3	105,893,631 (GRCm39)	missense	probably benign	0.00
R3894:Ovgp1	UTSW	3	105,893,912 (GRCm39)	unclassified	probably benign
R3894:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R3895:Ovgp1	UTSW	3	105,893,912 (GRCm39)	unclassified	probably benign
R4050:Ovgp1	UTSW	3	105,893,912 (GRCm39)	unclassified	probably benign
R4050:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R4467:Ovgp1	UTSW	3	105,885,027 (GRCm39)	missense	probably benign	0.04
R4611:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R4628:Ovgp1	UTSW	3	105,887,639 (GRCm39)	splice site	probably null
R4738:Ovgp1	UTSW	3	105,887,234 (GRCm39)	missense	probably damaging	1.00
R4944:Ovgp1	UTSW	3	105,887,269 (GRCm39)	missense	possibly damaging	0.66
R5110:Ovgp1	UTSW	3	105,885,099 (GRCm39)	missense	probably damaging	1.00
R6531:Ovgp1	UTSW	3	105,894,387 (GRCm39)	unclassified	probably benign
R6540:Ovgp1	UTSW	3	105,893,897 (GRCm39)	nonsense	probably null
R6562:Ovgp1	UTSW	3	105,887,589 (GRCm39)	missense	probably damaging	1.00
R6601:Ovgp1	UTSW	3	105,893,747 (GRCm39)	unclassified	probably benign
R6906:Ovgp1	UTSW	3	105,894,189 (GRCm39)	unclassified	probably benign
R7313:Ovgp1	UTSW	3	105,894,387 (GRCm39)	missense	unknown
R7430:Ovgp1	UTSW	3	105,893,619 (GRCm39)	missense	possibly damaging	0.62
R7430:Ovgp1	UTSW	3	105,893,618 (GRCm39)	missense	probably damaging	0.99
R7566:Ovgp1	UTSW	3	105,881,626 (GRCm39)	start gained	probably benign
R7684:Ovgp1	UTSW	3	105,887,272 (GRCm39)	missense	probably damaging	0.99
R7805:Ovgp1	UTSW	3	105,894,110 (GRCm39)	missense	unknown
R7820:Ovgp1	UTSW	3	105,893,837 (GRCm39)	unclassified	probably benign
R7919:Ovgp1	UTSW	3	105,888,601 (GRCm39)	missense	probably damaging	1.00
R8039:Ovgp1	UTSW	3	105,883,339 (GRCm39)	missense	probably benign	0.26
R8483:Ovgp1	UTSW	3	105,894,311 (GRCm39)	unclassified	probably benign
R9259:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R9261:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R9262:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R9359:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R9389:Ovgp1	UTSW	3	105,893,841 (GRCm39)	unclassified	probably benign
R9390:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R9444:Ovgp1	UTSW	3	105,893,841 (GRCm39)	unclassified	probably benign
R9445:Ovgp1	UTSW	3	105,893,883 (GRCm39)	unclassified	probably benign
R9466:Ovgp1	UTSW	3	105,887,484 (GRCm39)	missense
R9586:Ovgp1	UTSW	3	105,881,138 (GRCm39)	missense	probably damaging	0.96
Z1177:Ovgp1	UTSW	3	105,894,156 (GRCm39)	missense	unknown

Predicted Primers

PCR Primer
(F):5'- TGGATCTGTAACCCCTGGAGGAAC -3'
(R):5'- ATGCCAGTGGTGGTCTGAGAAATG -3'

Sequencing Primer
(F):5'- GAGGAACAGCATCTCCTCG -3'
(R):5'- TGGTGATCTTAGAAACCCCAGTG -3'

Posted On

2013-06-11