Mutagenetix > Incidental Mutation

Incidental Mutation 'R7340:Oga'

569815

Institutional Source

Beutler Lab

Gene Symbol

Oga

Ensembl Gene

ENSMUSG00000025220

Gene Name

O-GlcNAcase

Synonyms

4833427O07Rik, 5830447M11Rik, Mgea5, 2810009A20Rik, Hy5

MMRRC Submission

045430-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7340 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

45738698-45772274 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to A at 45755895 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamine to Stop codon at position 583 (Q583*)

Ref Sequence

ENSEMBL: ENSMUSP00000026243 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000026243]

AlphaFold

Q9EQQ9

Predicted Effect

probably null
Transcript: ENSMUST00000026243
AA Change: Q583*

SMART Domains

Protein: ENSMUSP00000026243
Gene: ENSMUSG00000025220
AA Change: Q583*

Domain	Start	End	E-Value	Type
low complexity region	44	57	N/A	INTRINSIC
Pfam:NAGidase	62	361	2.5e-84	PFAM
low complexity region	453	458	N/A	INTRINSIC
PDB:4BMH\|A	700	915	1e-13	PDB
SCOP:d1cjwa_	715	916	1e-3	SMART

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.7%
20x: 99.1%

Validation Efficiency

99% (83/84)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The dynamic modification of cytoplasmic and nuclear proteins by O-linked N-acetylglucosamine (O-GlcNAc) addition and removal on serine and threonine residues is catalyzed by OGT (MIM 300255), which adds O-GlcNAc, and MGEA5, a glycosidase that removes O-GlcNAc modifications (Gao et al., 2001 [PubMed 11148210]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Mice homozygous for a gene-trapped allele exhibit perinatal lethality associated with a developmental delay and respiratory failure. Mouse embryonic fibroblasts exhibit proliferative and mitotic defects, frequent cytokinesis failure, and loss of genomic stability. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 83 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb11	C	T	2: 69,130,211 (GRCm39)	D282N	probably damaging	Het
Adam30	A	T	3: 98,069,637 (GRCm39)	N490I	probably benign	Het
Ankrd55	A	T	13: 112,492,497 (GRCm39)	I223F	probably damaging	Het
Ano8	T	A	8: 71,935,655 (GRCm39)	E321V	probably damaging	Het
Apc2	A	G	10: 80,149,316 (GRCm39)	K1457E	probably benign	Het
Asb15	T	A	6: 24,558,513 (GRCm39)	V38E	probably benign	Het
Atp4a	T	C	7: 30,416,155 (GRCm39)	S417P	possibly damaging	Het
AY358078	A	G	14: 52,063,716 (GRCm39)	N454S	probably damaging	Het
Cables2	A	G	2: 179,903,450 (GRCm39)	Y245H		Het
Cactin	CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG	CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG	10: 81,157,152 (GRCm39)		probably benign	Het
Camsap3	G	A	8: 3,637,960 (GRCm39)		probably null	Het
Ccdc178	A	T	18: 22,150,518 (GRCm39)	V705E	probably benign	Het
Ccdc47	T	C	11: 106,091,799 (GRCm39)	Q472R	possibly damaging	Het
Ccdc62	A	G	5: 124,089,283 (GRCm39)	D307G	probably damaging	Het
Cdcp3	A	G	7: 130,879,344 (GRCm39)	T1788A	unknown	Het
Cdh23	A	G	10: 60,366,775 (GRCm39)	I235T	probably benign	Het
Cep89	G	A	7: 35,129,353 (GRCm39)	R630H	probably damaging	Het
Cfap65	T	C	1: 74,960,742 (GRCm39)	N743D	probably benign	Het
Cimap1b	T	A	15: 89,262,610 (GRCm39)	T116S	probably benign	Het
Clec16a	A	G	16: 10,398,827 (GRCm39)	N329S	probably null	Het
Col25a1	A	G	3: 130,340,006 (GRCm39)		probably null	Het
Daam1	T	G	12: 72,035,713 (GRCm39)	D969E	probably benign	Het
Dntt	A	C	19: 41,047,004 (GRCm39)		probably null	Het
Dsel	C	T	1: 111,789,303 (GRCm39)	G411S	probably damaging	Het
Dst	T	A	1: 34,229,810 (GRCm39)	Y2468N	probably benign	Het
Exosc9	A	G	3: 36,615,297 (GRCm39)	T262A	possibly damaging	Het
Exph5	G	A	9: 53,288,309 (GRCm39)	A1797T	probably damaging	Het
Fbp2	A	T	13: 62,985,061 (GRCm39)	Y287N	probably damaging	Het
Fmn2	CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC	CCCTCCTCTCCCTGGAATGGGAATACCTCCCCCACCTCCTCTCCCTGGAATGGGAATATCTCCCCTACCTCCTCTCCCTGGAATGGGAATACCTCC	1: 174,436,769 (GRCm39)		probably benign	Het
Fus	T	A	7: 127,581,123 (GRCm39)		probably null	Het
Galnt9	T	A	5: 110,762,054 (GRCm39)	N397K	probably damaging	Het
Gdi1	G	A	X: 73,350,461 (GRCm39)	R55H	probably benign	Het
Gga1	A	G	15: 78,775,651 (GRCm39)	T369A	probably benign	Het
Gp1ba	T	C	11: 70,531,119 (GRCm39)	I295T	unknown	Het
Hk2	T	C	6: 82,705,873 (GRCm39)	E810G	probably benign	Het
Igsf10	A	G	3: 59,233,189 (GRCm39)	V1848A	probably damaging	Het
Insrr	G	A	3: 87,721,623 (GRCm39)		probably null	Het
Ip6k3	T	A	17: 27,367,504 (GRCm39)	M231L	probably benign	Het
Itgb8	T	C	12: 119,155,939 (GRCm39)	N171S	probably benign	Het
Ldlrad3	T	C	2: 101,897,184 (GRCm39)		probably null	Het
Ltbp1	T	A	17: 75,634,223 (GRCm39)	C886*	probably null	Het
Mettl13	T	C	1: 162,366,547 (GRCm39)	D444G	probably benign	Het
Mns1	A	G	9: 72,356,025 (GRCm39)	Y224C	probably damaging	Het
Mri1	C	T	8: 84,983,525 (GRCm39)	R122Q	probably benign	Het
Ms4a6d	G	A	19: 11,567,437 (GRCm39)	Q155*	probably null	Het
Myo5c	A	C	9: 75,196,423 (GRCm39)	K1290Q	probably benign	Het
Nlrp12	T	G	7: 3,281,755 (GRCm39)	Q842H	possibly damaging	Het
Or14c44	T	C	7: 86,061,957 (GRCm39)	L129P	possibly damaging	Het
Or14j8	T	A	17: 38,263,413 (GRCm39)	R167S	probably benign	Het
Or2t1	A	T	14: 14,328,401 (GRCm38)	T97S	possibly damaging	Het
Or5d39	T	C	2: 87,979,620 (GRCm39)	T248A	possibly damaging	Het
Otoa	A	G	7: 120,729,288 (GRCm39)	T554A	probably benign	Het
Per1	A	G	11: 68,994,008 (GRCm39)	D438G	probably damaging	Het
Phactr3	G	A	2: 177,975,854 (GRCm39)	R533H	probably damaging	Het
Phykpl	T	C	11: 51,490,370 (GRCm39)	F417S	probably damaging	Het
Pole	A	T	5: 110,482,330 (GRCm39)	T2057S	probably benign	Het
Polq	A	G	16: 36,881,288 (GRCm39)	T1151A	probably benign	Het
Polr1g	T	C	7: 19,093,073 (GRCm39)	T36A	probably benign	Het
Rbm26	A	T	14: 105,389,976 (GRCm39)	V216E	possibly damaging	Het
Ryk	T	C	9: 102,775,737 (GRCm39)	I449T	probably damaging	Het
Sap25	A	G	5: 137,640,935 (GRCm39)	T225A	probably benign	Het
Sart3	A	G	5: 113,882,728 (GRCm39)	M864T	probably benign	Het
Sec31b	T	C	19: 44,517,161 (GRCm39)	S280G	probably benign	Het
Sema4d	A	T	13: 51,877,598 (GRCm39)	I78N	probably damaging	Het
Sgip1	G	C	4: 102,778,661 (GRCm39)	R419S	unknown	Het
Slc13a3	T	C	2: 165,272,210 (GRCm39)	I278V	probably benign	Het
Slc2a5	A	G	4: 150,224,439 (GRCm39)	D312G	probably benign	Het
Slc39a2	A	T	14: 52,131,660 (GRCm39)	Q77L	possibly damaging	Het
Srbd1	A	T	17: 86,443,782 (GRCm39)	V148E	probably benign	Het
Syngr2	A	G	11: 117,703,322 (GRCm39)	E46G	probably damaging	Het
Taok1	A	G	11: 77,470,643 (GRCm39)	V54A	possibly damaging	Het
Tas2r106	T	A	6: 131,655,185 (GRCm39)	H222L	probably damaging	Het
Tcaf3	A	G	6: 42,566,848 (GRCm39)	I747T	probably benign	Het
Tmem151b	G	T	17: 45,856,195 (GRCm39)	P415Q	probably benign	Het
Tmf1	T	C	6: 97,145,061 (GRCm39)	D659G	possibly damaging	Het
Tnn	G	T	1: 159,973,592 (GRCm39)	D258E	probably damaging	Het
Traj33	A	G	14: 54,422,862 (GRCm39)	I16V	unknown	Het
Ttll13	G	T	7: 79,906,772 (GRCm39)	C480F	probably damaging	Het
Ttn	T	C	2: 76,714,415 (GRCm39)	N8137S	unknown	Het
Vmn1r85	T	C	7: 12,819,073 (GRCm39)	N24D	probably damaging	Het
Wdr81	T	C	11: 75,335,525 (GRCm39)	Q649R	probably null	Het
Zan	T	C	5: 137,382,092 (GRCm39)	T5152A	unknown	Het
Zc3h6	A	G	2: 128,835,110 (GRCm39)	D82G	possibly damaging	Het

Other mutations in Oga

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00671:Oga	APN	19	45,753,979 (GRCm39)	missense	possibly damaging	0.89
IGL01845:Oga	APN	19	45,756,301 (GRCm39)	missense	probably benign	0.00
IGL02039:Oga	APN	19	45,762,142 (GRCm39)	missense	probably damaging	0.98
IGL02428:Oga	APN	19	45,753,940 (GRCm39)	missense	probably damaging	1.00
IGL02581:Oga	APN	19	45,740,630 (GRCm39)	missense	possibly damaging	0.53
IGL02971:Oga	APN	19	45,750,682 (GRCm39)	missense	probably damaging	1.00
R0127:Oga	UTSW	19	45,760,327 (GRCm39)	missense	probably damaging	1.00
R0815:Oga	UTSW	19	45,771,425 (GRCm39)	missense	probably benign	0.00
R0863:Oga	UTSW	19	45,771,425 (GRCm39)	missense	probably benign	0.00
R1127:Oga	UTSW	19	45,740,594 (GRCm39)	nonsense	probably null
R1501:Oga	UTSW	19	45,767,079 (GRCm39)	missense	probably null	1.00
R1514:Oga	UTSW	19	45,765,370 (GRCm39)	missense	probably damaging	1.00
R1586:Oga	UTSW	19	45,765,349 (GRCm39)	missense	possibly damaging	0.94
R1716:Oga	UTSW	19	45,740,613 (GRCm39)	missense	probably benign	0.35
R1755:Oga	UTSW	19	45,746,845 (GRCm39)	missense	possibly damaging	0.93
R1774:Oga	UTSW	19	45,765,423 (GRCm39)	missense	probably benign	0.37
R2152:Oga	UTSW	19	45,746,461 (GRCm39)	nonsense	probably null
R4403:Oga	UTSW	19	45,767,078 (GRCm39)	missense	probably damaging	1.00
R4664:Oga	UTSW	19	45,760,384 (GRCm39)	missense	probably benign	0.15
R4971:Oga	UTSW	19	45,758,485 (GRCm39)	splice site	probably null
R5377:Oga	UTSW	19	45,746,461 (GRCm39)	nonsense	probably null
R5571:Oga	UTSW	19	45,765,445 (GRCm39)	missense	probably benign
R5639:Oga	UTSW	19	45,765,438 (GRCm39)	missense	probably damaging	1.00
R5665:Oga	UTSW	19	45,765,436 (GRCm39)	missense	probably benign	0.00
R5776:Oga	UTSW	19	45,760,363 (GRCm39)	missense	probably damaging	1.00
R6050:Oga	UTSW	19	45,753,919 (GRCm39)	missense	possibly damaging	0.95
R6054:Oga	UTSW	19	45,764,571 (GRCm39)	missense	probably damaging	1.00
R6317:Oga	UTSW	19	45,760,119 (GRCm39)	critical splice donor site	probably null
R6410:Oga	UTSW	19	45,764,484 (GRCm39)	splice site	probably null
R6990:Oga	UTSW	19	45,755,915 (GRCm39)	missense	probably benign	0.00
R7103:Oga	UTSW	19	45,771,605 (GRCm39)	start gained	probably benign
R7437:Oga	UTSW	19	45,767,046 (GRCm39)	missense	possibly damaging	0.76
R7490:Oga	UTSW	19	45,755,886 (GRCm39)	nonsense	probably null
R7741:Oga	UTSW	19	45,764,501 (GRCm39)	missense	probably damaging	1.00
R7823:Oga	UTSW	19	45,765,354 (GRCm39)	missense	possibly damaging	0.51
R8017:Oga	UTSW	19	45,762,107 (GRCm39)	missense	probably damaging	1.00
R8019:Oga	UTSW	19	45,762,107 (GRCm39)	missense	probably damaging	1.00
R8066:Oga	UTSW	19	45,760,291 (GRCm39)	missense	probably damaging	0.99
R8075:Oga	UTSW	19	45,749,621 (GRCm39)	missense	probably damaging	0.97
R8172:Oga	UTSW	19	45,765,339 (GRCm39)	missense	probably damaging	0.99
R8558:Oga	UTSW	19	45,746,511 (GRCm39)	missense	probably benign	0.00
R9050:Oga	UTSW	19	45,756,354 (GRCm39)	missense	probably damaging	1.00
R9150:Oga	UTSW	19	45,771,421 (GRCm39)	missense	probably benign	0.00
R9404:Oga	UTSW	19	45,743,096 (GRCm39)	frame shift	probably null
R9562:Oga	UTSW	19	45,743,096 (GRCm39)	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- AAGGCCTCTGGGGAAACATG -3'
(R):5'- CTATGCAGACAGATGAGCAAAC -3'

Sequencing Primer
(F):5'- GAAGCCCTGTGTTGAAATACC -3'
(R):5'- ACACAGAAGGAGCAGTTTGTG -3'

Posted On

2019-09-13