Mutagenetix > Incidental Mutation

Incidental Mutation 'R0518:Ogfod1'

48308

Institutional Source

Beutler Lab

Gene Symbol

Ogfod1

Ensembl Gene

ENSMUSG00000033009

Gene Name

2-oxoglutarate and iron-dependent oxygenase domain containing 1

Synonyms

4930415J21Rik

MMRRC Submission

038711-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0518 (G1)

Quality Score

181

Status

Not validated

Chromosome

Chromosomal Location

94763826-94794549 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 94781876 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000105183 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000060632] [ENSMUST00000093301] [ENSMUST00000109556]

AlphaFold

Q3U0K8

Predicted Effect

probably null
Transcript: ENSMUST00000060632

SMART Domains

Protein: ENSMUSP00000051430
Gene: ENSMUSG00000033009

Domain	Start	End	E-Value	Type
P4Hc	46	223	4.87e-26	SMART
Pfam:Ofd1_CTDD	246	513	1.4e-50	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000093301

SMART Domains

Protein: ENSMUSP00000090991
Gene: ENSMUSG00000033009

Domain	Start	End	E-Value	Type
P4Hc	61	228	2.6e-12	SMART
low complexity region	328	353	N/A	INTRINSIC
low complexity region	375	389	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000109556

SMART Domains

Protein: ENSMUSP00000105183
Gene: ENSMUSG00000033009

Domain	Start	End	E-Value	Type
P4Hc	61	238	4.87e-26	SMART
Pfam:Ofd1_CTDD	261	528	7.2e-51	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000127634

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145717

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000172674

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211865

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.6%
20x: 93.5%

Validation Efficiency

MGI Phenotype

PHENOTYPE: Mice homozygous for a null allele are viable and fertile. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 82 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acaca	A	G	11: 84,181,112 (GRCm39)		probably null	Het
Acsbg3	T	A	17: 57,192,169 (GRCm39)	Y577*	probably null	Het
Acsm5	T	C	7: 119,135,023 (GRCm39)	V327A	possibly damaging	Het
Agt	C	A	8: 125,283,839 (GRCm39)	E427*	probably null	Het
Akr1c14	T	C	13: 4,131,016 (GRCm39)	L236S	probably damaging	Het
Ammecr1l	C	T	18: 31,904,954 (GRCm39)	S65L	probably benign	Het
Ankrd33b	T	C	15: 31,367,432 (GRCm39)	D36G	probably damaging	Het
Ano8	A	T	8: 71,931,902 (GRCm39)	C766S	probably benign	Het
Arhgef16	G	T	4: 154,375,491 (GRCm39)	P168T	probably damaging	Het
Asic1	C	T	15: 99,596,700 (GRCm39)	R499C	probably damaging	Het
Atpsckmt	T	G	15: 31,606,103 (GRCm39)	S20R	probably benign	Het
Bank1	C	T	3: 135,919,703 (GRCm39)	C364Y	probably damaging	Het
Bmerb1	T	A	16: 13,804,676 (GRCm39)	S8T	possibly damaging	Het
Cacna1s	C	A	1: 136,004,597 (GRCm39)	D132E	probably benign	Het
Capn5	C	T	7: 97,782,089 (GRCm39)	R217Q	probably damaging	Het
Clasrp	A	G	7: 19,322,528 (GRCm39)	I284T	probably benign	Het
Coa3	T	A	11: 101,169,716 (GRCm39)	K13M	probably damaging	Het
Col13a1	A	T	10: 61,698,525 (GRCm39)	M512K	unknown	Het
Colgalt2	G	T	1: 152,384,312 (GRCm39)	A551S	possibly damaging	Het
Crhbp	C	A	13: 95,580,403 (GRCm39)		probably null	Het
Cryba2	T	C	1: 74,929,284 (GRCm39)	Y153C	possibly damaging	Het
Cryzl2	T	C	1: 157,292,000 (GRCm39)	V93A	probably damaging	Het
Ctsl	G	A	13: 64,513,032 (GRCm39)	L297F	possibly damaging	Het
Cyp2r1	T	G	7: 114,152,135 (GRCm39)	H274P	probably benign	Het
Ddx4	A	T	13: 112,761,313 (GRCm39)		probably null	Het
Dnai4	A	C	4: 102,921,727 (GRCm39)	Y464*	probably null	Het
Dnd1	A	G	18: 36,897,096 (GRCm39)	V350A	possibly damaging	Het
Dsg1b	A	T	18: 20,521,221 (GRCm39)	Q26L	probably benign	Het
Fam20b	C	A	1: 156,515,026 (GRCm39)	V280F	possibly damaging	Het
Foxb2	G	T	19: 16,849,820 (GRCm39)	C395*	probably null	Het
Glb1	ACCC	ACC	9: 114,250,812 (GRCm39)		probably null	Het
Gm9930	A	T	10: 9,410,547 (GRCm39)		noncoding transcript	Het
Hdac7	G	A	15: 97,704,380 (GRCm39)	Q497*	probably null	Het
Hk3	C	T	13: 55,162,239 (GRCm39)		probably null	Het
Hsd3b7	A	G	7: 127,402,251 (GRCm39)	T330A	probably benign	Het
Il20ra	A	T	10: 19,635,388 (GRCm39)	Q543L	probably damaging	Het
Itk	T	A	11: 46,251,115 (GRCm39)	D163V	probably damaging	Het
Kcnu1	T	G	8: 26,400,916 (GRCm39)	L688R	probably damaging	Het
Kng1	G	A	16: 22,879,232 (GRCm39)	A45T	possibly damaging	Het
Kti12	T	A	4: 108,705,776 (GRCm39)	V230E	possibly damaging	Het
Lhfpl7	T	A	5: 113,383,873 (GRCm39)	L97*	probably null	Het
Mgat5	T	A	1: 127,312,584 (GRCm39)	I241N	probably damaging	Het
Mkln1	A	G	6: 31,445,067 (GRCm39)	N321S	probably benign	Het
Mllt10	T	G	2: 18,076,017 (GRCm39)		probably null	Het
Ms4a1	C	A	19: 11,236,043 (GRCm39)		probably null	Het
Ngly1	C	T	14: 16,290,774 (GRCm38)	Q419*	probably null	Het
Nipsnap3b	T	A	4: 53,021,343 (GRCm39)	F243I	probably damaging	Het
Or10a2	T	A	7: 106,673,965 (GRCm39)	L310Q	possibly damaging	Het
Or2y11	C	T	11: 49,443,291 (GRCm39)	T239M	probably damaging	Het
Or51v8	T	A	7: 103,319,696 (GRCm39)	I181F	possibly damaging	Het
Or8c20	A	C	9: 38,260,499 (GRCm39)	N40T	probably damaging	Het
P2ry14	T	A	3: 59,022,625 (GRCm39)	E287D	probably damaging	Het
Pank4	A	T	4: 155,061,082 (GRCm39)	R510S	possibly damaging	Het
Pcsk6	T	A	7: 65,629,915 (GRCm39)	V347E	possibly damaging	Het
Peg3	T	C	7: 6,714,427 (GRCm39)	E265G	probably damaging	Het
Pik3c2b	C	A	1: 133,033,730 (GRCm39)	P1578H	probably damaging	Het
Pkd1	A	G	17: 24,814,193 (GRCm39)	S4188G	probably benign	Het
Ppp1r26	A	G	2: 28,342,314 (GRCm39)	D648G	probably damaging	Het
Ptprs	A	G	17: 56,726,621 (GRCm39)		probably null	Het
Rab24	A	T	13: 55,468,738 (GRCm39)		probably null	Het
Rap1gap2	A	T	11: 74,332,592 (GRCm39)	M71K	probably damaging	Het
Rergl	T	G	6: 139,473,524 (GRCm39)	K42T	probably damaging	Het
Rigi	C	T	4: 40,216,354 (GRCm39)		probably null	Het
Septin5	T	C	16: 18,443,647 (GRCm39)	T92A	probably benign	Het
Ski	A	G	4: 155,243,743 (GRCm39)		probably null	Het
Slc17a8	A	G	10: 89,412,192 (GRCm39)	S414P	probably benign	Het
Slc25a36	A	T	9: 96,979,228 (GRCm39)	I71N	probably damaging	Het
Syne2	A	C	12: 76,155,636 (GRCm39)		probably null	Het
Tdrd5	C	A	1: 156,090,511 (GRCm39)	W845L	probably damaging	Het
Tfb2m	T	C	1: 179,365,389 (GRCm39)	I192V	possibly damaging	Het
Tll1	T	G	8: 64,551,505 (GRCm39)	D292A	probably damaging	Het
Trank1	A	C	9: 111,162,876 (GRCm39)	D45A	probably damaging	Het
Trim17	T	A	11: 58,859,320 (GRCm39)	V178E	probably damaging	Het
Trim9	A	T	12: 70,393,359 (GRCm39)	L195Q	probably damaging	Het
Ttc27	A	T	17: 75,163,544 (GRCm39)	R717S	possibly damaging	Het
Upk2	G	T	9: 44,365,418 (GRCm39)	P50Q	probably damaging	Het
Usp9y	A	T	Y: 1,307,880 (GRCm39)	C2319S	probably benign	Het
Vmn1r4	G	T	6: 56,933,883 (GRCm39)	C129F	probably benign	Het
Vmn2r100	A	T	17: 19,742,178 (GRCm39)	D184V	probably damaging	Het
Xpnpep3	T	G	15: 81,311,693 (GRCm39)	I133S	possibly damaging	Het
Zfp628	A	T	7: 4,922,939 (GRCm39)	Q387L	probably damaging	Het
Zic2	CCCACCACCACCATCACCACCACCACC	CCCACCATCACCACCACCACC	14: 122,713,776 (GRCm39)		probably benign	Het

Other mutations in Ogfod1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01074:Ogfod1	APN	8	94,789,634 (GRCm39)	missense	probably damaging	1.00
IGL01296:Ogfod1	APN	8	94,782,299 (GRCm39)	splice site	probably benign
IGL01369:Ogfod1	APN	8	94,789,719 (GRCm39)	critical splice donor site	probably null
IGL02113:Ogfod1	APN	8	94,790,841 (GRCm39)	missense	probably damaging	1.00
IGL02228:Ogfod1	APN	8	94,789,615 (GRCm39)	missense	probably benign	0.00
IGL03057:Ogfod1	APN	8	94,782,766 (GRCm39)	missense	possibly damaging	0.78
IGL03071:Ogfod1	APN	8	94,784,395 (GRCm39)	missense	probably damaging	1.00
R0391:Ogfod1	UTSW	8	94,789,651 (GRCm39)	missense	probably damaging	1.00
R0395:Ogfod1	UTSW	8	94,790,156 (GRCm39)	critical splice donor site	probably null
R0605:Ogfod1	UTSW	8	94,773,895 (GRCm39)	splice site	probably benign
R0708:Ogfod1	UTSW	8	94,765,673 (GRCm39)	missense	possibly damaging	0.89
R0763:Ogfod1	UTSW	8	94,782,264 (GRCm39)	missense	probably benign	0.03
R1101:Ogfod1	UTSW	8	94,790,932 (GRCm39)	missense	probably benign
R1244:Ogfod1	UTSW	8	94,763,999 (GRCm39)	missense	probably benign
R1332:Ogfod1	UTSW	8	94,784,727 (GRCm39)	missense	probably damaging	1.00
R1336:Ogfod1	UTSW	8	94,784,727 (GRCm39)	missense	probably damaging	1.00
R2301:Ogfod1	UTSW	8	94,763,996 (GRCm39)	missense	probably damaging	0.99
R3025:Ogfod1	UTSW	8	94,789,680 (GRCm39)	missense	probably damaging	1.00
R3710:Ogfod1	UTSW	8	94,784,380 (GRCm39)	nonsense	probably null
R4612:Ogfod1	UTSW	8	94,763,975 (GRCm39)	missense	possibly damaging	0.66
R5349:Ogfod1	UTSW	8	94,781,876 (GRCm39)	splice site	probably benign
R5495:Ogfod1	UTSW	8	94,790,906 (GRCm39)	missense	probably benign	0.30
R5690:Ogfod1	UTSW	8	94,784,769 (GRCm39)	missense	probably damaging	0.99
R6355:Ogfod1	UTSW	8	94,789,610 (GRCm39)	missense	probably benign
R7282:Ogfod1	UTSW	8	94,764,067 (GRCm39)	missense	possibly damaging	0.47
R7396:Ogfod1	UTSW	8	94,765,615 (GRCm39)	missense	probably benign	0.00
R7651:Ogfod1	UTSW	8	94,763,981 (GRCm39)	missense	probably benign	0.04
R8868:Ogfod1	UTSW	8	94,773,906 (GRCm39)	missense	probably damaging	1.00
X0027:Ogfod1	UTSW	8	94,764,032 (GRCm39)	missense	probably benign	0.08
Z1177:Ogfod1	UTSW	8	94,763,937 (GRCm39)	unclassified	probably benign

Predicted Primers

PCR Primer
(F):5'- GAATTAATGCGAGCCTGACAACCAC -3'
(R):5'- AGAGCAAGACCGTTGGCACATC -3'

Sequencing Primer
(F):5'- ATGAGTCTGCTAACAGCACTCTG -3'
(R):5'- TTTGAACCCATCGGGCTG -3'

Posted On

2013-06-12