Mutagenetix > Incidental Mutation

Incidental Mutation 'R7894:Nr2f2'

609519

Institutional Source

Beutler Lab

Gene Symbol

Nr2f2

Ensembl Gene

ENSMUSG00000030551

Gene Name

nuclear receptor subfamily 2, group F, member 2

Synonyms

COUP-TF2, EAR3, ARP-1, Tcfcoup2, 9430015G03Rik, COUP-TFII, Aporp1

MMRRC Submission

045946-MU

Accession Numbers

Essential gene?

Essential (E-score: 1.000) question?

Stock #

R7894 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

70001692-70016483 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 70009681 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 133 (Y133H)

Ref Sequence

ENSEMBL: ENSMUSP00000032768 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000032768] [ENSMUST00000089565] [ENSMUST00000208081]

AlphaFold

P43135

Predicted Effect

probably damaging
Transcript: ENSMUST00000032768
AA Change: Y133H

PolyPhen 2 Score 0.995 (Sensitivity: 0.68; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000032768
Gene: ENSMUSG00000030551
AA Change: Y133H

Domain	Start	End	E-Value	Type
low complexity region	21	75	N/A	INTRINSIC
ZnF_C4	76	147	4.57e-39	SMART
HOLI	214	374	1.29e-47	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000089565

SMART Domains

Protein: ENSMUSP00000086993
Gene: ENSMUSG00000030551

Domain	Start	End	E-Value	Type
HOLI	81	241	5.2e-50	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000208081

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.7%
20x: 98.9%

Validation Efficiency

99% (81/82)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the steroid thyroid hormone superfamily of nuclear receptors. The encoded protein is a ligand inducible transcription factor that is involved in the regulation of many different genes. Alternate splicing results in multiple transcript variants. [provided by RefSeq, Mar 2010]
PHENOTYPE: Homozygotes for a targeted null mutation exhibit impaired angiogenesis and heart development with hemorrhagic brains and hearts, and die around embryonic day 10. About 5% of heterozygotes share the hemorrhagic phenotype at embryonic day 9.5. [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
Abca9	A	G	11: 109,997,415 (GRCm39)	M1551T	possibly damaging	Het
Abcc9	A	G	6: 142,539,733 (GRCm39)	*1547Q	probably null	Het
Adamts20	A	C	15: 94,249,641 (GRCm39)	C459G	probably damaging	Het
Adamts5	C	T	16: 85,674,808 (GRCm39)	W452*	probably null	Het
Adcy8	G	T	15: 64,792,054 (GRCm39)	Q301K	possibly damaging	Het
Adgrv1	A	C	13: 81,715,570 (GRCm39)	C873G	probably benign	Het
Ak9	A	G	10: 41,296,535 (GRCm39)	D1427G	unknown	Het
Amy2a1	T	A	3: 113,324,190 (GRCm39)	M117L	possibly damaging	Het
Ap5z1	G	T	5: 142,452,039 (GRCm39)	R23L	probably benign	Het
Ap5z1	C	T	5: 142,456,191 (GRCm39)	Q337*	probably null	Het
Astn1	C	A	1: 158,429,508 (GRCm39)	Q759K	probably damaging	Het
Cd276	T	A	9: 58,444,762 (GRCm39)	T70S	possibly damaging	Het
Cd38	C	T	5: 44,057,746 (GRCm39)	T106I	probably damaging	Het
Cdon	C	G	9: 35,388,244 (GRCm39)	R740G	probably damaging	Het
Clk2	C	T	3: 89,076,201 (GRCm39)	R124W	possibly damaging	Het
Cyp1b1	C	T	17: 80,021,644 (GRCm39)	V33M	possibly damaging	Het
Dab1	T	A	4: 104,589,335 (GRCm39)	D547E	probably benign	Het
Degs1	A	T	1: 182,104,416 (GRCm39)	Y290N	probably damaging	Het
Degs1	G	C	1: 182,104,417 (GRCm39)	H289Q	probably benign	Het
Dop1b	T	A	16: 93,607,092 (GRCm39)	C2249S	probably benign	Het
Ecpas	T	C	4: 58,853,708 (GRCm39)	N361S	probably damaging	Het
Ehd4	A	C	2: 119,932,909 (GRCm39)	Y172*	probably null	Het
Erc2	A	G	14: 27,499,165 (GRCm39)	D347G	probably damaging	Het
Espl1	T	G	15: 102,212,460 (GRCm39)	V522G	probably damaging	Het
Fabp9	T	A	3: 10,262,227 (GRCm39)	T10S	probably benign	Het
Fam193a	T	C	5: 34,597,877 (GRCm39)	I558T	possibly damaging	Het
Fhod1	T	C	8: 106,057,789 (GRCm39)	E912G	probably damaging	Het
Gja1	T	C	10: 56,264,645 (GRCm39)	F335L	possibly damaging	Het
Gm29106	A	G	1: 118,127,265 (GRCm39)	H319R	probably damaging	Het
Hunk	C	T	16: 90,269,353 (GRCm39)	S299F	probably damaging	Het
Hydin	C	T	8: 111,239,642 (GRCm39)	T1974M	possibly damaging	Het
Ighv10-1	T	A	12: 114,442,650 (GRCm39)	T112S	probably damaging	Het
Ireb2	T	A	9: 54,789,620 (GRCm39)	V98E	probably damaging	Het
Irf4	A	C	13: 30,937,435 (GRCm39)	H167P	probably benign	Het
Irf6	C	T	1: 192,845,021 (GRCm39)	P164L	probably benign	Het
Josd1	A	G	15: 79,561,451 (GRCm39)	I119T	probably damaging	Het
Kcna5	G	T	6: 126,512,011 (GRCm39)	T39K	probably damaging	Het
Klhl24	A	G	16: 19,941,750 (GRCm39)	D566G	probably damaging	Het
Kmt2a	T	A	9: 44,761,154 (GRCm39)	K232*	probably null	Het
Krt36	A	G	11: 99,996,061 (GRCm39)	L121P	probably damaging	Het
Lama3	A	T	18: 12,595,864 (GRCm39)	H931L	probably benign	Het
Lamp3	A	T	16: 19,474,141 (GRCm39)	I411N	probably damaging	Het
Lingo3	C	T	10: 80,670,610 (GRCm39)	W440*	probably null	Het
Mia2	T	C	12: 59,236,433 (GRCm39)	Y712H	probably damaging	Het
Mlh1	T	A	9: 111,059,145 (GRCm39)		probably null	Het
Mta3	T	A	17: 84,070,363 (GRCm39)	S174T	probably benign	Het
Myo15a	A	G	11: 60,381,963 (GRCm39)	T347A		Het
Naaladl2	C	T	3: 23,900,718 (GRCm39)	R704H	possibly damaging	Het
Nfib	T	C	4: 82,246,030 (GRCm39)	N394S	probably benign	Het
Or2ak7	C	T	11: 58,575,500 (GRCm39)	S267F	possibly damaging	Het
Or2i1	C	T	17: 37,508,047 (GRCm39)	E196K	probably damaging	Het
Or4c115	A	G	2: 88,927,932 (GRCm39)	V113A	possibly damaging	Het
Or4f61	A	T	2: 111,922,822 (GRCm39)	C75S	probably benign	Het
Or5p62	T	A	7: 107,771,391 (GRCm39)	M187L	probably benign	Het
Phgdh	C	A	3: 98,247,124 (GRCm39)	V9L	probably damaging	Het
Pkd2	T	A	5: 104,628,103 (GRCm39)	D392E	probably damaging	Het
Plekhm3	A	G	1: 64,960,874 (GRCm39)	S461P	probably benign	Het
Prss39	A	G	1: 34,539,308 (GRCm39)	T183A	probably benign	Het
Pter	T	A	2: 12,999,566 (GRCm39)	I235K	probably damaging	Het
Ptp4a3	T	C	15: 73,628,756 (GRCm39)	V172A	probably benign	Het
Rasa2	T	C	9: 96,484,780 (GRCm39)	N145D	probably benign	Het
Rasal2	A	T	1: 157,071,218 (GRCm39)	H45Q	probably benign	Het
Rbm43	A	G	2: 51,815,909 (GRCm39)	V104A	probably damaging	Het
Rhbdd2	C	A	5: 135,667,969 (GRCm39)		probably null	Het
Rictor	C	T	15: 6,801,635 (GRCm39)	S441L	probably benign	Het
Rimbp2	T	A	5: 128,838,528 (GRCm39)	N1023I	probably damaging	Het
Rtl1	A	T	12: 109,561,031 (GRCm39)	D269E	possibly damaging	Het
Sbp	A	G	17: 24,161,163 (GRCm39)		probably benign	Het
Sorbs1	T	A	19: 40,316,020 (GRCm39)	T374S	probably benign	Het
Tgs1	A	T	4: 3,598,652 (GRCm39)	K655I	probably benign	Het
Thsd1	A	C	8: 22,749,585 (GRCm39)	T819P	probably damaging	Het
Tmprss11c	C	T	5: 86,379,655 (GRCm39)	V418M	probably damaging	Het
Top2a	A	T	11: 98,900,431 (GRCm39)	D645E	probably damaging	Het
Top2b	G	A	14: 16,413,081 (GRCm38)	V997I	possibly damaging	Het
Ttc34	A	G	4: 154,943,840 (GRCm39)	D118G	probably damaging	Het
Ttll5	A	G	12: 85,935,948 (GRCm39)	D353G	probably damaging	Het
Uba6	A	T	5: 86,265,924 (GRCm39)	Y994*	probably null	Het
Vinac1	A	C	2: 128,879,049 (GRCm39)	V959G	unknown	Het
Vmn1r189	A	T	13: 22,285,906 (GRCm39)	Y310*	probably null	Het
Vps13c	T	A	9: 67,834,265 (GRCm39)	I1644N	probably damaging	Het
Zfp811	T	C	17: 33,017,821 (GRCm39)	D73G	possibly damaging	Het
Zfp951	A	T	5: 104,962,838 (GRCm39)	C243S	probably benign	Het

Other mutations in Nr2f2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00672:Nr2f2	APN	7	70,007,514 (GRCm39)	missense	possibly damaging	0.88
IGL01736:Nr2f2	APN	7	70,004,446 (GRCm39)	missense	probably damaging	1.00
IGL02667:Nr2f2	APN	7	70,007,733 (GRCm39)	missense	probably damaging	1.00
R0149:Nr2f2	UTSW	7	70,007,810 (GRCm39)	missense	possibly damaging	0.90
R0206:Nr2f2	UTSW	7	70,009,923 (GRCm39)	missense	probably damaging	0.98
R0207:Nr2f2	UTSW	7	70,009,923 (GRCm39)	missense	probably damaging	0.98
R0240:Nr2f2	UTSW	7	70,009,923 (GRCm39)	missense	probably damaging	0.98
R0243:Nr2f2	UTSW	7	70,009,923 (GRCm39)	missense	probably damaging	0.98
R0361:Nr2f2	UTSW	7	70,007,810 (GRCm39)	missense	possibly damaging	0.90
R0540:Nr2f2	UTSW	7	70,004,460 (GRCm39)	missense	probably damaging	1.00
R0607:Nr2f2	UTSW	7	70,004,460 (GRCm39)	missense	probably damaging	1.00
R0741:Nr2f2	UTSW	7	70,007,745 (GRCm39)	missense	probably damaging	1.00
R1894:Nr2f2	UTSW	7	70,004,419 (GRCm39)	missense	probably benign	0.00
R1961:Nr2f2	UTSW	7	70,007,903 (GRCm39)	missense	possibly damaging	0.80
R3033:Nr2f2	UTSW	7	70,007,810 (GRCm39)	missense	possibly damaging	0.90
R3754:Nr2f2	UTSW	7	70,007,769 (GRCm39)	missense	probably benign	0.01
R4517:Nr2f2	UTSW	7	70,007,870 (GRCm39)	missense	probably benign	0.21
R6175:Nr2f2	UTSW	7	70,007,946 (GRCm39)	missense	probably damaging	1.00
R6226:Nr2f2	UTSW	7	70,009,744 (GRCm39)	missense	probably benign	0.00
R7544:Nr2f2	UTSW	7	70,004,499 (GRCm39)	missense	probably damaging	1.00
R7796:Nr2f2	UTSW	7	70,007,901 (GRCm39)	missense	probably benign	0.03
R9377:Nr2f2	UTSW	7	70,007,856 (GRCm39)	missense	probably damaging	1.00
R9411:Nr2f2	UTSW	7	70,007,525 (GRCm39)	missense
R9513:Nr2f2	UTSW	7	70,010,056 (GRCm39)	missense	probably damaging	0.98
Z1176:Nr2f2	UTSW	7	70,007,526 (GRCm39)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- GGTTCCTAGTACCAAATCCCC -3'
(R):5'- GCAATGGTAGTCAGCACGTG -3'

Sequencing Primer
(F):5'- TAGTACCAAATCCCCTCCGACTG -3'
(R):5'- GCAGCAGCAGCACATCGAG -3'

Posted On

2019-12-20