Mutagenetix > Incidental Mutation

Incidental Mutation 'R3770:Foxk2'

273233

Institutional Source

Beutler Lab

Gene Symbol

Foxk2

Ensembl Gene

ENSMUSG00000039275

Gene Name

forkhead box K2

Synonyms

1110054H05Rik, Ilf1, 5730434B08Rik

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R3770 (G1)

Quality Score

101

Status

Not validated

Chromosome

Chromosomal Location

121150816-121200722 bp(+) (GRCm39)

Type of Mutation

small insertion (1 aa in frame mutation)

DNA Base Change (assembly)

CGGGGGG to CGGGGGGGGG at 121151317 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000101719 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000103015] [ENSMUST00000106113]

AlphaFold

Q3UCQ1

Predicted Effect

probably benign
Transcript: ENSMUST00000103015

SMART Domains

Protein: ENSMUSP00000099304
Gene: ENSMUSG00000000056

Domain	Start	End	E-Value	Type
Pfam:Fe_hyd_lg_C	98	391	1e-75	PFAM
Fe_hyd_SSU	396	452	5.66e-19	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000106113

SMART Domains

Protein: ENSMUSP00000101719
Gene: ENSMUSG00000039275

Domain	Start	End	E-Value	Type
low complexity region	2	32	N/A	INTRINSIC
FHA	47	119	9.96e-10	SMART
FH	247	338	2.2e-52	SMART
low complexity region	440	465	N/A	INTRINSIC
low complexity region	486	498	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.2%
20x: 94.8%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains a fork head DNA binding domain. This protein can bind to the purine-rich motifs of the HIV long terminal repeat (LTR), and to the similar purine-rich motif in the interleukin 2 (IL2) promoter. It may be involved in the regulation of viral and cellular promoter elements. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 47 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acox1	T	C	11: 116,065,213 (GRCm39)	D578G	probably damaging	Het
Adgrb1	T	A	15: 74,460,157 (GRCm39)	I543N	probably damaging	Het
Agbl1	T	C	7: 76,075,677 (GRCm39)		probably null	Het
Ano1	A	G	7: 144,149,306 (GRCm39)	Y852H	probably damaging	Het
Apol9a	G	C	15: 77,288,596 (GRCm39)	T257S	probably benign	Het
Arhgap23	A	T	11: 97,366,932 (GRCm39)	D1071V	probably damaging	Het
Atp1a1	T	C	3: 101,488,510 (GRCm39)	D842G	probably benign	Het
Brd7	A	T	8: 89,066,035 (GRCm39)		probably null	Het
Btbd7	G	A	12: 102,761,451 (GRCm39)	P578L	probably damaging	Het
C3	C	T	17: 57,512,303 (GRCm39)	D1542N	possibly damaging	Het
Cfap54	C	T	10: 92,714,398 (GRCm39)	M2660I	unknown	Het
Dock7	T	C	4: 98,859,066 (GRCm39)	T1409A	probably benign	Het
Exoc3l4	A	G	12: 111,391,989 (GRCm39)	D410G	probably benign	Het
Herc2	A	G	7: 55,814,755 (GRCm39)	I2703V	probably benign	Het
Ifna7	T	C	4: 88,734,964 (GRCm39)	V167A	probably damaging	Het
Iqcg	G	A	16: 32,870,378 (GRCm39)		silent	Het
Klf3	A	G	5: 64,984,560 (GRCm39)		probably null	Het
Krtap12-1	G	T	10: 77,556,729 (GRCm39)	V91L	probably benign	Het
Lipo5	G	T	19: 33,445,200 (GRCm39)	T123N	unknown	Het
Macf1	A	G	4: 123,268,560 (GRCm39)	S4689P	probably damaging	Het
Map3k5	T	A	10: 19,900,765 (GRCm39)	V313D	probably damaging	Het
Mypn	C	A	10: 62,961,486 (GRCm39)	L1035F	possibly damaging	Het
Neurl1a	T	C	19: 47,228,328 (GRCm39)	L58P	probably damaging	Het
Or5aq1	C	T	2: 86,966,158 (GRCm39)	C169Y	probably damaging	Het
Pla2g5	C	G	4: 138,528,746 (GRCm39)	C70S	probably damaging	Het
Pole4	G	A	6: 82,599,095 (GRCm39)	R119C	possibly damaging	Het
Ppm1h	G	T	10: 122,740,027 (GRCm39)	L367F	probably damaging	Het
Ptpru	C	T	4: 131,535,735 (GRCm39)	C414Y	probably damaging	Het
Rasal3	A	T	17: 32,611,125 (GRCm39)	L912Q	probably damaging	Het
Reln	C	T	5: 22,153,564 (GRCm39)	V2247M	probably damaging	Het
Rhot2	T	C	17: 26,059,521 (GRCm39)	D407G	probably benign	Het
Rreb1	C	T	13: 38,113,579 (GRCm39)	R313W	possibly damaging	Het
Rufy4	T	C	1: 74,186,822 (GRCm39)	C537R	probably damaging	Het
Scn11a	T	A	9: 119,613,115 (GRCm39)	D825V	probably damaging	Het
Slc12a3	A	G	8: 95,079,668 (GRCm39)	H832R	probably benign	Het
Slc27a2	A	G	2: 126,409,718 (GRCm39)	D300G	possibly damaging	Het
Sos1	A	G	17: 80,705,737 (GRCm39)	V1278A	probably damaging	Het
Sstr3	C	A	15: 78,424,577 (GRCm39)	V57L	probably damaging	Het
Tex2	T	A	11: 106,435,078 (GRCm39)	R783W	unknown	Het
Tjp2	A	T	19: 24,078,190 (GRCm39)	I901N	probably benign	Het
Top1	A	T	2: 160,563,442 (GRCm39)	I758F	probably damaging	Het
Trim41	T	C	11: 48,699,911 (GRCm39)	E98G	possibly damaging	Het
Vmn2r65	A	T	7: 84,589,623 (GRCm39)	N764K	probably damaging	Het
Vmn2r81	A	T	10: 79,106,434 (GRCm39)	I471F	probably damaging	Het
Wdr25	G	A	12: 108,864,346 (GRCm39)	V164M	probably damaging	Het
Zdhhc13	T	A	7: 48,452,692 (GRCm39)	L5M	probably damaging	Het
Zfp747l1	A	G	7: 126,984,035 (GRCm39)		probably benign	Het

Other mutations in Foxk2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00339:Foxk2	APN	11	121,190,560 (GRCm39)	missense	probably damaging	1.00
IGL00502:Foxk2	APN	11	121,187,925 (GRCm39)	splice site	probably benign
IGL02619:Foxk2	APN	11	121,190,402 (GRCm39)	splice site	probably benign
IGL03067:Foxk2	APN	11	121,176,394 (GRCm39)	missense	possibly damaging	0.87
R1843:Foxk2	UTSW	11	121,176,363 (GRCm39)	missense	probably benign	0.01
R2153:Foxk2	UTSW	11	121,151,213 (GRCm39)	missense	probably benign	0.08
R2847:Foxk2	UTSW	11	121,151,317 (GRCm39)	small insertion	probably benign
R4024:Foxk2	UTSW	11	121,176,439 (GRCm39)	missense	possibly damaging	0.67
R6958:Foxk2	UTSW	11	121,190,563 (GRCm39)	missense	probably benign	0.16
R6968:Foxk2	UTSW	11	121,151,308 (GRCm39)	missense	possibly damaging	0.87
R7558:Foxk2	UTSW	11	121,178,884 (GRCm39)	missense	probably benign	0.00
R7736:Foxk2	UTSW	11	121,190,473 (GRCm39)	missense	possibly damaging	0.92
R7902:Foxk2	UTSW	11	121,190,553 (GRCm39)	missense	probably benign

Predicted Primers

PCR Primer
(F):5'- GTACCTCATGAAGAAGCGGTCG -3'
(R):5'- ATCAGGATCCCTCCCTGATG -3'

Sequencing Primer
(F):5'- TAGATGTGAGCATGGGCCACTC -3'
(R):5'- TCTGACCCTGCTCATGGGTAG -3'

Posted On

2015-03-25