Mutagenetix > Incidental Mutation

Incidental Mutation 'R0105:Fto'

33267

Institutional Source

Beutler Lab

Gene Symbol

Fto

Ensembl Gene

ENSMUSG00000055932

Gene Name

FTO alpha-ketoglutarate dependent dioxygenase

Synonyms

MMRRC Submission

038391-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R0105 (G1)

Quality Score

225

Status

Validated (trace)

Chromosome

Chromosomal Location

92040153-92395067 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 92249430 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Glutamic Acid to Lysine at position 421 (E421K)

Ref Sequence

ENSEMBL: ENSMUSP00000147548 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000069718] [ENSMUST00000128081]

AlphaFold

Q8BGW1

Predicted Effect

probably damaging
Transcript: ENSMUST00000069718
AA Change: E421K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

SMART Domains

Protein: ENSMUSP00000068380
Gene: ENSMUSG00000055932
AA Change: E421K

Domain	Start	End	E-Value	Type
low complexity region	7	24	N/A	INTRINSIC
FTO_NTD	35	323	2.71e-191	SMART
Pfam:FTO_CTD	326	495	1.1e-69	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000128081
AA Change: E421K

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140276

Meta Mutation Damage Score

0.2064

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.0%
20x: 94.9%

Validation Efficiency

100% (70/70)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA and RNA damage by oxidative demethylation. Studies in mice and humans indicate a role in nervous and cardiovascular systems and a strong association with body mass index, obesity risk, and type 2 diabetes. [provided by RefSeq, Jul 2011]
PHENOTYPE: Mice homozygous for an ENU-induced or targeted knock-out allele exhibit decreased body weight, adipose tissue, and body fat and increased metabolism, serum lipids, and serum glucagon that may be gender and diet dependent. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 66 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5530400C23Rik	G	A	6: 133,271,277 (GRCm39)	R107K	probably benign	Het
A530053G22Rik	T	C	6: 60,379,137 (GRCm39)		noncoding transcript	Het
Adcy9	A	G	16: 4,106,252 (GRCm39)	V954A	probably damaging	Het
Aldh8a1	T	A	10: 21,271,438 (GRCm39)	M388K	probably damaging	Het
Ankhd1	A	G	18: 36,779,819 (GRCm39)	I1720M	probably damaging	Het
Atp6v0a4	T	C	6: 38,030,064 (GRCm39)		probably benign	Het
C1qtnf4	T	A	2: 90,720,707 (GRCm39)	*327R	probably null	Het
C1s1	T	C	6: 124,518,277 (GRCm39)		probably benign	Het
Cdsn	A	C	17: 35,867,035 (GRCm39)	R521S	possibly damaging	Het
Cgnl1	T	C	9: 71,563,384 (GRCm39)	M848V	probably benign	Het
Cog3	A	G	14: 75,959,580 (GRCm39)	S591P	probably damaging	Het
Col6a3	A	G	1: 90,725,883 (GRCm39)	V1375A	possibly damaging	Het
Cplane1	T	A	15: 8,216,876 (GRCm39)	V698D	probably benign	Het
Cr1l	A	G	1: 194,794,720 (GRCm39)		probably benign	Het
Crmp1	T	A	5: 37,441,479 (GRCm39)	D520E	probably damaging	Het
Ctdspl2	T	A	2: 121,807,801 (GRCm39)		probably benign	Het
Dnah6	C	T	6: 73,132,262 (GRCm39)	A1147T	probably damaging	Het
Dsg2	T	C	18: 20,735,111 (GRCm39)	S1030P	probably benign	Het
Elavl3	C	A	9: 21,948,129 (GRCm39)	V12F	possibly damaging	Het
Fam20b	T	C	1: 156,518,140 (GRCm39)	E218G	probably damaging	Het
Fam227a	T	C	15: 79,505,033 (GRCm39)	D466G	possibly damaging	Het
Gab2	T	C	7: 96,948,279 (GRCm39)	Y290H	probably damaging	Het
Gm973	A	G	1: 59,621,633 (GRCm39)	Q591R	probably null	Het
Gsdmc2	T	C	15: 63,700,026 (GRCm39)	T249A	probably benign	Het
Il15ra	T	A	2: 11,735,459 (GRCm39)		probably null	Het
Il1rl1	CTTGTTGTTGTTGTTGTTG	CTTGTTGTTGTTGTTGTTGTTG	1: 40,481,734 (GRCm39)		probably benign	Het
Il6ra	A	G	3: 89,784,125 (GRCm39)	I382T	probably damaging	Het
Isy1	G	A	6: 87,796,167 (GRCm39)	R257W	probably damaging	Het
Krt76	T	C	15: 101,793,347 (GRCm39)	T564A	unknown	Het
Lhpp	T	C	7: 132,232,254 (GRCm39)	S57P	probably damaging	Het
Lrrk1	G	T	7: 65,942,089 (GRCm39)	D716E	probably damaging	Het
Mcm3ap	T	A	10: 76,335,368 (GRCm39)	D1263E	probably damaging	Het
Mogat1	A	G	1: 78,500,307 (GRCm39)	T124A	probably benign	Het
Mroh7	T	C	4: 106,568,467 (GRCm39)	T48A	possibly damaging	Het
Nccrp1	T	C	7: 28,246,463 (GRCm39)	D33G	probably benign	Het
Neurog1	G	T	13: 56,399,050 (GRCm39)	D232E	probably benign	Het
Or4a71	T	C	2: 89,358,707 (GRCm39)	T16A	probably benign	Het
Or4c105	T	A	2: 88,648,253 (GRCm39)	V246D	probably damaging	Het
Otog	C	A	7: 45,937,790 (GRCm39)	T1833K	possibly damaging	Het
Perm1	C	A	4: 156,302,682 (GRCm39)	H409N	probably benign	Het
Pik3r5	A	T	11: 68,381,337 (GRCm39)	E174D	probably damaging	Het
Pkhd1	G	A	1: 20,593,956 (GRCm39)	Q1386*	probably null	Het
Pla2r1	T	C	2: 60,345,325 (GRCm39)	R344G	possibly damaging	Het
Plekha5	G	A	6: 140,537,473 (GRCm39)	R646K	possibly damaging	Het
Plekhg4	G	A	8: 106,108,644 (GRCm39)	V1202M	possibly damaging	Het
Ppil4	A	G	10: 7,674,210 (GRCm39)	Y118C	probably damaging	Het
Prrc2b	G	T	2: 32,103,323 (GRCm39)	E934*	probably null	Het
Psmb9	A	G	17: 34,406,249 (GRCm39)	F12S	probably benign	Het
Ptdss2	T	C	7: 140,732,793 (GRCm39)	W183R	probably damaging	Het
Ptpn4	C	T	1: 119,615,335 (GRCm39)		probably null	Het
Reln	G	A	5: 22,253,813 (GRCm39)	R600W	probably damaging	Het
Scml4	T	A	10: 42,806,595 (GRCm39)	V161E	probably damaging	Het
Sdcbp2	A	T	2: 151,431,478 (GRCm39)	T284S	probably benign	Het
Slc22a29	T	C	19: 8,137,991 (GRCm39)		probably benign	Het
Slc35e1	T	C	8: 73,246,415 (GRCm39)		probably benign	Het
Spen	T	C	4: 141,197,121 (GRCm39)		probably benign	Het
Sumf2	T	A	5: 129,878,735 (GRCm39)		probably benign	Het
Tbx10	A	G	19: 4,043,121 (GRCm39)		probably benign	Het
Tex10	C	A	4: 48,468,957 (GRCm39)	V73F	probably damaging	Het
Tgm5	C	A	2: 120,907,493 (GRCm39)	G77W	probably damaging	Het
Tnfrsf21	T	A	17: 43,351,082 (GRCm39)		probably null	Het
Treml2	C	T	17: 48,609,856 (GRCm39)	T96I	probably damaging	Het
Trim65	T	C	11: 116,016,892 (GRCm39)	*523W	probably null	Het
Zcchc17	T	A	4: 130,243,099 (GRCm39)	D28V	probably benign	Het
Zhx2	T	C	15: 57,686,091 (GRCm39)	F487L	probably damaging	Het
Zkscan6	T	A	11: 65,712,811 (GRCm39)	L248Q	probably damaging	Het

Other mutations in Fto

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01458:Fto	APN	8	92,168,344 (GRCm39)	missense	probably benign	0.29
IGL01541:Fto	APN	8	92,136,376 (GRCm39)	missense	probably damaging	1.00
IGL01636:Fto	APN	8	92,135,969 (GRCm39)	missense	probably damaging	1.00
IGL01788:Fto	APN	8	92,136,359 (GRCm39)	missense	probably benign	0.25
IGL02016:Fto	APN	8	92,393,034 (GRCm39)	nonsense	probably null
IGL02365:Fto	APN	8	92,195,003 (GRCm39)	missense	probably damaging	1.00
IGL02639:Fto	APN	8	92,136,156 (GRCm39)	missense	probably damaging	1.00
IGL02926:Fto	APN	8	92,211,795 (GRCm39)	missense	probably damaging	1.00
IGL03194:Fto	APN	8	92,136,415 (GRCm39)	missense	probably damaging	1.00
R0091:Fto	UTSW	8	92,168,435 (GRCm39)	critical splice donor site	probably null
R0326:Fto	UTSW	8	92,136,155 (GRCm39)	missense	probably damaging	1.00
R0332:Fto	UTSW	8	92,128,518 (GRCm39)	splice site	probably benign
R0378:Fto	UTSW	8	92,200,940 (GRCm39)	missense	probably damaging	1.00
R0601:Fto	UTSW	8	92,128,430 (GRCm39)	splice site	probably null
R1526:Fto	UTSW	8	92,168,314 (GRCm39)	missense	possibly damaging	0.90
R2092:Fto	UTSW	8	92,136,315 (GRCm39)	nonsense	probably null
R4731:Fto	UTSW	8	92,136,342 (GRCm39)	missense	probably damaging	1.00
R4732:Fto	UTSW	8	92,136,342 (GRCm39)	missense	probably damaging	1.00
R4733:Fto	UTSW	8	92,136,342 (GRCm39)	missense	probably damaging	1.00
R5347:Fto	UTSW	8	92,118,107 (GRCm39)	intron	probably benign
R5840:Fto	UTSW	8	92,393,068 (GRCm39)	utr 3 prime	probably benign
R7213:Fto	UTSW	8	92,118,135 (GRCm39)	missense	probably benign	0.00
R7271:Fto	UTSW	8	92,211,818 (GRCm39)	missense	probably damaging	1.00
R7658:Fto	UTSW	8	92,392,950 (GRCm39)	missense	probably benign	0.34
R7763:Fto	UTSW	8	92,136,071 (GRCm39)	missense	probably damaging	0.99
R8110:Fto	UTSW	8	92,211,818 (GRCm39)	missense	probably damaging	1.00
R8700:Fto	UTSW	8	92,249,461 (GRCm39)	missense	probably damaging	0.96
R8915:Fto	UTSW	8	92,136,471 (GRCm39)	critical splice donor site	probably null
R9787:Fto	UTSW	8	92,211,886 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCACAGTGACCAGTCAGCGAAAATC -3'
(R):5'- AACCTTAGTTCTCTGAGCGGGACG -3'

Sequencing Primer
(F):5'- AATAGCTCATGGTAGGCAGTTCC -3'
(R):5'- TCTGAGCAGAACAAACCTGGC -3'

Posted On

2013-05-09