Mutagenetix > Incidental Mutation

Incidental Mutation 'R0064:Gm270'

16425

Institutional Source

Beutler Lab

Gene Symbol

Gm270

Ensembl Gene

Gene Name

predicted gene 270

Synonyms

LOC218241

MMRRC Submission

038356-MU

Accession Numbers

Essential gene?

Not available question?

Stock #

R0064 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

49917804-49918779 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

C to A at 49919367 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000223010

Coding Region Coverage

1x: 87.7%
3x: 83.1%
10x: 65.7%
20x: 35.9%

Validation Efficiency

92% (56/61)

Allele List at MGI

All alleles(1) : Gene trapped(1)

Other mutations in this stock

Total: 24 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abhd18	A	G	3: 40,888,288 (GRCm39)	I377M	probably benign	Het
Ccdc25	T	A	14: 66,091,561 (GRCm39)	I60K	possibly damaging	Het
Cdk1	T	C	10: 69,180,907 (GRCm39)	D101G	probably benign	Het
Cep126	A	T	9: 8,130,183 (GRCm39)		probably benign	Het
Col1a2	G	A	6: 4,518,822 (GRCm39)		probably benign	Het
Crlf3	A	G	11: 79,948,728 (GRCm39)	I239T	possibly damaging	Het
Cul1	A	G	6: 47,479,349 (GRCm39)		probably benign	Het
Fbp2	A	T	13: 63,001,862 (GRCm39)	F118I	probably damaging	Het
Fgd3	T	G	13: 49,449,901 (GRCm39)	D116A	possibly damaging	Het
Knl1	T	A	2: 118,906,724 (GRCm39)	N1604K	probably benign	Het
Lpl	A	G	8: 69,345,356 (GRCm39)	H120R	probably damaging	Het
Myo18a	G	T	11: 77,738,170 (GRCm39)	R1704L	probably damaging	Het
Nlrc3	G	T	16: 3,781,951 (GRCm39)	T486K	possibly damaging	Het
Obscn	A	C	11: 58,918,292 (GRCm39)	V6260G	probably damaging	Het
Or10a2	T	C	7: 106,673,487 (GRCm39)	F151L	probably benign	Het
Pmpca	C	A	2: 26,285,519 (GRCm39)	D498E	probably benign	Het
Pnpla7	G	T	2: 24,887,239 (GRCm39)	E28*	probably null	Het
Polg	C	A	7: 79,111,632 (GRCm39)	W206C	probably damaging	Het
Spata31	T	C	13: 65,069,912 (GRCm39)	Y687H	probably damaging	Het
Sybu	T	A	15: 44,536,389 (GRCm39)	T646S	probably benign	Het
Tns3	G	A	11: 8,385,856 (GRCm39)	Q1381*	probably null	Het
Trank1	A	G	9: 111,172,263 (GRCm39)	D84G	probably damaging	Het
Urb1	A	G	16: 90,576,028 (GRCm39)	F843L	probably benign	Het
Zfp287	A	T	11: 62,605,764 (GRCm39)	L370H	possibly damaging	Het

Other mutations in Gm270

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
3-1:Gm270	UTSW	13	49,918,539 (GRCm39)	exon	noncoding transcript

Posted On

2013-01-20