Mutagenetix > Incidental Mutation

Incidental Mutation 'R0024:Gm9457'

15161

Institutional Source

Beutler Lab

Gene Symbol

Gm9457

Ensembl Gene

ENSMUSG00000095600

Gene Name

predicted gene 9457

Synonyms

MMRRC Submission

038319-MU

Accession Numbers

Essential gene?

Not available question?

Stock #

R0024 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

4862761-4863166 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to C at 4863131 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: ENSMUST00000180176

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000207403

Coding Region Coverage

1x: 79.2%
3x: 69.7%
10x: 44.0%
20x: 23.5%

Validation Efficiency

95% (75/79)

Allele List at MGI

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgre5	T	C	8: 84,454,913 (GRCm39)	T260A	probably damaging	Het
Ahctf1	G	A	1: 179,580,001 (GRCm39)	T2067M	probably damaging	Het
Akip1	T	C	7: 109,303,345 (GRCm39)	S63P	probably benign	Het
Ankrd34c	G	A	9: 89,611,580 (GRCm39)	P254S	possibly damaging	Het
Aqp8	T	C	7: 123,066,663 (GRCm39)	I256T	probably benign	Het
Arnt2	A	G	7: 83,933,334 (GRCm39)	V308A	probably benign	Het
Astn1	G	A	1: 158,511,785 (GRCm39)	S1209N	probably damaging	Het
Atf7ip	T	C	6: 136,576,818 (GRCm39)		probably benign	Het
Bbx	T	A	16: 50,045,281 (GRCm39)	M427L	probably benign	Het
Cadm4	T	C	7: 24,202,169 (GRCm39)	L336P	probably benign	Het
Camk2d	A	G	3: 126,591,372 (GRCm39)	M281V	probably benign	Het
Dennd2b	T	C	7: 109,123,866 (GRCm39)	H1131R	probably damaging	Het
Dll3	A	G	7: 27,999,586 (GRCm39)		probably benign	Het
Dscam	G	A	16: 96,394,585 (GRCm39)	R1906*	probably null	Het
Dst	C	T	1: 34,228,200 (GRCm39)	P1606L	probably damaging	Het
Eif2ak3	A	G	6: 70,869,340 (GRCm39)	T676A	probably benign	Het
Entpd5	T	C	12: 84,420,507 (GRCm39)	M428T	probably benign	Het
Fry	T	G	5: 150,304,268 (GRCm39)	S553A	probably benign	Het
Gls2	G	A	10: 128,035,125 (GRCm39)	R86H	probably damaging	Het
Gm14340	T	A	2: 180,466,043 (GRCm39)		noncoding transcript	Het
Hfm1	T	C	5: 107,004,790 (GRCm39)	K1179E	probably benign	Het
Iqgap1	T	C	7: 80,401,687 (GRCm39)	T473A	probably benign	Het
Krt34	A	T	11: 99,931,863 (GRCm39)	C119S	probably benign	Het
Krt6a	A	G	15: 101,599,150 (GRCm39)		probably benign	Het
Lysmd4	A	G	7: 66,875,828 (GRCm39)	T164A	probably benign	Het
Mroh2b	T	A	15: 4,955,109 (GRCm39)	Y701N	probably damaging	Het
Pi4ka	T	C	16: 17,133,399 (GRCm39)		probably benign	Het
Plcb1	A	G	2: 135,204,345 (GRCm39)	S900G	probably benign	Het
Plxna2	T	A	1: 194,326,303 (GRCm39)	I79N	possibly damaging	Het
Prpf31	C	A	7: 3,639,658 (GRCm39)		probably null	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Rsc1a1	T	C	4: 141,412,583 (GRCm39)	K110E	probably benign	Het
Sin3a	T	A	9: 57,025,537 (GRCm39)		probably benign	Het
Slc24a2	T	C	4: 86,946,477 (GRCm39)		probably benign	Het
Slc6a3	A	T	13: 73,688,956 (GRCm39)		probably benign	Het
Sugct	G	A	13: 17,032,454 (GRCm39)	H433Y	probably benign	Het
Sycp2l	A	G	13: 41,295,264 (GRCm39)	I310M	probably damaging	Het
Tpm3	C	A	3: 89,994,756 (GRCm39)		probably null	Het
Ttc27	T	C	17: 75,077,259 (GRCm39)	F385L	possibly damaging	Het
Utrn	A	G	10: 12,281,755 (GRCm39)	V3301A	probably benign	Het

Posted On

2012-12-12