Mutagenetix > Incidental Mutation

Incidental Mutation 'P0026:Gm10440'

8145

Institutional Source

Beutler Lab

Gene Symbol

Gm10440

Ensembl Gene

Gene Name

predicted gene 10440

Synonyms

MMRRC Submission

038279-MU

Accession Numbers

Essential gene?

Not available question?

Stock #

P0026 (G1)

Quality Score

Status

Validated

Chromosome

Chromosomal Location

54507334-54515884 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 54513511 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197424

Coding Region Coverage

Validation Efficiency

97% (63/65)

Allele List at MGI

Other mutations in this stock

Total: 26 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abi2	A	G	1: 60,492,882 (GRCm39)	N182D	probably benign	Het
Acad10	T	C	5: 121,775,415 (GRCm39)	Y429C	probably damaging	Het
Aifm3	A	T	16: 17,324,981 (GRCm39)		probably benign	Het
Bud13	A	G	9: 46,199,656 (GRCm39)	H339R	probably benign	Het
Cpa1	T	A	6: 30,640,905 (GRCm39)	M132K	probably damaging	Het
Dapk1	T	A	13: 60,865,963 (GRCm39)		probably benign	Het
Dchs1	A	T	7: 105,407,612 (GRCm39)	N2073K	probably damaging	Het
Dnah2	A	T	11: 69,355,773 (GRCm39)	N2227K	probably damaging	Het
Dnpep	C	T	1: 75,285,329 (GRCm39)	V468I	probably benign	Het
Elf3	A	G	1: 135,183,711 (GRCm39)		probably null	Het
Fam124a	T	G	14: 62,843,571 (GRCm39)	L360V	probably damaging	Het
Fam20a	A	T	11: 109,566,667 (GRCm39)		probably null	Het
Fermt3	A	G	19: 6,991,792 (GRCm39)	S140P	probably damaging	Het
Il12rb1	A	G	8: 71,265,185 (GRCm39)	D167G	probably damaging	Het
Ints8	T	A	4: 11,225,788 (GRCm39)	K590*	probably null	Het
Kcnu1	T	C	8: 26,382,150 (GRCm39)	F500S	probably damaging	Het
Mrm3	T	C	11: 76,138,326 (GRCm39)	V238A	probably damaging	Het
Rap1gap2	A	G	11: 74,458,036 (GRCm39)		probably benign	Het
Rusc2	T	A	4: 43,415,840 (GRCm39)	V382E	possibly damaging	Het
Slc9a5	A	G	8: 106,081,923 (GRCm39)	N216S	probably damaging	Het
Snx7	A	T	3: 117,633,672 (GRCm39)	F63I	probably damaging	Het
Syne2	A	G	12: 75,926,994 (GRCm39)		probably benign	Het
Tenm4	T	C	7: 96,523,734 (GRCm39)	Y1751H	probably damaging	Het
Trappc9	G	A	15: 72,824,931 (GRCm39)	P366S	probably damaging	Het
Trim17	A	G	11: 58,862,084 (GRCm39)	D372G	possibly damaging	Het
Zfp354a	G	A	11: 50,952,325 (GRCm39)	G85R	probably null	Het

Posted On

2012-11-20