Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02230:Gm10030'

285666

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm10030

Ensembl Gene

ENSMUSG00000057802

Gene Name

predicted gene 10030

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.059) question?

Stock #

IGL02230

Quality Score

Status

Chromosome

Chromosomal Location

110818567-110837097 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to A at 110835458 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: ENSMUST00000080872

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197279

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000197321

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 33 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actn1	T	A	12: 80,218,604 (GRCm39)	T727S	probably benign	Het
Cyp4a12b	A	T	4: 115,291,193 (GRCm39)	I374F	probably damaging	Het
Ecel1	T	C	1: 87,079,916 (GRCm39)	N399S	probably damaging	Het
Fpr-rs3	T	C	17: 20,844,190 (GRCm39)	E317G	probably damaging	Het
Gm4884	A	T	7: 40,692,829 (GRCm39)	Q266L	probably damaging	Het
Gpr45	C	A	1: 43,071,816 (GRCm39)	A153E	probably damaging	Het
Hc	A	G	2: 34,903,682 (GRCm39)	F991L	probably benign	Het
Hif1a	T	G	12: 73,979,224 (GRCm39)	D249E	probably damaging	Het
Hsd17b12	A	G	2: 93,875,743 (GRCm39)	L194P	possibly damaging	Het
Hspg2	T	C	4: 137,245,956 (GRCm39)	S947P	probably damaging	Het
Kng1	G	T	16: 22,879,244 (GRCm39)		probably null	Het
Lpp	C	T	16: 24,580,895 (GRCm39)	R204W	probably damaging	Het
Lrrc4	T	A	6: 28,830,879 (GRCm39)	K245N	probably damaging	Het
Mdga2	G	A	12: 66,702,197 (GRCm39)	R335*	probably null	Het
Naa16	A	T	14: 79,614,801 (GRCm39)		probably benign	Het
Ncbp1	C	A	4: 46,165,272 (GRCm39)	N528K	probably benign	Het
Or10a2	A	G	7: 106,673,700 (GRCm39)	I222V	probably damaging	Het
Or7a41	T	A	10: 78,870,876 (GRCm39)	M82K	probably damaging	Het
Pipox	A	G	11: 77,772,032 (GRCm39)	L364P	probably damaging	Het
R3hdm4	C	A	10: 79,747,925 (GRCm39)	A206S	probably damaging	Het
Rasgrf2	A	G	13: 92,136,145 (GRCm39)	I589T	probably damaging	Het
Ror2	C	T	13: 53,264,764 (GRCm39)	S764N	probably damaging	Het
Sdr16c5	T	C	4: 4,016,354 (GRCm39)	E24G	probably damaging	Het
Sec24a	T	C	11: 51,599,861 (GRCm39)	I815V	possibly damaging	Het
Serpina16	A	G	12: 103,641,561 (GRCm39)	Y55H	probably damaging	Het
Sirt2	C	T	7: 28,478,371 (GRCm39)	R83C	probably damaging	Het
Sntg1	A	T	1: 8,752,195 (GRCm39)		probably null	Het
Stmn1	A	G	4: 134,200,224 (GRCm39)	E99G	probably damaging	Het
Tas2r103	T	C	6: 133,014,019 (GRCm39)	I16V	possibly damaging	Het
Vit	A	G	17: 78,927,056 (GRCm39)	K334E	probably damaging	Het
Washc4	T	C	10: 83,417,233 (GRCm39)	I876T	probably benign	Het
Wrn	A	T	8: 33,807,591 (GRCm39)	V289D	probably damaging	Het
Zfp318	C	T	17: 46,707,736 (GRCm39)	R265*	probably null	Het

Other mutations in Gm10030

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL03355:Gm10030	APN	9	110,835,841 (GRCm39)	splice site	noncoding transcript
R1834:Gm10030	UTSW	9	110,833,947 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16