Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02693:Gm5866'

303841

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5866

Ensembl Gene

ENSMUSG00000095078

Gene Name

predicted gene 5866

Synonyms

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.436) question?

Stock #

IGL02693

Quality Score

Status

Chromosome

Chromosomal Location

52739416-52740388 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to T at 52740558 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: ENSMUST00000177881

SMART Domains

Protein: ENSMUSP00000137023
Gene: ENSMUSG00000095078

Domain	Start	End	E-Value	Type
Pfam:Nuc_sug_transp	3	239	4.6e-32	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A830018L16Rik	A	G	1: 11,666,506 (GRCm39)	D271G	probably damaging	Het
Agl	A	T	3: 116,540,077 (GRCm39)	V1478E	possibly damaging	Het
Ckap5	C	T	2: 91,400,556 (GRCm39)	P636L	probably damaging	Het
Cnot1	A	G	8: 96,500,113 (GRCm39)	V127A	probably damaging	Het
Cs	A	G	10: 128,185,678 (GRCm39)		probably benign	Het
Fbln1	G	A	15: 85,113,775 (GRCm39)	E170K	probably benign	Het
Lpin3	T	C	2: 160,746,975 (GRCm39)	V794A	probably damaging	Het
Ly86	T	G	13: 37,559,005 (GRCm39)	I68S	probably damaging	Het
Mrps34	A	G	17: 25,114,172 (GRCm39)	I11V	probably benign	Het
Nsmce4a	A	G	7: 130,144,538 (GRCm39)	S122P	probably damaging	Het
Olfm1	A	G	2: 28,102,662 (GRCm39)	E112G	probably damaging	Het
Or5w20	T	G	2: 87,726,877 (GRCm39)	C111W	probably damaging	Het
Parp9	A	G	16: 35,777,340 (GRCm39)	E428G	probably benign	Het
Phkb	T	G	8: 86,668,863 (GRCm39)	F297V	probably damaging	Het
Pianp	T	G	6: 124,978,598 (GRCm39)	F268V	possibly damaging	Het
Polr1a	T	C	6: 71,940,830 (GRCm39)		probably benign	Het
Prune2	G	A	19: 17,101,855 (GRCm39)	G2453E	probably benign	Het
Ptpn4	T	C	1: 119,643,699 (GRCm39)	N350D	probably damaging	Het
Rbm12	C	T	2: 155,937,480 (GRCm39)		probably benign	Het
Rfc4	A	G	16: 22,932,960 (GRCm39)	S326P	probably damaging	Het
Rnf123	G	A	9: 107,945,501 (GRCm39)	R390*	probably null	Het
Slc35f1	A	T	10: 52,809,224 (GRCm39)	L70F	probably damaging	Het
Slc5a7	T	C	17: 54,583,947 (GRCm39)	T448A	probably benign	Het
Spata31h1	T	C	10: 82,121,092 (GRCm39)	I3973V	probably benign	Het
Spmip9	C	A	6: 70,890,488 (GRCm39)	R101S	possibly damaging	Het
Stoml1	T	A	9: 58,164,359 (GRCm39)	I149N	probably damaging	Het
Sytl1	A	T	4: 132,985,057 (GRCm39)	C180S	probably benign	Het
Traf6	T	C	2: 101,518,850 (GRCm39)	L113P	possibly damaging	Het
Trappc9	A	G	15: 72,835,542 (GRCm39)		probably benign	Het
Tubg2	T	C	11: 101,051,725 (GRCm39)	Y317H	probably damaging	Het
Zfp334	T	C	2: 165,222,433 (GRCm39)	T537A	possibly damaging	Het

Other mutations in Gm5866

Allele	Source	Chr	Coord	Type	Predicted Effect
R3771:Gm5866	UTSW	5	52,740,088 (GRCm39)	exon	noncoding transcript
R3772:Gm5866	UTSW	5	52,740,088 (GRCm39)	exon	noncoding transcript
R4657:Gm5866	UTSW	5	52,740,262 (GRCm39)	exon	noncoding transcript
R5052:Gm5866	UTSW	5	52,740,234 (GRCm39)	exon	noncoding transcript
R5120:Gm5866	UTSW	5	52,740,224 (GRCm39)	exon	noncoding transcript
R5874:Gm5866	UTSW	5	52,739,956 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16