Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02179:Gm5852'

283231

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5852

Ensembl Gene

ENSMUSG00000103210

Gene Name

predicted gene 5852

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02179

Quality Score

Status

Chromosome

Chromosomal Location

93634333-93635353 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

C to T at 93635023 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: ENSMUST00000193543

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194119

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 37 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abl1	C	A	2: 31,682,261 (GRCm39)	A385D	probably damaging	Het
Ace	A	G	11: 105,860,615 (GRCm39)	D174G	probably benign	Het
Aldh1l2	A	G	10: 83,358,701 (GRCm39)	V98A	probably benign	Het
AU040320	T	A	4: 126,729,405 (GRCm39)	F522L	probably benign	Het
Ccdc73	A	G	2: 104,737,913 (GRCm39)	D3G	probably damaging	Het
Cdk14	A	C	5: 5,153,845 (GRCm39)	L199V	probably damaging	Het
Cdk15	G	T	1: 59,370,100 (GRCm39)	A381S	possibly damaging	Het
Cyb5a	A	G	18: 84,891,280 (GRCm39)	I68V	probably benign	Het
Dock5	G	A	14: 68,043,945 (GRCm39)		probably benign	Het
Fbxw24	T	A	9: 109,438,973 (GRCm39)	K201*	probably null	Het
Gsdma3	A	G	11: 98,526,097 (GRCm39)	K274E	possibly damaging	Het
Hoxa7	T	A	6: 52,192,854 (GRCm39)	Q178L	probably damaging	Het
Itgae	G	T	11: 73,024,844 (GRCm39)	V992L	probably benign	Het
Klk1b26	A	G	7: 43,665,736 (GRCm39)	N183D	probably benign	Het
Krt39	A	T	11: 99,411,667 (GRCm39)	S140T	probably damaging	Het
Lama2	G	A	10: 26,946,360 (GRCm39)	T1953I	probably benign	Het
Mmp1a	G	A	9: 7,464,273 (GRCm39)	R26Q	probably benign	Het
Myh7b	A	C	2: 155,456,411 (GRCm39)	I175L	probably benign	Het
Nol11	A	G	11: 107,080,082 (GRCm39)	M1T	probably null	Het
Nrxn1	T	A	17: 90,937,511 (GRCm39)	I641F	probably damaging	Het
Or51ag1	A	C	7: 103,155,934 (GRCm39)	L73R	probably damaging	Het
Or8k3	A	T	2: 86,058,591 (GRCm39)	C241*	probably null	Het
Or9i2	T	C	19: 13,815,851 (GRCm39)	T229A	probably benign	Het
Parn	G	T	16: 13,485,456 (GRCm39)	H13Q	probably benign	Het
Pcnx1	T	C	12: 81,980,493 (GRCm39)		probably benign	Het
Pdcd10	T	C	3: 75,434,922 (GRCm39)	D60G	probably damaging	Het
Phka2	G	A	X: 159,337,376 (GRCm39)		probably null	Het
Ppargc1a	A	T	5: 51,631,053 (GRCm39)	D525E	possibly damaging	Het
Rad54l2	C	A	9: 106,597,589 (GRCm39)	R139L	probably damaging	Het
Rnf20	T	C	4: 49,638,712 (GRCm39)	V178A	probably benign	Het
Ror2	C	T	13: 53,264,764 (GRCm39)	S764N	probably damaging	Het
Sdccag8	C	T	1: 176,705,622 (GRCm39)	H479Y	probably benign	Het
Taf8	T	C	17: 47,813,158 (GRCm39)	T13A	probably benign	Het
Ttc8	T	C	12: 98,930,796 (GRCm39)	L270P	possibly damaging	Het
Ttn	G	A	2: 76,717,712 (GRCm39)	Q365*	probably null	Het
Uchl1	A	G	5: 66,833,637 (GRCm39)	Q2R	probably benign	Het
Ufl1	A	G	4: 25,254,896 (GRCm39)	V440A	probably damaging	Het

Other mutations in Gm5852

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00340:Gm5852	APN	3	93,634,501 (GRCm39)	exon	noncoding transcript
IGL01432:Gm5852	APN	3	93,635,086 (GRCm39)	missense	possibly damaging	0.86
IGL02345:Gm5852	APN	3	93,635,055 (GRCm39)	exon	noncoding transcript
IGL02366:Gm5852	APN	3	93,634,568 (GRCm39)	exon	noncoding transcript
IGL03279:Gm5852	APN	3	93,634,584 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16