Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02345:Gm5852'

289232

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 #

IGL02345

Quality Score

Status

Chromosome

Chromosomal Location

93634333-93635353 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to A at 93635055 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: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcc1	G	T	16: 14,214,215 (GRCm39)	D177Y	possibly damaging	Het
Casc3	T	C	11: 98,718,390 (GRCm39)		probably benign	Het
Catspere2	G	A	1: 177,842,754 (GRCm39)	V60I	possibly damaging	Het
Cnga1	C	T	5: 72,762,615 (GRCm39)	V300I	probably benign	Het
Dcun1d4	A	G	5: 73,668,495 (GRCm39)	D41G	probably damaging	Het
Dnm1l	T	C	16: 16,147,758 (GRCm39)	S181G	possibly damaging	Het
Dyrk1a	T	G	16: 94,472,221 (GRCm39)	S242A	possibly damaging	Het
Fcgbp	T	A	7: 27,771,068 (GRCm39)		probably benign	Het
Fibcd1	T	C	2: 31,706,604 (GRCm39)	Y409C	probably damaging	Het
Fig4	A	T	10: 41,143,770 (GRCm39)	W230R	probably null	Het
Flt1	T	C	5: 147,519,436 (GRCm39)	S960G	probably benign	Het
Fyb1	A	G	15: 6,649,143 (GRCm39)	S390G	possibly damaging	Het
Gbx2	T	C	1: 89,856,698 (GRCm39)	T231A	probably benign	Het
Lmo7	T	C	14: 102,124,909 (GRCm39)	V456A	probably damaging	Het
Mark3	A	G	12: 111,593,541 (GRCm39)	N191S	probably damaging	Het
Or7h8	C	A	9: 20,124,314 (GRCm39)	S223Y	possibly damaging	Het
Pik3c2a	C	T	7: 116,005,126 (GRCm39)	E381K	probably damaging	Het
Pik3r5	A	G	11: 68,383,552 (GRCm39)	D457G	probably benign	Het
Plcg2	T	C	8: 118,311,919 (GRCm39)	S404P	probably damaging	Het
Prr16	T	C	18: 51,436,301 (GRCm39)	F260S	probably damaging	Het
Psd4	T	C	2: 24,291,835 (GRCm39)		probably null	Het
Ptgs1	A	G	2: 36,132,983 (GRCm39)	D327G	probably null	Het
Rgsl1	C	T	1: 153,679,755 (GRCm39)		probably null	Het
Spart	T	A	3: 55,025,147 (GRCm39)		probably null	Het
Sugp1	A	G	8: 70,495,734 (GRCm39)		probably benign	Het
Tubgcp3	A	T	8: 12,675,056 (GRCm39)	I713N	probably damaging	Het
Usp19	A	G	9: 108,371,057 (GRCm39)	T240A	probably benign	Het
Vash2	A	G	1: 190,710,412 (GRCm39)	V81A	probably benign	Het
Vmn2r41	T	G	7: 8,141,767 (GRCm39)	N566H	probably damaging	Het
Wdr31	A	G	4: 62,377,083 (GRCm39)	I42T	possibly damaging	Het
Zfp292	C	T	4: 34,809,244 (GRCm39)	V1272I	possibly damaging	Het
Zfp638	C	T	6: 83,961,857 (GRCm39)	R1899C	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
IGL02179:Gm5852	APN	3	93,635,023 (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