Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03152:Gm4799'

411126

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm4799

Ensembl Gene

Gene Name

predicted gene 4799

Synonyms

Accession Numbers

Essential gene?

Probably essential (E-score: 0.862) question?

Stock #

IGL03152

Quality Score

Status

Chromosome

Chromosomal Location

82790178-82790834 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 82790797 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: ENSMUST00000095396

SMART Domains

Protein: ENSMUSP00000093045
Gene: ENSMUSG00000071151

Domain	Start	End	E-Value	Type
low complexity region	7	40	N/A	INTRINSIC
low complexity region	45	69	N/A	INTRINSIC
low complexity region	76	91	N/A	INTRINSIC
Pfam:TFIID_30kDa	128	177	2.1e-29	PFAM
low complexity region	181	192	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 23 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Cacna2d1	T	A	5: 16,527,566 (GRCm39)	N540K	probably benign	Het
Caln1	A	G	5: 130,646,693 (GRCm39)	E43G	probably damaging	Het
Car14	A	C	3: 95,806,157 (GRCm39)	C301W	probably damaging	Het
Clpx	G	A	9: 65,217,458 (GRCm39)	V9I	possibly damaging	Het
Edar	A	G	10: 58,445,817 (GRCm39)	F249S	possibly damaging	Het
Fads2b	A	G	2: 85,330,648 (GRCm39)	S220P	probably damaging	Het
Fhip2a	C	A	19: 57,367,264 (GRCm39)	T269K	probably damaging	Het
Grk4	T	C	5: 34,902,701 (GRCm39)	S418P	probably damaging	Het
Kcnh4	A	G	11: 100,636,598 (GRCm39)	S774P	probably benign	Het
Kif23	A	G	9: 61,837,058 (GRCm39)		probably benign	Het
Lyl1	C	T	8: 85,429,300 (GRCm39)	P3L	possibly damaging	Het
Myef2l	A	T	3: 10,153,334 (GRCm39)	K34N	probably benign	Het
Or5al1	A	T	2: 85,990,030 (GRCm39)	I228N	possibly damaging	Het
Pcgf6	A	T	19: 47,037,344 (GRCm39)		probably benign	Het
Ryr2	G	A	13: 11,868,036 (GRCm39)	R265C	probably damaging	Het
Smgc	A	G	15: 91,725,625 (GRCm39)	K2R	possibly damaging	Het
Stx5a	T	C	19: 8,727,138 (GRCm39)		probably null	Het
Syne2	A	T	12: 76,012,486 (GRCm39)	N2560I	probably benign	Het
Tuba3a	A	T	6: 125,258,300 (GRCm39)	L230Q	probably damaging	Het
Tubb4b-ps1	A	G	5: 7,230,001 (GRCm39)		probably benign	Het
Zfp217	A	G	2: 169,960,972 (GRCm39)	S452P	probably damaging	Het
Zfp764l1	A	G	7: 126,991,469 (GRCm39)	C173R	probably damaging	Het
Zzef1	G	A	11: 72,814,008 (GRCm39)		probably null	Het

Other mutations in Gm4799

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01396:Gm4799	APN	10	82,790,518 (GRCm39)	exon	noncoding transcript
IGL02152:Gm4799	APN	10	82,790,589 (GRCm39)	exon	noncoding transcript
R0611:Gm4799	UTSW	10	82,790,563 (GRCm39)	exon	noncoding transcript
R1501:Gm4799	UTSW	10	82,790,469 (GRCm39)	exon	noncoding transcript
R5869:Gm4799	UTSW	10	82,790,283 (GRCm39)	exon	noncoding transcript

Posted On

2016-08-02