Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02416:Gm5407'

292433

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5407

Ensembl Gene

ENSMUSG00000058176

Gene Name

predicted gene 5407

Synonyms

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.267) question?

Stock #

IGL02416

Quality Score

Status

Chromosome

Chromosomal Location

49117014-49118261 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 49117250 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000079520 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000080694]

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000080694

SMART Domains

Protein: ENSMUSP00000079520
Gene: ENSMUSG00000058176

Domain	Start	End	E-Value	Type
Pfam:Peptidase_C48	67	247	6.5e-43	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 39 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamdec1	T	C	14: 68,810,282 (GRCm39)	N227S	probably null	Het
Adgrf5	T	G	17: 43,755,871 (GRCm39)		probably null	Het
Arid2	G	A	15: 96,247,936 (GRCm39)	G116D	possibly damaging	Het
Arsa	T	A	15: 89,358,991 (GRCm39)	H225L	probably damaging	Het
Atf6	T	A	1: 170,574,726 (GRCm39)	K571*	probably null	Het
Bicdl1	A	C	5: 115,801,944 (GRCm39)	L38R	probably damaging	Het
Cct4	T	C	11: 22,952,868 (GRCm39)	S515P	probably damaging	Het
Celsr3	A	C	9: 108,709,318 (GRCm39)	D1388A	probably damaging	Het
Clca3a2	T	C	3: 144,790,777 (GRCm39)	T432A	probably benign	Het
Des	T	A	1: 75,339,372 (GRCm39)		probably null	Het
Dock11	T	A	X: 35,283,739 (GRCm39)	V1119E	probably damaging	Het
Dysf	A	G	6: 84,169,896 (GRCm39)	N1763S	possibly damaging	Het
Emilin1	A	G	5: 31,075,132 (GRCm39)	S458G	possibly damaging	Het
Fhdc1	T	G	3: 84,352,535 (GRCm39)	M897L	probably benign	Het
Foxj1	T	C	11: 116,222,829 (GRCm39)	S325G	probably benign	Het
Gm6576	T	C	15: 27,026,073 (GRCm39)		noncoding transcript	Het
Hells	G	A	19: 38,953,071 (GRCm39)	S743N	probably benign	Het
Ighv2-9-1	A	T	12: 113,733,731 (GRCm39)	L30Q	probably damaging	Het
Iqgap1	A	T	7: 80,375,786 (GRCm39)	L1363H	probably damaging	Het
Lrp2	T	C	2: 69,299,977 (GRCm39)	D3025G	probably damaging	Het
Mef2d	C	T	3: 88,063,809 (GRCm39)	R79C	probably damaging	Het
Mical1	G	T	10: 41,360,806 (GRCm39)		probably null	Het
Micu2	A	T	14: 58,161,422 (GRCm39)	V300E	probably damaging	Het
Mmgt2	T	C	11: 62,555,703 (GRCm39)	L17P	probably damaging	Het
Or4p21	A	G	2: 88,277,174 (GRCm39)	I36T	probably benign	Het
Or7c19	T	A	8: 85,957,662 (GRCm39)	C179*	probably null	Het
Or7e177	A	T	9: 20,211,541 (GRCm39)	E15V	probably benign	Het
Pigb	A	G	9: 72,924,714 (GRCm39)	S482P	probably benign	Het
Pkd1l2	T	A	8: 117,767,574 (GRCm39)	T1239S	possibly damaging	Het
Pou1f1	T	C	16: 65,328,842 (GRCm39)	I187T	probably damaging	Het
Prox1	C	T	1: 189,893,327 (GRCm39)	A373T	probably benign	Het
Rabgap1	T	C	2: 37,451,962 (GRCm39)	I954T	probably benign	Het
Scube3	T	G	17: 28,383,110 (GRCm39)	C429W	probably damaging	Het
Slco6b1	T	A	1: 96,852,058 (GRCm39)		noncoding transcript	Het
Strc	A	T	2: 121,199,539 (GRCm39)	I1300N	probably damaging	Het
Tdrd6	T	A	17: 43,935,629 (GRCm39)	R1806S	probably benign	Het
Trpm8	T	A	1: 88,288,438 (GRCm39)	L860Q	probably damaging	Het
Vmn1r8	A	G	6: 57,013,605 (GRCm39)	R219G	probably damaging	Het
Wdr48	A	G	9: 119,753,826 (GRCm39)	S649G	probably damaging	Het

Other mutations in Gm5407

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL03110:Gm5407	APN	16	49,117,757 (GRCm39)	exon	noncoding transcript
R1913:Gm5407	UTSW	16	49,117,283 (GRCm39)	exon	noncoding transcript
R2959:Gm5407	UTSW	16	49,117,326 (GRCm39)	exon	noncoding transcript
R4728:Gm5407	UTSW	16	49,117,283 (GRCm39)	exon	noncoding transcript
R5771:Gm5407	UTSW	16	49,117,229 (GRCm39)	exon	noncoding transcript
R8292:Gm5407	UTSW	16	49,117,550 (GRCm39)	missense	noncoding transcript

Posted On

2015-04-16