Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03073:4933440M02Rik'

417583

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4933440M02Rik

Ensembl Gene

ENSMUSG00000045928

Gene Name

RIKEN cDNA 4933440M02 gene

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.089) question?

Stock #

IGL03073

Quality Score

Status

Chromosome

Chromosomal Location

124930954-124948958 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 124930735 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: ENSMUST00000061823

SMART Domains

Protein: ENSMUSP00000058153
Gene: ENSMUSG00000045928

Domain	Start	End	E-Value	Type
low complexity region	106	117	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000205794

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000206609

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 33 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actr6	A	G	10: 89,562,556 (GRCm39)	S108P	probably damaging	Het
Adam34	A	T	8: 44,103,940 (GRCm39)	N568K	probably damaging	Het
Anpep	A	G	7: 79,488,703 (GRCm39)	L408P	probably damaging	Het
Atp13a1	T	C	8: 70,251,152 (GRCm39)	V459A	probably damaging	Het
Atp2b1	C	T	10: 98,835,713 (GRCm39)	T486M	probably damaging	Het
Cdc42bpa	T	A	1: 179,921,941 (GRCm39)		probably benign	Het
Espnl	T	C	1: 91,272,278 (GRCm39)	I502T	probably damaging	Het
Fancm	T	C	12: 65,148,406 (GRCm39)	Y674H	probably damaging	Het
Gnaq	T	A	19: 16,293,470 (GRCm39)	N137K	probably benign	Het
Igf1r	T	A	7: 67,864,791 (GRCm39)	D1196E	probably damaging	Het
Insrr	A	G	3: 87,717,245 (GRCm39)		probably benign	Het
Lypd9	A	T	11: 58,338,277 (GRCm39)	D38E	probably damaging	Het
Mcf2l	C	A	8: 13,050,004 (GRCm39)	H313N	probably damaging	Het
Mdh1b	C	T	1: 63,760,646 (GRCm39)		probably null	Het
Mrc1	G	A	2: 14,310,153 (GRCm39)	V805I	probably damaging	Het
Ncam2	T	G	16: 81,418,235 (GRCm39)	D763E	possibly damaging	Het
Ncapg2	T	G	12: 116,415,894 (GRCm39)	H1091Q	probably benign	Het
Or5b112	T	G	19: 13,319,386 (GRCm39)	I88R	probably benign	Het
Or8h8	A	G	2: 86,753,697 (GRCm39)	Y60H	probably damaging	Het
Pcdh18	T	A	3: 49,707,816 (GRCm39)	D886V	possibly damaging	Het
Pdlim4	A	G	11: 53,954,467 (GRCm39)	V21A	probably damaging	Het
Safb2	A	G	17: 56,878,289 (GRCm39)	S24P	probably benign	Het
Sec16a	A	G	2: 26,329,195 (GRCm39)	M940T	probably benign	Het
Snx14	A	G	9: 88,304,949 (GRCm39)		probably null	Het
Sox1	T	C	8: 12,446,625 (GRCm39)	W89R	probably damaging	Het
Stx12	T	C	4: 132,585,760 (GRCm39)	M207V	probably benign	Het
Tex14	A	G	11: 87,426,435 (GRCm39)	T1154A	probably damaging	Het
Tmcc3	T	G	10: 94,414,813 (GRCm39)	S172A	probably benign	Het
Tnc	T	A	4: 63,889,461 (GRCm39)	I1773F	possibly damaging	Het
Tshz3	A	T	7: 36,470,170 (GRCm39)	N720Y	probably damaging	Het
Usp19	G	A	9: 108,373,002 (GRCm39)		probably benign	Het
Vmn1r170	A	C	7: 23,306,273 (GRCm39)	Q225P	probably damaging	Het
Vmn2r89	A	G	14: 51,693,528 (GRCm39)	I293V	possibly damaging	Het

Other mutations in 4933440M02Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02104:4933440M02Rik	APN	7	124,930,714 (GRCm39)	unclassified	noncoding transcript
IGL02115:4933440M02Rik	APN	7	124,930,781 (GRCm39)	unclassified	noncoding transcript
IGL02977:4933440M02Rik	APN	7	124,930,874 (GRCm39)	unclassified	noncoding transcript
R0525:4933440M02Rik	UTSW	7	124,930,671 (GRCm39)	unclassified	noncoding transcript
R4787:4933440M02Rik	UTSW	7	124,930,714 (GRCm39)	unclassified	noncoding transcript

Posted On

2016-08-02