Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01113:4930544L04Rik'

51575

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4930544L04Rik

Ensembl Gene

ENSMUSG00000073803

Gene Name

RIKEN cDNA 4930544L04 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01113

Quality Score

Status

Chromosome

Chromosomal Location

134998064-135001273 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 134998871 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: ENSMUST00000097982

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000211181

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
Adam34l	T	C	8: 44,079,189 (GRCm39)	H345R	probably damaging	Het
Adgrv1	A	T	13: 81,637,147 (GRCm39)	F3431L	probably benign	Het
Adk	A	G	14: 21,142,461 (GRCm39)	N21S	probably damaging	Het
Cacna2d3	A	G	14: 29,022,688 (GRCm39)		probably benign	Het
Camk2d	C	A	3: 126,574,061 (GRCm39)	A156E	probably damaging	Het
Ccdc171	G	T	4: 83,580,047 (GRCm39)	W598L	probably damaging	Het
Cep85	C	T	4: 133,876,072 (GRCm39)	V445I	possibly damaging	Het
Cftr	A	G	6: 18,270,252 (GRCm39)	Y814C	probably damaging	Het
Dctn1	T	C	6: 83,156,879 (GRCm39)	S9P	probably benign	Het
Dmxl1	A	G	18: 50,045,818 (GRCm39)	K2409R	probably benign	Het
Dnaaf1	T	A	8: 120,309,317 (GRCm39)	I135N	probably damaging	Het
Eif3d	G	A	15: 77,847,515 (GRCm39)	T241M	probably damaging	Het
Etv1	T	C	12: 38,831,791 (GRCm39)		probably benign	Het
Gdpd3	C	A	7: 126,366,997 (GRCm39)	S182R	probably benign	Het
Gm12888	C	A	4: 121,175,521 (GRCm39)	C87F	probably damaging	Het
Gml	C	A	15: 74,685,576 (GRCm39)	M136I	probably benign	Het
Habp2	A	G	19: 56,298,548 (GRCm39)	T137A	probably benign	Het
Igkv6-25	C	T	6: 70,192,772 (GRCm39)	P60S	possibly damaging	Het
Mak	A	T	13: 41,195,619 (GRCm39)	W396R	probably damaging	Het
Mast4	C	A	13: 102,910,744 (GRCm39)	C441F	probably damaging	Het
Medag	T	C	5: 149,353,372 (GRCm39)	I189T	probably benign	Het
Myh1	A	G	11: 67,093,006 (GRCm39)	T71A	probably benign	Het
Nin	G	T	12: 70,078,553 (GRCm39)	L1678M	probably damaging	Het
Nol6	T	C	4: 41,115,749 (GRCm39)	D1081G	probably damaging	Het
Or1j4	A	T	2: 36,740,631 (GRCm39)	D191V	probably damaging	Het
Or6f1	A	T	7: 85,970,361 (GRCm39)	D266E	probably benign	Het
Ppp1r10	T	A	17: 36,240,451 (GRCm39)	N580K	probably damaging	Het
Rpgrip1l	T	C	8: 91,987,367 (GRCm39)		probably benign	Het
Serpinb3a	G	A	1: 106,978,789 (GRCm39)	Q57*	probably null	Het
Thumpd3	T	C	6: 113,037,021 (GRCm39)	S307P	probably benign	Het
Upf1	A	C	8: 70,790,934 (GRCm39)	D577E	probably benign	Het
Vmn2r99	T	C	17: 19,614,518 (GRCm39)	V746A	probably benign	Het
Wscd2	T	C	5: 113,708,800 (GRCm39)	V268A	probably damaging	Het

Posted On

2013-06-21