Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01149:4632415L05Rik'

50805

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4632415L05Rik

Ensembl Gene

ENSMUSG00000048106

Gene Name

RIKEN cDNA 4632415L05 gene

Synonyms

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.401) question?

Stock #

IGL01149

Quality Score

Status

Chromosome

Chromosomal Location

19949146-19950173 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to G at 19949276 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: ENSMUST00000059704

SMART Domains

Protein: ENSMUSP00000055285
Gene: ENSMUSG00000048106

Domain	Start	End	E-Value	Type
low complexity region	55	103	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198527

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 30 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aadacl4fm4	T	C	4: 144,400,349 (GRCm39)	D143G	probably benign	Het
Adcy1	A	C	11: 7,087,385 (GRCm39)	N420H	probably damaging	Het
Avp	T	C	2: 130,422,593 (GRCm39)		probably benign	Het
B3galnt2	A	T	13: 14,155,270 (GRCm39)	I216F	probably benign	Het
Cdc42bpa	T	C	1: 179,902,137 (GRCm39)	S465P	probably damaging	Het
Cdc42bpg	T	A	19: 6,362,235 (GRCm39)		probably benign	Het
Cdcp2	T	C	4: 106,964,308 (GRCm39)	F386S	probably benign	Het
Cdh4	A	G	2: 179,515,937 (GRCm39)	T372A	probably damaging	Het
Clspn	T	G	4: 126,466,971 (GRCm39)	M612R	probably damaging	Het
Dll4	T	C	2: 119,161,590 (GRCm39)	C391R	probably damaging	Het
Dll4	T	C	2: 119,163,226 (GRCm39)	Y616H	probably damaging	Het
Exoc1	A	G	5: 76,690,091 (GRCm39)		probably benign	Het
F830045P16Rik	A	G	2: 129,302,232 (GRCm39)		probably null	Het
Fhod1	A	G	8: 106,074,439 (GRCm39)		probably benign	Het
Fign	T	C	2: 63,810,104 (GRCm39)	R389G	possibly damaging	Het
Gm13941	T	A	2: 110,931,482 (GRCm39)	E50V	unknown	Het
Kit	C	T	5: 75,771,536 (GRCm39)	T231M	probably damaging	Het
Neu3	T	C	7: 99,463,087 (GRCm39)	H212R	probably benign	Het
Nup214	G	T	2: 31,924,712 (GRCm39)	S1747I	probably damaging	Het
Or4f4b	T	C	2: 111,314,446 (GRCm39)	S224P	probably damaging	Het
Or4q3	G	T	14: 50,583,071 (GRCm39)	A276E	probably damaging	Het
Or8b12i	G	T	9: 20,082,826 (GRCm39)	L14I	probably damaging	Het
Secisbp2	T	C	13: 51,830,491 (GRCm39)		probably null	Het
Slc26a10	G	A	10: 127,010,046 (GRCm39)		probably benign	Het
Slc7a6	T	C	8: 106,906,232 (GRCm39)	S155P	probably damaging	Het
Slf1	A	T	13: 77,260,767 (GRCm39)	I173N	probably damaging	Het
Tedc1	C	T	12: 113,126,808 (GRCm39)	R357*	probably null	Het
Tkfc	A	G	19: 10,578,015 (GRCm39)	L38P	probably damaging	Het
Tubgcp4	A	G	2: 121,015,264 (GRCm39)	D324G	probably null	Het
Zfyve16	T	C	13: 92,644,791 (GRCm39)	H1137R	probably damaging	Het

Other mutations in 4632415L05Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R5271:4632415L05Rik	UTSW	3	19,949,311 (GRCm39)	exon	noncoding transcript

Posted On

2013-06-21