Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01345:4930518I15Rik'

278296

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4930518I15Rik

Ensembl Gene

ENSMUSG00000074629

Gene Name

RIKEN cDNA 4930518I15 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01345

Quality Score

Status

Chromosome

Chromosomal Location

156698536-156700132 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to G at 156699020 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000096745 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073352] [ENSMUST00000081335] [ENSMUST00000099141]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000073352

SMART Domains

Protein: ENSMUSP00000073074
Gene: ENSMUSG00000062175

Domain	Start	End	E-Value	Type
HOX	18	83	1.51e-12	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000081335

SMART Domains

Protein: ENSMUSP00000096745
Gene: ENSMUSG00000062175

Domain	Start	End	E-Value	Type
HOX	18	83	1.51e-12	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000099141
AA Change: S39P

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000153616

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000175634

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000176134

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000176281

SMART Domains

Protein: ENSMUSP00000135007
Gene: ENSMUSG00000062175

Domain	Start	End	E-Value	Type
PDB:2LK2\|A	1	23	2e-7	PDB

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185402

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000187327

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000183465

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 22 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Atr	G	A	9: 95,823,002 (GRCm39)	C2323Y	probably damaging	Het
Ccdc107	T	A	4: 43,493,453 (GRCm39)	L8*	probably null	Het
Erc1	T	A	6: 119,738,224 (GRCm39)	K240*	probably null	Het
Gcat	T	C	15: 78,918,265 (GRCm39)		probably benign	Het
Gm4847	A	T	1: 166,462,541 (GRCm39)	D316E	probably damaging	Het
Gm8267	A	G	14: 44,962,412 (GRCm39)	S3P	probably damaging	Het
Gpr26	T	C	7: 131,569,161 (GRCm39)	F169L	possibly damaging	Het
Itgal	T	A	7: 126,900,128 (GRCm39)	F129I	possibly damaging	Het
Kcnk1	T	A	8: 126,752,146 (GRCm39)	C251S	possibly damaging	Het
Nfkb1	T	C	3: 135,300,742 (GRCm39)	D608G	probably damaging	Het
Nlrp2	T	C	7: 5,320,491 (GRCm39)	E882G	probably benign	Het
Odad2	T	C	18: 7,266,947 (GRCm39)	K385E	probably benign	Het
Pik3r5	G	A	11: 68,387,020 (GRCm39)	D854N	possibly damaging	Het
Rnf220	G	A	4: 117,130,467 (GRCm39)	R253*	probably null	Het
Slc22a15	A	C	3: 101,787,492 (GRCm39)	S259R	probably benign	Het
Tln1	G	A	4: 43,536,281 (GRCm39)	L2004F	probably damaging	Het
Tlnrd1	A	G	7: 83,532,054 (GRCm39)	S126P	probably damaging	Het
Ulk4	T	C	9: 121,037,228 (GRCm39)	T587A	possibly damaging	Het
Vasn	A	G	16: 4,466,232 (GRCm39)	I60V	probably benign	Het
Vps33a	G	T	5: 123,711,006 (GRCm39)	N13K	probably benign	Het
Zmiz2	A	G	11: 6,355,015 (GRCm39)	D862G	possibly damaging	Het
Zswim3	T	A	2: 164,662,057 (GRCm39)	L179H	probably damaging	Het

Other mutations in 4930518I15Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01344:4930518I15Rik	APN	2	156,699,020 (GRCm39)	unclassified	probably benign
R4604:4930518I15Rik	UTSW	2	156,699,074 (GRCm39)	unclassified	probably benign
R9061:4930518I15Rik	UTSW	2	156,699,133 (GRCm39)	start codon destroyed	probably null

Posted On

2015-04-16