Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03357:Gm4831'

419999

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm4831

Ensembl Gene

ENSMUSG00000092339

Gene Name

predicted gene 4831

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL03357

Quality Score

Status

Chromosome

Chromosomal Location

37424742-37425335 bp(+) (GRCm39)

Type of Mutation

utr 5 prime

DNA Base Change (assembly)

C to T at 37422879 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000150988 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000168659] [ENSMUST00000214994] [ENSMUST00000216341]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000168659

SMART Domains

Protein: ENSMUSP00000128393
Gene: ENSMUSG00000096477

Domain	Start	End	E-Value	Type
Pfam:7TM_GPCR_Srv	23	304	5.1e-7	PFAM
Pfam:7tm_4	29	306	3.4e-50	PFAM
Pfam:7tm_1	39	288	1.1e-26	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174626

Predicted Effect

probably benign
Transcript: ENSMUST00000214994

Predicted Effect

probably benign
Transcript: ENSMUST00000216341

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahnak	C	T	19: 8,986,689 (GRCm39)		probably benign	Het
Asah1	A	G	8: 41,799,233 (GRCm39)		probably benign	Het
Ces1d	C	A	8: 93,896,346 (GRCm39)		probably null	Het
Chd6	T	C	2: 160,859,936 (GRCm39)		probably benign	Het
Chn2	G	A	6: 54,171,062 (GRCm39)	R47Q	probably benign	Het
Clmp	A	G	9: 40,597,623 (GRCm39)		probably benign	Het
Col11a1	G	A	3: 113,987,740 (GRCm39)	G245R	probably damaging	Het
Cyp4a32	T	A	4: 115,468,798 (GRCm39)	S395T	probably benign	Het
Dcc	A	T	18: 71,460,625 (GRCm39)	I1155K	probably damaging	Het
Dpy19l4	G	A	4: 11,267,615 (GRCm39)	H442Y	probably damaging	Het
Dpys	T	C	15: 39,687,612 (GRCm39)	I395M	probably damaging	Het
Dpysl2	T	C	14: 67,050,736 (GRCm39)	K374E	probably damaging	Het
Fryl	A	T	5: 73,211,402 (GRCm39)	D660E	probably damaging	Het
Gabrb2	T	C	11: 42,482,771 (GRCm39)	F210L	probably damaging	Het
Igsf10	A	T	3: 59,243,632 (GRCm39)	M234K	probably benign	Het
Ints11	T	C	4: 155,956,581 (GRCm39)		probably benign	Het
Mex3a	T	A	3: 88,443,553 (GRCm39)	S210T	probably benign	Het
Or4k42	C	T	2: 111,320,289 (GRCm39)	M71I	probably benign	Het
Or4k52	G	A	2: 111,610,871 (GRCm39)	V69I	probably benign	Het
Pde1c	A	G	6: 56,157,078 (GRCm39)	V106A	probably damaging	Het
Pitpnm3	G	A	11: 71,961,716 (GRCm39)	Q284*	probably null	Het
Pkd1l2	A	G	8: 117,722,548 (GRCm39)	L2420P	probably damaging	Het
Prpf39	A	G	12: 65,108,211 (GRCm39)		probably benign	Het
Prss28	C	T	17: 25,528,669 (GRCm39)	T37I	probably benign	Het
Serpinb6c	A	T	13: 34,079,369 (GRCm39)	S108T	probably benign	Het
Snx7	T	C	3: 117,632,524 (GRCm39)	H131R	probably damaging	Het
Tex101	A	T	7: 24,367,758 (GRCm39)	I198K	probably damaging	Het
Thoc2l	T	G	5: 104,668,334 (GRCm39)	V952G	probably damaging	Het
Thumpd2	T	C	17: 81,351,519 (GRCm39)		probably benign	Het
Ubqln3	A	C	7: 103,791,763 (GRCm39)	I109S	probably benign	Het
Zfp212	A	T	6: 47,907,771 (GRCm39)	N250I	probably benign	Het

Posted On

2016-08-02