Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03142:Gm3115'

410740

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm3115

Ensembl Gene

ENSMUSG00000091022

Gene Name

predicted gene 3115

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL03142

Quality Score

Status

Chromosome

Chromosomal Location

18371507-18385609 bp(-) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to C at 4084302 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000136699 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000166928] [ENSMUST00000177660]

AlphaFold

L7N285

Predicted Effect

probably benign
Transcript: ENSMUST00000166928

SMART Domains

Protein: ENSMUSP00000127156
Gene: ENSMUSG00000091022

Domain	Start	End	E-Value	Type
Pfam:Takusan	48	128	1.2e-17	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000177660

SMART Domains

Protein: ENSMUSP00000136699
Gene: ENSMUSG00000091022

Domain	Start	End	E-Value	Type
Pfam:Takusan	46	129	3.8e-29	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 36 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ccdc88c	T	C	12: 100,913,457 (GRCm39)	S523G	probably damaging	Het
Ccnb1	A	T	13: 100,920,039 (GRCm39)	D157E	probably damaging	Het
Cep43	T	A	17: 8,411,041 (GRCm39)	S331R	probably damaging	Het
Cfap70	T	C	14: 20,447,283 (GRCm39)	T1055A	probably damaging	Het
Fn1	C	A	1: 71,676,455 (GRCm39)	R592L	probably damaging	Het
Frmpd4	T	A	X: 166,262,479 (GRCm39)	D550V	possibly damaging	Het
Gcm2	A	G	13: 41,256,711 (GRCm39)	V346A	probably benign	Het
Gm10112	C	T	X: 110,209,673 (GRCm39)	T4I	probably damaging	Het
Has2	A	T	15: 56,545,491 (GRCm39)	I37N	possibly damaging	Het
Hmgn3	A	G	9: 83,028,482 (GRCm39)		probably benign	Het
Klhl29	T	A	12: 5,187,603 (GRCm39)	N254Y	probably damaging	Het
Kti12	A	G	4: 108,705,362 (GRCm39)	Y92C	probably damaging	Het
Lyset	G	A	12: 102,710,933 (GRCm39)	S52N	probably damaging	Het
Mgat5	A	C	1: 127,339,960 (GRCm39)	Q447P	probably damaging	Het
Mlh3	C	A	12: 85,297,075 (GRCm39)		probably null	Het
Mrpl45	T	C	11: 97,206,751 (GRCm39)	W18R	probably benign	Het
Mtor	A	G	4: 148,538,356 (GRCm39)	D138G	probably benign	Het
Mycbp2	C	T	14: 103,536,212 (GRCm39)	C246Y	probably damaging	Het
Mylk4	A	T	13: 32,904,582 (GRCm39)	V415E	probably damaging	Het
Olfm3	A	T	3: 114,890,679 (GRCm39)	Q124L	probably damaging	Het
Or4d11	A	T	19: 12,013,752 (GRCm39)	M118K	probably damaging	Het
Pam	C	T	1: 97,822,111 (GRCm39)	G298R	probably damaging	Het
Pappa2	A	C	1: 158,682,501 (GRCm39)	I849R	probably damaging	Het
Pde3a	T	A	6: 141,438,025 (GRCm39)	D1031E	probably benign	Het
Pik3cb	A	T	9: 98,947,615 (GRCm39)	S521T	probably benign	Het
Pkn1	A	G	8: 84,397,652 (GRCm39)	F824L	possibly damaging	Het
Pspn	C	T	17: 57,306,566 (GRCm39)	R121Q	probably benign	Het
Ric1	A	G	19: 29,578,380 (GRCm39)	D1195G	possibly damaging	Het
Sin3b	A	G	8: 73,471,196 (GRCm39)	D381G	probably damaging	Het
Slc37a3	T	C	6: 39,336,919 (GRCm39)		probably null	Het
Smtn	T	A	11: 3,482,601 (GRCm39)	K124*	probably null	Het
Tbce	A	G	13: 14,194,449 (GRCm39)	V70A	possibly damaging	Het
Tti1	A	G	2: 157,842,597 (GRCm39)	Y811H	probably damaging	Het
Uggt2	T	C	14: 119,235,603 (GRCm39)	Y1424C	probably damaging	Het
Upf1	A	G	8: 70,785,977 (GRCm39)	V994A	probably benign	Het
Vmn2r121	T	C	X: 123,042,635 (GRCm39)	D174G	possibly damaging	Het

Other mutations in Gm3115

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01406:Gm3115	APN	14	4,087,137 (GRCm38)	unclassified	probably benign
IGL01671:Gm3115	APN	14	4,084,189 (GRCm38)	missense	probably benign	0.05
IGL02952:Gm3115	APN	14	4,084,302 (GRCm38)	splice site	probably benign

Posted On

2016-08-02