Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03072:Gm17093'

417562

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm17093

Ensembl Gene

ENSMUSG00000091429

Gene Name

predicted gene 17093

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.195) question?

Stock #

IGL03072

Quality Score

Status

Chromosome

Chromosomal Location

44755733-44760901 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

G to T at 44758129 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000170427

SMART Domains

Protein: ENSMUSP00000132075
Gene: ENSMUSG00000091429

Domain	Start	End	E-Value	Type
Pfam:Takusan	57	137	2.6e-27	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000227180

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 27 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2210408I21Rik	G	A	13: 77,408,116 (GRCm39)	V148I	probably benign	Het
Ahcyl2	T	C	6: 29,906,500 (GRCm39)		probably benign	Het
Ahnak	T	C	19: 8,983,872 (GRCm39)	S1719P	probably benign	Het
C2cd5	A	G	6: 143,025,609 (GRCm39)	I196T	possibly damaging	Het
Cdhr2	A	G	13: 54,874,474 (GRCm39)	I849V	probably benign	Het
Cpsf3	A	G	12: 21,345,089 (GRCm39)	K134E	possibly damaging	Het
Dnai1	A	G	4: 41,602,979 (GRCm39)	T161A	probably benign	Het
Igf2bp2	A	G	16: 21,886,891 (GRCm39)		probably null	Het
Lcor	T	C	19: 41,547,253 (GRCm39)	V279A	possibly damaging	Het
Myo9a	C	A	9: 59,716,725 (GRCm39)	T475K	possibly damaging	Het
Nat8f4	A	G	6: 85,877,836 (GRCm39)		probably benign	Het
Neto1	A	G	18: 86,516,714 (GRCm39)	T344A	probably benign	Het
Or6c203	A	T	10: 129,010,358 (GRCm39)	D177E	probably damaging	Het
Or7c19	A	G	8: 85,957,139 (GRCm39)	N5S	probably benign	Het
Or8k17	A	T	2: 86,066,804 (GRCm39)	M118K	probably damaging	Het
Pde8a	A	T	7: 80,958,557 (GRCm39)	I312F	probably damaging	Het
Ppp3cb	A	G	14: 20,581,793 (GRCm39)	I74T	probably damaging	Het
Prom1	T	C	5: 44,216,004 (GRCm39)		probably benign	Het
Psg29	T	C	7: 16,942,719 (GRCm39)	V240A	probably benign	Het
Reep4	T	C	14: 70,785,675 (GRCm39)	S238P	probably damaging	Het
Stxbp2	A	T	8: 3,691,971 (GRCm39)	I538F	probably benign	Het
Tmprss5	T	A	9: 49,020,318 (GRCm39)	N99K	possibly damaging	Het
Tph1	G	A	7: 46,302,283 (GRCm39)	T313M	probably damaging	Het
Tprn	T	C	2: 25,154,530 (GRCm39)	S611P	probably damaging	Het
Upp2	G	T	2: 58,645,435 (GRCm39)		probably null	Het
Vezt	C	A	10: 93,809,895 (GRCm39)	A549S	probably damaging	Het
Zfp786	A	G	6: 47,798,177 (GRCm39)	Y254H	probably benign	Het

Other mutations in Gm17093

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01401:Gm17093	APN	14	44,758,984 (GRCm39)	missense	unknown
IGL01431:Gm17093	APN	14	44,759,122 (GRCm39)	splice site	probably benign
IGL01911:Gm17093	APN	14	44,758,277 (GRCm39)	splice site	probably benign
IGL02324:Gm17093	APN	14	44,755,807 (GRCm39)	missense	unknown
IGL02418:Gm17093	APN	14	44,758,185 (GRCm39)	missense	unknown
R3419:Gm17093	UTSW	14	44,759,047 (GRCm39)	missense	unknown
R4838:Gm17093	UTSW	14	44,755,805 (GRCm39)	missense	unknown
R4994:Gm17093	UTSW	14	44,756,779 (GRCm39)	missense	probably damaging	1.00
R5819:Gm17093	UTSW	14	44,758,986 (GRCm39)	missense	unknown
R8167:Gm17093	UTSW	14	44,758,139 (GRCm39)	missense
R8962:Gm17093	UTSW	14	44,758,149 (GRCm39)	missense
R9757:Gm17093	UTSW	14	44,758,990 (GRCm39)	missense

Posted On

2016-08-02