Mutagenetix > Incidental Mutation

Incidental Mutation 'R3419:Gm17093'

475631

Institutional Source

Beutler Lab

Gene Symbol

Gm17093

Ensembl Gene

ENSMUSG00000091429

Gene Name

predicted gene 17093

Synonyms

MMRRC Submission

040637-MU

Accession Numbers

Essential gene?

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

Stock #

R3419 (G1)

Quality Score

Status

Not validated

Chromosome

Chromosomal Location

44755733-44760901 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 44759047 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Valine at position 190 (I190V)

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

unknown
Transcript: ENSMUST00000170427
AA Change: I190V

SMART Domains

Protein: ENSMUSP00000132075
Gene: ENSMUSG00000091429
AA Change: I190V

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

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000227180

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.0%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 50 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
5530400C23Rik	A	G	6: 133,271,082 (GRCm39)	Q42R	probably benign	Het
Ankrd26	A	G	6: 118,512,068 (GRCm39)	L518P	probably damaging	Het
Armc9	T	C	1: 86,122,060 (GRCm39)	L395P	probably damaging	Het
Baz1a	T	C	12: 54,993,684 (GRCm39)	K181E	probably benign	Het
Bend3	T	C	10: 43,385,978 (GRCm39)	S124P	probably damaging	Het
Cdh5	C	T	8: 104,856,002 (GRCm39)	R312C	probably damaging	Het
Col6a3	T	C	1: 90,731,813 (GRCm39)	D873G	probably benign	Het
Dmbx1	G	C	4: 115,777,873 (GRCm39)	R64G	probably benign	Het
Dpy19l2	T	C	9: 24,492,501 (GRCm39)	E699G	probably damaging	Het
Dync2i1	C	T	12: 116,188,597 (GRCm39)	V666I	probably benign	Het
Eef2k	T	A	7: 120,485,093 (GRCm39)	M320K	probably damaging	Het
Exoc5	A	T	14: 49,260,735 (GRCm39)	N377K	probably damaging	Het
Fam20c	A	T	5: 138,743,623 (GRCm39)	N220Y	probably damaging	Het
Fchsd2	T	A	7: 100,927,867 (GRCm39)		probably null	Het
Flrt2	A	G	12: 95,747,378 (GRCm39)	Y572C	probably damaging	Het
Gsto1	T	C	19: 47,846,344 (GRCm39)	F64L	probably benign	Het
Gucy1a1	A	G	3: 82,013,440 (GRCm39)	S401P	probably damaging	Het
Hoxd10	A	G	2: 74,522,921 (GRCm39)	K200E	probably benign	Het
Kcnj13	T	C	1: 87,314,641 (GRCm39)	T194A	probably benign	Het
Klk14	G	A	7: 43,341,501 (GRCm39)	C51Y	probably damaging	Het
Lacc1	T	G	14: 77,272,321 (GRCm39)	E158D	probably benign	Het
Lyn	A	T	4: 3,746,833 (GRCm39)	I204F	probably damaging	Het
Mapk6	T	C	9: 75,305,039 (GRCm39)	E126G	probably damaging	Het
Mbd6	C	G	10: 127,122,372 (GRCm39)	R152P	probably null	Het
Or2h1b	A	T	17: 37,462,242 (GRCm39)	V53E	probably damaging	Het
Or52e15	A	G	7: 104,645,727 (GRCm39)	I128T	probably damaging	Het
Or8g17	C	T	9: 38,930,372 (GRCm39)	C155Y	probably benign	Het
P2ry1	T	C	3: 60,911,133 (GRCm39)	F91L	probably damaging	Het
Paqr3	A	G	5: 97,247,559 (GRCm39)	L183P	probably damaging	Het
Pcdh15	C	A	10: 74,420,054 (GRCm39)	D1166E	probably benign	Het
Pik3r1	T	C	13: 101,828,723 (GRCm39)	D25G	probably benign	Het
Poc5	A	T	13: 96,540,925 (GRCm39)	T365S	possibly damaging	Het
Polr3a	A	G	14: 24,517,103 (GRCm39)	L716P	probably damaging	Het
Ppp1r3a	A	T	6: 14,719,413 (GRCm39)	D500E	probably benign	Het
Ptcd3	A	T	6: 71,860,470 (GRCm39)	I579K	possibly damaging	Het
Rnf168	A	G	16: 32,118,010 (GRCm39)	N524D	probably benign	Het
Scn7a	AT	ATT	2: 66,531,239 (GRCm39)		probably null	Het
Sel1l	A	G	12: 91,776,776 (GRCm39)	W689R	probably damaging	Het
Serpinb13	T	C	1: 106,926,657 (GRCm39)	S218P	probably damaging	Het
Serpini1	A	G	3: 75,547,589 (GRCm39)	Y367C	probably damaging	Het
Snrnp48	G	A	13: 38,405,335 (GRCm39)	D248N	possibly damaging	Het
St6galnac4	A	G	2: 32,485,743 (GRCm39)	T217A	probably damaging	Het
Tdrd1	T	A	19: 56,819,663 (GRCm39)	N54K	possibly damaging	Het
Tmem30c	A	G	16: 57,098,031 (GRCm39)	V130A	probably benign	Het
Trpa1	T	C	1: 14,944,605 (GRCm39)	I1046M	probably benign	Het
Tulp2	T	A	7: 45,168,176 (GRCm39)	M196K	possibly damaging	Het
Unc5b	G	A	10: 60,614,593 (GRCm39)	R235W	probably damaging	Het
Vmn1r175	A	T	7: 23,508,075 (GRCm39)	M184K	probably damaging	Het
Vmn2r2	A	T	3: 64,024,320 (GRCm39)	F754I	probably benign	Het
Vmn2r9	A	C	5: 108,994,299 (GRCm39)	M450R	probably damaging	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
IGL03072:Gm17093	APN	14	44,758,129 (GRCm39)	splice site	probably benign
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

Predicted Primers

Posted On

2017-05-11