Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03206:Gm12830'

413163

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm12830

Ensembl Gene

ENSMUSG00000055198

Gene Name

predicted gene 12830

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.140) question?

Stock #

IGL03206

Quality Score

Status

Chromosome

Chromosomal Location

114678919-114713363 bp(+) (GRCm39)

Type of Mutation

splice site

DNA Base Change (assembly)

T to A at 114702314 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: ENSMUST00000137570

SMART Domains

Protein: ENSMUSP00000120534
Gene: ENSMUSG00000055198

Domain	Start	End	E-Value	Type
transmembrane domain	15	34	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000155499

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000157298

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 45 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
A2ml1	T	A	6: 128,530,239 (GRCm39)	E939D	possibly damaging	Het
Aloxe3	C	A	11: 69,020,472 (GRCm39)	A172D	possibly damaging	Het
Bscl2	G	A	19: 8,820,453 (GRCm39)	R158Q	probably damaging	Het
Cdon	A	G	9: 35,414,602 (GRCm39)	D1159G	probably benign	Het
Cep164	A	G	9: 45,714,023 (GRCm39)	V203A	probably benign	Het
Chml	T	C	1: 175,515,303 (GRCm39)	D206G	probably benign	Het
E2f6	T	C	12: 16,872,090 (GRCm39)		probably benign	Het
Emilin3	T	A	2: 160,752,719 (GRCm39)	Y77F	probably damaging	Het
Fbxw15	A	T	9: 109,394,430 (GRCm39)	N128K	possibly damaging	Het
Gjd2	A	G	2: 113,842,204 (GRCm39)	L91P	probably damaging	Het
Gpr161	T	A	1: 165,149,218 (GRCm39)	L529Q	probably damaging	Het
Hoxd10	T	A	2: 74,522,776 (GRCm39)	Y151*	probably null	Het
Iars1	A	G	13: 49,846,546 (GRCm39)	D215G	possibly damaging	Het
Ift140	T	C	17: 25,311,800 (GRCm39)	V1241A	probably damaging	Het
Kdm5b	A	G	1: 134,555,055 (GRCm39)	N1321S	probably benign	Het
Lrat	T	A	3: 82,810,656 (GRCm39)	I122F	probably damaging	Het
Myl10	C	T	5: 136,726,796 (GRCm39)	Q106*	probably null	Het
Ncapd2	A	T	6: 125,148,660 (GRCm39)	Y1018N	possibly damaging	Het
Ndrg1	C	T	15: 66,814,936 (GRCm39)	W172*	probably null	Het
Nphs2	T	C	1: 156,153,701 (GRCm39)	M264T	probably damaging	Het
Nrxn3	A	T	12: 89,227,278 (GRCm39)	R677S	possibly damaging	Het
Nudt12	T	C	17: 59,314,667 (GRCm39)	T306A	probably benign	Het
Numb	A	G	12: 83,872,070 (GRCm39)		probably benign	Het
Or10h28	T	A	17: 33,487,725 (GRCm39)	I9K	possibly damaging	Het
Or2y1	A	T	11: 49,385,536 (GRCm39)	M59L	probably benign	Het
Or5p58	C	T	7: 107,694,261 (GRCm39)	C172Y	probably damaging	Het
Pbld2	T	A	10: 62,883,261 (GRCm39)	D94E	probably benign	Het
Pkd1l3	C	A	8: 110,350,345 (GRCm39)	Q397K	probably benign	Het
Ppp4r3a	A	T	12: 101,024,878 (GRCm39)	L207H	probably damaging	Het
Ranbp2	T	A	10: 58,301,369 (GRCm39)	I674N	probably damaging	Het
Retnlg	G	T	16: 48,694,655 (GRCm39)	C101F	probably damaging	Het
Rif1	T	A	2: 51,993,634 (GRCm39)	I849N	probably damaging	Het
Serpinb9d	T	C	13: 33,382,014 (GRCm39)	I161T	possibly damaging	Het
Slc17a6	T	C	7: 51,315,771 (GRCm39)		probably benign	Het
Smg8	A	C	11: 86,976,814 (GRCm39)		probably null	Het
Spata31d1c	C	A	13: 65,183,407 (GRCm39)	N316K	probably benign	Het
Tlr1	A	G	5: 65,082,400 (GRCm39)	S726P	probably damaging	Het
Trim69	A	C	2: 122,003,636 (GRCm39)	D195A	probably benign	Het
Ttc16	T	G	2: 32,661,897 (GRCm39)		probably null	Het
Usp53	T	A	3: 122,746,832 (GRCm39)	M405L	probably benign	Het
Ywhag	G	A	5: 135,939,914 (GRCm39)	R227*	probably null	Het
Zfp335	G	T	2: 164,734,601 (GRCm39)		probably benign	Het
Zfp607a	T	C	7: 27,577,248 (GRCm39)	I106T	possibly damaging	Het
Zfp959	T	C	17: 56,204,613 (GRCm39)	S214P	possibly damaging	Het
Zfyve9	T	C	4: 108,546,406 (GRCm39)	M868V	possibly damaging	Het

Other mutations in Gm12830

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01150:Gm12830	APN	4	114,702,261 (GRCm39)	missense	unknown
R0309:Gm12830	UTSW	4	114,702,173 (GRCm39)	splice site	probably benign
R5484:Gm12830	UTSW	4	114,702,248 (GRCm39)	missense	unknown
R5503:Gm12830	UTSW	4	114,678,936 (GRCm39)	missense	unknown
R6226:Gm12830	UTSW	4	114,702,246 (GRCm39)	missense	unknown
R6975:Gm12830	UTSW	4	114,702,246 (GRCm39)	missense
R9636:Gm12830	UTSW	4	114,698,859 (GRCm39)	missense

Posted On

2016-08-02