Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03407:Gm21726'

421646

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm21726

Ensembl Gene

ENSMUSG00000094277

Gene Name

predicted gene, 21726

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL03407

Quality Score

Status

Chromosome

Chromosomal Location

90731448-90731839 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 90731760 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000179654

SMART Domains

Protein: ENSMUSP00000136397
Gene: ENSMUSG00000094277

Domain	Start	End	E-Value	Type
Pfam:Ribosomal_L23	35	108	1.9e-10	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 30 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abcb5	A	G	12: 118,904,111 (GRCm39)	V198A	probably benign	Het
Acot3	A	T	12: 84,105,415 (GRCm39)	D294V	probably damaging	Het
Dnajc10	T	C	2: 80,176,985 (GRCm39)	Y647H	probably damaging	Het
Eml6	G	A	11: 29,856,330 (GRCm39)	L67F	probably damaging	Het
Fbxw8	A	G	5: 118,280,741 (GRCm39)	C139R	probably damaging	Het
Fscb	G	T	12: 64,520,269 (GRCm39)	A399D	probably damaging	Het
Lama2	A	T	10: 27,223,017 (GRCm39)	V423D	probably damaging	Het
Mctp2	A	T	7: 71,861,400 (GRCm39)	I415N	probably benign	Het
Myh13	A	G	11: 67,242,978 (GRCm39)	T964A	probably damaging	Het
Ncf4	A	G	15: 78,138,981 (GRCm39)		probably benign	Het
Nelfcd	G	A	2: 174,268,625 (GRCm39)	A559T	possibly damaging	Het
Or3a1d	G	T	11: 74,238,371 (GRCm39)	T13K	possibly damaging	Het
Or51m1	A	T	7: 103,578,158 (GRCm39)	N43Y	probably damaging	Het
Plch2	A	T	4: 155,074,255 (GRCm39)	V870E	probably damaging	Het
Prss55	A	T	14: 64,314,539 (GRCm39)	D210E	probably damaging	Het
Rad51ap2	A	G	12: 11,507,198 (GRCm39)	I373M	possibly damaging	Het
Rbm12	C	A	2: 155,939,484 (GRCm39)	G263*	probably null	Het
Rnf167	G	T	11: 70,541,879 (GRCm39)		probably null	Het
Scn10a	A	G	9: 119,477,237 (GRCm39)	I715T	probably damaging	Het
Spata31f1a	A	T	4: 42,850,528 (GRCm39)	W543R	probably benign	Het
St8sia1	T	C	6: 142,859,775 (GRCm39)	N118S	possibly damaging	Het
Tas1r3	A	G	4: 155,946,439 (GRCm39)		probably null	Het
Thbs2	A	G	17: 14,893,535 (GRCm39)	S882P	probably benign	Het
Tmem25	A	G	9: 44,707,636 (GRCm39)	S220P	probably damaging	Het
Tnpo1	C	T	13: 99,000,348 (GRCm39)	E340K	probably damaging	Het
Trex1	C	T	9: 108,887,395 (GRCm39)	G199S	probably damaging	Het
Ttn	T	C	2: 76,544,545 (GRCm39)	I32814V	probably damaging	Het
Vmn2r15	T	A	5: 109,434,185 (GRCm39)	R840*	probably null	Het
Vps13b	A	T	15: 35,640,012 (GRCm39)	Q1294L	possibly damaging	Het
Zdhhc7	T	C	8: 120,812,131 (GRCm39)	N164D	probably damaging	Het

Other mutations in Gm21726

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R1157:Gm21726	UTSW	13	90,731,724 (GRCm39)	exon	noncoding transcript

Posted On

2016-08-02