Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02400:Gm5828'

291864

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm5828

Ensembl Gene

ENSMUSG00000091020

Gene Name

predicted gene 5828

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.245) question?

Stock #

IGL02400

Quality Score

Status

Chromosome

Chromosomal Location

16838503-16840362 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

G to T at 16840042 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: ENSMUST00000071842

SMART Domains

Protein: ENSMUSP00000136559
Gene: ENSMUSG00000091020

Domain	Start	End	E-Value	Type
low complexity region	60	74	N/A	INTRINSIC
low complexity region	143	163	N/A	INTRINSIC
low complexity region	174	182	N/A	INTRINSIC
low complexity region	207	218	N/A	INTRINSIC
HMG	222	292	1.88e-17	SMART
low complexity region	307	339	N/A	INTRINSIC
low complexity region	435	481	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 28 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610028H24Rik	A	G	10: 76,290,644 (GRCm39)	I128V	possibly damaging	Het
Arfgef3	G	T	10: 18,522,005 (GRCm39)	Q674K	probably damaging	Het
Atp6v0a2	T	A	5: 124,798,849 (GRCm39)	N851K	probably benign	Het
Chrna7	A	G	7: 62,749,070 (GRCm39)	C471R	probably damaging	Het
Csgalnact1	C	A	8: 68,854,144 (GRCm39)	G219V	probably damaging	Het
Egflam	T	A	15: 7,276,534 (GRCm39)	K544M	probably benign	Het
Erbb3	A	C	10: 128,415,393 (GRCm39)	N385K	probably benign	Het
Fancm	A	G	12: 65,160,589 (GRCm39)	R1388G	probably damaging	Het
Gm10720	C	A	9: 3,016,900 (GRCm39)		probably null	Het
Gm20489	A	T	X: 100,306,944 (GRCm39)	N328K	possibly damaging	Het
Gnaq	T	C	19: 16,293,492 (GRCm39)	Y145H	probably damaging	Het
Itgbl1	A	G	14: 124,083,938 (GRCm39)	D148G	probably damaging	Het
Myc	T	G	15: 61,861,760 (GRCm39)		probably benign	Het
Or10d5	A	G	9: 39,861,635 (GRCm39)	V144A	probably benign	Het
Or5m3b	A	T	2: 85,872,420 (GRCm39)	I254F	probably benign	Het
Or6c211	A	G	10: 129,505,752 (GRCm39)	V212A	probably damaging	Het
Padi3	T	G	4: 140,516,179 (GRCm39)	K567T	probably benign	Het
Pi4ka	T	C	16: 17,111,748 (GRCm39)	T1576A	probably damaging	Het
Pikfyve	A	G	1: 65,291,728 (GRCm39)	R1316G	probably damaging	Het
Ryr2	A	G	13: 11,620,130 (GRCm39)		probably benign	Het
Sash1	G	A	10: 8,609,411 (GRCm39)	R713*	probably null	Het
Tmem214	G	A	5: 31,030,090 (GRCm39)	A296T	probably benign	Het
Tnfsf4	T	A	1: 161,223,276 (GRCm39)	C42S	possibly damaging	Het
Tpp1	A	G	7: 105,396,238 (GRCm39)	I487T	possibly damaging	Het
Trim43a	T	A	9: 88,464,165 (GRCm39)	N25K	probably benign	Het
Tuft1	T	C	3: 94,542,809 (GRCm39)		probably benign	Het
Usp46	T	C	5: 74,197,713 (GRCm39)	H26R	probably benign	Het
Zfp560	A	T	9: 20,261,896 (GRCm39)	I85N	possibly damaging	Het

Other mutations in Gm5828

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01143:Gm5828	APN	1	16,840,172 (GRCm39)	exon	noncoding transcript
IGL01751:Gm5828	APN	1	16,840,208 (GRCm39)	exon	noncoding transcript
IGL02275:Gm5828	APN	1	16,839,342 (GRCm39)	exon	noncoding transcript
IGL02480:Gm5828	APN	1	16,839,766 (GRCm39)	exon	noncoding transcript
R0143:Gm5828	UTSW	1	16,838,579 (GRCm39)	exon	noncoding transcript
R1245:Gm5828	UTSW	1	16,839,353 (GRCm39)	exon	noncoding transcript
R1405:Gm5828	UTSW	1	16,839,768 (GRCm39)	exon	noncoding transcript
R1514:Gm5828	UTSW	1	16,839,583 (GRCm39)	exon	noncoding transcript
R1644:Gm5828	UTSW	1	16,839,485 (GRCm39)	exon	noncoding transcript
R2118:Gm5828	UTSW	1	16,840,199 (GRCm39)	exon	noncoding transcript
R2290:Gm5828	UTSW	1	16,838,568 (GRCm39)	exon	noncoding transcript
R3428:Gm5828	UTSW	1	16,838,838 (GRCm39)	exon	noncoding transcript
R3962:Gm5828	UTSW	1	16,838,868 (GRCm39)	exon	noncoding transcript
R4657:Gm5828	UTSW	1	16,839,642 (GRCm39)	exon	noncoding transcript
R5067:Gm5828	UTSW	1	16,839,516 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16