Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01143:Gm5828'

50346

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 #

IGL01143

Quality Score

Status

Chromosome

Chromosomal Location

16838503-16840362 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 16840172 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: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abtb3	A	T	10: 85,490,335 (GRCm39)		probably benign	Het
Adgrl4	A	G	3: 151,205,866 (GRCm39)		probably null	Het
Adgrv1	A	C	13: 81,567,470 (GRCm39)	D5234E	probably benign	Het
Bmp7	G	T	2: 172,721,275 (GRCm39)	H267N	probably benign	Het
Ccdc113	T	C	8: 96,260,888 (GRCm39)	V30A	probably damaging	Het
Ccdc185	A	T	1: 182,575,417 (GRCm39)	L424Q	probably damaging	Het
Cep192	T	A	18: 67,937,445 (GRCm39)	D58E	probably damaging	Het
Ces1f	C	T	8: 93,998,458 (GRCm39)		probably null	Het
Chaf1a	T	A	17: 56,370,336 (GRCm39)	D600E	possibly damaging	Het
Cndp2	A	G	18: 84,695,442 (GRCm39)		probably null	Het
Dnah11	T	A	12: 117,976,475 (GRCm39)	D2727V	probably damaging	Het
Dync1li2	T	C	8: 105,156,085 (GRCm39)	D252G	probably damaging	Het
Ephx2	C	T	14: 66,326,971 (GRCm39)	R408Q	probably damaging	Het
Fat1	C	A	8: 45,488,569 (GRCm39)	T3427K	possibly damaging	Het
Gal3st4	A	G	5: 138,269,664 (GRCm39)	M1T	probably null	Het
Gm7694	C	T	1: 170,130,394 (GRCm39)	M1I	probably null	Het
Gpatch1	A	G	7: 35,000,997 (GRCm39)		probably benign	Het
Grik1	G	T	16: 87,754,488 (GRCm39)		probably null	Het
Gtf2ird2	A	G	5: 134,225,394 (GRCm39)	T161A	possibly damaging	Het
Hk2	T	C	6: 82,706,533 (GRCm39)	I790V	possibly damaging	Het
Ints9	G	A	14: 65,274,870 (GRCm39)	V609I	probably benign	Het
Kcnq4	T	G	4: 120,555,820 (GRCm39)	D585A	probably damaging	Het
Large2	T	C	2: 92,196,684 (GRCm39)	Y464C	probably damaging	Het
Lpar6	G	A	14: 73,476,077 (GRCm39)	D13N	probably damaging	Het
Morn1	T	C	4: 155,176,761 (GRCm39)	Y132H	probably damaging	Het
Nphp1	C	T	2: 127,622,056 (GRCm39)	V24I	probably benign	Het
Or5b104	A	T	19: 13,072,476 (GRCm39)	F179I	probably damaging	Het
Or5w17	T	C	2: 87,584,278 (GRCm39)	N20D	probably benign	Het
Or8b1c	G	T	9: 38,384,338 (GRCm39)	M98I	possibly damaging	Het
Pcdhb13	T	C	18: 37,575,690 (GRCm39)	W23R	probably benign	Het
Plekhg3	T	C	12: 76,611,756 (GRCm39)		probably null	Het
Slx4	T	C	16: 3,808,752 (GRCm39)	K396R	probably benign	Het
Snx13	A	G	12: 35,182,159 (GRCm39)	D736G	probably damaging	Het
Spag17	A	G	3: 99,846,614 (GRCm39)	D46G	probably benign	Het
Spata31	T	G	13: 65,068,630 (GRCm39)	Y259*	probably null	Het
Synj1	T	C	16: 90,748,864 (GRCm39)	E1064G	probably damaging	Het
Tom1	A	G	8: 75,785,085 (GRCm39)	T81A	probably benign	Het
Ttc23l	A	G	15: 10,530,775 (GRCm39)	I279T	probably damaging	Het
Ttc39a	T	C	4: 109,300,010 (GRCm39)		probably null	Het
Vmn2r108	C	A	17: 20,682,727 (GRCm39)	A826S	possibly damaging	Het
Zyg11b	A	T	4: 108,102,191 (GRCm39)	V510E	possibly damaging	Het

Other mutations in Gm5828

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01751:Gm5828	APN	1	16,840,208 (GRCm39)	exon	noncoding transcript
IGL02275:Gm5828	APN	1	16,839,342 (GRCm39)	exon	noncoding transcript
IGL02400:Gm5828	APN	1	16,840,042 (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

2013-06-21