Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02805:Gm1818'

360372

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm1818

Ensembl Gene

ENSMUSG00000091277

Gene Name

predicted gene 1818

Synonyms

LOC217536

Accession Numbers

Essential gene?

Probably essential (E-score: 0.897) question?

Stock #

IGL02805

Quality Score

Status

Chromosome

Chromosomal Location

48602091-48606668 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

C to T at 48602518 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: ENSMUST00000169406

SMART Domains

Protein: ENSMUSP00000131939
Gene: ENSMUSG00000091277

Domain	Start	End	E-Value	Type
low complexity region	1	22	N/A	INTRINSIC
Pfam:RrnaAD	78	377	4.3e-23	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 38 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acaca	T	C	11: 84,113,959 (GRCm39)		probably benign	Het
Ankdd1b	A	G	13: 96,580,810 (GRCm39)	S163P	probably benign	Het
Ap5z1	G	A	5: 142,456,038 (GRCm39)		probably benign	Het
Asb14	A	G	14: 26,623,144 (GRCm39)	N172S	possibly damaging	Het
Avil	G	A	10: 126,843,486 (GRCm39)	V139I	possibly damaging	Het
C130073F10Rik	A	T	4: 101,748,171 (GRCm39)	M1K	probably null	Het
Ccdc33	T	A	9: 58,005,874 (GRCm39)	I37F	probably benign	Het
Ccdc9	T	C	7: 16,009,199 (GRCm39)	M550V	probably benign	Het
Cfap119	T	C	7: 127,185,566 (GRCm39)	D121G	possibly damaging	Het
Cgn	T	A	3: 94,681,687 (GRCm39)	L469F	probably damaging	Het
Dnaaf3	C	T	7: 4,526,704 (GRCm39)	G458R	possibly damaging	Het
Dscaml1	T	A	9: 45,359,195 (GRCm39)	N151K	probably damaging	Het
Dsel	A	G	1: 111,790,046 (GRCm39)	V163A	probably damaging	Het
Epg5	A	G	18: 78,073,406 (GRCm39)		probably benign	Het
Fanca	A	T	8: 124,016,233 (GRCm39)	I670N	probably damaging	Het
Fsip2	T	C	2: 82,823,839 (GRCm39)	V6524A	probably benign	Het
Gm10985	T	C	3: 53,752,514 (GRCm39)		probably null	Het
Hars2	C	T	18: 36,920,630 (GRCm39)	R158*	probably null	Het
Htr5b	A	G	1: 121,455,617 (GRCm39)	V101A	probably damaging	Het
Ipp	A	G	4: 116,386,885 (GRCm39)	I356V	possibly damaging	Het
Itga8	T	A	2: 12,194,291 (GRCm39)	N703I	possibly damaging	Het
Or8b3	T	A	9: 38,315,132 (GRCm39)		probably benign	Het
Ppp6r3	T	C	19: 3,542,428 (GRCm39)	N406D	probably benign	Het
Rbbp6	G	A	7: 122,600,411 (GRCm39)		probably benign	Het
Rgs7	T	C	1: 174,977,262 (GRCm39)	Y114C	probably damaging	Het
Ripor1	A	G	8: 106,344,203 (GRCm39)	T446A	probably damaging	Het
Rnf213	A	G	11: 119,325,892 (GRCm39)	D1562G	probably damaging	Het
Scaf11	A	T	15: 96,318,063 (GRCm39)	D500E	possibly damaging	Het
Spock1	A	G	13: 58,055,391 (GRCm39)	I4T	possibly damaging	Het
Srebf2	C	A	15: 82,054,045 (GRCm39)	N35K	probably benign	Het
Srgap3	G	T	6: 112,704,224 (GRCm39)	H922N	probably damaging	Het
Stk32c	A	C	7: 138,701,762 (GRCm39)	H112Q	probably damaging	Het
Styxl2	T	C	1: 165,926,630 (GRCm39)	E994G	probably damaging	Het
Thumpd3	A	G	6: 113,043,758 (GRCm39)	D391G	probably damaging	Het
Vmn2r38	T	A	7: 9,078,546 (GRCm39)	H612L	probably damaging	Het
Vsig10l	T	G	7: 43,114,666 (GRCm39)	I289S	probably damaging	Het
Wwox	G	A	8: 115,438,753 (GRCm39)	G273E	probably damaging	Het
Zscan4d	T	G	7: 10,898,897 (GRCm39)		probably benign	Het

Other mutations in Gm1818

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01456:Gm1818	APN	12	48,602,583 (GRCm39)	exon	noncoding transcript
IGL01472:Gm1818	APN	12	48,603,072 (GRCm39)	exon	noncoding transcript
IGL01634:Gm1818	APN	12	48,602,992 (GRCm39)	exon	noncoding transcript
IGL01874:Gm1818	APN	12	48,602,973 (GRCm39)	exon	noncoding transcript
IGL02287:Gm1818	APN	12	48,602,505 (GRCm39)	exon	noncoding transcript
R1174:Gm1818	UTSW	12	48,602,982 (GRCm39)	exon	noncoding transcript
R1175:Gm1818	UTSW	12	48,602,982 (GRCm39)	exon	noncoding transcript
R1636:Gm1818	UTSW	12	48,602,550 (GRCm39)	exon	noncoding transcript
R4797:Gm1818	UTSW	12	48,602,393 (GRCm39)	exon	noncoding transcript
R4828:Gm1818	UTSW	12	48,602,409 (GRCm39)	exon	noncoding transcript
R4937:Gm1818	UTSW	12	48,606,607 (GRCm39)	exon	noncoding transcript
R5022:Gm1818	UTSW	12	48,602,318 (GRCm39)	exon	noncoding transcript
R5023:Gm1818	UTSW	12	48,602,318 (GRCm39)	exon	noncoding transcript
R5952:Gm1818	UTSW	12	48,602,719 (GRCm39)	exon	noncoding transcript
R6057:Gm1818	UTSW	12	48,602,346 (GRCm39)	exon	noncoding transcript
R6131:Gm1818	UTSW	12	48,602,319 (GRCm39)	exon	noncoding transcript
Z1088:Gm1818	UTSW	12	48,602,907 (GRCm39)	exon	noncoding transcript

Posted On

2015-12-18