Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01456:Gm1818'

84781

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 #

IGL01456

Quality Score

Status

Chromosome

Chromosomal Location

48602091-48606668 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

A to T at 48602583 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: 32 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam6b	T	A	12: 113,455,083 (GRCm39)	D633E	probably benign	Het
Akap13	T	C	7: 75,252,595 (GRCm39)	C242R	probably damaging	Het
Ap5z1	T	C	5: 142,453,791 (GRCm39)	L175P	probably damaging	Het
Arid1b	A	G	17: 5,341,510 (GRCm39)	E938G	probably damaging	Het
Arid4a	A	G	12: 71,114,036 (GRCm39)	N208D	probably benign	Het
Atr	A	G	9: 95,832,618 (GRCm39)	H2556R	possibly damaging	Het
Cald1	A	T	6: 34,741,931 (GRCm39)	D438V	probably damaging	Het
Dcbld2	C	T	16: 58,229,236 (GRCm39)	P40S	possibly damaging	Het
Dock8	G	A	19: 25,096,863 (GRCm39)	M590I	possibly damaging	Het
Hace1	A	G	10: 45,586,094 (GRCm39)		probably benign	Het
Igkv10-96	A	G	6: 68,609,086 (GRCm39)	Y70H	probably benign	Het
Kdm2a	G	T	19: 4,401,783 (GRCm39)	H200Q	probably damaging	Het
Ldha	A	G	7: 46,499,602 (GRCm39)	D111G	possibly damaging	Het
Map7	A	G	10: 20,149,550 (GRCm39)	E567G	unknown	Het
Nbeal1	G	T	1: 60,269,787 (GRCm39)	L375F	probably damaging	Het
Nectin3	T	C	16: 46,279,216 (GRCm39)	E254G	probably benign	Het
Nlrp4b	A	T	7: 10,448,150 (GRCm39)	I118F	probably benign	Het
Pkhd1	A	T	1: 20,269,683 (GRCm39)	V3287D	probably damaging	Het
Ptpre	T	G	7: 135,271,531 (GRCm39)	V375G	probably damaging	Het
Rabgap1	A	G	2: 37,431,187 (GRCm39)	E746G	probably damaging	Het
Sh2b2	C	T	5: 136,253,321 (GRCm39)	C311Y	probably damaging	Het
Skor1	G	A	9: 63,052,772 (GRCm39)	T399I	probably damaging	Het
Sptbn2	A	G	19: 4,796,777 (GRCm39)	T1792A	probably damaging	Het
Tiparp	G	T	3: 65,460,030 (GRCm39)	G442*	probably null	Het
Tln1	G	A	4: 43,543,432 (GRCm39)		probably benign	Het
Tmc7	C	A	7: 118,146,533 (GRCm39)		probably benign	Het
Top2a	A	T	11: 98,901,856 (GRCm39)	L458Q	probably damaging	Het
Tpte	A	G	8: 22,835,068 (GRCm39)		probably benign	Het
Unc13a	G	A	8: 72,097,211 (GRCm39)	R1228W	probably damaging	Het
Vipr1	C	T	9: 121,494,244 (GRCm39)	T275M	probably damaging	Het
Vmn1r177	G	T	7: 23,565,753 (GRCm39)	P41Q	possibly damaging	Het
Vmn2r4	A	T	3: 64,313,816 (GRCm39)	N388K	probably damaging	Het

Other mutations in Gm1818

Allele	Source	Chr	Coord	Type	Predicted Effect
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
IGL02805:Gm1818	APN	12	48,602,518 (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

2013-11-11