Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01874:Gm1818'

178796

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 #

IGL01874

Quality Score

Status

Chromosome

Chromosomal Location

48602091-48606668 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 48602973 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: 48 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts16	A	T	13: 70,916,823 (GRCm39)	V723D	possibly damaging	Het
Adgrb1	G	A	15: 74,413,423 (GRCm39)	V536I	possibly damaging	Het
Aox4	T	C	1: 58,291,243 (GRCm39)	L787S	probably damaging	Het
Atp2c1	A	C	9: 105,326,024 (GRCm39)	V293G	probably damaging	Het
Ccnb1	T	C	13: 100,920,001 (GRCm39)	D170G	probably damaging	Het
Cdc42	T	C	4: 137,063,381 (GRCm39)	I4V	probably benign	Het
Clip1	T	C	5: 123,741,729 (GRCm39)	Q1175R	possibly damaging	Het
Cox6a1	A	G	5: 115,483,904 (GRCm39)	*113Q	probably null	Het
Crtc2	C	T	3: 90,165,815 (GRCm39)	P139L	probably damaging	Het
Cyp8b1	A	T	9: 121,744,969 (GRCm39)	M121K	possibly damaging	Het
D630003M21Rik	C	A	2: 158,046,644 (GRCm39)	G778C	probably damaging	Het
Dgat1	A	G	15: 76,387,241 (GRCm39)	F349L	probably damaging	Het
Enox1	A	G	14: 77,816,602 (GRCm39)	Y194C	probably damaging	Het
Fam120b	T	A	17: 15,623,301 (GRCm39)	C426*	probably null	Het
Fxyd3	A	G	7: 30,770,318 (GRCm39)		probably benign	Het
Gin1	A	G	1: 97,710,797 (GRCm39)	Y160C	probably damaging	Het
Gm10718	A	T	9: 3,025,118 (GRCm39)	Y194F	probably benign	Het
Gm11110	T	A	17: 57,399,693 (GRCm39)		probably benign	Het
Gucy1a2	T	C	9: 3,797,343 (GRCm39)	S598P	probably damaging	Het
Hook3	T	A	8: 26,529,760 (GRCm39)	N199Y	possibly damaging	Het
Il10ra	A	G	9: 45,178,458 (GRCm39)	L41P	probably damaging	Het
Itgam	C	T	7: 127,714,338 (GRCm39)	T949I	probably damaging	Het
Kctd3	A	G	1: 188,729,188 (GRCm39)	V123A	probably damaging	Het
Krt84	G	A	15: 101,436,239 (GRCm39)	A450V	probably damaging	Het
Lrrc7	G	A	3: 157,946,080 (GRCm39)		probably benign	Het
Nckap1	A	G	2: 80,355,980 (GRCm39)	F608L	probably damaging	Het
Niban2	A	T	2: 32,795,779 (GRCm39)		probably null	Het
Nmbr	A	T	10: 14,642,696 (GRCm39)	Y85F	probably benign	Het
Nol6	A	C	4: 41,115,412 (GRCm39)	L1135R	probably damaging	Het
Ntan1	T	C	16: 13,653,077 (GRCm39)	F278L	probably benign	Het
Or2n1e	T	A	17: 38,586,408 (GRCm39)	S249T	probably benign	Het
Pcsk5	T	A	19: 17,573,041 (GRCm39)	T474S	probably damaging	Het
Pex11b	T	A	3: 96,550,883 (GRCm39)		probably null	Het
Pkhd1	G	T	1: 20,173,459 (GRCm39)	A3786E	probably benign	Het
Prkdc	T	C	16: 15,552,858 (GRCm39)	I2098T	possibly damaging	Het
Prl2c5	T	A	13: 13,365,362 (GRCm39)	S169R	probably benign	Het
Ptbp2	A	G	3: 119,541,449 (GRCm39)	V196A	probably damaging	Het
Rad17	T	C	13: 100,754,192 (GRCm39)		probably benign	Het
Skic2	T	C	17: 35,060,185 (GRCm39)	N114D	probably benign	Het
Slc47a2	T	A	11: 61,203,685 (GRCm39)		probably null	Het
Srcin1	A	T	11: 97,423,924 (GRCm39)	M684K	possibly damaging	Het
Sspo	T	A	6: 48,429,124 (GRCm39)	C298S	probably damaging	Het
Tenm3	G	T	8: 48,689,793 (GRCm39)	Y1915*	probably null	Het
Tnks1bp1	A	G	2: 84,888,791 (GRCm39)	T373A	probably benign	Het
Trp63	A	C	16: 25,701,335 (GRCm39)	N470H	possibly damaging	Het
Ttn	T	C	2: 76,628,907 (GRCm39)	N12703S	probably damaging	Het
Ubr4	T	C	4: 139,120,600 (GRCm39)		probably benign	Het
Vmn2r56	T	A	7: 12,449,602 (GRCm39)	Y212F	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
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

2014-05-07