Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL03217:Gm9755'

413512

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm9755

Ensembl Gene

Gene Name

predicted pseudogene 9755

Synonyms

Accession Numbers

Essential gene?

Probably essential (E-score: 0.928) question?

Stock #

IGL03217

Quality Score

Status

Chromosome

Chromosomal Location

67966887-67968242 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 67967035 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000032981

SMART Domains

Protein: ENSMUSP00000091180
Gene: ENSMUSG00000030735

Domain	Start	End	E-Value	Type
Pfam:GTP_EFTU	55	249	1.4e-55	PFAM
Pfam:GTP_EFTU_D2	272	341	4.8e-17	PFAM
Pfam:GTP_EFTU_D3	345	440	1.5e-25	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 21 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aaas	A	G	15: 102,258,430 (GRCm39)	I29T	probably damaging	Het
Adam2	G	A	14: 66,272,262 (GRCm39)	P640L	possibly damaging	Het
Ccl4	T	C	11: 83,553,504 (GRCm39)	S6P	unknown	Het
Cd300lf	T	A	11: 115,015,117 (GRCm39)	T151S	possibly damaging	Het
Elk4	A	G	1: 131,945,778 (GRCm39)	T219A	probably benign	Het
Eml1	G	T	12: 108,501,201 (GRCm39)	E680D	probably benign	Het
Hmcn1	A	T	1: 150,619,418 (GRCm39)	I1232N	possibly damaging	Het
Maml2	T	C	9: 13,531,295 (GRCm39)	S170P	probably damaging	Het
Mettl16	T	A	11: 74,708,529 (GRCm39)	M536K	probably damaging	Het
Nelfcd	G	A	2: 174,268,625 (GRCm39)	A559T	possibly damaging	Het
Nxf2	T	C	X: 133,856,281 (GRCm39)	I287V	probably benign	Het
Nyap2	A	G	1: 81,065,039 (GRCm39)	D17G	probably damaging	Het
Pde6b	T	C	5: 108,567,432 (GRCm39)	C270R	probably damaging	Het
Ptchd1	T	C	X: 154,356,955 (GRCm39)	D750G	probably damaging	Het
Rrn3	G	A	16: 13,626,875 (GRCm39)	E490K	possibly damaging	Het
Slc27a2	G	A	2: 126,428,172 (GRCm39)	G519D	possibly damaging	Het
Sox5	A	G	6: 143,853,223 (GRCm39)	S352P	probably damaging	Het
Spart	G	T	3: 55,035,912 (GRCm39)		probably benign	Het
Sult1e1	T	C	5: 87,737,947 (GRCm39)	T45A	possibly damaging	Het
Tat	G	A	8: 110,721,818 (GRCm39)	V242I	probably benign	Het
Zfp442	A	G	2: 150,251,714 (GRCm39)		probably benign	Het

Other mutations in Gm9755

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01655:Gm9755	APN	8	67,967,885 (GRCm39)	exon	noncoding transcript
IGL03229:Gm9755	APN	8	67,967,324 (GRCm39)	exon	noncoding transcript
R1110:Gm9755	UTSW	8	67,967,710 (GRCm39)	exon	noncoding transcript
R1630:Gm9755	UTSW	8	67,967,312 (GRCm39)	exon	noncoding transcript
R4257:Gm9755	UTSW	8	67,967,129 (GRCm39)	exon	noncoding transcript
R4743:Gm9755	UTSW	8	67,966,929 (GRCm39)	exon	noncoding transcript
R5960:Gm9755	UTSW	8	67,967,840 (GRCm39)	exon	noncoding transcript

Posted On

2016-08-02