Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01689:Gm11541'

104049

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm11541

Ensembl Gene

Gene Name

predicted gene 11541

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.133) question?

Stock #

IGL01689

Quality Score

Status

Chromosome

Chromosomal Location

94585324-94595325 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 94595020 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 16 (V16A)

Ref Sequence

ENSEMBL: ENSMUSP00000066721 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000069852]

Predicted Effect

unknown
Transcript: ENSMUST00000069852
AA Change: V16A

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 18 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aox4	A	G	1: 58,284,320 (GRCm39)		probably benign	Het
Arhgap10	A	G	8: 78,137,763 (GRCm39)		probably benign	Het
Armc9	T	C	1: 86,202,140 (GRCm39)	V766A	probably benign	Het
Asxl2	A	T	12: 3,546,425 (GRCm39)	Q403L	probably benign	Het
Cd244a	G	A	1: 171,410,462 (GRCm39)		probably benign	Het
Cdc34b	A	G	11: 94,633,345 (GRCm39)	K182E	probably benign	Het
Csnk1d	A	T	11: 120,862,393 (GRCm39)	F295L	probably benign	Het
Kdr	T	C	5: 76,097,500 (GRCm39)	D1252G	probably benign	Het
Kif14	A	G	1: 136,447,380 (GRCm39)	D1395G	probably damaging	Het
Lars1	T	A	18: 42,350,014 (GRCm39)	Q930L	probably benign	Het
Lypd5	A	G	7: 24,052,054 (GRCm39)		probably benign	Het
Or2w1b	G	A	13: 21,300,243 (GRCm39)	C127Y	probably damaging	Het
Paics	T	C	5: 77,109,138 (GRCm39)		probably null	Het
Pcnt	A	G	10: 76,247,487 (GRCm39)	V1015A	probably damaging	Het
Thada	C	T	17: 84,754,116 (GRCm39)	S285N	possibly damaging	Het
Tlr1	T	C	5: 65,083,122 (GRCm39)	D485G	probably damaging	Het
Vmn2r66	T	C	7: 84,657,033 (GRCm39)	N124S	probably damaging	Het
Zfyve26	T	C	12: 79,330,827 (GRCm39)	D464G	possibly damaging	Het

Other mutations in Gm11541

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01451:Gm11541	APN	11	94,586,495 (GRCm39)	missense	unknown
R2698:Gm11541	UTSW	11	94,586,441 (GRCm39)	nonsense	probably null
R4465:Gm11541	UTSW	11	94,595,048 (GRCm39)	missense	unknown
R5526:Gm11541	UTSW	11	94,594,944 (GRCm39)	missense	unknown
X0018:Gm11541	UTSW	11	94,586,451 (GRCm39)	missense	unknown

Posted On

2014-01-21