Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01341:Gm7094'

74847

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm7094

Ensembl Gene

ENSMUSG00000096375

Gene Name

predicted pseudogene 7094

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01341

Quality Score

Status

Chromosome

Chromosomal Location

21342627-21343130 bp(+) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

A to G at 21343107 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: ENSMUST00000178379

SMART Domains

Protein: ENSMUSP00000135993
Gene: ENSMUSG00000096375

Domain	Start	End	E-Value	Type
EFh	28	56	1.28e-8	SMART
EFh	64	92	7.82e-4	SMART
EFh	101	129	1.23e-1	SMART
EFh	137	165	3.37e-8	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185842

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ahnak	T	A	19: 8,989,067 (GRCm39)	H3450Q	probably benign	Het
Arcn1	A	G	9: 44,668,489 (GRCm39)	I249T	possibly damaging	Het
Arhgef5	G	A	6: 43,260,925 (GRCm39)	R1450H	probably damaging	Het
Cdh26	A	T	2: 178,099,240 (GRCm39)	D113V	probably damaging	Het
Cnot4	A	G	6: 35,047,189 (GRCm39)	V141A	probably damaging	Het
Cox6a1	C	A	5: 115,483,898 (GRCm39)		probably benign	Het
Ctsll3	C	T	13: 60,946,813 (GRCm39)	D269N	probably benign	Het
Dnttip2	T	C	3: 122,070,261 (GRCm39)	I492T	probably damaging	Het
Gimap8	A	G	6: 48,635,701 (GRCm39)	S489G	probably damaging	Het
Glra2	T	C	X: 164,107,562 (GRCm39)	D46G	probably damaging	Het
Gmps	T	C	3: 63,922,861 (GRCm39)	I608T	probably damaging	Het
Gzma	A	G	13: 113,230,418 (GRCm39)		probably benign	Het
H2-Q4	T	A	17: 35,601,978 (GRCm39)	V280E	probably damaging	Het
Jak1	C	T	4: 101,032,290 (GRCm39)	G439S	probably damaging	Het
Kars1	T	C	8: 112,721,606 (GRCm39)	I556V	probably benign	Het
Kifc2	T	C	15: 76,547,098 (GRCm39)		probably null	Het
Kit	T	C	5: 75,767,734 (GRCm39)	I39T	probably damaging	Het
Map3k6	G	T	4: 132,975,371 (GRCm39)	R702L	possibly damaging	Het
Marveld3	T	A	8: 110,675,049 (GRCm39)	T256S	possibly damaging	Het
Nkd1	G	A	8: 89,318,180 (GRCm39)		probably benign	Het
Or5aq6	T	A	2: 86,923,643 (GRCm39)	I33L	probably benign	Het
Or6c212	G	A	10: 129,558,747 (GRCm39)	T222I	possibly damaging	Het
Pax2	A	G	19: 44,779,127 (GRCm39)	S167G	probably damaging	Het
Pdlim3	T	A	8: 46,368,277 (GRCm39)	D258E	probably benign	Het
Ppip5k1	A	T	2: 121,173,691 (GRCm39)	C393*	probably null	Het
Pxdn	T	C	12: 30,052,486 (GRCm39)	S888P	probably damaging	Het
Relb	T	C	7: 19,350,298 (GRCm39)	I218V	probably benign	Het
Reln	T	A	5: 22,174,077 (GRCm39)	I2009F	probably damaging	Het
Sec23b	T	C	2: 144,427,653 (GRCm39)	S627P	probably benign	Het
Slc2a8	T	A	2: 32,866,003 (GRCm39)	Q39L	probably damaging	Het
Tmem143	T	C	7: 45,565,558 (GRCm39)	Y340H	probably damaging	Het
Ttn	A	G	2: 76,560,663 (GRCm39)	V29246A	probably damaging	Het
Wdr81	T	C	11: 75,336,427 (GRCm39)	D1654G	probably damaging	Het
Zbtb11	T	G	16: 55,811,294 (GRCm39)	L484R	possibly damaging	Het
Zcchc8	A	G	5: 123,842,632 (GRCm39)	V367A	probably benign	Het

Other mutations in Gm7094

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0166:Gm7094	UTSW	1	21,342,958 (GRCm39)	unclassified	noncoding transcript

Posted On

2013-10-07