Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02610:Gm6430'

300444

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm6430

Ensembl Gene

ENSMUSG00000044757

Gene Name

predicted gene 6430

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.236) question?

Stock #

IGL02610

Quality Score

Status

Chromosome

Chromosomal Location

96952406-96953653 bp(+) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

G to A at 96952560 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: ENSMUST00000054664

SMART Domains

Protein: ENSMUSP00000136398
Gene: ENSMUSG00000044757

Domain	Start	End	E-Value	Type
RRM	12	86	3.26e-5	SMART
RRM	112	184	2.38e-7	SMART
low complexity region	233	254	N/A	INTRINSIC
RRM	290	360	2.43e-13	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000188810

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 27 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Armc8	T	C	9: 99,409,122 (GRCm39)		probably benign	Het
Ccdc93	T	G	1: 121,420,700 (GRCm39)	V527G	probably benign	Het
Ctcfl	C	A	2: 172,947,819 (GRCm39)		probably benign	Het
Dmd	T	C	X: 82,707,762 (GRCm39)	S359P	probably damaging	Het
Drc3	T	C	11: 60,261,419 (GRCm39)	F190S	probably benign	Het
Dync1h1	A	T	12: 110,625,666 (GRCm39)	K3943*	probably null	Het
Dzip3	A	G	16: 48,772,016 (GRCm39)	V551A	probably damaging	Het
Ep300	T	A	15: 81,485,723 (GRCm39)	L237M	unknown	Het
Gab1	A	G	8: 81,526,728 (GRCm39)		probably null	Het
Ighv16-1	A	T	12: 114,032,733 (GRCm39)	V23E	probably damaging	Het
Ikbkb	T	A	8: 23,165,088 (GRCm39)		probably null	Het
Ncr1	A	T	7: 4,341,132 (GRCm39)	N41I	probably benign	Het
Nfkbib	T	C	7: 28,459,274 (GRCm39)	D319G	probably damaging	Het
Nkain3	T	C	4: 20,469,459 (GRCm39)	E85G	probably damaging	Het
Or51h1	G	A	7: 102,308,774 (GRCm39)	V249M	probably benign	Het
Pip5k1c	C	A	10: 81,153,155 (GRCm39)		probably null	Het
Ppp2r2b	A	G	18: 42,781,840 (GRCm39)		probably benign	Het
Rgs11	G	A	17: 26,426,605 (GRCm39)	V279I	probably benign	Het
Rhod	A	G	19: 4,476,203 (GRCm39)	F183L	probably damaging	Het
Slc35f3	A	T	8: 127,047,956 (GRCm39)	T99S	probably damaging	Het
Spata31e4	T	C	13: 50,855,748 (GRCm39)	V462A	possibly damaging	Het
Spock3	A	G	8: 63,798,771 (GRCm39)	Y264C	probably damaging	Het
Trnt1	T	C	6: 106,755,779 (GRCm39)	F278S	possibly damaging	Het
Ush2a	T	A	1: 188,176,663 (GRCm39)	Y1276N	probably damaging	Het
Veph1	A	G	3: 66,079,588 (GRCm39)	L309P	probably damaging	Het
Vmn1r7	G	T	6: 57,002,037 (GRCm39)	F74L	probably benign	Het
Vsnl1	C	T	12: 11,382,072 (GRCm39)	W103*	probably null	Het

Other mutations in Gm6430

Allele	Source	Chr	Coord	Type	Predicted Effect
R2225:Gm6430	UTSW	1	96,953,441 (GRCm39)	unclassified	noncoding transcript
R2906:Gm6430	UTSW	1	96,952,554 (GRCm39)	intron	noncoding transcript
R4258:Gm6430	UTSW	1	96,952,561 (GRCm39)	intron	noncoding transcript
R4407:Gm6430	UTSW	1	96,953,297 (GRCm39)	unclassified	noncoding transcript

Posted On

2015-04-16