Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01751:Gm6605'

153125

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Gm6605

Ensembl Gene

ENSMUSG00000094920

Gene Name

predicted gene 6605

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.095) question?

Stock #

IGL01751

Quality Score

Status

Chromosome

Chromosomal Location

38146045-38149848 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 38147630 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: ENSMUST00000031488

SMART Domains

Protein: ENSMUSP00000031488
Gene: ENSMUSG00000094920

Domain	Start	End	E-Value	Type
Pfam:DUF4629	426	526	7.6e-31	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000185975

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 31 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700018F24Rik	A	G	5: 144,979,981 (GRCm39)		probably null	Het
Abtb3	C	A	10: 85,490,366 (GRCm39)	Q1011K	probably damaging	Het
Aoc1l2	A	T	6: 48,907,522 (GRCm39)	H174L	possibly damaging	Het
Auts2	G	T	5: 131,501,198 (GRCm39)	Q72K	probably damaging	Het
Ccdc7b	A	T	8: 129,863,049 (GRCm39)		probably benign	Het
Frem3	A	G	8: 81,342,372 (GRCm39)	E1555G	probably benign	Het
Gm5263	T	G	1: 146,296,302 (GRCm39)		noncoding transcript	Het
Gm5828	A	G	1: 16,840,208 (GRCm39)		noncoding transcript	Het
Gvin3	T	A	7: 106,201,516 (GRCm39)	N576I	possibly damaging	Het
Hps3	T	C	3: 20,065,130 (GRCm39)	D638G	probably damaging	Het
Igdcc4	A	T	9: 65,039,014 (GRCm39)	N887I	probably damaging	Het
Itpkc	G	A	7: 26,912,491 (GRCm39)		probably benign	Het
Mfge8	A	G	7: 78,786,403 (GRCm39)		probably null	Het
Mrc2	G	T	11: 105,216,560 (GRCm39)	L116F	probably benign	Het
Necab1	T	C	4: 14,978,171 (GRCm39)	D226G	probably damaging	Het
Neurod2	T	C	11: 98,218,201 (GRCm39)	E321G	possibly damaging	Het
Obp2b	G	T	2: 25,627,760 (GRCm39)	V59L	possibly damaging	Het
Olr1	T	C	6: 129,465,811 (GRCm39)	N65S	possibly damaging	Het
Or14c39	A	T	7: 86,343,997 (GRCm39)	Q111L	probably benign	Het
Or2n1	G	T	17: 38,486,577 (GRCm39)	V201L	probably benign	Het
Or5d43	A	T	2: 88,104,977 (GRCm39)	C139S	possibly damaging	Het
Or8b48	C	T	9: 38,492,809 (GRCm39)	P79S	probably damaging	Het
Rock1	A	G	18: 10,079,113 (GRCm39)		probably null	Het
Scn3a	T	A	2: 65,291,596 (GRCm39)	M1717L	possibly damaging	Het
Smg7	T	C	1: 152,719,812 (GRCm39)	D903G	possibly damaging	Het
Tlr1	A	T	5: 65,083,290 (GRCm39)	L429*	probably null	Het
Ttll9	A	T	2: 152,825,025 (GRCm39)	N68I	probably damaging	Het
Ttn	A	G	2: 76,567,943 (GRCm39)	V25904A	possibly damaging	Het
Uaca	G	A	9: 60,777,139 (GRCm39)	V507M	probably damaging	Het
Vmn1r195	G	T	13: 22,463,421 (GRCm39)	C297F	probably benign	Het
Zdhhc2	G	A	8: 40,926,042 (GRCm39)	A346T	probably benign	Het

Other mutations in Gm6605

Allele	Source	Chr	Coord	Type	Predicted Effect
R0578:Gm6605	UTSW	7	38,147,699 (GRCm39)	exon	noncoding transcript
R0579:Gm6605	UTSW	7	38,147,699 (GRCm39)	exon	noncoding transcript
R0580:Gm6605	UTSW	7	38,147,699 (GRCm39)	exon	noncoding transcript
R0581:Gm6605	UTSW	7	38,147,699 (GRCm39)	exon	noncoding transcript
R0615:Gm6605	UTSW	7	38,147,699 (GRCm39)	exon	noncoding transcript
R0675:Gm6605	UTSW	7	38,147,699 (GRCm39)	exon	noncoding transcript
R2061:Gm6605	UTSW	7	38,147,706 (GRCm39)	exon	noncoding transcript
R5027:Gm6605	UTSW	7	38,149,683 (GRCm39)	exon	noncoding transcript

Posted On

2014-02-04