Mutagenetix > Incidental Mutation

Incidental Mutation 'R4391:6030469F06Rik'

326376

Institutional Source

Beutler Lab

Gene Symbol

6030469F06Rik

Ensembl Gene

ENSMUSG00000095953

Gene Name

RIKEN cDNA 6030469F06 gene

Synonyms

MMRRC Submission

041682-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.126) question?

Stock #

R4391 (G1)

Quality Score

123

Status

Not validated

Chromosome

Chromosomal Location

31218861-31235921 bp(+) (GRCm39)

Type of Mutation

intron

DNA Base Change (assembly)

A to T at 31234622 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: ENSMUST00000179160

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218473

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218642

Coding Region Coverage

1x: 99.6%
3x: 98.6%
10x: 96.4%
20x: 91.6%

Validation Efficiency

100% (40/40)

Allele List at MGI

Other mutations in this stock

Total: 35 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Actn2	C	T	13: 12,305,634 (GRCm39)	R394Q	probably damaging	Het
Atg16l1	A	G	1: 87,687,842 (GRCm39)	D62G	probably damaging	Het
Atp2b1	A	G	10: 98,839,076 (GRCm39)	T635A	probably benign	Het
Chil4	G	A	3: 106,111,043 (GRCm39)	P284S	possibly damaging	Het
Dnah1	G	A	14: 31,016,792 (GRCm39)	T1575I	probably damaging	Het
Dnah7b	A	G	1: 46,376,754 (GRCm39)		probably null	Het
Dnajc12	A	G	10: 63,242,838 (GRCm39)	T37A	probably benign	Het
Efcab5	T	A	11: 76,981,284 (GRCm39)	N1354I	probably damaging	Het
Epas1	T	C	17: 87,117,091 (GRCm39)	L218P	probably benign	Het
Fbxw15	T	A	9: 109,397,300 (GRCm39)		probably benign	Het
Filip1l	C	A	16: 57,391,155 (GRCm39)	S581*	probably null	Het
Focad	T	A	4: 88,104,195 (GRCm39)	I358K	probably damaging	Het
Gm382	T	A	X: 125,968,942 (GRCm39)	S376T	probably benign	Het
Gpsm1	C	T	2: 26,214,009 (GRCm39)	R179C	probably damaging	Het
Hjurp	A	G	1: 88,194,283 (GRCm39)		probably benign	Het
Homer3	G	A	8: 70,742,793 (GRCm39)		probably null	Het
Krt39	C	T	11: 99,405,578 (GRCm39)	A441T	probably benign	Het
Nrdc	T	A	4: 108,903,841 (GRCm39)	N662K	probably damaging	Het
Obox5	C	T	7: 15,491,899 (GRCm39)	Q105*	probably null	Het
Or56a3b	T	A	7: 104,770,793 (GRCm39)	M43K	possibly damaging	Het
Or5af1	T	A	11: 58,722,841 (GRCm39)	V287D	possibly damaging	Het
Or8c13	A	T	9: 38,091,645 (GRCm39)	V158D	probably damaging	Het
Pcdhb5	T	A	18: 37,455,789 (GRCm39)	L723Q	possibly damaging	Het
Pou3f3	G	T	1: 42,736,618 (GRCm39)	A105S	unknown	Het
Ppp1r3d	C	T	2: 178,055,880 (GRCm39)	D41N	probably damaging	Het
Ppp4r1	A	G	17: 66,131,749 (GRCm39)	N497S	probably benign	Het
Rad54b	T	G	4: 11,615,570 (GRCm39)	N859K	probably benign	Het
Sh3bp2	C	T	5: 34,707,062 (GRCm39)	S29L	probably benign	Het
Smarcad1	A	T	6: 65,033,443 (GRCm39)	N142I	probably benign	Het
Sp140l1	G	A	1: 85,062,852 (GRCm39)		probably benign	Het
Stat3	G	A	11: 100,796,378 (GRCm39)		probably benign	Het
Stmn3	T	C	2: 180,950,576 (GRCm39)	R77G	probably benign	Het
Ugt1a1	CAGAGAGAGAGAGA	CAGAGAGAGAGA	1: 88,139,706 (GRCm39)		probably benign	Het
Vmn2r79	A	G	7: 86,651,099 (GRCm39)	H166R	possibly damaging	Het
Xlr3a	T	C	X: 72,135,450 (GRCm39)	I87V	possibly damaging	Het

Other mutations in 6030469F06Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL01957:6030469F06Rik	APN	12	31,235,042 (GRCm39)	intron	noncoding transcript
R0411:6030469F06Rik	UTSW	12	31,234,730 (GRCm39)	intron	noncoding transcript
R1464:6030469F06Rik	UTSW	12	31,234,914 (GRCm39)	intron	noncoding transcript
R1464:6030469F06Rik	UTSW	12	31,234,914 (GRCm39)	intron	noncoding transcript
R3424:6030469F06Rik	UTSW	12	31,234,632 (GRCm39)	intron	noncoding transcript
R5524:6030469F06Rik	UTSW	12	31,234,862 (GRCm39)	intron	noncoding transcript
R8176:6030469F06Rik	UTSW	12	31,235,135 (GRCm39)	missense	noncoding transcript
R8296:6030469F06Rik	UTSW	12	31,235,058 (GRCm39)	missense	noncoding transcript

Predicted Primers

Posted On

2015-07-06