Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02451:B430305J03Rik'

293634

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

B430305J03Rik

Ensembl Gene

ENSMUSG00000053706

Gene Name

RIKEN cDNA B430305J03 gene

Synonyms

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.414) question?

Stock #

IGL02451

Quality Score

Status

Chromosome

Chromosomal Location

61269671-61273372 bp(-) (GRCm39)

Type of Mutation

utr 5 prime

DNA Base Change (assembly)

A to G at 61271562 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000038841 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049064] [ENSMUST00000066298]

AlphaFold

Q8BQQ8

Predicted Effect

probably benign
Transcript: ENSMUST00000049064

SMART Domains

Protein: ENSMUSP00000038841
Gene: ENSMUSG00000036894

Domain	Start	End	E-Value	Type
RAS	1	167	3.08e-111	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000066298
AA Change: V61A

SMART Domains

Protein: ENSMUSP00000070175
Gene: ENSMUSG00000053706
AA Change: V61A

Domain	Start	End	E-Value	Type
low complexity region	95	103	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194223

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 49 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700123K08Rik	T	G	5: 138,561,809 (GRCm39)	T126P	probably damaging	Het
Asic2	T	C	11: 80,782,563 (GRCm39)		probably benign	Het
Bbs7	A	G	3: 36,664,741 (GRCm39)	F47L	possibly damaging	Het
Bcl2l14	G	T	6: 134,400,804 (GRCm39)	G75V	probably benign	Het
Btnl4	T	C	17: 34,694,901 (GRCm39)	H4R	probably benign	Het
Champ1	C	A	8: 13,928,739 (GRCm39)	P299Q	probably damaging	Het
Cimap3	T	A	3: 105,921,820 (GRCm39)	E34D	probably benign	Het
Cldnd2	A	G	7: 43,091,082 (GRCm39)	K5E	probably benign	Het
Ctr9	T	A	7: 110,642,631 (GRCm39)	L401*	probably null	Het
Cyp2c29	G	A	19: 39,279,291 (GRCm39)	G96D	possibly damaging	Het
Enpp4	A	T	17: 44,412,315 (GRCm39)	L298H	probably damaging	Het
Git1	T	C	11: 77,391,513 (GRCm39)	C222R	possibly damaging	Het
Gpam	T	C	19: 55,076,635 (GRCm39)	T189A	probably damaging	Het
Hgfac	T	G	5: 35,201,158 (GRCm39)		probably null	Het
Hivep3	T	A	4: 119,991,162 (GRCm39)	S2221T	probably damaging	Het
Ifi47	T	C	11: 48,986,604 (GRCm39)	Y124H	probably damaging	Het
Il1a	T	C	2: 129,148,575 (GRCm39)	E45G	probably damaging	Het
Itga11	T	A	9: 62,642,635 (GRCm39)	I186N	probably damaging	Het
Krt16	A	T	11: 100,137,162 (GRCm39)		probably benign	Het
Mapk13	A	G	17: 28,995,387 (GRCm39)	T203A	probably damaging	Het
Mrpl37	T	A	4: 106,923,839 (GRCm39)	I52F	probably damaging	Het
Mtrex	C	T	13: 113,027,881 (GRCm39)	V660M	probably damaging	Het
Nr1i2	A	G	16: 38,069,654 (GRCm39)	F417L	probably benign	Het
Or10ag59	T	A	2: 87,405,576 (GRCm39)	S49R	probably benign	Het
Or6c215	G	A	10: 129,637,702 (GRCm39)	Q231*	probably null	Het
Osbpl1a	T	C	18: 13,047,550 (GRCm39)		probably benign	Het
Parg	C	T	14: 31,964,186 (GRCm39)	T112M	probably damaging	Het
Pou6f1	T	C	15: 100,477,821 (GRCm39)	T166A	possibly damaging	Het
Prtg	A	G	9: 72,764,281 (GRCm39)	I585V	possibly damaging	Het
Ptpru	T	G	4: 131,504,086 (GRCm39)		probably benign	Het
Rab6a	T	C	7: 100,285,970 (GRCm39)		probably null	Het
Rnf207	C	T	4: 152,396,869 (GRCm39)	R425H	probably benign	Het
Rusf1	A	G	7: 127,875,582 (GRCm39)	L257P	probably damaging	Het
Slc27a2	A	G	2: 126,420,912 (GRCm39)	M468V	probably benign	Het
Slc30a1	A	G	1: 191,639,441 (GRCm39)	H108R	possibly damaging	Het
Sned1	A	G	1: 93,163,930 (GRCm39)		probably benign	Het
Sptbn4	A	T	7: 27,065,014 (GRCm39)	F2095Y	probably null	Het
Sspo	A	T	6: 48,437,237 (GRCm39)		probably benign	Het
Tbx19	A	G	1: 164,967,740 (GRCm39)	S336P	probably benign	Het
Tmem101	T	A	11: 102,044,119 (GRCm39)	D256V	probably damaging	Het
Trbv20	T	G	6: 41,165,210 (GRCm39)	L2V	unknown	Het
Trpc7	A	G	13: 56,970,274 (GRCm39)	S382P	probably damaging	Het
Tut4	C	A	4: 108,386,473 (GRCm39)	Y1114*	probably null	Het
Uhmk1	T	C	1: 170,040,095 (GRCm39)	T91A	possibly damaging	Het
Vmn2r10	T	A	5: 109,143,788 (GRCm39)	R721*	probably null	Het
Vmn2r94	T	A	17: 18,478,453 (GRCm39)	Y98F	possibly damaging	Het
Zfp532	A	G	18: 65,756,672 (GRCm39)	R202G	probably damaging	Het
Zfp827	T	C	8: 79,787,601 (GRCm39)	S256P	probably damaging	Het
Zzef1	T	C	11: 72,792,214 (GRCm39)	I2266T	probably damaging	Het

Other mutations in B430305J03Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
R0400:B430305J03Rik	UTSW	3	61,271,556 (GRCm39)	utr 5 prime	probably benign
R0704:B430305J03Rik	UTSW	3	61,271,414 (GRCm39)	nonsense	probably null
R1133:B430305J03Rik	UTSW	3	61,271,430 (GRCm39)	nonsense	probably null
R1727:B430305J03Rik	UTSW	3	61,271,299 (GRCm39)	utr 5 prime	probably benign
R1735:B430305J03Rik	UTSW	3	61,271,361 (GRCm39)	utr 5 prime	probably benign
R4065:B430305J03Rik	UTSW	3	61,271,646 (GRCm39)	utr 5 prime	probably benign
R4978:B430305J03Rik	UTSW	3	61,271,440 (GRCm39)	start gained	probably benign
R7073:B430305J03Rik	UTSW	3	61,271,681 (GRCm39)	missense	unknown
R7242:B430305J03Rik	UTSW	3	61,271,256 (GRCm39)	missense	unknown
R7345:B430305J03Rik	UTSW	3	61,271,539 (GRCm39)	missense	unknown
R9624:B430305J03Rik	UTSW	3	61,271,408 (GRCm39)	missense	unknown

Posted On

2015-04-16