Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01518:4930447F04Rik'

89385

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

4930447F04Rik

Ensembl Gene

ENSMUSG00000031182

Gene Name

RIKEN cDNA 4930447F04 gene

Synonyms

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL01518

Quality Score

Status

Chromosome

Chromosomal Location

65346967-65347830 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to C at 65347660 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Glycine at position 16 (V16G)

Ref Sequence

ENSEMBL: ENSMUSP00000033525 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000033525]

AlphaFold

A2AFR2

Predicted Effect

unknown
Transcript: ENSMUST00000033525
AA Change: V16G

SMART Domains

Protein: ENSMUSP00000033525
Gene: ENSMUSG00000031182
AA Change: V16G

Domain	Start	End	E-Value	Type
low complexity region	56	68	N/A	INTRINSIC
low complexity region	86	101	N/A	INTRINSIC

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
4933427I04Rik	A	T	4: 123,754,494 (GRCm39)	E136V	probably benign	Het
Aadac	A	G	3: 59,943,320 (GRCm39)	D75G	probably damaging	Het
Arfgap1	T	A	2: 180,614,518 (GRCm39)	S125T	probably benign	Het
Atxn2	G	T	5: 121,949,042 (GRCm39)	A813S	probably damaging	Het
Cadps	C	A	14: 12,522,352 (GRCm38)	S604I	probably damaging	Het
Ces1a	G	T	8: 93,771,726 (GRCm39)	P24T	probably damaging	Het
Col4a4	T	A	1: 82,433,480 (GRCm39)	M1488L	unknown	Het
Fndc3c1	T	C	X: 105,475,029 (GRCm39)	N941S	probably damaging	Het
Fryl	T	C	5: 73,244,305 (GRCm39)	Y1172C	possibly damaging	Het
Gm1527	T	C	3: 28,949,737 (GRCm39)		probably benign	Het
Hsf2	T	C	10: 57,388,230 (GRCm39)	L458P	probably damaging	Het
Il2	T	C	3: 37,177,156 (GRCm39)	T127A	possibly damaging	Het
Inpp5e	A	G	2: 26,287,946 (GRCm39)	Y617H	probably damaging	Het
Isoc2b	G	A	7: 4,853,763 (GRCm39)	S137F	probably damaging	Het
Map2	C	T	1: 66,464,490 (GRCm39)	P241S	probably damaging	Het
Mfsd6	C	A	1: 52,748,481 (GRCm39)	R128L	probably damaging	Het
Mrnip	A	G	11: 50,088,462 (GRCm39)	T153A	probably damaging	Het
Or4x6	A	G	2: 89,949,315 (GRCm39)	F209S	possibly damaging	Het
Or8d1	A	T	9: 38,767,095 (GRCm39)	M246L	probably benign	Het
Pi4ka	T	C	16: 17,098,599 (GRCm39)	N2022S	probably benign	Het
Scrt2	C	A	2: 151,935,560 (GRCm39)	R238S	probably damaging	Het
St3gal6	T	A	16: 58,305,138 (GRCm39)	D108V	probably benign	Het
Tmem132b	C	T	5: 125,855,855 (GRCm39)	T529M	probably damaging	Het
Trappc11	T	C	8: 47,954,904 (GRCm39)		probably null	Het
Tspyl1	T	A	10: 34,159,195 (GRCm39)	S307T	possibly damaging	Het
Ush2a	A	G	1: 188,131,982 (GRCm39)	S735G	probably benign	Het
Wnk2	T	C	13: 49,221,668 (GRCm39)	M1186V	possibly damaging	Het

Other mutations in 4930447F04Rik

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R0454:4930447F04Rik	UTSW	X	65,347,274 (GRCm39)	missense	unknown

Posted On

2013-12-03