Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01566:E030025P04Rik'

90981

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

E030025P04Rik

Ensembl Gene

Gene Name

RIKEN cDNA E030025P04 gene

Synonyms

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.102) question?

Stock #

IGL01566

Quality Score

Status

Chromosome

Chromosomal Location

109030117-109035195 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 109034714 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Aspartic acid to Valine at position 58 (D58V)

Ref Sequence

ENSEMBL: ENSMUSP00000102321 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000106710]

Predicted Effect

unknown
Transcript: ENSMUST00000106710
AA Change: D58V

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 21 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
AB124611	T	C	9: 21,447,285 (GRCm39)	V149A	possibly damaging	Het
Casc3	T	C	11: 98,714,227 (GRCm39)		probably null	Het
Dhdds	T	C	4: 133,718,648 (GRCm39)	I162V	probably damaging	Het
Dsg1a	T	C	18: 20,469,840 (GRCm39)		probably benign	Het
Gcn1	A	G	5: 115,749,117 (GRCm39)	N1883S	probably damaging	Het
Gucy1a2	T	C	9: 3,634,661 (GRCm39)	L235P	probably damaging	Het
Jkampl	G	A	6: 73,445,673 (GRCm39)	T292I	probably damaging	Het
Kprp	T	C	3: 92,731,271 (GRCm39)	N593S	probably benign	Het
Mme	T	C	3: 63,269,350 (GRCm39)		probably benign	Het
Nr6a1	G	T	2: 38,617,901 (GRCm39)	Q419K	probably benign	Het
Pcolce	A	G	5: 137,603,422 (GRCm39)		probably benign	Het
Ppp2cb	C	A	8: 34,101,791 (GRCm39)	R110S	probably benign	Het
Slc35f1	A	G	10: 52,965,551 (GRCm39)	Y322C	probably damaging	Het
Slc5a3	T	C	16: 91,874,465 (GRCm39)	V174A	probably damaging	Het
St8sia4	G	T	1: 95,581,482 (GRCm39)	R87S	probably benign	Het
Tfdp2	A	G	9: 96,177,083 (GRCm39)	E5G	probably damaging	Het
Tmem161b	T	C	13: 84,442,881 (GRCm39)	I267T	probably benign	Het
Ttn	A	G	2: 76,782,365 (GRCm39)	L957P	probably damaging	Het
Ttn	A	G	2: 76,612,445 (GRCm39)		probably benign	Het
Ubqln1	A	T	13: 58,327,481 (GRCm39)		probably null	Het
Wdfy3	A	C	5: 102,044,454 (GRCm39)		probably benign	Het

Other mutations in E030025P04Rik

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02709:E030025P04Rik	APN	11	109,030,324 (GRCm39)	utr 3 prime	probably benign
Tipper	UTSW	11	109,030,425 (GRCm39)	missense	unknown
K3955:E030025P04Rik	UTSW	11	109,034,778 (GRCm39)	missense	unknown
R1842:E030025P04Rik	UTSW	11	109,030,396 (GRCm39)	missense	unknown
R1854:E030025P04Rik	UTSW	11	109,034,744 (GRCm39)	missense	unknown
R2382:E030025P04Rik	UTSW	11	109,034,880 (GRCm39)	nonsense	probably null
R6413:E030025P04Rik	UTSW	11	109,030,425 (GRCm39)	missense	unknown
R6870:E030025P04Rik	UTSW	11	109,030,993 (GRCm39)	missense	unknown
R9121:E030025P04Rik	UTSW	11	109,034,738 (GRCm39)	missense	unknown
R9344:E030025P04Rik	UTSW	11	109,030,454 (GRCm39)	critical splice acceptor site	probably null
R9381:E030025P04Rik	UTSW	11	109,030,384 (GRCm39)	missense	unknown
Z1176:E030025P04Rik	UTSW	11	109,034,797 (GRCm39)	missense	unknown

Posted On

2013-12-09