Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00517:Rpl21-ps4'

332546

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rpl21-ps4

Ensembl Gene

Gene Name

ribosomal protein L21, pseudogene 4

Synonyms

Gm5201

Accession Numbers

Essential gene?

Probably essential (E-score: 0.867) question?

Stock #

IGL00517

Quality Score

Status

Chromosome

Chromosomal Location

11241784-11242221 bp(-) (GRCm39)

Type of Mutation

unclassified

DNA Base Change (assembly)

T to C at 11227544 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000080237

SMART Domains

Protein: ENSMUSP00000079127
Gene: ENSMUSG00000072714

Domain	Start	End	E-Value	Type
Pfam:Ribosomal_L21e	3	99	1.5e-51	PFAM

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 25 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Arap1	C	T	7: 101,037,256 (GRCm39)	R180W	probably damaging	Het
Atg4a	T	A	X: 139,945,488 (GRCm39)	M345K	probably damaging	Het
Cacna1s	T	C	1: 136,015,077 (GRCm39)	V408A	probably damaging	Het
Ccdc141	C	T	2: 76,884,988 (GRCm39)	G551D	probably damaging	Het
Cdh2	A	C	18: 16,760,693 (GRCm39)	V558G	possibly damaging	Het
Col9a1	T	A	1: 24,234,615 (GRCm39)		probably benign	Het
Fbxo15	T	A	18: 84,977,225 (GRCm39)	F46I	probably damaging	Het
Gdpd4	T	C	7: 97,653,478 (GRCm39)	I497T	probably damaging	Het
Gtf2f2	A	G	14: 76,232,941 (GRCm39)	V75A	probably benign	Het
Hpse	T	C	5: 100,839,196 (GRCm39)	H384R	possibly damaging	Het
Lama2	T	A	10: 27,073,326 (GRCm39)	T1044S	probably benign	Het
Lamp2	T	C	X: 37,545,186 (GRCm39)		probably benign	Het
Lipe	C	A	7: 25,087,985 (GRCm39)		probably null	Het
Marf1	T	C	16: 13,933,606 (GRCm39)	E1594G	possibly damaging	Het
Mettl24	T	C	10: 40,686,496 (GRCm39)	V291A	probably benign	Het
Patj	G	T	4: 98,329,308 (GRCm39)	V521F	possibly damaging	Het
Prkg1	A	T	19: 30,872,068 (GRCm39)	D242E	probably benign	Het
Qsox2	T	C	2: 26,112,267 (GRCm39)	I92V	probably benign	Het
Rasgrf1	T	C	9: 89,852,534 (GRCm39)	Y367H	probably damaging	Het
Sigirr	T	C	7: 140,672,147 (GRCm39)	E266G	probably benign	Het
Slitrk6	T	C	14: 110,988,547 (GRCm39)	T387A	probably benign	Het
Smim22	T	C	16: 4,825,860 (GRCm39)	L54P	probably damaging	Het
Taf4	G	A	2: 179,566,206 (GRCm39)		probably benign	Het
Trappc14	A	G	5: 138,259,967 (GRCm39)	V363A	possibly damaging	Het
Zswim3	T	C	2: 164,663,011 (GRCm39)	L497S	probably damaging	Het

Other mutations in Rpl21-ps4

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL02608:Rpl21-ps4	APN	14	11,227,831 (GRCm38)	exon	noncoding transcript
IGL02641:Rpl21-ps4	APN	14	11,227,661 (GRCm38)	exon	noncoding transcript
IGL03352:Rpl21-ps4	APN	14	11,227,760 (GRCm38)	exon	noncoding transcript
R0255:Rpl21-ps4	UTSW	14	11,227,556 (GRCm38)	exon	noncoding transcript
R4418:Rpl21-ps4	UTSW	14	11,227,879 (GRCm38)	exon	noncoding transcript

Posted On

2015-08-05