Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02641:Rpl21-ps4'

301719

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rpl21-ps4

Ensembl Gene

ENSMUSG00000072714

Gene Name

ribosomal protein L21, pseudogene 4

Synonyms

Gm5201

Accession Numbers

Essential gene?

Probably essential (E-score: 0.867) question?

Stock #

IGL02641

Quality Score

Status

Chromosome

Chromosomal Location

11241784-11242221 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

G to A at 11227661 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

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: 30 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
3100002H09Rik	A	T	4: 124,504,510 (GRCm39)	M14K	unknown	Het
Arhgap24	T	C	5: 103,040,386 (GRCm39)	V441A	probably damaging	Het
Cdv3	G	T	9: 103,241,223 (GRCm39)	Q115K	probably damaging	Het
Clstn1	G	T	4: 149,713,968 (GRCm39)	G207C	probably null	Het
Col28a1	A	T	6: 8,014,794 (GRCm39)	Y870*	probably null	Het
Creb3	A	C	4: 43,563,311 (GRCm39)	H136P	probably benign	Het
Dcaf17	G	A	2: 70,912,375 (GRCm39)	C320Y	probably damaging	Het
Fbl	T	C	7: 27,874,471 (GRCm39)	S66P	probably damaging	Het
Fgfrl1	C	A	5: 108,853,731 (GRCm39)	S279R	probably damaging	Het
Gdpgp1	C	T	7: 79,888,796 (GRCm39)	R276*	probably null	Het
Hcfc2	A	G	10: 82,538,383 (GRCm39)	Y140C	probably damaging	Het
Ighg3	A	G	12: 113,323,818 (GRCm39)	I190T	unknown	Het
Itgav	T	C	2: 83,598,689 (GRCm39)		probably benign	Het
Lce1c	C	A	3: 92,587,845 (GRCm39)		probably benign	Het
Ldoc1	G	A	X: 60,753,419 (GRCm39)	C35Y	probably damaging	Het
Lrp10	T	A	14: 54,706,068 (GRCm39)	C419*	probably null	Het
Micall2	T	C	5: 139,705,094 (GRCm39)	D80G	probably damaging	Het
Or5b21	T	A	19: 12,839,566 (GRCm39)	C142*	probably null	Het
Pde3b	C	T	7: 114,130,052 (GRCm39)	T869I	probably damaging	Het
Pip5k1c	C	A	10: 81,153,155 (GRCm39)		probably null	Het
Pkhd1	G	A	1: 20,628,976 (GRCm39)	T657I	possibly damaging	Het
Pnisr	A	G	4: 21,860,908 (GRCm39)	N197S	probably benign	Het
Rtn4rl1	A	C	11: 75,156,650 (GRCm39)	T361P	probably damaging	Het
Spaca9	C	A	2: 28,585,963 (GRCm39)	E34*	probably null	Het
Trip10	T	A	17: 57,569,411 (GRCm39)	D478E	probably benign	Het
Tsc22d2	A	G	3: 58,323,576 (GRCm39)	D156G	probably damaging	Het
Ufc1	T	C	1: 171,117,764 (GRCm39)	D50G	probably damaging	Het
Vmn1r202	T	G	13: 22,686,274 (GRCm39)	I48L	probably benign	Het
Vmn2r111	A	T	17: 22,792,205 (GRCm39)	V17E	possibly damaging	Het
Vps13a	T	A	19: 16,676,185 (GRCm39)	M1263L	probably benign	Het

Other mutations in Rpl21-ps4

Allele	Source	Chr	Coord	Type	Predicted Effect
IGL00517:Rpl21-ps4	APN	14	11,227,544 (GRCm38)	unclassified	noncoding transcript
IGL02608:Rpl21-ps4	APN	14	11,227,831 (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

2015-04-16