Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL01517:Rpl28-ps4'

90442

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rpl28-ps4

Ensembl Gene

ENSMUSG00000090549

Gene Name

ribosomal protein L28, pseudogene 4

Synonyms

Gm4783

Accession Numbers

Essential gene?

Possibly essential (E-score: 0.713) question?

Stock #

IGL01517

Quality Score

Status

Chromosome

Chromosomal Location

117190651-117191027 bp(-) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 117190813 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

no structure available at present

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000170447

SMART Domains

Protein: ENSMUSP00000130197
Gene: ENSMUSG00000090549

Domain	Start	End	E-Value	Type
Pfam:Ribosomal_L28e	1	114	4.8e-30	PFAM
low complexity region	117	129	N/A	INTRINSIC

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 34 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adamts6	A	T	13: 104,526,700 (GRCm39)		probably benign	Het
Arpc1b	A	G	5: 145,064,679 (GRCm39)		probably benign	Het
Ccdc54	G	A	16: 50,410,280 (GRCm39)	L329F	possibly damaging	Het
Cdc42bpg	G	A	19: 6,368,467 (GRCm39)	R1055H	probably damaging	Het
Cylc1	A	G	X: 110,162,799 (GRCm39)	T29A	possibly damaging	Het
Ddx50	T	C	10: 62,482,911 (GRCm39)	T53A	probably benign	Het
Dmap1	G	A	4: 117,533,206 (GRCm39)	R283C	probably damaging	Het
Extl3	A	T	14: 65,314,156 (GRCm39)	L342H	probably damaging	Het
Gjb3	A	C	4: 127,219,914 (GRCm39)	I206S	probably damaging	Het
Gphn	T	A	12: 78,423,148 (GRCm39)	I53K	probably damaging	Het
Gpr22	C	T	12: 31,758,709 (GRCm39)		probably benign	Het
Inpp5b	T	A	4: 124,676,229 (GRCm39)	C362S	probably benign	Het
Iqgap3	C	A	3: 88,016,703 (GRCm39)	Q1062K	probably benign	Het
Kdm2a	A	G	19: 4,412,089 (GRCm39)		probably benign	Het
Ltbp3	A	G	19: 5,807,760 (GRCm39)	D1167G	possibly damaging	Het
Mpo	A	G	11: 87,686,647 (GRCm39)	N65D	possibly damaging	Het
Mrpl2	A	G	17: 46,960,909 (GRCm39)	R268G	probably damaging	Het
Nfkbia	C	T	12: 55,537,430 (GRCm39)	A220T	probably damaging	Het
Nlrc3	T	A	16: 3,765,351 (GRCm39)	I1091F	probably damaging	Het
Notch2	T	A	3: 98,045,971 (GRCm39)	S1674R	probably benign	Het
Or10h28	T	A	17: 33,488,629 (GRCm39)	N310K	probably benign	Het
Or14a257	T	C	7: 86,138,765 (GRCm39)		probably benign	Het
Pde8b	A	G	13: 95,237,395 (GRCm39)		probably null	Het
Pla2r1	A	G	2: 60,334,597 (GRCm39)	Y392H	probably damaging	Het
Plekhm1	A	T	11: 103,285,609 (GRCm39)	N275K	possibly damaging	Het
Prdm16	T	C	4: 154,412,882 (GRCm39)	H1041R	probably damaging	Het
Rapsn	C	A	2: 90,866,963 (GRCm39)	N88K	probably damaging	Het
Rasef	T	A	4: 73,688,059 (GRCm39)	Q31H	probably benign	Het
Trpc7	T	C	13: 57,008,878 (GRCm39)	Y263C	probably damaging	Het
Ttn	T	C	2: 76,577,940 (GRCm39)	T24318A	probably damaging	Het
Vmn1r35	T	C	6: 66,656,434 (GRCm39)	T79A	probably benign	Het
Vmn2r100	T	A	17: 19,742,225 (GRCm39)	S200T	probably benign	Het
Wnt9b	A	G	11: 103,621,907 (GRCm39)	V250A	probably benign	Het
Zyg11a	T	A	4: 108,058,391 (GRCm39)	K383M	probably null	Het

Other mutations in Rpl28-ps4

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
R2044:Rpl28-ps4	UTSW	6	117,190,856 (GRCm39)	exon	noncoding transcript

Posted On

2013-12-09