Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL02643:Rplp1rt'

301826

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Rplp1rt

Ensembl Gene

ENSMUSG00000091014

Gene Name

ribosomal protein lateral stalk subunit P1, retrotransposed

Synonyms

Gm5244

Accession Numbers

Essential gene?

Not available question?

Stock #

IGL02643

Quality Score

Status

Chromosome

Chromosomal Location

12824168-12824612 bp(+) (GRCm39)

Type of Mutation

exon

DNA Base Change (assembly)

T to C at 12824300 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Gene Model

predicted gene model for transcript(s):

AlphaFold

A0A494BA26

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000164001

SMART Domains

Protein: ENSMUSP00000127083
Gene: ENSMUSG00000091014

Domain	Start	End	E-Value	Type
Pfam:Ribosomal_60s	23	112	1.3e-23	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000189517

Coding Region Coverage

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 41 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acad10	T	G	5: 121,769,633 (GRCm39)	M608L	probably benign	Het
Adamts2	A	T	11: 50,679,527 (GRCm39)	M836L	probably benign	Het
Ankrd11	A	T	8: 123,619,061 (GRCm39)	M1597K	probably damaging	Het
Arhgef17	A	T	7: 100,533,089 (GRCm39)	F1145L	possibly damaging	Het
Atp13a3	A	T	16: 30,152,614 (GRCm39)	W32R	probably null	Het
Atp2a3	C	A	11: 72,866,165 (GRCm39)	H262N	probably benign	Het
Bod1l	T	A	5: 41,976,148 (GRCm39)	E1722V	possibly damaging	Het
Ceacam16	A	G	7: 19,595,086 (GRCm39)		probably benign	Het
Col14a1	T	A	15: 55,284,258 (GRCm39)	Y840N	unknown	Het
Dlg5	A	G	14: 24,241,250 (GRCm39)	C132R	probably damaging	Het
Dock4	T	A	12: 40,718,429 (GRCm39)	N242K	probably damaging	Het
Dsg3	G	A	18: 20,662,012 (GRCm39)	V426I	probably benign	Het
Dync1h1	T	C	12: 110,625,706 (GRCm39)		probably benign	Het
Flvcr2	T	A	12: 85,842,997 (GRCm39)	M357K	possibly damaging	Het
Gapvd1	A	G	2: 34,594,192 (GRCm39)	S932P	probably damaging	Het
Gata4	T	A	14: 63,442,204 (GRCm39)	D205V	possibly damaging	Het
Kcnk2	T	A	1: 188,990,976 (GRCm39)	I195L	possibly damaging	Het
Krt1	T	C	15: 101,755,479 (GRCm39)	I427V	probably benign	Het
Mapk1ip1l	T	A	14: 47,548,339 (GRCm39)	H162Q	possibly damaging	Het
Micu1	A	G	10: 59,675,558 (GRCm39)	D380G	probably damaging	Het
Mknk2	A	C	10: 80,504,435 (GRCm39)	L289R	probably damaging	Het
Mtcl2	A	G	2: 156,882,663 (GRCm39)	V463A	probably damaging	Het
Myo18a	A	T	11: 77,668,998 (GRCm39)	N286I	possibly damaging	Het
Or5ae2	A	T	7: 84,506,239 (GRCm39)	I221F	probably damaging	Het
Pdp1	C	T	4: 11,962,062 (GRCm39)	R83H	probably benign	Het
Ptafr	A	C	4: 132,307,437 (GRCm39)	I276L	probably benign	Het
Rab3gap2	A	T	1: 184,999,197 (GRCm39)	D968V	possibly damaging	Het
Samd8	T	A	14: 21,843,212 (GRCm39)	M447K	probably damaging	Het
Six5	G	T	7: 18,831,455 (GRCm39)	V649L	probably benign	Het
Slc1a2	T	A	2: 102,570,225 (GRCm39)	F168I	probably benign	Het
Slc1a7	G	A	4: 107,869,497 (GRCm39)	V521M	possibly damaging	Het
Sorbs1	T	C	19: 40,353,577 (GRCm39)	D206G	possibly damaging	Het
Stim2	T	C	5: 54,267,955 (GRCm39)	V417A	probably damaging	Het
Tbx20	A	G	9: 24,685,009 (GRCm39)		probably benign	Het
Tia1	A	G	6: 86,393,372 (GRCm39)	I71V	probably benign	Het
Ttc7	T	C	17: 87,648,327 (GRCm39)	S509P	possibly damaging	Het
Ttpal	A	G	2: 163,449,140 (GRCm39)		probably benign	Het
Tubgcp2	A	T	7: 139,576,067 (GRCm39)	N865K	probably damaging	Het
Wdr45	G	T	X: 7,593,288 (GRCm39)	E62*	probably null	Het
Zfp507	A	G	7: 35,494,656 (GRCm39)	F129S	probably damaging	Het
Zfp518b	T	A	5: 38,831,498 (GRCm39)	H169L	probably damaging	Het

Other mutations in Rplp1rt

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02217:Rplp1rt	APN	19	12,824,227 (GRCm39)	exon	noncoding transcript

Posted On

2015-04-16