Mutagenetix > Incidental Mutation

Incidental Mutation 'R0006:Rpp40'

43666

Institutional Source

Beutler Lab

Gene Symbol

Rpp40

Ensembl Gene

ENSMUSG00000021418

Gene Name

ribonuclease P 40 subunit

Synonyms

Rnasep1, D8Bwg1265e

MMRRC Submission

041980-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.924) question?

Stock #

R0006 (G1)

Quality Score

134

Status

Validated

Chromosome

Chromosomal Location

36077455-36090342 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 36080718 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Proline to Serine at position 339 (P339S)

Ref Sequence

ENSEMBL: ENSMUSP00000134228 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000171686] [ENSMUST00000174230]

AlphaFold

Q8R1F9

Predicted Effect

probably damaging
Transcript: ENSMUST00000171686
AA Change: P362S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000130290
Gene: ENSMUSG00000021418
AA Change: P362S

Domain	Start	End	E-Value	Type
Pfam:Ribonuc_P_40	75	346	1.9e-97	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000174230
AA Change: P339S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000134228
Gene: ENSMUSG00000021418
AA Change: P339S

Domain	Start	End	E-Value	Type
Pfam:Ribonuc_P_40	85	324	1.7e-83	PFAM

Predicted Effect

unknown
Transcript: ENSMUST00000174231
AA Change: P82S

SMART Domains

Protein: ENSMUSP00000134210
Gene: ENSMUSG00000021418
AA Change: P82S

Domain	Start	End	E-Value	Type
Pfam:Ribonuc_P_40	19	67	1.5e-19	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000174852

Meta Mutation Damage Score

0.0911

Coding Region Coverage

1x: 99.2%
3x: 98.4%
10x: 96.4%
20x: 93.3%

Validation Efficiency

97% (67/69)

Allele List at MGI

Other mutations in this stock

Total: 63 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aebp1	A	G	11: 5,813,935 (GRCm39)		probably benign	Het
Aldh3a1	G	A	11: 61,107,927 (GRCm39)	V324M	probably damaging	Het
Als2cl	T	A	9: 110,723,686 (GRCm39)	L694Q	possibly damaging	Het
Appl2	A	G	10: 83,438,762 (GRCm39)	F556L	probably damaging	Het
Atad2b	T	A	12: 4,992,030 (GRCm39)	S210T	possibly damaging	Het
Aurka	A	G	2: 172,201,673 (GRCm39)		probably null	Het
Boc	C	T	16: 44,316,812 (GRCm39)	V444I	probably benign	Het
Cfap61	G	A	2: 145,919,232 (GRCm39)	V655I	probably benign	Het
Chd8	A	G	14: 52,472,750 (GRCm39)	I351T	possibly damaging	Het
Chid1	T	A	7: 141,076,339 (GRCm39)		probably benign	Het
Cyp3a41a	T	A	5: 145,641,606 (GRCm39)	H288L	probably benign	Het
Dnase2b	T	A	3: 146,288,244 (GRCm39)	I284F	probably damaging	Het
Dock2	A	G	11: 34,262,453 (GRCm39)		probably benign	Het
Dst	C	T	1: 34,267,999 (GRCm39)	T5325I	probably benign	Het
Erbb3	A	G	10: 128,409,279 (GRCm39)		probably null	Het
Fancl	A	G	11: 26,419,695 (GRCm39)	N316S	possibly damaging	Het
Farsa	G	T	8: 85,587,934 (GRCm39)		probably benign	Het
Fibcd1	T	G	2: 31,728,599 (GRCm39)	D86A	probably damaging	Het
Gab1	A	T	8: 81,496,359 (GRCm39)	M617K	possibly damaging	Het
Gabrd	C	A	4: 155,473,058 (GRCm39)	V72L	probably damaging	Het
Ggh	C	A	4: 20,054,155 (GRCm39)	T150K	possibly damaging	Het
Gnb3	G	A	6: 124,812,767 (GRCm39)		probably benign	Het
Hephl1	T	A	9: 14,988,060 (GRCm39)	T683S	probably benign	Het
Hmcn1	G	A	1: 150,684,427 (GRCm39)	P381L	probably damaging	Het
Hspa8	T	G	9: 40,715,925 (GRCm39)	N544K	probably benign	Het
Hspg2	C	T	4: 137,247,242 (GRCm39)	T1155I	probably damaging	Het
Igdcc4	C	T	9: 65,042,382 (GRCm39)		probably benign	Het
Jazf1	A	G	6: 52,871,071 (GRCm39)		probably benign	Het
Kntc1	T	A	5: 123,927,201 (GRCm39)	S1219T	probably benign	Het
L3mbtl1	A	T	2: 162,806,489 (GRCm39)	Y460F	possibly damaging	Het
Lcor	A	G	19: 41,573,338 (GRCm39)	T698A	probably benign	Het
Lyrm7	T	A	11: 54,739,423 (GRCm39)	T76S	probably benign	Het
Map1b	C	T	13: 99,571,810 (GRCm39)	V304M	probably damaging	Het
Mcub	A	C	3: 129,727,414 (GRCm39)		probably benign	Het
Muc13	T	C	16: 33,623,518 (GRCm39)	S271P	probably damaging	Het
Myo16	A	G	8: 10,525,988 (GRCm39)	K843E	probably damaging	Het
Nav2	A	G	7: 49,102,978 (GRCm39)	E531G	possibly damaging	Het
Niban3	A	G	8: 72,057,688 (GRCm39)		probably benign	Het
Nup188	T	C	2: 30,212,035 (GRCm39)	V553A	probably benign	Het
Or1e16	A	G	11: 73,286,314 (GRCm39)	F178S	probably damaging	Het
Or1e1c	A	G	11: 73,266,414 (GRCm39)	M283V	possibly damaging	Het
Or52d1	A	G	7: 103,755,527 (GRCm39)	I14V	probably benign	Het
Or6z1	A	G	7: 6,504,610 (GRCm39)	I205T	possibly damaging	Het
Or8b9	T	A	9: 37,766,516 (GRCm39)	V134D	possibly damaging	Het
P4ha3	C	T	7: 99,968,155 (GRCm39)	R378*	probably null	Het
Rap1gds1	G	T	3: 138,689,632 (GRCm39)		probably null	Het
Rbfox1	T	A	16: 7,148,284 (GRCm39)	S244R	probably benign	Het
Rsph4a	T	C	10: 33,785,144 (GRCm39)	C148R	probably damaging	Het
Skint5	T	C	4: 113,751,059 (GRCm39)		probably benign	Het
Sptbn1	A	G	11: 30,073,855 (GRCm39)	S1405P	probably damaging	Het
Tex35	T	C	1: 156,927,314 (GRCm39)	K154E	possibly damaging	Het
Thada	T	C	17: 84,533,468 (GRCm39)	N1661S	probably benign	Het
Tle4	A	G	19: 14,444,078 (GRCm39)		probably benign	Het
Tnxb	T	C	17: 34,901,266 (GRCm39)	S1027P	probably benign	Het
Tpm3	T	A	3: 89,994,968 (GRCm39)		probably benign	Het
Ubr4	T	C	4: 139,158,960 (GRCm39)	F2438L	probably benign	Het
Uggt2	A	T	14: 119,287,075 (GRCm39)	F640L	probably benign	Het
Vmn1r20	T	G	6: 57,409,290 (GRCm39)	H205Q	probably damaging	Het
Wbp2	T	C	11: 115,970,614 (GRCm39)		probably null	Het
Xirp1	T	C	9: 119,846,520 (GRCm39)	I788V	probably benign	Het
Zc3hav1	A	G	6: 38,296,637 (GRCm39)		probably null	Het
Zfp687	A	G	3: 94,918,767 (GRCm39)	I335T	probably damaging	Het
Zfpm1	A	G	8: 123,061,227 (GRCm39)	Y264C	probably damaging	Het

Other mutations in Rpp40

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01072:Rpp40	APN	13	36,086,017 (GRCm39)	missense	probably damaging	1.00
IGL01550:Rpp40	APN	13	36,090,183 (GRCm39)	splice site	probably null
IGL03028:Rpp40	APN	13	36,088,494 (GRCm39)	missense	probably damaging	0.99
R0098:Rpp40	UTSW	13	36,082,970 (GRCm39)	missense	probably benign	0.06
R0098:Rpp40	UTSW	13	36,082,970 (GRCm39)	missense	probably benign	0.06
R0144:Rpp40	UTSW	13	36,085,352 (GRCm39)	missense	probably benign	0.00
R0799:Rpp40	UTSW	13	36,086,034 (GRCm39)	missense	probably benign
R1852:Rpp40	UTSW	13	36,080,897 (GRCm39)	missense	probably benign	0.06
R2083:Rpp40	UTSW	13	36,082,975 (GRCm39)	missense	probably benign	0.01
R2129:Rpp40	UTSW	13	36,082,604 (GRCm39)	nonsense	probably null
R4042:Rpp40	UTSW	13	36,082,549 (GRCm39)	missense	probably benign	0.00
R4044:Rpp40	UTSW	13	36,082,549 (GRCm39)	missense	probably benign	0.00
R4118:Rpp40	UTSW	13	36,080,787 (GRCm39)	missense	probably damaging	1.00
R5068:Rpp40	UTSW	13	36,082,681 (GRCm39)	missense	probably benign	0.00
R5181:Rpp40	UTSW	13	36,080,695 (GRCm39)	splice site	probably null
R7023:Rpp40	UTSW	13	36,082,889 (GRCm39)	missense	possibly damaging	0.66
R7916:Rpp40	UTSW	13	36,086,034 (GRCm39)	missense	probably benign	0.03
R9194:Rpp40	UTSW	13	36,080,898 (GRCm39)	missense	probably benign	0.02
Z1191:Rpp40	UTSW	13	36,080,739 (GRCm39)	missense	probably benign	0.33

Predicted Primers

PCR Primer
(F):5'- GATCGTAGGATAAGCAGCCAGTGC -3'
(R):5'- GCCCCACCTTAATAGAAGGGAAGC -3'

Sequencing Primer
(F):5'- ACTGTAGCAAGTCTGGGTGA -3'
(R):5'- CTTCGATGAACCAAAGTTGGCTC -3'

Posted On

2013-05-29