Mutagenetix > Incidental Mutation

Incidental Mutation 'R0552:Mppe1'

45264

Institutional Source

Beutler Lab

Gene Symbol

Mppe1

Ensembl Gene

ENSMUSG00000062526

Gene Name

metallophosphoesterase 1

Synonyms

Pgap5

MMRRC Submission

038744-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.112) question?

Stock #

R0552 (G1)

Quality Score

162

Status

Not validated

Chromosome

Chromosomal Location

67358119-67378901 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 67370419 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000072808 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000073054] [ENSMUST00000073054]

AlphaFold

no structure available at present

Predicted Effect

probably null
Transcript: ENSMUST00000073054

SMART Domains

Protein: ENSMUSP00000072808
Gene: ENSMUSG00000062526

Domain	Start	End	E-Value	Type
transmembrane domain	21	43	N/A	INTRINSIC
Pfam:Metallophos	68	308	3.3e-13	PFAM
transmembrane domain	358	380	N/A	INTRINSIC

Predicted Effect

probably null
Transcript: ENSMUST00000073054

SMART Domains

Protein: ENSMUSP00000072808
Gene: ENSMUSG00000062526

Domain	Start	End	E-Value	Type
transmembrane domain	21	43	N/A	INTRINSIC
Pfam:Metallophos	68	308	3.3e-13	PFAM
transmembrane domain	358	380	N/A	INTRINSIC

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 94.1%

Validation Efficiency

Allele List at MGI

Other mutations in this stock

Total: 40 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adam9	A	T	8: 25,453,026 (GRCm39)	N760K	probably benign	Het
Ahcyl	T	A	16: 45,974,955 (GRCm39)	T141S	probably benign	Het
Akr1b10	A	G	6: 34,369,920 (GRCm39)	T216A	possibly damaging	Het
Arsj	A	G	3: 126,232,993 (GRCm39)	R580G	probably benign	Het
C9	A	T	15: 6,474,918 (GRCm39)	I26F	probably damaging	Het
Cacna2d1	A	G	5: 16,533,041 (GRCm39)	E578G	probably damaging	Het
Clca4b	C	T	3: 144,622,536 (GRCm39)	V510I	probably benign	Het
Dab2	C	T	15: 6,464,895 (GRCm39)	T561I	possibly damaging	Het
Golga5	A	T	12: 102,450,752 (GRCm39)	E12D	possibly damaging	Het
Hsd17b12	A	T	2: 93,874,280 (GRCm39)	F208I	probably damaging	Het
Inf2	A	G	12: 112,579,008 (GRCm39)		probably benign	Het
Kcnh3	T	A	15: 99,127,337 (GRCm39)	W378R	probably damaging	Het
Klhdc8b	G	C	9: 108,326,422 (GRCm39)	R158G	possibly damaging	Het
Klhl41	G	A	2: 69,500,554 (GRCm39)	R5Q	probably benign	Het
Lcn3	T	C	2: 25,656,421 (GRCm39)		probably null	Het
Muc20	G	A	16: 32,614,300 (GRCm39)	A359V	probably damaging	Het
Myh14	T	C	7: 44,263,105 (GRCm39)	D1765G	probably damaging	Het
Or10j2	T	C	1: 173,098,372 (GRCm39)	M210T	probably benign	Het
Or4c10b	C	T	2: 89,711,235 (GRCm39)	Q22*	probably null	Het
Or5p58	A	G	7: 107,693,985 (GRCm39)	M264T	probably benign	Het
Pbrm1	T	A	14: 30,757,916 (GRCm39)	L182Q	probably damaging	Het
Pde8a	A	G	7: 80,967,095 (GRCm39)	N412S	probably benign	Het
Phyh	A	G	2: 4,940,912 (GRCm39)	T271A	probably damaging	Het
Pkhd1l1	T	C	15: 44,352,942 (GRCm39)	S258P	probably damaging	Het
Ptpro	T	A	6: 137,420,592 (GRCm39)	V1007D	probably damaging	Het
Pyroxd1	A	G	6: 142,291,463 (GRCm39)	E2G	probably benign	Het
Ralgapa1	G	T	12: 55,723,550 (GRCm39)	Q2115K	probably benign	Het
Rufy3	A	G	5: 88,732,129 (GRCm39)	E44G	possibly damaging	Het
Slit2	A	T	5: 48,395,721 (GRCm39)	N712I	probably damaging	Het
Sptbn1	A	G	11: 30,095,985 (GRCm39)	M303T	possibly damaging	Het
Ssbp4	A	G	8: 71,052,509 (GRCm39)	I154T	probably benign	Het
Syne2	A	G	12: 75,977,778 (GRCm39)	K1409E	probably benign	Het
Tfap2b	T	C	1: 19,304,449 (GRCm39)	Y420H	probably damaging	Het
Tlr5	A	G	1: 182,803,261 (GRCm39)		probably null	Het
Tmprss15	C	T	16: 78,821,637 (GRCm39)		probably null	Het
Tns1	A	T	1: 73,959,722 (GRCm39)	I418N	probably damaging	Het
Txlna	A	T	4: 129,522,984 (GRCm39)	V452D	probably benign	Het
Wdr17	C	T	8: 55,146,131 (GRCm39)	A90T	possibly damaging	Het
Zfp563	A	T	17: 33,323,659 (GRCm39)	S85C	possibly damaging	Het
Zfp764l1	A	T	7: 126,991,504 (GRCm39)	I161N	possibly damaging	Het

Other mutations in Mppe1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01129:Mppe1	APN	18	67,370,515 (GRCm39)	nonsense	probably null
IGL03028:Mppe1	APN	18	67,360,755 (GRCm39)	missense	probably damaging	1.00
R0087:Mppe1	UTSW	18	67,358,775 (GRCm39)	makesense	probably null
R0538:Mppe1	UTSW	18	67,370,548 (GRCm39)	missense	probably damaging	1.00
R1170:Mppe1	UTSW	18	67,360,777 (GRCm39)	missense	probably damaging	1.00
R1970:Mppe1	UTSW	18	67,362,843 (GRCm39)	missense	probably benign	0.07
R2229:Mppe1	UTSW	18	67,361,082 (GRCm39)	critical splice donor site	probably null
R3874:Mppe1	UTSW	18	67,358,957 (GRCm39)	critical splice acceptor site	probably null
R4194:Mppe1	UTSW	18	67,361,139 (GRCm39)	missense	probably benign	0.27
R4775:Mppe1	UTSW	18	67,359,930 (GRCm39)	missense	possibly damaging	0.96
R4940:Mppe1	UTSW	18	67,361,095 (GRCm39)	missense	probably damaging	1.00
R4974:Mppe1	UTSW	18	67,361,133 (GRCm39)	missense	probably benign
R4979:Mppe1	UTSW	18	67,362,773 (GRCm39)	missense	probably damaging	1.00
R5768:Mppe1	UTSW	18	67,358,889 (GRCm39)	missense	possibly damaging	0.87
R5784:Mppe1	UTSW	18	67,361,098 (GRCm39)	missense	probably benign	0.12
R5895:Mppe1	UTSW	18	67,358,834 (GRCm39)	missense	probably benign	0.00
R6547:Mppe1	UTSW	18	67,362,059 (GRCm39)	missense	probably benign
R7161:Mppe1	UTSW	18	67,362,842 (GRCm39)	missense	probably benign	0.10
R7580:Mppe1	UTSW	18	67,370,488 (GRCm39)	missense	probably damaging	0.99
R7699:Mppe1	UTSW	18	67,358,775 (GRCm39)	makesense	probably null
R7700:Mppe1	UTSW	18	67,358,775 (GRCm39)	makesense	probably null
R7908:Mppe1	UTSW	18	67,362,055 (GRCm39)	missense	probably benign	0.01
R8399:Mppe1	UTSW	18	67,358,946 (GRCm39)	missense	probably benign	0.17
R8896:Mppe1	UTSW	18	67,370,472 (GRCm39)	missense	probably damaging	1.00
R9002:Mppe1	UTSW	18	67,358,925 (GRCm39)	missense	possibly damaging	0.96

Predicted Primers

PCR Primer
(F):5'- AGCTTTGGTTGCCTGTACTAACCC -3'
(R):5'- GAGAGCGTTGCTGTTGAAACTCAC -3'

Sequencing Primer
(F):5'- GGTTGCCTGTACTAACCCAGTAG -3'
(R):5'- AGTTGTCATTATCTCTGTGCTTCTG -3'

Posted On

2013-06-11