Mutagenetix > Incidental Mutation

Incidental Mutation 'R4930:Apeh'

381164

Institutional Source

Beutler Lab

Gene Symbol

Apeh

Ensembl Gene

ENSMUSG00000032590

Gene Name

acylpeptide hydrolase

Synonyms

N-acylaminoacyl peptide hydrolase

MMRRC Submission

042531-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4930 (G1)

Quality Score

194

Status

Validated

Chromosome

Chromosomal Location

108085413-108094606 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 108087825 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 446 (S446P)

Ref Sequence

ENSEMBL: ENSMUSP00000141856 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000035211] [ENSMUST00000159372] [ENSMUST00000160249] [ENSMUST00000162886] [ENSMUST00000191985] [ENSMUST00000193254]

AlphaFold

Q8R146

Predicted Effect

probably benign
Transcript: ENSMUST00000035211

SMART Domains

Protein: ENSMUSP00000035211
Gene: ENSMUSG00000032591

Domain	Start	End	E-Value	Type
PAN_AP	21	104	2.65e-9	SMART
KR	108	188	3.13e-39	SMART
KR	189	270	8.57e-46	SMART
KR	290	372	7.94e-41	SMART
KR	377	459	6.59e-47	SMART
Tryp_SPc	488	709	2.27e-55	SMART

Predicted Effect

unknown
Transcript: ENSMUST00000081309
AA Change: S444P

SMART Domains

Protein: ENSMUSP00000080058
Gene: ENSMUSG00000032590
AA Change: S444P

Domain	Start	End	E-Value	Type
Pfam:DLH	485	721	2e-8	PFAM
Pfam:Abhydrolase_1	501	633	3.8e-9	PFAM
Pfam:Abhydrolase_5	501	708	5e-16	PFAM
Pfam:Peptidase_S9	516	732	1.6e-38	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000159372

Predicted Effect

probably benign
Transcript: ENSMUST00000160249

SMART Domains

Protein: ENSMUSP00000124548
Gene: ENSMUSG00000041528

Domain	Start	End	E-Value	Type
low complexity region	104	115	N/A	INTRINSIC
SPRY	132	253	1.52e-28	SMART
low complexity region	471	488	N/A	INTRINSIC
low complexity region	508	518	N/A	INTRINSIC
coiled coil region	1041	1061	N/A	INTRINSIC
low complexity region	1236	1245	N/A	INTRINSIC
RING	1254	1291	5.27e-4	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000161253

Predicted Effect

probably benign
Transcript: ENSMUST00000162886

SMART Domains

Protein: ENSMUSP00000125175
Gene: ENSMUSG00000032591

Domain	Start	End	E-Value	Type
PAN_AP	21	104	2.65e-9	SMART
KR	108	188	3.13e-39	SMART
KR	189	270	1.07e-46	SMART
KR	281	363	7.94e-41	SMART
KR	368	450	6.59e-47	SMART
Tryp_SPc	479	700	2.27e-55	SMART

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000191754

Predicted Effect

probably benign
Transcript: ENSMUST00000191985

SMART Domains

Protein: ENSMUSP00000142150
Gene: ENSMUSG00000032590

Domain	Start	End	E-Value	Type
low complexity region	3	19	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000192278

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000192916

Predicted Effect

probably benign
Transcript: ENSMUST00000193254
AA Change: S446P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)

SMART Domains

Protein: ENSMUSP00000141856
Gene: ENSMUSG00000032590
AA Change: S446P

Domain	Start	End	E-Value	Type
Pfam:DLH	485	721	4.8e-8	PFAM
Pfam:Abhydrolase_5	501	708	5.7e-16	PFAM
Pfam:Abhydrolase_6	503	714	6.2e-14	PFAM
Pfam:Peptidase_S9	515	732	1.4e-38	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194014

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194083

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000194915

Meta Mutation Damage Score

0.1014

Coding Region Coverage

1x: 99.0%
3x: 98.2%
10x: 95.9%
20x: 91.1%

Validation Efficiency

99% (88/89)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes the enzyme acylpeptide hydrolase, which catalyzes the hydrolysis of the terminal acetylated amino acid preferentially from small acetylated peptides. The acetyl amino acid formed by this hydrolase is further processed to acetate and a free amino acid by an aminoacylase. This gene is located within the same region of chromosome 3 (3p21) as the aminoacylase gene, and deletions at this locus are also associated with a decrease in aminoacylase activity. The acylpeptide hydrolase is a homotetrameric protein of 300 kDa with each subunit consisting of 732 amino acid residues. It can play an important role in destroying oxidatively damaged proteins in living cells. Deletions of this gene locus are found in various types of carcinomas, including small cell lung carcinoma and renal cell carcinoma. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 81 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930447C04Rik	C	T	12: 72,906,234 (GRCm38)	E242K	possibly damaging	Het
A930011G23Rik	A	G	5: 99,222,404 (GRCm38)	M499T	possibly damaging	Het
Abcb8	G	A	5: 24,400,781 (GRCm38)	V196M	possibly damaging	Het
Ahnak	T	C	19: 9,010,967 (GRCm38)	M3205T	possibly damaging	Het
Ankrd1	A	G	19: 36,115,033 (GRCm38)	Y265H	probably damaging	Het
Apip	C	A	2: 103,091,881 (GRCm38)	Y197*	probably null	Het
Arhgef11	T	G	3: 87,728,594 (GRCm38)	V925G	probably damaging	Het
Arid4b	T	C	13: 14,187,477 (GRCm38)	V929A	probably damaging	Het
Asah2	T	A	19: 32,052,906 (GRCm38)	D122V	probably benign	Het
B2m	A	T	2: 122,151,647 (GRCm38)	D116V	possibly damaging	Het
Bhmt-ps1	A	G	4: 26,369,184 (GRCm38)		noncoding transcript	Het
Cacna1g	T	A	11: 94,444,073 (GRCm38)	I803F	probably damaging	Het
Ccdc43	A	T	11: 102,690,285 (GRCm38)	V113E	probably damaging	Het
Cenpj	A	T	14: 56,534,781 (GRCm38)	Y388*	probably null	Het
Chd3	G	A	11: 69,354,208 (GRCm38)		probably benign	Het
Chil3	C	T	3: 106,164,208 (GRCm38)	D47N	possibly damaging	Het
Colgalt2	A	G	1: 152,499,959 (GRCm38)	T361A	possibly damaging	Het
Cops3	C	A	11: 59,835,367 (GRCm38)		probably benign	Het
Crb2	G	T	2: 37,783,314 (GRCm38)	G74V	probably damaging	Het
Cspg4b	G	T	13: 113,327,662 (GRCm38)	G1453C	probably damaging	Het
Cyp20a1	A	T	1: 60,366,719 (GRCm38)	Y224F	probably damaging	Het
Diaph3	A	G	14: 87,141,166 (GRCm38)		probably benign	Het
Dnah3	A	T	7: 119,951,681 (GRCm38)	Y3127*	probably null	Het
Eef1akmt3	A	C	10: 127,041,355 (GRCm38)	S14A	possibly damaging	Het
Ehf	C	A	2: 103,266,857 (GRCm38)	R250L	probably damaging	Het
Eps8l1	G	A	7: 4,460,916 (GRCm38)	R13Q	possibly damaging	Het
Frem2	A	C	3: 53,656,315 (GRCm38)	V257G	possibly damaging	Het
Gc	T	C	5: 89,439,589 (GRCm38)	T259A	probably benign	Het
Gm4952	A	T	19: 12,627,012 (GRCm38)	N263Y	probably benign	Het
Gpcpd1	T	A	2: 132,546,874 (GRCm38)	H326L	probably damaging	Het
Helz	T	C	11: 107,620,168 (GRCm38)	F617L	probably damaging	Het
Hoxb4	T	C	11: 96,318,836 (GRCm38)	Y23H	probably damaging	Het
Hsf4	T	A	8: 105,272,698 (GRCm38)		probably null	Het
Ift56	A	T	6: 38,391,540 (GRCm38)	Y174F	probably damaging	Het
Ighv1-81	T	C	12: 115,920,304 (GRCm38)	D109G	probably damaging	Het
Irx4	T	C	13: 73,268,913 (GRCm38)	V476A	probably benign	Het
Katnb1	T	A	8: 95,097,294 (GRCm38)		probably null	Het
L3mbtl1	A	G	2: 162,965,772 (GRCm38)	Y490C	probably damaging	Het
Lemd2	A	G	17: 27,193,832 (GRCm38)		probably null	Het
Lrrc38	A	T	4: 143,369,868 (GRCm38)	T250S	probably damaging	Het
Map3k8	A	T	18: 4,349,215 (GRCm38)	Y34*	probably null	Het
Mgst1	T	A	6: 138,153,509 (GRCm38)	F79I	probably benign	Het
Midn	T	C	10: 80,155,355 (GRCm38)	S357P	probably benign	Het
Mmp3	T	A	9: 7,447,640 (GRCm38)	D208E	probably benign	Het
Mrps26	A	G	2: 130,564,942 (GRCm38)	E163G	probably damaging	Het
Mycbpap	A	T	11: 94,503,157 (GRCm38)	M371K	probably benign	Het
Mynn	A	C	3: 30,607,042 (GRCm38)	N91T	probably damaging	Het
Nek11	A	G	9: 105,300,066 (GRCm38)	L292P	probably damaging	Het
Nid1	A	T	13: 13,510,011 (GRCm38)	R1228W	probably damaging	Het
Nphs2	T	C	1: 156,320,929 (GRCm38)	Y121H	probably damaging	Het
Or1f19	T	G	16: 3,592,435 (GRCm38)	L13R	probably damaging	Het
Or4p7	G	A	2: 88,391,940 (GRCm38)	R231H	probably benign	Het
Or5ac22	C	A	16: 59,314,873 (GRCm38)	C178F	probably damaging	Het
Or5ap2	T	A	2: 85,849,893 (GRCm38)	I147N	probably benign	Het
Or5d38	A	C	2: 88,124,340 (GRCm38)	I215S	probably benign	Het
Or7e176	T	C	9: 20,260,017 (GRCm38)	I59T	probably damaging	Het
Or9q2	T	C	19: 13,795,551 (GRCm38)	H20R	probably benign	Het
P2rx7	C	T	5: 122,670,479 (GRCm38)	T308M	probably damaging	Het
Prdx6	C	T	1: 161,241,693 (GRCm38)		probably benign	Het
Rad54b	T	A	4: 11,615,579 (GRCm38)	D862E	probably damaging	Het
Ripor1	A	G	8: 105,617,182 (GRCm38)	Y344C	probably damaging	Het
Rnf112	T	C	11: 61,453,465 (GRCm38)	M43V	probably benign	Het
Rp1l1	A	G	14: 64,032,206 (GRCm38)	N1747S	probably benign	Het
Rps27	A	G	3: 90,212,999 (GRCm38)	V22A	probably damaging	Het
Spaca1	A	G	4: 34,044,236 (GRCm38)	V86A	possibly damaging	Het
Spdef	A	G	17: 27,718,162 (GRCm38)	Y156H	probably damaging	Het
Specc1	A	C	11: 62,118,958 (GRCm38)	E433D	possibly damaging	Het
Srpra	T	A	9: 35,215,030 (GRCm38)	F506L	probably benign	Het
Stxbp5	A	G	10: 9,760,866 (GRCm38)		probably benign	Het
Syne1	C	T	10: 5,052,777 (GRCm38)	R8046Q	probably damaging	Het
Tbx5	T	A	5: 119,883,025 (GRCm38)	S365R	probably benign	Het
Terb1	G	T	8: 104,447,948 (GRCm38)	P698Q	probably benign	Het
Tmbim7	T	A	5: 3,661,948 (GRCm38)	Y27*	probably null	Het
Tmem106c	C	A	15: 97,965,028 (GRCm38)	A60E	possibly damaging	Het
Ttc6	T	A	12: 57,673,823 (GRCm38)		probably null	Het
Ttn	T	C	2: 76,732,370 (GRCm38)	I28747V	possibly damaging	Het
Unc13a	C	T	8: 71,630,504 (GRCm38)		probably null	Het
Wdr81	T	C	11: 75,451,924 (GRCm38)	D839G	probably benign	Het
Wfdc15a	G	C	2: 164,199,805 (GRCm38)	Q33E	probably benign	Het
Zfp456	T	C	13: 67,366,946 (GRCm38)	R214G	probably benign	Het
Zfp457	T	A	13: 67,294,100 (GRCm38)	Y137F	probably damaging	Het

Other mutations in Apeh

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01317:Apeh	APN	9	108,086,207 (GRCm38)	missense	probably benign
IGL02232:Apeh	APN	9	108,091,872 (GRCm38)	missense	probably benign	0.02
IGL02563:Apeh	APN	9	108,093,709 (GRCm38)	missense	possibly damaging	0.85
IGL02713:Apeh	APN	9	108,085,672 (GRCm38)	missense	probably damaging	1.00
IGL02794:Apeh	APN	9	108,092,010 (GRCm38)	missense	possibly damaging	0.94
IGL03355:Apeh	APN	9	108,086,445 (GRCm38)	missense	probably benign	0.00
R6807_Apeh_606	UTSW	9	108,092,679 (GRCm38)	missense	probably damaging	1.00
R0511:Apeh	UTSW	9	108,087,055 (GRCm38)	missense	probably benign
R1221:Apeh	UTSW	9	108,092,609 (GRCm38)	missense	probably benign
R1574:Apeh	UTSW	9	108,092,726 (GRCm38)	splice site	probably null
R1863:Apeh	UTSW	9	108,092,103 (GRCm38)	missense	possibly damaging	0.91
R2126:Apeh	UTSW	9	108,085,667 (GRCm38)	missense	probably damaging	1.00
R2353:Apeh	UTSW	9	108,086,292 (GRCm38)	missense	possibly damaging	0.84
R5156:Apeh	UTSW	9	108,094,287 (GRCm38)	missense	probably damaging	1.00
R5278:Apeh	UTSW	9	108,091,258 (GRCm38)	missense	probably benign	0.08
R5366:Apeh	UTSW	9	108,091,806 (GRCm38)	missense	probably benign	0.01
R5384:Apeh	UTSW	9	108,086,463 (GRCm38)	missense	probably damaging	1.00
R5940:Apeh	UTSW	9	108,091,899 (GRCm38)	splice site	probably null
R6102:Apeh	UTSW	9	108,086,439 (GRCm38)	missense	probably damaging	1.00
R6300:Apeh	UTSW	9	108,092,679 (GRCm38)	missense	probably damaging	1.00
R6368:Apeh	UTSW	9	108,087,243 (GRCm38)	missense	probably damaging	1.00
R6807:Apeh	UTSW	9	108,092,679 (GRCm38)	missense	probably damaging	1.00
R6809:Apeh	UTSW	9	108,092,679 (GRCm38)	missense	probably damaging	1.00
R6817:Apeh	UTSW	9	108,092,679 (GRCm38)	missense	probably damaging	1.00
R6828:Apeh	UTSW	9	108,087,038 (GRCm38)	missense	probably damaging	1.00
R6866:Apeh	UTSW	9	108,092,679 (GRCm38)	missense	probably damaging	1.00
R7034:Apeh	UTSW	9	108,094,271 (GRCm38)	missense	possibly damaging	0.70
R7036:Apeh	UTSW	9	108,094,271 (GRCm38)	missense	possibly damaging	0.70
R7139:Apeh	UTSW	9	108,092,146 (GRCm38)	missense	probably damaging	1.00
R8024:Apeh	UTSW	9	108,092,591 (GRCm38)	missense	probably benign	0.20
R8289:Apeh	UTSW	9	108,086,245 (GRCm38)	missense	probably damaging	0.99
R8731:Apeh	UTSW	9	108,087,223 (GRCm38)	missense	probably benign
R8957:Apeh	UTSW	9	108,092,373 (GRCm38)	missense	probably benign	0.21
R9055:Apeh	UTSW	9	108,085,846 (GRCm38)	missense	possibly damaging	0.64
R9569:Apeh	UTSW	9	108,094,410 (GRCm38)	missense	unknown
R9695:Apeh	UTSW	9	108,086,284 (GRCm38)	missense	probably damaging	0.99

Predicted Primers

PCR Primer
(F):5'- AAGCCTGCAATGGGAGCTAG -3'
(R):5'- AGTGTGCCTACAAAAGTGCCC -3'

Sequencing Primer
(F):5'- TAGGAAGGGCCACCACTGTG -3'
(R):5'- ACCTCGAAGCCAAGAAGTTG -3'

Posted On

2016-04-15