Mutagenetix > Incidental Mutation

Incidental Mutation 'R4019:Acy1'

312687

Institutional Source

Beutler Lab

Gene Symbol

Acy1

Ensembl Gene

ENSMUSG00000023262

Gene Name

aminoacylase 1

Synonyms

Acy-1, 1110014J22Rik

MMRRC Submission

040953-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R4019 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

106310180-106315518 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 106313978 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Threonine to Alanine at position 61 (T61A)

Ref Sequence

ENSEMBL: ENSMUSP00000149636 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000024031] [ENSMUST00000048685] [ENSMUST00000171678] [ENSMUST00000171925] [ENSMUST00000185334] [ENSMUST00000187001] [ENSMUST00000190972] [ENSMUST00000215395] [ENSMUST00000215506] [ENSMUST00000216400] [ENSMUST00000187983] [ENSMUST00000190803] [ENSMUST00000214275] [ENSMUST00000190900] [ENSMUST00000190798]

AlphaFold

no structure available at present

Predicted Effect

probably benign
Transcript: ENSMUST00000024031
AA Change: T61A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000024031
Gene: ENSMUSG00000023262
AA Change: T61A

Domain	Start	End	E-Value	Type
Pfam:Peptidase_M28	61	239	8.6e-8	PFAM
Pfam:Peptidase_M20	76	397	1.8e-38	PFAM
Pfam:M20_dimer	188	302	1.4e-17	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000048685

SMART Domains

Protein: ENSMUSP00000047322
Gene: ENSMUSG00000042210

Domain	Start	End	E-Value	Type
transmembrane domain	12	29	N/A	INTRINSIC
Pfam:Hydrolase_4	55	142	3.3e-10	PFAM
Pfam:Abhydrolase_5	73	227	8.1e-21	PFAM
Pfam:Abhydrolase_6	74	181	1e-14	PFAM
Pfam:Abhydrolase_6	176	238	1.4e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000171678

SMART Domains

Protein: ENSMUSP00000126101
Gene: ENSMUSG00000042210

Domain	Start	End	E-Value	Type
transmembrane domain	12	29	N/A	INTRINSIC
Pfam:Hydrolase_4	55	142	3.3e-10	PFAM
Pfam:Abhydrolase_5	73	227	8.1e-21	PFAM
Pfam:Abhydrolase_6	74	181	1e-14	PFAM
Pfam:Abhydrolase_6	176	238	1.4e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000171925

SMART Domains

Protein: ENSMUSP00000126916
Gene: ENSMUSG00000042210

Domain	Start	End	E-Value	Type
transmembrane domain	12	29	N/A	INTRINSIC
Pfam:Abhydrolase_5	73	245	7.9e-17	PFAM
low complexity region	253	265	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000185334

SMART Domains

Protein: ENSMUSP00000140345
Gene: ENSMUSG00000042210

Domain	Start	End	E-Value	Type
transmembrane domain	12	29	N/A	INTRINSIC
Pfam:Hydrolase_4	55	142	3.3e-10	PFAM
Pfam:Abhydrolase_5	73	227	8.1e-21	PFAM
Pfam:Abhydrolase_6	74	181	1e-14	PFAM
Pfam:Abhydrolase_6	176	238	1.4e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000187001

SMART Domains

Protein: ENSMUSP00000140042
Gene: ENSMUSG00000042210

Domain	Start	End	E-Value	Type
signal peptide	1	30	N/A	INTRINSIC
SCOP:d1imja_	51	110	1e-10	SMART
PDB:1IMJ\|A	58	110	6e-13	PDB

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000187324

Predicted Effect

probably benign
Transcript: ENSMUST00000190972
AA Change: T61A

PolyPhen 2 Score 0.002 (Sensitivity: 0.99; Specificity: 0.30)

SMART Domains

Protein: ENSMUSP00000139953
Gene: ENSMUSG00000023262
AA Change: T61A

Domain	Start	End	E-Value	Type
Pfam:Peptidase_M20	76	216	2.9e-24	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000190851

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000189097

Predicted Effect

probably benign
Transcript: ENSMUST00000215395
AA Change: T61A

PolyPhen 2 Score 0.007 (Sensitivity: 0.96; Specificity: 0.75)

Predicted Effect

probably benign
Transcript: ENSMUST00000215506
AA Change: T61A

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)

Predicted Effect

possibly damaging
Transcript: ENSMUST00000216400
AA Change: T61A

PolyPhen 2 Score 0.941 (Sensitivity: 0.80; Specificity: 0.94)

Predicted Effect

probably benign
Transcript: ENSMUST00000187983

SMART Domains

Protein: ENSMUSP00000140901
Gene: ENSMUSG00000042210

Domain	Start	End	E-Value	Type
signal peptide	1	30	N/A	INTRINSIC
Pfam:Abhydrolase_5	73	203	5.4e-12	PFAM
Pfam:Abhydrolase_6	74	197	1.4e-10	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000217531

Predicted Effect

probably benign
Transcript: ENSMUST00000190803

Predicted Effect

probably benign
Transcript: ENSMUST00000214275

Predicted Effect

probably benign
Transcript: ENSMUST00000190900

SMART Domains

Protein: ENSMUSP00000140582
Gene: ENSMUSG00000023262

Domain	Start	End	E-Value	Type
PDB:1Q7L\|C	1	50	9e-23	PDB

Predicted Effect

probably benign
Transcript: ENSMUST00000190798

SMART Domains

Protein: ENSMUSP00000141096
Gene: ENSMUSG00000042210

Domain	Start	End	E-Value	Type
signal peptide	1	30	N/A	INTRINSIC
Pfam:Hydrolase_4	55	142	1.7e-8	PFAM
Pfam:Abhydrolase_5	73	157	1.2e-8	PFAM
Pfam:Abhydrolase_6	74	157	1.4e-10	PFAM

Coding Region Coverage

1x: 99.1%
3x: 98.5%
10x: 97.0%
20x: 94.2%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a cytosolic, homodimeric, zinc-binding enzyme that catalyzes the hydrolysis of acylated L-amino acids to L-amino acids and an acyl group, and has been postulated to function in the catabolism and salvage of acylated amino acids. This gene is located on chromosome 3p21.1, a region reduced to homozygosity in small-cell lung cancer (SCLC), and its expression has been reported to be reduced or undetectable in SCLC cell lines and tumors. The amino acid sequence of human aminoacylase-1 is highly homologous to the porcine counterpart, and this enzyme is the first member of a new family of zinc-binding enzymes. Mutations in this gene cause aminoacylase-1 deficiency, a metabolic disorder characterized by central nervous system defects and increased urinary excretion of N-acetylated amino acids. Alternative splicing of this gene results in multiple transcript variants. Read-through transcription also exists between this gene and the upstream ABHD14A (abhydrolase domain containing 14A) gene, as represented in GeneID:100526760. A related pseudogene has been identified on chromosome 18. [provided by RefSeq, Nov 2010]

Allele List at MGI

Other mutations in this stock

Total: 43 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Ap4e1	C	T	2: 126,903,846 (GRCm39)	S916F	probably benign	Het
Brpf1	G	A	6: 113,287,243 (GRCm39)	R157Q	probably damaging	Het
Canx	A	T	11: 50,190,072 (GRCm39)	S429T	probably damaging	Het
Casz1	C	T	4: 149,017,335 (GRCm39)	P208L	probably benign	Het
Ctnnd1	C	T	2: 84,450,302 (GRCm39)	R306H	probably damaging	Het
Dip2c	T	C	13: 9,664,401 (GRCm39)	V909A	probably damaging	Het
Epg5	C	A	18: 78,073,665 (GRCm39)	Q2511K	probably damaging	Het
Ghitm	G	A	14: 36,852,651 (GRCm39)	A143V	probably damaging	Het
Gramd2b	T	C	18: 56,612,026 (GRCm39)		probably null	Het
Ifitm3	T	C	7: 140,589,772 (GRCm39)	T94A	possibly damaging	Het
Ift81	G	A	5: 122,731,192 (GRCm39)	T321M	probably benign	Het
Ikbkb	C	T	8: 23,161,728 (GRCm39)	V387I	probably benign	Het
Lct	T	C	1: 128,231,963 (GRCm39)	M629V	probably damaging	Het
Lpar5	A	G	6: 125,058,638 (GRCm39)	N120D	probably damaging	Het
Lrrc37	A	G	11: 103,506,119 (GRCm39)	S1950P	probably benign	Het
Lrrtm2	T	C	18: 35,345,923 (GRCm39)	I460V	possibly damaging	Het
Naip5	T	C	13: 100,359,883 (GRCm39)	E451G	probably benign	Het
Naip5	T	C	13: 100,359,902 (GRCm39)	I445V	probably benign	Het
Nbas	A	G	12: 13,532,520 (GRCm39)	R1743G	probably damaging	Het
Nherf4	A	T	9: 44,162,117 (GRCm39)		probably null	Het
Notch1	T	C	2: 26,371,154 (GRCm39)	T311A	probably benign	Het
Oplah	A	G	15: 76,181,476 (GRCm39)	Y1155H	probably damaging	Het
Or4c15	A	G	2: 88,760,080 (GRCm39)	I193T	probably benign	Het
Or52k2	T	C	7: 102,253,849 (GRCm39)	F96S	probably damaging	Het
Pcnx1	C	T	12: 81,965,018 (GRCm39)	T395I	probably damaging	Het
Pdgfb	A	C	15: 79,885,923 (GRCm39)	V108G	probably damaging	Het
Prpf40b	T	C	15: 99,214,357 (GRCm39)	S846P	probably benign	Het
Ptprc	T	A	1: 138,006,254 (GRCm39)	H752L	probably damaging	Het
Rin2	C	T	2: 145,702,366 (GRCm39)	T354I	probably benign	Het
Scn3a	A	G	2: 65,356,295 (GRCm39)		probably benign	Het
Sco1	T	G	11: 66,954,846 (GRCm39)	S284A	probably benign	Het
Slc25a10	T	A	11: 120,388,265 (GRCm39)	M227K	probably damaging	Het
Sox8	A	G	17: 25,789,271 (GRCm39)	Y76H	probably damaging	Het
Spdya	A	C	17: 71,863,309 (GRCm39)	K19N	possibly damaging	Het
Syngap1	C	T	17: 27,171,315 (GRCm39)		probably benign	Het
Sytl3	T	C	17: 7,003,892 (GRCm39)	S326P	probably damaging	Het
Tbl3	A	G	17: 24,923,695 (GRCm39)	V239A	probably damaging	Het
Tenm2	T	C	11: 35,937,901 (GRCm39)	I1592V	probably benign	Het
Vmn2r109	T	A	17: 20,774,074 (GRCm39)	D427V	probably benign	Het
Vmn2r115	A	G	17: 23,579,017 (GRCm39)	K830R	probably damaging	Het
Vmn2r45	A	T	7: 8,474,580 (GRCm39)	L816*	probably null	Het
Zfp335	C	T	2: 164,743,380 (GRCm39)	R536H	probably damaging	Het
Zfp777	T	A	6: 48,019,046 (GRCm39)	Q296L	probably damaging	Het

Other mutations in Acy1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01670:Acy1	APN	9	106,314,006 (GRCm39)	unclassified	probably benign
IGL03029:Acy1	APN	9	106,312,314 (GRCm39)	missense	probably damaging	0.98
IGL03304:Acy1	APN	9	106,312,665 (GRCm39)	critical splice donor site	probably null
R0691:Acy1	UTSW	9	106,313,070 (GRCm39)	splice site	probably null
R2152:Acy1	UTSW	9	106,312,816 (GRCm39)	missense	probably damaging	1.00
R3882:Acy1	UTSW	9	106,312,708 (GRCm39)	missense	possibly damaging	0.75
R4421:Acy1	UTSW	9	106,312,912 (GRCm39)	splice site	probably null
R4700:Acy1	UTSW	9	106,310,782 (GRCm39)	missense	probably benign	0.00
R4931:Acy1	UTSW	9	106,310,390 (GRCm39)	missense	probably damaging	1.00
R4934:Acy1	UTSW	9	106,312,321 (GRCm39)	missense	probably null	1.00
R5030:Acy1	UTSW	9	106,310,596 (GRCm39)	missense	probably benign	0.31
R5482:Acy1	UTSW	9	106,311,838 (GRCm39)	intron	probably benign
R5748:Acy1	UTSW	9	106,313,926 (GRCm39)	missense	probably damaging	1.00
R6932:Acy1	UTSW	9	106,314,826 (GRCm39)	critical splice donor site	probably null
R7468:Acy1	UTSW	9	106,314,921 (GRCm39)	start codon destroyed	probably null	0.64
R7768:Acy1	UTSW	9	106,310,817 (GRCm39)	missense	possibly damaging	0.90
R8144:Acy1	UTSW	9	106,313,319 (GRCm39)	splice site	probably null
R8226:Acy1	UTSW	9	106,314,857 (GRCm39)	missense	probably damaging	0.98
R8692:Acy1	UTSW	9	106,310,377 (GRCm39)	missense	probably damaging	1.00
R8774:Acy1	UTSW	9	106,313,913 (GRCm39)	missense	probably damaging	1.00
R8774-TAIL:Acy1	UTSW	9	106,313,913 (GRCm39)	missense	probably damaging	1.00
R9112:Acy1	UTSW	9	106,311,952 (GRCm39)	missense	probably benign	0.01
R9491:Acy1	UTSW	9	106,312,994 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CGAGAGTCAGTGGTGAGATC -3'
(R):5'- AGACAGCTATACATCTCTGGGCTG -3'

Sequencing Primer
(F):5'- TCAGTGGTGAGATCGGCAC -3'
(R):5'- ATACATCTCTGGGCTGCCTGG -3'

Posted On

2015-04-30