Mutagenetix > Incidental Mutation

Incidental Mutation 'IGL00332:Acp6'

8551

Institutional Source

Australian Phenomics Network (link to record)

Gene Symbol

Acp6

Ensembl Gene

ENSMUSG00000028093

Gene Name

acid phosphatase 6, lysophosphatidic

Synonyms

5730559A09Rik, ACPL1, mPACPL1

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.102) question?

Stock #

IGL00332

Quality Score

Status

Chromosome

Chromosomal Location

97066070-97083892 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

T to C at 97083737 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Histidine at position 404 (Y404H)

Ref Sequence

ENSEMBL: ENSMUSP00000088263 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000090759]

AlphaFold

Q8BP40

Predicted Effect

possibly damaging
Transcript: ENSMUST00000090759
AA Change: Y404H

PolyPhen 2 Score 0.944 (Sensitivity: 0.80; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000088263
Gene: ENSMUSG00000028093
AA Change: Y404H

Domain	Start	End	E-Value	Type
Pfam:His_Phos_2	42	228	4.6e-20	PFAM
Pfam:His_Phos_2	245	371	8e-9	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000139898

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000143234

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146143

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000198329

Coding Region Coverage

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the histidine acid phosphatase protein family. The encoded protein hydrolyzes lysophosphatidic acid, which is involved in G protein-coupled receptor signaling, lipid raft modulation, and in balancing lipid composition within the cell. Alternative splicing results in multiple transcript variants. [provided by RefSeq, May 2016]
PHENOTYPE: Phenotypic analysis of mice homozygous for a gene trap allele indicates this mutation has no notable phenotype in any parameter tested. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adgrv1	T	A	13: 81,620,996 (GRCm39)		probably benign	Het
Akap13	A	G	7: 75,378,667 (GRCm39)	K2107E	probably damaging	Het
Ankrd42	A	G	7: 92,233,662 (GRCm39)		probably benign	Het
Apba3	C	T	10: 81,108,901 (GRCm39)	P555S	probably damaging	Het
Aplnr	A	G	2: 84,967,985 (GRCm39)	S337G	probably benign	Het
Arhgef40	A	G	14: 52,226,417 (GRCm39)	N154D	probably damaging	Het
Asb14	A	G	14: 26,633,998 (GRCm39)	K401R	probably benign	Het
Aspn	C	A	13: 49,719,968 (GRCm39)	T328K	probably benign	Het
Barhl2	C	T	5: 106,603,365 (GRCm39)	A265T	possibly damaging	Het
Brca2	T	A	5: 150,463,363 (GRCm39)	H1042Q	probably benign	Het
C3	A	G	17: 57,533,004 (GRCm39)	L167P	probably benign	Het
Ccdc33	A	G	9: 57,977,257 (GRCm39)		probably benign	Het
Cdk10	T	A	8: 123,957,063 (GRCm39)	M222K	possibly damaging	Het
Cfap45	C	T	1: 172,362,912 (GRCm39)		probably benign	Het
Chil3	T	A	3: 106,056,017 (GRCm39)	N352I	probably damaging	Het
Chn2	G	T	6: 54,272,907 (GRCm39)		probably null	Het
Cimip2b	G	A	4: 43,428,158 (GRCm39)	R100W	possibly damaging	Het
Cpt1b	T	C	15: 89,305,066 (GRCm39)	E394G	probably benign	Het
Fcgr2b	T	A	1: 170,788,799 (GRCm39)	N273I	possibly damaging	Het
Fpr-rs7	G	A	17: 20,333,480 (GRCm39)	Q337*	probably null	Het
Fras1	T	A	5: 96,887,217 (GRCm39)	N2666K	possibly damaging	Het
Gfra3	C	T	18: 34,824,601 (GRCm39)		probably null	Het
Gm4553	T	C	7: 141,718,964 (GRCm39)	S155G	unknown	Het
Gpr75	C	T	11: 30,841,590 (GRCm39)	T165I	probably damaging	Het
Gzmd	A	T	14: 56,367,737 (GRCm39)	C179S	probably damaging	Het
Hand1	T	G	11: 57,722,575 (GRCm39)	H13P	probably damaging	Het
Irak3	C	T	10: 120,013,972 (GRCm39)		probably null	Het
Isl2	T	A	9: 55,452,253 (GRCm39)	L275Q	possibly damaging	Het
Itgb2	T	C	10: 77,393,240 (GRCm39)	V367A	probably damaging	Het
Katna1	T	C	10: 7,638,758 (GRCm39)		probably benign	Het
Myh6	A	G	14: 55,184,450 (GRCm39)	M1627T	probably benign	Het
Naprt	A	G	15: 75,765,164 (GRCm39)	Y187H	probably damaging	Het
Nedd4	T	A	9: 72,642,371 (GRCm39)	V550E	probably damaging	Het
Nt5c2	A	G	19: 46,884,954 (GRCm39)	V252A	possibly damaging	Het
Or8k39	T	C	2: 86,563,579 (GRCm39)	I126V	possibly damaging	Het
Or9i16	C	T	19: 13,864,945 (GRCm39)	V210I	probably benign	Het
P2ry2	A	G	7: 100,647,393 (GRCm39)	V304A	probably damaging	Het
Pde4dip	T	C	3: 97,674,593 (GRCm39)	N108D	probably benign	Het
Pdgfrl	A	G	8: 41,438,660 (GRCm39)	T199A	probably damaging	Het
Plaa	A	G	4: 94,470,844 (GRCm39)	Y431H	probably benign	Het
Pls1	A	T	9: 95,664,472 (GRCm39)	I177N	possibly damaging	Het
Plxna2	T	C	1: 194,472,138 (GRCm39)	F1035L	probably damaging	Het
Ppp6r3	A	T	19: 3,564,729 (GRCm39)		probably null	Het
Prpf4b	T	C	13: 35,067,890 (GRCm39)	S240P	probably benign	Het
Reg2	T	A	6: 78,383,204 (GRCm39)	Y50*	probably null	Het
Rev3l	C	T	10: 39,682,965 (GRCm39)	T361I	probably benign	Het
Rps4l	A	G	6: 148,256,383 (GRCm39)		probably benign	Het
Scn11a	A	T	9: 119,598,982 (GRCm39)	F1183I	probably damaging	Het
Sh2b2	T	C	5: 136,253,273 (GRCm39)	E327G	probably damaging	Het
Shank2	A	G	7: 143,965,584 (GRCm39)	K1057R	probably damaging	Het
Sim2	T	A	16: 93,915,803 (GRCm39)	Y255*	probably null	Het
Snx9	A	G	17: 5,949,636 (GRCm39)	N112S	probably benign	Het
Sphkap	T	A	1: 83,258,237 (GRCm39)	I169F	probably damaging	Het
Spink5	A	G	18: 44,100,111 (GRCm39)	T43A	probably benign	Het
Stac2	C	T	11: 97,932,005 (GRCm39)	S265N	probably benign	Het
Tbx20	A	G	9: 24,670,044 (GRCm39)	V91A	probably damaging	Het
Tgfbr2	C	T	9: 115,939,257 (GRCm39)	R190H	probably damaging	Het
Ubr2	A	G	17: 47,301,916 (GRCm39)		probably null	Het
Wdfy3	C	T	5: 102,063,204 (GRCm39)		probably null	Het
Wdr82	T	C	9: 106,061,449 (GRCm39)	V166A	probably benign	Het
Zfhx4	C	T	3: 5,307,401 (GRCm39)	A209V	probably damaging	Het
Zfp518b	T	A	5: 38,831,109 (GRCm39)	T299S	possibly damaging	Het

Other mutations in Acp6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01610:Acp6	APN	3	97,083,036 (GRCm39)	missense	possibly damaging	0.81
IGL01655:Acp6	APN	3	97,073,288 (GRCm39)	critical splice donor site	probably null
IGL01788:Acp6	APN	3	97,073,198 (GRCm39)	missense	probably damaging	1.00
IGL01845:Acp6	APN	3	97,081,123 (GRCm39)	missense	probably benign	0.00
IGL02978:Acp6	APN	3	97,073,875 (GRCm39)	missense	probably benign	0.30
IGL03180:Acp6	APN	3	97,082,951 (GRCm39)	missense	probably benign	0.15
R0144:Acp6	UTSW	3	97,073,145 (GRCm39)	splice site	probably benign
R0471:Acp6	UTSW	3	97,075,891 (GRCm39)	critical splice donor site	probably null
R1458:Acp6	UTSW	3	97,081,104 (GRCm39)	splice site	probably benign
R1889:Acp6	UTSW	3	97,073,201 (GRCm39)	missense	probably damaging	0.98
R1990:Acp6	UTSW	3	97,083,054 (GRCm39)	missense	probably damaging	1.00
R2051:Acp6	UTSW	3	97,075,333 (GRCm39)	missense	probably benign	0.00
R3786:Acp6	UTSW	3	97,066,605 (GRCm39)	missense	probably damaging	0.98
R3933:Acp6	UTSW	3	97,073,499 (GRCm39)	missense	probably benign	0.00
R4271:Acp6	UTSW	3	97,073,934 (GRCm39)	critical splice donor site	probably null
R4604:Acp6	UTSW	3	97,083,075 (GRCm39)	missense	probably benign	0.23
R4864:Acp6	UTSW	3	97,066,683 (GRCm39)	critical splice donor site	probably null
R4935:Acp6	UTSW	3	97,079,060 (GRCm39)	critical splice donor site	probably null
R5076:Acp6	UTSW	3	97,075,305 (GRCm39)	missense	probably benign	0.01
R5255:Acp6	UTSW	3	97,075,312 (GRCm39)	missense	probably benign	0.11
R5896:Acp6	UTSW	3	97,075,810 (GRCm39)	missense	probably benign	0.03
R5959:Acp6	UTSW	3	97,073,888 (GRCm39)	missense	probably damaging	1.00
R6004:Acp6	UTSW	3	97,082,997 (GRCm39)	missense	probably benign	0.11
R6938:Acp6	UTSW	3	97,082,949 (GRCm39)	missense	probably benign	0.04
R7593:Acp6	UTSW	3	97,073,266 (GRCm39)	missense	probably benign	0.30
R8485:Acp6	UTSW	3	97,066,302 (GRCm39)	start gained	probably benign
R8796:Acp6	UTSW	3	97,066,509 (GRCm39)	missense	probably benign	0.01
R8971:Acp6	UTSW	3	97,078,961 (GRCm39)	missense	probably damaging	1.00
X0067:Acp6	UTSW	3	97,073,273 (GRCm39)	nonsense	probably null

Posted On

2012-12-06