LYPLA1 (lysophospholipase 1) - Rat Genome Database

Name: LYPLA1
Creator: Rat Genome Database
License: Creative Commons CC BY 4.0
Keywords: Rat Gene RGD Genome

Gene: LYPLA1 (lysophospholipase 1) Homo sapiens

Analyze

Symbol:

LYPLA1

Name:

lysophospholipase 1

RGD ID:

735384

HGNC Page

HGNC:6737

Description:

Enables lysophospholipase activity and palmitoyl-(protein) hydrolase activity. Involved in fatty acid transport and negative regulation of aggrephagy. Located in several cellular components, including cytosol; endoplasmic reticulum; and nucleus. Is active in cell surface.

Type:

protein-coding

RefSeq Status:

REVIEWED

Previously known as:

acyl-protein thioesterase 1; acyl-protein thioesterase-1; APT-1; APT1; hAPT1; LOC105375839; LPL-I; LPL1; lysophospholipase I; lysophospholipid-specific lysophospholipase; LYSOPLA; lysoPLA I; palmitoyl-protein hydrolase; uncharacterized LOC105375839

RGD Orthologs

Alliance Orthologs

More Info

more info ...

More Info

Species	Gene symbol and name	Data Source	Assertion derived from	less info ...
Orthologs ¹				less info ...
Mus musculus (house mouse):	Lypla1 (lysophospholipase 1)	HGNC	EggNOG, Ensembl, HGNC, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Rattus norvegicus (Norway rat):	Lypla1 (lysophospholipase 1)	HGNC	EggNOG, Ensembl, HomoloGene, Inparanoid, NCBI, OMA, OrthoDB, Panther, PhylomeDB, Treefam
Chinchilla lanigera (long-tailed chinchilla):	Lypla1 (lysophospholipase 1)	NCBI	Ortholog
Pan paniscus (bonobo/pygmy chimpanzee):	LYPLA1 (lysophospholipase 1)	NCBI	Ortholog
Canis lupus familiaris (dog):	LYPLA1 (lysophospholipase 1)	HGNC	EggNOG, Ensembl, Inparanoid, NCBI, OMA, OrthoDB, Panther, Treefam
Ictidomys tridecemlineatus (thirteen-lined ground squirrel):	Lypla1 (lysophospholipase 1)	NCBI	Ortholog
Sus scrofa (pig):	LYPLA1 (lysophospholipase 1)	HGNC	EggNOG, Ensembl, NCBI, OMA, OrthoDB, Panther, Treefam
Chlorocebus sabaeus (green monkey):	LYPLA1 (lysophospholipase 1)	NCBI	Ortholog
Heterocephalus glaber (naked mole-rat):	Lypla1 (lysophospholipase 1)	NCBI	Ortholog
Other homologs ²
Rattus norvegicus (Norway rat):	LOC120099997 (acyl-protein thioesterase 1-like)	HGNC	Ensembl, Panther, Treefam
Rattus norvegicus (Norway rat):	Lypla2 (lysophospholipase 2)	HGNC	OrthoDB
Mus musculus (house mouse):	Lypla2 (lysophospholipase 2)	HGNC	OrthoDB
Sus scrofa (pig):	LYPLA2 (lysophospholipase 2)	HGNC	OrthoDB
Canis lupus familiaris (dog):	TCEA1 (transcription elongation factor A1)	HGNC	EggNOG
Alliance orthologs ³
Rattus norvegicus (Norway rat):	Lypla1 (lysophospholipase 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Mus musculus (house mouse):	Lypla1 (lysophospholipase 1)	Alliance	DIOPT (Ensembl Compara\|HGNC\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Danio rerio (zebrafish):	lypla1 (lysophospholipase 1)	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid\|ZFIN)
Drosophila melanogaster (fruit fly):	CG18815	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Saccharomyces cerevisiae (baker's yeast):	TML25	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|SonicParanoid)
Caenorhabditis elegans (roundworm):	ath-1	Alliance	DIOPT (Ensembl Compara\|Hieranoid\|InParanoid\|OMA\|OrthoFinder\|OrthoInspector\|PANTHER\|PhylomeDB\|SonicParanoid)
Rattus norvegicus (Norway rat):	LOC120099997 (acyl-protein thioesterase 1-like)	Alliance	DIOPT (Ensembl Compara\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus tropicalis (tropical clawed frog):	lypla1	Alliance	DIOPT (Ensembl Compara\|OMA\|OrthoFinder\|PANTHER\|PhylomeDB)
Xenopus laevis (African clawed frog):	lypla1.L	Alliance	DIOPT (Xenbase)
Xenopus laevis (African clawed frog):	lypla1.S	Alliance	DIOPT (Xenbase)

Related Pseudogenes:

LYPLA1P1 LYPLA1P2 LYPLA1P3

Allele / Splice:

See ClinVar data

Latest Assembly:

GRCh38 - Human Genome Assembly GRCh38

Position:

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	54,046,367 - 54,102,017 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	54,958,927 - 55,014,507 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	55,121,491 - 55,177,130 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	8	55,121,490 - 55,177,130	NCBI
Celera	8	50,949,236 - 51,005,140 (-)	NCBI		Celera
Cytogenetic Map	8	q11.23	NCBI
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI		HuRef
CHM1_1	8	55,010,550 - 55,065,879 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI		T2T-CHM13v2.0

JBrowse:

View Region in Genome Browser (JBrowse)

Model

Annotation Click to see Annotation Detail View

Disease Annotations Click to see Annotation Detail View

genetic disease (IAGP)

Gene-Chemical Interaction Annotations Click to see Annotation Detail View

(+)-schisandrin B (ISO)

1,1-dichloroethene (ISO)

1,2-dimethylhydrazine (ISO)

17alpha-ethynylestradiol (ISO)

2,2',4,4'-Tetrabromodiphenyl ether (EXP)

2,3,7,8-tetrachlorodibenzodioxine (EXP,ISO)

2,4,6-tribromophenol (EXP)

2-hydroxypropanoic acid (EXP)

3,3',4,4',5-pentachlorobiphenyl (ISO)

3H-1,2-dithiole-3-thione (ISO)

5-fluorouracil (EXP)

6-propyl-2-thiouracil (ISO)

9-cis-retinoic acid (ISO)

acetamide (ISO)

acrolein (EXP)

alpha-pinene (EXP)

ammonium chloride (ISO)

antirheumatic drug (EXP)

aristolochic acid A (EXP)

Aroclor 1254 (ISO)

arsane (EXP)

arsenic atom (EXP)

arsenous acid (EXP)

benzo[a]pyrene (EXP,ISO)

benzo[a]pyrene diol epoxide I (EXP)

bexarotene (ISO)

bisphenol A (EXP,ISO)

Bisphenol B (EXP)

bisphenol F (EXP)

C60 fullerene (ISO)

cadmium dichloride (ISO)

calcitriol (ISO)

calcium atom (ISO)

calcium(0) (ISO)

carbon nanotube (ISO)

cisplatin (ISO)

clofibrate (ISO)

copper(II) sulfate (EXP)

diarsenic trioxide (EXP)

Diisodecyl phthalate (ISO)

diquat (ISO)

diuron (ISO)

doxorubicin (EXP)

elemental selenium (EXP)

epoxiconazole (ISO)

ethanol (ISO)

fenvalerate (ISO)

flavonoids (ISO)

folic acid (ISO)

folpet (ISO)

gentamycin (ISO)

glafenine (ISO)

iron atom (ISO)

iron(0) (ISO)

ivermectin (EXP)

lithocholic acid (ISO)

methidathion (ISO)

methylseleninic acid (EXP)

N-nitrosodiethylamine (ISO)

nefazodone (ISO)

ozone (EXP)

paracetamol (EXP,ISO)

perfluorooctanoic acid (EXP)

phenylpropanolamine (ISO)

phenytoin (ISO)

pregnenolone 16alpha-carbonitrile (ISO)

rac-lactic acid (EXP)

rotenone (EXP)

selenium atom (EXP)

sodium dichromate (ISO)

sodium dodecyl sulfate (EXP)

tert-butyl hydroperoxide (ISO)

tetrachloromethane (ISO)

thapsigargin (ISO)

Tributyltin oxide (ISO)

triptonide (ISO)

undecane (ISO)

valproic acid (EXP)

zinc atom (ISO)

zinc(0) (ISO)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

fatty acid metabolic process (IEA)

fatty acid transport (IDA)

macromolecule depalmitoylation (IEA)

negative regulation of aggrephagy (IDA)

negative regulation of Golgi to plasma membrane protein transport (IEA,ISO)

Cellular Component

cytoplasm (IBA,IDA,IEA)

cytosol (IDA,IEA,TAS)

endoplasmic reticulum (IDA,IEA)

extracellular exosome (HDA)

membrane (IEA)

nuclear membrane (IDA,IEA)

nucleoplasm (IDA)

nucleus (IEA)

plasma membrane (IDA,IEA)

Molecular Function

carboxylic ester hydrolase activity (IBA,IEA)

hydrolase activity (IEA)

lipase activity (IDA)

lysophospholipase activity (IDA,ISO,TAS)

palmitoyl-(protein) hydrolase activity (IBA,IDA,IEA,IMP)

phospholipase activity (IDA)

protein binding (IPI)

Molecular Pathway Annotations Click to see Annotation Detail View

glycerophospholipid metabolic pathway (EXP,IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	GOAs Human GO annotations	GOA_HUMAN data from the GO Consortium
2.	KEGG Annotation Import Pipeline	Pipeline to import KEGG annotations from KEGG into RGD
3.	SMPDB Annotation Import Pipeline	Pipeline to import SMPDB annotations from SMPDB into RGD
4.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:1531641	PMID:7566098	PMID:8619474	PMID:9110174	PMID:10064899	PMID:10395961	PMID:10760470	PMID:11042152	PMID:11080636	PMID:12477932	PMID:15489334	PMID:16344560
PMID:18976975	PMID:19322201	PMID:19439193	PMID:19465924	PMID:19738201	PMID:20418879	PMID:20685872	PMID:21393252	PMID:21873635	PMID:22623428	PMID:23376485	PMID:23396970
PMID:23533145	PMID:24682756	PMID:25416956	PMID:25670628	PMID:25849916	PMID:26186194	PMID:26344197	PMID:27481942	PMID:28380382	PMID:28514442	PMID:29117863	PMID:29295957
PMID:29362370	PMID:29955894	PMID:30431103	PMID:30482805	PMID:31536960	PMID:32296183	PMID:32958780	PMID:33961781	PMID:34984578	PMID:35831314	PMID:35944360	PMID:36114006
PMID:36215168	PMID:36803235	PMID:36966971	PMID:37802024	PMID:38344800	PMID:38496616

Genomics

Comparative Map Data

LYPLA1
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	8	54,046,367 - 54,102,017 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	8	54,958,927 - 55,014,507 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	8	55,121,491 - 55,177,130 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	8	55,121,490 - 55,177,130	NCBI
Celera	8	50,949,236 - 51,005,140 (-)	NCBI		Celera
Cytogenetic Map	8	q11.23	NCBI
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI		HuRef
CHM1_1	8	55,010,550 - 55,065,879 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI		T2T-CHM13v2.0

Lypla1
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	1	4,878,046 - 4,916,958 (+)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	1	4,878,011 - 4,918,633 (+)	Ensembl		GRCm39 Ensembl
GRCm38	1	4,807,823 - 4,846,735 (+)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	1	4,807,788 - 4,848,410 (+)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	1	4,797,974 - 4,836,816 (+)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	1	4,797,974 - 4,836,816 (+)	NCBI		MGSCv36	mm8
Celera	1	4,819,711 - 4,858,108 (+)	NCBI		Celera
Cytogenetic Map	1	A1	NCBI
cM Map	1	1.79	NCBI

Lypla1
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	5	19,477,408 - 19,506,568 (-)	NCBI		GRCr8
mRatBN7.2	5	14,679,605 - 14,708,774 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	5	14,679,606 - 14,708,746 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	5	16,873,890 - 16,902,965 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	5	18,487,392 - 18,516,463 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	5	18,208,564 - 18,237,635 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	5	14,559,333 - 14,588,447 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	5	14,559,334 - 14,588,422 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	5	19,341,836 - 19,370,929 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	5	14,882,196 - 14,911,284 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
RGSC_v3.1	5	14,882,195 - 14,911,284 (-)	NCBI
Celera	5	14,050,814 - 14,079,913 (-)	NCBI		Celera
Cytogenetic Map	5	q12	NCBI

Lypla1
(Chinchilla lanigera - long-tailed chinchilla)

Chinchilla Assembly	Chr	Position (strand)	Source	Genome Browsers
Chinchilla Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChiLan1.0	NW_004955454	13,356,851 - 13,385,110 (-)	NCBI	ChiLan1.0	ChiLan1.0

LYPLA1
(Pan paniscus - bonobo/pygmy chimpanzee)

Bonobo Assembly	Chr	Position (strand)	Source	Genome Browsers
Bonobo Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
NHGRI_mPanPan1-v2	7	69,685,881 - 69,740,846 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	8	45,410,670 - 45,465,681 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	8	50,474,238 - 50,529,167 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	8	47,850,592 - 47,905,377 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	8	47,850,592 - 47,905,367 (-)	Ensembl	panpan1.1		panPan2

LYPLA1
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	29	5,656,376 - 5,696,901 (-)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	29	5,616,961 - 5,697,284 (-)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	29	6,031,347 - 6,072,546 (-)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	29	5,732,636 - 5,773,863 (-)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	29	5,691,587 - 5,773,875 (-)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	29	5,669,309 - 5,710,546 (-)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	29	5,874,942 - 5,916,139 (-)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	29	5,957,952 - 5,999,169 (-)	NCBI		UU_Cfam_GSD_1.0

Lypla1
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)

Squirrel Assembly	Chr	Position (strand)	Source	Genome Browsers
Squirrel Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HiC_Itri_2	NW_024405303	73,814,174 - 73,848,519 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936496	936,763 - 971,710 (-)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936496	937,918 - 971,315 (-)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

LYPLA1
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	4	77,083,548 - 77,102,408 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	4	77,083,624 - 77,102,407 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	4	84,154,849 - 84,172,657 (+)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

LYPLA1
(Chlorocebus sabaeus - green monkey)

Green Monkey Assembly	Chr	Position (strand)	Source	Genome Browsers
Green Monkey Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
ChlSab1.1	8	50,120,930 - 50,171,517 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
Vero_WHO_p1.0	NW_023666039	91,764,068 - 91,814,847 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Lypla1
(Heterocephalus glaber - naked mole-rat)

Naked Mole-Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Naked Mole-Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
HetGla 1.0	NW_004624735	1,582,169 - 1,622,307 (+)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in LYPLA1
12 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145049449)x3	copy number gain	See cases [RCV000051206]	Chr8:241530..145049449 [GRCh38] Chr8:191530..146274835 [GRCh37] Chr8:181530..146245639 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:244417-145054775)x3	copy number gain	Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053604]\|See cases [RCV000053604]	Chr8:244417..145054775 [GRCh38] Chr8:194417..146280161 [GRCh37] Chr8:184417..146250965 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000053602]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q11.1-13.2(chr8:46031334-69303787)x3	copy number gain	See cases [RCV000133720]	Chr8:46031334..69303787 [GRCh38] Chr8:46942956..70216022 [GRCh37] Chr8:47062121..70378576 [NCBI36] Chr8:8q11.1-13.2	pathogenic
GRCh38/hg38 8q11.23(chr8:53790469-54207499)x3	copy number gain	See cases [RCV000135369]	Chr8:53790469..54207499 [GRCh38] Chr8:54703029..55120059 [GRCh37] Chr8:54865582..55282612 [NCBI36] Chr8:8q11.23	uncertain significance
GRCh38/hg38 8q11.23-12.1(chr8:53996579-56163431)x1	copy number loss	See cases [RCV000135764]	Chr8:53996579..56163431 [GRCh38] Chr8:54909139..57075990 [GRCh37] Chr8:55071692..57238544 [NCBI36] Chr8:8q11.23-12.1	likely pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241605-145054781)x3	copy number gain	See cases [RCV000138643]	Chr8:241605..145054781 [GRCh38] Chr8:191605..146280167 [GRCh37] Chr8:181605..146250971 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q11.1-24.3(chr8:46031340-139285494)x3	copy number gain	See cases [RCV000139539]	Chr8:46031340..139285494 [GRCh38] Chr8:46942962..140297737 [GRCh37] Chr8:47062127..140366919 [NCBI36] Chr8:8q11.1-24.3	pathogenic
GRCh38/hg38 8p12-q12.1(chr8:36580103-59618998)x3	copy number gain	See cases [RCV000139582]	Chr8:36580103..59618998 [GRCh38] Chr8:36437621..60531557 [GRCh37] Chr8:36556779..60694111 [NCBI36] Chr8:8p12-q12.1	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:208048-145070385)x3	copy number gain	See cases [RCV000141808]	Chr8:208048..145070385 [GRCh38] Chr8:158048..146295771 [GRCh37] Chr8:148048..146266575 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8p21.3-q24.3(chr8:21291522-145070385)x3	copy number gain	See cases [RCV000142021]	Chr8:21291522..145070385 [GRCh38] Chr8:21149033..146295771 [GRCh37] Chr8:21193313..146266575 [NCBI36] Chr8:8p21.3-q24.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:226452-145068712)x3	copy number gain	See cases [RCV000142858]	Chr8:226452..145068712 [GRCh38] Chr8:176452..146294098 [GRCh37] Chr8:166452..146264902 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh38/hg38 8q11.21-12.1(chr8:49471778-57825470)x1	copy number loss	See cases [RCV000142642]	Chr8:49471778..57825470 [GRCh38] Chr8:50384337..58738029 [GRCh37] Chr8:50546890..58900583 [NCBI36] Chr8:8q11.21-12.1	pathogenic\|likely pathogenic
GRCh38/hg38 8q11.23-12.3(chr8:53325389-61863018)x1	copy number loss	See cases [RCV000143182]	Chr8:53325389..61863018 [GRCh38] Chr8:54237949..62775577 [GRCh37] Chr8:54400502..62938131 [NCBI36] Chr8:8q11.23-12.3	pathogenic
GRCh38/hg38 8p23.3-q24.3(chr8:241530-145054634)x3	copy number gain	See cases [RCV000148092]	Chr8:241530..145054634 [GRCh38] Chr8:191530..146280020 [GRCh37] Chr8:181530..146250824 [NCBI36] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q11.23-12.3(chr8:53436131-65195953)x3	copy number gain	See cases [RCV000239428]	Chr8:53436131..65195953 [GRCh37] Chr8:8q11.23-12.3	pathogenic
GRCh37/hg19 8p21.2-q12.1(chr8:24772064-24813176)x3	copy number gain	See cases [RCV000446588]	Chr8:24772064..24813176 [GRCh37] Chr8:8p21.2-q12.1	uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158991-146280828)x3	copy number gain	See cases [RCV000447507]	Chr8:158991..146280828 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q11.23-12.1(chr8:54661151-57790737)x3	copy number gain	See cases [RCV000445710]	Chr8:54661151..57790737 [GRCh37] Chr8:8q11.23-12.1	uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)	copy number gain	See cases [RCV000510234]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158049-146295771)x3	copy number gain	See cases [RCV000511095]	Chr8:158049..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
NM_006330.4(LYPLA1):c.37A>G (p.Ile13Val)	single nucleotide variant	Inborn genetic diseases [RCV003248489]	Chr8:54101787 [GRCh38] Chr8:55014347 [GRCh37] Chr8:8q11.23	uncertain significance
GRCh37/hg19 8p23.1-q24.3(chr8:12490999-146295771)x3	copy number gain	See cases [RCV000512169]	Chr8:12490999..146295771 [GRCh37] Chr8:8p23.1-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:164984-146293414)x3	copy number gain	not provided [RCV000747254]	Chr8:164984..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:10213-146293414)x3	copy number gain	not provided [RCV000747248]	Chr8:10213..146293414 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q11.21-12.1(chr8:49822483-58822602)x1	copy number loss	not provided [RCV000747540]	Chr8:49822483..58822602 [GRCh37] Chr8:8q11.21-12.1	pathogenic
NM_006330.4(LYPLA1):c.457C>T (p.Pro153Ser)	single nucleotide variant	not provided [RCV000965077]	Chr8:54052660 [GRCh38] Chr8:54965220 [GRCh37] Chr8:8q11.23	benign
GRCh37/hg19 8p12-q24.3(chr8:31936551-146295771)x3	copy number gain	not provided [RCV000848192]	Chr8:31936551..146295771 [GRCh37] Chr8:8p12-q24.3	pathogenic
GRCh37/hg19 8p11.22-q12.3(chr8:39555657-64049089)x3	copy number gain	not provided [RCV000846266]	Chr8:39555657..64049089 [GRCh37] Chr8:8p11.22-q12.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not provided [RCV000848478]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
GRCh37/hg19 8q11.1-11.23(chr8:46863521-55218838)x3	copy number gain	not provided [RCV000683033]	Chr8:46863521..55218838 [GRCh37] Chr8:8q11.1-11.23	uncertain significance
NC_000008.10:g.(?_54978308)_(56436786_?)dup	duplication	not provided [RCV001033025]	Chr8:54978308..56436786 [GRCh37] Chr8:8q11.23-12.1	uncertain significance
NC_000008.10:g.(?_54978308)_(56436786_?)dup	duplication	not provided [RCV001323424]	Chr8:54978308..56436786 [GRCh37] Chr8:8q11.23-12.1	uncertain significance
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)	copy number gain	Polydactyly [RCV002280629]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic
NM_006330.4(LYPLA1):c.322A>G (p.Ile108Val)	single nucleotide variant	Inborn genetic diseases [RCV002902521]	Chr8:54055098 [GRCh38] Chr8:54967658 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.422C>G (p.Ala141Gly)	single nucleotide variant	Inborn genetic diseases [RCV002798585]	Chr8:54052695 [GRCh38] Chr8:54965255 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.43C>T (p.Pro15Ser)	single nucleotide variant	Inborn genetic diseases [RCV002887774]	Chr8:54101781 [GRCh38] Chr8:55014341 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.7G>A (p.Gly3Ser)	single nucleotide variant	Inborn genetic diseases [RCV002785026]	Chr8:54101817 [GRCh38] Chr8:55014377 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.625A>T (p.Ser209Cys)	single nucleotide variant	Inborn genetic diseases [RCV002804337]	Chr8:54051026 [GRCh38] Chr8:54963586 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.145A>G (p.Ile49Val)	single nucleotide variant	Inborn genetic diseases [RCV002718238]	Chr8:54065770 [GRCh38] Chr8:54978330 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.308A>T (p.Glu103Val)	single nucleotide variant	Inborn genetic diseases [RCV002920486]	Chr8:54055112 [GRCh38] Chr8:54967672 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.472G>A (p.Gly158Ser)	single nucleotide variant	Inborn genetic diseases [RCV003184357]	Chr8:54051179 [GRCh38] Chr8:54963739 [GRCh37] Chr8:8q11.23	likely benign
GRCh37/hg19 8q11.23(chr8:54906222-55166087)x3	copy number gain	not provided [RCV003484741]	Chr8:54906222..55166087 [GRCh37] Chr8:8q11.23	uncertain significance
GRCh37/hg19 8q11.23(chr8:54906222-55183775)x3	copy number gain	not provided [RCV003484740]	Chr8:54906222..55183775 [GRCh37] Chr8:8q11.23	uncertain significance
GRCh37/hg19 8q11.23(chr8:54798193-55200535)x3	copy number gain	not provided [RCV003484739]	Chr8:54798193..55200535 [GRCh37] Chr8:8q11.23	uncertain significance
NM_006330.4(LYPLA1):c.510C>T (p.His170=)	single nucleotide variant	not provided [RCV003435494]	Chr8:54051141 [GRCh38] Chr8:54963701 [GRCh37] Chr8:8q11.23	likely benign
GRCh37/hg19 8p21.2-q21.3(chr8:27024288-89410121)x3	copy number gain	not specified [RCV003986754]	Chr8:27024288..89410121 [GRCh37] Chr8:8p21.2-q21.3	pathogenic
GRCh37/hg19 8p23.3-q24.3(chr8:158048-146295771)x3	copy number gain	not specified [RCV003986742]	Chr8:158048..146295771 [GRCh37] Chr8:8p23.3-q24.3	pathogenic

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1612
Count of miRNA genes:	826
Interacting mature miRNAs:	940
Transcripts:	ENST00000316963, ENST00000343231, ENST00000517297, ENST00000518546, ENST00000519272, ENST00000519891, ENST00000519926, ENST00000520718, ENST00000520896, ENST00000521352, ENST00000521856, ENST00000521898, ENST00000522007
Prediction methods:	Microtar, Miranda, Rnahybrid
Result types:	miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region

RH80504

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	54,958,981 - 54,959,216	UniSTS	GRCh37
GRCh37	6	71,876,881 - 71,877,116	UniSTS	GRCh37
Build 36	6	71,933,602 - 71,933,837	RGD	NCBI36
Celera	8	50,949,279 - 50,949,514	UniSTS
Celera	6	72,265,528 - 72,265,763	RGD
Cytogenetic Map	8	q11.23	UniSTS
Cytogenetic Map	6	q13	UniSTS
HuRef	8	50,427,376 - 50,427,611	UniSTS
HuRef	6	69,074,818 - 69,075,053	UniSTS

LYPLA1__7347

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	8	54,958,870 - 54,959,706	UniSTS	GRCh37
Build 36	8	55,121,423 - 55,122,259	RGD	NCBI36
Celera	8	50,949,168 - 50,950,004	RGD
HuRef	8	50,427,265 - 50,428,101	UniSTS

Expression

RNA-SEQ Expression

High: > 1000 TPM value Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system

circulatory system

endocrine system

exocrine system

hemolymphoid system

hepatobiliary system

integumental system

musculoskeletal system

nervous system

renal system

reproductive system

respiratory system

sensory system

visual system

adipose tissue

appendage

entire extraembryonic component

pharyngeal arch

High

Medium

2248

2051

1564

610

1524

450

4124

1804

1344

392

1367

1575

174

1164

2585

Low

191

937

162

425

233

392

2390

203

Below cutoff

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001279356	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001279357	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001279358	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001279359	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001279360	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_001425837	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_006330	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_005251127	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012956	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012957	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012958	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012959	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_017012960	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421223	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421224	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421225	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421226	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421227	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_047421228	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359536	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359537	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359538	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359539	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359540	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359541	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359542	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359543	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359544	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359545	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XM_054359546	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001745453	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_001745454	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_928895	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	XR_928896	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AA307642	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AA827237	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC100821	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF035293	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF052112	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF077198	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF077199	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF081281	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF291053	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK289400	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK298206	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK307277	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK313739	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC008652	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC010397	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC039537	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471068	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068270	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CR457103	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA817192	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA881616	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DA883059	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000316963 ⟹ ENSP00000320043

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,046,367 - 54,101,947 (-)	Ensembl

RefSeq Acc Id:

ENST00000343231 ⟹ ENSP00000344477

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,047,407 - 54,101,828 (-)	Ensembl

RefSeq Acc Id:

ENST00000517297

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,054,453 - 54,101,854 (-)	Ensembl

RefSeq Acc Id:

ENST00000518546 ⟹ ENSP00000428729

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,051,011 - 54,101,977 (-)	Ensembl

RefSeq Acc Id:

ENST00000519272

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,047,792 - 54,101,444 (-)	Ensembl

RefSeq Acc Id:

ENST00000519891

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,051,125 - 54,101,554 (-)	Ensembl

RefSeq Acc Id:

ENST00000519926

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,053,198 - 54,101,849 (-)	Ensembl

RefSeq Acc Id:

ENST00000520718

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,047,963 - 54,052,898 (-)	Ensembl

RefSeq Acc Id:

ENST00000520896

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,055,102 - 54,101,554 (-)	Ensembl

RefSeq Acc Id:

ENST00000521352 ⟹ ENSP00000428306

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,052,654 - 54,101,535 (-)	Ensembl

RefSeq Acc Id:

ENST00000521856

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,100,350 - 54,101,928 (-)	Ensembl

RefSeq Acc Id:

ENST00000521898 ⟹ ENSP00000430791

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,052,742 - 54,101,858 (-)	Ensembl

RefSeq Acc Id:

ENST00000522007 ⟹ ENSP00000427967

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,051,072 - 54,101,855 (-)	Ensembl

RefSeq Acc Id:

ENST00000618741 ⟹ ENSP00000484280

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,046,368 - 54,101,554 (-)	Ensembl

RefSeq Acc Id:

ENST00000618914 ⟹ ENSP00000482430

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	8	54,046,368 - 54,102,017 (-)	Ensembl

RefSeq Acc Id:

NM_001279356 ⟹ NP_001266285

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI
GRCh37	8	54,958,927 - 55,014,577 (-)	NCBI
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI
CHM1_1	8	55,010,550 - 55,065,879 (-)	NCBI
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

Sequence:

show sequence

GTTGGCGCGCACGCGCCTGAGCGTGCGCCCGGTGGGGCCGGCCGGGACTCGCCGCTCGCACGCC
CTTGGGCCGCGGCCGGGCGCCCGCTCTTCCTTCCGCTTGCGCTGTGAGCTGAGGCGGTGTATGT
GCGGCAATAACATGTCAACCCCGCTGCCCGCCATCGTGCCCGCCGCCCGGAAGGCCACCGCTGC
GGTGATTTTCCTGCATGGATTGGGAGATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGTATC
AGAAGTTCACATATCAAATATATCTGCCCGCATGCGCCTGTTAGGCCTGTTACATTAAATATGA
ACGTGGCTATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTCACAGGAGGATGAATC
TGGGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAAGTGAAGAATGGCATT
CCTTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGTCCTATCGGTGGTGCTAATAGAGATA
TTTCTATTCTCCAGTGCCACGGGGATTGTGACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTAC
GGTGGAAAAACTAAAAACATTGGTGAATCCAGCCAATGTGACCTTTAAAACCTATGAAGGTATG
ATGCACAGTTCGTGTCAACAGGAAATGATGGATGTCAAGCAATTCATTGATAAACTCCTACCTC
CAATTGATTGACGTCACTAAGAGGCCTTGTGTAGAAGTACACCAGCATCATTGTAGTAGAGTGT
AAACCTTTTCCCATGCCCAGTCTTCAAATTTCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAA
TACATGCCAATAACACAGATCAAATAATATCTCCTCATGAGAAATTTATGATCTTTTAAGTTTC
TATACATGTATTCTTATAAGACGACCCAGGATCTACTATATTAGAATAGATGAAGCAGGTAGCT
TCTTTTTTCTCAAATGTAATTCAGCAAAATAATACAGTACTGCCACCAGATTTTTTATTACATC
ATTTGAAAATTAGCAGTATGCTTAATGAAAATTTGTTCAGGTATAAATGAGCAGTTAAGATATA
AACAATTTATGCATGCTGTGACTTAGTCTATGGATTTATTCCAAAATTGCTTAGTCACCATGCA
GTGTCTGTATTTTTATATATGTGTTCATATATACATAATGATTATAATACATAATAAGAATGAG
GTGGTATTACATTATTCCTAATAATAGGGATAATGCTGTTTATTGTCAAGAAAAAGTAAAATCG
TTCTCTTCAATTAATGGCCCTTTTATTTTGGGACCAGGCTTTTATTTTCCCTGATATTATTTCT
ATTTAATACTCTTTTCTCTCAAGAAAAAAAAAAAAGTTTGTTTTTTCTTTATTGTCCTTCATAG
CAGGCCAAGTATTGCCTCTCTGCAATAGACAGCTACTGTCAATACATGCTGTAATTTGACATTC
TGGGTCACAGATATAAGGTATTTAAAATCTATTTATGCTTTATAGAGAAACCAGACATTAAAAC
TTCATGCACTACTTATTTCGAATTACTGTACCTTATCCAAATTTACACCTAGCTATTAGGATCT
TCAACCCAGGTAACAGGAATAATTCTGTGGTTTCATTTTTCTGTAAACAACTGAAAGAATAATT
AGATCATATTCTAGTATGTTCTGAAATATCTTTAAGACTGATCTTAAAAACTAACTTCTAAGAT
GATTTCATCTTCTCATAGTATAGAGTTTACTTTGTACACGTTTGAAACCAACTACTGTAGAAGA
TGAGGAATCTATTGTAATTTTTTGCTTTATTTTCATCTGCCAGTGGACTTATTTGAAATTTTCA
CTTTAGTCAAATTATTTTTTGTATTAGTTTTTGATGCAGACATAAAAATAGCAATCATTTTAAA
TTGTCAAAATTTCCAGATTACTGGTAAAAATTATTTGAAAACAAACTTATGGGTAATAAAGGCT
AGTCAGAACCCTATACCATAAAGTGTAGTTACCATACAGATTAATATGTAGCAAAAATGTATGC
TTGATATTTCTCAACTGTGTTAATTTTTCTGCTGTATTCCAGCTGACCAAAACAATATTAAGAA
TGCATCTTTATAAATGGGTGCTAATTGATAATGGAAATAATTTAGTAATGGACTATACAGGATG
TTAATAATGAAGCCATATGTTTATGTCTGGATTTAAAAATTTTAAACAATCATTTACTATGTCA
TTTTTCTTTACCTTGAAGAACATAAACTGTTATTTCACTTCTACAAATCAGCAAGATATTATTT
ATGGCAAGAAATATTCCATTGAAATATTGTGCTGTAACATGGGAAAGTGTAAATGTTTTTCATG
GTTTCTATCAATGTGAAATAAAATTTAATTCTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

NM_001279357 ⟹ NP_001266286

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI
GRCh37	8	54,958,927 - 55,014,577 (-)	NCBI
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI
CHM1_1	8	55,010,550 - 55,065,879 (-)	NCBI
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

Sequence:

show sequence

GTTGGCGCGCACGCGCCTGAGCGTGCGCCCGGTGGGGCCGGCCGGGACTCGCCGCTCGCACGCC
CTTGGGCCGCGGCCGGGCGCCCGCTCTTCCTTCCGCTTGCGCTGTGAGCTGAGGCGGTGTATGT
GCGGCAATAACATGTCAACCCCGCTGCCCGCCATCGTGCCCGCCGCCCGGAAGGCCACCGCTGC
GGTGATTTTCCTGCATGGATTGGGAGATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGTATC
AGAAGTTCACATATCAAATATATCTGCCCGCATGCGTTTGATATTATTGGGCTTTCACCAGATT
CACAGGAGGATGAATCTGGGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGA
AGTGAAGAATGGCATTCCTTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTA
TCTTTATATACTGCCCTTACCACACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGC
TTCCACTTCGGGCTTCCTTTCCACAGGGTCCTATCGGTGGTGCTAATAGAGATATTTCTATTCT
CCAGTGCCACGGGGATTGTGACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTACGGTGGAAAAA
CTAAAAACATTGGTGAATCCAGCCAATGTGACCTTTAAAACCTATGAAGGTATGATGCACAGTT
CGTGTCAACAGGAAATGATGGATGTCAAGCAATTCATTGATAAACTCCTACCTCCAATTGATTG
ACGTCACTAAGAGGCCTTGTGTAGAAGTACACCAGCATCATTGTAGTAGAGTGTAAACCTTTTC
CCATGCCCAGTCTTCAAATTTCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAATACATGCCAA
TAACACAGATCAAATAATATCTCCTCATGAGAAATTTATGATCTTTTAAGTTTCTATACATGTA
TTCTTATAAGACGACCCAGGATCTACTATATTAGAATAGATGAAGCAGGTAGCTTCTTTTTTCT
CAAATGTAATTCAGCAAAATAATACAGTACTGCCACCAGATTTTTTATTACATCATTTGAAAAT
TAGCAGTATGCTTAATGAAAATTTGTTCAGGTATAAATGAGCAGTTAAGATATAAACAATTTAT
GCATGCTGTGACTTAGTCTATGGATTTATTCCAAAATTGCTTAGTCACCATGCAGTGTCTGTAT
TTTTATATATGTGTTCATATATACATAATGATTATAATACATAATAAGAATGAGGTGGTATTAC
ATTATTCCTAATAATAGGGATAATGCTGTTTATTGTCAAGAAAAAGTAAAATCGTTCTCTTCAA
TTAATGGCCCTTTTATTTTGGGACCAGGCTTTTATTTTCCCTGATATTATTTCTATTTAATACT
CTTTTCTCTCAAGAAAAAAAAAAAAGTTTGTTTTTTCTTTATTGTCCTTCATAGCAGGCCAAGT
ATTGCCTCTCTGCAATAGACAGCTACTGTCAATACATGCTGTAATTTGACATTCTGGGTCACAG
ATATAAGGTATTTAAAATCTATTTATGCTTTATAGAGAAACCAGACATTAAAACTTCATGCACT
ACTTATTTCGAATTACTGTACCTTATCCAAATTTACACCTAGCTATTAGGATCTTCAACCCAGG
TAACAGGAATAATTCTGTGGTTTCATTTTTCTGTAAACAACTGAAAGAATAATTAGATCATATT
CTAGTATGTTCTGAAATATCTTTAAGACTGATCTTAAAAACTAACTTCTAAGATGATTTCATCT
TCTCATAGTATAGAGTTTACTTTGTACACGTTTGAAACCAACTACTGTAGAAGATGAGGAATCT
ATTGTAATTTTTTGCTTTATTTTCATCTGCCAGTGGACTTATTTGAAATTTTCACTTTAGTCAA
ATTATTTTTTGTATTAGTTTTTGATGCAGACATAAAAATAGCAATCATTTTAAATTGTCAAAAT
TTCCAGATTACTGGTAAAAATTATTTGAAAACAAACTTATGGGTAATAAAGGCTAGTCAGAACC
CTATACCATAAAGTGTAGTTACCATACAGATTAATATGTAGCAAAAATGTATGCTTGATATTTC
TCAACTGTGTTAATTTTTCTGCTGTATTCCAGCTGACCAAAACAATATTAAGAATGCATCTTTA
TAAATGGGTGCTAATTGATAATGGAAATAATTTAGTAATGGACTATACAGGATGTTAATAATGA
AGCCATATGTTTATGTCTGGATTTAAAAATTTTAAACAATCATTTACTATGTCATTTTTCTTTA
CCTTGAAGAACATAAACTGTTATTTCACTTCTACAAATCAGCAAGATATTATTTATGGCAAGAA
ATATTCCATTGAAATATTGTGCTGTAACATGGGAAAGTGTAAATGTTTTTCATGGTTTCTATCA
ATGTGAAATAAAATTTAATTCTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

NM_001279358 ⟹ NP_001266287

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI
GRCh37	8	54,958,927 - 55,014,577 (-)	NCBI
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI
CHM1_1	8	55,010,550 - 55,065,879 (-)	NCBI
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

Sequence:

show sequence

GTTGGCGCGCACGCGCCTGAGCGTGCGCCCGGTGGGGCCGGCCGGGACTCGCCGCTCGCACGCC
CTTGGGCCGCGGCCGGGCGCCCGCTCTTCCTTCCGCTTGCGCTGTGAGCTGAGGCGGTGTATGT
GCGGCAATAACATGTCAACCCCGCTGCCCGCCATCGTGCCCGCCGCCCGGAAGGCCACCGCTGC
GGTGATTTTCCTGCATGGATTGGGAGATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGTATC
AGAAGTTCACATATCAAATATATCTGCCCGCATGCGCCTGTTAGGCCTGTTACATTAAATATGA
ACGTGGCTATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTCACAGGAGGATGAATC
TGGGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAAGTGAAGAATGGCATT
CCTTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTATCTTTATATACTGCCC
TTACCACACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGCTTCCACTTCGGGCTTC
CTTTCCACAGTGCCACGGGGATTGTGACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTACGGTG
GAAAAACTAAAAACATTGGTGAATCCAGCCAATGTGACCTTTAAAACCTATGAAGGTATGATGC
ACAGTTCGTGTCAACAGGAAATGATGGATGTCAAGCAATTCATTGATAAACTCCTACCTCCAAT
TGATTGACGTCACTAAGAGGCCTTGTGTAGAAGTACACCAGCATCATTGTAGTAGAGTGTAAAC
CTTTTCCCATGCCCAGTCTTCAAATTTCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAATACA
TGCCAATAACACAGATCAAATAATATCTCCTCATGAGAAATTTATGATCTTTTAAGTTTCTATA
CATGTATTCTTATAAGACGACCCAGGATCTACTATATTAGAATAGATGAAGCAGGTAGCTTCTT
TTTTCTCAAATGTAATTCAGCAAAATAATACAGTACTGCCACCAGATTTTTTATTACATCATTT
GAAAATTAGCAGTATGCTTAATGAAAATTTGTTCAGGTATAAATGAGCAGTTAAGATATAAACA
ATTTATGCATGCTGTGACTTAGTCTATGGATTTATTCCAAAATTGCTTAGTCACCATGCAGTGT
CTGTATTTTTATATATGTGTTCATATATACATAATGATTATAATACATAATAAGAATGAGGTGG
TATTACATTATTCCTAATAATAGGGATAATGCTGTTTATTGTCAAGAAAAAGTAAAATCGTTCT
CTTCAATTAATGGCCCTTTTATTTTGGGACCAGGCTTTTATTTTCCCTGATATTATTTCTATTT
AATACTCTTTTCTCTCAAGAAAAAAAAAAAAGTTTGTTTTTTCTTTATTGTCCTTCATAGCAGG
CCAAGTATTGCCTCTCTGCAATAGACAGCTACTGTCAATACATGCTGTAATTTGACATTCTGGG
TCACAGATATAAGGTATTTAAAATCTATTTATGCTTTATAGAGAAACCAGACATTAAAACTTCA
TGCACTACTTATTTCGAATTACTGTACCTTATCCAAATTTACACCTAGCTATTAGGATCTTCAA
CCCAGGTAACAGGAATAATTCTGTGGTTTCATTTTTCTGTAAACAACTGAAAGAATAATTAGAT
CATATTCTAGTATGTTCTGAAATATCTTTAAGACTGATCTTAAAAACTAACTTCTAAGATGATT
TCATCTTCTCATAGTATAGAGTTTACTTTGTACACGTTTGAAACCAACTACTGTAGAAGATGAG
GAATCTATTGTAATTTTTTGCTTTATTTTCATCTGCCAGTGGACTTATTTGAAATTTTCACTTT
AGTCAAATTATTTTTTGTATTAGTTTTTGATGCAGACATAAAAATAGCAATCATTTTAAATTGT
CAAAATTTCCAGATTACTGGTAAAAATTATTTGAAAACAAACTTATGGGTAATAAAGGCTAGTC
AGAACCCTATACCATAAAGTGTAGTTACCATACAGATTAATATGTAGCAAAAATGTATGCTTGA
TATTTCTCAACTGTGTTAATTTTTCTGCTGTATTCCAGCTGACCAAAACAATATTAAGAATGCA
TCTTTATAAATGGGTGCTAATTGATAATGGAAATAATTTAGTAATGGACTATACAGGATGTTAA
TAATGAAGCCATATGTTTATGTCTGGATTTAAAAATTTTAAACAATCATTTACTATGTCATTTT
TCTTTACCTTGAAGAACATAAACTGTTATTTCACTTCTACAAATCAGCAAGATATTATTTATGG
CAAGAAATATTCCATTGAAATATTGTGCTGTAACATGGGAAAGTGTAAATGTTTTTCATGGTTT
CTATCAATGTGAAATAAAATTTAATTCTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

NM_001279359 ⟹ NP_001266288

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI
GRCh37	8	54,958,927 - 55,014,577 (-)	NCBI
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI
CHM1_1	8	55,010,550 - 55,065,879 (-)	NCBI
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

Sequence:

show sequence

GTTGGCGCGCACGCGCCTGAGCGTGCGCCCGGTGGGGCCGGCCGGGACTCGCCGCTCGCACGCC
CTTGGGCCGCGGCCGGGCGCCCGCTCTTCCTTCCGCTTGCGCTGTGAGCTGAGGCGGTGTATGT
GCGGCAATAACATGTCAACCCCGCTGCCCGCCATCGTGCCCGCCGCCCGGAAGGCCACCGCTGC
GGTGATTTTCCTGCATGGATTGGGAGATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGCCTG
TTAGGCCTGTTACATTAAATATGAACGTGGCTATGCCTTCATGGTTTGATATTATTGGGCTTTC
ACCAGATTCACAGGAGGATGAATCTGGGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATT
GATCAAGAAGTGAAGAATGGCATTCCTTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAG
GAGCTTTATCTTTATATACTGCCCTTACCACACAGCAGAAACTGGCAGGTGTCACTGCACTCAG
TTGCTGGCTTCCACTTCGGGCTTCCTTTCCACAGGGTCCTATCGGTGGTGCTAATAGAGATATT
TCTATTCTCCAGTGCCACGGGGATTGTGACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTACGG
TGGAAAAACTAAAAACATTGGTGAATCCAGCCAATGTGACCTTTAAAACCTATGAAGGTATGAT
GCACAGTTCGTGTCAACAGGAAATGATGGATGTCAAGCAATTCATTGATAAACTCCTACCTCCA
ATTGATTGACGTCACTAAGAGGCCTTGTGTAGAAGTACACCAGCATCATTGTAGTAGAGTGTAA
ACCTTTTCCCATGCCCAGTCTTCAAATTTCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAATA
CATGCCAATAACACAGATCAAATAATATCTCCTCATGAGAAATTTATGATCTTTTAAGTTTCTA
TACATGTATTCTTATAAGACGACCCAGGATCTACTATATTAGAATAGATGAAGCAGGTAGCTTC
TTTTTTCTCAAATGTAATTCAGCAAAATAATACAGTACTGCCACCAGATTTTTTATTACATCAT
TTGAAAATTAGCAGTATGCTTAATGAAAATTTGTTCAGGTATAAATGAGCAGTTAAGATATAAA
CAATTTATGCATGCTGTGACTTAGTCTATGGATTTATTCCAAAATTGCTTAGTCACCATGCAGT
GTCTGTATTTTTATATATGTGTTCATATATACATAATGATTATAATACATAATAAGAATGAGGT
GGTATTACATTATTCCTAATAATAGGGATAATGCTGTTTATTGTCAAGAAAAAGTAAAATCGTT
CTCTTCAATTAATGGCCCTTTTATTTTGGGACCAGGCTTTTATTTTCCCTGATATTATTTCTAT
TTAATACTCTTTTCTCTCAAGAAAAAAAAAAAAGTTTGTTTTTTCTTTATTGTCCTTCATAGCA
GGCCAAGTATTGCCTCTCTGCAATAGACAGCTACTGTCAATACATGCTGTAATTTGACATTCTG
GGTCACAGATATAAGGTATTTAAAATCTATTTATGCTTTATAGAGAAACCAGACATTAAAACTT
CATGCACTACTTATTTCGAATTACTGTACCTTATCCAAATTTACACCTAGCTATTAGGATCTTC
AACCCAGGTAACAGGAATAATTCTGTGGTTTCATTTTTCTGTAAACAACTGAAAGAATAATTAG
ATCATATTCTAGTATGTTCTGAAATATCTTTAAGACTGATCTTAAAAACTAACTTCTAAGATGA
TTTCATCTTCTCATAGTATAGAGTTTACTTTGTACACGTTTGAAACCAACTACTGTAGAAGATG
AGGAATCTATTGTAATTTTTTGCTTTATTTTCATCTGCCAGTGGACTTATTTGAAATTTTCACT
TTAGTCAAATTATTTTTTGTATTAGTTTTTGATGCAGACATAAAAATAGCAATCATTTTAAATT
GTCAAAATTTCCAGATTACTGGTAAAAATTATTTGAAAACAAACTTATGGGTAATAAAGGCTAG
TCAGAACCCTATACCATAAAGTGTAGTTACCATACAGATTAATATGTAGCAAAAATGTATGCTT
GATATTTCTCAACTGTGTTAATTTTTCTGCTGTATTCCAGCTGACCAAAACAATATTAAGAATG
CATCTTTATAAATGGGTGCTAATTGATAATGGAAATAATTTAGTAATGGACTATACAGGATGTT
AATAATGAAGCCATATGTTTATGTCTGGATTTAAAAATTTTAAACAATCATTTACTATGTCATT
TTTCTTTACCTTGAAGAACATAAACTGTTATTTCACTTCTACAAATCAGCAAGATATTATTTAT
GGCAAGAAATATTCCATTGAAATATTGTGCTGTAACATGGGAAAGTGTAAATGTTTTTCATGGT
TTCTATCAATGTGAAATAAAATTTAATTCTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

NM_001279360 ⟹ NP_001266289

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,474 (-)	NCBI
GRCh37	8	54,958,927 - 55,014,577 (-)	NCBI
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI
CHM1_1	8	55,010,550 - 55,065,416 (-)	NCBI
T2T-CHM13v2.0	8	54,423,759 - 54,478,554 (-)	NCBI

Sequence:

show sequence

CTCTGCAGCGTGTTTCTGCCTGGTGTGTGGGTGAGGGAAACCTAAGTCCGCCAGGAAATCGCCT
TATTGTCACCTCGCACTCTTATCCTCAATGAAAGAAGTTTGAAGATTGAGTGTCCTACAAGGTG
ATTTTCCTGCATGGATTGGGAGATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGTATCAGAA
GTTCACATATCAAATATATCTGCCCGCATGCGCCTGTTAGGCCTGTTACATTAAATATGAACGT
GGCTATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTCACAGGAGGATGAATCTGGG
ATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAAGTGAAGAATGGCATTCCTT
CTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTATCTTTATATACTGCCCTTAC
CACACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGCTTCCACTTCGGGCTTCCTTT
CCACAGGGTCCTATCGGTGGTGCTAATAGAGATATTTCTATTCTCCAGTGCCACGGGGATTGTG
ACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTACGGTGGAAAAACTAAAAACATTGGTGAATCC
AGCCAATGTGACCTTTAAAACCTATGAAGGTATGATGCACAGTTCGTGTCAACAGGAAATGATG
GATGTCAAGCAATTCATTGATAAACTCCTACCTCCAATTGATTGACGTCACTAAGAGGCCTTGT
GTAGAAGTACACCAGCATCATTGTAGTAGAGTGTAAACCTTTTCCCATGCCCAGTCTTCAAATT
TCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAATACATGCCAATAACACAGATCAAATAATAT
CTCCTCATGAGAAATTTATGATCTTTTAAGTTTCTATACATGTATTCTTATAAGACGACCCAGG
ATCTACTATATTAGAATAGATGAAGCAGGTAGCTTCTTTTTTCTCAAATGTAATTCAGCAAAAT
AATACAGTACTGCCACCAGATTTTTTATTACATCATTTGAAAATTAGCAGTATGCTTAATGAAA
ATTTGTTCAGGTATAAATGAGCAGTTAAGATATAAACAATTTATGCATGCTGTGACTTAGTCTA
TGGATTTATTCCAAAATTGCTTAGTCACCATGCAGTGTCTGTATTTTTATATATGTGTTCATAT
ATACATAATGATTATAATACATAATAAGAATGAGGTGGTATTACATTATTCCTAATAATAGGGA
TAATGCTGTTTATTGTCAAGAAAAAGTAAAATCGTTCTCTTCAATTAATGGCCCTTTTATTTTG
GGACCAGGCTTTTATTTTCCCTGATATTATTTCTATTTAATACTCTTTTCTCTCAAGAAAAAAA
AAAAAGTTTGTTTTTTCTTTATTGTCCTTCATAGCAGGCCAAGTATTGCCTCTCTGCAATAGAC
AGCTACTGTCAATACATGCTGTAATTTGACATTCTGGGTCACAGATATAAGGTATTTAAAATCT
ATTTATGCTTTATAGAGAAACCAGACATTAAAACTTCATGCACTACTTATTTCGAATTACTGTA
CCTTATCCAAATTTACACCTAGCTATTAGGATCTTCAACCCAGGTAACAGGAATAATTCTGTGG
TTTCATTTTTCTGTAAACAACTGAAAGAATAATTAGATCATATTCTAGTATGTTCTGAAATATC
TTTAAGACTGATCTTAAAAACTAACTTCTAAGATGATTTCATCTTCTCATAGTATAGAGTTTAC
TTTGTACACGTTTGAAACCAACTACTGTAGAAGATGAGGAATCTATTGTAATTTTTTGCTTTAT
TTTCATCTGCCAGTGGACTTATTTGAAATTTTCACTTTAGTCAAATTATTTTTTGTATTAGTTT
TTGATGCAGACATAAAAATAGCAATCATTTTAAATTGTCAAAATTTCCAGATTACTGGTAAAAA
TTATTTGAAAACAAACTTATGGGTAATAAAGGCTAGTCAGAACCCTATACCATAAAGTGTAGTT
ACCATACAGATTAATATGTAGCAAAAATGTATGCTTGATATTTCTCAACTGTGTTAATTTTTCT
GCTGTATTCCAGCTGACCAAAACAATATTAAGAATGCATCTTTATAAATGGGTGCTAATTGATA
ATGGAAATAATTTAGTAATGGACTATACAGGATGTTAATAATGAAGCCATATGTTTATGTCTGG
ATTTAAAAATTTTAAACAATCATTTACTATGTCATTTTTCTTTACCTTGAAGAACATAAACTGT
TATTTCACTTCTACAAATCAGCAAGATATTATTTATGGCAAGAAATATTCCATTGAAATATTGT
GCTGTAACATGGGAAAGTGTAAATGTTTTTCATGGTTTCTATCAATGTGAAATAAAATTTAATT
CTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

NM_006330 ⟹ NP_006321

RefSeq Status:

REVIEWED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI
GRCh37	8	54,958,927 - 55,014,577 (-)	NCBI
Build 36	8	55,121,491 - 55,177,130 (-)	NCBI Archive
HuRef	8	50,427,322 - 50,482,732 (-)	NCBI
CHM1_1	8	55,010,550 - 55,065,879 (-)	NCBI
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

Sequence:

show sequence

GTTGGCGCGCACGCGCCTGAGCGTGCGCCCGGTGGGGCCGGCCGGGACTCGCCGCTCGCACGCC
CTTGGGCCGCGGCCGGGCGCCCGCTCTTCCTTCCGCTTGCGCTGTGAGCTGAGGCGGTGTATGT
GCGGCAATAACATGTCAACCCCGCTGCCCGCCATCGTGCCCGCCGCCCGGAAGGCCACCGCTGC
GGTGATTTTCCTGCATGGATTGGGAGATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGTATC
AGAAGTTCACATATCAAATATATCTGCCCGCATGCGCCTGTTAGGCCTGTTACATTAAATATGA
ACGTGGCTATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTCACAGGAGGATGAATC
TGGGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAAGTGAAGAATGGCATT
CCTTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTATCTTTATATACTGCCC
TTACCACACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGCTTCCACTTCGGGCTTC
CTTTCCACAGGGTCCTATCGGTGGTGCTAATAGAGATATTTCTATTCTCCAGTGCCACGGGGAT
TGTGACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTACGGTGGAAAAACTAAAAACATTGGTGA
ATCCAGCCAATGTGACCTTTAAAACCTATGAAGGTATGATGCACAGTTCGTGTCAACAGGAAAT
GATGGATGTCAAGCAATTCATTGATAAACTCCTACCTCCAATTGATTGACGTCACTAAGAGGCC
TTGTGTAGAAGTACACCAGCATCATTGTAGTAGAGTGTAAACCTTTTCCCATGCCCAGTCTTCA
AATTTCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAATACATGCCAATAACACAGATCAAATA
ATATCTCCTCATGAGAAATTTATGATCTTTTAAGTTTCTATACATGTATTCTTATAAGACGACC
CAGGATCTACTATATTAGAATAGATGAAGCAGGTAGCTTCTTTTTTCTCAAATGTAATTCAGCA
AAATAATACAGTACTGCCACCAGATTTTTTATTACATCATTTGAAAATTAGCAGTATGCTTAAT
GAAAATTTGTTCAGGTATAAATGAGCAGTTAAGATATAAACAATTTATGCATGCTGTGACTTAG
TCTATGGATTTATTCCAAAATTGCTTAGTCACCATGCAGTGTCTGTATTTTTATATATGTGTTC
ATATATACATAATGATTATAATACATAATAAGAATGAGGTGGTATTACATTATTCCTAATAATA
GGGATAATGCTGTTTATTGTCAAGAAAAAGTAAAATCGTTCTCTTCAATTAATGGCCCTTTTAT
TTTGGGACCAGGCTTTTATTTTCCCTGATATTATTTCTATTTAATACTCTTTTCTCTCAAGAAA
AAAAAAAAAGTTTGTTTTTTCTTTATTGTCCTTCATAGCAGGCCAAGTATTGCCTCTCTGCAAT
AGACAGCTACTGTCAATACATGCTGTAATTTGACATTCTGGGTCACAGATATAAGGTATTTAAA
ATCTATTTATGCTTTATAGAGAAACCAGACATTAAAACTTCATGCACTACTTATTTCGAATTAC
TGTACCTTATCCAAATTTACACCTAGCTATTAGGATCTTCAACCCAGGTAACAGGAATAATTCT
GTGGTTTCATTTTTCTGTAAACAACTGAAAGAATAATTAGATCATATTCTAGTATGTTCTGAAA
TATCTTTAAGACTGATCTTAAAAACTAACTTCTAAGATGATTTCATCTTCTCATAGTATAGAGT
TTACTTTGTACACGTTTGAAACCAACTACTGTAGAAGATGAGGAATCTATTGTAATTTTTTGCT
TTATTTTCATCTGCCAGTGGACTTATTTGAAATTTTCACTTTAGTCAAATTATTTTTTGTATTA
GTTTTTGATGCAGACATAAAAATAGCAATCATTTTAAATTGTCAAAATTTCCAGATTACTGGTA
AAAATTATTTGAAAACAAACTTATGGGTAATAAAGGCTAGTCAGAACCCTATACCATAAAGTGT
AGTTACCATACAGATTAATATGTAGCAAAAATGTATGCTTGATATTTCTCAACTGTGTTAATTT
TTCTGCTGTATTCCAGCTGACCAAAACAATATTAAGAATGCATCTTTATAAATGGGTGCTAATT
GATAATGGAAATAATTTAGTAATGGACTATACAGGATGTTAATAATGAAGCCATATGTTTATGT
CTGGATTTAAAAATTTTAAACAATCATTTACTATGTCATTTTTCTTTACCTTGAAGAACATAAA
CTGTTATTTCACTTCTACAAATCAGCAAGATATTATTTATGGCAAGAAATATTCCATTGAAATA
TTGTGCTGTAACATGGGAAAGTGTAAATGTTTTTCATGGTTTCTATCAATGTGAAATAAAATTT
AATTCTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

XM_005251127 ⟹ XP_005251184

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,474 (-)	NCBI
GRCh37	8	54,958,927 - 55,014,577 (-)	NCBI

Sequence:

show sequence

GTGTGTGGGTGAGGGAAACCTAAGTCCGCCAGGAAATCGCCTTATTGTCACCTCGCACTCTTAT
CCTCAATGAAAGAAGTTTGAAGATTGAGTGTCCTACAAGGTGATTTTCCTGCATGGATTGGGAG
ATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGCCTGTTAGGCCTGTTACATTAAATATGAAC
GTGGCTATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTCACAGGAGGATGAATCTG
GGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAAGTGAAGAATGGCATTCC
TTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTATCTTTATATACTGCCCTT
ACCACACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGCTTCCACTTCGGGCTTCCT
TTCCACAGGGTCCTATCGGTGGTGCTAATAGAGATATTTCTATTCTCCAGTGCCACGGGGATTG
TGACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTACGGTGGAAAAACTAAAAACATTGGTGAAT
CCAGCCAATGTGACCTTTAAAACCTATGAAGGTATGATGCACAGTTCGTGTCAACAGGAAATGA
TGGATGTCAAGCAATTCATTGATAAACTCCTACCTCCAATTGATTGACGTCACTAAGAGGCCTT
GTGTAGAAGTACACCAGCATCATTGTAGTAGAGTGTAAACCTTTTCCCATGCCCAGTCTTCAAA
TTTCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAATACATGCCAATAACACAGATCAAATAAT
ATCTCCTCATGAGAAATTTATGATCTTTTAAGTTTCTATACATGTATTCTTATAAGACGACCCA
GGATCTACTATATTAGAATAGATGAAGCAGGTAGCTTCTTTTTTCTCAAATGTAATTCAGCAAA
ATAATACAGTACTGCCACCAGATTTTTTATTACATCATTTGAAAATTAGCAGTATGCTTAATGA
AAATTTGTTCAGGTATAAATGAGCAGTTAAGATATAAACAATTTATGCATGCTGTGACTTAGTC
TATGGATTTATTCCAAAATTGCTTAGTCACCATGCAGTGTCTGTATTTTTATATATGTGTTCAT
ATATACATAATGATTATAATACATAATAAGAATGAGGTGGTATTACATTATTCCTAATAATAGG
GATAATGCTGTTTATTGTCAAGAAAAAGTAAAATCGTTCTCTTCAATTAATGGCCCTTTTATTT
TGGGACCAGGCTTTTATTTTCCCTGATATTATTTCTATTTAATACTCTTTTCTCTCAA

hide sequence

RefSeq Acc Id:

XM_017012956 ⟹ XP_016868445

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI

Sequence:

show sequence

CGCGCACGCGCCTGAGCGTGCGCCCGGTGGGGCCGGCCGGGACTCGCCGCTCGCACGCCCTTGG
GCCGCGGCCGGGCGCCCGCTCTTCCTTCCGCTTGCGCTGTGAGCTGAGGCGGTGTATGTGCGGC
AATAACATGTCAACCCCGCTGCCCGCCATCGTGCCCGCCGCCCGGAAGGCCACCGCTGCGGTGA
TTTTCCTGCATGGATTGGGAGATACTGGGCCTGTTAGGCCTGTTACATTAAATATGAACGTGGC
TATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTCACAGGAGGATGAATCTGGGATT
AAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAAGTGAAGAATGGCATTCCTTCTA
ACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTATCTTTATATACTGCCCTTACCAC
ACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGCTTCCACTTCGGGCTTCCTTTCCA
CAGGGTCCTATCGGTGGTGCTAATAGAGATATTTCTATTCTCCAGTGCCACGGGGATTGTGACC
CTTTGGTTCCCCTGATGTTTGGTTCTCTTACGGTGGAAAAACTAAAAACATTGGTGAATCCAGC
CAATGTGACCTTTAAAACCTATGAAGGTATGATGCACAGTTCGTGTCAACAGGAAATGATGGAT
GTCAAGCAATTCATTGATAAACTCCTACCTCCAATTGATTGACGTCACTAAGAGGCCTTGTGTA
GAAGTACACCAGCATCATTGTAGTAGAGTGTAAACCTTTTCCCATGCCCAGTCTTCAAATTTCT
AATGTTTTGCAGTGTTAAAATGTTTTGCAAATACATGCCAATAACACAGATCAAATAATATCTC
CTCATGAGAAATTTATGATCTTTTAAGTTTCTATACATGTATTCTTATAAGACGACCCAGGATC
TACTATATTAGAATAGATGAAGCAGGTAGCTTCTTTTTTCTCAAATGTAATTCAGCAAAATAAT
ACAGTACTGCCACCAGATTTTTTATTACATCATTTGAAAATTAGCAGTATGCTTAATGAAAATT
TGTTCAGGTATAAATGAGCAGTTAAGATATAAACAATTTATGCATGCTGTGACTTAGTCTATGG
ATTTATTCCAAAATTGCTTAGTCACCATGCAGTGTCTGTATTTTTATATATGTGTTCATATATA
CATAATGATTATAATACATAATAAGAATGAGGTGGTATTACATTATTCCTAATAATAGGGATAA
TGCTGTTTATTGTCAAGAAAAAGTAAAATCGTTCTCTTCAATTAATGGCCCTTTTATTTTGGGA
CCAGGCTTTTATTTTCCCTGATATTATTTCTATTTAATACTCTTTTCTCTCAAGAAAAAAAAAA
AAGTTTGTTTTTTCTTTATTGTCCTTCATAGCAGGCCAAGTATTGCCTCTCTGCAATAGACAGC
TACTGTCAATACATGCTGTAATTTGACATTCTGGGTCACAGATATAAGGTATTTAAAATCTATT
TATGCTTTATAGAGAAACCAGACATTAAAACTTCATGCACTACTTATTTCGAATTACTGTACCT
TATCCAAATTTACACCTAGCTATTAGGATCTTCAACCCAGGTAACAGGAATAATTCTGTGGTTT
CATTTTTCTGTAAACAACTGAAAGAATAATTAGATCATATTCTAGTATGTTCTGAAATATCTTT
AAGACTGATCTTAAAAACTAACTTCTAAGATGATTTCATCTTCTCATAGTATAGAGTTTACTTT
GTACACGTTTGAAACCAACTACTGTAGAAGATGAGGAATCTATTGTAATTTTTTGCTTTATTTT
CATCTGCCAGTGGACTTATTTGAAATTTTCACTTTAGTCAAATTATTTTTTGTATTAGTTTTTG
ATGCAGACATAAAAATAGCAATCATTTTAAATTGTCAAAATTTCCAGATTACTGGTAAAAATTA
TTTGAAAACAAACTTATGGGTAATAAAGGCTAGTCAGAACCCTATACCATAAAGTGTAGTTACC
ATACAGATTAATATGTAGCAAAAATGTATGCTTGATATTTCTCAACTGTGTTAATTTTTCTGCT
GTATTCCAGCTGACCAAAACAATATTAAGAATGCATCTTTATAAATGGGTGCTAATTGATAATG
GAAATAATTTAGTAATGGACTATACAGGATGTTAATAATGAAGCCATATGTTTATGTCTGGATT
TAAAAATTTTAAACAATCATTTACTATGTCATTTTTCTTTACCTTGAAGAACATAAACTGTTAT
TTCACTTCTACAAATCAGCAAGATATTATTTATGGCAAGAAATATTCCATTGAAATATTGTGCT
GTAACATGGGAAAGTGTAAATGTTTTTCATGGT

hide sequence

RefSeq Acc Id:

XM_017012958 ⟹ XP_016868447

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI

Sequence:

show sequence

CGCCTGAGCGTGCGCCCGGTGGGGCCGGCCGGGACTCGCCGCTCGCACGCCCTTGGGCCGCGGC
CGGGCGCCCGCTCTTCCTTCCGCTTGCGCTGTGAGCTGAGGCGGTGTATGTGCGGCAATAACAT
GTCAACCCCGCTGCCCGCCATCGTGCCCGCCGCCCGGAAGGCCACCGCTGCGGTGATTTTCCTG
CATGGATTGGGAGATACTGGGCACGGATGGGCAGAAGCCTTTGCAGGCCTGTTAGGCCTGTTAC
ATTAAATATGAACGTGGCTATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTCACAG
GAGGATGAATCTGGGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAAGTGA
AGAATGGCATTCCTTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTATCTTT
ATATACTGCCCTTACCACACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGCTTCCA
CTTCGGGCTTCCTTTCCACAGTGCCACGGGGATTGTGACCCTTTGGTTCCCCTGATGTTTGGTT
CTCTTACGGTGGAAAAACTAAAAACATTGGTGAATCCAGCCAATGTGACCTTTAAAACCTATGA
AGGTATGATGCACAGTTCGTGTCAACAGGAAATGATGGATGTCAAGCAATTCATTGATAAACTC
CTACCTCCAATTGATTGACGTCACTAAGAGGCCTTGTGTAGAAGTACACCAGCATCATTGTAGT
AGAGTGTAAACCTTTTCCCATGCCCAGTCTTCAAATTTCTAATGTTTTGCAGTGTTAAAATGTT
TTGCAAATACATGCCAATAACACAGATCAAATAATATCTCCTCATGAGAAATTTATGATCTTTT
AAGTTTCTATACATGTATTCTTATAAGACGACCCAGGATCTACTATATTAGAATAGATGAAGCA
GGTAGCTTCTTTTTTCTCAAATGTAATTCAGCAAAATAATACAGTACTGCCACCAGATTTTTTA
TTACATCATTTGAAAATTAGCAGTATGCTTAATGAAAATTTGTTCAGGTATAAATGAGCAGTTA
AGATATAAACAATTTATGCATGCTGTGACTTAGTCTATGGATTTATTCCAAAATTGCTTAGTCA
CCATGCAGTGTCTGTATTTTTATATATGTGTTCATATATACATAATGATTATAATACATAATAA
GAATGAGGTGGTATTACATTATTCCTAATAATAGGGATAATGCTGTTTATTGTCAAGAAAAAGT
AAAATCGTTCTCTTCAATTAATGGCCCTTTTATTTTGGGACCAGGCTTTTATTTTCCCTGATAT
TATTTCTATTTAATACTCTTTTCTCTCAAGAAAAAAAAAAAAGTTTGTTTTTTCTTTATTGTCC
TTCATAGCAGGCCAAGTATTGCCTCTCTGCAATAGACAGCTACTGTCAATACATGCTGTAATTT
GACATTCTGGGTCACAGATATAAGGTATTTAAAATCTATTTATGCTTTATAGAGAAACCAGACA
TTAAAACTTCATGCACTACTTATTTCGAATTACTGTACCTTATCCAAATTTACACCTAGCTATT
AGGATCTTCAACCCAGGTAACAGGAATAATTCTGTGGTTTCATTTTTCTGTAAACAACTGAAAG
AATAATTAGATCATATTCTAGTATGTTCTGAAATATCTTTAAGACTGATCTTAAAAACTAACTT
CTAAGATGATTTCATCTTCTCATAGTATAGAGTTTACTTTGTACACGTTTGAAACCAACTACTG
TAGAAGATGAGGAATCTATTGTAATTTTTTGCTTTATTTTCATCTGCCAGTGGACTTATTTGAA
ATTTTCACTTTAGTCAAATTATTTTTTGTATTAGTTTTTGATGCAGACATAAAAATAGCAATCA
TTTTAAATTGTCAAAATTTCCAGATTACTGGTAAAAATTATTTGAAAACAAACTTATGGGTAAT
AAAGGCTAGTCAGAACCCTATACCATAAAGTGTAGTTACCATACAGATTAATATGTAGCAAAAA
TGTATGCTTGATATTTCTCAACTGTGTTAATTTTTCTGCTGTATTCCAGCTGACCAAAACAATA
TTAAGAATGCATCTTTATAAATGGGTGCTAATTGATAATGGAAATAATTTAGTAATGGACTATA
CAGGATGTTAATAATGAAGCCATATGTTTATGTCTGGATTTAAAAATTTTAAACAATCATTTAC
TATGTCATTTTTCTTTACCTTGAAGAACATAAACTGTTATTTCACTTCTACAAATCAGCAAGAT
ATTATTTATGGCAAGAAATATTCCATTGAAATATTGTGCTGTAACATGGGAAAGTGTAAATGTT
TTTCATGGTTTCTATCAATGTGAAATAAAATTTAATTCTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

XM_017012960 ⟹ XP_016868449

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,474 (-)	NCBI

Sequence:

show sequence

GGCCTAGGGCACGGCGTCAGCCTCTGCAGCGTGTTTCTGCCTGGTGTGTGGGTGAGGGAAACCT
AAGTCCGCCAGGAAATCGCCTTATTGTCACCTCGCACTCTTATCCTCAATGAAAGAAGTTTGAA
GATTGAGTGTCCTACAAGGTGATTTTCCTGCATGGATTGGGAGATACTGGGCCTGTTAGGCCTG
TTACATTAAATATGAACGTGGCTATGCCTTCATGGTTTGATATTATTGGGCTTTCACCAGATTC
ACAGGAGGATGAATCTGGGATTAAACAGGCAGCAGAAAATATAAAAGCTTTGATTGATCAAGAA
GTGAAGAATGGCATTCCTTCTAACAGAATTATTTTGGGAGGGTTTTCTCAGGGAGGAGCTTTAT
CTTTATATACTGCCCTTACCACACAGCAGAAACTGGCAGGTGTCACTGCACTCAGTTGCTGGCT
TCCACTTCGGGCTTCCTTTCCACAGGGTCCTATCGGTGGTGCTAATAGAGATATTTCTATTCTC
CAGTGCCACGGGGATTGTGACCCTTTGGTTCCCCTGATGTTTGGTTCTCTTACGGTGGAAAAAC
TAAAAACATTGGTGAATCCAGCCAATGTGACCTTTAAAACCTATGAAGGTATGATGCACAGTTC
GTGTCAACAGGAAATGATGGATGTCAAGCAATTCATTGATAAACTCCTACCTCCAATTGATTGA
CGTCACTAAGAGGCCTTGTGTAGAAGTACACCAGCATCATTGTAGTAGAGTGTAAACCTTTTCC
CATGCCCAGTCTTCAAATTTCTAATGTTTTGCAGTGTTAAAATGTTTTGCAAATACATGCCAAT
AACACAGATCAAATAATATCTCCTCATGAGAAATTTATGATCTTTTAAGTTTCTATACATGTAT
TCTTATAAGACGACCCAGGATCTACTATATTAGAATAGATGAAGCAGGTAGCTTCTTTTTTCTC
AAATGTAATTCAGCAAAATAATACAGTACTGCCACCAGATTTTTTATTACATCATTTGAAAATT
AGCAGTATGCTTAATGAAAATTTGTTCAGGTATAAATGAGCAGTTAAGATATAAACAATTTATG
CATGCTGTGACTTAGTCTATGGATTTATTCCAAAATTGCTTAGTCACCATGCAGTGTCTGTATT
TTTATATATGTGTTCATATATACATAATGATTATAATACATAATAAGAATGAGGTGGTATTACA
TTATTCCTAATAATAGGGATAATGCTGTTTATTGTCAAGAAAAAGTAAAATCGTTCTCTTCAAT
TAATGGCCCTTTTATTTTGGGACCAGGCTTTTATTTTCCCTGATATTATTTCTATTTAATACTC
TTTTCTCTCAAGAAAAAAAAAAAAGTTTGTTTTTTCTTTATTGTCCTTCATAGCAGGCCAAGTA
TTGCCTCTCTGCAATAGACAGCTACTGTCAATACATGCTGTAATTTGACATTCTGGGTCACAGA
TATAAGGTATTTAAAATCTATTTATGCTTTATAGAGAAACCAGACATTAAAACTTCATGCACTA
CTTATTTCGAATTACTGTACCTTATCCAAATTTACACCTAGCTATTAGGATCTTCAACCCAGGT
AACAGGAATAATTCTGTGGTTTCATTTTTCTGTAAACAACTGAAAGAATAATTAGATCATATTC
TAGTATGTTCTGAAATATCTTTAAGACTGATCTTAAAAACTAACTTCTAAGATGATTTCATCTT
CTCATAGTATAGAGTTTACTTTGTACACGTTTGAAACCAACTACTGTAGAAGATGAGGAATCTA
TTGTAATTTTTTGCTTTATTTTCATCTGCCAGTGGACTTATTTGAAATTTTCACTTTAGTCAAA
TTATTTTTTGTATTAGTTTTTGATGCAGACATAAAAATAGCAATCATTTTAAATTGTCAAAATT
TCCAGATTACTGGTAAAAATTATTTGAAAACAAACTTATGGGTAATAAAGGCTAGTCAGAACCC
TATACCATAAAGTGTAGTTACCATACAGATTAATATGTAGCAAAAATGTATGCTTGATATTTCT
CAACTGTGTTAATTTTTCTGCTGTATTCCAGCTGACCAAAACAATATTAAGAATGCATCTTTAT
AAATGGGTGCTAATTGATAATGGAAATAATTTAGTAATGGACTATACAGGATGTTAATAATGAA
GCCATATGTTTATGTCTGGATTTAAAAATTTTAAACAATCATTTACTATGTCATTTTTCTTTAC
CTTGAAGAACATAAACTGTTATTTCACTTCTACAAATCAGCAAGATATTATTTATGGCAAGAAA
TATTCCATTGAAATATTGTGCTGTAACATGGGAAAGTGTAAATGTTTTTCATGGTTTCTATCAA
TGTGAAATAAAATTTAATTCTGACTTTTCTGTGA

hide sequence

RefSeq Acc Id:

XM_047421223 ⟹ XP_047277179

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,474 (-)	NCBI

RefSeq Acc Id:

XM_047421224 ⟹ XP_047277180

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,474 (-)	NCBI

RefSeq Acc Id:

XM_047421225 ⟹ XP_047277181

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI

RefSeq Acc Id:

XM_047421226 ⟹ XP_047277182

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,474 (-)	NCBI

RefSeq Acc Id:

XM_047421227 ⟹ XP_047277183

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,474 (-)	NCBI

RefSeq Acc Id:

XM_047421228 ⟹ XP_047277184

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,046,367 - 54,101,947 (-)	NCBI

RefSeq Acc Id:

XM_054359536 ⟹ XP_054215511

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,478,554 (-)	NCBI

RefSeq Acc Id:

XM_054359537 ⟹ XP_054215512

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,478,554 (-)	NCBI

RefSeq Acc Id:

XM_054359538 ⟹ XP_054215513

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,458,930 (-)	NCBI

RefSeq Acc Id:

XM_054359539 ⟹ XP_054215514

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

RefSeq Acc Id:

XM_054359540 ⟹ XP_054215515

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

RefSeq Acc Id:

XM_054359541 ⟹ XP_054215516

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,478,554 (-)	NCBI

RefSeq Acc Id:

XM_054359542 ⟹ XP_054215517

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,478,554 (-)	NCBI

RefSeq Acc Id:

XM_054359543 ⟹ XP_054215518

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

RefSeq Acc Id:

XM_054359544 ⟹ XP_054215519

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,478,554 (-)	NCBI

RefSeq Acc Id:

XM_054359545 ⟹ XP_054215520

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,478,554 (-)	NCBI

RefSeq Acc Id:

XM_054359546 ⟹ XP_054215521

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
T2T-CHM13v2.0	8	54,423,759 - 54,479,027 (-)	NCBI

Protein Sequences


Protein RefSeqs	NP_001266285	(Get FASTA)	NCBI Sequence Viewer
	NP_001266286	(Get FASTA)	NCBI Sequence Viewer
	NP_001266287	(Get FASTA)	NCBI Sequence Viewer
	NP_001266288	(Get FASTA)	NCBI Sequence Viewer
	NP_001266289	(Get FASTA)	NCBI Sequence Viewer
	NP_001412766	(Get FASTA)	NCBI Sequence Viewer
	NP_006321	(Get FASTA)	NCBI Sequence Viewer
	XP_005251184	(Get FASTA)	NCBI Sequence Viewer
	XP_016868445	(Get FASTA)	NCBI Sequence Viewer
	XP_016868447	(Get FASTA)	NCBI Sequence Viewer
	XP_016868449	(Get FASTA)	NCBI Sequence Viewer
	XP_047277179	(Get FASTA)	NCBI Sequence Viewer
	XP_047277180	(Get FASTA)	NCBI Sequence Viewer
	XP_047277181	(Get FASTA)	NCBI Sequence Viewer
	XP_047277182	(Get FASTA)	NCBI Sequence Viewer
	XP_047277183	(Get FASTA)	NCBI Sequence Viewer
	XP_047277184	(Get FASTA)	NCBI Sequence Viewer
	XP_054215511	(Get FASTA)	NCBI Sequence Viewer
	XP_054215512	(Get FASTA)	NCBI Sequence Viewer
	XP_054215513	(Get FASTA)	NCBI Sequence Viewer
	XP_054215514	(Get FASTA)	NCBI Sequence Viewer
	XP_054215515	(Get FASTA)	NCBI Sequence Viewer
	XP_054215516	(Get FASTA)	NCBI Sequence Viewer
	XP_054215517	(Get FASTA)	NCBI Sequence Viewer
	XP_054215518	(Get FASTA)	NCBI Sequence Viewer
	XP_054215519	(Get FASTA)	NCBI Sequence Viewer
	XP_054215520	(Get FASTA)	NCBI Sequence Viewer
	XP_054215521	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAB88180	(Get FASTA)	NCBI Sequence Viewer
	AAC31610	(Get FASTA)	NCBI Sequence Viewer
	AAD26993	(Get FASTA)	NCBI Sequence Viewer
	AAD26994	(Get FASTA)	NCBI Sequence Viewer
	AAG10063	(Get FASTA)	NCBI Sequence Viewer
	AAH08652	(Get FASTA)	NCBI Sequence Viewer
	AAH10397	(Get FASTA)	NCBI Sequence Viewer
	BAF82089	(Get FASTA)	NCBI Sequence Viewer
	BAG36480	(Get FASTA)	NCBI Sequence Viewer
	BAG60476	(Get FASTA)	NCBI Sequence Viewer
	CAG33384	(Get FASTA)	NCBI Sequence Viewer
	EAW86742	(Get FASTA)	NCBI Sequence Viewer
	EAW86743	(Get FASTA)	NCBI Sequence Viewer
	EAW86744	(Get FASTA)	NCBI Sequence Viewer
	EAW86745	(Get FASTA)	NCBI Sequence Viewer
	EAW86746	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000320043
	ENSP00000320043.3
	ENSP00000344477
	ENSP00000344477.6
	ENSP00000427967.1
	ENSP00000428306.1
	ENSP00000428729.1
	ENSP00000430791.2
	ENSP00000482430
	ENSP00000482430.1
	ENSP00000484280
	ENSP00000484280.1
GenBank Protein	O75608	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_006321 ⟸ NM_006330
- Peptide Label:	isoform 1
- UniProtKB:	O43202 (UniProtKB/Swiss-Prot), Q9UQF9 (UniProtKB/Swiss-Prot), O75608 (UniProtKB/Swiss-Prot), Q6IAQ1 (UniProtKB/TrEMBL), B4DJV9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MCGNNMSTPLPAIVPAARKATAAVIFLHGLGDTGHGWAEAFAGIRSSHIKYICPHAPVRPVTLN MNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRIILGGFSQGGALSLYT ALTTQQKLAGVTALSCWLPLRASFPQGPIGGANRDISILQCHGDCDPLVPLMFGSLTVEKLKTL VNPANVTFKTYEGMMHSSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	NP_001266288 ⟸ NM_001279359
- Peptide Label:	isoform 5
- UniProtKB:	O75608 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MGRSLCRPVRPVTLNMNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRI ILGGFSQGGALSLYTALTTQQKLAGVTALSCWLPLRASFPQGPIGGANRDISILQCHGDCDPLV PLMFGSLTVEKLKTLVNPANVTFKTYEGMMHSSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	NP_001266286 ⟸ NM_001279357
- Peptide Label:	isoform 3
- UniProtKB:	E5RGR0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MCGNNMSTPLPAIVPAARKATAAVIFLHGLGDTGHGWAEAFAGIRSSHIKYICPHAFDIIGLSP DSQEDESGIKQAAENIKALIDQEVKNGIPSNRIILGGFSQGGALSLYTALTTQQKLAGVTALSC WLPLRASFPQGPIGGANRDISILQCHGDCDPLVPLMFGSLTVEKLKTLVNPANVTFKTYEGMMH SSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	NP_001266285 ⟸ NM_001279356
- Peptide Label:	isoform 2
- UniProtKB:	B4DP64 (UniProtKB/TrEMBL), E5RGR0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MCGNNMSTPLPAIVPAARKATAAVIFLHGLGDTGHGWAEAFAGIRSSHIKYICPHAPVRPVTLN MNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRIILGGFSQGPIGGANR DISILQCHGDCDPLVPLMFGSLTVEKLKTLVNPANVTFKTYEGMMHSSCQQEMMDVKQFIDKLL PPID hide sequence

RefSeq Acc Id:	NP_001266287 ⟸ NM_001279358
- Peptide Label:	isoform 4
- UniProtKB:	B4DJV9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MCGNNMSTPLPAIVPAARKATAAVIFLHGLGDTGHGWAEAFAGIRSSHIKYICPHAPVRPVTLN MNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRIILGGFSQGGALSLYT ALTTQQKLAGVTALSCWLPLRASFPQCHGDCDPLVPLMFGSLTVEKLKTLVNPANVTFKTYEGM MHSSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	NP_001266289 ⟸ NM_001279360
- Peptide Label:	isoform 6
- UniProtKB:	A0A087X1K9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRIILGGFSQGGALSLYT ALTTQQKLAGVTALSCWLPLRASFPQGPIGGANRDISILQCHGDCDPLVPLMFGSLTVEKLKTL VNPANVTFKTYEGMMHSSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	XP_005251184 ⟸ XM_005251127
- Peptide Label:	isoform X5
- Sequence:	show sequence MGRSLCRPVRPVTLNMNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRI ILGGFSQGGALSLYTALTTQQKLAGVTALSCWLPLRASFPQGPIGGANRDISILQCHGDCDPLV PLMFGSLTVEKLKTLVNPANVTFKTYEGMMHSSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	XP_016868447 ⟸ XM_017012958
- Peptide Label:	isoform X6
- Sequence:	show sequence MGRSLCRPVRPVTLNMNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRI ILGGFSQGGALSLYTALTTQQKLAGVTALSCWLPLRASFPQCHGDCDPLVPLMFGSLTVEKLKT LVNPANVTFKTYEGMMHSSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	XP_016868449 ⟸ XM_017012960
- Peptide Label:	isoform X7
- UniProtKB:	A0A087X1K9 (UniProtKB/TrEMBL)
- Sequence:	show sequence MNVAMPSWFDIIGLSPDSQEDESGIKQAAENIKALIDQEVKNGIPSNRIILGGFSQGGALSLYT ALTTQQKLAGVTALSCWLPLRASFPQGPIGGANRDISILQCHGDCDPLVPLMFGSLTVEKLKTL VNPANVTFKTYEGMMHSSCQQEMMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:	XP_016868445 ⟸ XM_017012956
- Peptide Label:	isoform X3
- UniProtKB:	E5RGR0 (UniProtKB/TrEMBL)
- Sequence:	show sequence MCGNNMSTPLPAIVPAARKATAAVIFLHGLGDTGPVRPVTLNMNVAMPSWFDIIGLSPDSQEDE SGIKQAAENIKALIDQEVKNGIPSNRIILGGFSQGGALSLYTALTTQQKLAGVTALSCWLPLRA SFPQGPIGGANRDISILQCHGDCDPLVPLMFGSLTVEKLKTLVNPANVTFKTYEGMMHSSCQQE MMDVKQFIDKLLPPID hide sequence

RefSeq Acc Id:

ENSP00000428729 ⟸ ENST00000518546

RefSeq Acc Id:

ENSP00000428306 ⟸ ENST00000521352

RefSeq Acc Id:

ENSP00000430791 ⟸ ENST00000521898

RefSeq Acc Id:

ENSP00000427967 ⟸ ENST00000522007

RefSeq Acc Id:

ENSP00000484280 ⟸ ENST00000618741

RefSeq Acc Id:

ENSP00000482430 ⟸ ENST00000618914

RefSeq Acc Id:

ENSP00000320043 ⟸ ENST00000316963

RefSeq Acc Id:

ENSP00000344477 ⟸ ENST00000343231

RefSeq Acc Id:	XP_047277181 ⟸ XM_047421225
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_047277184 ⟸ XM_047421228
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_047277182 ⟸ XM_047421226
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_047277183 ⟸ XM_047421227
- Peptide Label:	isoform X7
- UniProtKB:	A0A087X1K9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_047277180 ⟸ XM_047421224
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_047277179 ⟸ XM_047421223
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054215515 ⟸ XM_054359540
- Peptide Label:	isoform X4

RefSeq Acc Id:	XP_054215514 ⟸ XM_054359539
- Peptide Label:	isoform X3

RefSeq Acc Id:	XP_054215518 ⟸ XM_054359543
- Peptide Label:	isoform X6

RefSeq Acc Id:	XP_054215521 ⟸ XM_054359546
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054215520 ⟸ XM_054359545
- Peptide Label:	isoform X7
- UniProtKB:	A0A087X1K9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054215516 ⟸ XM_054359541
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054215517 ⟸ XM_054359542
- Peptide Label:	isoform X5

RefSeq Acc Id:	XP_054215519 ⟸ XM_054359544
- Peptide Label:	isoform X7
- UniProtKB:	A0A087X1K9 (UniProtKB/TrEMBL)

RefSeq Acc Id:	XP_054215512 ⟸ XM_054359537
- Peptide Label:	isoform X2

RefSeq Acc Id:	XP_054215511 ⟸ XM_054359536
- Peptide Label:	isoform X1

RefSeq Acc Id:	XP_054215513 ⟸ XM_054359538
- Peptide Label:	isoform X8

Protein Domains

Phospholipase/carboxylesterase/thioesterase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-O75608-F1-model_v2	AlphaFold	O75608	1-230	view protein structure

Promoters

RGD ID:

7213317

Promoter ID:

EPDNEW_H12403

Type:

initiation region

Name:

LYPLA1_1

Description:

lysophospholipase I

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H12404

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,101,854 - 54,101,914	EPDNEW

RGD ID:

7213315

Promoter ID:

EPDNEW_H12404

Type:

initiation region

Name:

LYPLA1_2

Description:

lysophospholipase I

SO ACC ID:

SO:0000170

Source:

EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)

Alternative Promoters:

null; see alsoEPDNEW_H12403

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	8	54,101,960 - 54,102,020	EPDNEW

RGD ID:

6806858

Promoter ID:

HG_KWN:61298

Type:

CpG-Island

SO ACC ID:

SO:0000170

Source:

MPROMDB

Tissues & Cell Lines:

CD4+TCell, CD4+TCell_12Hour, HeLa_S3, Jurkat, K562, Lymphoblastoid, NB4

Transcripts:

NM_006330, UC003XRZ.1

Position:

Human Assembly	Chr	Position (strand)	Source
Build 36	8	55,176,854 - 55,177,354 (-)	MPROMDB

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:6737	AgrOrtholog
COSMIC	LYPLA1	COSMIC
Ensembl Genes	ENSG00000120992	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000316963	ENTREZGENE
	ENST00000316963.8	UniProtKB/Swiss-Prot
	ENST00000343231	ENTREZGENE
	ENST00000343231.10	UniProtKB/Swiss-Prot
	ENST00000518546.5	UniProtKB/TrEMBL
	ENST00000521352.5	UniProtKB/TrEMBL
	ENST00000521898.5	UniProtKB/TrEMBL
	ENST00000522007.5	UniProtKB/TrEMBL
	ENST00000618741	ENTREZGENE
	ENST00000618741.1	UniProtKB/TrEMBL
	ENST00000618914	ENTREZGENE
	ENST00000618914.4	UniProtKB/TrEMBL
Gene3D-CATH	3.40.50.1820	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx	ENSG00000120992	GTEx
HGNC ID	HGNC:6737	ENTREZGENE
Human Proteome Map	LYPLA1	Human Proteome Map
InterPro	AB_hydrolase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	PLipase/COase/thioEstase	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report	hsa:10434	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene	10434	ENTREZGENE
OMIM	605599	OMIM
PANTHER	ACYL-PROTEIN THIOESTERASE 1	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
	LYSOPHOSPHOLIPASE-RELATED	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam	Abhydrolase_2	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB	PA30499	PharmGKB
Superfamily-SCOP	SSF53474	UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt	A0A087X1K9	ENTREZGENE, UniProtKB/TrEMBL
	B4DJV9	ENTREZGENE, UniProtKB/TrEMBL
	B4DP64	ENTREZGENE, UniProtKB/TrEMBL
	E5RFT6_HUMAN	UniProtKB/TrEMBL
	E5RGR0	ENTREZGENE, UniProtKB/TrEMBL
	E5RI35_HUMAN	UniProtKB/TrEMBL
	E5RJ48_HUMAN	UniProtKB/TrEMBL
	LYPA1_HUMAN	UniProtKB/Swiss-Prot
	O43202	ENTREZGENE
	O75608	ENTREZGENE
	Q6IAQ1	ENTREZGENE, UniProtKB/TrEMBL
	Q9UQF9	ENTREZGENE
UniProt Secondary	O43202	UniProtKB/Swiss-Prot
	Q9UQF9	UniProtKB/Swiss-Prot

Nomenclature History

Date	Current Symbol	Current Name	Previous Symbol	Previous Name	Description	Reference	Status
2023-11-30	LYPLA1	lysophospholipase 1	LOC105375839	uncharacterized LOC105375839	GeneMerge from RGD:38655295	737654	PROVISIONAL
2018-10-30	LYPLA1	lysophospholipase 1		lysophospholipase I	Symbol and/or name change	5135510	APPROVED

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Imported Disease Annotations - ClinVar

Imported Annotations - SMPDB

Imported Annotations - KEGG (archival)

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Imported Disease Annotations - ClinVar

Imported Annotations - SMPDB

Imported Annotations - KEGG (archival)