PGLYRP2 (peptidoglycan recognition protein 2)

Gene: PGLYRP2 (peptidoglycan recognition protein 2) Homo sapiens

Analyze

Symbol:

PGLYRP2

Name:

peptidoglycan recognition protein 2

RGD ID:

1346354

HGNC Page

HGNC:30013

Description:

Enables N-acetylmuramoyl-L-alanine amidase activity; peptidoglycan binding activity; and peptidoglycan immune receptor activity. Involved in defense response to Gram-positive bacterium and detection of bacterium. Located in extracellular exosome.

Type:

protein-coding

RefSeq Status:

VALIDATED

Previously known as:

HMFT0141; N-acetylmuramoyl-L-alanine amidase; peptidoglycan recognition protein L; peptidoglycan recognition protein long; peptidoglycan recognition protein-like; PGLYRPL; PGRP-L; PGRPL; tagL; tagL-alpha; tagl-beta; TAGL-like

RGD Orthologs

Alliance Genes

More Info

more info ...

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	19	15,468,645 - 15,479,501 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	15,468,645 - 15,498,956 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	15,579,456 - 15,590,312 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	15,440,456 - 15,451,315 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	15,440,462 - 15,451,312	NCBI
Celera	19	15,476,268 - 15,487,143 (-)	NCBI		Celera
Cytogenetic Map	19	p13.12	NCBI
HuRef	19	15,147,207 - 15,158,066 (-)	NCBI		HuRef
CHM1_1	19	15,579,067 - 15,589,927 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	15,593,641 - 15,604,523 (-)	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

(1->4)-beta-D-glucan (ISO)

1,2-dimethylhydrazine (ISO)

17beta-estradiol (EXP)

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

2-hydroxypropanoic acid (EXP)

aflatoxin B1 (EXP,ISO)

Aflatoxin B2 alpha (EXP)

arsane (EXP)

arsenic atom (EXP)

benzo[a]pyrene (EXP,ISO)

benzo[e]pyrene (EXP)

Benzo[k]fluoranthene (ISO)

bosentan (EXP)

buta-1,3-diene (ISO)

chromium(6+) (ISO)

copper atom (EXP)

copper(0) (EXP)

cyclosporin A (EXP,ISO)

diazinon (EXP)

endosulfan (EXP)

gentamycin (ISO)

inulin (ISO)

Lasiocarpine (EXP)

lipopolysaccharide (EXP)

methapyrilene (EXP)

nickel atom (EXP)

O-methyleugenol (EXP)

paracetamol (EXP,ISO)

perfluorononanoic acid (EXP)

perfluorooctane-1-sulfonic acid (EXP,ISO)

phenobarbital (ISO)

pirinixic acid (ISO)

potassium dichromate (ISO)

propiconazole (ISO)

rac-lactic acid (EXP)

rotenone (ISO)

S-(1,2-dichlorovinyl)-L-cysteine (EXP)

silicon dioxide (ISO)

sodium arsenite (EXP)

tetrachloromethane (ISO)

thioacetamide (ISO)

titanium dioxide (ISO)

trichloroethene (ISO)

triptonide (ISO)

valproic acid (EXP,ISO)

zinc atom (EXP)

zinc(0) (EXP)

Gene Ontology Annotations Click to see Annotation Detail View

Biological Process

biological process involved in interaction with host (IEA,ISO)

defense response to Gram-positive bacterium (IBA,IDA,IEA)

detection of bacterium (IBA,IDA,IEA)

immune system process (IEA)

innate immune response (NAS)

negative regulation of natural killer cell differentiation involved in immune response (IEA,ISO)

negative regulation of type II interferon production (IEA,ISO)

peptide amidation (NAS)

peptidoglycan catabolic process (IEA)

regulation of inflammatory response (IEA,ISO)

Cellular Component

extracellular exosome (HDA)

extracellular region (IEA,TAS)

membrane (IEA,NAS)

Molecular Function

hydrolase activity (IEA)

metal ion binding (IEA)

N-acetylmuramoyl-L-alanine amidase activity (IDA,IEA,TAS)

peptidoglycan binding (IBA,IDA,IEA)

peptidoglycan immune receptor activity (IBA,IDA,IEA)

protein binding (IPI)

zinc ion binding (IEA)

References

References - curated

#	Reference Title	Reference Citation
1.	ClinVar Automated Import and Annotation Pipeline	RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2.	Data Import for Chemical-Gene Interactions	RGD automated import pipeline for gene-chemical interactions

Additional References at PubMed

PMID:7663175	PMID:11441184	PMID:11461926	PMID:11752456	PMID:12477932	PMID:12669421	PMID:12754519	PMID:12975309	PMID:14506276	PMID:14702039	PMID:15221005	PMID:15340057
PMID:15340161	PMID:16054449	PMID:16239516	PMID:16335952	PMID:16344560	PMID:16714290	PMID:17975119	PMID:18649358	PMID:19023099	PMID:20237496	PMID:21873635	PMID:23376485
PMID:23533145	PMID:24838182	PMID:25544563	PMID:26039076	PMID:29914927	PMID:31479523	PMID:32296183	PMID:32967043	PMID:33427621	PMID:34461924	PMID:35218888

Genomics

Comparative Map Data

PGLYRP2
(Homo sapiens - human)

Human Assembly	Chr	Position (strand)	Source	Genome Browsers
Human Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCh38	19	15,468,645 - 15,479,501 (-)	NCBI	GRCh38	GRCh38	hg38	GRCh38
GRCh38.p14 Ensembl	19	15,468,645 - 15,498,956 (-)	Ensembl	GRCh38		hg38	GRCh38
GRCh37	19	15,579,456 - 15,590,312 (-)	NCBI	GRCh37	GRCh37	hg19	GRCh37
Build 36	19	15,440,456 - 15,451,315 (-)	NCBI	NCBI36	Build 36	hg18	NCBI36
Build 34	19	15,440,462 - 15,451,312	NCBI
Celera	19	15,476,268 - 15,487,143 (-)	NCBI		Celera
Cytogenetic Map	19	p13.12	NCBI
HuRef	19	15,147,207 - 15,158,066 (-)	NCBI		HuRef
CHM1_1	19	15,579,067 - 15,589,927 (-)	NCBI		CHM1_1
T2T-CHM13v2.0	19	15,593,641 - 15,604,523 (-)	NCBI		T2T-CHM13v2.0

Pglyrp2
(Mus musculus - house mouse)

Mouse Assembly	Chr	Position (strand)	Source	Genome Browsers
Mouse Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCm39	17	32,631,433 - 32,643,157 (-)	NCBI	GRCm39	GRCm39	mm39
GRCm39 Ensembl	17	32,631,433 - 32,643,141 (-)	Ensembl		GRCm39 Ensembl
GRCm38	17	32,412,459 - 32,424,219 (-)	NCBI	GRCm38	GRCm38	mm10	GRCm38
GRCm38.p6 Ensembl	17	32,412,459 - 32,424,167 (-)	Ensembl	GRCm38		mm10	GRCm38
MGSCv37	17	32,550,045 - 32,557,920 (-)	NCBI	GRCm37	MGSCv37	mm9	NCBIm37
MGSCv36	17	32,550,306 - 32,561,112 (-)	NCBI		MGSCv36	mm8
Celera	17	33,325,622 - 33,333,482 (-)	NCBI		Celera
Cytogenetic Map	17	B1	NCBI
cM Map	17	17.56	NCBI

Pglyrp2
(Rattus norvegicus - Norway rat)

Rat Assembly	Chr	Position (strand)	Source	Genome Browsers
Rat Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
GRCr8	7	12,069,414 - 12,082,437 (-)	NCBI		GRCr8
mRatBN7.2	7	11,418,674 - 11,432,162 (-)	NCBI	mRatBN7.2	mRatBN7.2
mRatBN7.2 Ensembl	7	11,418,880 - 11,427,773 (-)	Ensembl		mRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx	7	14,237,304 - 14,246,286 (-)	NCBI	Rnor_SHR	UTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0	7	16,114,726 - 16,123,712 (-)	NCBI	Rnor_SHRSP	UTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0	7	13,986,312 - 13,995,267 (-)	NCBI	Rnor_WKY	UTH_Rnor_WKY_Bbb_1.0
Rnor_6.0	7	14,426,481 - 14,435,987 (-)	NCBI	Rnor6.0	Rnor_6.0	rn6	Rnor6.0
Rnor_6.0 Ensembl	7	14,429,701 - 14,435,967 (-)	Ensembl	Rnor6.0		rn6	Rnor6.0
Rnor_5.0	7	14,580,379 - 14,588,764 (-)	NCBI	Rnor5.0	Rnor_5.0	rn5	Rnor5.0
RGSC_v3.4	7	12,995,858 - 12,996,949 (-)	NCBI	RGSC3.4	RGSC_v3.4	rn4	RGSC3.4
Celera	7	9,530,143 - 9,537,285 (-)	NCBI		Celera
Cytogenetic Map	7	q11	NCBI

Pglyrp2
(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 Ensembl	NW_004955495	7,785,193 - 7,796,210 (+)	Ensembl	ChiLan1.0
ChiLan1.0	NW_004955495	7,785,398 - 7,792,158 (+)	NCBI	ChiLan1.0	ChiLan1.0

PGLYRP2
(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	20	20,378,029 - 20,396,483 (-)	NCBI		NHGRI_mPanPan1-v2
NHGRI_mPanPan1	19	19,380,830 - 19,399,218 (-)	NCBI		NHGRI_mPanPan1
Mhudiblu_PPA_v0	19	14,999,893 - 15,012,376 (-)	NCBI	Mhudiblu_PPA_v0	Mhudiblu_PPA_v0	panPan3
PanPan1.1	19	15,986,083 - 15,997,726 (-)	NCBI	panpan1.1	PanPan1.1	panPan2
PanPan1.1 Ensembl	19	15,986,090 - 15,997,726 (-)	Ensembl	panpan1.1		panPan2

PGLYRP2
(Canis lupus familiaris - dog)

Dog Assembly	Chr	Position (strand)	Source	Genome Browsers
Dog Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
CanFam3.1	20	46,724,906 - 46,730,227 (+)	NCBI	CanFam3.1	CanFam3.1	canFam3	CanFam3.1
CanFam3.1 Ensembl	20	46,726,224 - 46,730,321 (+)	Ensembl	CanFam3.1		canFam3	CanFam3.1
Dog10K_Boxer_Tasha	20	46,572,665 - 46,577,974 (+)	NCBI		Dog10K_Boxer_Tasha
ROS_Cfam_1.0	20	47,211,739 - 47,217,048 (+)	NCBI		ROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl	20	47,210,950 - 47,217,128 (+)	Ensembl		ROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1	20	46,446,615 - 46,451,923 (+)	NCBI		UMICH_Zoey_3.1
UNSW_CanFamBas_1.0	20	46,863,271 - 46,868,579 (+)	NCBI		UNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0	20	47,136,764 - 47,142,073 (+)	NCBI		UU_Cfam_GSD_1.0

Pglyrp2
(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_024405118	205,489,000 - 205,495,525 (+)	NCBI		HiC_Itri_2
SpeTri2.0 Ensembl	NW_004936596	5,038,452 - 5,044,569 (+)	Ensembl	SpeTri2.0	SpeTri2.0 Ensembl
SpeTri2.0	NW_004936596	5,038,452 - 5,043,172 (+)	NCBI	SpeTri2.0	SpeTri2.0		SpeTri2.0

PGLYRP2
(Sus scrofa - pig)

Pig Assembly	Chr	Position (strand)	Source	Genome Browsers
Pig Assembly	Chr	Position (strand)	Source	JBrowse	NCBI	UCSC	Ensembl
Sscrofa11.1 Ensembl	2	62,134,533 - 62,140,184 (+)	Ensembl	Sscrofa11.1		susScr11	Sscrofa11.1
Sscrofa11.1	2	62,135,578 - 62,140,180 (+)	NCBI	Sscrofa11.1	Sscrofa11.1	susScr11	Sscrofa11.1
Sscrofa10.2	2	61,567,649 - 61,572,250 (-)	NCBI	Sscrofa10.2	Sscrofa10.2	susScr3

PGLYRP2
(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	6	14,072,310 - 14,084,014 (-)	NCBI	ChlSab1.1	ChlSab1.1	chlSab2
ChlSab1.1 Ensembl	6	14,072,423 - 14,082,798 (-)	Ensembl	ChlSab1.1	ChlSab1.1 Ensembl	chlSab2
Vero_WHO_p1.0	NW_023666074	5,424,409 - 5,435,504 (+)	NCBI	Vero_WHO_p1.0	Vero_WHO_p1.0

Pglyrp2
(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_female_1.0 Ensembl	NW_004624901	2,554,048 - 2,561,826 (-)	Ensembl	HetGla_female_1.0	HetGla_female_1.0 Ensembl	hetGla2
HetGla 1.0	NW_004624901	2,554,303 - 2,562,436 (-)	NCBI	HetGla_female_1.0	HetGla 1.0	hetGla2

Variants

Variants in PGLYRP2
31 total Variants

Clinical Variants

Name	Type	Condition(s)	Position(s)	Clinical significance
GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3	copy number gain	See cases [RCV000052912]	Chr19:13974677..27839676 [GRCh38] Chr19:14085489..28330584 [GRCh37] Chr19:13946489..33022424 [NCBI36] Chr19:19p13.12-q11	pathogenic
GRCh38/hg38 19p13.12(chr19:15227306-15496644)x3	copy number gain	See cases [RCV000054146]	Chr19:15227306..15496644 [GRCh38] Chr19:15338117..15607455 [GRCh37] Chr19:15199117..15468455 [NCBI36] Chr19:19p13.12	uncertain significance
NM_052890.3(PGLYRP2):c.606C>T (p.Ser202=)	single nucleotide variant	Malignant melanoma [RCV000071966]	Chr19:15476064 [GRCh38] Chr19:15586875 [GRCh37] Chr19:15447875 [NCBI36] Chr19:19p13.12	not provided
GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	copy number gain	See cases [RCV000133888]	Chr19:11227942..44626354 [GRCh38] Chr19:11338618..45129651 [GRCh37] Chr19:11199618..49821491 [NCBI36] Chr19:19p13.2-q13.31	pathogenic
GRCh38/hg38 19p13.12-13.11(chr19:14154962-16914313)x1	copy number loss	See cases [RCV000134176]	Chr19:14154962..16914313 [GRCh38] Chr19:14265774..17025123 [GRCh37] Chr19:14126774..16886123 [NCBI36] Chr19:19p13.12-13.11	pathogenic
GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3	copy number gain	See cases [RCV000136696]	Chr19:15133594..24193591 [GRCh38] Chr19:15244405..24376393 [GRCh37] Chr19:15105405..24168233 [NCBI36] Chr19:19p13.12-12	pathogenic\|likely pathogenic
GRCh37/hg19 19p13.12-13.11(chr19:14124666-16431349)x1	copy number loss	See cases [RCV000448818]	Chr19:14124666..16431349 [GRCh37] Chr19:19p13.12-13.11	pathogenic
GRCh37/hg19 19p13.12-13.11(chr19:14883158-16788770)x1	copy number loss	See cases [RCV000511367]	Chr19:14883158..16788770 [GRCh37] Chr19:19p13.12-13.11	pathogenic
NM_052890.4(PGLYRP2):c.325G>T (p.Gly109Trp)	single nucleotide variant	Inborn genetic diseases [RCV003247505]	Chr19:15476345 [GRCh38] Chr19:15587156 [GRCh37] Chr19:19p13.12	uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	copy number gain	See cases [RCV000511289]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic\|uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	copy number gain	See cases [RCV000512296]	Chr19:260912..58956888 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3	copy number gain	not provided [RCV000752439]	Chr19:68029..59110290 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3	copy number gain	not provided [RCV000752444]	Chr19:260912..59097160 [GRCh37] Chr19:19p13.3-q13.43	pathogenic
GRCh37/hg19 19p13.12(chr19:15246479-15683078)x3	copy number gain	not provided [RCV000740052]	Chr19:15246479..15683078 [GRCh37] Chr19:19p13.12	benign
GRCh37/hg19 19p13.12(chr19:15278099-15710360)x3	copy number gain	not provided [RCV000740056]	Chr19:15278099..15710360 [GRCh37] Chr19:19p13.12	benign
GRCh37/hg19 19p13.12(chr19:15338105-15668026)x1	copy number loss	not provided [RCV000847812]	Chr19:15338105..15668026 [GRCh37] Chr19:19p13.12	uncertain significance
GRCh37/hg19 19p13.12(chr19:14368330-15712368)x1	copy number loss	not provided [RCV001007034]	Chr19:14368330..15712368 [GRCh37] Chr19:19p13.12	pathogenic
NM_052890.4(PGLYRP2):c.493G>A (p.Val165Ile)	single nucleotide variant	Inborn genetic diseases [RCV003273408]	Chr19:15476177 [GRCh38] Chr19:15586988 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.701G>T (p.Gly234Val)	single nucleotide variant	not provided [RCV000894148]	Chr19:15475969 [GRCh38] Chr19:15586780 [GRCh37] Chr19:19p13.12	benign
GRCh37/hg19 19p13.12-12(chr19:14286624-20956753)x3	copy number gain	not provided [RCV001259370]	Chr19:14286624..20956753 [GRCh37] Chr19:19p13.12-12	pathogenic
GRCh37/hg19 19p13.12(chr19:15184922-15582812)	copy number gain	not specified [RCV002052676]	Chr19:15184922..15582812 [GRCh37] Chr19:19p13.12	uncertain significance
GRCh37/hg19 19p13.12-13.11(chr19:14124666-16431349)	copy number loss	not specified [RCV002052675]	Chr19:14124666..16431349 [GRCh37] Chr19:19p13.12-13.11	pathogenic
NC_000019.9:g.(?_14847048)_(17394124_?)del	deletion	not provided [RCV003116664]	Chr19:14847048..17394124 [GRCh37] Chr19:19p13.12-13.11	uncertain significance
NM_052890.4(PGLYRP2):c.698G>C (p.Arg233Pro)	single nucleotide variant	Inborn genetic diseases [RCV002841324]	Chr19:15475972 [GRCh38] Chr19:15586783 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.1492A>G (p.Thr498Ala)	single nucleotide variant	Inborn genetic diseases [RCV002990325]	Chr19:15469781 [GRCh38] Chr19:15580592 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.1447G>A (p.Val483Met)	single nucleotide variant	Inborn genetic diseases [RCV002911840]	Chr19:15469826 [GRCh38] Chr19:15580637 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.1678A>G (p.Arg560Gly)	single nucleotide variant	Inborn genetic diseases [RCV002743228]	Chr19:15468716 [GRCh38] Chr19:15579527 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.877C>T (p.Arg293Trp)	single nucleotide variant	Inborn genetic diseases [RCV002955802]	Chr19:15475793 [GRCh38] Chr19:15586604 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.1295T>G (p.Met432Arg)	single nucleotide variant	Inborn genetic diseases [RCV002929830]	Chr19:15471938 [GRCh38] Chr19:15582749 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.595G>A (p.Val199Ile)	single nucleotide variant	Inborn genetic diseases [RCV002983914]	Chr19:15476075 [GRCh38] Chr19:15586886 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.674G>A (p.Gly225Glu)	single nucleotide variant	Inborn genetic diseases [RCV002696671]	Chr19:15475996 [GRCh38] Chr19:15586807 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.1400G>A (p.Gly467Asp)	single nucleotide variant	Inborn genetic diseases [RCV002875318]	Chr19:15469873 [GRCh38] Chr19:15580684 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.1668T>G (p.Ser556Arg)	single nucleotide variant	Inborn genetic diseases [RCV002697164]	Chr19:15468726 [GRCh38] Chr19:15579537 [GRCh37] Chr19:19p13.12	likely benign
NM_052890.4(PGLYRP2):c.1199T>C (p.Leu400Pro)	single nucleotide variant	Inborn genetic diseases [RCV002747190]	Chr19:15472034 [GRCh38] Chr19:15582845 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.304G>A (p.Val102Ile)	single nucleotide variant	Inborn genetic diseases [RCV002652742]	Chr19:15476366 [GRCh38] Chr19:15587177 [GRCh37] Chr19:19p13.12	uncertain significance
GRCh38/hg38 19p13.12-13.11(chr19:15014099-16261691)	copy number loss	Chromosome 19p13.13 deletion syndrome [RCV003223562]	Chr19:15014099..16261691 [GRCh38] Chr19:19p13.12-13.11	pathogenic\|uncertain significance
NM_052890.4(PGLYRP2):c.404G>A (p.Arg135His)	single nucleotide variant	Inborn genetic diseases [RCV003202923]	Chr19:15476266 [GRCh38] Chr19:15587077 [GRCh37] Chr19:19p13.12	likely benign
NM_052890.4(PGLYRP2):c.325G>C (p.Gly109Arg)	single nucleotide variant	Inborn genetic diseases [RCV003217131]	Chr19:15476345 [GRCh38] Chr19:15587156 [GRCh37] Chr19:19p13.12	uncertain significance
NM_052890.4(PGLYRP2):c.1025T>G (p.Leu342Arg)	single nucleotide variant	Inborn genetic diseases [RCV003376353]	Chr19:15475645 [GRCh38] Chr19:15586456 [GRCh37] Chr19:19p13.12	uncertain significance
GRCh37/hg19 19p13.12-13.11(chr19:14888106-17360864)x3	copy number gain	not provided [RCV003485195]	Chr19:14888106..17360864 [GRCh37] Chr19:19p13.12-13.11	uncertain significance
GRCh37/hg19 19p13.13-13.11(chr19:13970692-18139376)x3	copy number gain	not specified [RCV003986122]	Chr19:13970692..18139376 [GRCh37] Chr19:19p13.13-13.11	uncertain significance
GRCh37/hg19 19p13.12(chr19:15263384-15683826)x3	copy number gain	not specified [RCV003986112]	Chr19:15263384..15683826 [GRCh37] Chr19:19p13.12	uncertain significance

miRNA Target Status

Predicted Target Of

	Summary Value
Count of predictions:	1195
Count of miRNA genes:	723
Interacting mature miRNAs:	814
Transcripts:	ENST00000292609, ENST00000340880, ENST00000594637, ENST00000601792
Prediction methods:	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

PGLYRP2_3637

Human Assembly	Chr	Position (strand)	Source	JBrowse
GRCh37	19	15,579,384 - 15,580,182	UniSTS	GRCh37
Build 36	19	15,440,384 - 15,441,182	RGD	NCBI36
Celera	19	15,476,196 - 15,476,994	RGD
HuRef	19	15,147,135 - 15,147,933	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

adipose tissue

appendage

High

Medium

375

120

Low

105

153

350

Below cutoff

1391

1761

840

152

1414

2575

838

1482

148

621

1120

136

841

1585

View RNA-SEQ Expression Data

Sequence

Nucleotide Sequences


RefSeq Transcripts	NM_001363546	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	NM_052890	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
GenBank Nucleotide	AB073610	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AC011492	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AF384856	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK055882	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK289415	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AK292292	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	AY358156	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC136551	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC136552	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	BC144238	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CH471106	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	CP068259	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles
	DB041324	(Get FASTA)	NCBI Sequence Viewer	Search GEO for Microarray Profiles

RefSeq Acc Id:

ENST00000292609 ⟹ ENSP00000292609

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	15,468,645 - 15,479,501 (-)	Ensembl

RefSeq Acc Id:

ENST00000340880 ⟹ ENSP00000345968

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	15,468,645 - 15,479,501 (-)	Ensembl

RefSeq Acc Id:

ENST00000594637 ⟹ ENSP00000470112

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	15,476,353 - 15,479,831 (-)	Ensembl

RefSeq Acc Id:

ENST00000601792 ⟹ ENSP00000472856

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38.p14 Ensembl	19	15,476,235 - 15,498,956 (-)	Ensembl

RefSeq Acc Id:

NM_001363546 ⟹ NP_001350475

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	15,468,645 - 15,479,501 (-)	NCBI
T2T-CHM13v2.0	19	15,593,641 - 15,604,523 (-)	NCBI

Sequence:

show sequence

ATTCGCCGCTGGACTTTGACAGTGGTCAAAGGCTCTGCTCAGTTCTCTGTGCCTGTCTCCCTCC
AGCACTGCCGAGGTTCTCTGCCGAGGCCAACCAGAAATACCCCTTGGAAGCTGGAATCCTGCAA
CAATGGCCCAGGGTGTCCTCTGGATCCTACTCGGATTGCTACTGTGGTCAGACCCAGGGACAGC
CTCCCTGCCCCTGCTCATGGACTCTGTCATCCAGGCCCTGGCTGAGCTGGAGCAGAAAGTGCCA
GCTGCCAAGACCAGACACACAGCTTCTGCGTGGCTGATGTCAGCTCCAAACTCTGGCCCCCACA
ATCGCCTCTACCACTTCCTGCTGGGGGCATGGAGCCTCAATGCTACAGAGTTGGATCCCTGCCC
ACTAAGCCCAGAGCTGTTAGGCCTGACCAAGGAGGTGGCCCGACATGACGTACGAGAAGGGAAG
GAATATGGGGTGGTGCTGGCACCTGATGGCTCGACCGTGGCTGTGGAGCCTCTGCTGGCGGGGC
TGGAGGCAGGGCTGCAAGGGCGCAGGGTCATAAATTTGCCCTTGGACAGCATGGCTGCCCCTTG
GGAGACTGGAGATACCTTTCCAGATGTTGTGGCCATTGCTCCAGATGTAAGAGCCACCTCCTCC
CCAGGACTCAGGGATGGCTCTCCAGATGTCACCACTGCAGATATTGGAGCCAACACTCCAGATG
CTACAAAAGGCTGTCCAGATGTCCAAGCTTCCTTGCCAGATGCCAAAGCCAAGTCCCCACCGAC
CATGGTGGACAGCCTCCTGGCAGTCACCCTGGCTGGAAACCTGGGCCTGACCTTCCTCCGAGGT
TCCCAGACCCAGAGCCATCCAGACCTGGGAACTGAGGGCTGCTGGGACCAGCTCTCTGCCCCTC
GGACCTTTACGCTTTTGGACCCCAAGGCATCTCTGTTAACCATGGCCTTCCTCAATGGCGCCCT
GGATGGGGTCATCCTTGGAGACTACCTGAGCCGGACTCCTGAGCCCCGGCCATCCCTCAGCCAC
TTGCTGAGCCAGTACTATGGGGCTGGGGTGGCCAGAGACCCAGGGTTCCGCAGCAACTTCCGAC
GGCAGAACGGTGCTGCTCTGACTTCAGCCTCCATCCTGGCCCAGCAGGTGTGGGGAACCCTTGT
CCTTCTACAGAGGCTGGAGCCAGTACACCTCCAGCTTCAGTGCATGAGCCAAGAACAGCTGGCC
CAGGTGGCTGCCAATGCTACCAAGGAATTCACTGAGGCCTTCCTGGGATGCCCGGCCATCCACC
CCCGCTGCCGCTGGGGAGCGGCGCCTTATCGGGGCCGCCCGAAGCTGCTGCAGCTGCCGCTGGG
ATTCTTGTACGTGCATCACACCTACGTGCCTGCACCACCCTGCACGGACTTCACGCGCTGCGCA
GCCAACATGCGCTCCATGCAGCGCTACCACCAGGACACGCAAGGCTGGGGAGACATCGGCTACA
GTTTCGTGGTGGGCTCGGACGGCTACGTGTACGAGGGACGCGGCTGGCACTGGGTGGGCGCCCA
CACGCTCGGCCACAACTCCCGGGGCTTCGGCGTGGCCATAGTGGGCAACTACACCGCGGCGCTG
CCCACCGAGGCCGCTCTGCGCACGGTGCGCGACACGCTCCCGAGTTGTGCGGTGCGCGCCGGCC
TCCTGCGGCCAGACTACGCGCTGCTGGGCCACCGCCAGCTGGTGCGCACCGACTGCCCCGGCGA
CGCGCTCTTCGACCTGCTGCGCACCTGGCCGCACTTCACCGCGGTGAGTCTTCGCAGCCTGCAC
TACACGGCCCGCCGCCCCTCCGTCTACACAAGCTCCACGAGGCCCCTGCCCCCTGCCTGTAACA
GCTGTGCCCGCACAGCCTCAGCCAGGCCCCCAACTTCCCGGCGGCACGTCTATTCAGGAAACCT
AGGCCCAGCCTTTGCGGGTCACTCTGCGGGCAACATCCCTGATCCTGTGACTTCTGCCTATGCA
GCCTCAGCTCAGCCCCAGACCCAGCCAGCCTGTCCTTTCCCCAGCTCCTAATACCTCTACCTTT
CCAGCCAAGGCATGGACCCTGACACCTGCCAACAGCCCCTCTGCCCTCACAACCTCAGCCTGGC
CTTCATGACTTCTCTACCCAAGTCACAACCTGTCAGGCTGCACCACCTCATCCTGGCCCGCCGA
ACCTTGACCTCACCCCTGCCCCTACCCGAAGGCCCTCTGTCCACACAACATGAACCTAGGCTGT
GACCTTTTGCCTTCACAACCTCTGTCCAGTCCTTAATCCTGTGTTGCAATTCTCTGTCCAGACA
ATCTCAACTCTGAGGTTGCTTGTTTCGTCCCTGACTCCTTAACCCCTGATGACAACTCTTATGC
CAGCACAACTTTGACCTGATGACCTCATCCCAGCCCTTGATCGCCATCACTAAAACAATTTTAG
AATCACACCTGGACAATCTCGTGCTACCTACATACTGCCACTCCATTTCATTAAGCTATTGACT
AGCACATCCATCTCGGCCTATAGTTGGCTTTGTCCTCACTCTCTCACTTTGGGCCACTGTCCCC
TCCCTGATCCAGGGTTCCACCACCAGGAGGGCAGACCCAGCCACATACCACAACCACCCCCAAG
CCTCACACTCCCTTGTCTTTTTCCAGACTGTTAAGCCAAGACCTGCCAGGAGTGTCTCTAAGAG
ATCCAGGAGGGAGCCACCCCCAAGGACCCTGCCAGCCACAGACCTCCAATAAAGACAGCATGGA
AACAAA

hide sequence

RefSeq Acc Id:

NM_052890 ⟹ NP_443122

RefSeq Status:

VALIDATED

Type:

CODING

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	15,468,645 - 15,479,501 (-)	NCBI
GRCh37	19	15,579,456 - 15,590,315 (-)	ENTREZGENE
Build 36	19	15,440,456 - 15,451,315 (-)	NCBI Archive
HuRef	19	15,147,207 - 15,158,066 (-)	ENTREZGENE
CHM1_1	19	15,579,067 - 15,589,927 (-)	NCBI
T2T-CHM13v2.0	19	15,593,641 - 15,604,523 (-)	NCBI

Sequence:

show sequence

ATTCGCCGCTGGACTTTGACAGTGGTCAAAGGCTCTGCTCAGTTCTCTGTGCCTGTCTCCCTCC
AGCACTGCCGAGGTTCTCTGCCGAGGCCAACCAGAAATACCCCTTGGAAGCTGGAATCCTGCAA
CAATGGCCCAGGGTGTCCTCTGGATCCTACTCGGATTGCTACTGTGGTCAGACCCAGGGACAGC
CTCCCTGCCCCTGCTCATGGACTCTGTCATCCAGGCCCTGGCTGAGCTGGAGCAGAAAGTGCCA
GCTGCCAAGACCAGACACACAGCTTCTGCGTGGCTGATGTCAGCTCCAAACTCTGGCCCCCACA
ATCGCCTCTACCACTTCCTGCTGGGGGCATGGAGCCTCAATGCTACAGAGTTGGATCCCTGCCC
ACTAAGCCCAGAGCTGTTAGGCCTGACCAAGGAGGTGGCCCGACATGACGTACGAGAAGGGAAG
GAATATGGGGTGGTGCTGGCACCTGATGGCTCGACCGTGGCTGTGGAGCCTCTGCTGGCGGGGC
TGGAGGCAGGGCTGCAAGGGCGCAGGGTCATAAATTTGCCCTTGGACAGCATGGCTGCCCCTTG
GGAGACTGGAGATACCTTTCCAGATGTTGTGGCCATTGCTCCAGATGTAAGAGCCACCTCCTCC
CCAGGACTCAGGGATGGCTCTCCAGATGTCACCACTGCAGATATTGGAGCCAACACTCCAGATG
CTACAAAAGGCTGTCCAGATGTCCAAGCTTCCTTGCCAGATGCCAAAGCCAAGTCCCCACCGAC
CATGGTGGACAGCCTCCTGGCAGTCACCCTGGCTGGAAACCTGGGCCTGACCTTCCTCCGAGGT
TCCCAGACCCAGAGCCATCCAGACCTGGGAACTGAGGGCTGCTGGGACCAGCTCTCTGCCCCTC
GGACCTTTACGCTTTTGGACCCCAAGGCATCTCTGTTAACCATGGCCTTCCTCAATGGCGCCCT
GGATGGGGTCATCCTTGGAGACTACCTGAGCCGGACTCCTGAGCCCCGGCCATCCCTCAGCCAC
TTGCTGAGCCAGTACTATGGGGCTGGGGTGGCCAGAGACCCAGGGTTCCGCAGCAACTTCCGAC
GGCAGAACGGTGCTGCTCTGACTTCAGCCTCCATCCTGGCCCAGCAGGTGTGGGGAACCCTTGT
CCTTCTACAGAGGCTGGAGCCAGTACACCTCCAGCTTCAGTGCATGAGCCAAGAACAGCTGGCC
CAGGTGGCTGCCAATGCTACCAAGGAATTCACTGAGGCCTTCCTGGGATGCCCGGCCATCCACC
CCCGCTGCCGCTGGGGAGCGGCGCCTTATCGGGGCCGCCCGAAGCTGCTGCAGCTGCCGCTGGG
ATTCTTGTACGTGCATCACACCTACGTGCCTGCACCACCCTGCACGGACTTCACGCGCTGCGCA
GCCAACATGCGCTCCATGCAGCGCTACCACCAGGACACGCAAGGCTGGGGAGACATCGGCTACA
GTTTCGTGGTGGGCTCGGACGGCTACGTGTACGAGGGACGCGGCTGGCACTGGGTGGGCGCCCA
CACGCTCGGCCACAACTCCCGGGGCTTCGGCGTGGCCATAGTGGGCAACTACACCGCGGCGCTG
CCCACCGAGGCCGCTCTGCGCACGGTGCGCGACACGCTCCCGAGTTGTGCGGTGCGCGCCGGCC
TCCTGCGGCCAGACTACGCGCTGCTGGGCCACCGCCAGCTGGTGCGCACCGACTGCCCCGGCGA
CGCGCTCTTCGACCTGCTGCGCACCTGGCCGCACTTCACCGCGACTGTTAAGCCAAGACCTGCC
AGGAGTGTCTCTAAGAGATCCAGGAGGGAGCCACCCCCAAGGACCCTGCCAGCCACAGACCTCC
AATAAAGACAGCATGGAAACAAA

hide sequence

Protein Sequences


Protein RefSeqs	NP_001350475	(Get FASTA)	NCBI Sequence Viewer
	NP_443122	(Get FASTA)	NCBI Sequence Viewer
GenBank Protein	AAI36552	(Get FASTA)	NCBI Sequence Viewer
	AAI36553	(Get FASTA)	NCBI Sequence Viewer
	AAI44239	(Get FASTA)	NCBI Sequence Viewer
	AAL05629	(Get FASTA)	NCBI Sequence Viewer
	AAQ88523	(Get FASTA)	NCBI Sequence Viewer
	BAB71034	(Get FASTA)	NCBI Sequence Viewer
	BAD38647	(Get FASTA)	NCBI Sequence Viewer
	BAF82104	(Get FASTA)	NCBI Sequence Viewer
	BAF84981	(Get FASTA)	NCBI Sequence Viewer
	EAW84482	(Get FASTA)	NCBI Sequence Viewer
	EAW84483	(Get FASTA)	NCBI Sequence Viewer
Ensembl Protein	ENSP00000292609
	ENSP00000292609.3
	ENSP00000345968
	ENSP00000345968.4
	ENSP00000470112.1
	ENSP00000472856.2
GenBank Protein	Q96PD5	(Get FASTA)	NCBI Sequence Viewer

RefSeq Acc Id:	NP_443122 ⟸ NM_052890
- Peptide Label:	isoform 1 precursor
- UniProtKB:	Q96N74 (UniProtKB/Swiss-Prot), Q68CK1 (UniProtKB/Swiss-Prot), B7ZM33 (UniProtKB/Swiss-Prot), B2RMZ2 (UniProtKB/Swiss-Prot), A8K8C7 (UniProtKB/Swiss-Prot), A8K050 (UniProtKB/Swiss-Prot), Q9UC60 (UniProtKB/Swiss-Prot), Q96PD5 (UniProtKB/Swiss-Prot)
- Sequence:	show sequence MAQGVLWILLGLLLWSDPGTASLPLLMDSVIQALAELEQKVPAAKTRHTASAWLMSAPNSGPHN RLYHFLLGAWSLNATELDPCPLSPELLGLTKEVARHDVREGKEYGVVLAPDGSTVAVEPLLAGL EAGLQGRRVINLPLDSMAAPWETGDTFPDVVAIAPDVRATSSPGLRDGSPDVTTADIGANTPDA TKGCPDVQASLPDAKAKSPPTMVDSLLAVTLAGNLGLTFLRGSQTQSHPDLGTEGCWDQLSAPR TFTLLDPKASLLTMAFLNGALDGVILGDYLSRTPEPRPSLSHLLSQYYGAGVARDPGFRSNFRR QNGAALTSASILAQQVWGTLVLLQRLEPVHLQLQCMSQEQLAQVAANATKEFTEAFLGCPAIHP RCRWGAAPYRGRPKLLQLPLGFLYVHHTYVPAPPCTDFTRCAANMRSMQRYHQDTQGWGDIGYS FVVGSDGYVYEGRGWHWVGAHTLGHNSRGFGVAIVGNYTAALPTEAALRTVRDTLPSCAVRAGL LRPDYALLGHRQLVRTDCPGDALFDLLRTWPHFTATVKPRPARSVSKRSRREPPPRTLPATDLQ hide sequence

RefSeq Acc Id:	NP_001350475 ⟸ NM_001363546
- Peptide Label:	isoform 2 precursor

RefSeq Acc Id:

ENSP00000470112 ⟸ ENST00000594637

RefSeq Acc Id:

ENSP00000292609 ⟸ ENST00000292609

RefSeq Acc Id:

ENSP00000472856 ⟸ ENST00000601792

RefSeq Acc Id:

ENSP00000345968 ⟸ ENST00000340880

Protein Domains

N-acetylmuramoyl-L-alanine amidase

Protein Structures

Name	Modeler	Protein Id	AA Range	Protein Structure
AF-Q96PD5-F1-model_v2	AlphaFold	Q96PD5	1-576	view protein structure

Promoters

RGD ID:

7238905

Promoter ID:

EPDNEW_H25198

Type:

initiation region

Name:

PGLYRP2_1

Description:

peptidoglycan recognition protein 2

SO ACC ID:

SO:0000170

Source:

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

Experiment Methods:

Single-end sequencing.

Position:

Human Assembly	Chr	Position (strand)	Source
GRCh38	19	15,479,501 - 15,479,561	EPDNEW

Additional Information

External Database Links

Database	Acc Id	Source(s)
AGR Gene	HGNC:30013	AgrOrtholog
COSMIC	PGLYRP2	COSMIC
Ensembl Genes	ENSG00000161031	Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript	ENST00000292609	ENTREZGENE
	ENST00000292609.8	UniProtKB/Swiss-Prot
	ENST00000340880	ENTREZGENE
	ENST00000340880.5	UniProtKB/Swiss-Prot
	ENST00000594637.1	UniProtKB/TrEMBL
	ENST00000601792.1	UniProtKB/TrEMBL
Gene3D-CATH	3.40.80.10	UniProtKB/Swiss-Prot
GTEx	ENSG00000161031	GTEx
HGNC ID	HGNC:30013	ENTREZGENE
Human Proteome Map	PGLYRP2	Human Proteome Map
InterPro	Amidase/PGRP_sf	UniProtKB/Swiss-Prot
	Amidase_domain	UniProtKB/Swiss-Prot
	PGRP	UniProtKB/Swiss-Prot
	PGRP_domain_met/bac	UniProtKB/Swiss-Prot
KEGG Report	hsa:114770	UniProtKB/Swiss-Prot
NCBI Gene	114770	ENTREZGENE
OMIM	608199	OMIM
PANTHER	N-ACETYLMURAMOYL-L-ALANINE AMIDASE	UniProtKB/Swiss-Prot
	PTHR11022	UniProtKB/Swiss-Prot
Pfam	Amidase_2	UniProtKB/Swiss-Prot
PharmGKB	PA134929965	PharmGKB
SMART	Ami_2	UniProtKB/Swiss-Prot
	PGRP	UniProtKB/Swiss-Prot
Superfamily-SCOP	SSF55846	UniProtKB/Swiss-Prot
UniProt	A8K050	ENTREZGENE
	A8K8C7	ENTREZGENE
	B2RMZ2	ENTREZGENE
	B7ZM33	ENTREZGENE
	M0QYW3_HUMAN	UniProtKB/TrEMBL
	M0R2W8_HUMAN	UniProtKB/TrEMBL
	PGRP2_HUMAN	UniProtKB/Swiss-Prot
	Q68CK1	ENTREZGENE
	Q96N74	ENTREZGENE
	Q96PD5	ENTREZGENE
	Q9UC60	ENTREZGENE
UniProt Secondary	A8K050	UniProtKB/Swiss-Prot
	A8K8C7	UniProtKB/Swiss-Prot
	B2RMZ2	UniProtKB/Swiss-Prot
	B7ZM33	UniProtKB/Swiss-Prot
	Q68CK1	UniProtKB/Swiss-Prot
	Q96N74	UniProtKB/Swiss-Prot
	Q9UC60	UniProtKB/Swiss-Prot

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)

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Imported Disease Annotations - ClinVar