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Category Symbol Source: HGNC EntrezGene Ensembl GeneCards RNA genes CroW21

GIFtS
-

NINJ2 Gene

protein-coding GIFtS: 47
GCID: GC12M000673

ninjurin 2

Explore 5 diseases affiliated with
NINJ2 via

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Human Malady Compendium

(According to ¹HGNC, ²Entrez Gene,
³UniProtKB/Swiss-Prot, ⁴UniProtKB/TrEMBL, ⁵OMIM, ⁶GeneLoc, ⁷Ensembl, ⁸DME, ⁹miRBase, and/or ¹⁰fRNAdb)
About This Section

Aliases
Ninjurin 2¹ ²
Nerve Injury-Induced Protein 2² ³
Ninjurin-2¹

External Ids:	HGNC: 7825¹	Entrez Gene: 4815²	Ensembl: ENSG00000171840⁷	OMIM: 607297⁵	UniProtKB: Q9NZG7³

Export aliases for NINJ2 gene to outside databases

Previous GC identifers: GC12M000526 GC12M000543

(According to Entrez Gene, Tocris Bioscience, Wikipedia's Gene Wiki, PharmGKB,
UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL)
About This Section

Entrez Gene summary for NINJ2:

The protein encoded by this gene belongs to the ninjurin (for nerve injury induced) family. It is a cell surface

adhesion protein that is upregulated in Schwann cells surrounding the distal segment of injured nerve, and promotes

neurite outgrowth, thus may have a role in nerve regeneration after nerve injury. (provided by RefSeq, Oct 2011)

UniProtKB/Swiss-Prot: NINJ2_HUMAN, Q9NZG7

Function: Homophilic cell adhesion molecule that promotes axonal growth. May play a role in nerve regeneration and in

the formation and function of other tissues

(According to GeneLoc and/or HGNC, and/or
Entrez Gene (NCBI build 37),
and/or miRBase,
Genomic Views according to UCSC (hg19) and Ensembl (release 69), Regulatory elements and Epigenetics data according to QIAGEN, SABiosciences, and/or SwitchGear Genomics)
About This Section

RefSeq DNA sequence:

NC_000012.11 NC_018923.1 NT_009759.16

Regulatory elements:

SABiosciences Regulatory transcription factor binding sites in the NINJ2 gene promoter:
Bach2 Brachyury FOXO3 GATA-1 C/EBPalpha FOXO3b HOXA5 FOXO4 FOXO3a FOXO1
Other transcription factors

SwitchGear Promoter luciferase reporter plasmid: NINJ2 promoter sequence

Search SABiosciences Chromatin IP Primers for NINJ2

Epigenetics:

QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat NINJ2

Genomic Location:
Genomic View: UCSC Golden Path with GeneCards custom track

Entrez Gene cytogenetic band: 12p13 Ensembl cytogenetic band: 12p13.33 HGNC cytogenetic band: 12p13

NINJ2 Gene in genomic location: bands according to Ensembl, locations according to (and/or Entrez Gene and/or Ensembl if different)
NINJ2 gene location

GeneLoc information about chromosome 12 GeneLoc Exon Structure

GeneLoc location for GC12M000673: view genomic region (about GC identifiers)

Start:	673,462 bp from pter	End:	772,945 bp from pter
Size:	99,484 bases	Orientation:	minus strand

(According to ¹UniProtKB, HORDE, neXtProt, Ensembl, and/or Reactome, Modification sites according to ²PhosphoSitePlus, Specific Peptides from DME, Protein expression images according to data from SPIRE MOPED and PaxDb, RefSeq according to NCBI, PDB rendering according to OCA and/or Proteopedia, Recombinant Proteins from EMD Millipore, R&D Systems, GenScript, Enzo Life Sciences, OriGene, Novus Biologicals, Sino Biological, ProSpec, and/or Uscn,
Biochemical Assays by EMD Millipore, R&D Systems, OriGene, GenScript, Cell Signaling Technology, Enzo Life Sciences, and/or Uscn, Ontologies according to Gene Ontology Consortium 01 Mar 2013 and Entrez Gene, Antibodies by EMD Millipore, R&D Systems, GenScript, Cell Signaling Technology, OriGene, Novus Biologicals, Thermo Fisher Scientific, Abcam, and/or Uscn)
About This Section

UniProtKB/Swiss-Prot: NINJ2_HUMAN, Q9NZG7 (See protein sequence)

Recommended Name: Ninjurin-2

Size: 142 amino acids; 15680 Da

Subcellular location: Membrane; Multi-pass membrane protein

Sequence caution: Sequence=AAH57766.2; Type=Erroneous initiation; Note=Translation N-terminally shortened;

Explore the universe of human proteins at neXtProt for NINJ2: NX_Q9NZG7

NINJ2 Protein expression data from MOPED and PaxDb: About this image

REFSEQ proteins: NP_057617.2

ENSEMBL proteins:

ENSP00000307552 ENSP00000380435 ENSP00000438831 ENSP00000415158

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Gene Ontology (GO): 2 cellular component terms (GO ID links to tree view): About this table

GO ID	Qualified GO term	Evidence	PubMed IDs
GO:0005887	integral to plasma membrane	TAS	10627596
GO:0016021	integral to membrane	--	--

NINJ2 for ontologies About GeneDecksing

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(According to InterPro, ProtoNet, UniProtKB, and/or BLOCKS, Sets of similar genes according to GeneDecks)
About This Section

NINJ2 for domains About GeneDecksing

1 InterPro domain/family:

IPR007007 Ninjurin

Graphical View of Domain Structure for InterPro Entry Q9NZG7

ProtoNet protein and cluster: Q9NZG7

1 Blocks protein family: IPB007007 Ninjurin

UniProtKB/Swiss-Prot: NINJ2_HUMAN, Q9NZG7

Similarity: Belongs to the ninjurin family

(According to ¹UniProtKB, Genatlas, LifeMap Discovery™, IUBMB, and/or ²DME, Human phenotypes from GenomeRNAi, Animal models from MGI Mar 06 2013,
bound targets from SABiosciences, miRNA Gene Targets from miRTarBase shRNA from OriGene, RNAi from EMD Millipore, siRNAs from OriGene, QIAGEN, microRNA from QIAGEN, Gene Editing from DNA2.0, Clones from EMD Millipore, OriGene, SwitchGear Genomics, GenScript, Sino Biological, DNA2.0, and Vector BioLabs, Cell Lines from GenScript, LifeMap BioReagents, In Situ Hybridization Assays from Advanced Cell Diagnostics, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene.)
About This Section

Function Summary:

UniProtKB/Swiss-Prot: NINJ2_HUMAN, Q9NZG7

Function: Homophilic cell adhesion molecule that promotes axonal growth. May play a role in nerve regeneration and in

the formation and function of other tissues

Induction: By nerve injury; in Schwann cells

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In Situ Assay
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3 GenomeRNAi human phenotypes for NINJ2:

Decreased homologous recombina

Increased G1 DNA content

Increased gamma-H2AX phosphory

(Pathways according to EMD Millipore, R&D Systems, Cell Signaling Technology, KEGG, PharmGKB, BioSystems, Reactome, Tocris Bioscience, GeneGo (Thomson Reuters), QIAGEN, and/or UniProtKB, Sets of similar genes according to GeneDecks, Interaction Networks according to SABiosciences, and/or STRING, Interactions according to ¹UniProtKB, ²MINT, ³I2D, and/or ⁴STRING, with links to IntAct and Ensembl, Ontologies according to Gene Ontology Consortium 01 Mar 2013 via Entrez Gene).
About This Section

Interactions:

Search SABiosciences Gene Network Central^TM Interacting Genes and Proteins Networks for NINJ2

Gene Ontology (GO): 4 biological process terms (GO ID links to tree view): About this table

GO ID	Qualified GO term	Evidence	PubMed IDs
GO:0007155	cell adhesion	--	--
GO:0007158	neuron cell-cell adhesion	TAS	10627596
GO:0007399	nervous system development	TAS	10627596
GO:0042246	tissue regeneration	IEA	--

NINJ2 for ontologies About GeneDecksing

(Chemical Compounds according to UniProtKB, Enzo Life Sciences, EMD Millipore, Tocris Bioscience HMDB, BitterDB, and/or Novoseek, and Drugs according to DrugBank, Enzo Life Sciences, and/or PharmGKB, with drugs/clinical trials/news search links to CenterWatch)
About This Section

Browse Small Molecules at EMD Millipore

Browse drugs & compounds from Enzo Life Sciences

Browse Tocris compounds for NINJ2
Search CenterWatch for drugs/clinical trials and news about NINJ2

(Secondary structures according to fRNAdb,
GenBank/EMBL/DDBJ Accessions according to
Unigene (Build 235 Homo sapiens; Mar 10 2013) or GenBank,
RefSeq according to Entrez Gene,
DOTS (version 10), and/or AceView, transcript ids from Ensembl with links to UCSC,
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About This Section

REFSEQ mRNAs for NINJ2 gene:

NM_016533.4

Unigene Cluster for NINJ2:

Ninjurin 2

Hs.656450 [show with all ESTs]

Unigene Representative Sequence: AK296012

5 Ensembl transcripts including schematic representations, and UCSC links where relevant:

ENST00000305108(uc001qil.3) ENST00000397265 ENST00000542920 ENST00000433832(uc010sdr.2 uc010sds.2)

ENST00000537416

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Additional cDNA sequence:

AF205633.1 AK296012.1 AK298043.1 AK315995.1 BC057766.1

3 DOTS entries:

DT.212267 DT.95364223 DT.91828925

24/72 AceView cDNA sequences (see all 72):

R06257 AW016477 AI393003 BU660855 CA446244 AA450074 AA743532 BM354140

NM_016533 AA769168 AI333512 CA431480 W38567 CB243438 AI218723 BC057766

BU953992 BM127826 BI598565 BU624562 BI603068 CB995632 AW016351 BG706186

GeneLoc Exon Structure

(RNA expression data according to H-InvDB, NONCODE, miRBase, and RNAdb, Expression images according to data from BioGPS, Illumina Human BodyMap, and CGAP SAGE, Sets of similar genes according to GeneDecks, in vivo and in vitro expression data from LifeMap Discovery™, plus additional links to Genevestigator, and/or SOURCE, and/or BioGPS, and/or UniProtKB,
PCR Arrays from SABiosciences, Primers from OriGene, SABiosciences, and/or QIAGEN, In Situ Hybridization Assays from Advanced Cell Diagnostics)
About This Section

NINJ2 expression in normal human tissues (normalized intensities)
See probesets specificity/sensitivity at GeneAnnot
About this imageBioGPS
CGAP TAG: TCTGTCTAAG

About this image

NINJ2 expression in embryonic tissues and stem cells

Expression by the Database of Embryonic development, Stem cell research, and Regenerative medicine About this table

1 LifeMap In Vivo Development Anatomical Compartment/Cell

Tissue

Anatomical Compartment

Cell

Category (developmental path)

Umbilical Cord

Umbilical Veins

Umbilical Cord

Expression:

Positive

Negative

Selective marker

Experimental details:

Curated

Microarrays

In-situ hybridization

Stem Cell Differentiation: 4 LifeMap Cells

Name

Category

HyStem+TGF?3+GDF5-induced SK11 cells (HyStem+TGF?3+GDF5 in...)

Bone, Cartilage

HyStem+TGF?3+GDF5-induced SM30 cells (HyStem+TGF?3+GDF5 in...)

Bone, Cartilage

HyStem+TGF?3+GDF5-induced 7PEND24 cells (HyStem+TGF?3+GDF5 in...)

Bone

HyStem+TGF?3+GDF5-induced E15 cells (HyStem+TGF?3+GDF5 in...)

Bone, Cartilage

See NINJ2 Protein Expression from SPIRE MOPED and PaxDB
Genevestigator expression for NINJ2

SOURCE GeneReport for Unigene cluster: Hs.656450

UniProtKB/Swiss-Prot: NINJ2_HUMAN, Q9NZG7

Tissue specificity: Widely expressed. In adult, higher expression in the bone marrow and peripheral blood lymphocytes,

medium in the lung, lymph node, thyroid, uterus, thymus, spleen, prostate and skeletal muscle, lower in the liver,

placenta, brain, heart and kidney. In embryo, higher expression in the thymus, heart and liver, lower in the spleen,

lung, brain and kidney

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In Situ
Assay Products:

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(Orthologs according to ^1,2HomoloGene (²older version, for species not in ¹newer version), ³euGenes, ⁴SGD , ⁵MGI Mar 06 2013, with possible further links to Flybase and/or WormBase, and/or ⁶Ensembl pan taxonomic compara , Gene Trees according to Ensembl and TreeFam)
About This Section

This gene was present in the common ancestor of animals.

Orthologs for NINJ2 gene from 6/15 species (see all 15) About this table

Organism	Taxonomic classification	Gene	Description	Human Similarity	Orthology Type	Details
mouse (Mus musculus)	Mammalia	Ninj2^{1 , 5}	ninjurin 2^{1, 5}	77.93(n)¹ 73.24(a)¹		6 (56.90 cM)⁵ 29862¹ NM_016718.2¹ NP_057927.1¹ 120093350⁵
chicken (Gallus gallus)	Aves	NINJ2¹	ninjurin 2	68.11(n) 65.47(a)		418151 XM_416382.3 XP_416382.2
lizard (Anolis carolinensis)	Reptilia	NINJ2⁶	--	56(a)	1 ↔ 1	5(12084631-12091608)
African clawed frog (Xenopus laevis)	Amphibia	CD360436.1²	--	75.52(n)		CD360436.1
zebrafish (Danio rerio)	Actinopterygii	LOC799267¹	ninjurin-1-like	67.51(n) 63.03(a)		799267 XM_001339607.2 XP_001339643.2
fruit fly (Drosophila melanogaster)	Insecta	CG14394⁶ CG11637⁶ (see all 3)	--	34(a) 19(a) (see all 3)	many ↔ many many ↔ many (see all 3)	3R(8520868-8523265) 3L(18885483-18886378)

ENSEMBL Gene Tree for NINJ2 (if available)
TreeFam Gene Tree for NINJ2 (if available)

(Paralogs according to ¹HomoloGene,
²Ensembl, and ³SIMAP, Pseudogenes according to ⁴Pseudogene.org Build 68)
About This Section

Paralogs for NINJ2 gene

NINJ1²

1 SIMAP similar gene for NINJ2 using alignment to 4 protein entries: NINJ2_HUMAN (see all proteins):

NINJ1

NINJ2 for paralogs About GeneDecksing

(SNPs/Variants according to the ¹NCBI SNP Database, ²Ensembl, ³PupaSUITE, UniProtKB, and DNA2.0, Linkage Disequilibrium by HapMap, Structural Variations(CNVs/InDels/Inversions) from the Database of Genomic Variants, Mutations from the Human Gene Mutation Database (HGMD) and the Locus Specific Mutation Databases (LSDB), Blood group antigen gene mutations by BGMUT, Resequencing Primers from QIAGEN, Cancer Mutation PCR Arrays and Assays and Copy Number PCR Arrays from SABiosciences)
About This Section

SNP ID	Valid	Clinical significance	Chr 12 pos	Sequence	#	AA Chg	Type	More	#	Allele freq	Pop	Total sample	More
Genomic Data					Transcription Related Data				Allele Frequencies
				--	--	--		--	--
rs73598112^1,2	C,	--	592095(+)	`TCCCCA/TGGAGA`	1	--	us2k¹		2		WA NA	122
rs57671584^1,2	C,	--	592786(+)	`GCACAG/AACCCA`	1	--	us2k¹		2		CSA WA	120
rs73598116^1,2	C,	--	593213(+)	`CCTGGG/AGTATG`	1	--	int¹		1		WA	2
rs7956216^1,2	A	--	594060(+)	`CATGGA/GGGACC`	1	--	int¹		0	--	--	--	--
rs79332231^1,2	C,F,	--	594080(+)	`GAAGTC/TTGAAC`	1	--	int¹		1		WA	118
rs7956326^1,2	A	--	594112(+)	`AGATTC/GAGTAA`	1	--	int¹		0	--	--	--	--
rs7956334^1,2	A	--	594142(+)	`TTAAAC/GTCCTA`	1	--	spa¹		0	--	--	--	--
rs73598117^1,2	C,F,	--	594239(+)	`CTTTGC/TTTGTC`	1	--	int¹		2		WA CSA	4
rs7976830^1,2	A	--	594394(+)	`TGCACC/TCTGGA`	1	--	int¹		0	--	--	--	--
rs58723372^1,2	F,	--	594886(+)	`CAAAAG/AGTTAG`	1	--	int¹		1		WA	118

HapMap Linkage Disequilibrium report for NINJ2 (673462 - 772945 bp)
Structural Variations (Copy Number Variations, Insertions/Deletions, Inversions)
Database of Genomic Variants (DGV): 9 variations for NINJ2
3 CNVs: 53493 9677 3871
6 Indels: 25042 45062 86134 25039 71423 75893

SABiosciences Cancer Mutation PCR Assays

QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing NINJ2

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(in which this Gene is Involved, According to MalaCards, OMIM, UniProtKB, the University of Copenhagen DISEASES database, Genatlas, GeneTests, GAD, HuGE Navigator, and/or TGDB.)
About This Section

NINJ2 for disorders           About GeneDecksing

OMIM gene information: 607297    OMIM disorders: --

5 diseases for NINJ2:    About MalaCards

acrocallosal syndrome alzheimer's disease thyroiditis prostatitis

neuronitis

1 disease from the University of Copenhagen DISEASES database for NINJ2:

Acrocallosal syndrome

Human Genome Epidemiology (HuGE) Navigator: NINJ2 (4 documents)

Export disorders for NINJ2 gene to outside databases

(in PubMed. Associations of this gene to articles via ¹Entrez Gene, ²UniProtKB/Swiss-Prot, ³HGNC, ⁴GAD, ⁵PharmGKB, ⁶HMDB, ⁷DrugBank, ⁸UniProtKB/TrEMBL, ⁹ Novoseek, and/or ¹⁰fRNAdb)
About This Section

PubMed articles for NINJ2 gene, integrated from 9 sources (see all 13):
(articles sorted by number of sources associating them with NINJ2)

Utopia: connect your pdf to the dynamic
world of online information

Ninjurin2, a novel homophilic adhesion molecule, is expressed in mature sensory and enteric neurons and promotes neurite outgrowth. (PubMed id 10627596)^{1, 2, 3} Araki T. and Milbrandt J. (2000)
The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). (PubMed id 15489334)^{1, 2} Gerhard D.S....Malek J. (2004)
The rs11833579 and rs12425791 polymorphisms and risk o f ischemic stroke in an Asian population: a meta-analysis. (PubMed id 22795341)¹ Lian G....Li S. (2012)
Association between 12p13 SNPs rs11833579/rs12425791 n ear NINJ2 gene and ischemic stroke in East Asian population: evidence from a met a-analysis. (PubMed id 22297388)¹ Li B.H....Li J.C. (2012)
Genetic polymorphisms of a novel vascular susceptibil ity gene, Ninjurin2 (NINJ2), are associated with a decreased risk of Alzheimer' s disease. (PubMed id 21674003)¹ Lin K.P....Chen Y.C. (2011)
No evidence for association of 12p13 SNPs rs11833579 and rs12425791 within NINJ2 gene with ischemic stroke in Chinese Han population . (PubMed id 21376321)¹ Ding H....Wang D.W. (2011)
NINJ2 polymorphism is associated with ischemic stroke in Chinese Han population. (PubMed id 21722921)¹ Wan X.H....Wang X.F. (2011)
Failure to validate association between 12p13 variant s and ischemic stroke. (PubMed id 20410525)¹ (2010)
[Strong association between the NINJ2 gene polymorphi sm and the susceptibility of stroke in Chinese Han population in Fangshan distr ict]. (PubMed id 20957003)¹ Chen K....Qiu C.C. (2010)
Genomewide association studies of stroke. (PubMed id 19369658)¹ Ikram M.A....Wolf P.A. (2009)

(in PubMed, OMIM, and NCBI Bookshelf)
About This Section

		AND	OR
Aliases
Free Text

Query String		PubMed OMIM NCBI Bookshelf
	(Note: In FireFox, select the above section and copy using Ctrl-C)

(According to Entrez Gene, HGNC, AceView, euGenes, Ensembl, miRBase, ECgene, Kegg, and/or H-InvDB)
About This Section

Entrez Gene: 4815	HGNC: 7825	AceView: NINJ2	Ensembl:ENSG00000171840	euGenes: HUgn4815
ECgene: NINJ2	H-InvDB: NINJ2

(According to HUGE)
About This Section

(According to PharmGKB, ATLAS, HORDE, IMGT, LEIDEN, UniProtKB/Swiss-Prot, and/or UniProtKB/TrEMBL,
Wikipedia and/or GeneReviews via UniProtKB/Swiss-Prot)
About This Section

Name	Description
PharmGKB entry for NINJ2	Pharmacogenomics, SNPs, Pathways

Intellectual Property for NINJ2 gene
(Patent information from GeneIP, Licensable technologies from WIS Yeda, Salk, Tufts, IP news from LifeMap Sciences, Inc.)

About This Section

Patent Information for NINJ2 gene:
Search GeneIP for patents involving NINJ2

GeneCards and IP:
Japan Patent Office Licenses GeneCards European Patent Office Licenses GeneCards Improving the IP Search

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In Situ Hybridization Assays from
Advanced Cell Diagnostics
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	Antibodies for NINJ2 (Ninjurin-2)		Browse Cell Culture Products
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	Browse OriGene Antibodies		OriGene shRNA RFP for NINJ2
	OriGene 29mer shRNA kits in GFP-retroviral vector in human, mouse, rat for NINJ2		OriGene genome-wide validated SYBR primer pairs in human, mouse, rat for NINJ2
	OriGene Protein Over-expression Lysate for NINJ2		Browse OriGene Fluorogenic Cell Assay Kits
	OriGene siRNA for NINJ2		Browse 3'-UTR reporter clones for miRNA target validation
	OriGene untagged cDNA clones in CMV expression vector in human, mouse, rat for NINJ2		OriGene Myc/DDK tagged cDNA clones in CMV expression vector in human, mouse, rat for NINJ2
	Browse OriGene GFP tagged cDNA clones in CMV expression vector		Browse OriGene MicroRNA Expression Plasmids
	Browse OriGene basic RS shRNAs		Browse OriGene validated miRNA SYBR primer pairs
	OriGene Purified Protein for NINJ2		OriGene custom cloning services - gene synthesis, subcloning, mutagenesis, variant library, vector shuttling
	OriGene Custom Antibody Services for NINJ2		OriGene Custom Protein Services for NINJ2
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	QIAGEN Custom miScript Target Protector blocks miRNA-binding site of in human, mouse, rat NINJ2
	QIAGEN SeqTarget long-range PCR primers in human, mouse, rat for resequencing NINJ2
	QIAGEN PyroMark CpG Assay predesigned Pyrosequencing DNA Methylation assays in human, mouse, rat NINJ2
	QIAGEN FlexiTube/FlexiPlate siRNA for gene silencing in human, mouse, rat NINJ2
	QIAGEN QuantiFast Probe-based Assays in human, mouse, rat NINJ2
	QIAGEN QuantiTect SYBR Green Assays in human, mouse, rat NINJ2

	GenScript Custom Purified and Recombinant Proteins Services for NINJ2		GenScript cDNA clones with any tag delivered in your preferred vector for NINJ2
	GenScript Custom Assay Services for NINJ2		GenScript Custom Superior Antibodies Services for NINJ2
	GenScript Custom overexpressing Cell Line Services for NINJ2		CloneReady with Over 120,000 Genes
	Gene Synthesis: Any Gene in Any Vector		Vector-based siRNA and miRNA, Ready for Transfection
	Gene Mutant Library, Variants up to 10^11		Plasmid Preparation
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	Search for Antibodies for NINJ2 at Abcam
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Advanced Cell Diagnostics RNAscope RNA in situ hybridization assays for NINJ2

	SwitchGear 3'UTR luciferase reporter plasmids for NINJ2
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Vector BioLabs ready-to-use adenovirus/AAV for human, mouse, rat NINJ2

GeneCards Homepage - Last full update: 18 Mar 2013 - Incrementals: 21 Mar 2013 , 15 Apr 2013 , 26 Apr 2013

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Category			VWF (GIFTS: 73) von Willebrand factor
GIFtS Group

The GeneCards human gene database gene index: 1 3 5 6 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z

The GeneCards Human Gene Database

Developed at the Crown Human Genome Center, Department of Molecular Genetics, the Weizmann Institute of Science

Hot genes Disease genes NINJ2 gene at Home site.

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NINJ2 Gene

ninjurin 2

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NINJ2 Gene

ninjurin 2

Aliasesfor NINJ2 gene

Summariesfor NINJ2 gene

Genomic Viewsfor NINJ2 gene

Proteinsfor NINJ2 gene

Protein Domains /Familiesfor NINJ2 gene

Functionfor NINJ2 gene

Pathways & Interactionsfor NINJ2 gene

Drugs & Compoundsfor NINJ2 gene

Transcriptsfor NINJ2 gene

Expression for NINJ2 gene

Orthologsfor NINJ2 gene

Paralogsfor NINJ2 gene

Genomic Variantsfor NINJ2 gene

Disorders / Diseasesfor NINJ2 gene

Publicationsfor NINJ2 gene

External Searches for NINJ2 gene

Genome Databases showing NINJ2 gene

Other Databases showing NINJ2 gene

Specialized Databases showing NINJ2 gene

Intellectual Propertyfor NINJ2 gene

Productsfor NINJ2 gene

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Aliases
for NINJ2 gene

Summaries
for NINJ2 gene

Genomic Views
for NINJ2 gene

Proteins
for NINJ2 gene

Protein Domains /
Families
for NINJ2 gene

Function
for NINJ2 gene

Pathways & Interactions
for NINJ2 gene

Drugs & Compounds
for NINJ2 gene

Transcripts
for NINJ2 gene

Expression
for NINJ2 gene

Orthologs
for NINJ2 gene

Paralogs
for NINJ2 gene

Genomic Variants
for NINJ2 gene

Disorders / Diseases
for NINJ2 gene

Publications
for NINJ2 gene

Intellectual Property
for NINJ2 gene

Products
for NINJ2 gene