DNAJB2 (DnaJ heat shock protein family (Hsp40) member B2)

Gene

• Entrez ID: 3300
• Gene name: DnaJ heat shock protein family (Hsp40) member B2
• Gene symbol: DNAJB2
• Synonyms (NCBI Gene): CMT2T, DSMA5, HMNR5, HSJ-1, HSJ1, HSPF3
• Chromosome: 2
• Chromosome location: 2q35
• Summary: This gene is almost exclusively expressed in the brain, mainly in the neuronal layers. It encodes a protein that shows sequence similarity to bacterial DnaJ protein and the yeast homologs. In bacteria, this protein is implicated in protein folding and pro

SNPs

SNP ID	Visualize variation	Clinical significance	Consequence
rs369661561	A>G	Likely-pathogenic	Splice acceptor variant
rs562669797	T>A	Likely-pathogenic	Splice donor variant
rs730882139	G>A	Pathogenic, conflicting-interpretations-of-pathogenicity	Splice donor variant
rs730882140	A>G	Pathogenic, conflicting-interpretations-of-pathogenicity	Missense variant, coding sequence variant
rs756614404	G>A	Pathogenic, uncertain-significance	Splice donor variant
rs758322672	A>G	Likely-pathogenic	Splice acceptor variant
rs764813110	G>A	Pathogenic	Splice acceptor variant
rs797045039	G>T	Pathogenic	Coding sequence variant, stop gained
rs879253868	C>-	Likely-pathogenic	Frameshift variant, coding sequence variant

miRNA

miRTarBase ID	miRNA	Experiments	Reference
MIRT042091	hsa-miR-484	CLASH	23622248
MIRT614188	hsa-miR-141-5p	HITS-CLIP	23824327
MIRT614187	hsa-miR-338-3p	HITS-CLIP	23824327
MIRT614186	hsa-miR-6788-3p	HITS-CLIP	23824327
MIRT614185	hsa-miR-1238-3p	HITS-CLIP	23824327
MIRT614188	hsa-miR-141-5p	HITS-CLIP	23824327
MIRT614187	hsa-miR-338-3p	HITS-CLIP	23824327
MIRT614186	hsa-miR-6788-3p	HITS-CLIP	23824327
MIRT614185	hsa-miR-1238-3p	HITS-CLIP	23824327
MIRT614188	hsa-miR-141-5p	HITS-CLIP	23824327
MIRT614187	hsa-miR-338-3p	HITS-CLIP	23824327
MIRT614186	hsa-miR-6788-3p	HITS-CLIP	23824327
MIRT614185	hsa-miR-1238-3p	HITS-CLIP	23824327
MIRT614188	hsa-miR-141-5p	HITS-CLIP	23824327
MIRT614187	hsa-miR-338-3p	HITS-CLIP	23824327
MIRT614186	hsa-miR-6788-3p	HITS-CLIP	23824327
MIRT614185	hsa-miR-1238-3p	HITS-CLIP	23824327
MIRT940172	hsa-miR-1275	CLIP-seq
MIRT940173	hsa-miR-4271	CLIP-seq
MIRT940174	hsa-miR-4525	CLIP-seq
MIRT940175	hsa-miR-4665-5p	CLIP-seq
MIRT940176	hsa-miR-4723-5p	CLIP-seq
MIRT940177	hsa-miR-4725-3p	CLIP-seq
MIRT940178	hsa-miR-4747-5p	CLIP-seq
MIRT940179	hsa-miR-524-3p	CLIP-seq
MIRT940180	hsa-miR-525-3p	CLIP-seq
MIRT940181	hsa-miR-625	CLIP-seq
MIRT940182	hsa-miR-3620	CLIP-seq
MIRT940183	hsa-miR-3656	CLIP-seq
MIRT940184	hsa-miR-378g	CLIP-seq
MIRT940185	hsa-miR-4292	CLIP-seq
MIRT940186	hsa-miR-4432	CLIP-seq
MIRT940187	hsa-miR-4438	CLIP-seq
MIRT940188	hsa-miR-4693-3p	CLIP-seq
MIRT940189	hsa-miR-4732-3p	CLIP-seq
MIRT940190	hsa-miR-499-5p	CLIP-seq
MIRT1978039	hsa-miR-1202	CLIP-seq
MIRT1978040	hsa-miR-1283	CLIP-seq
MIRT1978041	hsa-miR-146b-3p	CLIP-seq
MIRT1978042	hsa-miR-1913	CLIP-seq
MIRT1978043	hsa-miR-1915	CLIP-seq
MIRT1978044	hsa-miR-205	CLIP-seq
MIRT1978045	hsa-miR-2277-5p	CLIP-seq
MIRT1978046	hsa-miR-3173-5p	CLIP-seq
MIRT1978047	hsa-miR-3194-3p	CLIP-seq
MIRT1978048	hsa-miR-3194-5p	CLIP-seq
MIRT1978049	hsa-miR-324-3p	CLIP-seq
MIRT1978050	hsa-miR-3972	CLIP-seq
MIRT1978051	hsa-miR-4283	CLIP-seq
MIRT940185	hsa-miR-4292	CLIP-seq
MIRT1978052	hsa-miR-4479	CLIP-seq
MIRT1978053	hsa-miR-4489	CLIP-seq
MIRT1978054	hsa-miR-451b	CLIP-seq
MIRT1978055	hsa-miR-4696	CLIP-seq
MIRT1978056	hsa-miR-4726-3p	CLIP-seq
MIRT1978057	hsa-miR-621	CLIP-seq
MIRT1978058	hsa-miR-760	CLIP-seq
MIRT1978059	hsa-miR-764	CLIP-seq
MIRT1978060	hsa-miR-874	CLIP-seq
MIRT1978061	hsa-miR-941	CLIP-seq
MIRT2213558	hsa-miR-29a	CLIP-seq
MIRT2213559	hsa-miR-29b	CLIP-seq
MIRT2213560	hsa-miR-29c	CLIP-seq
MIRT2213561	hsa-miR-3065-3p	CLIP-seq
MIRT1978048	hsa-miR-3194-5p	CLIP-seq
MIRT1978048	hsa-miR-3194-5p	CLIP-seq
MIRT2386959	hsa-miR-186	CLIP-seq
MIRT2386960	hsa-miR-3978	CLIP-seq
MIRT2386961	hsa-miR-4679	CLIP-seq
MIRT2386962	hsa-miR-4781-3p	CLIP-seq
MIRT1978039	hsa-miR-1202	CLIP-seq
MIRT2517336	hsa-miR-1207-5p	CLIP-seq
MIRT2517337	hsa-miR-1249	CLIP-seq
MIRT2517338	hsa-miR-1321	CLIP-seq
MIRT2517339	hsa-miR-1343	CLIP-seq
MIRT2517340	hsa-miR-1827	CLIP-seq
MIRT2517341	hsa-miR-2355-5p	CLIP-seq
MIRT2517342	hsa-miR-2682	CLIP-seq
MIRT2517343	hsa-miR-3150b-3p	CLIP-seq
MIRT1978048	hsa-miR-3194-5p	CLIP-seq
MIRT940184	hsa-miR-378g	CLIP-seq
MIRT1978050	hsa-miR-3972	CLIP-seq
MIRT2517344	hsa-miR-4252	CLIP-seq
MIRT2517345	hsa-miR-4270	CLIP-seq
MIRT940185	hsa-miR-4292	CLIP-seq
MIRT2517346	hsa-miR-4308	CLIP-seq
MIRT2517347	hsa-miR-4326	CLIP-seq
MIRT2517348	hsa-miR-4437	CLIP-seq
MIRT2517349	hsa-miR-4441	CLIP-seq
MIRT2517350	hsa-miR-449c	CLIP-seq
MIRT2517351	hsa-miR-4514	CLIP-seq
MIRT2517352	hsa-miR-4645-5p	CLIP-seq
MIRT2517353	hsa-miR-4673	CLIP-seq
MIRT2517354	hsa-miR-4674	CLIP-seq
MIRT2517355	hsa-miR-4692	CLIP-seq
MIRT2517356	hsa-miR-4701-5p	CLIP-seq
MIRT2517357	hsa-miR-4722-3p	CLIP-seq
MIRT2517358	hsa-miR-4739	CLIP-seq
MIRT2517359	hsa-miR-4756-5p	CLIP-seq
MIRT2517360	hsa-miR-4763-3p	CLIP-seq
MIRT2517361	hsa-miR-4784	CLIP-seq
MIRT2517362	hsa-miR-588	CLIP-seq
MIRT2517363	hsa-miR-765	CLIP-seq
MIRT2517364	hsa-miR-940	CLIP-seq
MIRT2517336	hsa-miR-1207-5p	CLIP-seq
MIRT2517338	hsa-miR-1321	CLIP-seq
MIRT2517340	hsa-miR-1827	CLIP-seq
MIRT2517341	hsa-miR-2355-5p	CLIP-seq
MIRT2517342	hsa-miR-2682	CLIP-seq
MIRT2517343	hsa-miR-3150b-3p	CLIP-seq
MIRT940184	hsa-miR-378g	CLIP-seq
MIRT2517344	hsa-miR-4252	CLIP-seq
MIRT2517345	hsa-miR-4270	CLIP-seq
MIRT940185	hsa-miR-4292	CLIP-seq
MIRT2517346	hsa-miR-4308	CLIP-seq
MIRT2517348	hsa-miR-4437	CLIP-seq
MIRT2517349	hsa-miR-4441	CLIP-seq
MIRT2517350	hsa-miR-449c	CLIP-seq
MIRT2517351	hsa-miR-4514	CLIP-seq
MIRT2517352	hsa-miR-4645-5p	CLIP-seq
MIRT2517353	hsa-miR-4673	CLIP-seq
MIRT2517354	hsa-miR-4674	CLIP-seq
MIRT2517355	hsa-miR-4692	CLIP-seq
MIRT2517356	hsa-miR-4701-5p	CLIP-seq
MIRT2517358	hsa-miR-4739	CLIP-seq
MIRT2517359	hsa-miR-4756-5p	CLIP-seq
MIRT2517360	hsa-miR-4763-3p	CLIP-seq
MIRT2517361	hsa-miR-4784	CLIP-seq
MIRT2517362	hsa-miR-588	CLIP-seq
MIRT2517363	hsa-miR-765	CLIP-seq
MIRT2517364	hsa-miR-940	CLIP-seq

Gene ontology (GO)

GO ID	Ontology	Definition	Evidence	Reference
GO:0000502	Component	Proteasome complex	IDA	15936278
GO:0001671	Function	ATPase activator activity	IBA
GO:0001671	Function	ATPase activator activity	IDA	7957263, 22219199
GO:0005515	Function	Protein binding	IPI	12754272, 15936278, 21625540, 21719532, 24023695, 25036637, 33961781
GO:0005634	Component	Nucleus	IDA	12754272
GO:0005634	Component	Nucleus	IDA	12754272, 21231916, 28031292
GO:0005634	Component	Nucleus	IEA
GO:0005737	Component	Cytoplasm	IDA	12754272, 21625540, 28031292
GO:0005737	Component	Cytoplasm	IEA
GO:0005783	Component	Endoplasmic reticulum	IEA
GO:0005789	Component	Endoplasmic reticulum membrane	IDA	12754272
GO:0005789	Component	Endoplasmic reticulum membrane	IEA
GO:0005829	Component	Cytosol	IBA
GO:0005829	Component	Cytosol	IDA	21231916
GO:0006457	Process	Protein folding	IBA
GO:0006457	Process	Protein folding	IMP	24023695
GO:0006986	Process	Response to unfolded protein	TAS	1599432
GO:0008285	Process	Negative regulation of cell population proliferation	IGI	9553041
GO:0016020	Component	Membrane	IEA
GO:0016234	Component	Inclusion body	IDA	15936278
GO:0030308	Process	Negative regulation of cell growth	IGI	9553041
GO:0030544	Function	Hsp70 protein binding	IBA
GO:0030544	Function	Hsp70 protein binding	IDA	21625540
GO:0030544	Function	Hsp70 protein binding	IEA
GO:0030544	Function	Hsp70 protein binding	IPI	15936278, 22219199
GO:0031396	Process	Regulation of protein ubiquitination	IMP	24023695
GO:0031398	Process	Positive regulation of protein ubiquitination	IDA	15936278
GO:0031593	Function	Polyubiquitin modification-dependent protein binding	IDA	15936278, 21625540
GO:0031625	Function	Ubiquitin protein ligase binding	IPI	20889486
GO:0031965	Component	Nuclear membrane	IDA
GO:0032091	Process	Negative regulation of protein binding	IDA	7957263
GO:0032436	Process	Positive regulation of proteasomal ubiquitin-dependent protein catabolic process	IDA	15936278
GO:0032436	Process	Positive regulation of proteasomal ubiquitin-dependent protein catabolic process	TAS	28031292
GO:0032781	Process	Positive regulation of ATP-dependent activity	IDA	7957263, 22219199
GO:0032880	Process	Regulation of protein localization	IMP	20889486
GO:0036503	Process	ERAD pathway	IDA	15936278
GO:0042026	Process	Protein refolding	IBA
GO:0042026	Process	Protein refolding	IDA	21231916
GO:0043130	Function	Ubiquitin binding	IDA	28031292
GO:0043161	Process	Proteasome-mediated ubiquitin-dependent protein catabolic process	IMP	21625540
GO:0048471	Component	Perinuclear region of cytoplasm	IDA	28031292
GO:0051082	Function	Unfolded protein binding	IBA
GO:0051082	Function	Unfolded protein binding	IDA	21231916, 24023695
GO:0051082	Function	Unfolded protein binding	IEA
GO:0051087	Function	Protein-folding chaperone binding	IEA
GO:0051087	Function	Protein-folding chaperone binding	IPI	21231916
GO:0070050	Process	Neuron cellular homeostasis	TAS	28031292
GO:0070628	Function	Proteasome binding	IDA	15936278
GO:0090084	Process	Negative regulation of inclusion body assembly	IDA	15936278, 21231916
GO:0090084	Process	Negative regulation of inclusion body assembly	IEA
GO:0090084	Process	Negative regulation of inclusion body assembly	IMP	20889486
GO:0090086	Process	Negative regulation of protein deubiquitination	IDA	15936278
GO:0098554	Component	Cytoplasmic side of endoplasmic reticulum membrane	TAS	28031292
GO:0120283	Function	Protein serine/threonine kinase binding	IPI	28031292
GO:0140036	Function	Ubiquitin-modified protein reader activity	IDA	28031292
GO:0140318	Function	Protein transporter activity	TAS	28031292
GO:1903332	Process	Regulation of protein folding	IDA	7957263

Other IDs

• MIM: 604139
• HGNC: 5228
• e!Ensembl: ENSG00000135924

Protein

• UniProt ID: P25686
• Protein name: DnaJ homolog subfamily B member 2 (Heat shock 40 kDa protein 3) (Heat shock protein J1) (HSJ-1)
• Protein function: Functions as a co-chaperone, regulating the substrate binding and activating the ATPase activity of chaperones of the HSP70/heat shock protein 70 family (PubMed:22219199, PubMed:7957263). In parallel, also contributes to the ubiquitin-dependent
• PDB: 2LGW
• Family and domains:

  Pfam

  Accession	ID	Position in sequence	Description	Type
  PF00226	DnaJ	3 → 66	DnaJ domain	Domain

• Tissue specificity: TISSUE SPECIFICITY: More abundantly expressed in neocortex, cerebellum, spinal cord and retina where it is expressed by neuronal cells (at protein level) (PubMed:12754272, PubMed:1599432). Detected at much lower level in non-neuronal tissues including kid
• Sequence:

  MASYYEILDVPRSASADDIKKAYRRKALQWHPDKNPDNKEFAEKKFKEVAEAYEVLSDKH
  KREIYDRYGREGLTGTGTGPSRAEAGSGGPGFTFTFRSPEEVFREFFGSGDPFAELFDDL
  GPFSELQNRGSRHSGPFFTFSSSFPGHSDFSSSSFSFSPGAGAFRSVSTSTTFVQGRRIT
  TRRIMENGQERVEVEEDGQLKSVTINGVPDDLALGLELSRREQQPSVTSRSGGTQVQQTP
  ASCPLDSDLSEDEDLQLAMAYSLSEMEAAGKKPAGGREAQHRRQGRPKAQHQDPGLGGTQ
  EGARGEATKRSPSPEEKASRCLIL

• Sequence length: 324

Pathways

KEGG:

Protein processing in endoplasmic reticulum

Associated diseases

Evidence Score:

• ★☆☆☆☆  Gene-disease association found in Text Mining only
• ★★☆☆☆  Found in Text Mining and Unknown/Other Associations
• ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources
• ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants)
• ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)

Causal
Phenotype Name	Clinical Significance	dbSNP ID	RCV Accession	Evidence Score
Autosomal recessive distal spinal muscular atrophy 2	Pathogenic; Likely pathogenic	rs730882139, rs730882140, rs756614404	RCV003447120 RCV003447121 RCV003447123	★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Charcot-Marie-Tooth disease	Pathogenic; Likely pathogenic	rs730882139, rs730882140, rs756614404	RCV000192265 RCV000192266 RCV000789088	★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Charcot-Marie-Tooth disease axonal type 2T	Pathogenic	rs797045039	RCV000191078	★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Charcot-Marie-Tooth disease X-linked dominant 1	Pathogenic	rs756614404	RCV002051587	★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
DNAJB2-related disorder	Pathogenic; Likely pathogenic	rs756614404, rs2545028296	RCV003407713 RCV003412413	★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Neuronopathy, distal hereditary motor, autosomal recessive 5	Pathogenic; Likely pathogenic	rs2125081805, rs2125082259, rs2125082935, rs1951889033, rs730882139, rs730882140, rs936213383, rs756614404, rs879253868, rs764813110, rs368547938, rs918395100, rs758322672, rs562669797, rs1182614290, rs1018405924	RCV001941373 RCV001999715 RCV001956956 RCV002290280 RCV000161908 RCV000161909 RCV002571696 RCV000201941 RCV000235093 RCV000235055 RCV003536105 RCV003651121 RCV000761527 RCV000808455 RCV001072057 RCV001095531	★★★★★ ClinVar: Pathogenic / Likely Pathogenic (≥5 Variants)

Unknown / Other Associations
Phenotype Name	Clinical Significance	Source	Evidence Score
Acute myeloid leukemia	Benign	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Cervical cancer	Conflicting classifications of pathogenicity	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Charcot-Marie-Tooth disease type 2	Conflicting classifications of pathogenicity	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
CHARCOT-MARIE-TOOTH DISEASE, X-LINKED, 1	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DNAJ HEAT SHOCK PROTEIN FAMILY MEMBER B2-RELATED CHARCOT-MARIE-TOOTH DISEASE TYPE 2	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DNAJB2-RELATED CHARCOT-MARIE-TOOTH DISEASE TYPE 2	—	Orphanet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Familial cancer of breast	Conflicting classifications of pathogenicity	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant lymphoma, large B-cell, diffuse	Uncertain significance; Benign	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus	Uncertain significance	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Ovarian serous cystadenocarcinoma	Benign	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Sarcoma	Benign	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
SPINAL MUSCULAR ATROPHY, JERASH TYPE	—	Disgenet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Thymoma	Benign	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Thyroid cancer, nonmedullary, 1	Conflicting classifications of pathogenicity	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine carcinosarcoma	Benign	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine corpus endometrial carcinoma	Uncertain significance	ClinVar	★★☆☆☆ Found in Text Mining + Unknown/Other Associations
YOUNG ADULT-ONSET DISTAL HEREDITARY MOTOR NEUROPATHY	—	Disgenet, Orphanet Disgenet, Orphanet	★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Associations from Text Mining
Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Amyotrophic Lateral Sclerosis	Amyotrophic Lateral Sclerosis	BEFREE	24023695, 28031292		★☆☆☆☆ Found in Text Mining only
Amyotrophic Lateral Sclerosis	Amyotrophic lateral sclerosis	Pubtator	28031292	Associate	★☆☆☆☆ Found in Text Mining only
Amyotrophy, monomelic	Monomelic Amyotrophy	BEFREE	19412816		★☆☆☆☆ Found in Text Mining only
Bulbo-Spinal Atrophy, X-Linked	Bulbospinal Atrophy, X-Linked	BEFREE	20395441		★☆☆☆☆ Found in Text Mining only
Charcot-Marie-Tooth Disease	Charcot-Marie-Tooth Disease	BEFREE	28031292		★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Charcot-Marie-Tooth Disease	Charcot-Marie-Tooth Disease	CLINVAR_DG			★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
CHARCOT-MARIE-TOOTH DISEASE, AXONAL, TYPE 2T	Charcot-Marie-Tooth Disease	CLINVAR_DG	26633545		★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Distal Hereditary Motor Neuropathy Type II	Distal hereditary motor neuropathy	Pubtator	28031292	Associate	★☆☆☆☆ Found in Text Mining only
DNAJB2-related Charcot-Marie-Tooth disease type 2	Charcot-Marie-Tooth Disease	Orphanet			★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Hearing Loss	Hearing loss	Pubtator	35286755	Associate	★☆☆☆☆ Found in Text Mining only
Hereditary Motor and Sensory Neuropathies	Hereditary motor and sensory neuropathy	BEFREE	25274842		★☆☆☆☆ Found in Text Mining only
Hereditary Motor and Sensory-Neuropathy Type II	Dysautonomia	BEFREE	25274842		★☆☆☆☆ Found in Text Mining only
Hereditary Sensory and Motor Neuropathy	Hereditary sensory and motor neuropathy	Pubtator	35286755	Associate	★☆☆☆☆ Found in Text Mining only
Huntington Disease	Huntington Disease	LHGDN	16604191		★☆☆☆☆ Found in Text Mining only
Motor Neuron Disease, Lower	Motor Neuron Disease	BEFREE	22522442		★☆☆☆☆ Found in Text Mining only
Muscular Atrophy Spinal	Spinal muscular atrophy	Pubtator	27449489, 28031292	Associate	★☆☆☆☆ Found in Text Mining only
Muscular Dystrophy, Duchenne	Duchenne Muscular Dystrophy	BEFREE	20395441		★☆☆☆☆ Found in Text Mining only
Myopathy	Myopathy	BEFREE	20395441		★☆☆☆☆ Found in Text Mining only
Nervous System Diseases	Nervous system disease	Pubtator	35286755	Associate	★☆☆☆☆ Found in Text Mining only
Neurodegenerative Diseases	Neurodegenerative disorder	Pubtator	28031292	Associate	★☆☆☆☆ Found in Text Mining only
Neurodegenerative Disorders	Neurodegenerative Disorders	BEFREE	20395441, 28031292		★☆☆☆☆ Found in Text Mining only
Neuropathy	Neuropathy	BEFREE	25274842		★☆☆☆☆ Found in Text Mining only
Parkinson Disease	Parkinson disease	Pubtator	35286755	Associate	★☆☆☆☆ Found in Text Mining only
Parkinson Disease Secondary	Secondary parkinson disease	Pubtator	27449489, 28031292, 35286755, 37070754	Associate	★☆☆☆☆ Found in Text Mining only
Parkinsonian Disorders	Parkinson Disease	BEFREE	27449489		★☆☆☆☆ Found in Text Mining only
Peripheral motor neuropathy	Motor nerve neuritis	BEFREE	22522442, 25274842		★☆☆☆☆ Found in Text Mining only
Peripheral Nervous System Diseases	Peripheral nervous system disease	Pubtator	26556829, 37070754	Associate	★☆☆☆☆ Found in Text Mining only
Spastic Paraplegia Hereditary	Hereditary spastic paraplegia	Pubtator	26556829	Associate	★☆☆☆☆ Found in Text Mining only
Spinal Muscular Atrophy	Spinal Muscular Atrophy	BEFREE	27449489		★☆☆☆☆ Found in Text Mining only
Spinal Muscular Atrophy	Spinal Muscular Atrophy	HPO_DG			★☆☆☆☆ Found in Text Mining only
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5	Spinal Muscular Atrophy,Distal	ORPHANET_DG	22522442		★☆☆☆☆ Found in Text Mining only
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5	Spinal Muscular Atrophy,Distal	GENOMICS_ENGLAND_DG	22522442		★☆☆☆☆ Found in Text Mining only
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5	Spinal Muscular Atrophy,Distal	CLINVAR_DG	22522442, 25274842, 26257172, 27083531		★☆☆☆☆ Found in Text Mining only
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5	Spinal Muscular Atrophy,Distal	UNIPROT_DG	22522442, 24627108, 25274842		★☆☆☆☆ Found in Text Mining only
SPINAL MUSCULAR ATROPHY, DISTAL, AUTOSOMAL RECESSIVE, 5	Spinal Muscular Atrophy,Distal	CTD_human_DG			★☆☆☆☆ Found in Text Mining only
Vacuolar Neuromyopathy	Vacuolar neuromyopathy	Pubtator	37070754	Associate	★☆☆☆☆ Found in Text Mining only
Young adult-onset distal hereditary motor neuropathy	Distal Hereditary Motor Neuronopathy	Orphanet			★★☆☆☆ Found in Text Mining + Unknown/Other Associations