Gene Gene information from NCBI Gene database. Download as csv Download as pdf
Entrez ID	55746
Gene name	Nucleoporin 133
Gene symbol	NUP133
Synonyms (NCBI Gene)	GAMOS8NPHS18hNUP133
Chromosome	1
Chromosome location	1q42.13
Summary	The nuclear envelope creates distinct nuclear and cytoplasmic compartments in eukaryotic cells. It consists of two concentric membranes perforated by nuclear pores, large protein complexes that form aqueous channels to regulate the flow of macromolecules

SNP ID	Visualize variation	Clinical significance	Consequence
rs376476266	A>G	Likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant
rs1433513056	A>G,T	Pathogenic	Intron variant
rs1558091788	A>C	Likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant
rs1558108130	G>C	Likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant

163 Show/Hide all (163)

miRTarBase ID	miRNA	Experiments	Reference
MIRT035996	hsa-miR-1301-3p	CLASH	23622248
MIRT461348	hsa-miR-590-3p	PAR-CLIP	23592263
MIRT461347	hsa-miR-3120-3p	PAR-CLIP	23592263
MIRT461346	hsa-miR-3126-3p	PAR-CLIP	23592263
MIRT461345	hsa-miR-1298-3p	PAR-CLIP	23592263
MIRT461344	hsa-miR-1289	PAR-CLIP	23592263
MIRT461342	hsa-miR-4294	PAR-CLIP	23592263
MIRT461343	hsa-miR-516b-5p	PAR-CLIP	23592263
MIRT461341	hsa-miR-3198	PAR-CLIP	23592263
MIRT461340	hsa-miR-4309	PAR-CLIP	23592263
MIRT461339	hsa-miR-1303	PAR-CLIP	23592263
MIRT440074	ebv-miR-BART10-3p	HITS-CLIP	22473208
MIRT440074	ebv-miR-BART10-3p	HITS-CLIP	22473208
MIRT727057	hsa-miR-27a-3p	HITS-CLIP	22473208
MIRT727056	hsa-miR-27b-3p	HITS-CLIP	22473208
MIRT461348	hsa-miR-590-3p	PAR-CLIP	23592263
MIRT461347	hsa-miR-3120-3p	PAR-CLIP	23592263
MIRT461346	hsa-miR-3126-3p	PAR-CLIP	23592263
MIRT461345	hsa-miR-1298-3p	PAR-CLIP	23592263
MIRT461344	hsa-miR-1289	PAR-CLIP	23592263
MIRT461342	hsa-miR-4294	PAR-CLIP	23592263
MIRT461343	hsa-miR-516b-5p	PAR-CLIP	23592263
MIRT461341	hsa-miR-3198	PAR-CLIP	23592263
MIRT461340	hsa-miR-4309	PAR-CLIP	23592263
MIRT461339	hsa-miR-1303	PAR-CLIP	23592263
MIRT1198986	hsa-miR-3607-5p	CLIP-seq
MIRT1198987	hsa-miR-4468	CLIP-seq
MIRT1198988	hsa-miR-4666-5p	CLIP-seq
MIRT1198989	hsa-miR-516b	CLIP-seq
MIRT1198990	hsa-miR-646	CLIP-seq
MIRT2057678	hsa-miR-128	CLIP-seq
MIRT2057679	hsa-miR-130a	CLIP-seq
MIRT2057680	hsa-miR-130b	CLIP-seq
MIRT2057681	hsa-miR-142-5p	CLIP-seq
MIRT2057682	hsa-miR-224	CLIP-seq
MIRT2057683	hsa-miR-27a	CLIP-seq
MIRT2057684	hsa-miR-27b	CLIP-seq
MIRT2057685	hsa-miR-301a	CLIP-seq
MIRT2057686	hsa-miR-301b	CLIP-seq
MIRT2057687	hsa-miR-340	CLIP-seq
MIRT2057688	hsa-miR-3649	CLIP-seq
MIRT2057689	hsa-miR-3666	CLIP-seq
MIRT2057690	hsa-miR-3685	CLIP-seq
MIRT2057691	hsa-miR-4295	CLIP-seq
MIRT2057692	hsa-miR-454	CLIP-seq
MIRT2057693	hsa-miR-4729	CLIP-seq
MIRT2057694	hsa-miR-489	CLIP-seq
MIRT2057695	hsa-miR-516a-3p	CLIP-seq
MIRT2057696	hsa-miR-545	CLIP-seq
MIRT2057697	hsa-miR-548aa	CLIP-seq
MIRT2057698	hsa-miR-548p	CLIP-seq
MIRT2057699	hsa-miR-570	CLIP-seq
MIRT2057700	hsa-miR-656	CLIP-seq
MIRT2057701	hsa-miR-659	CLIP-seq
MIRT2057702	hsa-miR-9	CLIP-seq
MIRT2057703	hsa-miR-935	CLIP-seq
MIRT2286039	hsa-miR-1236	CLIP-seq
MIRT2286040	hsa-miR-125a-3p	CLIP-seq
MIRT2057679	hsa-miR-130a	CLIP-seq
MIRT2057680	hsa-miR-130b	CLIP-seq
MIRT2286041	hsa-miR-148a	CLIP-seq
MIRT2286042	hsa-miR-148b	CLIP-seq
MIRT2286043	hsa-miR-152	CLIP-seq
MIRT2286044	hsa-miR-19a	CLIP-seq
MIRT2286045	hsa-miR-19b	CLIP-seq
MIRT2057682	hsa-miR-224	CLIP-seq
MIRT2057685	hsa-miR-301a	CLIP-seq
MIRT2057686	hsa-miR-301b	CLIP-seq
MIRT2286046	hsa-miR-3148	CLIP-seq
MIRT2057689	hsa-miR-3666	CLIP-seq
MIRT2286047	hsa-miR-376a	CLIP-seq
MIRT2286048	hsa-miR-376b	CLIP-seq
MIRT2286049	hsa-miR-3934	CLIP-seq
MIRT2286050	hsa-miR-3973	CLIP-seq
MIRT2286051	hsa-miR-4276	CLIP-seq
MIRT2057691	hsa-miR-4295	CLIP-seq
MIRT2057692	hsa-miR-454	CLIP-seq
MIRT2286052	hsa-miR-4717-3p	CLIP-seq
MIRT2286053	hsa-miR-4753-3p	CLIP-seq
MIRT1198989	hsa-miR-516b	CLIP-seq
MIRT2286054	hsa-miR-518a-5p	CLIP-seq
MIRT2286055	hsa-miR-527	CLIP-seq
MIRT2057697	hsa-miR-548aa	CLIP-seq
MIRT2286056	hsa-miR-548l	CLIP-seq
MIRT2057699	hsa-miR-570	CLIP-seq
MIRT2286057	hsa-miR-642b	CLIP-seq
MIRT2286058	hsa-miR-764	CLIP-seq
MIRT2057703	hsa-miR-935	CLIP-seq
MIRT2286040	hsa-miR-125a-3p	CLIP-seq
MIRT2286046	hsa-miR-3148	CLIP-seq
MIRT2286049	hsa-miR-3934	CLIP-seq
MIRT2286057	hsa-miR-642b	CLIP-seq
MIRT2286058	hsa-miR-764	CLIP-seq
MIRT2286039	hsa-miR-1236	CLIP-seq
MIRT2286040	hsa-miR-125a-3p	CLIP-seq
MIRT2057678	hsa-miR-128	CLIP-seq
MIRT2057679	hsa-miR-130a	CLIP-seq
MIRT2057680	hsa-miR-130b	CLIP-seq
MIRT2286041	hsa-miR-148a	CLIP-seq
MIRT2286042	hsa-miR-148b	CLIP-seq
MIRT2286043	hsa-miR-152	CLIP-seq
MIRT2286044	hsa-miR-19a	CLIP-seq
MIRT2286045	hsa-miR-19b	CLIP-seq
MIRT2057682	hsa-miR-224	CLIP-seq
MIRT2057683	hsa-miR-27a	CLIP-seq
MIRT2057684	hsa-miR-27b	CLIP-seq
MIRT2057685	hsa-miR-301a	CLIP-seq
MIRT2057686	hsa-miR-301b	CLIP-seq
MIRT2286046	hsa-miR-3148	CLIP-seq
MIRT2583972	hsa-miR-325	CLIP-seq
MIRT2057689	hsa-miR-3666	CLIP-seq
MIRT2286047	hsa-miR-376a	CLIP-seq
MIRT2286048	hsa-miR-376b	CLIP-seq
MIRT2286049	hsa-miR-3934	CLIP-seq
MIRT2286050	hsa-miR-3973	CLIP-seq
MIRT2286051	hsa-miR-4276	CLIP-seq
MIRT2057691	hsa-miR-4295	CLIP-seq
MIRT2057692	hsa-miR-454	CLIP-seq
MIRT2583973	hsa-miR-4671-3p	CLIP-seq
MIRT2286053	hsa-miR-4753-3p	CLIP-seq
MIRT2583974	hsa-miR-4775	CLIP-seq
MIRT2583975	hsa-miR-494	CLIP-seq
MIRT1198989	hsa-miR-516b	CLIP-seq
MIRT2286054	hsa-miR-518a-5p	CLIP-seq
MIRT2286055	hsa-miR-527	CLIP-seq
MIRT2057697	hsa-miR-548aa	CLIP-seq
MIRT2286056	hsa-miR-548l	CLIP-seq
MIRT2057699	hsa-miR-570	CLIP-seq
MIRT2583976	hsa-miR-628-3p	CLIP-seq
MIRT2286057	hsa-miR-642b	CLIP-seq
MIRT2286058	hsa-miR-764	CLIP-seq
MIRT2057703	hsa-miR-935	CLIP-seq
MIRT2286039	hsa-miR-1236	CLIP-seq
MIRT2286040	hsa-miR-125a-3p	CLIP-seq
MIRT2057678	hsa-miR-128	CLIP-seq
MIRT2057679	hsa-miR-130a	CLIP-seq
MIRT2057680	hsa-miR-130b	CLIP-seq
MIRT2286041	hsa-miR-148a	CLIP-seq
MIRT2286042	hsa-miR-148b	CLIP-seq
MIRT2286043	hsa-miR-152	CLIP-seq
MIRT2286044	hsa-miR-19a	CLIP-seq
MIRT2286045	hsa-miR-19b	CLIP-seq
MIRT2057683	hsa-miR-27a	CLIP-seq
MIRT2057684	hsa-miR-27b	CLIP-seq
MIRT2057685	hsa-miR-301a	CLIP-seq
MIRT2057686	hsa-miR-301b	CLIP-seq
MIRT2286046	hsa-miR-3148	CLIP-seq
MIRT2057689	hsa-miR-3666	CLIP-seq
MIRT2286049	hsa-miR-3934	CLIP-seq
MIRT2286050	hsa-miR-3973	CLIP-seq
MIRT2286051	hsa-miR-4276	CLIP-seq
MIRT2057691	hsa-miR-4295	CLIP-seq
MIRT2057692	hsa-miR-454	CLIP-seq
MIRT2286053	hsa-miR-4753-3p	CLIP-seq
MIRT2583975	hsa-miR-494	CLIP-seq
MIRT2286054	hsa-miR-518a-5p	CLIP-seq
MIRT2286055	hsa-miR-527	CLIP-seq
MIRT2057697	hsa-miR-548aa	CLIP-seq
MIRT2286056	hsa-miR-548l	CLIP-seq
MIRT2057699	hsa-miR-570	CLIP-seq
MIRT2286057	hsa-miR-642b	CLIP-seq
MIRT2286058	hsa-miR-764	CLIP-seq
MIRT2057703	hsa-miR-935	CLIP-seq

35 Show/Hide all (35)

GO ID	Ontology	Definition	Evidence	Reference
GO:0000775	Component	Chromosome, centromeric region	IEA
GO:0000776	Component	Kinetochore	IDA	17098863
GO:0000776	Component	Kinetochore	IEA
GO:0000972	Process	Transcription-dependent tethering of RNA polymerase II gene DNA at nuclear periphery	IBA
GO:0005515	Function	Protein binding	IPI	11564755, 15146057, 17363900, 24315095, 24725412, 24947832, 26411495, 26496610, 27194810, 30179222, 31046837, 33961781, 34819669, 35271311
GO:0005634	Component	Nucleus	IEA
GO:0005635	Component	Nuclear envelope	IDA	24315095
GO:0005635	Component	Nuclear envelope	TAS
GO:0005643	Component	Nuclear pore	IDA	11564755, 11684705, 17098863
GO:0005643	Component	Nuclear pore	IEA
GO:0005643	Component	Nuclear pore	NAS	24315095
GO:0005694	Component	Chromosome	IEA
GO:0005829	Component	Cytosol	TAS
GO:0006406	Process	MRNA export from nucleus	IDA	11684705
GO:0006606	Process	Protein import into nucleus	IBA
GO:0006913	Process	Nucleocytoplasmic transport	NAS	27016207
GO:0006999	Process	Nuclear pore organization	IMP	15146057
GO:0015031	Process	Protein transport	IEA
GO:0016020	Component	Membrane	HDA	19946888
GO:0016973	Process	Poly(A)+ mRNA export from nucleus	IBA
GO:0017056	Function	Structural constituent of nuclear pore	IBA
GO:0017056	Function	Structural constituent of nuclear pore	IDA	11684705
GO:0017056	Function	Structural constituent of nuclear pore	IEA
GO:0021915	Process	Neural tube development	IEA
GO:0022008	Process	Neurogenesis	IEA
GO:0031080	Component	Nuclear pore outer ring	IBA
GO:0031080	Component	Nuclear pore outer ring	IDA	15146057, 17360435
GO:0031080	Component	Nuclear pore outer ring	NAS	17363900
GO:0031965	Component	Nuclear membrane	IDA
GO:0048339	Process	Paraxial mesoderm development	IEA
GO:0048513	Process	Animal organ development	IEA
GO:0048731	Process	System development	IEA
GO:0051028	Process	MRNA transport	IEA
GO:0061053	Process	Somite development	IEA
GO:0072006	Process	Nephron development	IMP	30179222

MIM	HGNC	e!Ensembl
607613	18016	ENSG00000069248

Q8WUM0

Protein name

Nuclear pore complex protein Nup133 (133 kDa nucleoporin) (Nucleoporin Nup133)

Protein function

Involved in poly(A)+ RNA transport. Involved in nephrogenesis (PubMed:30179222).

PDB

1XKS , 3CQC , 3CQG , 3I4R , 5A9Q , 7PEQ , 7R5J , 7R5K

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF03177	Nucleoporin_C	594 → 1024	Non-repetitive/WGA-negative nucleoporin C-terminal	Family

Tissue specificity

TISSUE SPECIFICITY: Widely expressed in fetal and adult tissues. Expressed in the brain and kidney. {ECO:0000269|PubMed:30427554}.

Sequence

MFPAAPSPRTPGTGSRRGPLAGLGPGSTPRTASRKGLPLGSAVSSPVLFSPVGRRSSLSS
RGTPTRMFPHHSITESVNYDVKTFGSSLPVKVMEALTLAEVDDQLTINIDEGGWACLVCK
EKLIIWKIALSPITKLSVCKELQLPPSDFHWSADLVALSYSSPSGEAHSTQAVAVMVATR
EGSIRYWPSLAGEDTYTEAFVDSGGDKTYSFLTAVQGGSFILSSSGSQLIRLIPESSGKI
HQHILPQGQGMLSGIGRKVSSLFGILSPSSDLTLSSVLWDRERSSFYSLTSSNISKWELD
DSSEKHAYSWDINRALKENITDAIWGSESNYEAIKEGVNIRYLDLKQNCDGLVILAAAWH
SADNPCLIYYSLITIEDNGCQMSDAVTVEVTQYNPPFQSEDLILCQLTVPNFSNQTAYLY
NESAVYVCSTGTGKFSLPQEKIVFNAQGDSVLGAGACGGVPIIFSRNSGLVSITSRENVS
ILAEDLEGSLASSVAGPNSESMIFETTTKNETIAQEDKIKLLKAAFLQYCRKDLGHAQMV
VDELFSSHSDLDSDSELDRAVTQISVDLMDDYPASDPRWAESVPEEAPGFSNTSLIILHQ
LEDKMKAHSFLMDFIHQVGLFGRLGSFPVRGTPMATRLLLCEHAEKLSAAIVLKNHHSRL
SDLVNTAILIALNKREYEIPSNLTPADVFFREVSQVDTICECLLEHEEQVLRDAPMDSIE
WAEVVINVNNILKDMLQAASHYRQNRNSLYRREESLEKEPEYVPWTATSGPGGIRTVIIR
QHEIVLKVAYPQADSNLRNIVTEQLVALIDCFLDGYVSQLKSVDKSSNRERYDNLEMEYL
QKRSDLLSPLLSLGQYLWAASLAEKYCDFDILVQMCEQTDNQSRLQRYMTQFADQNFSDF
LFRWYLEKGKRGKLLSQPISQHGQLANFLQAHEHLSWLHEINSQELEKAHATLLGLANME
TRYFAKKKTLLGLSKLAALASDFSEDMLQEKIEEMAEQERFLLHQETLPEQLLAEKQLNL
SAMPVLTAPQLIGLYICEENRRANEYDFKKALDLLEYIDEEEDININDLKLEILCKALQR
DNWSSSDGKDDPIEVSKDSIFVKILQKLLKDGIQLSEYLPEVKDLLQADQLGSLKSNPYF
EFVLKANYEYYVQGQI

Sequence length

1156

Interactions

View interactions

KEGG Pathway	Reactome Pathway
Nucleocytoplasmic transport	ISG15 antiviral mechanism
Amyotrophic lateral sclerosis	Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal
	Transport of the SLBP independent Mature mRNA
	Transport of the SLBP Dependant Mature mRNA
	Transport of Mature mRNA Derived from an Intronless Transcript
	Transport of Mature mRNA derived from an Intron-Containing Transcript
	Rev-mediated nuclear export of HIV RNA
	Transport of Ribonucleoproteins into the Host Nucleus
	NS1 Mediated Effects on Host Pathways
	Viral Messenger RNA Synthesis
	NEP/NS2 Interacts with the Cellular Export Machinery
	Regulation of Glucokinase by Glucokinase Regulatory Protein
	Vpr-mediated nuclear import of PICs
	snRNP Assembly
	Separation of Sister Chromatids
	Resolution of Sister Chromatid Cohesion
	SUMOylation of DNA damage response and repair proteins
	SUMOylation of ubiquitinylation proteins
	Nuclear Pore Complex (NPC) Disassembly
	Regulation of HSF1-mediated heat shock response
	SUMOylation of SUMOylation proteins
	SUMOylation of chromatin organization proteins
	SUMOylation of RNA binding proteins
	SUMOylation of DNA replication proteins
	Transcriptional regulation by small RNAs
	Defective TPR may confer susceptibility towards thyroid papillary carcinoma (TPC)
	RHO GTPases Activate Formins
	tRNA processing in the nucleus
	Mitotic Prometaphase
	HCMV Early Events
	HCMV Late Events
	Postmitotic nuclear pore complex (NPC) reformation
	EML4 and NUDC in mitotic spindle formation

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)

Phenotype Name	Clinical Significance	dbSNP ID	RCV Accession	Evidence Score
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Galloway-Mowat syndrome 8	Pathogenic; Likely pathogenic	rs1433513056, rs1660478193	RCV000760137 RCV001291775	★★★★★ ★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Nephrotic syndrome, type 18	Likely pathogenic	rs760521214, rs1558108130, rs1558091788	RCV001808225 RCV000721158 RCV000721160	★★★★★ ★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)

Phenotype Name	Clinical Significance	Source	Reference	Evidence Score
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal. Show/Hide Unknown Diseases (22)
Acute myeloid leukemia	Benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Chronic lymphocytic leukemia/small lymphocytic lymphoma	Benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Clear cell carcinoma of kidney	Benign; Likely benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Colon adenocarcinoma	Likely benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Colorectal cancer	Uncertain significance	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
DIABETES MELLITUS	—	GWAS catalog	39024449	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
FAMILIAL IDIOPATHIC STEROID-RESISTANT NEPHROTIC SYNDROME	—	GWAS catalog	30179222	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
focal and segmental glomerulosclerosis	Uncertain significance	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
GALLOWAY MOWAT SYNDROME	—	Disgenet	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Galloway-Mowat syndrome	Uncertain significance	ClinVar CTD, Orphanet CTD, Orphanet	30427554, 30427554	★★★★★ ★★★☆☆ Reported in Unknown/Other Associations (≥2 sources)
Gastric cancer	Benign; Likely benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
GENETIC STEROID-RESISTANT NEPHROTIC SYNDROME	—	Disgenet	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Hepatocellular carcinoma	Likely benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
HEREDITARY STEROID-RESISTANT NEPHROTIC SYNDROME	—	Orphanet	30179222	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Malignant tumor of esophagus	Benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
NUP133-related disorder	Likely benign; Benign; Uncertain significance	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
POST-TRAUMATIC STRESS DISORDER	—	GWAS catalog	33510476	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Sarcoma	Benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Thymoma	Benign; Likely benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS	—	GWAS catalog	32499647	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine carcinosarcoma	Benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Uterine corpus endometrial carcinoma	Benign; Likely benign	ClinVar	—	★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations

Disease Name	Disease (Merged)	Source	PMID	Relationship Type	Evidence Score
Associations from Text Mining Disease associations identified through text mining Show/Hide Text Mining Associations (35)
Aqueductal Stenosis	Aqueductal Stenosis	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Brain Diseases	Brain disease	Pubtator	36755238	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Chronic kidney disease stage 5	Kidney Disease	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Dental Enamel Hypoplasia	Dental Enamel Hypoplasia	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Dwarfism	Dwarfism	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Focal cortical dysplasia	Focal cortical dysplasia	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Focal glomerulosclerosis	Glomerulosclerosis	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Galloway Mowat syndrome	Galloway-Mowat Syndrome	BEFREE	30427554		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Galloway Mowat syndrome	Galloway-Mowat Syndrome	ORPHANET_DG	30427554		★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Galloway-Mowat syndrome	Galloway-Mowat Syndrome	Orphanet			★★★★★ ★★★☆☆ Reported in Unknown/Other Associations (≥2 sources)
Genetic steroid-resistant nephrotic syndrome	Genetic Steroid-Resistant Nephrotic Syndrome	Orphanet			★★★★★ ★★☆☆☆ Found in Text Mining + Unknown/Other Associations
Global developmental delay	Developmental Delay	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Glomerulosclerosis Focal Segmental	Focal segmental glomerulosclerosis	Pubtator	37565816	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Hemiplegia/hemiparesis	Hemiplegia/hemiparesis	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Hiatal Hernia	Hiatal Hernia	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Hypoalbuminemia	Hypoalbuminemia	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Impaired cognition	Impaired Cognition	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Kidney Diseases	Kidney Disease	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Macrotia	Macrotia	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Malignant neoplasm of breast	Breast Cancer	UNIPROT_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Microcephaly	Microcephaly	BEFREE	30427554		★★★★★ ★☆☆☆☆ Found in Text Mining only
Microcephaly	Microcephaly	Pubtator	36755238	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Microcephaly	Microcephaly	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Micrognathism	Micrognathism	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Multiple Myeloma	Multiple myeloma	BEFREE	29861858		★★★★★ ★☆☆☆☆ Found in Text Mining only
Nephrotic Syndrome	Nephrotic Syndrome	BEFREE	30894603		★★★★★ ★☆☆☆☆ Found in Text Mining only
Nephrotic Syndrome	Nephrotic syndrome	Pubtator	35455939	Associate	★★★★★ ★☆☆☆☆ Found in Text Mining only
Nephrotic Syndrome	Nephrotic Syndrome	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
NEPHROTIC SYNDROME, STEROID-RESISTANT, AUTOSOMAL RECESSIVE	Nephritis	ORPHANET_DG	30179222		★★★★★ ★☆☆☆☆ Found in Text Mining only
NEPHROTIC SYNDROME, TYPE 18	Nephrotic Syndrome	UNIPROT_DG	30179222		★★★★★ ★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
NEPHROTIC SYNDROME, TYPE 18	Nephrotic Syndrome	CLINVAR_DG	30179222		★★★★★ ★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
NEPHROTIC SYNDROME, TYPE 18	Nephrotic Syndrome	GENOMICS_ENGLAND_DG	30179222, 30427554		★★★★★ ★★★★☆ ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Pachygyria	Pachygyria	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Steroid resistant nephrotic syndrome of childhood	Steroid resistant nephrotic syndrome	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only
Strabismus	Strabismus	HPO_DG			★★★★★ ★☆☆☆☆ Found in Text Mining only

Related Gene	Shared Diseases	Shared Disease Names	Shared Pathways	Shared Pathway Names	Shared Evidence Sources	Shared Evidence Names
NUP107	5	["Idiopathic steroid-resistant nephrotic syndrome","Galloway-mowat syndrome","Genetic steroid-resistant nephrotic syndrome","Hereditary steroid-resistant nephrotic syndrome","Nephrotic syndrome"]	34	["Nucleocytoplasmic transport","Regulation of HSF1-mediated heat shock response","Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal","Separation of Sister Chromatids","Resolution of Sister Chromatid Cohesion","RHO GTPases Activate Formins","Mitotic Prometaphase","EML4 and NUDC in mitotic spindle formation","HCMV Late Events","SUMOylation of DNA damage response and repair proteins","SUMOylation of chromatin organization proteins","SUMOylation of RNA binding proteins"]	10	["Disgenet (Galloway-mowat syndrome)","CTD (Galloway-mowat syndrome)","Orphanet (Galloway-mowat syndrome)","ClinVar (Galloway-mowat syndrome)","HPO (Galloway-mowat syndrome)","Disgenet (Genetic steroid-resistant nephrotic syndrome)","Orphanet (Hereditary steroid-resistant nephrotic syndrome)","Disgenet (Nephrotic syndrome)","ClinVar (Nephrotic syndrome)","HPO (Nephrotic syndrome)"]
NUP205	4	["Idiopathic steroid-resistant nephrotic syndrome","Genetic steroid-resistant nephrotic syndrome","Hereditary steroid-resistant nephrotic syndrome","Nephrotic syndrome"]	28	["Nucleocytoplasmic transport","Regulation of HSF1-mediated heat shock response","HCMV Late Events","SUMOylation of DNA damage response and repair proteins","SUMOylation of chromatin organization proteins","SUMOylation of RNA binding proteins","snRNP Assembly","HCMV Early Events","Transport of the SLBP independent Mature mRNA","Transport of the SLBP Dependant Mature mRNA","Transport of Mature mRNA Derived from an Intronless Transcript","Transport of Mature mRNA derived from an Intron-Containing Transcript"]	8	["GWAS catalog (Idiopathic steroid-resistant nephrotic syndrome)","Disgenet (Genetic steroid-resistant nephrotic syndrome)","Orphanet (Hereditary steroid-resistant nephrotic syndrome)","ClinGen (Nephrotic syndrome)","Disgenet (Nephrotic syndrome)","GWAS catalog (Nephrotic syndrome)","ClinVar (Nephrotic syndrome)","HPO (Nephrotic syndrome)"]
NUP160	4	["Idiopathic steroid-resistant nephrotic syndrome","Genetic steroid-resistant nephrotic syndrome","Hereditary steroid-resistant nephrotic syndrome","Nephrotic syndrome"]	34	["Nucleocytoplasmic transport","Regulation of HSF1-mediated heat shock response","Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal","Separation of Sister Chromatids","Resolution of Sister Chromatid Cohesion","RHO GTPases Activate Formins","Mitotic Prometaphase","EML4 and NUDC in mitotic spindle formation","HCMV Late Events","SUMOylation of DNA damage response and repair proteins","SUMOylation of chromatin organization proteins","SUMOylation of RNA binding proteins"]	6	["Disgenet (Genetic steroid-resistant nephrotic syndrome)","Orphanet (Hereditary steroid-resistant nephrotic syndrome)","ClinGen (Nephrotic syndrome)","Disgenet (Nephrotic syndrome)","ClinVar (Nephrotic syndrome)","HPO (Nephrotic syndrome)"]
NUP85	4	["Idiopathic steroid-resistant nephrotic syndrome","Genetic steroid-resistant nephrotic syndrome","Hereditary steroid-resistant nephrotic syndrome","Nephrotic syndrome"]	34	["Nucleocytoplasmic transport","Regulation of HSF1-mediated heat shock response","Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal","Separation of Sister Chromatids","Resolution of Sister Chromatid Cohesion","RHO GTPases Activate Formins","Mitotic Prometaphase","EML4 and NUDC in mitotic spindle formation","HCMV Late Events","SUMOylation of DNA damage response and repair proteins","SUMOylation of chromatin organization proteins","SUMOylation of RNA binding proteins"]	5	["Disgenet (Genetic steroid-resistant nephrotic syndrome)","Orphanet (Hereditary steroid-resistant nephrotic syndrome)","Disgenet (Nephrotic syndrome)","ClinVar (Nephrotic syndrome)","HPO (Nephrotic syndrome)"]
NUP93	4	["Idiopathic steroid-resistant nephrotic syndrome","Genetic steroid-resistant nephrotic syndrome","Hereditary steroid-resistant nephrotic syndrome","Nephrotic syndrome"]	28	["Nucleocytoplasmic transport","Regulation of HSF1-mediated heat shock response","HCMV Late Events","SUMOylation of DNA damage response and repair proteins","SUMOylation of chromatin organization proteins","SUMOylation of RNA binding proteins","snRNP Assembly","HCMV Early Events","Transport of the SLBP independent Mature mRNA","Transport of the SLBP Dependant Mature mRNA","Transport of Mature mRNA Derived from an Intronless Transcript","Transport of Mature mRNA derived from an Intron-Containing Transcript"]	6	["Disgenet (Genetic steroid-resistant nephrotic syndrome)","Orphanet (Hereditary steroid-resistant nephrotic syndrome)","ClinGen (Nephrotic syndrome)","Disgenet (Nephrotic syndrome)","ClinVar (Nephrotic syndrome)","HPO (Nephrotic syndrome)"]

NUP133 (nucleoporin 133)

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