ConVarT

Nup98 (GeneID: 269966) | Mus musculus

Description:	nucleoporin 98 [Source:MGI Symbol;Acc:MGI:109404]
Synonyms:	4732457F17, Nup96, AI849286
Other ID(s):	ENSMUSG00000063550, MGI:109404
Protein Accession Numbers:	NP_001274094, XP_030098484, XP_006507959, NP_001274096, NP_001274093, XP_030098483, XP_006507958, NP_001274095, XP_006507960, NP_075355
Statistics:

∙ Please click the name of species for the protein accession number used in the alignment.
∙ A p letter used as a pointer to positions of post translational modifications in human.
∙ Protein domains illustrated above belong to Homo sapiens (Human).
∙ ClinVar stacked bar chart represents whole protein isoforms of the gene. Please, check the other protein isoforms of the gene below.
∙ If more than one transcripts below are active (with blue background color), it means all the active transcripts have the same sequence.
ENST00000355260 ENST00000359171 ENST00000397004 ENST00000397007 ENST00000397013 ENST00000429801 ENST00000524563 ENST00000527104 ENST00000529063 ENST00000529379 ENST00000532475 ENST00000533346 NP_001352054 NP_001352055 NP_001352056 NP_001352057 NP_001352058 NP_005378 NP_057404 NP_624357 NP_624358 ">ENST00000324932

ClinVar Data

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Variation ID	Allele ID	RS Number	Variant Type	Record	Alteration	Clinicial Sig.	Last Update	Phenotypes	Cytogenetic	Review Status	RCV Acc.N.

gnomAD

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Variant ID	Transcript ID	Alteration	Annotation	Allele C.	Allele N.	Allele F.	rsNumber	Flags	Filter
No data available in table

Showing 0 to 0 of 0 entries

Post-translational Modifications (PTMs)

Gene Name	ACC ID	PTM Type	Position	Mod-rsd	Site +/-7 Aa	Mw_kd	Site grpID

Catalogue of Somatic Mutations in Cancer (COSMIC)

Gene Name	Transcript ID	Sample name	Primary Site	Primary Histology	Mutation ID	Mutation CDS	Mutation Aa	Mutation Desc.	FATHMM Prediction	FATHMM Score	Mutation Somatic Status	PUBMED PMID	Tumor Origin	Position

dbSNP

Gene ID	Transcript ID	Consequence	Position	HGVSp	Impact

Protein Domains (PFAM)

Pfam Domain	Domain Name	Description	Positions	Clan	Clan Name	Organism
NO RESULT FOUND
PF04096	Nucleoporin2	Nucleoporin autopeptidase	777-924	CL0661	Gain	Caenorhabditis elegans
PF12110	Nup96	Nuclear protein 96	1253-1515			Caenorhabditis elegans
PF13634	Nucleoporin_FG	Nucleoporin FG repeat region	59-138	CL0647	FG_rpt	Caenorhabditis elegans
PF13634	Nucleoporin_FG	Nucleoporin FG repeat region	275-362	CL0647	FG_rpt	Caenorhabditis elegans
PF13634	Nucleoporin_FG	Nucleoporin FG repeat region	198-278	CL0647	FG_rpt	Caenorhabditis elegans
PF13634	Nucleoporin_FG	Nucleoporin FG repeat region	1-86	CL0647	FG_rpt	Caenorhabditis elegans
PF13634	Nucleoporin_FG	Nucleoporin FG repeat region	418-494	CL0647	FG_rpt	Caenorhabditis elegans
PF13634	Nucleoporin_FG	Nucleoporin FG repeat region	359-424	CL0647	FG_rpt	Caenorhabditis elegans

List of the diseases from DisGeNET

Disease Name	Disease Category	DSI*	DPI**
Anemia	Hemic and Lymphatic Diseases ;	0.586	0.414
Malignant neoplasm of breast	Neoplasms ; Skin and Connective Tissue Diseases ;	0.586	0.414
Leukemia, Myelocytic, Acute	Neoplasms ;	0.586	0.414
Lymphopenia	Hemic and Lymphatic Diseases ; Immune System Diseases ;	0.586	0.414
Acute Myeloid Leukemia, M1	Neoplasms ;	0.586	0.414
Neutropenia	Hemic and Lymphatic Diseases ;	0.586	0.414
Acute Myeloid Leukemia (AML-M2)	Neoplasms ;	0.586	0.414
NO RESULT FOUND