Gene Gene information from NCBI Gene database.
Entrez ID 29978
Gene name Ubiquilin 2
Gene symbol UBQLN2
Synonyms (NCBI Gene)
ALS15CHAP1DSK2HRIHFB2157N4BP4PLIC2
Chromosome X
Chromosome location Xp11.21
Summary This gene encodes an ubiquitin-like protein (ubiquilin) that shares high degree of similarity with related products in yeast, rat and frog. Ubiquilins contain a N-terminal ubiquitin-like domain and a C-terminal ubiquitin-associated domain. They physically
SNPs SNP information provided by dbSNP.
6
SNP ID Visualize variation Clinical significance Consequence
rs45559331 C>A,T Likely-benign, conflicting-interpretations-of-pathogenicity, benign Coding sequence variant, synonymous variant
rs369947678 C>A,G,T Benign, pathogenic, pathogenic-likely-pathogenic Missense variant, coding sequence variant
rs387906709 C>A,T Pathogenic Missense variant, coding sequence variant
rs387906710 C>T Pathogenic Missense variant, coding sequence variant
rs387906711 C>A,T Pathogenic Missense variant, coding sequence variant
miRNA miRNA information provided by mirtarbase database.
306
miRTarBase ID miRNA Experiments Reference
MIRT020846 hsa-miR-155-5p Proteomics 18668040
MIRT025411 hsa-miR-34a-5p Proteomics 21566225
MIRT025411 hsa-miR-34a-5p Proteomics 21566225
MIRT025411 hsa-miR-34a-5p Proteomics 21566225
MIRT041770 hsa-miR-484 CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
28
GO ID Ontology Definition Evidence Reference
GO:0000045 Process Autophagosome assembly IBA
GO:0005515 Function Protein binding IPI 15231748, 17098253, 18199683, 18307982, 18497817, 20059542, 21988832, 23459205, 23541532, 24215460, 24811749, 25616961, 32296183, 32814053, 35914814, 36217029
GO:0005634 Component Nucleus IEA
GO:0005737 Component Cytoplasm IDA 18199683
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
300264 12509 ENSG00000188021
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9UHD9
Protein name Ubiquilin-2 (Chap1) (DSK2 homolog) (Protein linking IAP with cytoskeleton 2) (PLIC-2) (hPLIC-2) (Ubiquitin-like product Chap1/Dsk2)
Protein function Plays an important role in the regulation of different protein degradation mechanisms and pathways including ubiquitin-proteasome system (UPS), autophagy and the endoplasmic reticulum-associated protein degradation (ERAD) pathway. Mediates the p
PDB 1J8C , 2NBV , 6MUN , 7F7X
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00240 ubiquitin 33 105 Ubiquitin family Domain
PF00627 UBA 581 618 UBA/TS-N domain Domain
Sequence
MAENGESSGPPRPSRGPAAAQGSAAAPAEPKIIKVTVKTPKEKEEFAVPENSSVQQFKEA
ISKRFKSQTDQLVLIFAGKILKDQDTLIQHGIHDGLTVHLVIKSQ
NRPQGQSTQPSNAAG
TNTTSASTPRSNSTPISTNSNPFGLGSLGGLAGLSSLGLSSTNFSELQSQMQQQLMASPE
MMIQIMENPFVQSMLSNPDLMRQLIMANPQMQQLIQRNPEISHLLNNPDIMRQTLEIARN
PAMMQEMMRNQDLALSNLESIPGGYNALRRMYTDIQEPMLNAAQEQFGGNPFASVGSSSS
SGEGTQPSRTENRDPLPNPWAPPPATQSSATTSTTTSTGSGSGNSSSNATGNTVAAANYV
ASIFSTPGMQSLLQQITENPQLIQNMLSAPYMRSMMQSLSQNPDLAAQMMLNSPLFTANP
QLQEQMRPQLPAFLQQMQNPDTLSAMSNPRAMQALMQIQQGLQTLATEAPGLIPSFTPGV
GVGVLGTAIGPVGPVTPIGPIGPIVPFTPIGPIGPIGPTGPAAPPGSTGSGGPTGPTVSS
AAPSETTSPTSESGPNQQFIQQMVQALAGANAPQLPNPEVRFQQQLEQLNAMGFLNREAN
LQALIATGGDINAAIERL
LGSQPS
Sequence length 624
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG  Reactome
  Protein processing in endoplasmic reticulum
Amyotrophic lateral sclerosis
  Cargo recognition for clathrin-mediated endocytosis
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
178
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Amyotrophic lateral sclerosis type 15 Pathogenic rs387906709, rs387906710, rs387906711 RCV000022842
RCV000022843
RCV000022844
UBQLN2-related disorder Likely pathogenic rs2519963370 RCV003402318
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Amyotrophic lateral sclerosis Conflicting classifications of pathogenicity rs369947678 RCV000625776
Amyotrophic Lateral Sclerosis, Dominant Conflicting classifications of pathogenicity; Benign; Likely benign; Uncertain significance rs45559331, rs192883799, rs1057515975, rs1057515980, rs1057515973, rs778382794, rs142250604, rs1057515977, rs41306757, rs1057515974, rs1057515976, rs990201540, rs1057515979 RCV000399814
RCV000294537
RCV000349652
RCV000303430
RCV000325002
RCV000385557
RCV000336836
RCV000297168
RCV000358178
RCV000388853
RCV000281846
RCV000342793
RCV000400643
Vascular dementia Uncertain significance rs771147923 RCV002051769
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Adenocarcinoma of Lung Associate 35063704
Alzheimer Disease Inhibit 24086754
Alzheimer Disease Associate 34130600
Amyotrophic Lateral Sclerosis Associate 21857683, 22426854, 22766032, 23541532, 24086754, 25681989, 26075709, 28125704, 28430856, 28716533, 30442662, 30982635, 31167121, 32413959, 32731393
View all (8 more)
Amyotrophic lateral sclerosis 1 Associate 21857683, 23541532, 24086754, 25681989, 28125704, 36232630, 37257946
Ataxia Associate 34130600
Brain Diseases Associate 34130600
Carcinoma Hepatocellular Associate 32293796
Chediak Higashi Syndrome Associate 34130600
Chronic Kidney Diseases of Uncertain Etiology Associate 28125704