USP17L21

gene
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Summary

USP17L21 (ubiquitin specific peptidase 17 like family member 21, HGNC:44449) is a protein-coding gene on chromosome 4p16.1, encoding Ubiquitin carboxyl-terminal hydrolase 17-like protein 21 (D6R901). Deubiquitinating enzyme that removes conjugated ubiquitin from specific proteins to regulate different cellular processes that may include cell proliferation, progression through the cell cycle, apoptosis, cell migration, and the cellular response to viral infection.

Predicted to enable cysteine-type deubiquitinase activity. Predicted to be involved in regulation of apoptotic process and regulation of protein stability. Predicted to be located in endoplasmic reticulum. Predicted to be active in cytosol and nucleus.

Source: NCBI Gene 100287478 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001256862

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:44449
Approved symbolUSP17L21
Nameubiquitin specific peptidase 17 like family member 21
Location4p16.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000249811
Ensembl biotypeprotein_coding
Entrez100287478

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000506414

RefSeq mRNA: 1 — MANE Select: NM_001256862 NM_001256862

CCDS: CCDS59462

Canonical transcript exons

ENST00000506414 — 1 exons

ExonStartEnd
ENSE0000205291792628729264464

Expression profiles

Bgee: expression breadth not_expressed, 0 present calls, max score 37.20.

Top tissues by expression

130 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039737.20gold quality
ganglionic eminenceUBERON:000402337.12gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
bone marrowUBERON:000237132.78gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
muscle tissueUBERON:000238531.06gold quality
sural nerveUBERON:001548830.93gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.34gold quality
liverUBERON:000210728.78gold quality
lymph nodeUBERON:000002928.67gold quality
duodenumUBERON:000211428.14gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.88gold quality
vermiform appendixUBERON:000115426.42gold quality
bloodUBERON:000017826.07gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
muscle of legUBERON:000138325.61gold quality
leukocyteCL:000073824.80gold quality
primary visual cortexUBERON:000243624.61gold quality
monocyteCL:000057624.52gold quality
kidneyUBERON:000211324.51gold quality
gastrocnemiusUBERON:000138824.49gold quality
right lobe of liverUBERON:000111424.28gold quality
superior frontal gyrusUBERON:000266124.08gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

Cross-species orthologs

0 orthologs

Paralogs (71): USP2 (ENSG00000036672), USP28 (ENSG00000048028), USP36 (ENSG00000055483), USP13 (ENSG00000058056), USP33 (ENSG00000077254), USP40 (ENSG00000085982), USP48 (ENSG00000090686), USP14 (ENSG00000101557), USP11 (ENSG00000102226), USP10 (ENSG00000103194), USP31 (ENSG00000103404), USP42 (ENSG00000106346), USP5 (ENSG00000111667), USP4 (ENSG00000114316), USP9Y (ENSG00000114374), USP34 (ENSG00000115464), USP35 (ENSG00000118369), USP45 (ENSG00000123552), USP22 (ENSG00000124422), USP9X (ENSG00000124486), USP6 (ENSG00000129204), USP29 (ENSG00000131864), USP26 (ENSG00000134588), USP30 (ENSG00000135093), USP15 (ENSG00000135655), USP37 (ENSG00000135913), USP44 (ENSG00000136014), USP20 (ENSG00000136878), USP8 (ENSG00000138592), USP3 (ENSG00000140455), USP21 (ENSG00000143258), USP43 (ENSG00000154914), USP25 (ENSG00000155313), USP16 (ENSG00000156256), USP24 (ENSG00000162402), USP1 (ENSG00000162607), USP49 (ENSG00000164663), USP38 (ENSG00000170185), USP50 (ENSG00000170236), USP47 (ENSG00000170242)

Protein

Protein identifiers

Ubiquitin carboxyl-terminal hydrolase 17-like protein 21D6R901 (reviewed: D6R901)

All UniProt accessions (1): D6R901

UniProt curated annotations — full annotation on UniProt →

Function. Deubiquitinating enzyme that removes conjugated ubiquitin from specific proteins to regulate different cellular processes that may include cell proliferation, progression through the cell cycle, apoptosis, cell migration, and the cellular response to viral infection.

Subcellular location. Nucleus. Endoplasmic reticulum.

Similarity. Belongs to the peptidase C19 family. USP17 subfamily.

RefSeq proteins (1): NP_001243791* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR001394Peptidase_C19_UCHDomain
IPR018200USP_CSConserved_site
IPR028889USPDomain
IPR038765Papain-like_cys_pep_sfHomologous_superfamily
IPR050164Peptidase_C19Family

Pfam: PF00443

UniProt features (10 total): compositionally biased region 4, region of interest 2, active site 2, chain 1, domain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-D6R901-F167.770.44

Functional residue map

Curated UniProt residues grouped by drug-discovery relevance — catalytic, ligand-binding, modification, and mutation-validated positions. Source: UniProtKB sequence features.

Catalytic / active sites (2): 89 (nucleophile); 334 (proton acceptor)

Function

Pathways and Gene Ontology

Reactome pathways

1 pathways

IDPathway
R-HSA-5689880Ub-specific processing proteases

MSigDB gene sets: 14 (showing top): GOBP_PROTEIN_MODIFICATION_BY_SMALL_PROTEIN_REMOVAL, GOMF_CYSTEINE_TYPE_PEPTIDASE_ACTIVITY, chr4p16, GOBP_POST_TRANSLATIONAL_PROTEIN_MODIFICATION, GOBP_REGULATION_OF_PROTEIN_STABILITY, GOBP_PROTEOLYSIS, GOMF_PEPTIDASE_ACTIVITY, GOMF_UBIQUITIN_LIKE_PROTEIN_PEPTIDASE_ACTIVITY, REACTOME_POST_TRANSLATIONAL_PROTEIN_MODIFICATION, REACTOME_DEUBIQUITINATION, REACTOME_UB_SPECIFIC_PROCESSING_PROTEASES, GOBP_REGULATION_OF_PROGRAMMED_CELL_DEATH, GOBP_PROTEIN_MODIFICATION_PROCESS, GOMF_DEUBIQUITINASE_ACTIVITY

GO Biological Process (4): proteolysis (GO:0006508), protein deubiquitination (GO:0016579), regulation of protein stability (GO:0031647), regulation of apoptotic process (GO:0042981)

GO Molecular Function (4): cysteine-type deubiquitinase activity (GO:0004843), peptidase activity (GO:0008233), cysteine-type peptidase activity (GO:0008234), hydrolase activity (GO:0016787)

GO Cellular Component (3): nucleus (GO:0005634), endoplasmic reticulum (GO:0005783), cytosol (GO:0005829)

Reactome top-level categories

Rollup of top-1 pathways:

CategoryPathways
Deubiquitination1

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
intracellular membrane-bounded organelle2
cytoplasm2
protein metabolic process1
cysteine-type deubiquitinase activity1
protein modification by small protein removal1
regulation of biological quality1
apoptotic process1
regulation of programmed cell death1
cysteine-type peptidase activity1
deubiquitinase activity1
hydrolase activity1
catalytic activity, acting on a protein1
peptidase activity1
catalytic activity1
endomembrane system1
cellular anatomical structure1

Protein interactions and networks

STRING

46 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
USP17L21RCE1Q9Y256112
USP17L21USP17L22D6RA6164
USP17L21SUN3Q8TAQ90
USP17L21CDC25AP303040
USP17L21USP17L2Q6R6M40
USP17L21RIGIO957860
USP17L21USP17L12C9JPN90
USP17L21USP17L11C9JVI00
USP17L21USP17L10C9JJH30
USP17L21USP17L13C9JLJ40
USP17L21USP17L25Q0WX570
USP17L21USP17L3A6NCW00
USP17L21USP17L4A6NCW70
USP17L21USP17L5A8MUK10
USP17L21USP17L15C9J2P70
USP17L21USP17L18D6R9N70
USP17L21USP17L17D6RBQ60
USP17L21USP17L19D6RCP70
USP17L21USP17L20D6RJB60
USP17L21USP17L8P0C7I00

IntAct

2 interactions, top by confidence:

ABTypeScore
Mpsi-mi:“MI:0914”(association)0.350

BioGRID (5): USP17L21 (Positive Genetic), USP17L21 (Synthetic Lethality), USP17L21 (Affinity Capture-MS), USP17L21 (Affinity Capture-MS), USP17L21 (Affinity Capture-MS)

ESM2 similar proteins: A2A5N8, A6NCW0, A6NCW7, A8MUK1, B1AQJ2, B2RQC2, C9J2P7, C9JJH3, C9JLJ4, C9JPN9, C9JVI0, D3ZWK4, D6R901, D6R9N7, D6RA61, D6RBM5, D6RBQ6, D6RCP7, D6RJB6, E9Q9U0, G5E8G2, G5E8I7, O94966, P0C7H9, P0C7I0, P35125, P51784, Q0E2F9, Q0WX57, Q2TAC6, Q3UJD6, Q4KLL9, Q5R7G8, Q5TKR9, Q61068, Q66HE5, Q6J1Y9, Q6PFD6, Q6QN14, Q6R6M4

Diamond homologs: A1L1K8, A6NCW0, A6NCW7, A8MUK1, C9J2P7, C9JJH3, C9JLJ4, C9JPN9, C9JVI0, D6R901, D6R9N7, D6RA61, D6RBQ6, D6RCP7, D6RJB6, G1SW77, P0C7H9, P0C7I0, Q0WX57, Q5JVS0, Q5XJA5, Q6AXS5, Q6NRY1, Q6PB22, Q6R6M4, Q7RTZ2, Q8NC51, Q9CY58, Q9I9R0, Q9JKS5, A0JM59, A5PMR2, A5PN09, A6H8I0, A6NNY8, A6QNM7, A7Z056, B1AY13, B1WBD7, D3ZJ96

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

0 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

72 predictions. Top by Δscore:

VariantEffectΔscore
4:9264162:G:GTdonor_gain0.5500
4:9264163:A:Tdonor_gain0.5300
4:9264145:TGGA:Tdonor_gain0.4900
4:9264236:CGAAG:Cdonor_loss0.4700
4:9264237:GAAG:Gdonor_loss0.4700
4:9264238:AAG:Adonor_loss0.4700
4:9264239:AG:Adonor_loss0.4700
4:9264240:GGTAC:Gdonor_loss0.4700
4:9264241:G:GAdonor_loss0.4700
4:9264242:T:Adonor_loss0.4700
4:9264089:A:Tdonor_gain0.4500
4:9264235:TCGAA:Tdonor_loss0.4400
4:9264243:A:Cdonor_loss0.4300
4:9263615:A:Tdonor_gain0.3900
4:9264075:C:Tdonor_gain0.3900
4:9264235:TCGA:Tdonor_gain0.3900
4:9263970:GCC:Gdonor_gain0.3800
4:9262986:G:GCacceptor_gain0.3700
4:9263989:T:Gacceptor_gain0.3600
4:9264146:GGAA:Gdonor_gain0.3300
4:9264148:A:Tdonor_gain0.3300
4:9264209:G:GTdonor_gain0.3300
4:9263079:C:CGdonor_gain0.3200
4:9263079:C:Gdonor_gain0.3100
4:9264132:G:GTdonor_gain0.3100
4:9263853:TG:Tdonor_gain0.2900
4:9263854:GG:Gdonor_gain0.2900
4:9263988:A:AGacceptor_gain0.2900
4:9263993:GAAGA:Gacceptor_gain0.2900
4:9264267:A:AGdonor_gain0.2900

AlphaMissense

3494 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
4:9263923:A:TD351V0.996
4:9263924:T:AD351E0.995
4:9263924:T:GD351E0.995
4:9263718:T:CF283L0.994
4:9263720:C:AF283L0.994
4:9263720:C:GF283L0.994
4:9263361:T:CF164L0.992
4:9263363:T:AF164L0.992
4:9263363:T:GF164L0.992
4:9263873:T:AH334Q0.992
4:9263873:T:GH334Q0.992
4:9263123:T:AN84K0.991
4:9263123:T:GN84K0.991
4:9263907:T:AW346R0.991
4:9263907:T:CW346R0.991
4:9263922:G:CD351H0.990
4:9263923:A:CD351A0.990
4:9263871:C:GH334D0.989
4:9263136:T:CC89R0.986
4:9263147:C:AN92K0.986
4:9263147:C:GN92K0.986
4:9263351:T:AD160E0.986
4:9263351:T:GD160E0.986
4:9263122:A:CN84T0.985
4:9263138:C:GC89W0.985
4:9263869:G:AG333E0.985
4:9263137:G:AC89Y0.984
4:9263132:T:AN87K0.983
4:9263132:T:GN87K0.983
4:9263162:C:GC97W0.983

dbSNP variants (sampled 300 via entrez): RS1157242058 (4:9262737 G>A,T), RS1158170475 (4:9262294 G>T), RS1162539879 (4:9262484 A>G), RS1163330742 (4:9262542 C>A,T), RS1163971336 (4:9262123 G>A), RS1171929195 (4:9262108 C>G), RS1174095841 (4:9262378 C>G,T), RS1174149792 (4:9262190 G>A,T), RS1174383123 (4:9262436 ACACG>A), RS1175878637 (4:9262428 A>C,T), RS1176407077 (4:9262365 C>A,G,T), RS1183752149 (4:9262240 C>A,G), RS1186384917 (4:9262091 C>A), RS1187143343 (4:9262368 A>C,G), RS1189602824 (4:9262570 A>G)

Disease associations

OMIM: gene `` | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

2 total (human), top 2 by PubMed support.

ChemicalActions (top 5)PubMed papers
2-methyl-4-isothiazolin-3-oneincreases expression1
2-palmitoylglycerolincreases expression1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.