HNRNPCL3
gene geneOn this page
Summary
HNRNPCL3 (heterogeneous nuclear ribonucleoprotein C like 3, HGNC:51235) is a protein-coding gene on chromosome 1p36.21, encoding Heterogeneous nuclear ribonucleoprotein C-like 3 (B7ZW38).
Predicted to enable RNA binding activity. Predicted to be active in nucleus.
Source: NCBI Gene 649330 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001382358
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:51235 |
| Approved symbol | HNRNPCL3 |
| Name | heterogeneous nuclear ribonucleoprotein C like 3 |
| Location | 1p36.21 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000277058 |
| Ensembl biotype | protein_coding |
| Entrez | 649330 |
Gene structure
Transcript identifiers
Ensembl transcripts: 2 — 2 protein_coding
ENST00000617807, ENST00000681473
RefSeq mRNA: 1 — MANE Select: NM_001382358
NM_001382358
CCDS: CCDS72705
Canonical transcript exons
ENST00000617044 — 0 exons
Expression profiles
Bgee: expression breadth tissue_specific, 4 present calls, max score 45.74.
Top tissues by expression
121 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 45.74 | silver quality |
| cortical plate | UBERON:0005343 | 41.25 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 39.91 | silver quality |
| sural nerve | UBERON:0015488 | 39.39 | gold quality |
| bone marrow cell | CL:0002092 | 38.00 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 35.72 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 34.82 | gold quality |
| bone marrow | UBERON:0002371 | 32.68 | gold quality |
| right uterine tube | UBERON:0001302 | 32.31 | gold quality |
| muscle tissue | UBERON:0002385 | 32.12 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| liver | UBERON:0002107 | 29.42 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.04 | gold quality |
| placenta | UBERON:0001987 | 28.66 | silver quality |
| leukocyte | CL:0000738 | 28.56 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| monocyte | CL:0000576 | 28.10 | gold quality |
| blood | UBERON:0000178 | 27.58 | silver quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| urinary bladder | UBERON:0001255 | 26.78 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 25.89 | gold quality |
| gastrocnemius | UBERON:0001388 | 25.43 | gold quality |
| right adrenal gland cortex | UBERON:0035827 | 24.89 | gold quality |
| calcaneal tendon | UBERON:0003701 | 24.81 | gold quality |
Single-cell (SCXA)
Detected in 2 experiment(s), a significant marker in 1.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-GEOD-36552 | yes | 1870.63 |
| E-ANND-3 | no | 0.16 |
Regulation
Is transcription factor: no
Cross-species orthologs
2 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Hnrnpc | ENSMUSG00000060373 |
| rattus_norvegicus | LOC100911576 | ENSRNOG00000011621 |
Paralogs (6): HNRNPC (ENSG00000092199), RALY (ENSG00000125970), HNRNPCL1 (ENSG00000179172), HNRNPCL4 (ENSG00000179412), RALYL (ENSG00000184672), HNRNPCL2 (ENSG00000275774)
Protein
Protein identifiers
Heterogeneous nuclear ribonucleoprotein C-like 3 — B7ZW38 (reviewed: B7ZW38)
All UniProt accessions (1): B7ZW38
UniProt curated annotations — full annotation on UniProt →
Subcellular location. Nucleus.
Similarity. Belongs to the RRM HNRPC family. RALY subfamily.
RefSeq proteins (1): NP_001369287* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR000504 | RRM_dom | Domain |
| IPR012677 | Nucleotide-bd_a/b_plait_sf | Homologous_superfamily |
| IPR017347 | hnRNP_C | Family |
| IPR035979 | RBD_domain_sf | Homologous_superfamily |
| IPR051186 | RRM_HNRPC/RALY_subfam | Family |
Pfam: PF00076
UniProt features (9 total): compositionally biased region 4, region of interest 2, chain 1, domain 1, coiled-coil region 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-B7ZW38-F1 | 70.54 | 0.33 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 4 (showing top):
chr1p36, MANNO_MIDBRAIN_NEUROTYPES_HRGL3, MANNO_MIDBRAIN_NEUROTYPES_HGABA, KANNAN_BLOOD_2012_2013_TIV_AGE_65PLS_REVACCINATED_IN_6_9_MO_VS_REVACCINATED_IN_12_13_MOS_DN
GO Biological Process (0):
GO Molecular Function (2): RNA binding (GO:0003723), nucleic acid binding (GO:0003676)
GO Cellular Component (1): nucleus (GO:0005634)
GO top-level categories
Rollup of top GO terms by namespace:
| Category | Terms |
|---|---|
| nucleic acid binding | 1 |
| binding | 1 |
| intracellular membrane-bounded organelle | 1 |
Protein interactions and networks
STRING
1256 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| HNRNPCL3 | PRAMEF18 | Q5VWM3 | 522 |
| HNRNPCL3 | PRAMEF7 | Q5VXH5 | 507 |
| HNRNPCL3 | OR52N5 | Q8NH56 | 475 |
| HNRNPCL3 | RALYL | Q86SE5 | 439 |
| HNRNPCL3 | FAM131C | Q96AQ9 | 417 |
| HNRNPCL3 | ATP5MC3 | P48201 | 399 |
| HNRNPCL3 | ATP5MC1 | P05496 | 392 |
| HNRNPCL3 | OR4K1 | Q8NGD4 | 391 |
| HNRNPCL3 | PRAMEF1 | O95521 | 370 |
| HNRNPCL3 | PRAMEF2 | O60811 | 366 |
| HNRNPCL3 | TIGD3 | Q6B0B8 | 366 |
| HNRNPCL3 | ATP5ME | P56385 | 364 |
| HNRNPCL3 | OR8U1 | Q8NH10 | 348 |
| HNRNPCL3 | SCGB1C1 | Q8TD33 | 339 |
| HNRNPCL3 | SCGB1C2 | P0DMR2 | 338 |
IntAct
3 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| DYRK2 | HNRNPCL2 | psi-mi:“MI:2364”(proximity) | 0.270 |
| MST1R | SHTN1 | psi-mi:“MI:2364”(proximity) | 0.270 |
BioGRID (29): HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Proximity Label-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPCL3 (Affinity Capture-MS), HNRNPC (Cross-Linking-MS (XL-MS)), HNRNPCL1 (Cross-Linking-MS (XL-MS)), RALYL (Cross-Linking-MS (XL-MS)), HNRNPCL3 (Cross-Linking-MS (XL-MS))
ESM2 similar proteins: B2RXH8, B7ZW38, C0SUW7, F4JP52, F4JQZ3, F4JTI1, F4KIA8, G3V9R8, O48802, O60812, O77768, P07910, P0DMR1, P19600, P93831, Q08BJ2, Q08DJ0, Q0VFL3, Q0VFL7, Q0WNR6, Q0WUR5, Q10MI4, Q149C2, Q3ED78, Q41583, Q5DU00, Q5RA82, Q5VN06, Q5XIN3, Q64012, Q6K641, Q84PB3, Q84UI6, Q86SE5, Q86XZ4, Q8BTF8, Q8K1N4, Q8RWQ4, Q8S4P4, Q8S4P6
Diamond homologs: B2RXH8, B7ZW38, G3V9R8, O60812, O77768, P07910, P0DMR1, P19600, Q08DJ0, Q0VFL7, Q5RA82, Q64012, Q86SE5, Q8BTF8, Q9UKM9, Q9V3V0, Q9Z204, Q16629, Q3T106, Q8BL97, Q9W4D2, P38996, Q13247, Q29RT0, Q3B7L6, Q9WX39, F4JHI7, O22315, P84103, P84104, Q10145, Q3SZR8, Q74ZS6, Q94901, Q9FYB7, Q9LIS2, Q9XFR5, G3V6S8, Q3TWW8, Q6IQ97
SIGNOR signaling
0 interactions.
Disease & clinical
Clinical variants and AI predictions
ClinVar
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
0 predictions. Top by Δscore:
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 300 via entrez): RS1156987081 (1:13061374 G>A), RS1157098195 (1:13059144 T>C), RS1157417399 (1:13062154 C>A,T), RS1158702556 (1:13058820 A>G), RS1159218843 (1:13060855 C>T), RS1159632543 (1:13061686 G>A), RS1161426347 (1:13059275 C>G), RS1161833828 (1:13061397 A>C,G), RS1162411667 (1:13061759 C>T), RS1163544956 (1:13058898 G>A), RS1164036819 (1:13060887 T>C), RS1165896881 (1:13061476 G>T), RS1165919202 (1:13061008 C>T), RS1166013106 (1:13058900 G>C,T), RS1166184706 (1:13059288 G>A,C,T)
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
1 total (human), top 1 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| 4-(4-((5-(4,5-dimethyl-2-nitrophenyl)-2-furanyl)methylene)-4,5-dihydro-3-methyl-5-oxo-1H-pyrazol-1-yl)benzoic acid | decreases expression | 1 |
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.