HNRNPCL3

gene
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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

FieldValue
HGNC IDHGNC:51235
Approved symbolHNRNPCL3
Nameheterogeneous nuclear ribonucleoprotein C like 3
Location1p36.21
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000277058
Ensembl biotypeprotein_coding
Entrez649330

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):

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099145.74silver quality
cortical plateUBERON:000534341.25gold quality
hindlimb stylopod muscleUBERON:000425239.91silver quality
sural nerveUBERON:001548839.39gold quality
bone marrow cellCL:000209238.00gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
mucosa of transverse colonUBERON:000499135.72gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113434.82gold quality
bone marrowUBERON:000237132.68gold quality
right uterine tubeUBERON:000130232.31gold quality
muscle tissueUBERON:000238532.12gold quality
stromal cell of endometriumCL:000225529.87gold quality
liverUBERON:000210729.42gold quality
prefrontal cortexUBERON:000045129.04gold quality
placentaUBERON:000198728.66silver quality
leukocyteCL:000073828.56gold quality
duodenumUBERON:000211428.14gold quality
monocyteCL:000057628.10gold quality
bloodUBERON:000017827.58silver quality
lymph nodeUBERON:000002927.57gold quality
tonsilUBERON:000237227.05gold quality
urinary bladderUBERON:000125526.78gold quality
vermiform appendixUBERON:000115426.42gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
gastrocnemiusUBERON:000138825.43gold quality
right adrenal gland cortexUBERON:003582724.89gold quality
calcaneal tendonUBERON:000370124.81gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-GEOD-36552yes1870.63
E-ANND-3no0.16

Regulation

Is transcription factor: no

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusHnrnpcENSMUSG00000060373
rattus_norvegicusLOC100911576ENSRNOG00000011621

Paralogs (6): HNRNPC (ENSG00000092199), RALY (ENSG00000125970), HNRNPCL1 (ENSG00000179172), HNRNPCL4 (ENSG00000179412), RALYL (ENSG00000184672), HNRNPCL2 (ENSG00000275774)

Protein

Protein identifiers

Heterogeneous nuclear ribonucleoprotein C-like 3B7ZW38 (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)

IDNameType
IPR000504RRM_domDomain
IPR012677Nucleotide-bd_a/b_plait_sfHomologous_superfamily
IPR017347hnRNP_CFamily
IPR035979RBD_domain_sfHomologous_superfamily
IPR051186RRM_HNRPC/RALY_subfamFamily

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)

ModelpLDDTFraction very-high
AF-B7ZW38-F170.540.33

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:

CategoryTerms
nucleic acid binding1
binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

1256 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
HNRNPCL3PRAMEF18Q5VWM3522
HNRNPCL3PRAMEF7Q5VXH5507
HNRNPCL3OR52N5Q8NH56475
HNRNPCL3RALYLQ86SE5439
HNRNPCL3FAM131CQ96AQ9417
HNRNPCL3ATP5MC3P48201399
HNRNPCL3ATP5MC1P05496392
HNRNPCL3OR4K1Q8NGD4391
HNRNPCL3PRAMEF1O95521370
HNRNPCL3PRAMEF2O60811366
HNRNPCL3TIGD3Q6B0B8366
HNRNPCL3ATP5MEP56385364
HNRNPCL3OR8U1Q8NH10348
HNRNPCL3SCGB1C1Q8TD33339
HNRNPCL3SCGB1C2P0DMR2338

IntAct

3 interactions, top by confidence:

ABTypeScore
DYRK2HNRNPCL2psi-mi:“MI:2364”(proximity)0.270
MST1RSHTN1psi-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):

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

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.

ChemicalActions (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 aciddecreases 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.