HNRNPC - heterogeneous nuclear ribonucleoprotein C Gene

Also Known as C1; C2; HNRNP; HNRPC; SNRPC

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 3183

About HNRNPC

Cytogenetic location: 14q11.2 Genomic coordinates (GRCh38): 14:21,209,147-21,269,442 (from NCBI)

This gene has 32 transcripts (splice variants), 97 orthologues and 6 paralogues. Ubiquitous expression in lymph node (RPKM 82.0), bone marrow (RPKM 78.3) and 25 other tissues.

Summary

This gene belongs to the subfamily of ubiquitously expressed heterogeneous nuclear ribonucleoproteins (hnRNPs). The hnRNPs are RNA binding proteins and they complex with heterogeneous nuclear RNA (hnRNA). These proteins are associated with pre-mRNAs in the nucleus and appear to influence pre-mRNA processing and Other aspects of mRNA metabolism and transport. While all of the hnRNPs are present in the nucleus, some seem to shuttle between the nucleus and the cytoplasm. The hnRNP proteins have distinct nucleic acid binding properties. The protein encoded by this gene can act as a tetramer and is involved in the assembly of 40S hnRNP particles. Multiple transcript variants encoding at least two different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]

HNRNPC Products (4)

mRNA Protein Name
NM_001077442.2 NP_001070910.1 heterogeneous nuclear ribonucleoproteins C1/C2 isoform a
NM_001077443.2 NP_001070911.1 heterogeneous nuclear ribonucleoproteins C1/C2 isoform b
NM_004500.4 NP_004491.2 heterogeneous nuclear ribonucleoproteins C1/C2 isoform b
NM_031314.3 NP_112604.2 heterogeneous nuclear ribonucleoproteins C1/C2 isoform a
Molecular Function GO Annotation Evidence References Source
enables N6-methyladenosine-containing RNA reader activity IDA
IDA: Inferred from direct assay
25719671 GOA
enables RNA binding IPI
IPI: Inferred from physical interaction
18082603 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables mRNA 3'-UTR binding IDA
IDA: Inferred from direct assay
16010978 GOA
enables poly(U) RNA binding IDA
IDA: Inferred from direct assay
16010978 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
11546873 GOA
enables telomerase RNA binding IPI
IPI: Inferred from physical interaction
18082603 GOA
Biological Process GO Annotation Evidence References Source
involved in 3'-UTR-mediated mRNA stabilization IMP
IMP: Inferred from mutant phenotype
16010978 GOA
involved in mRNA splicing, via spliceosome IMP
IMP: Inferred from mutant phenotype
25719671 GOA
involved in negative regulation of telomere maintenance via telomerase IMP
IMP: Inferred from mutant phenotype
18082603 GOA
Cellular Component GO Annotation Evidence References Source
located in actin cytoskeleton IDA
IDA: Inferred from direct assay
11687588 GOA
part of catalytic step 2 spliceosome IDA
IDA: Inferred from direct assay
11991638 GOA
located in cytosol IDA
IDA: Inferred from direct assay
16010978 GOA
located in nucleus IDA
IDA: Inferred from direct assay
11687588 GOA
part of protein-containing complex IDA
IDA: Inferred from direct assay
11687588 GOA
part of spliceosomal complex IDA
IDA: Inferred from direct assay
9731529 GOA
part of telomerase holoenzyme complex IDA
IDA: Inferred from direct assay
18082603 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

HNRNPC Protein Structure

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (18 - 80)

  • 0
  • 100
  • 200
  • 306 a.a.
Protein Preferred Names Protein Names

heterogeneous nuclear ribonucleoproteins C1/C2

  • heterogeneous nuclear ribonucleoprotein C (C1/C2)

HNRNPC Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
HNRNPC P07910 SUMO1P1 Homo sapiens G2XKQ0 25416956
Intra
HNRNPC P07910 SUMO1P1 Homo sapiens G2XKQ0 25416956
Intra
HNRNPC P07910 UBE2I Homo sapiens Q7KZS0 25416956
Intra
HNRNPC P07910 HNRNPCL1 Homo sapiens O60812 33961781
Intra
HNRNPC P07910 HNRNPCL1 Homo sapiens O60812 32296183
Intra
HNRNPC P07910 HNRNPCL1 Homo sapiens O60812 32296183
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5-3 32296183
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5-3 32296183
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5-3 32296183
Intra
HNRNPC P07910 RBPMS2 Homo sapiens Q6ZRY4 32296183
Intra
HNRNPC P07910 RBPMS2 Homo sapiens Q6ZRY4 32296183
Intra
HNRNPC P07910 RBPMS2 Homo sapiens Q6ZRY4 32296183
Intra
HNRNPC P07910 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
HNRNPC P07910 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
HNRNPC P07910 DISC1 Homo sapiens Q9NRI5-2 32296183
Intra
HNRNPC P07910 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HNRNPC P07910 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HNRNPC P07910 MEOX2 Homo sapiens Q6FHY5 32296183
Intra
HNRNPC P07910 SHANK3 Homo sapiens Q9BYB0 21653829
Intra
HNRNPC P07910 SHANK3 Homo sapiens Q9BYB0 21653829
Intra
HNRNPC P07910 RNF4 Homo sapiens P78317 32296183
Intra
HNRNPC P07910 RNF4 Homo sapiens P78317 32296183
Intra
HNRNPC P07910 RNF4 Homo sapiens P78317 32296183
Intra
HNRNPC P07910 HNRNPA2B1 Homo sapiens P22626 30021884
Intra
HNRNPC P07910 HNRNPA2B1 Homo sapiens P22626 35271311
Intra
HNRNPC P07910 HNRNPD Homo sapiens Q14103 35271311
Intra
HNRNPC P07910 YWHAZ Homo sapiens P63104 15161933
Intra
HNRNPC P07910 KPNA2 Homo sapiens P52292 25416956
Intra
HNRNPC P07910 HNRNPA1 Homo sapiens P09651 35271311
Intra
HNRNPC P07910 HNRNPA1 Homo sapiens P09651 30021884
Intra
HNRNPC P07910 HNRNPA1 Homo sapiens P09651 11546873
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910 16189514
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910 32296183
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910 25416956
Intra
HNRNPC P07910 KPNA4 Homo sapiens O00629 35271311
Intra
HNRNPC P07910 KPNA4 Homo sapiens O00629 32296183
Intra
HNRNPC P07910 KPNA4 Homo sapiens O00629
FPS
35044719
Intra
HNRNPC P07910 KPNA3 Homo sapiens O00505 25416956
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910 16189514
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910 32296183
Intra
HNRNPC P07910 KPNA3 Homo sapiens O00505 35271311
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910
Y2H
22365833
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910 32296183
Intra
HNRNPC P07910 KPNA4 Homo sapiens O00629 25416956
Intra
HNRNPC P07910 KPNA4 Homo sapiens O00629 32296183
Intra
HNRNPC P07910 KPNA3 Homo sapiens O00505 16189514
Intra
HNRNPC P07910 KPNA3 Homo sapiens O00505 19447967
Intra
HNRNPC P07910 HNRNPC Homo sapiens P07910
Y2H
21516116
Intra
HNRNPC P07910 TARDBP Homo sapiens Q13148 32814053
Intra
HNRNPC P07910 TARDBP Homo sapiens Q13148 32814053
Intra
HNRNPC P07910 TARDBP Homo sapiens Q13148 32814053
Intra
HNRNPC P07910 CDC5L Homo sapiens Q99459 33961781
Intra
HNRNPC P07910 EPS8 Homo sapiens Q12929 25416956
Intra
HNRNPC P07910 HTT Homo sapiens P42858 32814053
Intra
HNRNPC P07910 HTT Homo sapiens P42858 17500595
Intra
HNRNPC P07910 HTT Homo sapiens P42858 32814053
Intra
HNRNPC P07910 HTT Homo sapiens P42858 32814053
Intra
HNRNPC P07910 KPNA5 Homo sapiens O15131 32296183
Intra
HNRNPC P07910 KPNA5 Homo sapiens O15131 32296183
Intra
HNRNPC P07910 SRPK2 Homo sapiens P78362 23602568
Intra
HNRNPC P07910 RALY Homo sapiens Q9UKM9 33961781
Intra
HNRNPC P07910 SDCBP Homo sapiens O00560 32296183
Intra
HNRNPC P07910 SDCBP Homo sapiens O00560 25416956
Intra
HNRNPC P07910 SDCBP Homo sapiens O00560 32296183
Intra
HNRNPC P07910 LMO2 Homo sapiens P25791 25416956
Intra
HNRNPC P07910 RBM41 Homo sapiens Q96IZ5 16189514
Intra
HNRNPC P07910 RBM41 Homo sapiens Q96IZ5 25416956
Intra
HNRNPC P07910 RBM41 Homo sapiens Q96IZ5
Y2H
21516116
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5 25416956
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5 19447967
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5 25416956
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5 25416956
Intra
HNRNPC P07910 RALYL Homo sapiens Q86SE5 16189514
Intra
HNRNPC P07910 PAX6 Homo sapiens P26367 32296183
Intra
HNRNPC P07910 PAX6 Homo sapiens P26367 32296183
Intra
HNRNPC P07910 PAX6 Homo sapiens P26367 32296183
Intra
HNRNPC P07910 SUMO1 Homo sapiens P63165 25416956
Intra
HNRNPC P07910 SUMO1 Homo sapiens P63165 32296183
Intra
HNRNPC P07910 SUMO1 Homo sapiens P63165 32296183
Intra
HNRNPC P07910 SUMO1 Homo sapiens P63165 32296183
Intra
HNRNPC P07910 ZFYVE26 Homo sapiens Q68DK2-5 25416956
Intra
HNRNPC P07910 ZFYVE26 Homo sapiens Q68DK2-5 25416956
Intra
HNRNPC P07910 HNRNPCL2 Homo sapiens B2RXH8 32296183
Intra
HNRNPC P07910 HNRNPCL2 Homo sapiens B2RXH8 32296183
Intra
HNRNPC P07910 RALY Homo sapiens Q53GL6 32296183
Intra
HNRNPC P07910 RALY Homo sapiens Q53GL6 32296183
Intra
HNRNPC P07910 RALY Homo sapiens Q53GL6 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

HNRNPC Antibodies

Cat. No. Product Name Application Reactivity
HY-P82129 hnRNP C1/C2 Antibody (YA1874) WB, IHC-P, ICC/IF, IP, FC Human, Mouse, Rat
HY-P85884 hnRNP C1/C2 Antibody (YA5576) WB, ICC/IF, ELISA Human, Mouse, Rat, Monkey, Rabbit, Orangutan

Related Diseases

Diseases Alias
Mixed Connective Tissue Disease
  • Sharp Syndrome

  • Mctd

  • Connective Tissue Disease Overlap Syndrome

  • Mixed Collagen Vascular Disease

  • Mctd - [Mixed Connective Tissue Disease]

Oculopharyngeal Muscular Dystrophy
  • OPMD

  • Muscular Dystrophy, Oculopharyngeal

  • Dystrophy, Oculopharyngeal Muscular

  • Oculopharyngeal Dystrophy

  • Progressive Muscular Dystrophy, Oculopharyngeal Type

  • Muscular Dystrophy Oculopharyngeal

  • Dystrophy, Muscular, Oculopharyngeal

Connective Tissue Disease
  • Connective Tissue Diseases

  • Connective Tissue Disorder

  • Abnormality Of Connective Tissue

  • Disorder Of Connective Tissue

  • Connective Tissue Disorders

Multisystem Proteinopathy
Muscular Atrophy
  • Muscle Wasting

  • Amyotrophia

  • Wasting - Muscle

  • Skeletal Muscle Atrophy

Fragile X-Associated Tremor/Ataxia Syndrome
  • Fxtas Syndrome

  • Fragile X Tremor/Ataxia Syndrome

  • Fxtas

Muscular Dystrophy
  • Muscular Dystrophies

  • Congenital Md

  • Congenital Muscular Dystrophy

  • Cmd

  • Mdc

  • Dystrophy, Muscular

  • Gower'S Muscular Dystrophy

  • Progressive Musclular Dystrophy

  • Pseudohypertrophic Atrophy

  • Pseudohypertrophic Muscle Paralysis

  • Pseudohypertrophic Muscular Atrophy

  • Pseudohypertrophic Muscular Dystrophy

  • Pseudohypertrophic Paralysis

  • Pseudomuscular Hypertrophy

Systemic Lupus Erythematosus
  • Lupus Nephritis

  • SLE

  • Disseminated Lupus Erythematosus

  • Systemic Lupus Erythematosus, Susceptibility To

  • Lupus Erythematosus, Systemic

  • Lupus Nephritis, Susceptibility To

  • Libman-Sacks Disease

  • Systemic Lupus Erythematosus Susceptibility To

  • Sle - Lupus Erythematosus, Systemic

  • Le Syndrome

  • Lupus

  • Lupus Erythematosus Systemic

  • Lupus Erythematosus, Systemic, Susceptibility To

  • Lupus Vulgaris

  • Lupus Erythematosus, Discoid

  • Lupus Erythematosus

  • Systemic Lupus Erythematosus Nos

  • Sle - [Systemic Lupus Erythematosus]

Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis 1
  • FTDALS1

  • Frontotemporal Dementia And/Or Motor Neuron Disease

  • Ftdmnd

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia

  • Alsftd

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And/Or Amyotrophic Lateral Sclerosis-1

  • Frontotemporal Dementia With Motor Neuron Disease

  • Ftdals

  • Ftd-Als

  • Ftd-Mnd

  • Frontotemporal Dementia With Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis With Frontotemporal Dementia 1

  • Amyotrophic Lateral Sclerosis/Frontotemporal Dementia

  • Dementia, Frontotemporal, And/Or Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis And/Or Frontotemporal Dementia 1

  • Frontotemporal Lobar Degeneration

  • Grn-Related Frontotemporal Dementia

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

Wilms Tumor 1
  • Nephroblastoma

  • Wilms Tumor

  • WT1

  • Wilms' Tumor

  • Bilateral Wilms Tumor

  • Wilms Tumor, Type 1

  • Wilms Tumor, Somatic

  • Adult Nephroblastoma

  • Wt1 Disorder

  • Renal Embryonic Tumor

  • Adult Kidney Wilms Tumor

  • Childhood Kidney Wilms Tumor

  • Nonanaplastic Kidney Wilms Tumor

Amyotrophic Lateral Sclerosis 1
  • Amyotrophic Lateral Sclerosis

  • ALS

  • Lou Gehrig Disease

  • Amyotrophic Lateral Sclerosis Type 1

  • Charcot Disease

  • ALS1

  • Amyotrophic Lateral Sclerosis, Susceptibility To

  • Fals

  • Lou Gehrig'S Disease

  • Mnd

  • Motor Neuron Disease

  • Familial Amyotrophic Lateral Sclerosis

  • Amyotrophic Lateral Sclerosis 1, Familial

  • Amyotrophic Lateral Sclerosis 1, Autosomal Dominant

  • Motor Neuron Disease, Bulbar

  • Motor Neurone Disease

  • Amyotrophic Lateral Sclerosis With Dementia

  • Dementia With Amyotrophic Lateral Sclerosis

  • Motor Neuron Disease, Amyotrophic Lateral Sclerosis

  • Sclerosis, Lateral, Amyotrophic

  • Sclerosis, Lateral, Amyotrophic, Type 1

  • Amyotrophic Sclerosis

  • Als - [Amyotrophic Lateral Sclerosis]

  • Wasting Palsy

  • Amyotrophic Paralysis

  • Amyotrophy Lateral Sclerosis

  • Wasting Paralysis

  • Spinal Progressive Amyotrophy

  • Progressive Atrophic Paralysis

Retinitis Pigmentosa
  • RP

  • Rod-Cone Dystrophy

  • Autosomal Recessive Retinitis Pigmentosa

  • Non-Syndromic Retinitis Pigmentosa

  • Pericentral Pigmentary Retinopathy

  • Pigmentary Retinopathy

  • Tapetoretinal Degeneration

  • Rcd

  • Retinitis Pigmentosa Autosomal Recessive

  • ARRP

  • Retinitis Pigmentosa, Autosomal Recessive

  • Retinitis Pigmentosa 1

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus HNRNPC RGD RGD:1309982
Mus musculus HNRNPC MGD MGI:107795
Macaca mulatta HNRNPC VGNC VGNC:84348