HNRNPA2B1
heterogeneous nuclear ribonucleoprotein A2/B1 | HNRNPA2, HNRNPB1, HNRPA2B1

This gene belongs to the A/B 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 has two repeats of quasi-RRM domains that bind to RNAs. This gene has been described to generate two alternatively spliced transcript variants which encode different isoforms. [provided by RefSeq, Jul 2008]

Member of: DE-11 DE-11.6
Biological processes 46 terms
Cajal body (GO:0015030)DNA geometric change (GO:0032392)DNA polymerase binding (GO:0070182)G-rich strand telomeric DNA binding (GO:0098505)N6-methyladenosine-containing RNA reader activity (GO:1990247)RNA binding (GO:0003723)RNA binding (GO:0003723)RNA binding (GO:0003723)RNA binding (GO:0003723)RNA transport (GO:0050658)catalytic step 2 spliceosome (GO:0071013)catalytic step 2 spliceosome (GO:0071013)chromosome, telomeric region (GO:0000781)cytoplasm (GO:0005737)cytoplasm (GO:0005737)extracellular exosome (GO:0070062)extracellular exosome (GO:0070062)extracellular region (GO:0005576)identical protein binding (GO:0042802)mRNA 3'-UTR binding (GO:0003730)mRNA 3'-UTR binding (GO:0003730)mRNA export from nucleus (GO:0006406)mRNA processing (GO:0006397)mRNA splicing, via spliceosome (GO:0000398)mRNA splicing, via spliceosome (GO:0000398)mRNA splicing, via spliceosome (GO:0000398)mRNA transport (GO:0051028)membrane (GO:0016020)miRNA binding (GO:0035198)miRNA transport (GO:1990428)molecular condensate scaffold activity (GO:0140693)nuclear matrix (GO:0016363)nucleic acid binding (GO:0003676)nucleoplasm (GO:0005654)nucleoplasm (GO:0005654)nucleoplasm (GO:0005654)nucleus (GO:0005634)nucleus (GO:0005634)positive regulation of telomere maintenance via telomere lengthening (GO:1904358)pre-mRNA intronic binding (GO:0097157)primary miRNA processing (GO:0031053)protein binding (GO:0005515)ribonucleoprotein complex (GO:1990904)single-stranded telomeric DNA binding (GO:0043047)single-stranded telomeric DNA binding (GO:0043047)spliceosomal complex (GO:0005681)
Expression (TPM)
HNRNPA2B1 — as a Regulated Gene

TFs regulating HNRNPA2B1 0 TFs

Transcription factors with Perturb-seq knockdown data for HNRNPA2B1. The Binding column indicates whether any binding evidence exists for this TF–gene pair (ChIP-seq or motif footprint peaks). The Mean coef is the average Perturb-seq regression coefficient across active gRNAs (positive = HNRNPA2B1 upregulated upon KD; negative = downregulated). The Outlier column indicates whether this gene is in the top or bottom 5% of all TF knockdown effects.

Data: Effect:
TF Mean coef Binding Outlier TF→Gene link

Elements linked to HNRNPA2B1

Open chromatin peaks (ATAC-seq) in the genomic neighbourhood of HNRNPA2B1, linked by TSS proximity or chromatin conformation (Multiome / HiCAR). Each element overlaps at least one TF ChIP-seq binding site — the TFs column shows how many distinct TFs bind that element.

Accessibility Element Dist. to TSS Link type TFs
chr7:25,950,166–25,951,811 249.5 kb Distal (>10kb) Multiome 777
chr7:26,151,798–26,154,281 48.6 kb Distal (>10kb) Multiome 635
chr7:26,199,573–26,202,470 222 bp At TSS Multiome 1167
chr7:26,291,673–26,292,388 91.2 kb Distal (>10kb) Multiome 647
chr7:26,375,964–26,377,507 176.3 kb Distal (>10kb) Multiome 698
chr7:26,397,280–26,399,477 197.8 kb Distal (>10kb) Multiome 678

Genome Browser

Genomic view of the HNRNPA2B1 locus showing ATAC-seq accessibility and RNA-seq expression across the ESC → DE time course, together with TF binding peaks and element-to-TSS loop connections.

chr7:25,940,166 – 26,409,477
Proximal 1 kb Distal 10 kb Multiome HiCAR ATAC-seq RNA-seq