HNRNPAB

Heterogeneous Nuclear Ribonucleoprotein A/B

Gene Information Card

Symbol HNRNPAB
Full Name Heterogeneous Nuclear Ribonucleoprotein A/B
Gene Type Protein coding
Chromosomal Location 5q35.3
NCBI Gene ID 3188 ncbi.nlm.nih.gov/gene/3188
Ensembl ID ENSG00000113595
UniProt ID Q99729
OMIM ID 604629
HGNC ID 5034
Aliases ABBP1, HNRPAB, hnRNP A/B, APOBEC1-binding protein 1

Description

HNRNPAB encodes a member of the heterogeneous nuclear ribonucleoprotein (hnRNP) family, which binds RNA and participates in pre-mRNA processing, alternative splicing, and mRNA transport. The protein contains two RNA recognition motifs and a glycine-rich domain. It is ubiquitously expressed and has been implicated in transcriptional regulation, including as a co-repressor of APOBEC1 editing. HNRNPAB is associated with various cancers and autoimmune disorders.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
Breast cancer Overexpression promotes cell proliferation and invasion via alternative splicing regulation PMID: 25605242
Hepatocellular carcinoma Upregulation correlates with poor prognosis and metastasis PMID: 29351289
Systemic lupus erythematosus Autoantibodies against HNRNPAB detected in patient sera PMID: 10775190
Colorectal cancer HNRNPAB knockdown reduces tumor growth in xenograft models PMID: 31019238

Expression Profile

Tissue Expression
Tissue nTPM level
Brain 12.5 Medium
Lung 15.3 Medium
Liver 18.7 Medium
Breast 14.2 Medium
Colon 16.1 Medium
Cell Line Expression
Cell Line nTPM Notes
HeLa 20.5 Cervical cancer cell line
HepG2 22.3 Hepatocellular carcinoma cell line
MCF7 18.9 Breast cancer cell line
A549 17.4 Lung cancer cell line
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
c.457G>A (p.Glu153Lys) Missense <0.1% (COSMIC) Unknown functional impact
c.784C>T (p.Arg262Trp) Missense <0.1% (COSMIC) Unknown functional impact
Mutation functional classification

Loss of Function (LOF)

No confirmed loss-of-function mutations reported in major databases.

Gain of Function (GOF)

No confirmed gain-of-function mutations reported.

Dominant Negative (DN)

No evidence for dominant-negative effects.

Pathways

Processing of Capped Intron-Containing Pre-mRNA (Reactome: R-HSA-72203)
mRNA Splicing - Major Pathway (Reactome: R-HSA-72163)

Protein Summary

HNRNPAB is a 331-amino acid protein with two RNA recognition motifs (RRM1 and RRM2) and a C-terminal glycine-rich domain. It shuttles between the nucleus and cytoplasm, binding to poly(A) and poly(U) sequences. The protein is involved in pre-mRNA splicing, stability, and transport. It also interacts with APOBEC1 to modulate RNA editing. Post-translational modifications include phosphorylation and arginine methylation, which regulate its localization and function.

Related Products

Product name Cat.No. Species Gene ID
HNRNPAB Knockout HEK293 Cell Line EDJ-KQ2201 Human 3182 Details Get a Quote
HNRNPAB Knockout A-549 Cell Line EDJ-KQ22443 Human 3182 Details Get a Quote
HNRNPAB Knockout HCT 116 Cell Line EDJ-KQ22444 Human 3182 Details Get a Quote
HNRNPAB Knockout HeLa Cell Line EDJ-KQ22445 Human 3182 Details Get a Quote
Displaying Records 1 To 4 Of 4 Records
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