MYCBPAP

MYCBP Associated Protein

Gene Information Card

Symbol MYCBPAP
Full Name MYCBP associated protein
Gene Type protein-coding
Chromosomal Location 17q21.33
NCBI Gene ID 84073 ncbi.nlm.nih.gov/gene/84073
Ensembl ID ENSG00000141510
UniProt ID Q9H0R8
OMIM ID 617760
HGNC ID HGNC:28987
Aliases FLJ20607, MGC138290

Description

MYCBPAP (MYCBP associated protein) is a protein-coding gene located on chromosome 17q21.33. It encodes a protein that may interact with MYCBP (MYC binding protein), potentially involved in transcriptional regulation. Limited functional data are available; further studies are needed to clarify its biological role.

Disease Associations

Disease category Pathophysiological mechanism Genomic evidence
No specific disease association Unknown No evidence from ClinVar, OMIM, or COSMIC

Expression Profile

Tissue Expression
Tissue nTPM level
Testis 2.5 Low
Brain 1.2 Low
Lung 0.8 Not detected
Cell Line Expression
Cell Line nTPM Notes
HEK293 1.0 Low expression
HeLa 0.5 Not detected
Data source:Human Protein Atlas(proteinatlas.org)

Mutations & Variants

Hotspot Mutations
Variant Type Frequency Functional Description
No reported mutations N/A N/A N/A
Mutation functional classification

Loss of Function (LOF)

No data

Gain of Function (GOF)

No data

Dominant Negative (DN)

No data

Gene Ontology (GO)

• No GO terms assigned

Pathways

• No known pathways

Protein Summary

The MYCBPAP protein is predicted to be a cytoplasmic or nuclear protein with no characterized domains. Its function remains largely unknown, with no experimental validation of interactions or activity.

Related Products

Product name Cat.No. Species Gene ID
MYCBPAP Knockout HEK293 Cell Line EDJ-KQ9970 Human 84073 Details Get a Quote
MYCBPAP Knockout A-549 Cell Line EDJ-KQ36903 Human 84073 Details Get a Quote
MYCBPAP Knockout HeLa Cell Line EDJ-KQ57528 Human 84073 Details Get a Quote
MYCBPAP Knockout HCT 116 Cell Line EDJ-KQ74450 Human 84073 Details Get a Quote
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