PAXIP1 PAX interacting protein 1
Gene ID: 22976, updated on 16-Apr-2024Gene type: protein coding
Also known as: PTIP; TNRC2; CAGF28; CAGF29; PACIP1; PAXIP1L
- See all available tests in GTR for this gene
- Go to complete Gene record for PAXIP1
- Go to Variation Viewer for PAXIP1 variants
Summary
This gene is a member of the paired box (PAX) gene family and encodes a nuclear protein with six BRCT (breast cancer carboxy-terminal) domains. This protein plays a critical role in maintaining genome stability, condensation of chromatin and progression through mitosis. [provided by RefSeq, Jul 2008]
Associated conditions
See all available tests in GTR for this gene
| Description | Tests |
|---|---|
| Genome-wide interaction study of smoking and bladder cancer risk. GeneReviews: Not available |
Genomic context
- Location:
- 7q36.2
- Sequence:
- Chromosome: 7; NC_000007.14 (154943690..155003411, complement)
- Total number of exons:
- 24
Variation
| Resource | Links for this gene |
|---|---|
| ClinVar | Variants reported to ClinVar |
| dbVar | Studies and variants |
| SNP | Variation Viewer for PAXIP1 variants |
| Genome viewer | Explore NCBI-annotated and select non-NCBI annotated genome assemblies |
- ClinVarRelated medical variations
- dbVarLink from Gene to dbVar
- OMIMLink to related OMIM entry
- PAXIP1 database
- PubMed (OMIM)Gene links to PubMed derived from omim_pubmed_cited links
- RefSeq RNAsLink to Nucleotide RefSeq RNAs
- RefSeqGeneLink to Nucleotide RefSeqGenes
- Variation ViewerRelated Variants
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