Hs04800997_cn

• Gene Symbol: FIP1L1
• Assay Reference Genome Location: Chr.4:53417170 on build GRCh38
• Cytoband: 4q12

Target Gene Details

• Entrez Gene ID: 81608
• Gene Name: factor interacting with PAPOLA and CPSF1
• Gene Aliases: FIP1, Rhe, hFip1
• Location: Chr.4:53377572-53462611 on Build GRCh38
• Assay Gene Location: Within Intron 11

Gene Symbol	Transcript Accession	Exon Location	Assay Transcript Location	Protein ID
FIP1L1	NM_001134937.1			NP_001128409.1
	NM_001134938.1			NP_001128410.1
	NM_030917.3			NP_112179.2
	XM_005265769.4			XP_005265826.1
	XM_005265773.4			XP_005265830.1
	XM_005265774.4			XP_005265831.1
	XM_005265778.4			XP_005265835.1
	XM_005265779.4			XP_005265836.1
	XM_005265781.4			XP_005265838.1
	XM_005265782.4			XP_005265839.1
	XM_017008662.1			XP_016864151.1
	XM_017008663.1			XP_016864152.1
	XM_017008664.1			XP_016864153.1
	XM_017008665.1			XP_016864154.1
	XM_017008666.1			XP_016864155.1
	XM_017008667.1			XP_016864156.1
	XM_017008668.1			XP_016864157.1
	XM_017008669.1			XP_016864158.1
	XM_017008670.1			XP_016864159.1
	XM_017008671.1			XP_016864160.1
	AK123992.1
	AK295737.1
	AK300398.1
	AK308145.1
	AL136910.1			CAB66844.1
	AY366510.1			AAQ88277.1
	BC011543.1			AAH11543.1
	BC017724.1			AAH17724.1
	BC024016.1			AAH24016.1
	BC052959.1			AAH52959.1
	BC110383.1

More Information

Additional Information:

For this assay, SNP(s) [rs79559383] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

• Set Membership: Intragenic, Intronic, Non-exonic, non-DGV Variation

Gene Ontology Categories:

Process(es)

mRNA splicing, via spliceosome
termination of RNA polymerase II transcription
mRNA export from nucleus
mRNA 3'-end processing

Function(s)

protein binding
poly(A) RNA binding