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TFIP11 tuftelin interacting protein 11 [ Homo sapiens (human) ]

Gene ID: 24144, updated on 2-Nov-2024

Summary

Official Symbol
TFIP11provided by HGNC
Official Full Name
tuftelin interacting protein 11provided by HGNC
Primary source
HGNC:HGNC:17165
See related
Ensembl:ENSG00000100109 MIM:612747; AllianceGenome:HGNC:17165
Gene type
protein coding
RefSeq status
REVIEWED
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
NTR1; STIP; TIP39; STIP-1; Spp382; bK445C9.6
Summary
This gene encodes a protein component of the spliceosome that promotes the release of the lariat-intron during late-stage splicing through the recruitment of a pre-mRNA splicing factor called DEAH-box helicase 15. The encoded protein contains a G-patch domain, a hallmark of RNA-processing proteins, that binds DEAH-box helicase 15. This protein contains an atypical nuclear localization sequence as well as a nuclear speckle-targeting sequence, enabling it to localize to distinct speckled regions within the cell nucleus. Polymorphisms in this gene are associated with dental caries suggesting a role in amelogenesis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2016]
Expression
Ubiquitous expression in testis (RPKM 20.2), bone marrow (RPKM 19.7) and 25 other tissues See more
Orthologs
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Genomic context

See TFIP11 in Genome Data Viewer
Location:
22q12.1
Exon count:
16
Annotation release Status Assembly Chr Location
RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 22 NC_000022.11 (26491240..26512473, complement)
RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 22 NC_060946.1 (26953642..26974877, complement)
RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 22 NC_000022.10 (26887206..26908439, complement)

Chromosome 22 - NC_000022.11Genomic Context describing neighboring genes Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13567 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13568 Neighboring gene Sharpr-MPRA regulatory region 14748 Neighboring gene RPS3A pseudogene 55 Neighboring gene ReSE screen-validated silencer GRCh37_chr22:26836513-26836669 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr22:26837982-26839181 Neighboring gene aspartate beta-hydroxylase domain containing 2 Neighboring gene HPS4 biogenesis of lysosomal organelles complex 3 subunit 2 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr22:26866926-26868125 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13569 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 18791 Neighboring gene MED14-independent group 3 enhancer GRCh37_chr22:26889254-26890453 Neighboring gene SRR1 domain containing Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 13570 Neighboring gene BRD4-independent group 4 enhancer GRCh37_chr22:26902046-26903245 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 18792 Neighboring gene H3K27ac hESC enhancer GRCh37_chr22:26908724-26909261 Neighboring gene TFIP11 divergent transcript Neighboring gene tyrosylprotein sulfotransferase 2 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:26937311-26937812 Neighboring gene Sharpr-MPRA regulatory region 3066 Neighboring gene microRNA 548j

Genomic regions, transcripts, and products

Expression

  • Project title: HPA RNA-seq normal tissues HPA RNA-seq normal tissues
  • Description: RNA-seq was performed of tissue samples from 95 human individuals representing 27 different tissues in order to determine tissue-specificity of all protein-coding genes
  • BioProject: PRJEB4337
  • Publication: PMID 24309898
  • Analysis date: Wed Apr 4 07:08:55 2018

Bibliography

GeneRIFs: Gene References Into Functions

What's a GeneRIF?

Pathways from PubChem

Interactions

Products Interactant Other Gene Complex Source Pubs Description

General gene information

Markers

Clone Names

  • FLJ22086

Gene Ontology Provided by GOA

Function Evidence Code Pubs
enables nucleic acid binding IEA
Inferred from Electronic Annotation
more info
 
enables protein binding IPI
Inferred from Physical Interaction
more info
PubMed 
Component Evidence Code Pubs
part_of U2-type post-mRNA release spliceosomal complex IBA
Inferred from Biological aspect of Ancestor
more info
 
part_of U2-type post-mRNA release spliceosomal complex IDA
Inferred from Direct Assay
more info
PubMed 
part_of catalytic step 2 spliceosome IDA
Inferred from Direct Assay
more info
PubMed 
located_in chromosome, telomeric region IDA
Inferred from Direct Assay
more info
PubMed 
located_in cytoplasm IEA
Inferred from Electronic Annotation
more info
 
located_in extracellular matrix IEA
Inferred from Electronic Annotation
more info
 
located_in nuclear speck IDA
Inferred from Direct Assay
more info
 
located_in nucleolus IDA
Inferred from Direct Assay
more info
PubMed 
located_in nucleoplasm TAS
Traceable Author Statement
more info
 
part_of spliceosomal complex IDA
Inferred from Direct Assay
more info
PubMed 

General protein information

Preferred Names
tuftelin-interacting protein 11
Names
septin and tuftelin-interacting protein 1
sip1/tuftelin interacting protein

NCBI Reference Sequences (RefSeq)

NEW Try the new Transcript table

RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001008697.3NP_001008697.1  tuftelin-interacting protein 11 isoform 1

    See identical proteins and their annotated locations for NP_001008697.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (1) encodes isoform 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, AL050258, CT841511, Z95115
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000384297.1, ENST00000405938.5
    Conserved Domains (3) summary
    pfam01585
    Location:149191
    G-patch; G-patch domain
    pfam07842
    Location:397666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23104
    TIP_N; Tuftelin interacting protein N terminal
  2. NM_001346857.2NP_001333786.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (3) uses an alternate splice site in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Conserved Domains (3) summary
    pfam01585
    Location:149191
    G-patch; G-patch domain
    pfam07842
    Location:397666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23104
    TIP_N; Tuftelin interacting protein N terminal
  3. NM_001346858.2NP_001333787.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (4) uses an alternate splice site in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Conserved Domains (3) summary
    pfam01585
    Location:149191
    G-patch; G-patch domain
    pfam07842
    Location:397666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23104
    TIP_N; Tuftelin interacting protein N terminal
  4. NM_001346859.2NP_001333788.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (5) differs in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, DC411331, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000385861.1, ENST00000407148.5
    Conserved Domains (3) summary
    pfam01585
    Location:149191
    G-patch; G-patch domain
    pfam07842
    Location:397666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23104
    TIP_N; Tuftelin interacting protein N terminal
  5. NM_001346861.2NP_001333790.1  tuftelin-interacting protein 11 isoform 1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (6) differs in the 5' UTR, compared to variant 1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, Z95115, Z99714
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000480171.1, ENST00000619735.4
    Conserved Domains (3) summary
    pfam01585
    Location:149191
    G-patch; G-patch domain
    pfam07842
    Location:397666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23104
    TIP_N; Tuftelin interacting protein N terminal
  6. NM_001346862.2NP_001333791.1  tuftelin-interacting protein 11 isoform 2

    Status: REVIEWED

    Description
    Transcript Variant: This variant (7) differs in the 5' UTR, lacks an in-frame portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (2) is shorter and has a distinct N-terminus, compared to isoform 1.
    Source sequence(s)
    AI468631, Z95115, Z99714
    UniProtKB/TrEMBL
    Q8N523
  7. NM_012143.4NP_036275.1  tuftelin-interacting protein 11 isoform 1

    See identical proteins and their annotated locations for NP_036275.1

    Status: REVIEWED

    Description
    Transcript Variant: This variant (2) lacks an exon in the 5' UTR, compared to variant1. Variants 1-6 encode the same isoform (1).
    Source sequence(s)
    AI468631, AL050258, DC411331
    Consensus CDS
    CCDS13838.1
    UniProtKB/Swiss-Prot
    O95908, Q20WL0, Q5H8V8, Q9UBB9, Q9UGV7, Q9Y2Q8
    UniProtKB/TrEMBL
    Q8N523
    Related
    ENSP00000384421.1, ENST00000407690.6
    Conserved Domains (3) summary
    pfam01585
    Location:149191
    G-patch; G-patch domain
    pfam07842
    Location:397666
    GCFC; GC-rich sequence DNA-binding factor-like protein
    pfam12457
    Location:23104
    TIP_N; Tuftelin interacting protein N terminal

RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference GRCh38.p14 Primary Assembly

Genomic

  1. NC_000022.11 Reference GRCh38.p14 Primary Assembly

    Range
    26491240..26512473 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

Alternate T2T-CHM13v2.0

Genomic

  1. NC_060946.1 Alternate T2T-CHM13v2.0

    Range
    26953642..26974877 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)