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  2. CSTF2T - cleavage stimulation factor subunit 2 tau variant Gene

CSTF2T - cleavage stimulation factor subunit 2 tau variant Gene

Homo sapiens

Also known as CstF-64T

Gene ID: 23283 | Gene type: protein coding

About CSTF2T

Cytogenetic location: 10q21.1 Genomic coordinates (GRCh38): 10:51,695,486-51,699,595 (from NCBI)

This gene has 1 transcript (splice variant), 106 orthologues and 5 paralogues.

Summary

Enables RNA binding activity. Predicted to be involved in pre-mRNA cleavage required for polyadenylation. Located in nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

CSTF2T Products(1)

mRNA Protein Name
NM_015235.3 NP_056050.1 cleavage stimulation factor subunit 2 tau variant
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CSTF2T Protein Structure

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (18 - 88)

CSTF2_hinge

CSTF2_hinge: Hinge domain of cleavage stimulation factor subunit 2 (112 - 192)

CSTF_C

CSTF_C: Transcription termination and cleavage factor C-terminal (570 - 613)

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  • 500
  • 616 a.a.
Protein Preferred Names Protein Names

cleavage stimulation factor subunit 2 tau variant

CF-1 64 kDa subunit tau

CSTF2T Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CSTF2T Q9H0L4 TLE5 Homo sapiens Q08117-2 32296183
Intra
CSTF2T Q9H0L4 TLE5 Homo sapiens Q08117-2 32296183
Intra
CSTF2T Q9H0L4 CTAG1A Homo sapiens P78358 32296183
Intra
CSTF2T Q9H0L4 CTAG1A Homo sapiens P78358 32296183
Intra
CSTF2T Q9H0L4 SPAG8 Homo sapiens Q99932-2 32296183
Intra
CSTF2T Q9H0L4 SPAG8 Homo sapiens Q99932-2 32296183
Intra
CSTF2T Q9H0L4 FOXI1 Homo sapiens Q12951-2 32296183
Intra
CSTF2T Q9H0L4 FOXI1 Homo sapiens Q12951-2 32296183
Intra
CSTF2T Q9H0L4 FAM168B Homo sapiens A1KXE4-2 32296183
Intra
CSTF2T Q9H0L4 FAM168B Homo sapiens A1KXE4-2 32296183
Intra
CSTF2T Q9H0L4 ATP23 Homo sapiens Q9Y6H3 32296183
Intra
CSTF2T Q9H0L4 ATP23 Homo sapiens Q9Y6H3 32296183
Intra
CSTF2T Q9H0L4 ATP23 Homo sapiens Q9Y6H3 32296183
Intra
CSTF2T Q9H0L4 TOX2 Homo sapiens Q96NM4-3 32296183
Intra
CSTF2T Q9H0L4 TOX2 Homo sapiens Q96NM4-3 32296183
Intra
CSTF2T Q9H0L4 STH Homo sapiens Q8IWL8 32296183
Intra
CSTF2T Q9H0L4 STH Homo sapiens Q8IWL8 32296183
Intra
CSTF2T Q9H0L4 a0a1u9x8x8_human Homo sapiens A0A1U9X8X8 32296183
Intra
CSTF2T Q9H0L4 a0a1u9x8x8_human Homo sapiens A0A1U9X8X8 32296183
Intra
CSTF2T Q9H0L4 COL17A1 Homo sapiens Q9UMD9 32296183
Intra
CSTF2T Q9H0L4 COL17A1 Homo sapiens Q9UMD9 32296183
Intra
CSTF2T Q9H0L4 COL17A1 Homo sapiens Q9UMD9 32296183
Intra
CSTF2T Q9H0L4 PKNOX2 Homo sapiens Q96KN3 32296183
Intra
CSTF2T Q9H0L4 PKNOX2 Homo sapiens Q96KN3 32296183
Intra
CSTF2T Q9H0L4 FOXJ2 Homo sapiens Q9P0K8 32296183
Intra
CSTF2T Q9H0L4 FOXJ2 Homo sapiens Q9P0K8 32296183
Intra
CSTF2T Q9H0L4 SMYD3 Homo sapiens Q9H7B4 32296183
Intra
CSTF2T Q9H0L4 SMYD3 Homo sapiens Q9H7B4 32296183
Intra
CSTF2T Q9H0L4 SMYD3 Homo sapiens Q9H7B4 32296183
Intra
CSTF2T Q9H0L4 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
CSTF2T Q9H0L4 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
CSTF2T Q9H0L4 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
CSTF2T Q9H0L4 HGS Homo sapiens O14964 25416956
Intra
CSTF2T Q9H0L4 HGS Homo sapiens O14964 25416956
Intra
CSTF2T Q9H0L4 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
CSTF2T Q9H0L4 UBQLN1 Homo sapiens Q9UMX0 25416956
Intra
CSTF2T Q9H0L4 UBQLN1 Homo sapiens Q9UMX0 16189514
Intra
CSTF2T Q9H0L4 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
CSTF2T Q9H0L4 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
CSTF2T Q9H0L4 CTDSP1 Homo sapiens Q9GZU7 32296183
Intra
CSTF2T Q9H0L4 CTDSP1 Homo sapiens Q9GZU7 32296183
Intra
CSTF2T Q9H0L4 LASP1 Homo sapiens Q14847-2 32296183
Intra
CSTF2T Q9H0L4 LASP1 Homo sapiens Q14847-2 32296183
Intra
CSTF2T Q9H0L4 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
CSTF2T Q9H0L4 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
CSTF2T Q9H0L4 UBQLN2 Homo sapiens Q9UHD9 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Oligoasthenoteratozoospermia

Oat

Oligoasthenoteratospermia

Oculopharyngeal Muscular Dystrophy

OPMD

Muscular Dystrophy, Oculopharyngeal

Dystrophy, Oculopharyngeal Muscular

Oculopharyngeal Dystrophy

Progressive Muscular Dystrophy, Oculopharyngeal Type

Muscular Dystrophy Oculopharyngeal

Dystrophy, Muscular, Oculopharyngeal

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Mus musculus CSTF2T MGD MGI:1932622
Rattus norvegicus CSTF2T RGD RGD:1310026
Macaca mulatta CSTF2T VGNC VGNC:106027
Bos taurus CSTF2T VGNC VGNC:27782