1. Gene
  2. CSTF2 - cleavage stimulation factor subunit 2 Gene

CSTF2 - cleavage stimulation factor subunit 2 Gene

Homo sapiens

Also known as CstF-64

Gene ID: 1478 | Gene type: protein coding

About CSTF2

Cytogenetic location: Xq22.1 Genomic coordinates (GRCh38): X:100,820,391-100,841,520 (from NCBI)

This gene has 4 transcripts (splice variants), 204 orthologues and 5 paralogues. Ubiquitous expression in esophagus (RPKM 6.8), testis (RPKM 6.5) and 24 other tissues.

Summary

This gene encodes a nuclear protein with an RRM (RNA recognition motif) domain. The protein is a member of the cleavage stimulation factor (CSTF) complex that is involved in the 3' end cleavage and polyadenylation of pre-mRNAs. Specifically, this protein binds GU-rich elements within the 3'-untranslated region of mRNAs. [provided by RefSeq, Jul 2008]

CSTF2 Products(3)

mRNA Protein Name
NM_001306206.2 NP_001293135.1 cleavage stimulation factor subunit 2 isoform 1
NM_001306209.2 NP_001293138.1 cleavage stimulation factor subunit 2 isoform 3
NM_001325.3 NP_001316.1 cleavage stimulation factor subunit 2 isoform 2
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables RNA binding IDA
IDA: Inferred from direct assay
1741396 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
10477523 GOA
Biological Process GO Annotation Evidence Reference Source
involved in mRNA 3'-end processing IMP
IMP: Inferred from mutant phenotype
32816001 GOA
Cellular Component GO Annotation Evidence Reference Source
located in cleavage body IDA
IDA: Inferred from direct assay
11598190 GOA
part of mRNA cleavage and polyadenylation specificity factor complex IDA
IDA: Inferred from direct assay
18305108 GOA
located in nucleus IMP
IMP: Inferred from mutant phenotype
32816001 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

CSTF2 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 (111 - 192)

CSTF_C

CSTF_C: Transcription termination and cleavage factor C-terminal (531 - 574)

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  • 577 a.a.
Protein Preferred Names Protein Names

cleavage stimulation factor subunit 2

CF-1 64 kDa subunit

CSTF2 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
CSTF2 P33240 CTBP2 Homo sapiens P56545-3 32296183
Intra
CSTF2 P33240 CTBP2 Homo sapiens P56545-3 32296183
Intra
CSTF2 P33240 CTBP2 Homo sapiens P56545-3 32296183
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0-2 25416956
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0-2 25416956
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0-2 25416956
Intra
CSTF2 P33240 METTL15 Homo sapiens A6NJ78-4 32296183
Intra
CSTF2 P33240 METTL15 Homo sapiens A6NJ78-4 32296183
Intra
CSTF2 P33240 CPSF2 Homo sapiens Q9P2I0 18688255
Intra
CSTF2 P33240 PRDM6 Homo sapiens Q9NQX0 32296183
Intra
CSTF2 P33240 PRDM6 Homo sapiens Q9NQX0 32296183
Intra
CSTF2 P33240 PRDM6 Homo sapiens Q9NQX0 32296183
Intra
CSTF2 P33240 TLE5 Homo sapiens Q08117-2 32296183
Intra
CSTF2 P33240 TLE5 Homo sapiens Q08117-2 32296183
Intra
CSTF2 P33240 TLE5 Homo sapiens Q08117-2 32296183
Intra
CSTF2 P33240 SPAG8 Homo sapiens Q99932-2 32296183
Intra
CSTF2 P33240 SPAG8 Homo sapiens Q99932-2 32296183
Intra
CSTF2 P33240 SPAG8 Homo sapiens Q99932-2 32296183
Intra
CSTF2 P33240 USP54 Homo sapiens Q70EL1-9 32296183
Intra
CSTF2 P33240 USP54 Homo sapiens Q70EL1-9 32296183
Intra
CSTF2 P33240 USP54 Homo sapiens Q70EL1-9 32296183
Intra
CSTF2 P33240 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
CSTF2 P33240 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
CSTF2 P33240 SAXO4 Homo sapiens Q7Z5V6-2 32296183
Intra
CSTF2 P33240 TLE3 Homo sapiens Q04726-4 32296183
Intra
CSTF2 P33240 TLE3 Homo sapiens Q04726-4 32296183
Intra
CSTF2 P33240 TLE3 Homo sapiens Q04726-4 32296183
Intra
CSTF2 P33240 POU6F2 Homo sapiens P78424 32296183
Intra
CSTF2 P33240 POU6F2 Homo sapiens P78424 32296183
Intra
CSTF2 P33240 POU6F2 Homo sapiens P78424 32296183
Intra
CSTF2 P33240 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
CSTF2 P33240 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
CSTF2 P33240 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
CSTF2 P33240 ANKRD10 Homo sapiens Q9NXR5-2 32296183
Intra
CSTF2 P33240 ANKRD10 Homo sapiens Q9NXR5-2 32296183
Intra
CSTF2 P33240 ANKRD10 Homo sapiens Q9NXR5-2 32296183
Intra
CSTF2 P33240 FAM168B Homo sapiens A1KXE4-2 32296183
Intra
CSTF2 P33240 FAM168B Homo sapiens A1KXE4-2 32296183
Intra
CSTF2 P33240 ABHD11 Homo sapiens Q8NFV4-4 32296183
Intra
CSTF2 P33240 ABHD11 Homo sapiens Q8NFV4-4 32296183
Intra
CSTF2 P33240 ABHD11 Homo sapiens Q8NFV4-4 32296183
Intra
CSTF2 P33240 TSC1 Homo sapiens Q86WV8 32296183
Intra
CSTF2 P33240 TSC1 Homo sapiens Q86WV8 32296183
Intra
CSTF2 P33240 TSC1 Homo sapiens Q86WV8 32296183
Intra
CSTF2 P33240 ATP23 Homo sapiens Q9Y6H3 32296183
Intra
CSTF2 P33240 ATP23 Homo sapiens Q9Y6H3 32296183
Intra
CSTF2 P33240 ATP23 Homo sapiens Q9Y6H3 32296183
Intra
CSTF2 P33240 STH Homo sapiens Q8IWL8 32296183
Intra
CSTF2 P33240 STH Homo sapiens Q8IWL8 32296183
Intra
CSTF2 P33240 STH Homo sapiens Q8IWL8 32296183
Intra
CSTF2 P33240 a0a1u9x8x8_human Homo sapiens A0A1U9X8X8 32296183
Intra
CSTF2 P33240 a0a1u9x8x8_human Homo sapiens A0A1U9X8X8 32296183
Intra
CSTF2 P33240 TFG Homo sapiens Q92734 32296183
Intra
CSTF2 P33240 TFG Homo sapiens Q92734 25416956
Intra
CSTF2 P33240 TFG Homo sapiens Q92734 32296183
Intra
CSTF2 P33240 TFG Homo sapiens Q92734 32296183
Intra
CSTF2 P33240 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
CSTF2 P33240 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
CSTF2 P33240 AKAP8L Homo sapiens Q9ULX6 32296183
Intra
CSTF2 P33240 PARN Homo sapiens O95453 20379136
Intra
CSTF2 P33240 CEACAM6 Homo sapiens P40199 32296183
Intra
CSTF2 P33240 CEACAM6 Homo sapiens P40199 32296183
Intra
CSTF2 P33240 CEACAM6 Homo sapiens P40199 32296183
Intra
CSTF2 P33240 BARD1 Homo sapiens Q99728 20379136
Intra
CSTF2 P33240 BARD1 Homo sapiens Q99728 10477523
Intra
CSTF2 P33240 INCA1 Homo sapiens Q0VD86 32296183
Intra
CSTF2 P33240 INCA1 Homo sapiens Q0VD86 32296183
Intra
CSTF2 P33240 INCA1 Homo sapiens Q0VD86 32296183
Intra
CSTF2 P33240 HGS Homo sapiens O14964 25416956
Intra
CSTF2 P33240 HGS Homo sapiens O14964 32296183
Intra
CSTF2 P33240 HGS Homo sapiens O14964 32296183
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0 16189514
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0 25416956
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0 32296183
Intra
CSTF2 P33240 UBQLN1 Homo sapiens Q9UMX0 25416956
Intra
CSTF2 P33240 CNOT2 Homo sapiens Q9NZN8 32296183
Intra
CSTF2 P33240 CNOT2 Homo sapiens Q9NZN8 32296183
Intra
CSTF2 P33240 CNOT2 Homo sapiens Q9NZN8 32296183
Intra
CSTF2 P33240 HDHD3 Homo sapiens Q9BSH5 32296183
Intra
CSTF2 P33240 HDHD3 Homo sapiens Q9BSH5 32296183
Intra
CSTF2 P33240 HDHD3 Homo sapiens Q9BSH5 32296183
Intra
CSTF2 P33240 RFX6 Homo sapiens Q8HWS3 32296183
Intra
CSTF2 P33240 RFX6 Homo sapiens Q8HWS3 32296183
Intra
CSTF2 P33240 RFX6 Homo sapiens Q8HWS3 32296183
Intra
CSTF2 P33240 METTL27 Homo sapiens Q8N6F8 32296183
Intra
CSTF2 P33240 METTL27 Homo sapiens Q8N6F8 32296183
Intra
CSTF2 P33240 METTL27 Homo sapiens Q8N6F8 32296183
Intra
CSTF2 P33240 ZNF341 Homo sapiens Q9BYN7 25416956
Intra
CSTF2 P33240 ZNF341 Homo sapiens Q9BYN7 25416956
Intra
CSTF2 P33240 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
CSTF2 P33240 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
CSTF2 P33240 UBQLN2 Homo sapiens Q9UHD9 32296183
Intra
CSTF2 P33240 SPAG8 Homo sapiens Q99932 25416956
Intra
CSTF2 P33240 SPAG8 Homo sapiens Q99932 25416956
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
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
Canis familiaris CSTF2 VGNC VGNC:39683
Macaca mulatta CSTF2 VGNC VGNC:71536
Mus musculus CSTF2 MGD MGI:1343054
Rattus norvegicus CSTF2 RGD RGD:1596566
Bos taurus CSTF2 VGNC VGNC:27781
Felis catus CSTF2 VGNC VGNC:61240