SRSF7 - serine and arginine rich splicing factor 7 Gene

Also Known as 9G8; AAG3; SFRS7

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6432

About SRSF7

Cytogenetic location: 2p22.1 Genomic coordinates (GRCh38): 2:38,743,599-38,751,494 (from NCBI)

This gene has 12 transcripts (splice variants), 232 orthologues and 8 paralogues. Ubiquitous expression in bone marrow (RPKM 57.8), lymph node (RPKM 43.5) and 25 other tissues.

Summary

The protein encoded by this gene is a member of the serine/arginine (SR)-rich family of pre-mRNA splicing factors, which constitute part of the spliceosome. Each of these factors contains an N-terminal RNA recognition motif (RRM) for binding RNA and a C-terminal RS domain for binding Other proteins. The RS domain is rich in serine and arginine residues and facilitates interaction between different SR splicing factors. In addition to being critical for mRNA splicing, the SR proteins have also been shown to be involved in mRNA export from the nucleus and in translation. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, May 2018]

SRSF7 Products (3)

mRNA Protein Name
NM_001031684.3 NP_001026854.1 serine/arginine-rich splicing factor 7 isoform 1
NM_001195446.2 NP_001182375.1 serine/arginine-rich splicing factor 7 isoform 2
NM_001363802.1 NP_001350731.1 serine/arginine-rich splicing factor 7 isoform 3
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
10749975 GOA
enables protein domain specific binding IPI
IPI: Inferred from physical interaction
10749975 GOA
Biological Process GO Annotation Evidence References Source
involved in RNA splicing IDA
IDA: Inferred from direct assay
8013463 GOA
involved in negative regulation of mRNA splicing, via spliceosome IDA
IDA: Inferred from direct assay
15009664 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

SRSF7 Protein Structure

RRM_1

RRM_1: RNA recognition motif. (a.k.a. RRM, RBD, or RNP domain) (13 - 77)

  • 0
  • 100
  • 200
  • 238 a.a.
Protein Preferred Names Protein Names

serine/arginine-rich splicing factor 7

  • SR splicing factor 7

SRSF7 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
SRSF7 Q16629 RBBP6 Homo sapiens Q7Z6E9 33961781
Intra
SRSF7 Q16629 RBBP6 Homo sapiens Q7Z6E9 18624398
Intra
SRSF7 Q16629 LUC7L2 Homo sapiens Q9Y383 31515488
Intra
SRSF7 Q16629 LUC7L2 Homo sapiens Q9Y383 25416956
Intra
SRSF7 Q16629 LUC7L2 Homo sapiens Q9Y383 25416956
Intra
SRSF7 Q16629 LUC7L2 Homo sapiens Q9Y383 32296183
Intra
SRSF7 Q16629 LUC7L2 Homo sapiens Q9Y383 25416956
Intra
SRSF7 Q16629 RNPS1 Homo sapiens Q15287 33961781
Intra
SRSF7 Q16629 NXF1 Homo sapiens Q9UBU9 17036044
Intra
SRSF7 Q16629 NXF1 Homo sapiens Q9UBU9 15184380
Intra
SRSF7 Q16629 SRPK1 Homo sapiens Q96SB4 33961781
Intra
SRSF7 Q16629 SRPK1 Homo sapiens Q96SB4 23602568
Intra
SRSF7 Q16629 SRPK2 Homo sapiens P78362 33961781
Intra
SRSF7 Q16629 LUC7L Homo sapiens Q9NQ29-3 32296183
Intra
SRSF7 Q16629 PRPF38A Homo sapiens Q8NAV1 32296183
Intra
SRSF7 Q16629 SDCBP Homo sapiens O00560 25416956
Intra
SRSF7 Q16629 SDCBP Homo sapiens O00560 25416956
Cross
SRSF7 Q16629 Srek1 Rattus norvegicus Q9JKL7 14559993
Cross: Cross-species interaction Intra: Intraspecies interaction

SRSF7 Antibodies

Cat. No. Product Name Application Reactivity
HY-P811025 SRSF7 Antibody WB, IHC-P, ICC/IF Human, Mouse, Rat

Related Diseases

Diseases Alias
Allergic Bronchopulmonary Aspergillosis
  • Aspergillosis, Allergic Bronchopulmonary

  • Abpa

  • Allergic Bronchopulmonary Mycosis

  • Hinson-Pepys Disease

  • Pulmonary Aspergillus Disease

  • Allergic Aspergillosis

  • Aspergillosis Allergic Bronchopulmonary

Frontotemporal Dementia
  • Pallidopontonigral Degeneration

  • Frontotemporal Lobar Degeneration

  • Semantic Dementia

  • FTD

  • Frontotemporal Lobe Dementia

  • Multiple System Tauopathy With Presenile Dementia

  • Dementia, Frontotemporal

  • Frontotemporal Dementia With Parkinsonism

  • Mstd

  • Frontotemporal Lobar Degeneration With Tau Inclusions

  • Ftld With Tau Inclusions

  • Dementia, Frontotemporal, With Parkinsonism

  • Fldem

  • Ftdp17

  • Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex

  • Ddpac

  • Wilhelmsen-Lynch Disease

  • Wld

  • Ppnd

  • Dementia, Frontotemporal, With Or Without Parkinsonism

  • Semantic Primary Progressive Aphasia

  • Semantic Variant Ppa

  • Wilhemsen-Lynch Disease

  • Frontotemporal Dementia-Amyotrophic Lateral Sclerosis

  • Frontotemporal Dementia And Parkinsonism Linked To Chromosome 17

  • Ftd-Als

  • Ftld

  • Pick Complex

  • Pick Disease Of The Brain

  • Frontotemporal Dementia With Parkinsonism-17

  • Grn-Related Frontotemporal Dementia

  • Frontotemporal Dementia With Motor Neuron Disease

  • Dementia In Fronto-Temporal Lobar Degeneration

  • Ftd - [Frontotemporal Dementia]

  • Temple Dementia

  • Frontal Lobe Dementia

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
Macaca mulatta SRSF7 VGNC VGNC:77822
Felis catus SRSF7 VGNC VGNC:81226
Canis familiaris SRSF7 VGNC VGNC:46821
Rattus norvegicus SRSF7 RGD RGD:1307425
Mus musculus SRSF7 MGD MGI:1926232
Bos taurus SRSF7 VGNC VGNC:35303
Others SRSF7 NCBI