APOBEC3F - apolipoprotein B mRNA editing enzyme catalytic subunit 3F Gene

Also Known as A3F; KA6; ARP8; BK150C2.4.MRNA

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 200316

About APOBEC3F

Cytogenetic location: 22q13.1 Genomic coordinates (GRCh38): 22:39,040,864-39,055,972 (from NCBI)

This gene has 4 transcripts (splice variants), 52 orthologues and 9 paralogues. Broad expression in lymph node (RPKM 2.8), ovary (RPKM 2.8) and 24 other tissues.

Summary

This gene is a member of the cytidine deaminase gene family. It is one of seven related genes or pseudogenes found in a cluster, thought to result from gene duplication, on chromosome 22. Members of the cluster encode proteins that are structurally and functionally related to the C to U RNA-editing cytidine deaminase APOBEC1. It is thought that the proteins may be RNA editing Enzymes and have roles in growth or cell cycle control. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Jul 2008]

APOBEC3F Products (2)

mRNA Protein Name
NM_001006666.2 NP_001006667.1 DNA dC->dU-editing enzyme APOBEC-3F isoform b
NM_145298.6 NP_660341.2 DNA dC->dU-editing enzyme APOBEC-3F isoform a
Molecular Function GO Annotation Evidence References Source
enables RNA binding IDA
IDA: Inferred from direct assay
11863358 GOA
enables cytidine deaminase activity IDA
IDA: Inferred from direct assay
17121840 GOA
enables identical protein binding IPI
IPI: Inferred from physical interaction
23685212 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16699599 GOA
enables zinc ion binding IDA
IDA: Inferred from direct assay
11863358 GOA
Cellular Component GO Annotation Evidence References Source
located in P-body IDA
IDA: Inferred from direct assay
16699599 GOA
located in cytoplasm IDA
IDA: Inferred from direct assay
16527742 GOA
part of ribonucleoprotein complex IDA
IDA: Inferred from direct assay
16699599 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

APOBEC3F Protein Structure

APOBEC_N

APOBEC_N: APOBEC-like N-terminal domain (23 - 183)

APOBEC_N

APOBEC_N: APOBEC-like N-terminal domain (200 - 371)

  • 0
  • 100
  • 200
  • 300
  • 373 a.a.
Protein Preferred Names Protein Names

DNA dC->dU-editing enzyme APOBEC-3F

  • apolipoprotein B editing enzyme catalytic polypeptide-like 3F

APOBEC3F Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
APOBEC3F Q8IUX4 APOBEC3F Homo sapiens Q8IUX4 23685212
Intra
APOBEC3F Q8IUX4 APOBEC3F Homo sapiens Q8IUX4
DLS
23685212
Intra
APOBEC3F Q8IUX4 TINF2 Homo sapiens Q9BSI4 21044950
Intra
APOBEC3F Q8IUX4 APOBEC3G Homo sapiens Q9HC16 15152192
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Immune Deficiency Disease
  • Immunodeficiency

  • Primary Immunodeficiency

  • Primary Immunodeficiency Disease

  • Immunologic Deficiency Syndromes

  • Hypoimmunity

  • Immune Deficiency Disorder

  • Immunodeficiency Syndrome

  • Immune Disorder

  • Primary Immune Deficiency Disorder

  • Immune System Diseases

  • Human Immunodeficiency Virus Infection

  • Hiv - [Human Immunodeficiency Virus Infection]

  • Hiv Positive Nos

  • Hiv Disease

  • Acquired Immune Deficiency Syndrome-Related Complex

  • Aids-Like Syndrome

  • Aids-Related Complex Nos

  • Arc - [Aids-Related Complex]

  • Immunodeficiency Due To Human Immunodeficiency Virus Infection

  • Unspecified Human Immunodeficiency Virus Disease

  • Hiv Disease Nos

  • Human Immunodeficiency Virus Positive Nos

  • Hiv Nos

  • Deficiency Of Complement Initial Pathway

  • Deficiency Of Complement Terminal Pathway

  • Cfdd - [Complement Factor D Deficiency]

  • Immunodeficiency With Nk-Cell - [Natural-Killer Cell] Deficiency

  • Nonfamilial Hypogammaglobulinaemia

  • Common Variable Immune Deficiency

  • Nonfamilial Agammaglobulinaemia

  • Common Variable Agammaglobulinaemia

  • Agammaglobulinaemia Nos

  • Agammaglobulinaemia Antibody Deficiency Syndrome

  • Hypogammaglobulinaemia Antibody Deficiency Syndrome

  • Acquired Agammaglobulinaemia Nos

  • Hypogammaglobulinaemia Nos

  • Hyper Igm

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 APOBEC3F MGD MGI:1933111