ABCF2 - ATP binding cassette subfamily F member 2 Gene

Also Known as ABC28; HUSSY18; HUSSY-18; EST133090

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 10061

About ABCF2

Cytogenetic location: 7q36.1 Genomic coordinates (GRCh38): 7:151,211,484-151,227,205 (from NCBI)

Ubiquitous expression in testis (RPKM 10.6), brain (RPKM 8.3) and 25 other tissues.

Summary

This gene encodes a member of the ATP-binding cassette (ABC) transporter superfamily. ATP-binding cassette proteins transport various molecules across extra- and intracellular membranes. Alterations in this gene may be involved in Cancer progression. Related pseudogenes have been identified on chromosomes 3 and 7. [provided by RefSeq, Mar 2019]

ABCF2 Products (1)

mRNA Protein Name
NM_007189.3 NP_009120.1 ATP-binding cassette sub-family F member 2

ABCF2 Protein Structure

ABC_tran

ABC_tran: ABC transporter (101 - 257)

ABC_tran_Xtn

ABC_tran_Xtn: ABC transporter (296 - 368)

ABC_tran

ABC_tran: ABC transporter (413 - 545)

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  • 623 a.a.
Protein Preferred Names Protein Names

ATP-binding cassette sub-family F member 2

  • ABC-type transport protein

Related Diseases

Diseases Alias
Cystic Fibrosis
  • Mucoviscidosis

  • CF

  • Pseudomonas Aeruginosa, Susceptibility To Chronic Infection By, In Cystic Fibrosis

  • Pseudomonas Aeruginosa Chronic Infection By, In Cystic Fibrosis

  • Cystic Fibrosis Lung Disease, Modifier Of

  • Cystic Fibrosis Of Pancreas

  • Fibrocystic Disease Of Pancreas

  • Cf - [Cystic Fibrosis]

  • Cystic Fibrosis Nos

  • Fibrocystic Disease

  • Fibrocystic Disease Of The Pancreas

  • Mucoviscidosis Of Pancreas

  • Nonproliferative Fibrocystic Disease

  • Pancreatic Cystic Fibrosis

Osteogenesis Imperfecta, Type I
  • Osteogenesis Imperfecta Type I

  • OI1

  • Oi, Type I

  • Osteogenesis Imperfecta Tarda

  • Osteogenesis Imperfecta With Blue Sclerae

  • Osteogenesis Imperfecta Type 1

  • Adair-Dighton Syndrome

  • Mild Osteogenesis Imperfecta

  • Non-Deforming Osteogenesis Imperfecta

  • Oi Type 1

  • Van Der Hoeve Syndrome

  • Classic Non-Deforming Oi With Blue Sclerae

  • Osteogenesis Imperfecta 1

  • Oi-I

  • Osteopenic Non-Fracture Syndrome

  • Osteogenesis Imperfecta, Mild

  • Osteogenesis Imperfecta

  • Lobstein'S Disease

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 ABCF2 MGD MGI:1351657
Rattus norvegicus ABCF2 RGD RGD:1304942
Macaca mulatta ABCF2 VGNC VGNC:81285
Bos taurus ABCF2 VGNC VGNC:25481
Felis catus ABCF2 VGNC VGNC:69337
Others ABCF2 NCBI