1. Gene
  2. ABCF2 - ATP binding cassette subfamily F member 2 Gene

ABCF2 - ATP binding cassette subfamily F member 2 Gene

Homo sapiens

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

Gene ID: 10061 | Gene type: protein coding

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