1. Gene
  2. SLC35F6 - solute carrier family 35 member F6 Gene

SLC35F6 - solute carrier family 35 member F6 Gene

Homo sapiens

Also known as ANT2BP; TANGO9; C2orf18

Gene ID: 54978 | Gene type: protein coding

About SLC35F6

Cytogenetic location: 2p23.3 Genomic coordinates (GRCh38): 2:26,764,284-26,781,231 (from NCBI)

This gene has 4 transcripts (splice variants) and 195 orthologues. Ubiquitous expression in thyroid (RPKM 11.5), skin (RPKM 10.8) and 25 other tissues.

Summary

Predicted to enable transmembrane transporter activity. Involved in negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway and positive regulation of cell population proliferation. Located in several cellular components, including lysosomal membrane; mitochondrion; and nucleoplasm. [provided by Alliance of Genome Resources, Apr 2022]

SLC35F6 Products(1)

mRNA Protein Name
NM_017877.4 NP_060347.2 solute carrier family 35 member F6 precursor
Gene Ontology
  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence Reference Source
enables protein binding IPI
IPI: Inferred from physical interaction
19154410 GOA
Biological Process GO Annotation Evidence Reference Source
involved in negative regulation of mitochondrial outer membrane permeabilization involved in apoptotic signaling pathway IMP
IMP: Inferred from mutant phenotype
19154410 GOA
involved in positive regulation of cell population proliferation IMP
IMP: Inferred from mutant phenotype
19154410 GOA
Cellular Component GO Annotation Evidence Reference Source
located in lysosomal membrane IDA
IDA: Inferred from direct assay
20957757 GOA
located in mitochondrion IDA
IDA: Inferred from direct assay
19154410 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

SLC35F6 Protein Structure

SLC35F

SLC35F: Solute carrier family 35 (95 - 224)

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

solute carrier family 35 member F6

ANT2-binding protein

Related Diseases

Diseases Alias
Pancreatic Ductal Adenocarcinoma

Ductal Adenocarcinoma Of The Pancreas

Gingival Fibromatosis

Hereditary Gingival Fibromatosis

Hereditary Gingival Hyperplasia

Autosomal Dominant Gingival Fibromatosis

Autosomal Dominant Gingival Hyperplasia

Fibromatosis, Gingival, Hereditary

Fibromatosis, Gingival

Mitochondrial Complex I Deficiency, Nuclear Type 1

Mitochondrial Complex I Deficiency

Nadh:Q(1) Oxidoreductase Deficiency

MC1DN1

Nadh-Coenzyme Q Reductase Deficiency

Isolated Mitochondrial Respiratory Chain Complex I Deficiency

Isolated Nadh-Coenzyme Q Reductase Deficiency

Isolated Nadh-Coq Reductase Deficiency

Isolated Nadh-Ubiquinone Reductase Deficiency

Mitochondrial Nadh Dehydrogenase Component Of Complex I, Deficiency Of

Nuclear Type Mitochondrial Complex I Deficiency 1

Isolated Complex I Deficiency

Complex 1 Mitochondrial Respiratory Chain Deficiency

Nadh Coenzyme Q Reductase Deficiency

Complex I Mitochondrial Respiratory Chain Deficiency

Deficiency Of Mitochondrial Nadh Dehydrogenase Component Of Complex I

Nadh:Ubiquinone Oxidoreductase Deficiency

Complex I, Mitochondrial Respiratory Chain, Deficiency Of

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
Rattus norvegicus SLC35F6 RGD RGD:1309228
Macaca mulatta SLC35F6 VGNC VGNC:106219
Felis catus SLC35F6 VGNC VGNC:65336
Bos taurus SLC35F6 VGNC VGNC:34836
Canis familiaris SLC35F6 VGNC VGNC:46380
Mus musculus SLC35F6 MGD MGI:1922169