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slc25a12.L solute carrier family 25 member 12 L homeolog [ Xenopus laevis (African clawed frog) ]

Gene ID: 443574, updated on 4-Nov-2024

Summary

Official Symbol
slc25a12.L
Official Full Name
solute carrier family 25 member 12 L homeolog
Primary source
Xenbase:XB-GENE-1002106
Locus tag
XELAEV_18044692mg
See related
EnsemblRapid:ENSXLAG00005030192 AllianceGenome:Xenbase:XB-GENE-1002106
Gene type
protein coding
RefSeq status
PROVISIONAL
Organism
Xenopus laevis
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Amphibia; Batrachia; Anura; Pipoidea; Pipidae; Xenopodinae; Xenopus; Xenopus
Also known as
slc25a12
Summary
Predicted to enable L-aspartate transmembrane transporter activity; L-glutamate transmembrane transporter activity; and calcium ion binding activity. Predicted to act upstream of or within L-glutamate transmembrane transport; aspartate transmembrane transport; and malate-aspartate shuttle. Predicted to be located in mitochondrial inner membrane. Human ortholog(s) of this gene implicated in Asperger syndrome; autistic disorder; and developmental and epileptic encephalopathy 39. Orthologous to human SLC25A12 (solute carrier family 25 member 12). [provided by Alliance of Genome Resources, Nov 2024]
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Genomic context

See slc25a12.L in Genome Data Viewer
Location:
chromosome: 9_10L
Exon count:
19
Annotation release Status Assembly Chr Location
101 current Xenopus_laevis_v10.1 (GCF_017654675.1) 9_10L NC_054387.1 (76003448..76112179, complement)
100 previous assembly Xenopus_laevis_v2 (GCF_001663975.1) 9_10L NC_030740.1 (65487732..65597354, complement)

Chromosome 9_10L - NC_054387.1Genomic Context describing neighboring genes Neighboring gene cytochrome b reductase 1 L homeolog Neighboring gene dynein, cytoplasmic 1, intermediate chain 2 L homeolog Neighboring gene histone acetyltransferase 1 L homeolog Neighboring gene methionyl aminopeptidase type 1D (mitochondrial) L homeolog

Genomic regions, transcripts, and products

General gene information

Gene Ontology Provided by Xenbase

Function Evidence Code Pubs
enables L-aspartate transmembrane transporter activity IEA
Inferred from Electronic Annotation
more info
 
enables L-glutamate transmembrane transporter activity IEA
Inferred from Electronic Annotation
more info
 
enables calcium ion binding IEA
Inferred from Electronic Annotation
more info
 
enables metal ion binding IEA
Inferred from Electronic Annotation
more info
 
Process Evidence Code Pubs
acts_upstream_of_or_within L-glutamate transmembrane transport IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within aspartate transmembrane transport IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within malate-aspartate shuttle IEA
Inferred from Electronic Annotation
more info
 
acts_upstream_of_or_within transmembrane transport IEA
Inferred from Electronic Annotation
more info
 
Component Evidence Code Pubs
located_in membrane IEA
Inferred from Electronic Annotation
more info
 
located_in mitochondrial inner membrane IEA
Inferred from Electronic Annotation
more info
 

General protein information

Preferred Names
solute carrier family 25 member 12 L homeolog
Names
solute carrier family 25 (aspartate/glutamate carrier), member 12 L homeolog
solute carrier family 25 (mitochondrial carrier, Aralar), member 12

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

  1. NM_001091799.1NP_001085268.1  solute carrier family 25 member 12 L homeolog

    See identical proteins and their annotated locations for NP_001085268.1

    Status: PROVISIONAL

    Source sequence(s)
    BC094139
    UniProtKB/TrEMBL
    A0A974BZ77, Q52KY7, Q6INL0
    Related
    ENSXLAP00005090747.1, ENSXLAT00005092427.1
    Conserved Domains (4) summary
    PTZ00168
    Location:324585
    PTZ00168; mitochondrial carrier protein; Provisional
    pfam00153
    Location:326417
    Mito_carr; Mitochondrial carrier protein
    pfam13499
    Location:1478
    EF-hand_7; EF-hand domain pair
    cl08302
    Location:1678
    EFh; EF-hand, calcium binding motif; A diverse superfamily of calcium sensors and calcium signal modulators; most examples in this alignment model have 2 active canonical EF hands. Ca2+ binding induces a conformational change in the EF-hand motif, leading to ...

RefSeqs of Annotated Genomes: Xenopus laevis Annotation Release 101 details...Open this link in a new tab

The following sections contain reference sequences that belong to a specific genome build. Explain

Reference Xenopus_laevis_v10.1 Primary Assembly

Genomic

  1. NC_054387.1 Reference Xenopus_laevis_v10.1 Primary Assembly

    Range
    76003448..76112179 complement
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_018234284.2XP_018089773.1  solute carrier family 25 member 12 L homeolog isoform X1

    UniProtKB/TrEMBL
    A0A1L8EW72, A0A974BZA1, Q6INL0
    Related
    ENSXLAP00005091090.1, ENSXLAT00005092769.1