SLC25A2 (solute carrier family 25 member 2) - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Gene: SLC25A2 (solute carrier family 25 member 2) Homo sapiens
Analyze
Symbol: SLC25A2
Name: solute carrier family 25 member 2
RGD ID: 1347291
HGNC Page HGNC:22921
Description: Enables L-arginine transmembrane transporter activity; L-lysine transmembrane transporter activity; and L-ornithine transmembrane transporter activity. Involved in L-alpha-amino acid transmembrane transport and ornithine metabolic process. Located in mitochondrion.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: MGC119151; MGC119153; mitochondrial ornithine transporter 2; ORC2; ornithine transporter 2; ORNT2; solute carrier family 25 (mitochondrial carrier, ornithine transporter) member 2
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385141,302,635 - 141,304,049 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5141,302,635 - 141,304,049 (-)EnsemblGRCh38hg38GRCh38
GRCh375140,682,202 - 140,683,616 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,662,380 - 140,663,796 (-)NCBINCBI36Build 36hg18NCBI36
Build 345140,662,379 - 140,663,616NCBI
Celera5136,759,021 - 136,760,437 (-)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,827,253 - 135,828,669 (-)NCBIHuRef
CHM1_15140,115,401 - 140,116,817 (-)NCBICHM1_1
T2T-CHM13v2.05141,827,934 - 141,829,348 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Function

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:10380929   PMID:10716726   PMID:11004451   PMID:11230163   PMID:12477932   PMID:12807890   PMID:12948741   PMID:19240061   PMID:20877624   PMID:21873635   PMID:22262851   PMID:23251661  
PMID:23266187   PMID:26403849   PMID:28514442   PMID:32296183   PMID:33845483   PMID:33961781   PMID:36217029  


Genomics

Comparative Map Data
SLC25A2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385141,302,635 - 141,304,049 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5141,302,635 - 141,304,049 (-)EnsemblGRCh38hg38GRCh38
GRCh375140,682,202 - 140,683,616 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,662,380 - 140,663,796 (-)NCBINCBI36Build 36hg18NCBI36
Build 345140,662,379 - 140,663,616NCBI
Celera5136,759,021 - 136,760,437 (-)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,827,253 - 135,828,669 (-)NCBIHuRef
CHM1_15140,115,401 - 140,116,817 (-)NCBICHM1_1
T2T-CHM13v2.05141,827,934 - 141,829,348 (-)NCBIT2T-CHM13v2.0
Slc25a2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391837,770,431 - 37,771,776 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1837,770,431 - 37,771,776 (-)EnsemblGRCm39 Ensembl
GRCm381837,637,378 - 37,638,723 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1837,637,378 - 37,638,723 (-)EnsemblGRCm38mm10GRCm38
GRCm38.p6 Ensembl1837,637,377 - 37,638,745 (-)EnsemblGRCm38mm10GRCm38
MGSCv371837,797,032 - 37,798,377 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361837,763,352 - 37,764,697 (-)NCBIMGSCv36mm8
Celera1838,969,866 - 38,971,211 (-)NCBICelera
Cytogenetic Map18B3NCBI
cM Map1819.54NCBI
Slc25a2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr81829,704,182 - 29,707,563 (-)NCBIGRCr8
mRatBN7.21829,452,943 - 29,456,324 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1829,453,582 - 29,460,383 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1829,557,293 - 29,560,674 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.01830,319,302 - 30,322,683 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.01829,654,627 - 29,658,008 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.01830,774,205 - 30,775,401 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1830,774,205 - 30,775,401 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01830,470,432 - 30,471,628 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41830,536,488 - 30,537,684 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11830,563,379 - 30,564,385 (-)NCBI
Celera1829,102,009 - 29,103,205 (-)NCBICelera
Cytogenetic Map18p11NCBI
SLC25A2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24136,552,172 - 136,557,044 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15134,691,724 - 134,695,284 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05136,664,485 - 136,666,344 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15142,778,348 - 142,779,770 (-)NCBIpanpan1.1PanPan1.1panPan2
SLC25A2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1236,286,080 - 36,287,619 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl236,286,584 - 36,287,489 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha233,337,980 - 33,339,519 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0236,740,699 - 36,742,238 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl236,741,203 - 36,742,108 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1233,814,742 - 33,816,281 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0234,625,750 - 34,627,289 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0235,433,398 - 35,434,937 (-)NCBIUU_Cfam_GSD_1.0
SLC25A2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl2142,944,078 - 142,944,980 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.12142,943,565 - 142,947,313 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.22149,142,741 - 149,144,549 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SLC25A2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.12343,922,525 - 43,924,166 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl2343,922,816 - 43,923,721 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366603433,930,087 - 33,931,925 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Slc25a2
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_004624774541,115 - 542,020 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_004624774540,820 - 542,200 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SLC25A2
11 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 copy number gain See cases [RCV000051193] Chr5:130860928..155321811 [GRCh38]
Chr5:130196621..154701371 [GRCh37]
Chr5:130224520..154681564 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-32(chr5:138871137-145812309)x1 copy number loss See cases [RCV000052142] Chr5:138871137..145812309 [GRCh38]
Chr5:138206826..145191872 [GRCh37]
Chr5:138234725..145172065 [NCBI36]
Chr5:5q31.2-32
pathogenic
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 copy number loss See cases [RCV000053524] Chr5:106619588..156124387 [GRCh38]
Chr5:105955289..155551397 [GRCh37]
Chr5:105983188..155483975 [NCBI36]
Chr5:5q21.3-33.2
pathogenic
GRCh38/hg38 5q31.3(chr5:140963199-142322798)x1 copy number loss See cases [RCV000136949] Chr5:140963199..142322798 [GRCh38]
Chr5:140453735..141702363 [GRCh37]
Chr5:140322968..141682547 [NCBI36]
Chr5:5q31.3
uncertain significance
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 copy number gain See cases [RCV000138808] Chr5:129847794..153353546 [GRCh38]
Chr5:129183487..152733106 [GRCh37]
Chr5:129211386..152713299 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.3-32(chr5:141089988-149530678)x3 copy number gain See cases [RCV000139504] Chr5:141089988..149530678 [GRCh38]
Chr5:140469572..148910241 [GRCh37]
Chr5:140449756..148890434 [NCBI36]
Chr5:5q31.3-32
pathogenic
GRCh38/hg38 5q31.2-31.3(chr5:138942857-144605017)x3 copy number gain See cases [RCV000142806] Chr5:138942857..144605017 [GRCh38]
Chr5:138278546..143984580 [GRCh37]
Chr5:138306445..143964773 [NCBI36]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3
likely benign
NC_000005.9:g.(?_86400000)_(154000000_?)del deletion Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] Chr5:86400000..154000000 [GRCh37]
Chr5:5q14.3-33.2
pathogenic
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3
pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NM_031947.4(SLC25A2):c.473A>G (p.Lys158Arg) single nucleotide variant Inborn genetic diseases [RCV003254461] Chr5:141303393 [GRCh38]
Chr5:140682960 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.203G>A (p.Gly68Asp) single nucleotide variant Inborn genetic diseases [RCV003257142] Chr5:141303663 [GRCh38]
Chr5:140683230 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q31.3(chr5:140676272-140929172)x3 copy number gain See cases [RCV000512526] Chr5:140676272..140929172 [GRCh37]
Chr5:5q31.3
likely benign
GRCh37/hg19 5q31.2-31.3(chr5:139147238-141540491)x1 copy number loss not provided [RCV000682600] Chr5:139147238..141540491 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32
uncertain significance
NM_031947.4(SLC25A2):c.485A>C (p.Lys162Thr) single nucleotide variant Inborn genetic diseases [RCV003270618] Chr5:141303381 [GRCh38]
Chr5:140682948 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q31.3-32(chr5:140424333-148985999)x3 copy number gain not provided [RCV000848228] Chr5:140424333..148985999 [GRCh37]
Chr5:5q31.3-32
uncertain significance
NC_000005.9:g.(?_136633338)_(140998481_?)dup duplication PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] Chr5:136633338..140998481 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) copy number gain not specified [RCV002053526] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
GRCh37/hg19 5q31.3(chr5:140082762-140773954)x3 copy number gain not provided [RCV002474614] Chr5:140082762..140773954 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.436A>C (p.Ile146Leu) single nucleotide variant Inborn genetic diseases [RCV002773443] Chr5:141303430 [GRCh38]
Chr5:140682997 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.311T>G (p.Leu104Arg) single nucleotide variant Inborn genetic diseases [RCV002818295] Chr5:141303555 [GRCh38]
Chr5:140683122 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.819G>A (p.Met273Ile) single nucleotide variant Inborn genetic diseases [RCV003000275] Chr5:141303047 [GRCh38]
Chr5:140682614 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.200C>A (p.Thr67Asn) single nucleotide variant Inborn genetic diseases [RCV002826807] Chr5:141303666 [GRCh38]
Chr5:140683233 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.56G>C (p.Gly19Ala) single nucleotide variant Inborn genetic diseases [RCV002764932] Chr5:141303810 [GRCh38]
Chr5:140683377 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.512A>G (p.His171Arg) single nucleotide variant Inborn genetic diseases [RCV003218610] Chr5:141303354 [GRCh38]
Chr5:140682921 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.572A>G (p.Tyr191Cys) single nucleotide variant Inborn genetic diseases [RCV003189695] Chr5:141303294 [GRCh38]
Chr5:140682861 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.413A>G (p.Tyr138Cys) single nucleotide variant Inborn genetic diseases [RCV003341060] Chr5:141303453 [GRCh38]
Chr5:140683020 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.308A>G (p.Lys103Arg) single nucleotide variant Inborn genetic diseases [RCV003378905] Chr5:141303558 [GRCh38]
Chr5:140683125 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.352G>A (p.Ala118Thr) single nucleotide variant Inborn genetic diseases [RCV003378102] Chr5:141303514 [GRCh38]
Chr5:140683081 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.350C>T (p.Ser117Phe) single nucleotide variant Inborn genetic diseases [RCV003370332] Chr5:141303516 [GRCh38]
Chr5:140683083 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_031947.4(SLC25A2):c.254A>G (p.Tyr85Cys) single nucleotide variant Inborn genetic diseases [RCV003371296] Chr5:141303612 [GRCh38]
Chr5:140683179 [GRCh37]
Chr5:5q31.3
uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:183
Count of miRNA genes:172
Interacting mature miRNAs:175
Transcripts:ENST00000239451
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
RH92610  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,682,286 - 140,682,436UniSTSGRCh37
Build 365140,662,470 - 140,662,620RGDNCBI36
Celera5136,759,111 - 136,759,261RGD
Cytogenetic Map5q31UniSTS
HuRef5135,827,343 - 135,827,493UniSTS
GeneMap99-GB4 RH Map5528.69UniSTS
SLC25A2__6844  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,682,085 - 140,682,830UniSTSGRCh37
Build 365140,662,269 - 140,663,014RGDNCBI36
Celera5136,758,910 - 136,759,655RGD
HuRef5135,827,142 - 135,827,887UniSTS
UniSTS:480968  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh375140,682,477 - 140,683,432UniSTSGRCh37
Celera5136,759,302 - 136,760,257UniSTS
HuRef5135,827,534 - 135,828,489UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system adipose tissue appendage entire extraembryonic component
High
Medium 280
Low 58 98 301 29 136 19 539 29 411 16 299 219 10 23 382 1
Below cutoff 1773 1943 1158 442 1118 300 2856 1291 2593 248 709 1133 150 941 1799 2

Sequence


RefSeq Acc Id: ENST00000239451   ⟹   ENSP00000239451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5141,302,635 - 141,304,049 (-)Ensembl
RefSeq Acc Id: NM_031947   ⟹   NP_114153
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385141,302,635 - 141,304,049 (-)NCBI
GRCh375140,682,196 - 140,683,612 (-)RGD
Build 365140,662,380 - 140,663,796 (-)NCBI Archive
Celera5136,759,021 - 136,760,437 (-)RGD
HuRef5135,827,253 - 135,828,669 (-)ENTREZGENE
CHM1_15140,115,401 - 140,116,835 (-)NCBI
T2T-CHM13v2.05141,827,934 - 141,829,348 (-)NCBI
Sequence:
RefSeq Acc Id: NP_114153   ⟸   NM_031947
- UniProtKB: Q6XUI0 (UniProtKB/Swiss-Prot),   Q496C1 (UniProtKB/Swiss-Prot),   Q8NFZ2 (UniProtKB/Swiss-Prot),   Q9BXI2 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: ENSP00000239451   ⟸   ENST00000239451

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BXI2-F1-model_v2 AlphaFold Q9BXI2 1-301 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:22921 AgrOrtholog
COSMIC SLC25A2 COSMIC
Ensembl Genes ENSG00000120329 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000239451 ENTREZGENE
  ENST00000239451.7 UniProtKB/Swiss-Prot
Gene3D-CATH 1.50.40.10 UniProtKB/Swiss-Prot
GTEx ENSG00000120329 GTEx
HGNC ID HGNC:22921 ENTREZGENE
Human Proteome Map SLC25A2 Human Proteome Map
InterPro Mitochondrial_sb/sol_carrier UniProtKB/Swiss-Prot
  Mt_carrier_dom_sf UniProtKB/Swiss-Prot
KEGG Report hsa:83884 UniProtKB/Swiss-Prot
NCBI Gene 83884 ENTREZGENE
OMIM 608157 OMIM
PANTHER MITOCHONDRIAL BASIC AMINO ACIDS TRANSPORTER-RELATED UniProtKB/Swiss-Prot
  MITOCHONDRIAL ORNITHINE TRANSPORTER 2 UniProtKB/Swiss-Prot
Pfam Mito_carr UniProtKB/Swiss-Prot
PharmGKB PA134910073 PharmGKB
PROSITE SOLCAR UniProtKB/Swiss-Prot
Superfamily-SCOP SSF103506 UniProtKB/Swiss-Prot
UniProt ORNT2_HUMAN UniProtKB/Swiss-Prot
  Q496C1 ENTREZGENE
  Q6XUI0 ENTREZGENE
  Q8NFZ2 ENTREZGENE
  Q9BXI2 ENTREZGENE
UniProt Secondary Q496C1 UniProtKB/Swiss-Prot
  Q6XUI0 UniProtKB/Swiss-Prot
  Q8NFZ2 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-03-08 SLC25A2  solute carrier family 25 member 2  SLC25A2  solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 2  Symbol and/or name change 5135510 APPROVED