SLC25A23 (solute carrier family 25 member 23) - Rat Genome Database

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Gene: SLC25A23 (solute carrier family 25 member 23) Homo sapiens
Analyze
Symbol: SLC25A23
Name: solute carrier family 25 member 23
RGD ID: 1343183
HGNC Page HGNC:19375
Description: Enables ADP:inorganic phosphate antiporter activity and ATP:inorganic phosphate antiporter activity. Involved in mitochondrial transmembrane transport; positive regulation of mitochondrial calcium ion concentration; and regulation of cellular hyperosmotic salinity response. Located in mitochondrion.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: APC2; calcium-binding mitochondrial carrier protein SCaMC-3; MCSC2; MGC2615; mitochondrial adenyl nucleotide antiporter SLC25A23; mitochondrial ATP-Mg/Pi carrier protein 2; mitochondrial Ca(2+)-dependent solute carrier protein 2; mitochondrial Ca2+-dependent solute carrier protein 2; SCaMC-3; SCAMC3; short calcium-binding mitochondrial carrier 3; short calcium-binding mitochondrial carrier protein 3; small calcium-binding mitochondrial carrier protein 3; solute carrier family 25 (mitochondrial carrier, phosphate carrier), member 23
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
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
GRCh38196,436,081 - 6,459,792 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl196,436,079 - 6,465,203 (-)EnsemblGRCh38hg38GRCh38
GRCh37196,440,075 - 6,459,803 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36196,391,075 - 6,410,781 (-)NCBINCBI36Build 36hg18NCBI36
Build 34196,391,074 - 6,410,781NCBI
Celera196,379,913 - 6,399,607 (-)NCBICelera
Cytogenetic Map19p13.3NCBI
HuRef196,200,943 - 6,222,762 (-)NCBIHuRef
CHM1_1196,439,650 - 6,459,340 (-)NCBICHM1_1
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
1,2-dichloroethane  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (ISO)
3,3',5,5'-tetrabromobisphenol A  (ISO)
3-chloropropane-1,2-diol  (ISO)
4-hydroxyphenyl retinamide  (ISO)
5-fluorouracil  (EXP)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acrylamide  (EXP)
aflatoxin B1  (ISO)
amitrole  (ISO)
antirheumatic drug  (EXP)
atrazine  (EXP)
benzo[a]pyrene  (EXP,ISO)
bisphenol A  (ISO)
carbon nanotube  (ISO)
choline  (ISO)
cisplatin  (ISO)
cobalt dichloride  (ISO)
cocaine  (EXP)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
copper(II) sulfate  (EXP)
crocidolite asbestos  (ISO)
cyclosporin A  (EXP)
decabromodiphenyl ether  (ISO)
dicrotophos  (EXP)
dioxygen  (ISO)
dorsomorphin  (EXP)
doxorubicin  (EXP)
endosulfan  (ISO)
ethanol  (ISO)
fenthion  (ISO)
fluoranthene  (ISO)
flutamide  (ISO)
folic acid  (ISO)
furan  (ISO)
gallic acid  (EXP)
gentamycin  (ISO)
heroin  (EXP)
hydrogen peroxide  (EXP)
L-methionine  (ISO)
lead(0)  (EXP)
methimazole  (ISO)
methyl methanesulfonate  (EXP)
methylmercury chloride  (EXP)
nefazodone  (ISO)
nickel atom  (EXP)
nimesulide  (ISO)
ochratoxin A  (ISO)
p-chloromercuribenzoic acid  (EXP)
paracetamol  (EXP,ISO)
paraquat  (ISO)
perfluorooctanoic acid  (ISO)
phenformin  (ISO)
pirinixic acid  (ISO)
pregnenolone 16alpha-carbonitrile  (ISO)
resveratrol  (EXP)
rotenone  (ISO)
SB 431542  (EXP)
silicon dioxide  (EXP)
sodium dichromate  (ISO)
succimer  (ISO)
sulfadimethoxine  (ISO)
sunitinib  (EXP)
tetrachloromethane  (ISO)
thimerosal  (EXP)
thioacetamide  (ISO)
toluene  (ISO)
trichloroethene  (ISO)
troglitazone  (ISO)
tungsten  (ISO)
tunicamycin  (EXP)
valdecoxib  (ISO)
valproic acid  (EXP,ISO)

References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:14702039   PMID:15054102   PMID:15123600   PMID:15716113   PMID:15801905   PMID:17207965   PMID:19322201   PMID:20020773   PMID:20877624   PMID:21145461   PMID:21873635  
PMID:23266187   PMID:24430870   PMID:25416956   PMID:26186194   PMID:26975899   PMID:27993893   PMID:28514442   PMID:28695448   PMID:33961781   PMID:34048709   PMID:36736316  


Genomics

Comparative Map Data
SLC25A23
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38196,436,081 - 6,459,792 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl196,436,079 - 6,465,203 (-)EnsemblGRCh38hg38GRCh38
GRCh37196,440,075 - 6,459,803 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36196,391,075 - 6,410,781 (-)NCBINCBI36Build 36hg18NCBI36
Build 34196,391,074 - 6,410,781NCBI
Celera196,379,913 - 6,399,607 (-)NCBICelera
Cytogenetic Map19p13.3NCBI
HuRef196,200,943 - 6,222,762 (-)NCBIHuRef
CHM1_1196,439,650 - 6,459,340 (-)NCBICHM1_1
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBIT2T-CHM13v2.0
Slc25a23
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391757,350,711 - 57,366,863 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1757,350,711 - 57,366,863 (-)EnsemblGRCm39 Ensembl
GRCm381757,043,711 - 57,059,909 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1757,043,711 - 57,059,863 (-)EnsemblGRCm38mm10GRCm38
MGSCv371757,183,134 - 57,199,286 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361756,728,621 - 56,745,010 (-)NCBIMGSCv36mm8
Celera1761,391,640 - 61,407,783 (-)NCBICelera
Cytogenetic Map17DNCBI
cM Map1729.64NCBI
Slc25a23
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr891,969,633 - 1,985,365 (-)NCBIGRCr8
mRatBN7.291,882,636 - 1,898,369 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl91,882,621 - 1,898,561 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx92,318,184 - 2,332,116 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.097,667,541 - 7,681,473 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.096,623,402 - 6,637,334 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.099,987,988 - 10,003,599 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl99,988,055 - 10,001,962 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.098,988,689 - 9,004,249 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera96,619,249 - 6,633,160 (+)NCBICelera
Cytogenetic Map9q11NCBI
Slc25a23
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554953,155,224 - 3,170,369 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554953,155,024 - 3,171,279 (+)NCBIChiLan1.0ChiLan1.0
SLC25A23
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v22010,849,590 - 10,867,823 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11910,075,652 - 10,093,741 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v0195,474,538 - 5,487,364 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.1196,388,937 - 6,410,481 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl196,388,937 - 6,410,480 (-)Ensemblpanpan1.1panPan2
SLC25A23
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12053,722,841 - 53,736,205 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2053,722,320 - 53,733,331 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2053,469,862 - 53,483,134 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02054,376,787 - 54,390,281 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2054,376,781 - 54,390,615 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12053,443,639 - 53,456,913 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02053,892,079 - 53,905,333 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02054,121,061 - 54,134,550 (+)NCBIUU_Cfam_GSD_1.0
Slc25a23
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405118214,028,801 - 214,045,845 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365883,792,778 - 3,808,593 (-)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365883,792,760 - 3,804,788 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SLC25A23
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl272,625,583 - 72,641,791 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1272,625,544 - 72,643,572 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2272,958,959 - 72,965,057 (-)NCBISscrofa10.2Sscrofa10.2susScr3
SLC25A23
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.166,042,186 - 6,063,969 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl66,044,516 - 6,063,842 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660811,934,087 - 1,959,948 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Slc25a23
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248283,559,813 - 3,572,395 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248283,558,034 - 3,572,426 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SLC25A23
29 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 19p13.3-13.2(chr19:1972245-9648879)x3 copy number gain See cases [RCV000052879] Chr19:1972245..9648879 [GRCh38]
Chr19:1972244..9759555 [GRCh37]
Chr19:1923244..9620555 [NCBI36]
Chr19:19p13.3-13.2
pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:4039158-9176125)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052881]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052881]|See cases [RCV000052881] Chr19:4039158..9176125 [GRCh38]
Chr19:4039156..9286801 [GRCh37]
Chr19:3990156..9147801 [NCBI36]
Chr19:19p13.3-13.2
pathogenic
GRCh38/hg38 19p13.3(chr19:4934885-6501642)x3 copy number gain See cases [RCV000052882] Chr19:4934885..6501642 [GRCh38]
Chr19:4934897..6501653 [GRCh37]
Chr19:4885897..6452653 [NCBI36]
Chr19:19p13.3
pathogenic
GRCh38/hg38 19p13.3-13.2(chr19:265917-8564134)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052876]|See cases [RCV000052876] Chr19:265917..8564134 [GRCh38]
Chr19:265917..8629018 [GRCh37]
Chr19:216917..8535018 [NCBI36]
Chr19:19p13.3-13.2
pathogenic
NM_024103.2(SLC25A23):c.1039C>T (p.Pro347Ser) single nucleotide variant Malignant melanoma [RCV000072431] Chr19:6452344 [GRCh38]
Chr19:6452355 [GRCh37]
Chr19:6403355 [NCBI36]
Chr19:19p13.3
not provided
NM_024103.2(SLC25A23):c.994C>T (p.Arg332Cys) single nucleotide variant Malignant melanoma [RCV000072432] Chr19:6452389 [GRCh38]
Chr19:6452400 [GRCh37]
Chr19:6403400 [NCBI36]
Chr19:19p13.3
not provided
NM_024103.2(SLC25A23):c.993C>T (p.Pro331=) single nucleotide variant Malignant melanoma [RCV000072433] Chr19:6452390 [GRCh38]
Chr19:6452401 [GRCh37]
Chr19:6403401 [NCBI36]
Chr19:19p13.3
not provided
GRCh38/hg38 19p13.3-13.2(chr19:5905175-6916287)x3 copy number gain See cases [RCV000139338] Chr19:5905175..6916287 [GRCh38]
Chr19:5905186..6916298 [GRCh37]
Chr19:5856186..6867298 [NCBI36]
Chr19:19p13.3-13.2
uncertain significance
GRCh38/hg38 19p13.3(chr19:259395-6795611)x3 copy number gain See cases [RCV000142627] Chr19:259395..6795611 [GRCh38]
Chr19:259395..6795622 [GRCh37]
Chr19:210395..6746622 [NCBI36]
Chr19:19p13.3
pathogenic
NM_024103.3(SLC25A23):c.664C>T (p.Arg222Trp) single nucleotide variant Inborn genetic diseases [RCV003310815] Chr19:6454454 [GRCh38]
Chr19:6454465 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.1163C>A (p.Thr388Asn) single nucleotide variant Inborn genetic diseases [RCV003242260] Chr19:6444210 [GRCh38]
Chr19:6444221 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888) copy number gain See cases [RCV000512296] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
NM_024103.3(SLC25A23):c.1126A>G (p.Ile376Val) single nucleotide variant Inborn genetic diseases [RCV003273727] Chr19:6444247 [GRCh38]
Chr19:6444258 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3 copy number gain See cases [RCV000511289] Chr19:260912..58956888 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic|uncertain significance
GRCh37/hg19 19p13.3-13.2(chr19:3120160-9732820)x3 copy number gain not provided [RCV000684096] Chr19:3120160..9732820 [GRCh37]
Chr19:19p13.3-13.2
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:260912-59097160)x3 copy number gain not provided [RCV000752444] Chr19:260912..59097160 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
GRCh37/hg19 19p13.3-q13.43(chr19:68029-59110290)x3 copy number gain not provided [RCV000752439] Chr19:68029..59110290 [GRCh37]
Chr19:19p13.3-q13.43
pathogenic
NM_024103.3(SLC25A23):c.970C>T (p.Arg324Cys) single nucleotide variant Inborn genetic diseases [RCV003245349] Chr19:6452413 [GRCh38]
Chr19:6452424 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.1068C>T (p.Tyr356=) single nucleotide variant not provided [RCV000884130] Chr19:6452315 [GRCh38]
Chr19:6452326 [GRCh37]
Chr19:19p13.3
benign
NM_024103.3(SLC25A23):c.728G>A (p.Arg243His) single nucleotide variant Inborn genetic diseases [RCV003243716] Chr19:6454390 [GRCh38]
Chr19:6454401 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3(chr19:5949772-6699729)x3 copy number gain not provided [RCV001007028] Chr19:5949772..6699729 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.757G>A (p.Ala253Thr) single nucleotide variant not provided [RCV001249340] Chr19:6454361 [GRCh38]
Chr19:6454372 [GRCh37]
Chr19:19p13.3
not provided
NM_024103.3(SLC25A23):c.342G>A (p.Ser114=) single nucleotide variant not provided [RCV000957847] Chr19:6457532 [GRCh38]
Chr19:6457543 [GRCh37]
Chr19:19p13.3
benign
NM_024103.3(SLC25A23):c.192C>T (p.Gly64=) single nucleotide variant not provided [RCV000957848] Chr19:6458289 [GRCh38]
Chr19:6458300 [GRCh37]
Chr19:19p13.3
benign
GRCh37/hg19 19p13.3(chr19:6246138-6823741)x3 copy number gain not provided [RCV001007029] Chr19:6246138..6823741 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3(chr19:6096399-6699729)x3 copy number gain not provided [RCV001259930] Chr19:6096399..6699729 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3(chr19:6394117-6469834) copy number loss not specified [RCV002052673] Chr19:6394117..6469834 [GRCh37]
Chr19:19p13.3
uncertain significance
NC_000019.9:g.(?_6361586)_(8212364_?)del deletion Mucolipidosis type IV [RCV003109715] Chr19:6361586..8212364 [GRCh37]
Chr19:19p13.3-13.2
pathogenic
NM_024103.3(SLC25A23):c.503G>A (p.Cys168Tyr) single nucleotide variant Inborn genetic diseases [RCV003258252] Chr19:6454698 [GRCh38]
Chr19:6454709 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.320G>A (p.Arg107Gln) single nucleotide variant Inborn genetic diseases [RCV002906800] Chr19:6457554 [GRCh38]
Chr19:6457565 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.242G>A (p.Arg81His) single nucleotide variant Inborn genetic diseases [RCV002991027] Chr19:6458239 [GRCh38]
Chr19:6458250 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.1258G>T (p.Gly420Cys) single nucleotide variant Inborn genetic diseases [RCV002739298] Chr19:6442124 [GRCh38]
Chr19:6442135 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.611C>G (p.Ala204Gly) single nucleotide variant Inborn genetic diseases [RCV002910783] Chr19:6454590 [GRCh38]
Chr19:6454601 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.256T>G (p.Phe86Val) single nucleotide variant Inborn genetic diseases [RCV002668223] Chr19:6458225 [GRCh38]
Chr19:6458236 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.730G>A (p.Gly244Ser) single nucleotide variant Inborn genetic diseases [RCV002826170] Chr19:6454388 [GRCh38]
Chr19:6454399 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.658A>G (p.Thr220Ala) single nucleotide variant Inborn genetic diseases [RCV002915264] Chr19:6454460 [GRCh38]
Chr19:6454471 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.1294C>T (p.Arg432Trp) single nucleotide variant Inborn genetic diseases [RCV002983321] Chr19:6442088 [GRCh38]
Chr19:6442099 [GRCh37]
Chr19:19p13.3
likely benign
NM_024103.3(SLC25A23):c.499G>A (p.Glu167Lys) single nucleotide variant Inborn genetic diseases [RCV002850092] Chr19:6454702 [GRCh38]
Chr19:6454713 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.929G>A (p.Arg310His) single nucleotide variant Inborn genetic diseases [RCV002897095] Chr19:6452454 [GRCh38]
Chr19:6452465 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.665G>A (p.Arg222Gln) single nucleotide variant Inborn genetic diseases [RCV002960122] Chr19:6454453 [GRCh38]
Chr19:6454464 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.482C>T (p.Thr161Met) single nucleotide variant Inborn genetic diseases [RCV002835715] Chr19:6456421 [GRCh38]
Chr19:6456432 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.416G>A (p.Arg139His) single nucleotide variant Inborn genetic diseases [RCV003200001] Chr19:6456487 [GRCh38]
Chr19:6456498 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.83G>A (p.Arg28His) single nucleotide variant Inborn genetic diseases [RCV003208418] Chr19:6459546 [GRCh38]
Chr19:6459557 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.631G>T (p.Val211Phe) single nucleotide variant Inborn genetic diseases [RCV003186284] Chr19:6454570 [GRCh38]
Chr19:6454581 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.199G>A (p.Asp67Asn) single nucleotide variant Inborn genetic diseases [RCV003302642] Chr19:6458282 [GRCh38]
Chr19:6458293 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.1358A>G (p.Tyr453Cys) single nucleotide variant Inborn genetic diseases [RCV003378920] Chr19:6442024 [GRCh38]
Chr19:6442035 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.1306C>T (p.Arg436Trp) single nucleotide variant Inborn genetic diseases [RCV003371888] Chr19:6442076 [GRCh38]
Chr19:6442087 [GRCh37]
Chr19:19p13.3
uncertain significance
NM_024103.3(SLC25A23):c.1030G>T (p.Gly344Cys) single nucleotide variant Inborn genetic diseases [RCV003386441] Chr19:6452353 [GRCh38]
Chr19:6452364 [GRCh37]
Chr19:19p13.3
uncertain significance
GRCh37/hg19 19p13.3-13.2(chr19:260912-7246777)x3 copy number gain not provided [RCV003485190] Chr19:260912..7246777 [GRCh37]
Chr19:19p13.3-13.2
pathogenic
NM_024103.3(SLC25A23):c.678T>C (p.Leu226=) single nucleotide variant not provided [RCV003423262] Chr19:6454440 [GRCh38]
Chr19:6454451 [GRCh37]
Chr19:19p13.3
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4197
Count of miRNA genes:1037
Interacting mature miRNAs:1268
Transcripts:ENST00000264088, ENST00000301454, ENST00000334510, ENST00000414491, ENST00000593600, ENST00000595267, ENST00000595810, ENST00000597039, ENST00000597307, ENST00000598704, ENST00000598908, ENST00000600682, ENST00000601322, ENST00000601760
Prediction methods:Microtar, 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
RH78554  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh37196,440,430 - 6,440,554UniSTSGRCh37
GRCh373118,113,400 - 118,113,524UniSTSGRCh37
Build 363119,596,090 - 119,596,214RGDNCBI36
Celera3116,521,408 - 116,521,532RGD
Celera196,380,268 - 6,380,392UniSTS
Cytogenetic Map19p13.3UniSTS
HuRef196,201,298 - 6,201,422UniSTS
HuRef3115,489,062 - 115,489,186UniSTS


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 visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 2434 2128 1622 535 1029 376 4305 2099 3720 411 1349 1594 174 1 1135 2786 2 2
Low 5 815 104 89 870 89 52 96 14 8 111 19 1 69 2 4
Below cutoff 48 51 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_024103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528275 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528277 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528278 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528279 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528280 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528281 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528282 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528283 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528284 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011528285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027285 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027286 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027287 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027288 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027289 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027290 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027291 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017027292 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439403 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439404 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439405 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439406 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439407 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439408 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439409 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439410 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439411 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439412 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047439413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322085 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322086 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322087 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322088 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322089 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322091 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322093 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322094 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322095 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322096 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322098 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322099 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322100 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322102 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322103 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322104 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322105 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322106 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322107 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322108 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322109 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322110 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322111 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322112 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054322113 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC010503 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC011539 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ512835 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ619962 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ619988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ879080 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ879081 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ879082 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ879083 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK027562 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK054901 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK074579 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK294514 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK295484 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AW379976 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY750170 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC001656 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BG706035 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471139 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068259 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

RefSeq Acc Id: ENST00000264088   ⟹   ENSP00000264088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,436,081 - 6,459,751 (-)Ensembl
RefSeq Acc Id: ENST00000301454   ⟹   ENSP00000301454
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,440,064 - 6,459,792 (-)Ensembl
RefSeq Acc Id: ENST00000334510   ⟹   ENSP00000334537
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,443,562 - 6,459,735 (-)Ensembl
RefSeq Acc Id: ENST00000593600   ⟹   ENSP00000470757
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,441,342 - 6,454,405 (-)Ensembl
RefSeq Acc Id: ENST00000595267
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,456,303 - 6,459,770 (-)Ensembl
RefSeq Acc Id: ENST00000595810   ⟹   ENSP00000472590
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,436,079 - 6,454,009 (-)Ensembl
RefSeq Acc Id: ENST00000597039
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,441,930 - 6,452,601 (-)Ensembl
RefSeq Acc Id: ENST00000597307   ⟹   ENSP00000472177
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,456,420 - 6,465,203 (-)Ensembl
RefSeq Acc Id: ENST00000598704   ⟹   ENSP00000472517
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,436,079 - 6,452,388 (-)Ensembl
RefSeq Acc Id: ENST00000598908   ⟹   ENSP00000472153
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,436,081 - 6,454,670 (-)Ensembl
RefSeq Acc Id: ENST00000600682   ⟹   ENSP00000470589
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,441,474 - 6,454,670 (-)Ensembl
RefSeq Acc Id: ENST00000601322   ⟹   ENSP00000470688
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,436,192 - 6,454,376 (-)Ensembl
RefSeq Acc Id: ENST00000601760
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl196,436,421 - 6,444,279 (-)Ensembl
RefSeq Acc Id: NM_024103   ⟹   NP_077008
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,440,064 - 6,459,792 (-)NCBI
GRCh37196,436,092 - 6,460,232 (-)NCBI
Build 36196,391,075 - 6,410,781 (-)NCBI Archive
Celera196,379,913 - 6,399,607 (-)RGD
HuRef196,200,943 - 6,222,762 (-)ENTREZGENE
CHM1_1196,439,650 - 6,459,340 (-)NCBI
T2T-CHM13v2.0196,429,579 - 6,449,293 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528274   ⟹   XP_011526576
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528275   ⟹   XP_011526577
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528276   ⟹   XP_011526578
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528277   ⟹   XP_011526579
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528278   ⟹   XP_011526580
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528279   ⟹   XP_011526581
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528280   ⟹   XP_011526582
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528282   ⟹   XP_011526584
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528283   ⟹   XP_011526585
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528284   ⟹   XP_011526586
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011528285   ⟹   XP_011526587
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,440,064 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027285   ⟹   XP_016882774
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027286   ⟹   XP_016882775
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027287   ⟹   XP_016882776
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027288   ⟹   XP_016882777
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027289   ⟹   XP_016882778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,440,064 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027290   ⟹   XP_016882779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,440,064 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027291   ⟹   XP_016882780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,440,064 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017027292   ⟹   XP_016882781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047439403   ⟹   XP_047295359
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,438,191 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439404   ⟹   XP_047295360
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439405   ⟹   XP_047295361
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439406   ⟹   XP_047295362
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439407   ⟹   XP_047295363
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439408   ⟹   XP_047295364
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439409   ⟹   XP_047295365
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439410   ⟹   XP_047295366
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439411   ⟹   XP_047295367
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439412   ⟹   XP_047295368
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_047439413   ⟹   XP_047295369
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,436,081 - 6,459,792 (-)NCBI
RefSeq Acc Id: XM_054322084   ⟹   XP_054178059
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322085   ⟹   XP_054178060
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322086   ⟹   XP_054178061
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322087   ⟹   XP_054178062
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322088   ⟹   XP_054178063
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322089   ⟹   XP_054178064
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,427,704 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322090   ⟹   XP_054178065
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322091   ⟹   XP_054178066
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322092   ⟹   XP_054178067
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322093   ⟹   XP_054178068
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322094   ⟹   XP_054178069
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322095   ⟹   XP_054178070
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322096   ⟹   XP_054178071
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322097   ⟹   XP_054178072
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322098   ⟹   XP_054178073
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322099   ⟹   XP_054178074
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322100   ⟹   XP_054178075
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322101   ⟹   XP_054178076
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,429,579 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322102   ⟹   XP_054178077
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322103   ⟹   XP_054178078
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322104   ⟹   XP_054178079
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,429,579 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322105   ⟹   XP_054178080
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322106   ⟹   XP_054178081
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322107   ⟹   XP_054178082
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,429,579 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322108   ⟹   XP_054178083
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322109   ⟹   XP_054178084
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322110   ⟹   XP_054178085
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322111   ⟹   XP_054178086
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,429,579 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322112   ⟹   XP_054178087
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
RefSeq Acc Id: XM_054322113   ⟹   XP_054178088
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.0196,425,594 - 6,449,293 (-)NCBI
Protein Sequences
Protein RefSeqs NP_077008 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526576 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526577 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526578 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526579 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526580 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526581 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526582 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526584 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526585 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526586 (Get FASTA)   NCBI Sequence Viewer  
  XP_011526587 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882774 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882775 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882776 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882777 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882778 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882779 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882780 (Get FASTA)   NCBI Sequence Viewer  
  XP_016882781 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295359 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295360 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295361 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295362 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295363 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295364 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295365 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295366 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295367 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295368 (Get FASTA)   NCBI Sequence Viewer  
  XP_047295369 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178059 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178060 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178061 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178062 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178063 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178064 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178065 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178066 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178067 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178068 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178069 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178070 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178071 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178072 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178073 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178074 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178075 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178076 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178077 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178078 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178079 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178080 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178081 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178082 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178083 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178084 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178085 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178086 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178087 (Get FASTA)   NCBI Sequence Viewer  
  XP_054178088 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH01656 (Get FASTA)   NCBI Sequence Viewer  
  AAU95077 (Get FASTA)   NCBI Sequence Viewer  
  BAB70825 (Get FASTA)   NCBI Sequence Viewer  
  BAC11071 (Get FASTA)   NCBI Sequence Viewer  
  BAG57727 (Get FASTA)   NCBI Sequence Viewer  
  BAG58407 (Get FASTA)   NCBI Sequence Viewer  
  CAD55563 (Get FASTA)   NCBI Sequence Viewer  
  CAF04059 (Get FASTA)   NCBI Sequence Viewer  
  CAF04494 (Get FASTA)   NCBI Sequence Viewer  
  CAI51682 (Get FASTA)   NCBI Sequence Viewer  
  CAI51683 (Get FASTA)   NCBI Sequence Viewer  
  CAI51684 (Get FASTA)   NCBI Sequence Viewer  
  CAI51685 (Get FASTA)   NCBI Sequence Viewer  
  EAW69087 (Get FASTA)   NCBI Sequence Viewer  
  EAW69088 (Get FASTA)   NCBI Sequence Viewer  
  EAW69089 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000264088
  ENSP00000264088.3
  ENSP00000301454
  ENSP00000301454.3
  ENSP00000334537
  ENSP00000334537.4
  ENSP00000470589.1
  ENSP00000470688.1
  ENSP00000470757.1
  ENSP00000472153.1
  ENSP00000472177.1
  ENSP00000472517.1
  ENSP00000472590.1
GenBank Protein Q9BV35 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_077008   ⟸   NM_024103
- UniProtKB: Q8N2N4 (UniProtKB/Swiss-Prot),   Q86Y43 (UniProtKB/Swiss-Prot),   Q705K3 (UniProtKB/Swiss-Prot),   Q4LBC2 (UniProtKB/Swiss-Prot),   B4DGB6 (UniProtKB/Swiss-Prot),   Q96NQ4 (UniProtKB/Swiss-Prot),   Q9BV35 (UniProtKB/Swiss-Prot)
- Sequence:
RefSeq Acc Id: XP_011526577   ⟸   XM_011528275
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: XP_011526581   ⟸   XM_011528279
- Peptide Label: isoform X9
- Sequence:
RefSeq Acc Id: XP_011526578   ⟸   XM_011528276
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011526584   ⟸   XM_011528282
- Peptide Label: isoform X12
- Sequence:
RefSeq Acc Id: XP_011526582   ⟸   XM_011528280
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: XP_011526576   ⟸   XM_011528274
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011526586   ⟸   XM_011528284
- Peptide Label: isoform X17
- Sequence:
RefSeq Acc Id: XP_011526579   ⟸   XM_011528277
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011526585   ⟸   XM_011528283
- Peptide Label: isoform X13
- Sequence:
RefSeq Acc Id: XP_011526580   ⟸   XM_011528278
- Peptide Label: isoform X7
- Sequence:
RefSeq Acc Id: XP_011526587   ⟸   XM_011528285
- Peptide Label: isoform X18
- Sequence:
RefSeq Acc Id: XP_016882776   ⟸   XM_017027287
- Peptide Label: isoform X14
- Sequence:
RefSeq Acc Id: XP_016882781   ⟸   XM_017027292
- Peptide Label: isoform X29
- Sequence:
RefSeq Acc Id: XP_016882775   ⟸   XM_017027286
- Peptide Label: isoform X11
- Sequence:
RefSeq Acc Id: XP_016882777   ⟸   XM_017027288
- Peptide Label: isoform X15
- Sequence:
RefSeq Acc Id: XP_016882774   ⟸   XM_017027285
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_016882780   ⟸   XM_017027291
- Peptide Label: isoform X28
- Sequence:
RefSeq Acc Id: XP_016882779   ⟸   XM_017027290
- Peptide Label: isoform X24
- Sequence:
RefSeq Acc Id: XP_016882778   ⟸   XM_017027289
- Peptide Label: isoform X21
- Sequence:
RefSeq Acc Id: ENSP00000472590   ⟸   ENST00000595810
RefSeq Acc Id: ENSP00000472177   ⟸   ENST00000597307
RefSeq Acc Id: ENSP00000472153   ⟸   ENST00000598908
RefSeq Acc Id: ENSP00000334537   ⟸   ENST00000334510
RefSeq Acc Id: ENSP00000472517   ⟸   ENST00000598704
RefSeq Acc Id: ENSP00000470589   ⟸   ENST00000600682
RefSeq Acc Id: ENSP00000470688   ⟸   ENST00000601322
RefSeq Acc Id: ENSP00000301454   ⟸   ENST00000301454
RefSeq Acc Id: ENSP00000264088   ⟸   ENST00000264088
RefSeq Acc Id: ENSP00000470757   ⟸   ENST00000593600
RefSeq Acc Id: XP_047295369   ⟸   XM_047439413
- Peptide Label: isoform X30
RefSeq Acc Id: XP_047295368   ⟸   XM_047439412
- Peptide Label: isoform X27
RefSeq Acc Id: XP_047295366   ⟸   XM_047439410
- Peptide Label: isoform X25
RefSeq Acc Id: XP_047295363   ⟸   XM_047439407
- Peptide Label: isoform X20
RefSeq Acc Id: XP_047295364   ⟸   XM_047439408
- Peptide Label: isoform X22
RefSeq Acc Id: XP_047295362   ⟸   XM_047439406
- Peptide Label: isoform X19
RefSeq Acc Id: XP_047295367   ⟸   XM_047439411
- Peptide Label: isoform X26
RefSeq Acc Id: XP_047295365   ⟸   XM_047439409
- Peptide Label: isoform X23
RefSeq Acc Id: XP_047295361   ⟸   XM_047439405
- Peptide Label: isoform X16
RefSeq Acc Id: XP_047295360   ⟸   XM_047439404
- Peptide Label: isoform X8
RefSeq Acc Id: XP_047295359   ⟸   XM_047439403
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054178088   ⟸   XM_054322113
- Peptide Label: isoform X30
RefSeq Acc Id: XP_054178085   ⟸   XM_054322110
- Peptide Label: isoform X27
RefSeq Acc Id: XP_054178072   ⟸   XM_054322097
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054178087   ⟸   XM_054322112
- Peptide Label: isoform X29
RefSeq Acc Id: XP_054178083   ⟸   XM_054322108
- Peptide Label: isoform X25
RefSeq Acc Id: XP_054178078   ⟸   XM_054322103
- Peptide Label: isoform X20
RefSeq Acc Id: XP_054178069   ⟸   XM_054322094
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054178080   ⟸   XM_054322105
- Peptide Label: isoform X22
RefSeq Acc Id: XP_054178077   ⟸   XM_054322102
- Peptide Label: isoform X19
RefSeq Acc Id: XP_054178073   ⟸   XM_054322098
- Peptide Label: isoform X15
RefSeq Acc Id: XP_054178060   ⟸   XM_054322085
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054178084   ⟸   XM_054322109
- Peptide Label: isoform X26
RefSeq Acc Id: XP_054178067   ⟸   XM_054322092
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054178081   ⟸   XM_054322106
- Peptide Label: isoform X23
RefSeq Acc Id: XP_054178074   ⟸   XM_054322099
- Peptide Label: isoform X16
RefSeq Acc Id: XP_054178061   ⟸   XM_054322086
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054178075   ⟸   XM_054322100
- Peptide Label: isoform X17
RefSeq Acc Id: XP_054178070   ⟸   XM_054322095
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054178068   ⟸   XM_054322093
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054178071   ⟸   XM_054322096
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054178066   ⟸   XM_054322091
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054178062   ⟸   XM_054322087
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054178065   ⟸   XM_054322090
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054178063   ⟸   XM_054322088
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054178059   ⟸   XM_054322084
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054178064   ⟸   XM_054322089
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054178086   ⟸   XM_054322111
- Peptide Label: isoform X28
RefSeq Acc Id: XP_054178082   ⟸   XM_054322107
- Peptide Label: isoform X24
RefSeq Acc Id: XP_054178079   ⟸   XM_054322104
- Peptide Label: isoform X21
RefSeq Acc Id: XP_054178076   ⟸   XM_054322101
- Peptide Label: isoform X18
Protein Domains
EF-hand

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9BV35-F1-model_v2 AlphaFold Q9BV35 1-468 view protein structure

Promoters
RGD ID:6815251
Promoter ID:HG_MRA:7729
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:HeLa_S3
Transcripts:AK054901
Position:
Human AssemblyChrPosition (strand)Source
Build 36196,409,986 - 6,410,486 (-)MPROMDB
RGD ID:6795434
Promoter ID:HG_KWN:28657
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   CD4+TCell_2Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000334510,   NM_024103,   UC002MEV.2
Position:
Human AssemblyChrPosition (strand)Source
Build 36196,410,701 - 6,411,707 (-)MPROMDB
RGD ID:7238217
Promoter ID:EPDNEW_H24855
Type:initiation region
Name:SLC25A23_1
Description:solute carrier family 25 member 23
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh38196,459,770 - 6,459,830EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:19375 AgrOrtholog
COSMIC SLC25A23 COSMIC
Ensembl Genes ENSG00000125648 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000264088 ENTREZGENE
  ENST00000264088.8 UniProtKB/Swiss-Prot
  ENST00000301454 ENTREZGENE
  ENST00000301454.9 UniProtKB/Swiss-Prot
  ENST00000334510 ENTREZGENE
  ENST00000334510.9 UniProtKB/Swiss-Prot
  ENST00000593600.5 UniProtKB/TrEMBL
  ENST00000595810.5 UniProtKB/TrEMBL
  ENST00000597307.1 UniProtKB/TrEMBL
  ENST00000598704.5 UniProtKB/TrEMBL
  ENST00000598908.5 UniProtKB/TrEMBL
  ENST00000600682.5 UniProtKB/TrEMBL
  ENST00000601322.5 UniProtKB/TrEMBL
Gene3D-CATH 1.50.40.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF-hand UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000125648 GTEx
HGNC ID HGNC:19375 ENTREZGENE
Human Proteome Map SLC25A23 Human Proteome Map
InterPro EF-hand-dom_pair UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_Hand_1_Ca_BS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_hand_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Mit_carrier UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Mitochondrial_sb/sol_carrier UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Mt_carrier_dom_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:79085 UniProtKB/Swiss-Prot
NCBI Gene 79085 ENTREZGENE
OMIM 608746 OMIM
PANTHER CALCIUM-BINDING MITOCHONDRIAL CARRIER PROTEIN SCAMC-3 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SOLUTE CARRIER FAMILY 25 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam EF-hand_7 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Mito_carr UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134932456 PharmGKB
PRINTS MITOCARRIER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE EF_HAND_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  EF_HAND_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SOLCAR UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART EFh UniProtKB/Swiss-Prot
Superfamily-SCOP SSF103506 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SSF47473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt B4DGB6 ENTREZGENE
  M0QZJ5_HUMAN UniProtKB/TrEMBL
  M0QZP9_HUMAN UniProtKB/TrEMBL
  M0QZT4_HUMAN UniProtKB/TrEMBL
  M0R1W8_HUMAN UniProtKB/TrEMBL
  M0R1X8_HUMAN UniProtKB/TrEMBL
  M0R2F3_HUMAN UniProtKB/TrEMBL
  M0R2I4_HUMAN UniProtKB/TrEMBL
  Q4LBC2 ENTREZGENE
  Q4LBC4_HUMAN UniProtKB/TrEMBL
  Q4LBC5_HUMAN UniProtKB/TrEMBL
  Q705K3 ENTREZGENE
  Q86Y43 ENTREZGENE
  Q8N2N4 ENTREZGENE
  Q96NQ4 ENTREZGENE
  Q9BV35 ENTREZGENE, UniProtKB/Swiss-Prot
UniProt Secondary B4DGB6 UniProtKB/Swiss-Prot
  Q4LBC2 UniProtKB/Swiss-Prot
  Q705K3 UniProtKB/Swiss-Prot
  Q86Y43 UniProtKB/Swiss-Prot
  Q8N2N4 UniProtKB/Swiss-Prot
  Q96NQ4 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-23 SLC25A23  solute carrier family 25 member 23    solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23  Symbol and/or name change 5135510 APPROVED