SLC16A14 (solute carrier family 16 member 14) - Rat Genome Database

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Gene: SLC16A14 (solute carrier family 16 member 14) Homo sapiens
Analyze
Symbol: SLC16A14
Name: solute carrier family 16 member 14
RGD ID: 1320146
HGNC Page HGNC:26417
Description: Predicted to enable monocarboxylic acid transmembrane transporter activity. Predicted to be involved in monocarboxylic acid transport. Predicted to be located in membrane. Predicted to be active in plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: FLJ30794; MCT 14; MCT14; monocarboxylate transporter 14; monocarboxylic acid transporter 14; solute carrier family 16 (monocarboxylic acid transporters), member 14; solute carrier family 16, member 14 (monocarboxylic acid transporter 14)
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Related Pseudogenes: SLC16A14P1  
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382230,034,982 - 230,068,924 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2230,034,982 - 230,068,993 (-)EnsemblGRCh38hg38GRCh38
GRCh372230,899,698 - 230,933,640 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362230,607,942 - 230,641,863 (-)NCBINCBI36Build 36hg18NCBI36
Build 342230,725,204 - 230,759,124NCBI
Celera2224,675,617 - 224,709,637 (-)NCBICelera
Cytogenetic Map2q36.3NCBI
HuRef2222,739,435 - 222,773,253 (-)NCBIHuRef
CHM1_12230,905,955 - 230,939,983 (-)NCBICHM1_1
T2T-CHM13v2.02230,517,639 - 230,551,553 (-)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
(-)-demecolcine  (EXP)
17beta-estradiol  (EXP,ISO)
2,2',5,5'-tetrachlorobiphenyl  (EXP)
2,3',4,4',5-Pentachlorobiphenyl  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
3-chloropropane-1,2-diol  (ISO)
4,4'-sulfonyldiphenol  (ISO)
6-propyl-2-thiouracil  (ISO)
aflatoxin B1  (EXP)
aldehydo-D-glucose  (ISO)
all-trans-retinoic acid  (EXP)
arsane  (EXP)
arsenic atom  (EXP)
belinostat  (EXP)
benzo[a]pyrene  (ISO)
benzo[a]pyrene diol epoxide I  (EXP)
bis(2-ethylhexyl) phthalate  (EXP)
bisphenol A  (EXP,ISO)
butan-1-ol  (EXP)
calcitriol  (EXP)
cefaloridine  (ISO)
CGP 52608  (EXP)
chlorpyrifos  (ISO)
copper atom  (EXP,ISO)
copper(0)  (EXP,ISO)
Cuprizon  (ISO)
cyclosporin A  (EXP)
D-glucose  (ISO)
dorsomorphin  (EXP)
endosulfan  (ISO)
entinostat  (EXP)
ethanol  (EXP)
ethyl methanesulfonate  (EXP)
fenfluramine  (EXP)
formaldehyde  (EXP)
fructose  (ISO)
glucose  (ISO)
GW 4064  (ISO)
leflunomide  (EXP)
lipopolysaccharide  (EXP)
methyl methanesulfonate  (EXP)
methylmercury chloride  (EXP)
N-methyl-4-phenylpyridinium  (EXP,ISO)
niclosamide  (EXP)
ochratoxin A  (ISO)
orphenadrine  (ISO)
ozone  (EXP,ISO)
panobinostat  (EXP)
paracetamol  (ISO)
paraquat  (ISO)
potassium chromate  (EXP)
rotenone  (EXP)
S-(1,2-dichlorovinyl)-L-cysteine  (EXP)
SB 431542  (EXP)
sodium arsenite  (EXP)
sulforaphane  (EXP)
sunitinib  (EXP)
temozolomide  (EXP)
testosterone  (EXP)
thimerosal  (EXP)
titanium dioxide  (ISO)
trichloroethene  (ISO)
trichostatin A  (EXP)
valproic acid  (EXP)
vinclozolin  (ISO)
vincristine  (EXP)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
membrane  (IEA)
plasma membrane  (IBA,IEA)

Molecular Function

References

References - curated
# Reference Title Reference Citation
1. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
2. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:12477932   PMID:12739169   PMID:14702039   PMID:16344560   PMID:21873635   PMID:26186194   PMID:27364523   PMID:27433848   PMID:28514442   PMID:28611215  


Genomics

Comparative Map Data
SLC16A14
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh382230,034,982 - 230,068,924 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl2230,034,982 - 230,068,993 (-)EnsemblGRCh38hg38GRCh38
GRCh372230,899,698 - 230,933,640 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 362230,607,942 - 230,641,863 (-)NCBINCBI36Build 36hg18NCBI36
Build 342230,725,204 - 230,759,124NCBI
Celera2224,675,617 - 224,709,637 (-)NCBICelera
Cytogenetic Map2q36.3NCBI
HuRef2222,739,435 - 222,773,253 (-)NCBIHuRef
CHM1_12230,905,955 - 230,939,983 (-)NCBICHM1_1
T2T-CHM13v2.02230,517,639 - 230,551,553 (-)NCBIT2T-CHM13v2.0
Slc16a14
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39184,881,344 - 84,912,927 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl184,883,619 - 84,912,855 (-)EnsemblGRCm39 Ensembl
GRCm38184,905,488 - 84,935,281 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl184,905,898 - 84,935,134 (-)EnsemblGRCm38mm10GRCm38
MGSCv37184,903,280 - 84,931,658 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36184,785,730 - 84,814,108 (-)NCBIMGSCv36mm8
Celera184,966,975 - 84,995,452 (-)NCBICelera
Cytogenetic Map1C5NCBI
cM Map143.43NCBI
Slc16a14
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr8993,558,144 - 93,585,396 (-)NCBIGRCr8
mRatBN7.2986,110,066 - 86,137,546 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl986,112,894 - 86,137,318 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx994,526,927 - 94,554,181 (-)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0999,655,421 - 99,682,679 (-)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.0998,038,816 - 98,066,050 (-)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.0992,503,602 - 92,531,163 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl992,503,597 - 92,530,938 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0992,234,657 - 92,262,771 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.4984,170,601 - 84,195,055 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.1984,354,585 - 84,372,280 (-)NCBI
Celera983,536,267 - 83,560,596 (-)NCBICelera
Cytogenetic Map9q35NCBI
Slc16a14
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_0049554535,017,347 - 5,044,259 (+)EnsemblChiLan1.0
ChiLan1.0NW_0049554535,011,638 - 5,044,259 (+)NCBIChiLan1.0ChiLan1.0
SLC16A14
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v213132,661,964 - 132,695,610 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan12B132,676,931 - 132,710,577 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v02B117,287,105 - 117,320,771 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.12B236,089,949 - 236,123,451 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl2B236,089,949 - 236,123,451 (-)Ensemblpanpan1.1panPan2
SLC16A14
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.12542,316,294 - 42,373,862 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl2542,318,457 - 42,354,370 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2542,941,535 - 42,972,390 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.02542,572,552 - 42,603,488 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl2542,572,554 - 42,603,761 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.12542,502,842 - 42,533,655 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.02542,344,506 - 42,375,280 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02542,499,740 - 42,530,578 (-)NCBIUU_Cfam_GSD_1.0
Slc16a14
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024405303184,496,691 - 184,526,011 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365256,413,583 - 6,443,568 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365256,413,606 - 6,443,004 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SLC16A14
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl15131,026,230 - 131,080,893 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.115131,042,367 - 131,080,931 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.215144,741,376 - 144,770,756 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SLC16A14
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.110116,059,296 - 116,092,297 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl10116,061,700 - 116,088,548 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604083,356,732 - 83,391,379 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Slc16a14
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248433,794,531 - 3,819,184 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248433,793,309 - 3,825,153 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in SLC16A14
21 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 2q32.3-37.3(chr2:194898783-236473913)x3 copy number gain See cases [RCV000051119] Chr2:194898783..236473913 [GRCh38]
Chr2:195763507..237382556 [GRCh37]
Chr2:195471752..237047295 [NCBI36]
Chr2:2q32.3-37.3		 pathogenic
GRCh38/hg38 2q36.3-37.2(chr2:227343278-235339168)x1 copy number loss See cases [RCV000052638] Chr2:227343278..235339168 [GRCh38]
Chr2:228207994..236247812 [GRCh37]
Chr2:227916238..235912551 [NCBI36]
Chr2:2q36.3-37.2		 pathogenic
GRCh38/hg38 2q36.3-37.3(chr2:226978129-236886599)x1 copy number loss See cases [RCV000052637] Chr2:226978129..236886599 [GRCh38]
Chr2:227842845..237795242 [GRCh37]
Chr2:227551089..237459981 [NCBI36]
Chr2:2q36.3-37.3		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:188818195-242065208)x3 copy number gain See cases [RCV000052958] Chr2:188818195..242065208 [GRCh38]
Chr2:189682921..243007359 [GRCh37]
Chr2:189391166..242656032 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3 copy number gain See cases [RCV000052959] Chr2:190310736..241892770 [GRCh38]
Chr2:191175462..242834921 [GRCh37]
Chr2:190883707..242483594 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q32.3-37.3(chr2:193122313-241074980)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052960]|See cases [RCV000052960] Chr2:193122313..241074980 [GRCh38]
Chr2:193987039..242014395 [GRCh37]
Chr2:193695284..241663068 [NCBI36]
Chr2:2q32.3-37.3		 pathogenic
GRCh38/hg38 2q36.1-37.3(chr2:223992431-242126245)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052972]|See cases [RCV000052972] Chr2:223992431..242126245 [GRCh38]
Chr2:224857148..243059659 [GRCh37]
Chr2:224565392..242717069 [NCBI36]
Chr2:2q36.1-37.3		 pathogenic
GRCh38/hg38 2q36.3-37.3(chr2:227803148-242086301)x3 copy number gain See cases [RCV000052973] Chr2:227803148..242086301 [GRCh38]
Chr2:228667864..243028452 [GRCh37]
Chr2:228376108..242677125 [NCBI36]
Chr2:2q36.3-37.3		 pathogenic
NM_152527.4(SLC16A14):c.1042G>T (p.Glu348Ter) single nucleotide variant Malignant melanoma [RCV000065455] Chr2:230046084 [GRCh38]
Chr2:230910800 [GRCh37]
Chr2:230619044 [NCBI36]
Chr2:2q36.3		 not provided
NM_152527.4(SLC16A14):c.781G>A (p.Asp261Asn) single nucleotide variant Malignant melanoma [RCV000065456] Chr2:230046345 [GRCh38]
Chr2:230911061 [GRCh37]
Chr2:230619305 [NCBI36]
Chr2:2q36.3		 not provided
NM_152527.4(SLC16A14):c.739G>A (p.Glu247Lys) single nucleotide variant Malignant melanoma [RCV000065457] Chr2:230046387 [GRCh38]
Chr2:230911103 [GRCh37]
Chr2:230619347 [NCBI36]
Chr2:2q36.3		 not provided
NM_152527.4(SLC16A14):c.498G>A (p.Thr166=) single nucleotide variant Malignant melanoma [RCV000060511] Chr2:230046628 [GRCh38]
Chr2:230911344 [GRCh37]
Chr2:230619588 [NCBI36]
Chr2:2q36.3		 not provided
GRCh38/hg38 2q36.3-37.3(chr2:228723579-241404867)x3 copy number gain See cases [RCV000134169] Chr2:228723579..241404867 [GRCh38]
Chr2:229588295..242344282 [GRCh37]
Chr2:229296539..241992955 [NCBI36]
Chr2:2q36.3-37.3		 pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:230411764-232019784)x1 copy number loss not specified [RCV000515677] Chr2:230411764..232019784 [GRCh37]
Chr2:2q36.3-37.1		 uncertain significance
GRCh38/hg38 2q36.3(chr2:229854662-230035411)x3 copy number gain See cases [RCV000135270] Chr2:229854662..230035411 [GRCh38]
Chr2:230719378..230900127 [GRCh37]
Chr2:230427622..230608371 [NCBI36]
Chr2:2q36.3		 likely benign
GRCh38/hg38 2q34-37.3(chr2:210579676-242126245)x3 copy number gain See cases [RCV000135934] Chr2:210579676..242126245 [GRCh38]
Chr2:211444400..243059659 [GRCh37]
Chr2:211152645..242717069 [NCBI36]
Chr2:2q34-37.3		 pathogenic
GRCh38/hg38 2q36.3-37.2(chr2:228014149-234976424)x3 copy number gain See cases [RCV000136967] Chr2:228014149..234976424 [GRCh38]
Chr2:228878865..235885068 [GRCh37]
Chr2:228587109..235549807 [NCBI36]
Chr2:2q36.3-37.2		 pathogenic
GRCh38/hg38 2q36.3(chr2:229648729-230055624)x1 copy number loss See cases [RCV000141450] Chr2:229648729..230055624 [GRCh38]
Chr2:230513445..230920340 [GRCh37]
Chr2:230221689..230628584 [NCBI36]
Chr2:2q36.3		 uncertain significance
GRCh38/hg38 2q32.2-37.3(chr2:189436149-241841232)x3 copy number gain See cases [RCV000142307] Chr2:189436149..241841232 [GRCh38]
Chr2:190300875..242783384 [GRCh37]
Chr2:190009120..242432057 [NCBI36]
Chr2:2q32.2-37.3		 pathogenic
GRCh38/hg38 2q35-37.3(chr2:218101759-242126245)x3 copy number gain See cases [RCV000143216] Chr2:218101759..242126245 [GRCh38]
Chr2:218966482..243059659 [GRCh37]
Chr2:218674727..242717069 [NCBI36]
Chr2:2q35-37.3		 pathogenic
GRCh37/hg19 2q35-37.3(chr2:219966808-237815985)x3 copy number gain See cases [RCV000448049] Chr2:219966808..237815985 [GRCh37]
Chr2:2q35-37.3		 pathogenic
GRCh37/hg19 2q36.1-37.1(chr2:223378640-232061074)x1 copy number loss See cases [RCV000448773] Chr2:223378640..232061074 [GRCh37]
Chr2:2q36.1-37.1		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384) copy number gain See cases [RCV000512056] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q34-37.3(chr2:213518431-242783384)x3 copy number gain See cases [RCV000512009] Chr2:213518431..242783384 [GRCh37]
Chr2:2q34-37.3		 pathogenic
GRCh37/hg19 2q36.1-37.3(chr2:222077224-239394441)x3 copy number gain See cases [RCV000511816] Chr2:222077224..239394441 [GRCh37]
Chr2:2q36.1-37.3		 pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:230491213-231404389)x1 copy number loss See cases [RCV000511869] Chr2:230491213..231404389 [GRCh37]
Chr2:2q36.3-37.1		 likely pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:12771-242783384)x3 copy number gain See cases [RCV000511212] Chr2:12771..242783384 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
NM_152527.5(SLC16A14):c.890T>C (p.Phe297Ser) single nucleotide variant Inborn genetic diseases [RCV003279592] Chr2:230046236 [GRCh38]
Chr2:230910952 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.205C>T (p.Arg69Cys) single nucleotide variant Inborn genetic diseases [RCV003251063] Chr2:230059148 [GRCh38]
Chr2:230923864 [GRCh37]
Chr2:2q36.3		 uncertain significance
GRCh37/hg19 2q36.3(chr2:230489419-230906744)x3 copy number gain not provided [RCV000659204] Chr2:230489419..230906744 [GRCh37]
Chr2:2q36.3		 uncertain significance
GRCh37/hg19 2q35-37.3(chr2:219225872-242016876)x3 copy number gain not provided [RCV000682170] Chr2:219225872..242016876 [GRCh37]
Chr2:2q35-37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:14238-243048760)x3 copy number gain not provided [RCV000752802] Chr2:14238..243048760 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:15672-243101834)x3 copy number gain not provided [RCV000752804] Chr2:15672..243101834 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:228966709-231528909)x1 copy number loss not provided [RCV000740932] Chr2:228966709..231528909 [GRCh37]
Chr2:2q36.3-37.1		 pathogenic
GRCh37/hg19 2p25.3-q37.3(chr2:1-243199373) copy number gain Mosaic trisomy 2 [RCV002280628] Chr2:1..243199373 [GRCh37]
Chr2:2p25.3-q37.3		 pathogenic
GRCh37/hg19 2q34-37.3(chr2:210779657-239879183)x3 copy number gain See cases [RCV000790568] Chr2:210779657..239879183 [GRCh37]
Chr2:2q34-37.3		 pathogenic
GRCh37/hg19 2q36.3(chr2:230713968-230904798)x4 copy number gain not provided [RCV000848464] Chr2:230713968..230904798 [GRCh37]
Chr2:2q36.3		 uncertain significance
GRCh37/hg19 2q36.3-37.3(chr2:230814690-242783384)x3 copy number gain not provided [RCV001007519] Chr2:230814690..242783384 [GRCh37]
Chr2:2q36.3-37.3		 pathogenic
NM_152527.5(SLC16A14):c.906G>A (p.Ser302=) single nucleotide variant not provided [RCV000946690] Chr2:230046220 [GRCh38]
Chr2:230910936 [GRCh37]
Chr2:2q36.3		 benign
GRCh37/hg19 2q36.3-37.1(chr2:230783729-231016862)x3 copy number gain not provided [RCV001007518] Chr2:230783729..231016862 [GRCh37]
Chr2:2q36.3-37.1		 uncertain significance
GRCh37/hg19 2q31.2-37.3(chr2:178397959-243007457)x3 copy number gain See cases [RCV001263052] Chr2:178397959..243007457 [GRCh37]
Chr2:2q31.2-37.3		 pathogenic
NM_152527.5(SLC16A14):c.217G>A (p.Ala73Thr) single nucleotide variant Inborn genetic diseases [RCV003197137] Chr2:230059136 [GRCh38]
Chr2:230923852 [GRCh37]
Chr2:2q36.3		 uncertain significance
GRCh37/hg19 2q36.1-37.1(chr2:223378640-232061074) copy number loss not specified [RCV002053287] Chr2:223378640..232061074 [GRCh37]
Chr2:2q36.1-37.1		 pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:229968217-231883182) copy number loss not specified [RCV002053293] Chr2:229968217..231883182 [GRCh37]
Chr2:2q36.3-37.1		 pathogenic
GRCh37/hg19 2q35-37.3(chr2:219606537-239217703) copy number loss not specified [RCV002053285] Chr2:219606537..239217703 [GRCh37]
Chr2:2q35-37.3		 pathogenic
GRCh37/hg19 2q36.3-37.1(chr2:228807574-235475892) copy number loss not specified [RCV002053291] Chr2:228807574..235475892 [GRCh37]
Chr2:2q36.3-37.1		 pathogenic
NM_152527.5(SLC16A14):c.366C>A (p.Asn122Lys) single nucleotide variant Inborn genetic diseases [RCV002837178] Chr2:230049798 [GRCh38]
Chr2:230914514 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.1211C>T (p.Thr404Met) single nucleotide variant Inborn genetic diseases [RCV002752062] Chr2:230045915 [GRCh38]
Chr2:230910631 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.1061C>T (p.Pro354Leu) single nucleotide variant Inborn genetic diseases [RCV002737274] Chr2:230046065 [GRCh38]
Chr2:230910781 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.1123G>A (p.Asp375Asn) single nucleotide variant Inborn genetic diseases [RCV002868786] Chr2:230046003 [GRCh38]
Chr2:230910719 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.1067C>T (p.Thr356Met) single nucleotide variant Inborn genetic diseases [RCV002874556] Chr2:230046059 [GRCh38]
Chr2:230910775 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.831G>A (p.Met277Ile) single nucleotide variant Inborn genetic diseases [RCV002674159] Chr2:230046295 [GRCh38]
Chr2:230911011 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.42T>G (p.Asp14Glu) single nucleotide variant Inborn genetic diseases [RCV002747894] Chr2:230059311 [GRCh38]
Chr2:230924027 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.1028T>C (p.Leu343Ser) single nucleotide variant Inborn genetic diseases [RCV002656860] Chr2:230046098 [GRCh38]
Chr2:230910814 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.279C>G (p.Phe93Leu) single nucleotide variant Inborn genetic diseases [RCV003201683] Chr2:230049885 [GRCh38]
Chr2:230914601 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.1162G>T (p.Ala388Ser) single nucleotide variant Inborn genetic diseases [RCV003192251] Chr2:230045964 [GRCh38]
Chr2:230910680 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.631C>T (p.Pro211Ser) single nucleotide variant Inborn genetic diseases [RCV003195279] Chr2:230046495 [GRCh38]
Chr2:230911211 [GRCh37]
Chr2:2q36.3		 uncertain significance
NM_152527.5(SLC16A14):c.1210A>G (p.Thr404Ala) single nucleotide variant Inborn genetic diseases [RCV003309633] Chr2:230045916 [GRCh38]
Chr2:230910632 [GRCh37]
Chr2:2q36.3		 uncertain significance
GRCh37/hg19 2q35-37.3(chr2:218376403-242783384)x3 copy number gain not provided [RCV003484087] Chr2:218376403..242783384 [GRCh37]
Chr2:2q35-37.3		 pathogenic
GRCh37/hg19 2q36.3(chr2:230714245-230903875)x3 copy number gain not provided [RCV003484096] Chr2:230714245..230903875 [GRCh37]
Chr2:2q36.3		 uncertain significance
Single allele duplication not provided [RCV003448672] Chr2:230077026..243049549 [GRCh37]
Chr2:2q36.3-37.3		 pathogenic
GRCh37/hg19 2q36.3(chr2:230603619-230947503)x3 copy number gain not provided [RCV000740940] Chr2:230603619..230947503 [GRCh37]
Chr2:2q36.3		 benign
GRCh37/hg19 2q36.3(chr2:230877172-230899765)x1 copy number loss not provided [RCV000740945] Chr2:230877172..230899765 [GRCh37]
Chr2:2q36.3		 benign
GRCh37/hg19 2q36.2-37.3(chr2:225995545-237594511)x3 copy number gain not provided [RCV003484091] Chr2:225995545..237594511 [GRCh37]
Chr2:2q36.2-37.3		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1740
Count of miRNA genes:941
Interacting mature miRNAs:1074
Transcripts:ENST00000295190, ENST00000412034, ENST00000425822, ENST00000436869, ENST00000457406
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
D2S2317  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372230,909,303 - 230,909,510UniSTSGRCh37
Build 362230,617,547 - 230,617,754RGDNCBI36
Celera2224,685,230 - 224,685,437RGD
Cytogenetic Map2q36.3UniSTS
HuRef2222,749,109 - 222,749,304UniSTS
Marshfield Genetic Map2233.62RGD
Marshfield Genetic Map2233.62UniSTS
Genethon Genetic Map2240.9UniSTS
deCODE Assembly Map2235.6UniSTS
Whitehead-YAC Contig Map2 UniSTS
SHGC-152545  
Human AssemblyChrPosition (strand)SourceJBrowse
Build 362230,617,506 - 230,617,697RGDNCBI36
Celera2224,685,189 - 224,685,380RGD
Cytogenetic Map2q36.3UniSTS
TNG Radiation Hybrid Map273786.0UniSTS
D2S247E  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh372230,911,846 - 230,911,977UniSTSGRCh37
Build 362230,620,090 - 230,620,221RGDNCBI36
Celera2224,687,773 - 224,687,904RGD
Cytogenetic Map2q36.3UniSTS
HuRef2222,751,442 - 222,751,573UniSTS


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 31 5 18 37 71 12 323 10 662 25 178 124 28 40 168
Low 2285 2223 1558 447 915 312 3306 1477 3025 338 1233 1430 143 1164 1970 2 2
Below cutoff 101 714 140 134 845 134 677 691 34 42 27 29 3 1 650

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_152527 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005246353 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510751 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011510752 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017003480 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047443523 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340803 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340804 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340805 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340806 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054340807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC093171 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055317 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK055356 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK123207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK292873 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL833470 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX512919 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AX512921 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC034382 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC065524 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BN000146 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX093330 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BX648181 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471063 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA044472 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000295190   ⟹   ENSP00000295190
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,034,982 - 230,068,924 (-)Ensembl
RefSeq Acc Id: ENST00000412034   ⟹   ENSP00000395775
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,045,670 - 230,068,548 (-)Ensembl
RefSeq Acc Id: ENST00000425822   ⟹   ENSP00000389726
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,059,227 - 230,068,289 (-)Ensembl
RefSeq Acc Id: ENST00000436869   ⟹   ENSP00000396834
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,059,299 - 230,068,993 (-)Ensembl
RefSeq Acc Id: ENST00000457406   ⟹   ENSP00000400352
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl2230,045,657 - 230,068,907 (-)Ensembl
RefSeq Acc Id: NM_152527   ⟹   NP_689740
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,034,982 - 230,068,924 (-)NCBI
GRCh372230,899,690 - 230,933,715 (-)RGD
Build 362230,607,942 - 230,641,863 (-)NCBI Archive
Celera2224,675,617 - 224,709,637 (-)RGD
HuRef2222,739,435 - 222,773,253 (-)ENTREZGENE
CHM1_12230,905,955 - 230,939,983 (-)NCBI
T2T-CHM13v2.02230,517,639 - 230,551,553 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005246353   ⟹   XP_005246410
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,034,982 - 230,068,924 (-)NCBI
GRCh372230,899,690 - 230,933,715 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011510751   ⟹   XP_011509053
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,034,982 - 230,067,504 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011510752   ⟹   XP_011509054
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,041,562 - 230,068,924 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017003480   ⟹   XP_016858969
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,034,982 - 230,068,053 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047443523   ⟹   XP_047299479
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh382230,034,982 - 230,068,201 (-)NCBI
RefSeq Acc Id: XM_054340803   ⟹   XP_054196778
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02230,517,639 - 230,550,682 (-)NCBI
RefSeq Acc Id: XM_054340804   ⟹   XP_054196779
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02230,517,639 - 230,550,504 (-)NCBI
RefSeq Acc Id: XM_054340805   ⟹   XP_054196780
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02230,524,225 - 230,551,553 (-)NCBI
RefSeq Acc Id: XM_054340806   ⟹   XP_054196781
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02230,517,639 - 230,551,553 (-)NCBI
RefSeq Acc Id: XM_054340807   ⟹   XP_054196782
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.02230,517,639 - 230,550,830 (-)NCBI
Protein Sequences
Protein RefSeqs NP_689740 (Get FASTA)   NCBI Sequence Viewer  
  XP_005246410 (Get FASTA)   NCBI Sequence Viewer  
  XP_011509053 (Get FASTA)   NCBI Sequence Viewer  
  XP_011509054 (Get FASTA)   NCBI Sequence Viewer  
  XP_016858969 (Get FASTA)   NCBI Sequence Viewer  
  XP_047299479 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196778 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196779 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196780 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196781 (Get FASTA)   NCBI Sequence Viewer  
  XP_054196782 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH34382 (Get FASTA)   NCBI Sequence Viewer  
  AAH65524 (Get FASTA)   NCBI Sequence Viewer  
  AAY24109 (Get FASTA)   NCBI Sequence Viewer  
  BAB70909 (Get FASTA)   NCBI Sequence Viewer  
  BAC85558 (Get FASTA)   NCBI Sequence Viewer  
  BAF85562 (Get FASTA)   NCBI Sequence Viewer  
  BAG51499 (Get FASTA)   NCBI Sequence Viewer  
  CAD52855 (Get FASTA)   NCBI Sequence Viewer  
  CAD52856 (Get FASTA)   NCBI Sequence Viewer  
  CAD80157 (Get FASTA)   NCBI Sequence Viewer  
  EAW70913 (Get FASTA)   NCBI Sequence Viewer  
  EAW70914 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000295190
  ENSP00000295190.4
  ENSP00000389726.1
  ENSP00000395775.1
  ENSP00000396834.1
  ENSP00000400352
  ENSP00000400352.1
GenBank Protein Q7RTX9 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_689740   ⟸   NM_152527
- UniProtKB: Q53R92 (UniProtKB/Swiss-Prot),   A8KA08 (UniProtKB/Swiss-Prot),   Q96NI7 (UniProtKB/Swiss-Prot),   Q7RTX9 (UniProtKB/Swiss-Prot),   Q6ZWE5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005246410   ⟸   XM_005246353
- Peptide Label: isoform X3
- UniProtKB: Q6ZWE5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011509053   ⟸   XM_011510751
- Peptide Label: isoform X1
- UniProtKB: Q53R92 (UniProtKB/Swiss-Prot),   A8KA08 (UniProtKB/Swiss-Prot),   Q96NI7 (UniProtKB/Swiss-Prot),   Q7RTX9 (UniProtKB/Swiss-Prot),   Q6ZWE5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011509054   ⟸   XM_011510752
- Peptide Label: isoform X2
- UniProtKB: Q6ZWE5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_016858969   ⟸   XM_017003480
- Peptide Label: isoform X1
- UniProtKB: Q53R92 (UniProtKB/Swiss-Prot),   A8KA08 (UniProtKB/Swiss-Prot),   Q96NI7 (UniProtKB/Swiss-Prot),   Q7RTX9 (UniProtKB/Swiss-Prot),   Q6ZWE5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000389726   ⟸   ENST00000425822
RefSeq Acc Id: ENSP00000395775   ⟸   ENST00000412034
RefSeq Acc Id: ENSP00000295190   ⟸   ENST00000295190
RefSeq Acc Id: ENSP00000400352   ⟸   ENST00000457406
RefSeq Acc Id: ENSP00000396834   ⟸   ENST00000436869
RefSeq Acc Id: XP_047299479   ⟸   XM_047443523
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054196781   ⟸   XM_054340806
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054196782   ⟸   XM_054340807
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054196778   ⟸   XM_054340803
- Peptide Label: isoform X1
- UniProtKB: Q7RTX9 (UniProtKB/Swiss-Prot),   Q53R92 (UniProtKB/Swiss-Prot),   A8KA08 (UniProtKB/Swiss-Prot),   Q96NI7 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054196779   ⟸   XM_054340804
- Peptide Label: isoform X1
- UniProtKB: Q7RTX9 (UniProtKB/Swiss-Prot),   Q53R92 (UniProtKB/Swiss-Prot),   A8KA08 (UniProtKB/Swiss-Prot),   Q96NI7 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054196780   ⟸   XM_054340805
- Peptide Label: isoform X2
Protein Domains
Major facilitator superfamily (MFS) profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q7RTX9-F1-model_v2 AlphaFold Q7RTX9 1-510 view protein structure

Promoters
RGD ID:6863034
Promoter ID:EPDNEW_H4682
Type:initiation region
Name:SLC16A14_1
Description:solute carrier family 16 member 14
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
GRCh382230,068,924 - 230,068,984EPDNEW
RGD ID:6798169
Promoter ID:HG_KWN:37609
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   Lymphoblastoid
Transcripts:NM_152527,   OTTHUMT00000332364,   OTTHUMT00000332366,   OTTHUMT00000332367,   UC002VQE.2
Position:
Human AssemblyChrPosition (strand)Source
Build 362230,641,111 - 230,641,817 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:26417 AgrOrtholog
COSMIC SLC16A14 COSMIC
Ensembl Genes ENSG00000163053 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000295190 ENTREZGENE
  ENST00000295190.9 UniProtKB/Swiss-Prot
  ENST00000412034.5 UniProtKB/TrEMBL
  ENST00000425822.5 UniProtKB/TrEMBL
  ENST00000436869.1 UniProtKB/TrEMBL
  ENST00000457406 ENTREZGENE
  ENST00000457406.5 UniProtKB/TrEMBL
Gene3D-CATH 1.20.1250.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000163053 GTEx
HGNC ID HGNC:26417 ENTREZGENE
Human Proteome Map SLC16A14 Human Proteome Map
InterPro MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_trans_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:151473 UniProtKB/Swiss-Prot
NCBI Gene 151473 ENTREZGENE
PANTHER MONOCARBOXYLATE TRANSPORTER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MONOCARBOXYLATE TRANSPORTER 14 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MFS_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134983567 PharmGKB
PROSITE MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF103473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A8KA08 ENTREZGENE
  C9JIV1_HUMAN UniProtKB/TrEMBL
  C9JME4_HUMAN UniProtKB/TrEMBL
  E7EMG7_HUMAN UniProtKB/TrEMBL
  MOT14_HUMAN UniProtKB/Swiss-Prot
  Q05BQ4_HUMAN UniProtKB/TrEMBL
  Q53R92 ENTREZGENE
  Q6ZWE5 ENTREZGENE, UniProtKB/TrEMBL
  Q7RTX9 ENTREZGENE
  Q96NI7 ENTREZGENE
UniProt Secondary A8KA08 UniProtKB/Swiss-Prot
  Q53R92 UniProtKB/Swiss-Prot
  Q96NI7 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-08 SLC16A14  solute carrier family 16 member 14    solute carrier family 16, member 14  Symbol and/or name change 5135510 APPROVED
2013-07-23 SLC16A14  solute carrier family 16, member 14    solute carrier family 16, member 14 (monocarboxylic acid transporter 14)  Symbol and/or name change 5135510 APPROVED