SLC22A16 (solute carrier family 22 member 16) - Rat Genome Database

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Gene: SLC22A16 (solute carrier family 22 member 16) Homo sapiens
Analyze
Symbol: SLC22A16
Name: solute carrier family 22 member 16
RGD ID: 1344136
HGNC Page HGNC:20302
Description: Enables amine transmembrane transporter activity; carnitine transmembrane transporter activity; and spermidine transmembrane transporter activity. Involved in several processes, including acid secretion; flagellated sperm motility; and organic cation transport. Acts upstream of or within carnitine transport. Located in cytosol and plasma membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: carnitine transporter 2; CT2; dJ261K5.1; epididymis secretory protein Li 18; flipt 2; FLIPT2; fly-like putative organic ion transporter 2; fly-like putative transporter 2; HEL-S-18; OAT6; OCT6; OKB1; organic cation transporter 6; organic cation transporter OKB1; organic cation/carnitine transporter 6; solute carrier family 22 (organic cation transporter), member 16; solute carrier family 22 (organic cation/carnitine transporter), member 16; WUGSC:RG331P03.1
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Squirrel
Pig
Green Monkey
Alliance Orthologs
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386110,424,687 - 110,476,613 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6110,424,687 - 110,476,641 (-)EnsemblGRCh38hg38GRCh38
GRCh376110,745,890 - 110,797,816 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366110,852,599 - 110,904,537 (-)NCBINCBI36Build 36hg18NCBI36
Build 346110,852,602 - 110,904,537NCBI
Celera6111,492,526 - 111,544,454 (-)NCBICelera
Cytogenetic Map6q21NCBI
HuRef6108,312,812 - 108,364,722 (-)NCBIHuRef
CHM1_16111,009,079 - 111,061,055 (-)NCBICHM1_1
T2T-CHM13v2.06111,603,183 - 111,655,121 (-)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
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component
cytosol  (IDA)
membrane  (IDA,IEA)
plasma membrane  (IC,IDA,IEA,TAS)

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. SMPDB Annotation Import Pipeline Pipeline to import SMPDB annotations from SMPDB into RGD
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
4. Doxorubicin pathways: pharmacodynamics and adverse effects. Thorn CF, etal., Pharmacogenet Genomics. 2011 Jul;21(7):440-6. doi: 10.1097/FPC.0b013e32833ffb56.
5. Transcriptomic characteristics of bronchoalveolar lavage fluid and peripheral blood mononuclear cells in COVID-19 patients. Xiong Y, etal., Emerg Microbes Infect. 2020 Dec;9(1):761-770. doi: 10.1080/22221751.2020.1747363.
Additional References at PubMed
PMID:12089149   PMID:12372408   PMID:12384147   PMID:12477932   PMID:14702039   PMID:15963465   PMID:17197897   PMID:17473959   PMID:17559346   PMID:17581421   PMID:20037140   PMID:20179710  
PMID:20453000   PMID:21873635   PMID:23503679   PMID:25772757   PMID:25998464   PMID:26314988   PMID:26499074   PMID:28036387   PMID:28514442   PMID:29676528   PMID:29698084   PMID:31182584  
PMID:32727751   PMID:33961781  


Genomics

Comparative Map Data
SLC22A16
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh386110,424,687 - 110,476,613 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl6110,424,687 - 110,476,641 (-)EnsemblGRCh38hg38GRCh38
GRCh376110,745,890 - 110,797,816 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 366110,852,599 - 110,904,537 (-)NCBINCBI36Build 36hg18NCBI36
Build 346110,852,602 - 110,904,537NCBI
Celera6111,492,526 - 111,544,454 (-)NCBICelera
Cytogenetic Map6q21NCBI
HuRef6108,312,812 - 108,364,722 (-)NCBIHuRef
CHM1_16111,009,079 - 111,061,055 (-)NCBICHM1_1
T2T-CHM13v2.06111,603,183 - 111,655,121 (-)NCBIT2T-CHM13v2.0
Slc22a16
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391040,446,317 - 40,480,128 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1040,446,332 - 40,480,128 (+)EnsemblGRCm39 Ensembl
GRCm381040,570,321 - 40,604,132 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1040,570,336 - 40,604,132 (+)EnsemblGRCm38mm10GRCm38
MGSCv371040,290,168 - 40,323,938 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361040,259,752 - 40,293,557 (+)NCBIMGSCv36mm8
Celera1041,459,880 - 41,493,899 (+)NCBICelera
Cytogenetic Map10B1NCBI
cM Map1021.99NCBI
Slc22a16
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82045,527,275 - 45,647,675 (+)NCBIGRCr8
mRatBN7.22043,972,808 - 44,068,447 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2043,972,836 - 44,065,019 (+)EnsemblmRatBN7.2 Ensembl
Rnor_6.02045,658,398 - 45,669,192 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02047,377,218 - 47,389,105 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera2044,675,285 - 44,692,225 (+)NCBICelera
Cytogenetic Map20q12NCBI
SLC22A16
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v25130,438,134 - 130,490,825 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan16128,324,168 - 128,376,849 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v06108,232,950 - 108,332,469 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.16112,302,079 - 112,354,629 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl6112,302,265 - 112,354,829 (-)Ensemblpanpan1.1panPan2
SLC22A16
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.11267,110,606 - 67,167,812 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl1267,110,606 - 67,149,880 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha1266,930,237 - 66,986,909 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.01267,995,002 - 68,050,363 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl1267,995,015 - 68,037,024 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.11267,346,263 - 67,401,153 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.01267,192,304 - 67,247,319 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.01267,464,534 - 67,521,660 (-)NCBIUU_Cfam_GSD_1.0
Slc22a16
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024404946102,036,912 - 102,078,052 (-)NCBIHiC_Itri_2
SpeTri2.0NW_0049365646,311,934 - 6,352,759 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
SLC22A16
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl176,423,355 - 76,467,575 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1176,423,386 - 76,468,267 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2186,021,436 - 86,064,197 (+)NCBISscrofa10.2Sscrofa10.2susScr3
SLC22A16
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11363,422,540 - 63,474,920 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl1363,442,867 - 63,474,874 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604035,665,444 - 35,767,647 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in SLC22A16
34 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 6q21-23.2(chr6:108944899-132067720)x1 copy number loss See cases [RCV000051196] Chr6:108944899..132067720 [GRCh38]
Chr6:109266102..132388860 [GRCh37]
Chr6:109372795..132430553 [NCBI36]
Chr6:6q21-23.2		 pathogenic
NM_033125.3(SLC22A16):c.792C>T (p.Val264=) single nucleotide variant Malignant melanoma [RCV000067068] Chr6:110442635 [GRCh38]
Chr6:110763838 [GRCh37]
Chr6:110870531 [NCBI36]
Chr6:6q21		 not provided
GRCh38/hg38 6q16.3-21(chr6:102356502-111049879)x1 copy number loss See cases [RCV000134806] Chr6:102356502..111049879 [GRCh38]
Chr6:102804377..111371082 [GRCh37]
Chr6:102911070..111477775 [NCBI36]
Chr6:6q16.3-21		 pathogenic
GRCh38/hg38 6q21-22.1(chr6:107370141-115827482)x1 copy number loss See cases [RCV000138006] Chr6:107370141..115827482 [GRCh38]
Chr6:107691345..116148646 [GRCh37]
Chr6:107798038..116255339 [NCBI36]
Chr6:6q21-22.1		 pathogenic
GRCh38/hg38 6q13-24.1(chr6:74382807-142040500)x3 copy number gain See cases [RCV000139729] Chr6:74382807..142040500 [GRCh38]
Chr6:75092523..142361637 [GRCh37]
Chr6:75149243..142403330 [NCBI36]
Chr6:6q13-24.1		 pathogenic
GRCh38/hg38 6q16.1-22.31(chr6:96609994-122161548)x1 copy number loss See cases [RCV000139465] Chr6:96609994..122161548 [GRCh38]
Chr6:97057870..122482694 [GRCh37]
Chr6:97164591..122524393 [NCBI36]
Chr6:6q16.1-22.31		 pathogenic
GRCh38/hg38 6q21(chr6:107445281-110547907)x1 copy number loss See cases [RCV000141382] Chr6:107445281..110547907 [GRCh38]
Chr6:107766485..110869110 [GRCh37]
Chr6:107873178..110975803 [NCBI36]
Chr6:6q21		 pathogenic
GRCh38/hg38 6q21-22.31(chr6:106503719-125781219)x1 copy number loss See cases [RCV000141587] Chr6:106503719..125781219 [GRCh38]
Chr6:106951594..126102365 [GRCh37]
Chr6:107058287..126144058 [NCBI36]
Chr6:6q21-22.31		 pathogenic
GRCh38/hg38 6q21(chr6:110020558-111200711)x3 copy number gain See cases [RCV000141546] Chr6:110020558..111200711 [GRCh38]
Chr6:110341761..111521914 [GRCh37]
Chr6:110448454..111628607 [NCBI36]
Chr6:6q21		 uncertain significance
GRCh38/hg38 6q16.3-21(chr6:103279465-113934239)x1 copy number loss See cases [RCV000142287] Chr6:103279465..113934239 [GRCh38]
Chr6:103727340..114255403 [GRCh37]
Chr6:103834033..114362096 [NCBI36]
Chr6:6q16.3-21		 pathogenic
GRCh38/hg38 6q16.3-22.31(chr6:100054889-120488154)x1 copy number loss See cases [RCV000143227] Chr6:100054889..120488154 [GRCh38]
Chr6:100502765..120809300 [GRCh37]
Chr6:100609486..120850999 [NCBI36]
Chr6:6q16.3-22.31		 pathogenic
GRCh37/hg19 6q21(chr6:109564793-112223595)x1 copy number loss See cases [RCV000447293] Chr6:109564793..112223595 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q14.3-22.31(chr6:85988428-120548687)x1 copy number loss See cases [RCV000445666] Chr6:85988428..120548687 [GRCh37]
Chr6:6q14.3-22.31		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3 copy number gain See cases [RCV000512067] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:156975-170919482) copy number gain See cases [RCV000510595] Chr6:156975..170919482 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6q16.1-22.1(chr6:95549951-116684929)x1 copy number loss not provided [RCV000682693] Chr6:95549951..116684929 [GRCh37]
Chr6:6q16.1-22.1		 pathogenic
GRCh37/hg19 6q21(chr6:110419878-111698827)x1 copy number loss not provided [RCV000682707] Chr6:110419878..111698827 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6p25.3-q27(chr6:60107-171054786)x3 copy number gain not provided [RCV000745400] Chr6:60107..171054786 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:108666-170980171)x3 copy number gain not provided [RCV000745403] Chr6:108666..170980171 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
GRCh37/hg19 6p25.3-q27(chr6:165632-170919470)x3 copy number gain not provided [RCV000745404] Chr6:165632..170919470 [GRCh37]
Chr6:6p25.3-q27		 pathogenic
NM_033125.4(SLC22A16):c.1294G>A (p.Val432Ile) single nucleotide variant not provided [RCV000884537] Chr6:110438737 [GRCh38]
Chr6:110759940 [GRCh37]
Chr6:6q21		 benign
NM_033125.4(SLC22A16):c.888C>G (p.Leu296=) single nucleotide variant not provided [RCV000965734] Chr6:110442539 [GRCh38]
Chr6:110763742 [GRCh37]
Chr6:6q21		 benign
NM_033125.4(SLC22A16):c.817A>T (p.Ile273Phe) single nucleotide variant Inborn genetic diseases [RCV003274806] Chr6:110442610 [GRCh38]
Chr6:110763813 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q21(chr6:109564694-112232351)x1 copy number loss not provided [RCV001007557] Chr6:109564694..112232351 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q16.3-22.1(chr6:101296547-117004249)x3 copy number gain Microcephaly [RCV001251053] Chr6:101296547..117004249 [GRCh37]
Chr6:6q16.3-22.1		 pathogenic
GRCh37/hg19 6q16.1-21(chr6:98949950-114533905)x1 copy number loss Deletion 6q16 q21 [RCV001263224] Chr6:98949950..114533905 [GRCh37]
Chr6:6q16.1-21		 pathogenic
GRCh37/hg19 6q21(chr6:110288308-110768384)x3 copy number gain not provided [RCV001259394] Chr6:110288308..110768384 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q21(chr6:110720327-111091182)x3 copy number gain Seizure [RCV002284260] Chr6:110720327..111091182 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q21(chr6:109796301-113083437)x3 copy number gain See cases [RCV001353182] Chr6:109796301..113083437 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q15-22.2(chr6:92054891-118329651) copy number loss not specified [RCV002053598] Chr6:92054891..118329651 [GRCh37]
Chr6:6q15-22.2		 pathogenic
GRCh37/hg19 6q21-22.1(chr6:110472732-114762836) copy number loss not specified [RCV002053609] Chr6:110472732..114762836 [GRCh37]
Chr6:6q21-22.1		 uncertain significance
GRCh37/hg19 6q14.3-22.31(chr6:85988428-120548687) copy number loss not specified [RCV002053595] Chr6:85988428..120548687 [GRCh37]
Chr6:6q14.3-22.31		 pathogenic
GRCh37/hg19 6q21(chr6:109564793-112223595) copy number loss not specified [RCV002053608] Chr6:109564793..112223595 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1363G>A (p.Gly455Arg) single nucleotide variant Inborn genetic diseases [RCV002968880] Chr6:110435910 [GRCh38]
Chr6:110757113 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.314A>G (p.Lys105Arg) single nucleotide variant Inborn genetic diseases [RCV002752822] Chr6:110456757 [GRCh38]
Chr6:110777960 [GRCh37]
Chr6:6q21		 likely benign
NM_033125.4(SLC22A16):c.445G>C (p.Asp149His) single nucleotide variant Inborn genetic diseases [RCV002682551] Chr6:110456626 [GRCh38]
Chr6:110777829 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1138T>C (p.Ser380Pro) single nucleotide variant Inborn genetic diseases [RCV002974289] Chr6:110442289 [GRCh38]
Chr6:110763492 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1669A>G (p.Thr557Ala) single nucleotide variant Inborn genetic diseases [RCV002661919] Chr6:110424938 [GRCh38]
Chr6:110746141 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1700C>T (p.Ala567Val) single nucleotide variant Inborn genetic diseases [RCV002926077] Chr6:110424907 [GRCh38]
Chr6:110746110 [GRCh37]
Chr6:6q21		 likely benign
NM_033125.4(SLC22A16):c.1454G>T (p.Cys485Phe) single nucleotide variant Inborn genetic diseases [RCV002822789] Chr6:110431238 [GRCh38]
Chr6:110752441 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1346T>G (p.Val449Gly) single nucleotide variant Inborn genetic diseases [RCV002884816] Chr6:110435927 [GRCh38]
Chr6:110757130 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1456C>T (p.Arg486Cys) single nucleotide variant Inborn genetic diseases [RCV003001333] Chr6:110431236 [GRCh38]
Chr6:110752439 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.724G>A (p.Ala242Thr) single nucleotide variant Inborn genetic diseases [RCV002707127] Chr6:110442703 [GRCh38]
Chr6:110763906 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1429G>A (p.Ala477Thr) single nucleotide variant Inborn genetic diseases [RCV002874719] Chr6:110431263 [GRCh38]
Chr6:110752466 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.396C>G (p.Asp132Glu) single nucleotide variant Inborn genetic diseases [RCV002674675] Chr6:110456675 [GRCh38]
Chr6:110777878 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.858G>C (p.Trp286Cys) single nucleotide variant Inborn genetic diseases [RCV002670689] Chr6:110442569 [GRCh38]
Chr6:110763772 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1012C>T (p.Pro338Ser) single nucleotide variant Inborn genetic diseases [RCV002936175] Chr6:110442415 [GRCh38]
Chr6:110763618 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.973C>A (p.Leu325Ile) single nucleotide variant Inborn genetic diseases [RCV002655688] Chr6:110442454 [GRCh38]
Chr6:110763657 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.596C>A (p.Ala199Glu) single nucleotide variant Inborn genetic diseases [RCV002814139] Chr6:110446928 [GRCh38]
Chr6:110768131 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1169A>G (p.Asn390Ser) single nucleotide variant Inborn genetic diseases [RCV003180598] Chr6:110442258 [GRCh38]
Chr6:110763461 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.1222G>C (p.Ala408Pro) single nucleotide variant Inborn genetic diseases [RCV003188878] Chr6:110438809 [GRCh38]
Chr6:110760012 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.541C>A (p.Arg181Ser) single nucleotide variant Inborn genetic diseases [RCV003372408] Chr6:110446983 [GRCh38]
Chr6:110768186 [GRCh37]
Chr6:6q21		 uncertain significance
NM_033125.4(SLC22A16):c.313A>G (p.Lys105Glu) single nucleotide variant Inborn genetic diseases [RCV003383059] Chr6:110456758 [GRCh38]
Chr6:110777961 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q21(chr6:110683352-111350364)x3 copy number gain not specified [RCV003986664] Chr6:110683352..111350364 [GRCh37]
Chr6:6q21		 uncertain significance
GRCh37/hg19 6q21-23.2(chr6:110546061-131896074)x3 copy number gain not specified [RCV003986625] Chr6:110546061..131896074 [GRCh37]
Chr6:6q21-23.2		 likely pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1325
Count of miRNA genes:764
Interacting mature miRNAs:878
Transcripts:ENST00000330550, ENST00000368919, ENST00000424139, ENST00000434949, ENST00000437378, ENST00000439654, ENST00000451557, ENST00000456137, ENST00000460159, ENST00000461487
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
SHGC-143321  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376110,778,002 - 110,778,298UniSTSGRCh37
Build 366110,884,695 - 110,884,991RGDNCBI36
Celera6111,524,624 - 111,524,920RGD
Cytogenetic Map6q21-q22.1UniSTS
Cytogenetic Map6q22.1UniSTS
HuRef6108,344,938 - 108,345,234UniSTS
TNG Radiation Hybrid Map653085.0UniSTS
A010A38  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376110,758,057 - 110,758,260UniSTSGRCh37
Build 366110,864,750 - 110,864,953RGDNCBI36
Celera6111,504,677 - 111,504,880RGD
Cytogenetic Map6q21-q22.1UniSTS
Cytogenetic Map6q22.1UniSTS
HuRef6108,324,974 - 108,325,177UniSTS
GeneMap99-GB4 RH Map6464.69UniSTS
NCBI RH Map61401.4UniSTS
G17048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376110,790,199 - 110,790,413UniSTSGRCh37
Build 366110,896,892 - 110,897,106RGDNCBI36
Celera6111,536,825 - 111,537,039RGD
Cytogenetic Map6q21-q22.1UniSTS
Cytogenetic Map6q22.1UniSTS
HuRef6108,357,107 - 108,357,321UniSTS
RH17540  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376110,758,111 - 110,758,285UniSTSGRCh37
Build 366110,864,804 - 110,864,978RGDNCBI36
Celera6111,504,731 - 111,504,905RGD
Cytogenetic Map6q21-q22.1UniSTS
Cytogenetic Map6q22.1UniSTS
HuRef6108,325,028 - 108,325,202UniSTS
GeneMap99-GB4 RH Map6462.63UniSTS
G33056  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh376110,758,057 - 110,758,260UniSTSGRCh37
Celera6111,504,677 - 111,504,880UniSTS
Cytogenetic Map6q21-q22.1UniSTS
Cytogenetic Map6q22.1UniSTS
HuRef6108,324,974 - 108,325,177UniSTS


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 1 10 10 28 10 2 315
Low 25 706 10 18 741 3 179 17 41 30 246 214 15 156 45 1
Below cutoff 1795 1673 1131 366 599 227 3073 1422 2828 211 646 950 141 987 1909 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_033125 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005267184 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536204 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536205 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536206 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536207 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536208 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536209 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536210 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536211 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011536212 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047419435 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054356634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB055798 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC002464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF268892 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI632467 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK057306 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK304546 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AL050350 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY145502 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC012014 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC037247 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC047565 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471051 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  GQ472228 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF458253 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000330550   ⟹   ENSP00000328583
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,424,756 - 110,476,204 (-)Ensembl
RefSeq Acc Id: ENST00000368919   ⟹   ENSP00000357915
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,424,687 - 110,476,613 (-)Ensembl
RefSeq Acc Id: ENST00000424139   ⟹   ENSP00000401007
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,446,873 - 110,476,396 (-)Ensembl
RefSeq Acc Id: ENST00000434949   ⟹   ENSP00000409306
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,438,720 - 110,476,440 (-)Ensembl
RefSeq Acc Id: ENST00000437378   ⟹   ENSP00000416310
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,442,244 - 110,476,398 (-)Ensembl
RefSeq Acc Id: ENST00000451557   ⟹   ENSP00000395642
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,424,687 - 110,456,821 (-)Ensembl
RefSeq Acc Id: ENST00000460159
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,424,687 - 110,425,382 (-)Ensembl
RefSeq Acc Id: ENST00000461487
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl6110,455,429 - 110,476,641 (-)Ensembl
RefSeq Acc Id: NM_033125   ⟹   NP_149116
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,613 (-)NCBI
GRCh376110,745,890 - 110,797,844 (-)NCBI
Build 366110,852,599 - 110,904,537 (-)NCBI Archive
HuRef6108,312,812 - 108,364,722 (-)NCBI
CHM1_16111,009,079 - 111,061,055 (-)NCBI
T2T-CHM13v2.06111,603,183 - 111,655,121 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536204   ⟹   XP_011534506
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,452 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536205   ⟹   XP_011534507
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,613 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536206   ⟹   XP_011534508
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,613 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536207   ⟹   XP_011534509
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,452 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536208   ⟹   XP_011534510
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,613 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536209   ⟹   XP_011534511
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,613 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536210   ⟹   XP_011534512
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,431,183 - 110,476,613 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536211   ⟹   XP_011534513
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,613 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011536212   ⟹   XP_011534514
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,456,611 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047419435   ⟹   XP_047275391
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh386110,424,687 - 110,476,613 (-)NCBI
RefSeq Acc Id: XM_054356626   ⟹   XP_054212601
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,183 - 111,654,966 (-)NCBI
RefSeq Acc Id: XM_054356627   ⟹   XP_054212602
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,199 - 111,655,121 (-)NCBI
RefSeq Acc Id: XM_054356628   ⟹   XP_054212603
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,183 - 111,655,121 (-)NCBI
RefSeq Acc Id: XM_054356629   ⟹   XP_054212604
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,183 - 111,655,121 (-)NCBI
RefSeq Acc Id: XM_054356630   ⟹   XP_054212605
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,183 - 111,655,121 (-)NCBI
RefSeq Acc Id: XM_054356631   ⟹   XP_054212606
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,609,679 - 111,655,121 (-)NCBI
RefSeq Acc Id: XM_054356632   ⟹   XP_054212607
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,183 - 111,655,121 (-)NCBI
RefSeq Acc Id: XM_054356633   ⟹   XP_054212608
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,199 - 111,655,121 (-)NCBI
RefSeq Acc Id: XM_054356634   ⟹   XP_054212609
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.06111,603,183 - 111,635,151 (-)NCBI
Protein Sequences
Protein RefSeqs NP_149116 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534506 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534507 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534508 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534509 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534510 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534511 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534512 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534513 (Get FASTA)   NCBI Sequence Viewer  
  XP_011534514 (Get FASTA)   NCBI Sequence Viewer  
  XP_047275391 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212601 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212602 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212603 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212604 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212605 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212606 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212607 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212608 (Get FASTA)   NCBI Sequence Viewer  
  XP_054212609 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB67044 (Get FASTA)   NCBI Sequence Viewer  
  AAH12014 (Get FASTA)   NCBI Sequence Viewer  
  AAH47565 (Get FASTA)   NCBI Sequence Viewer  
  AAK58593 (Get FASTA)   NCBI Sequence Viewer  
  AAN52928 (Get FASTA)   NCBI Sequence Viewer  
  ACV87203 (Get FASTA)   NCBI Sequence Viewer  
  BAB71419 (Get FASTA)   NCBI Sequence Viewer  
  BAC23062 (Get FASTA)   NCBI Sequence Viewer  
  BAG65342 (Get FASTA)   NCBI Sequence Viewer  
  EAW48313 (Get FASTA)   NCBI Sequence Viewer  
  EAW48314 (Get FASTA)   NCBI Sequence Viewer  
  EAW48315 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000328583.4
  ENSP00000357915
  ENSP00000357915.3
  ENSP00000395642
  ENSP00000395642.1
  ENSP00000401007.1
  ENSP00000409306.1
  ENSP00000416310
  ENSP00000416310.1
GenBank Protein Q86VW1 (Get FASTA)   NCBI Sequence Viewer  
Reference Protein Sequences
RefSeq Acc Id: NP_149116   ⟸   NM_033125
- UniProtKB: Q96M90 (UniProtKB/Swiss-Prot),   Q8IZD5 (UniProtKB/Swiss-Prot),   Q8IUG8 (UniProtKB/Swiss-Prot),   Q5JXM1 (UniProtKB/Swiss-Prot),   O14567 (UniProtKB/Swiss-Prot),   Q96RU0 (UniProtKB/Swiss-Prot),   Q86VW1 (UniProtKB/Swiss-Prot),   A0A0K0K1K9 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011534507   ⟸   XM_011536205
- Peptide Label: isoform X2
- UniProtKB: X6RE50 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011534513   ⟸   XM_011536211
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_011534510   ⟸   XM_011536208
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011534508   ⟸   XM_011536206
- Peptide Label: isoform X3
- Sequence:
RefSeq Acc Id: XP_011534511   ⟸   XM_011536209
- Peptide Label: isoform X6
- Sequence:
RefSeq Acc Id: XP_011534506   ⟸   XM_011536204
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011534509   ⟸   XM_011536207
- Peptide Label: isoform X4
- Sequence:
RefSeq Acc Id: XP_011534514   ⟸   XM_011536212
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: XP_011534512   ⟸   XM_011536210
- Peptide Label: isoform X7
- UniProtKB: C9JGT0 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000401007   ⟸   ENST00000424139
RefSeq Acc Id: ENSP00000395642   ⟸   ENST00000451557
RefSeq Acc Id: ENSP00000357915   ⟸   ENST00000368919
RefSeq Acc Id: ENSP00000409306   ⟸   ENST00000434949
RefSeq Acc Id: ENSP00000416310   ⟸   ENST00000437378
RefSeq Acc Id: ENSP00000328583   ⟸   ENST00000330550
RefSeq Acc Id: XP_047275391   ⟸   XM_047419435
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054212607   ⟸   XM_054356632
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054212604   ⟸   XM_054356629
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054212603   ⟸   XM_054356628
- Peptide Label: isoform X3
RefSeq Acc Id: XP_054212605   ⟸   XM_054356630
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054212601   ⟸   XM_054356626
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054212609   ⟸   XM_054356634
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054212608   ⟸   XM_054356633
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054212602   ⟸   XM_054356627
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054212606   ⟸   XM_054356631
- Peptide Label: isoform X7
Protein Domains
Major facilitator superfamily (MFS) profile

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q86VW1-F1-model_v2 AlphaFold Q86VW1 1-577 view protein structure

Promoters
RGD ID:7208883
Promoter ID:EPDNEW_H10187
Type:initiation region
Name:SLC22A16_1
Description:solute carrier family 22 member 16
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
GRCh386110,476,613 - 110,476,673EPDNEW
RGD ID:6804795
Promoter ID:HG_KWN:54633
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:ENST00000330550
Position:
Human AssemblyChrPosition (strand)Source
Build 366110,903,156 - 110,903,656 (-)MPROMDB
RGD ID:6804796
Promoter ID:HG_KWN:54634
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:OTTHUMT00000043428,   OTTHUMT00000043431,   OTTHUMT00000043432,   OTTHUMT00000043433,   OTTHUMT00000043434,   UC003PUE.1
Position:
Human AssemblyChrPosition (strand)Source
Build 366110,903,856 - 110,904,356 (-)MPROMDB

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:20302 AgrOrtholog
COSMIC SLC22A16 COSMIC
Ensembl Genes ENSG00000004809 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000330550.8 UniProtKB/Swiss-Prot
  ENST00000368919 ENTREZGENE
  ENST00000368919.8 UniProtKB/Swiss-Prot
  ENST00000424139.1 UniProtKB/TrEMBL
  ENST00000434949.5 UniProtKB/TrEMBL
  ENST00000437378 ENTREZGENE
  ENST00000437378.5 UniProtKB/TrEMBL
  ENST00000451557 ENTREZGENE
  ENST00000451557.5 UniProtKB/TrEMBL
Gene3D-CATH 1.20.1250.20 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000004809 GTEx
HGNC ID HGNC:20302 ENTREZGENE
Human Proteome Map SLC22A16 Human Proteome Map
InterPro MFS_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_sugar_transport-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MFS_trans_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:85413 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 85413 ENTREZGENE
OMIM 608276 OMIM
PANTHER SOLUTE CARRIER FAMILY 22 MEMBER UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  SOLUTE CARRIER FAMILY 22 MEMBER 16 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Sugar_tr UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134911502 PharmGKB, RGD
PROSITE MFS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF103473 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0K0K1K9 ENTREZGENE, UniProtKB/TrEMBL
  C9JGT0 ENTREZGENE, UniProtKB/TrEMBL
  C9JTF8_HUMAN UniProtKB/TrEMBL
  C9JU94_HUMAN UniProtKB/TrEMBL
  O14567 ENTREZGENE
  Q5JXM1 ENTREZGENE
  Q86VW1 ENTREZGENE
  Q8IUG8 ENTREZGENE
  Q8IZD5 ENTREZGENE
  Q96ER0_HUMAN UniProtKB/TrEMBL
  Q96M90 ENTREZGENE
  Q96RU0 ENTREZGENE
  S22AG_HUMAN UniProtKB/Swiss-Prot
  X6RE50 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary O14567 UniProtKB/Swiss-Prot
  Q5JXM1 UniProtKB/Swiss-Prot
  Q8IUG8 UniProtKB/Swiss-Prot
  Q8IZD5 UniProtKB/Swiss-Prot
  Q96M90 UniProtKB/Swiss-Prot
  Q96RU0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-02-23 SLC22A16  solute carrier family 22 member 16    solute carrier family 22 (organic cation/carnitine transporter), member 16  Symbol and/or name change 5135510 APPROVED