AQP6 (aquaporin 6) - Rat Genome Database

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Gene: AQP6 (aquaporin 6) Homo sapiens
Analyze
Symbol: AQP6
Name: aquaporin 6
RGD ID: 737143
HGNC Page HGNC:639
Description: Enables water channel activity. Involved in odontogenesis and renal water transport. Predicted to be located in cytoplasmic vesicle membrane. Predicted to be active in apical plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: AQP-6; AQP2L; aquaporin 2-like, kidney specific; aquaporin 6, kidney specific; aquaporin-2-like; aquaporin-6; aquaporin-6, kidney specific; hKID; KID; kidney-specific aquaporin
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
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
GRCh381249,972,947 - 49,977,139 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1249,967,194 - 49,977,139 (+)EnsemblGRCh38hg38GRCh38
GRCh371250,366,730 - 50,370,922 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361248,652,887 - 48,657,189 (+)NCBINCBI36Build 36hg18NCBI36
Build 341248,652,891 - 48,657,189NCBI
Celera1249,162,741 - 49,167,043 (+)NCBICelera
Cytogenetic Map12q13.12NCBI
HuRef1247,398,122 - 47,402,424 (+)NCBIHuRef
CHM1_11250,332,778 - 50,337,080 (+)NCBICHM1_1
T2T-CHM13v2.01249,935,958 - 49,940,150 (+)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
Gene Ontology Annotations     Click to see Annotation Detail View

Cellular Component

Molecular Pathway Annotations     Click to see Annotation Detail View
References

References - curated
# Reference Title Reference Citation
1. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
2. Aquaporins in the kidney. Kwon TH, etal., Handb Exp Pharmacol. 2009;(190):95-132. doi: 10.1007/978-3-540-79885-9_5.
3. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:8812490   PMID:9268644   PMID:12177001   PMID:12477932   PMID:12522663   PMID:19680475   PMID:20461409   PMID:21873635   PMID:26779650   PMID:32296183   PMID:33961781   PMID:36724073  
PMID:36949045  


Genomics

Comparative Map Data
AQP6
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381249,972,947 - 49,977,139 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1249,967,194 - 49,977,139 (+)EnsemblGRCh38hg38GRCh38
GRCh371250,366,730 - 50,370,922 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361248,652,887 - 48,657,189 (+)NCBINCBI36Build 36hg18NCBI36
Build 341248,652,891 - 48,657,189NCBI
Celera1249,162,741 - 49,167,043 (+)NCBICelera
Cytogenetic Map12q13.12NCBI
HuRef1247,398,122 - 47,402,424 (+)NCBIHuRef
CHM1_11250,332,778 - 50,337,080 (+)NCBICHM1_1
T2T-CHM13v2.01249,935,958 - 49,940,150 (+)NCBIT2T-CHM13v2.0
Aqp6
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm391599,495,891 - 99,503,359 (+)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl1599,499,281 - 99,503,358 (+)EnsemblGRCm39 Ensembl
GRCm381599,598,468 - 99,605,478 (+)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl1599,601,400 - 99,605,477 (+)EnsemblGRCm38mm10GRCm38
MGSCv371599,431,831 - 99,435,908 (+)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv361599,429,434 - 99,433,511 (+)NCBIMGSCv36mm8
Celera15101,756,793 - 101,760,851 (+)NCBICelera
Cytogenetic Map15F1NCBI
cM Map1556.13NCBI
Aqp6
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr87132,611,069 - 132,614,004 (+)NCBIGRCr8
mRatBN7.27130,732,216 - 130,735,149 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl7130,633,579 - 130,735,194 (+)EnsemblmRatBN7.2 Ensembl
mRatBN7.2 Ensembl7130,633,579 - 130,735,194 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx7132,535,805 - 132,538,735 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.07134,761,384 - 134,764,315 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.07134,673,911 - 134,676,841 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.07141,258,585 - 141,261,518 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl7141,258,584 - 141,261,735 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.0X115,763,288 - 115,766,221 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.47138,347,266 - 138,350,199 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.17138,423,702 - 138,426,636 (+)NCBI
Celera7127,213,574 - 127,216,507 (+)NCBICelera
Cytogenetic Map7q36NCBI
Aqp6
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955547567,152 - 571,895 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955547567,152 - 570,880 (+)NCBIChiLan1.0ChiLan1.0
AQP6
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21044,172,566 - 44,216,164 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11244,169,328 - 44,212,932 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01238,739,047 - 38,782,659 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11239,672,067 - 39,676,636 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1239,672,067 - 39,676,636 (-)Ensemblpanpan1.1panPan2
AQP6
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1274,727,732 - 4,731,828 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl274,727,725 - 4,731,316 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha2741,527,817 - 41,531,698 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0274,775,594 - 4,779,476 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl274,776,786 - 4,789,859 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1274,740,579 - 4,744,460 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0274,730,402 - 4,734,285 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.02741,922,470 - 41,926,347 (+)NCBIUU_Cfam_GSD_1.0
Aqp6
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440494565,511,431 - 65,514,075 (-)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365127,650,724 - 7,653,274 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365127,650,755 - 7,653,399 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
AQP6
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl515,887,966 - 15,890,805 (+)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1515,888,080 - 15,892,113 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2516,068,162 - 16,071,435 (-)NCBISscrofa10.2Sscrofa10.2susScr3
AQP6
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.11146,199,907 - 46,207,010 (+)NCBIChlSab1.1ChlSab1.1chlSab2
Vero_WHO_p1.0NW_023666037199,914,619 - 199,919,218 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Aqp6
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248162,316,668 - 2,319,650 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248162,314,660 - 2,319,649 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in AQP6
27 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 12q13.12(chr12:49840075-50315208)x3 copy number gain See cases [RCV000051958] Chr12:49840075..50315208 [GRCh38]
Chr12:50233858..50708991 [GRCh37]
Chr12:48520125..48995258 [NCBI36]
Chr12:12q13.12		 uncertain significance
GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3 copy number gain See cases [RCV000139555] Chr12:121271..133196807 [GRCh38]
Chr12:282465..133773393 [GRCh37]
Chr12:100698..132283466 [NCBI36]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3 copy number gain See cases [RCV000258805] Chr12:1..133851895 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic|likely pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3 copy number gain See cases [RCV000510482] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902) copy number gain See cases [RCV000511643] Chr12:173787..133777902 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
NC_000012.11:g.26370251_54361538inv inversion not specified [RCV000714265] Chr12:26370251..54361538 [GRCh37]
Chr12:12p12.1-q13.13		 uncertain significance
GRCh37/hg19 12p13.33-q24.33(chr12:191619-133777645)x3 copy number gain not provided [RCV000750246] Chr12:191619..133777645 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
GRCh37/hg19 12p13.33-q24.33(chr12:621220-133779118)x3 copy number gain not provided [RCV000750253] Chr12:621220..133779118 [GRCh37]
Chr12:12p13.33-q24.33		 pathogenic
NM_001652.4(AQP6):c.57T>C (p.Leu19=) single nucleotide variant not provided [RCV000967265] Chr12:49973230 [GRCh38]
Chr12:50367013 [GRCh37]
Chr12:12q13.12		 benign
NM_001652.4(AQP6):c.496C>G (p.Arg166Gly) single nucleotide variant not provided [RCV000967266] Chr12:49974417 [GRCh38]
Chr12:50368200 [GRCh37]
Chr12:12q13.12		 benign
NM_001652.4(AQP6):c.48G>A (p.Ala16=) single nucleotide variant not provided [RCV000959266] Chr12:49973221 [GRCh38]
Chr12:50367004 [GRCh37]
Chr12:12q13.12		 benign
NM_001652.4(AQP6):c.479T>C (p.Phe160Ser) single nucleotide variant not specified [RCV004332815] Chr12:49974400 [GRCh38]
Chr12:50368183 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.561+5G>A single nucleotide variant not provided [RCV000970247] Chr12:49974487 [GRCh38]
Chr12:50368270 [GRCh37]
Chr12:12q13.12		 benign
GRCh37/hg19 12q13.12(chr12:50331947-50439383)x3 copy number gain not provided [RCV002291539] Chr12:50331947..50439383 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.253G>A (p.Val85Met) single nucleotide variant not specified [RCV004333946] Chr12:49973426 [GRCh38]
Chr12:50367209 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.497G>A (p.Arg166His) single nucleotide variant not specified [RCV004085944] Chr12:49974418 [GRCh38]
Chr12:50368201 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.821C>T (p.Ser274Leu) single nucleotide variant not specified [RCV004086143] Chr12:49975643 [GRCh38]
Chr12:50369426 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.151G>A (p.Ala51Thr) single nucleotide variant not specified [RCV004178312] Chr12:49973324 [GRCh38]
Chr12:50367107 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.733C>T (p.Arg245Trp) single nucleotide variant not specified [RCV004205277] Chr12:49975555 [GRCh38]
Chr12:50369338 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.47C>T (p.Ala16Val) single nucleotide variant not specified [RCV004147620] Chr12:49973220 [GRCh38]
Chr12:50367003 [GRCh37]
Chr12:12q13.12		 likely benign
NM_001652.4(AQP6):c.757G>A (p.Val253Ile) single nucleotide variant not specified [RCV004225202] Chr12:49975579 [GRCh38]
Chr12:50369362 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.431C>T (p.Ala144Val) single nucleotide variant not specified [RCV004185540] Chr12:49974352 [GRCh38]
Chr12:50368135 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.329G>A (p.Gly110Glu) single nucleotide variant not specified [RCV004148827] Chr12:49973502 [GRCh38]
Chr12:50367285 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.380G>A (p.Arg127Gln) single nucleotide variant not specified [RCV004097265] Chr12:49973553 [GRCh38]
Chr12:50367336 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.163G>A (p.Val55Met) single nucleotide variant not specified [RCV004230673] Chr12:49973336 [GRCh38]
Chr12:50367119 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.712G>A (p.Asp238Asn) single nucleotide variant not specified [RCV004219720] Chr12:49975534 [GRCh38]
Chr12:50369317 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.250G>A (p.Ala84Thr) single nucleotide variant not specified [RCV004254981] Chr12:49973423 [GRCh38]
Chr12:50367206 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.115T>C (p.Phe39Leu) single nucleotide variant not specified [RCV004279645] Chr12:49973288 [GRCh38]
Chr12:50367071 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.107T>C (p.Leu36Pro) single nucleotide variant not specified [RCV004420048] Chr12:49973280 [GRCh38]
Chr12:50367063 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.127G>T (p.Gly43Cys) single nucleotide variant not specified [RCV004420049] Chr12:49973300 [GRCh38]
Chr12:50367083 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.271G>A (p.Val91Ile) single nucleotide variant not specified [RCV004420052] Chr12:49973444 [GRCh38]
Chr12:50367227 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.218C>T (p.Thr73Ile) single nucleotide variant not specified [RCV004420051] Chr12:49973391 [GRCh38]
Chr12:50367174 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.545T>A (p.Leu182Gln) single nucleotide variant not specified [RCV004664792] Chr12:49974466 [GRCh38]
Chr12:50368249 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.685C>G (p.Leu229Val) single nucleotide variant not specified [RCV004664781] Chr12:49975507 [GRCh38]
Chr12:50369290 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.557T>C (p.Ile186Thr) single nucleotide variant not specified [RCV004656049] Chr12:49974478 [GRCh38]
Chr12:50368261 [GRCh37]
Chr12:12q13.12		 uncertain significance
NM_001652.4(AQP6):c.817G>A (p.Gly273Ser) single nucleotide variant not specified [RCV004656064] Chr12:49975639 [GRCh38]
Chr12:50369422 [GRCh37]
Chr12:12q13.12		 likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:877
Count of miRNA genes:454
Interacting mature miRNAs:517
Transcripts:ENST00000315520, ENST00000489786, ENST00000551733
Prediction methods:Miranda, Rnahybrid, Targetscan
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
RH98915  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371250,370,665 - 50,370,849UniSTSGRCh37
Build 361248,656,932 - 48,657,116RGDNCBI36
Celera1249,166,786 - 49,166,970RGD
Cytogenetic Map12q13UniSTS
HuRef1247,402,167 - 47,402,351UniSTS
GeneMap99-GB4 RH Map12226.06UniSTS
RH98744  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371250,370,757 - 50,370,837UniSTSGRCh37
Build 361248,657,024 - 48,657,104RGDNCBI36
Celera1249,166,878 - 49,166,958RGD
Cytogenetic Map12q13UniSTS
HuRef1247,402,259 - 47,402,339UniSTS
GeneMap99-GB4 RH Map12226.26UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
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Cytogenetic Map5q33.2UniSTS
Cytogenetic Map13q32.2UniSTS
Cytogenetic Map14q23.1UniSTS
Cytogenetic Map8q21.2UniSTS
Cytogenetic Map2q24.1UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map2q23.3UniSTS
Cytogenetic Map19p13.1UniSTS
Cytogenetic Map15q14-q15UniSTS
Cytogenetic Map1q42.13UniSTS
Cytogenetic Map14q31UniSTS
Cytogenetic Map7p21.1UniSTS
Cytogenetic Map8p12-p11UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map7p11.1UniSTS
Cytogenetic Map1q31-q32UniSTS
Cytogenetic Map2q12UniSTS
Cytogenetic Map3p21.32UniSTS
Cytogenetic Map2p24.2UniSTS
Cytogenetic Map2q33-q34UniSTS
Cytogenetic Map6q24.1UniSTS
Cytogenetic Map4q22.1UniSTS
Cytogenetic Map15q13.3UniSTS
Cytogenetic Map10q26.11UniSTS
Cytogenetic Map7p15.3UniSTS
Cytogenetic Map10q23.33UniSTS
Cytogenetic Map12p12.1UniSTS
Cytogenetic Map7p13-p12UniSTS
Cytogenetic MapXq25UniSTS
Cytogenetic Map17q11-q21UniSTS
Cytogenetic Map12q23UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map14q23.2UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map15q21.2UniSTS
Cytogenetic Map3p26.1-p25.1UniSTS
Cytogenetic Map5q35UniSTS
Cytogenetic Map3q13.2UniSTS
Cytogenetic Map4p15.2UniSTS
Cytogenetic Map6q16.3UniSTS
Cytogenetic Map17q24-q25UniSTS
Cytogenetic MapXq12UniSTS
Cytogenetic MapXq27.1UniSTS
Cytogenetic Map8q12.3UniSTS
Cytogenetic Map5q21.2UniSTS
Cytogenetic Map5q15UniSTS
Cytogenetic Map5q35.1UniSTS
Cytogenetic Map4q13.3UniSTS
Cytogenetic Map4q35.2UniSTS
Cytogenetic Map3p26.1UniSTS
Cytogenetic Map3p11.1UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map2q21.2UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map18q12.3UniSTS
Cytogenetic Map18p11.3UniSTS
Cytogenetic Map17q11.1UniSTS
Cytogenetic Map15q25.1UniSTS
Cytogenetic Map13q12.3UniSTS
Cytogenetic Map12q23.2UniSTS
Cytogenetic Map12q12-q13UniSTS
Cytogenetic Map12q14UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map2q32-q34UniSTS
Cytogenetic Map16q22.3UniSTS
Cytogenetic Map2p15-p13UniSTS
Cytogenetic MapXp11.4UniSTS
Cytogenetic Map19q13.33-q13.41UniSTS
Cytogenetic Map20p11UniSTS
Cytogenetic Map6q23-q24UniSTS
Cytogenetic Map2p12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map13q11-q12UniSTS
Cytogenetic Map6p12.3-p11.2UniSTS
Cytogenetic Map6q16.1-q16.3UniSTS
Cytogenetic Map22q11UniSTS
Cytogenetic Map7q31.2UniSTS
Cytogenetic Map10q21.3UniSTS
Cytogenetic Map3q25.2UniSTS
Cytogenetic Map3p21.1-p14.3UniSTS
Cytogenetic Map6p12.1UniSTS
Cytogenetic Map3q23-q24UniSTS
Cytogenetic Map3q12UniSTS
Cytogenetic Map7q11.1UniSTS
Cytogenetic Map3q22.3UniSTS
Cytogenetic Map7q21.3UniSTS
Cytogenetic Map4q31.1UniSTS
Cytogenetic Map22q12-q13UniSTS
Cytogenetic Map4q23UniSTS
Cytogenetic MapXp22.12UniSTS
Cytogenetic Map6q16.1UniSTS
Cytogenetic Map13q14.13UniSTS
Cytogenetic Map18q21.3UniSTS
Cytogenetic Map9q33.2UniSTS
Cytogenetic Map11q21UniSTS
Cytogenetic Map8q12UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map17q24.3UniSTS
Cytogenetic Map6p23UniSTS
Cytogenetic Map8p11UniSTS
Cytogenetic Map5q34UniSTS
Cytogenetic Map1q24.3UniSTS
Cytogenetic Map9q33.1UniSTS
Cytogenetic Map1q23.3UniSTS
Cytogenetic Map2p16.2UniSTS
Cytogenetic Map9q22.31UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map7q35UniSTS
Cytogenetic Map1p36.2UniSTS
Cytogenetic Map11q22.3UniSTS
Cytogenetic Map16p12UniSTS
Cytogenetic Map1q22-q23UniSTS
Cytogenetic Map13q22.1UniSTS
Cytogenetic Map2q12.2UniSTS
Cytogenetic Map8p12UniSTS
Cytogenetic Map4q21UniSTS
Cytogenetic Map13q12.2UniSTS
Cytogenetic Map9q31-q33UniSTS
Cytogenetic Map6p24.1UniSTS
Cytogenetic Map1q23UniSTS
Cytogenetic Map11q12-q13UniSTS
Cytogenetic Map11q13.3UniSTS
Cytogenetic Map11q24.2UniSTS
Cytogenetic Map11q12.1UniSTS
Cytogenetic Map3p26UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21UniSTS
Cytogenetic Map19q13.1-q13.2UniSTS
Cytogenetic Map1p33-p32UniSTS
Cytogenetic Map7q36.2UniSTS
Cytogenetic Map4q32.3UniSTS
Cytogenetic Map16p13.2UniSTS
Cytogenetic Map14q32UniSTS
Cytogenetic Map10q11.23UniSTS
Cytogenetic Map10q26.1UniSTS
Cytogenetic Map9q32-q33.3UniSTS
Cytogenetic Map9q22.1-q22.2UniSTS
Cytogenetic Map3q26.1-q26.2UniSTS
Cytogenetic Map5q31-q34UniSTS
Cytogenetic Map9q33-q34UniSTS
Cytogenetic Map5q11.2-q13.2UniSTS
Cytogenetic Map13q32UniSTS
Cytogenetic Map9q22.32UniSTS
Cytogenetic Map1p36.3UniSTS
Cytogenetic Map1p36.3-p36.2UniSTS
Cytogenetic Map4q28.1UniSTS
Cytogenetic Map5q22UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic MapXq13.3UniSTS
Cytogenetic Map9q31.3UniSTS
Cytogenetic Map3p26.3UniSTS
Cytogenetic Map2q11.1UniSTS
Cytogenetic Map21q11.2UniSTS
Cytogenetic Map18q21.32UniSTS
Cytogenetic Map15q26.2UniSTS
Cytogenetic Map12q24.23UniSTS
Cytogenetic Map10q25.3UniSTS
Cytogenetic Map20q11.23UniSTS
Cytogenetic Map20p12.1UniSTS
Cytogenetic Map2q31.1-q31.2UniSTS
Cytogenetic MapXp22.31UniSTS
Cytogenetic MapXp21.3UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map4q28.2UniSTS
Cytogenetic Map3p14.2UniSTS
Cytogenetic Map3q24UniSTS
Cytogenetic Map2q13UniSTS
Cytogenetic Map20q13.2UniSTS
Cytogenetic Map14q11.2-q12UniSTS
Cytogenetic Map3p24UniSTS
Cytogenetic Map12q23.3UniSTS
Cytogenetic Map11q24.3UniSTS
Cytogenetic Map11q14.3UniSTS
Cytogenetic Map10q25.2UniSTS
Cytogenetic Map3q25.1UniSTS
Cytogenetic Map8q13UniSTS
Cytogenetic Map1p22.2UniSTS
Cytogenetic Map3p22.3UniSTS
Cytogenetic Map18q11.1UniSTS
Cytogenetic Map8q23.3UniSTS
Cytogenetic Map15q24UniSTS
Cytogenetic Map11cen-q12UniSTS
Cytogenetic Map11q25UniSTS
Cytogenetic Map3p22.2UniSTS
Cytogenetic MapXp21.1UniSTS
Cytogenetic Map7q36UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map12q21UniSTS
Cytogenetic Map7p15UniSTS
Cytogenetic Map7q22-q31UniSTS
Cytogenetic Map11q22UniSTS
Cytogenetic Map5p15.3UniSTS
Cytogenetic Map20q13.3-qterUniSTS
Cytogenetic Map1p35-p34UniSTS
Cytogenetic Map4p13-p12UniSTS
Cytogenetic Map10q21-q22UniSTS
Cytogenetic Map4q22UniSTS
Cytogenetic Map7p13-p11.1UniSTS
Cytogenetic Map9q31-q34UniSTS
Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression

RNA-SEQ Expression

adipose tissue
alimentary part of gastrointestinal system
appendage
circulatory system
ectoderm
endocrine system
endoderm
entire extraembryonic component
exocrine system
hemolymphoid system
hepatobiliary system
integumental system
mesenchyme
mesoderm
musculoskeletal system
nervous system
renal system
reproductive system
respiratory system
sensory system
visual system
1024 2381 2185 1899 4838 1522 2075 3 509 870 353 2063 5217 4784 51 3704 762 1636 1462 169 1

Sequence


Ensembl Acc Id: ENST00000315520   ⟹   ENSP00000320247
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1249,972,947 - 49,977,139 (+)Ensembl
Ensembl Acc Id: ENST00000489786
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1249,967,194 - 49,977,139 (+)Ensembl
Ensembl Acc Id: ENST00000551733   ⟹   ENSP00000449830
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1249,967,239 - 49,975,695 (+)Ensembl
Ensembl Acc Id: ENST00000615425   ⟹   ENSP00000477688
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1249,973,174 - 49,977,139 (+)Ensembl
Ensembl Acc Id: ENST00000618286   ⟹   ENSP00000477759
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1249,972,837 - 49,974,007 (+)Ensembl
RefSeq Acc Id: NM_001652   ⟹   NP_001643
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381249,972,947 - 49,977,139 (+)NCBI
GRCh371250,360,874 - 50,370,922 (+)NCBI
Build 361248,652,887 - 48,657,189 (+)NCBI Archive
Celera1249,162,741 - 49,167,043 (+)RGD
HuRef1247,398,122 - 47,402,424 (+)RGD
CHM1_11250,332,778 - 50,337,080 (+)NCBI
T2T-CHM13v2.01249,935,958 - 49,940,150 (+)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001643 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAB41566 (Get FASTA)   NCBI Sequence Viewer  
  AAB41567 (Get FASTA)   NCBI Sequence Viewer  
  CAB70889 (Get FASTA)   NCBI Sequence Viewer  
  EAW58111 (Get FASTA)   NCBI Sequence Viewer  
Ensembl Protein ENSP00000320247
  ENSP00000320247.5
  ENSP00000449830.1
  ENSP00000477759.1
GenBank Protein Q13520 (Get FASTA)   NCBI Sequence Viewer  
RefSeq Acc Id: NP_001643   ⟸   NM_001652
- UniProtKB: Q13520 (UniProtKB/Swiss-Prot)
- Sequence:
Ensembl Acc Id: ENSP00000477688   ⟸   ENST00000615425
Ensembl Acc Id: ENSP00000477759   ⟸   ENST00000618286
Ensembl Acc Id: ENSP00000320247   ⟸   ENST00000315520
Ensembl Acc Id: ENSP00000449830   ⟸   ENST00000551733

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q13520-F1-model_v2 AlphaFold Q13520 1-282 view protein structure

Promoters
RGD ID:6789657
Promoter ID:HG_KWN:15589
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:OTTHUMT00000257529,   UC001RVP.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361248,647,146 - 48,647,732 (+)MPROMDB
RGD ID:7223867
Promoter ID:EPDNEW_H17679
Type:initiation region
Name:AQP6_1
Description:aquaporin 6
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
GRCh381249,972,983 - 49,973,043EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:639 AgrOrtholog
COSMIC AQP6 COSMIC
Ensembl Genes ENSG00000086159 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000315520 ENTREZGENE
  ENST00000315520.10 UniProtKB/Swiss-Prot
  ENST00000551733.5 UniProtKB/TrEMBL
  ENST00000618286.1 UniProtKB/TrEMBL
Gene3D-CATH 1.20.1080.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000086159 GTEx
HGNC ID HGNC:639 ENTREZGENE
Human Proteome Map AQP6 Human Proteome Map
InterPro Aquaporin-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Aquaporin_6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Aquaporin_transptr UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIP_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:363 UniProtKB/Swiss-Prot
NCBI Gene 363 ENTREZGENE
OMIM 601383 OMIM
PANTHER PTHR19139 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR19139:SF113 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA24924 PharmGKB
PRINTS AQUAPORIN6 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MINTRINSICP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE MIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF81338 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt AQP6_HUMAN UniProtKB/Swiss-Prot
  F8VW87_HUMAN UniProtKB/TrEMBL
  Q13520 ENTREZGENE
  Q9NSV5_HUMAN UniProtKB/TrEMBL


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-01 AQP6  aquaporin 6  AQP6  aquaporin 6, kidney specific  Symbol and/or name change 5135510 APPROVED