AQP10 (aquaporin 10) - Rat Genome Database

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Gene: AQP10 (aquaporin 10) Homo sapiens
Analyze
Symbol: AQP10
Name: aquaporin 10
RGD ID: 1344809
HGNC Page HGNC:16029
Description: Enables glycerol channel activity and water channel activity. Involved in several processes, including cellular response to acidic pH; glycerol transmembrane transport; and protein homotetramerization. Located in intracellular membrane-bounded organelle and plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: AQP-10; AQPA_HUMAN; aquaglyceroporin-10; aquaporin-10; small intestine 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
GRCh381154,321,093 - 154,325,325 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1154,321,090 - 154,325,325 (+)EnsemblGRCh38hg38GRCh38
GRCh371154,293,569 - 154,297,801 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361152,560,216 - 152,564,425 (+)NCBINCBI36Build 36hg18NCBI36
Build 341151,106,664 - 151,110,873NCBI
Celera1127,365,303 - 127,369,516 (+)NCBICelera
Cytogenetic Map1q21.3NCBI
HuRef1125,657,284 - 125,661,501 (+)NCBIHuRef
CHM1_11155,689,895 - 155,694,130 (+)NCBICHM1_1
T2T-CHM13v2.01153,458,259 - 153,462,492 (+)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 Function

Molecular Pathway Annotations     Click to see Annotation Detail View
Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
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:1373524   PMID:1510932   PMID:7530250   PMID:9369468   PMID:9405233   PMID:9806845   PMID:9829975   PMID:10318966   PMID:10510269   PMID:10564231   PMID:11001937   PMID:11034202  
PMID:11076974   PMID:11573934   PMID:12084581   PMID:12477932   PMID:14701836   PMID:15489334   PMID:15898950   PMID:15948717   PMID:16596446   PMID:17178220   PMID:17207965   PMID:17575980  
PMID:17975119   PMID:18202181   PMID:18501347   PMID:18511455   PMID:18678926   PMID:18762715   PMID:19023099   PMID:19204726   PMID:19913121   PMID:20628086   PMID:21251984   PMID:21691092  
PMID:21733844   PMID:21873635   PMID:23382902   PMID:24623722   PMID:26313002   PMID:26810286   PMID:30420639   PMID:32296183   PMID:34699768  


Genomics

Comparative Map Data
AQP10
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381154,321,093 - 154,325,325 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1154,321,090 - 154,325,325 (+)EnsemblGRCh38hg38GRCh38
GRCh371154,293,569 - 154,297,801 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361152,560,216 - 152,564,425 (+)NCBINCBI36Build 36hg18NCBI36
Build 341151,106,664 - 151,110,873NCBI
Celera1127,365,303 - 127,369,516 (+)NCBICelera
Cytogenetic Map1q21.3NCBI
HuRef1125,657,284 - 125,661,501 (+)NCBIHuRef
CHM1_11155,689,895 - 155,694,130 (+)NCBICHM1_1
T2T-CHM13v2.01153,458,259 - 153,462,492 (+)NCBIT2T-CHM13v2.0
Aqp10-ps
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39389,870,751 - 89,877,041 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl389,872,016 - 89,875,998 (-)EnsemblGRCm39 Ensembl
GRCm38389,963,444 - 89,969,734 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl389,964,709 - 89,968,658 (-)EnsemblGRCm38mm10GRCm38
MGSCv37389,767,366 - 89,773,656 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv36390,091,325 - 90,092,558 (-)NCBIMGSCv36mm8
Celera389,999,953 - 90,006,243 (-)NCBICelera
Cytogenetic Map3F1NCBI
cM Map339.19NCBI
Aqp10
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr82177,699,717 - 177,704,620 (-)NCBIGRCr8
mRatBN7.22175,402,609 - 175,407,677 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl2175,403,263 - 175,406,815 (-)EnsemblmRatBN7.2 Ensembl
Rnor_6.02189,309,151 - 189,314,092 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.02208,732,677 - 208,734,879 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
Celera2169,344,930 - 169,349,241 (-)NCBICelera
Cytogenetic Map2q34NCBI
Aqp10
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_004955545845,749 - 848,738 (+)EnsemblChiLan1.0
ChiLan1.0NW_004955545845,749 - 848,738 (+)NCBIChiLan1.0ChiLan1.0
AQP10
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v2195,506,299 - 95,511,820 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan1195,241,532 - 95,247,053 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01129,677,969 - 129,682,681 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11133,291,027 - 133,295,265 (+)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1133,291,027 - 133,295,265 (+)Ensemblpanpan1.1panPan2
AQP10
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1742,961,041 - 42,964,053 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha742,451,365 - 42,454,540 (-)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0742,830,882 - 42,834,057 (-)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl742,830,139 - 42,833,937 (-)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1742,609,750 - 42,613,405 (-)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0742,663,571 - 42,666,669 (-)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0742,947,589 - 42,950,761 (-)NCBIUU_Cfam_GSD_1.0
Aqp10
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440505824,950,993 - 24,954,469 (+)NCBIHiC_Itri_2
SpeTri2.0 EnsemblNW_0049365803,980,659 - 3,984,394 (+)EnsemblSpeTri2.0SpeTri2.0 Ensembl
SpeTri2.0NW_0049365803,981,254 - 3,984,895 (+)NCBISpeTri2.0SpeTri2.0SpeTri2.0
AQP10
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl495,450,150 - 95,453,256 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1495,449,268 - 95,453,663 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.24104,328,003 - 104,332,534 (-)NCBISscrofa10.2Sscrofa10.2susScr3
AQP10
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1209,489,562 - 9,506,229 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl209,492,846 - 9,496,367 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_0236660388,845,092 - 8,858,410 (-)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Aqp10
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_0046248853,014,351 - 3,022,248 (-)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_0046248853,014,853 - 3,032,920 (-)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in AQP10
9 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3 copy number gain See cases [RCV000143515] Chr1:149854269..180267197 [GRCh38]
Chr1:149825831..180236332 [GRCh37]
Chr1:148092455..178502955 [NCBI36]
Chr1:1q21.2-25.2		 pathogenic
Single allele inversion Pediatric metastatic thyroid tumour [RCV000585807] Chr1:154130985..156843877 [GRCh37]
Chr1:1q21.3-23.1		 likely pathogenic
GRCh37/hg19 1q21.3-23.1(chr1:153751465-156660462)x3 copy number gain not provided [RCV000585385] Chr1:153751465..156660462 [GRCh37]
Chr1:1q21.3-23.1		 likely pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3 copy number gain See cases [RCV000510383] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:849467-249224684) copy number gain See cases [RCV000510926] Chr1:849467..249224684 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q21.3(chr1:150853044-154647786)x3 copy number gain not provided [RCV000684655] Chr1:150853044..154647786 [GRCh37]
Chr1:1q21.3		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:47851-249228449)x3 copy number gain not provided [RCV000736295] Chr1:47851..249228449 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1p36.33-q44(chr1:82154-249218992)x3 copy number gain not provided [RCV000736305] Chr1:82154..249218992 [GRCh37]
Chr1:1p36.33-q44		 pathogenic
GRCh37/hg19 1q21.3(chr1:154213874-154331789)x3 copy number gain not provided [RCV000847973] Chr1:154213874..154331789 [GRCh37]
Chr1:1q21.3		 uncertain significance
GRCh37/hg19 1q21.3(chr1:153659094-154307972)x3 copy number gain not provided [RCV001005142] Chr1:153659094..154307972 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_080429.3(AQP10):c.105+10A>G single nucleotide variant not provided [RCV000958270] Chr1:154321270 [GRCh38]
Chr1:154293746 [GRCh37]
Chr1:1q21.3		 benign
NC_000001.10:g.(?_130980840)_(248900000_?)dup duplication Gastrointestinal stromal tumor [RCV001300221]|Parathyroid carcinoma [RCV001341077] Chr1:130980840..248900000 [GRCh37]
Chr1:1q12-44		 uncertain significance
NC_000001.10:g.(?_154141761)_(156851434_?)dup duplication Charcot-Marie-Tooth disease type 2 [RCV001990060] Chr1:154141761..156851434 [GRCh37]
Chr1:1q21.3-23.1		 uncertain significance
NC_000001.10:g.(?_149895434)_(156851434_?)dup duplication Autosomal recessive mendelian susceptibility to mycobacterial diseases due to complete RORgamma receptor deficiency [RCV001958273]|Congenital neutropenia-myelofibrosis-nephromegaly syndrome [RCV001958271]|Kostmann syndrome [RCV003120769]|MHC class II deficiency [RCV001992607] Chr1:149895434..156851434 [GRCh37]
Chr1:1q21.2-23.1		 uncertain significance
NC_000001.10:g.(?_153963273)_(154580482_?)del deletion Kostmann syndrome [RCV003116530] Chr1:153963273..154580482 [GRCh37]
Chr1:1q21.3		 pathogenic
NM_080429.3(AQP10):c.385T>A (p.Tyr129Asn) single nucleotide variant not specified [RCV004283727] Chr1:154323255 [GRCh38]
Chr1:154295731 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_080429.3(AQP10):c.887T>C (p.Met296Thr) single nucleotide variant not specified [RCV004132642] Chr1:154324461 [GRCh38]
Chr1:154296937 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_080429.3(AQP10):c.20C>T (p.Pro7Leu) single nucleotide variant not specified [RCV004080788] Chr1:154321175 [GRCh38]
Chr1:154293651 [GRCh37]
Chr1:1q21.3		 likely benign
NM_080429.3(AQP10):c.139A>G (p.Thr47Ala) single nucleotide variant not specified [RCV004183961] Chr1:154321966 [GRCh38]
Chr1:154294442 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_080429.3(AQP10):c.642C>A (p.Asn214Lys) single nucleotide variant not specified [RCV004279407] Chr1:154323741 [GRCh38]
Chr1:154296217 [GRCh37]
Chr1:1q21.3		 uncertain significance
GRCh37/hg19 1q12-23.1(chr1:142535935-157648813)x3 copy number gain Chromosome 1q21.1 duplication syndrome [RCV003329522] Chr1:142535935..157648813 [GRCh37]
Chr1:1q12-23.1		 pathogenic
NM_080429.3(AQP10):c.628G>A (p.Gly210Arg) single nucleotide variant not specified [RCV004350124] Chr1:154323727 [GRCh38]
Chr1:154296203 [GRCh37]
Chr1:1q21.3		 uncertain significance
GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3 copy number gain not specified [RCV003986717] Chr1:144368497..158992086 [GRCh37]
Chr1:1q21.1-23.1		 pathogenic
GRCh37/hg19 1q21.3(chr1:154089394-154912611)x3 copy number gain not specified [RCV003986629] Chr1:154089394..154912611 [GRCh37]
Chr1:1q21.3		 uncertain significance
GRCh37/hg19 1q21.1-23.1(chr1:146577511-157155587)x3 copy number gain not specified [RCV003987261] Chr1:146577511..157155587 [GRCh37]
Chr1:1q21.1-23.1		 pathogenic
NM_080429.3(AQP10):c.542G>A (p.Arg181Gln) single nucleotide variant not specified [RCV004420009] Chr1:154323641 [GRCh38]
Chr1:154296117 [GRCh37]
Chr1:1q21.3		 uncertain significance
NM_080429.3(AQP10):c.50G>A (p.Arg17His) single nucleotide variant not specified [RCV004420008] Chr1:154321205 [GRCh38]
Chr1:154293681 [GRCh37]
Chr1:1q21.3		 uncertain significance
NC_000001.10:g.(?_153782653)_(154580482_?)dup duplication Symmetrical dyschromatosis of extremities [RCV004584092] Chr1:153782653..154580482 [GRCh37]
Chr1:1q21.3		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:1317
Count of miRNA genes:562
Interacting mature miRNAs:637
Transcripts:ENST00000324978, ENST00000355197, ENST00000484864
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.


QTLs in Region (GRCh38)
The following QTLs overlap with this region.    Full Report CSV TAB Printer Gviewer
RGD IDSymbolNameLODP ValueTraitSub TraitChrStartStopSpecies
1357381BW57_HBody weight QTL 57 (human)10.0001Body weightfat free mass after exercise training1140630236166630236Human


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 7 55 3 3 61 3 2 1 3 3
Low 48 658 24 23 825 23 31 24 22 8 376 407 4 10 13 1
Below cutoff 1751 1770 888 286 403 179 2990 1547 2169 126 746 672 110 982 1872 1

Sequence


Ensembl Acc Id: ENST00000324978   ⟹   ENSP00000318355
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,321,093 - 154,325,325 (+)Ensembl
Ensembl Acc Id: ENST00000355197
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,321,090 - 154,324,042 (+)Ensembl
Ensembl Acc Id: ENST00000484864   ⟹   ENSP00000420341
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1154,321,120 - 154,325,325 (+)Ensembl
RefSeq Acc Id: NM_080429   ⟹   NP_536354
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,321,093 - 154,325,325 (+)NCBI
GRCh371154,293,592 - 154,297,801 (+)RGD
Build 361152,560,216 - 152,564,425 (+)NCBI Archive
Celera1127,365,303 - 127,369,516 (+)RGD
HuRef1125,657,284 - 125,661,501 (+)RGD
CHM1_11155,689,895 - 155,694,130 (+)NCBI
T2T-CHM13v2.01153,458,259 - 153,462,492 (+)NCBI
Sequence:
RefSeq Acc Id: XM_011510104   ⟹   XP_011508406
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,321,093 - 154,325,325 (+)NCBI
Sequence:
RefSeq Acc Id: XM_047433547   ⟹   XP_047289503
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,321,093 - 154,325,325 (+)NCBI
RefSeq Acc Id: XM_054339481   ⟹   XP_054195456
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,458,259 - 153,462,492 (+)NCBI
RefSeq Acc Id: XM_054339482   ⟹   XP_054195457
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01153,458,259 - 153,462,492 (+)NCBI
RefSeq Acc Id: NP_536354   ⟸   NM_080429
- UniProtKB: Q5VYD4 (UniProtKB/Swiss-Prot),   Q5VYD3 (UniProtKB/Swiss-Prot),   Q8NG70 (UniProtKB/Swiss-Prot),   Q96PS8 (UniProtKB/Swiss-Prot),   B2RC92 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011508406   ⟸   XM_011510104
- Peptide Label: isoform X1
- UniProtKB: B2RC92 (UniProtKB/TrEMBL)
- Sequence:
Ensembl Acc Id: ENSP00000318355   ⟸   ENST00000324978
Ensembl Acc Id: ENSP00000420341   ⟸   ENST00000484864
RefSeq Acc Id: XP_047289503   ⟸   XM_047433547
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054195456   ⟸   XM_054339481
- Peptide Label: isoform X1
- UniProtKB: B2RC92 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054195457   ⟸   XM_054339482
- Peptide Label: isoform X2

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q96PS8-F1-model_v2 AlphaFold Q96PS8 1-301 view protein structure

Promoters
RGD ID:6784615
Promoter ID:HG_KWN:5281
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:NM_080429,   OTTHUMT00000087662,   UC001FEV.2
Position:
Human AssemblyChrPosition (strand)Source
Build 361152,560,011 - 152,560,511 (+)MPROMDB
RGD ID:6857336
Promoter ID:EPDNEW_H1833
Type:initiation region
Name:AQP10_1
Description:aquaporin 10
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381154,321,116 - 154,321,176EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:16029 AgrOrtholog
COSMIC AQP10 COSMIC
Ensembl Genes ENSG00000143595 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000324978 ENTREZGENE
  ENST00000324978.8 UniProtKB/Swiss-Prot
  ENST00000484864.1 UniProtKB/Swiss-Prot
Gene3D-CATH 1.20.1080.10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000143595 GTEx
HGNC ID HGNC:16029 ENTREZGENE
Human Proteome Map AQP10 Human Proteome Map
InterPro Aquaporin-like UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Aquaporin_10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIP/Aquaporin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MIP_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:89872 UniProtKB/Swiss-Prot
NCBI Gene 89872 ENTREZGENE
OMIM 606578 OMIM
PANTHER AQUAPORIN OR AQUAGLYCEROPORIN RELATED UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  AQUAPORIN-10 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam MIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA24919 PharmGKB
PRINTS AQUAPORIN10M UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  MINTRINSICP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE MIP UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Aquaporin-like UniProtKB/TrEMBL, UniProtKB/Swiss-Prot
UniProt AQP10_HUMAN UniProtKB/Swiss-Prot
  B2RC92 ENTREZGENE, UniProtKB/TrEMBL
  Q5VYD3 ENTREZGENE
  Q5VYD4 ENTREZGENE
  Q8NG70 ENTREZGENE
  Q96PS8 ENTREZGENE
UniProt Secondary Q5VYD3 UniProtKB/Swiss-Prot
  Q5VYD4 UniProtKB/Swiss-Prot
  Q8NG70 UniProtKB/Swiss-Prot