ANPEP (alanyl aminopeptidase, membrane) - Rat Genome Database

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Gene: ANPEP (alanyl aminopeptidase, membrane) Homo sapiens
Analyze
Symbol: ANPEP
Name: alanyl aminopeptidase, membrane
RGD ID: 737099
HGNC Page HGNC
Description: Predicted to have metalloaminopeptidase activity; peptide binding activity; and zinc ion binding activity. Predicted to be involved in several processes, including peptide catabolic process; proteolysis; and regulation of blood pressure. Localizes to endoplasmic reticulum-Golgi intermediate compartment; extracellular exosome; and plasma membrane. Biomarker of severe acute respiratory syndrome.
Type: protein-coding
RefSeq Status: REVIEWED
Also known as: alanyl (membrane) aminopeptidase; alanyl (membrane) aminopeptidase (aminopeptidase N, aminopeptidase M, microsomal aminopeptidase, CD13, p150); alanyl aminopeptidase; aminopeptidase M; aminopeptidase N; AP-M; AP-N; APN; CD13; GP150; hAPN; LAP1; membrane alanyl aminopeptidase; microsomal aminopeptidase; myeloid plasma membrane glycoprotein CD13; P150; PEPN
RGD Orthologs
Mouse
Rat
Chinchilla
Bonobo
Dog
Squirrel
Pig
Green Monkey
Naked Mole-Rat
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
NCBI Annotation Information: Note: This gene has been reviewed for its involvement in coronavirus biology, and is relevant for disease process.
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1589,784,895 - 89,815,401 (-)EnsemblGRCh38hg38GRCh38
GRCh381589,784,895 - 89,814,852 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371590,328,126 - 90,358,084 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361588,129,130 - 88,159,076 (-)NCBINCBI36hg18NCBI36
Build 341588,129,130 - 88,150,938NCBI
Celera1566,730,914 - 66,760,859 (-)NCBI
Cytogenetic Map15q26.1NCBI
HuRef1566,440,812 - 66,470,613 (-)NCBIHuRef
CHM1_11590,169,132 - 90,199,097 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene-Chemical Interaction Annotations     Click to see Annotation Detail View
(+)-schisandrin B  (ISO)
1,10-phenanthroline  (EXP)
1,2-dimethylhydrazine  (ISO)
17beta-estradiol  (EXP,ISO)
2,2,2-tetramine  (ISO)
2,3,7,8-tetrachlorodibenzodioxine  (EXP,ISO)
3,3',4,4'-tetrachlorobiphenyl  (ISO)
4,4'-sulfonyldiphenol  (ISO)
4-hydroxyphenyl retinamide  (EXP)
5-aza-2'-deoxycytidine  (EXP)
6-propyl-2-thiouracil  (ISO)
acetamide  (ISO)
acetylsalicylic acid  (EXP)
aflatoxin B1  (EXP)
ammonium chloride  (ISO)
antirheumatic drug  (EXP)
Aroclor 1254  (ISO)
arsane  (EXP,ISO)
arsenic atom  (EXP,ISO)
arsenous acid  (EXP)
benzene  (EXP,ISO)
benzo[a]pyrene  (EXP,ISO)
benzo[b]fluoranthene  (ISO)
bisphenol A  (EXP,ISO)
bisphenol F  (ISO)
buta-1,3-diene  (ISO)
C60 fullerene  (ISO)
cadmium atom  (EXP)
cadmium dichloride  (EXP)
carbon nanotube  (ISO)
chromium(6+)  (ISO)
chrysene  (ISO)
cisplatin  (EXP)
cobalt dichloride  (EXP,ISO)
copper atom  (ISO)
copper(0)  (ISO)
copper(II) chloride  (EXP)
copper(II) sulfate  (EXP)
crocidolite asbestos  (EXP,ISO)
cyclosporin A  (EXP,ISO)
daidzein  (EXP)
daidzein 7-O-beta-D-glucoside  (EXP)
DDT  (ISO)
deoxynivalenol  (EXP)
diarsenic trioxide  (EXP)
dicrotophos  (EXP)
diethylstilbestrol  (EXP)
diuron  (ISO)
elemental selenium  (EXP)
endosulfan  (ISO)
ethylenediaminetetraacetic acid  (EXP)
flutamide  (ISO)
folic acid  (ISO)
furan  (ISO)
genistein  (EXP)
genistein 7-O-beta-D-glucoside  (EXP)
gentamycin  (EXP)
glycitein  (EXP)
glycitin  (EXP)
GW 4064  (ISO)
L-ascorbic acid  (EXP)
methotrexate  (EXP)
methylmercury chloride  (EXP)
methylmercury(1+)  (ISO)
mifepristone  (EXP)
nefazodone  (ISO)
nickel atom  (EXP)
nickel sulfate  (ISO)
nimesulide  (ISO)
paracetamol  (EXP,ISO)
PD 0325901  (EXP)
perfluorooctane-1-sulfonic acid  (ISO)
phenobarbital  (ISO)
pirimiphos-methyl  (ISO)
pirinixic acid  (ISO)
porphyrins  (EXP)
potassium chromate  (EXP)
pregnenolone 16alpha-carbonitrile  (ISO)
quercetin  (EXP)
rotenone  (EXP)
selenium atom  (EXP)
serpentine asbestos  (EXP)
silicon dioxide  (EXP,ISO)
simvastatin  (ISO)
sodium arsenate  (ISO)
sodium arsenite  (ISO)
Soman  (ISO)
streptozocin  (ISO)
succimer  (ISO)
tacrolimus hydrate  (ISO)
tamoxifen  (ISO)
tert-butyl hydroperoxide  (EXP)
Tesaglitazar  (ISO)
tetrachloromethane  (ISO)
tetraphene  (ISO)
thimerosal  (EXP)
titanium dioxide  (ISO)
tobramycin  (ISO)
toluene  (ISO)
trichloroethene  (ISO)
Triptolide  (ISO)
triptonide  (ISO)
troglitazone  (EXP)
valproic acid  (EXP)
vinclozolin  (ISO)
vorinostat  (EXP)
zinc atom  (ISO)
zinc(0)  (ISO)
zoledronic acid  (EXP)

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
Colon cancer  (IAGP)
References

Additional References at PubMed
PMID:1675638   PMID:1705556   PMID:1977688   PMID:2428842   PMID:2564851   PMID:2901990   PMID:2903074   PMID:6149934   PMID:7576235   PMID:7902291   PMID:8102610   PMID:8105105  
PMID:8887485   PMID:9056417   PMID:9367365   PMID:9634079   PMID:10605003   PMID:10676659   PMID:10734069   PMID:11140838   PMID:11384645   PMID:11559807   PMID:11774469   PMID:11999577  
PMID:12406907   PMID:12443882   PMID:12473585   PMID:12477932   PMID:12551991   PMID:12634402   PMID:12675232   PMID:14507917   PMID:14767532   PMID:15084671   PMID:15166647   PMID:15234325  
PMID:15280478   PMID:15308636   PMID:15326289   PMID:15489334   PMID:15758076   PMID:15812828   PMID:15840518   PMID:15883031   PMID:15916720   PMID:16216591   PMID:16335952   PMID:16466852  
PMID:16469741   PMID:16502470   PMID:16533817   PMID:16572171   PMID:16685268   PMID:16778789   PMID:16818694   PMID:17192395   PMID:17329256   PMID:17363734   PMID:17363739   PMID:17636545  
PMID:17655775   PMID:17662271   PMID:17888402   PMID:17897319   PMID:17897790   PMID:17953966   PMID:17999179   PMID:18008160   PMID:18085638   PMID:18366676   PMID:18431797   PMID:18495788  
PMID:18605079   PMID:18677709   PMID:18794057   PMID:19056867   PMID:19199708   PMID:19236378   PMID:19330903   PMID:19373777   PMID:19562339   PMID:19597336   PMID:19908113   PMID:20064928  
PMID:20360068   PMID:20379614   PMID:20689807   PMID:21048031   PMID:21082674   PMID:21376765   PMID:21611838   PMID:21873635   PMID:21879266   PMID:21881118   PMID:22040956   PMID:22065384  
PMID:22079983   PMID:22199357   PMID:22307972   PMID:22544935   PMID:22932899   PMID:23206754   PMID:23322201   PMID:23376485   PMID:23488598   PMID:23500679   PMID:23533145   PMID:23643324  
PMID:23677132   PMID:24063007   PMID:24411984   PMID:24627994   PMID:24816252   PMID:24991573   PMID:25219368   PMID:25246708   PMID:25340499   PMID:25461922   PMID:25645918   PMID:25682862  
PMID:25879366   PMID:25885470   PMID:25929234   PMID:26208633   PMID:26311161   PMID:26449746   PMID:26514774   PMID:26655501   PMID:26771355   PMID:26845356   PMID:27377895   PMID:27467268  
PMID:28323433   PMID:28387421   PMID:28708295   PMID:28739875   PMID:28986522   PMID:29048432   PMID:29110838   PMID:29145632   PMID:29789790   PMID:30097533   PMID:30198568   PMID:30994973  
PMID:31040262   PMID:31056265   PMID:31343991   PMID:31650956   PMID:32199615   PMID:32249333   PMID:32360796   PMID:32457292  


Genomics

Comparative Map Data
ANPEP
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1589,784,895 - 89,815,401 (-)EnsemblGRCh38hg38GRCh38
GRCh381589,784,895 - 89,814,852 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371590,328,126 - 90,358,084 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361588,129,130 - 88,159,076 (-)NCBINCBI36hg18NCBI36
Build 341588,129,130 - 88,150,938NCBI
Celera1566,730,914 - 66,760,859 (-)NCBI
Cytogenetic Map15q26.1NCBI
HuRef1566,440,812 - 66,470,613 (-)NCBIHuRef
CHM1_11590,169,132 - 90,199,097 (-)NCBICHM1_1
Anpep
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm39779,471,551 - 79,497,958 (-)NCBIGRCm39mm39
GRCm39 Ensembl779,471,551 - 79,510,807 (-)Ensembl
GRCm38779,821,803 - 79,848,210 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl779,821,803 - 79,861,059 (-)EnsemblGRCm38mm10GRCm38
MGSCv37786,966,689 - 86,987,238 (-)NCBIGRCm37mm9NCBIm37
MGSCv36779,695,316 - 79,715,797 (-)NCBImm8
Celera777,221,100 - 77,243,027 (-)NCBICelera
Cytogenetic Map7D2NCBI
Anpep
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21133,767,332 - 133,810,137 (-)NCBI
Rnor_6.0 Ensembl1141,561,334 - 141,604,273 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_6.01141,561,364 - 141,604,249 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_5.01142,522,426 - 142,565,721 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41135,600,751 - 135,619,208 (-)NCBIRGSC3.4rn4RGSC3.4
RGSC_v3.11135,679,156 - 135,697,614 (-)NCBI
Celera1125,830,648 - 125,849,086 (-)NCBICelera
RH 3.4 Map11063.2RGD
Cytogenetic Map1q31NCBI
Anpep
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495541615,424,932 - 15,444,075 (+)EnsemblChiLan1.0
ChiLan1.0NW_00495541615,415,981 - 15,442,032 (+)NCBIChiLan1.0ChiLan1.0
ANPEP
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
PanPan1.11587,681,826 - 87,703,713 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1587,681,826 - 87,703,713 (-)Ensemblpanpan1.1panPan2
Mhudiblu_PPA_v01568,479,349 - 68,509,238 (-)NCBIMhudiblu_PPA_v0panPan3
ANPEP
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1352,764,418 - 52,779,516 (-)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl352,764,418 - 52,779,746 (-)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha355,398,319 - 55,413,377 (-)NCBI
ROS_Cfam_1.0353,181,131 - 53,196,208 (-)NCBI
UMICH_Zoey_3.1352,702,917 - 52,717,931 (-)NCBI
UNSW_CanFamBas_1.0352,912,916 - 52,927,956 (-)NCBI
UU_Cfam_GSD_1.0353,253,252 - 53,268,352 (-)NCBI
LOC101972738
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_024408640130,745,212 - 130,770,994 (+)NCBI
SpeTri2.0NW_00493648315,563,540 - 15,582,521 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
ANPEP
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl755,351,083 - 55,373,881 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1755,351,081 - 55,373,856 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2760,240,144 - 60,262,909 (-)NCBISscrofa10.2Sscrofa10.2susScr3
Pig Cytomap7cen-q21NCBI
LOC103231162
(Chlorocebus sabaeus - African green monkey)
Vervet AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1298,324,094 - 8,354,491 (-)NCBI
ChlSab1.1 Ensembl298,323,797 - 8,346,581 (-)Ensembl
Vero_WHO_p1.0NW_02366605938,429,007 - 38,487,801 (+)NCBI
Anpep
(Heterocephalus glaber - naked mole-rat)
Molerat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla 1.0NW_00462476816,840,743 - 16,856,158 (-)NCBI

Position Markers
STS-F04048  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371756,172,600 - 56,172,652UniSTSGRCh37
GRCh371590,338,918 - 90,339,313UniSTSGRCh37
Build 361588,139,922 - 88,140,317RGDNCBI36
Celera1566,741,706 - 66,742,101RGD
Celera1752,634,383 - 52,634,435UniSTS
HuRef1751,533,431 - 51,533,483UniSTS
HuRef1566,451,508 - 66,451,903UniSTS
GeneMap99-GB4 RH Map17369.89UniSTS
ANPEP_1718  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371590,328,094 - 90,328,728UniSTSGRCh37
Build 361588,129,098 - 88,129,732RGDNCBI36
Celera1566,730,882 - 66,731,516RGD
HuRef1566,440,780 - 66,441,414UniSTS
D2S2822  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371590,328,249 - 90,328,426UniSTSGRCh37
Build 361588,129,253 - 88,129,430RGDNCBI36
Celera1566,731,037 - 66,731,214RGD
Cytogenetic Map15q25-q26UniSTS
HuRef1566,440,935 - 66,441,112UniSTS
D15S1289  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371590,340,702 - 90,340,850UniSTSGRCh37
Build 361588,141,706 - 88,141,854RGDNCBI36
Celera1566,743,490 - 66,743,638RGD
Cytogenetic Map15q25-q26UniSTS
HuRef1566,453,292 - 66,453,440UniSTS
D15S1186  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371590,328,176 - 90,328,290UniSTSGRCh37
Build 361588,129,180 - 88,129,294RGDNCBI36
Celera1566,730,964 - 66,731,078RGD
Cytogenetic Map15q25-q26UniSTS
HuRef1566,440,862 - 66,440,976UniSTS
GeneMap99-GB4 RH Map15320.51UniSTS
Whitehead-RH Map15337.3UniSTS
NCBI RH Map15627.9UniSTS
MARC_3220-3221:991936916:1  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371590,347,183 - 90,347,585UniSTSGRCh37
Build 361588,148,187 - 88,148,589RGDNCBI36
Celera1566,749,971 - 66,750,373RGD
HuRef1566,459,777 - 66,460,179UniSTS

miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2665
Count of miRNA genes:962
Interacting mature miRNAs:1200
Transcripts:ENST00000300060, ENST00000558177, ENST00000558740, ENST00000559761, ENST00000559874, ENST00000559887, ENST00000560028, ENST00000560030, ENST00000560137
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.


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 94 4 4 82 4 1 4 6 3
Medium 835 1712 1043 601 1164 446 3055 285 671 305 606 1179 161 1172 1763 1
Low 1436 1254 668 15 243 13 1218 1847 2828 80 754 303 7 32 986 3
Below cutoff 57 13 4 2 306 2 70 57 210 24 76 99 2 39 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001150 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381923 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001381924 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AB209918 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC018988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC079075 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF527789 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ421875 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ421876 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ426050 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ426067 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ427985 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ427986 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ427987 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ427988 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298134 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298242 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298339 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK300946 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC058928 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BQ879097 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  JC231878 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KF510413 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  M22324 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  X13276 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000300060   ⟹   ENSP00000300060
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,784,895 - 89,814,852 (-)Ensembl
RefSeq Acc Id: ENST00000558177
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,797,575 - 89,802,736 (-)Ensembl
RefSeq Acc Id: ENST00000558740
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,790,953 - 89,793,187 (-)Ensembl
RefSeq Acc Id: ENST00000559761
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,797,445 - 89,799,560 (-)Ensembl
RefSeq Acc Id: ENST00000559874   ⟹   ENSP00000452934
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,806,273 - 89,815,401 (-)Ensembl
RefSeq Acc Id: ENST00000559887
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,803,985 - 89,804,851 (-)Ensembl
RefSeq Acc Id: ENST00000560028   ⟹   ENSP00000453405
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,804,277 - 89,805,372 (-)Ensembl
RefSeq Acc Id: ENST00000560030   ⟹   ENSP00000453545
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,797,659 - 89,803,969 (-)Ensembl
RefSeq Acc Id: ENST00000560137   ⟹   ENSP00000453413
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,806,401 - 89,814,864 (-)Ensembl
RefSeq Acc Id: ENST00000679248   ⟹   ENSP00000502886
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1589,784,895 - 89,814,852 (-)Ensembl
RefSeq Acc Id: NM_001150   ⟹   NP_001141
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381589,784,895 - 89,814,852 (-)NCBI
GRCh371590,328,126 - 90,358,119 (-)NCBI
Build 361588,129,130 - 88,159,076 (-)NCBI Archive
HuRef1566,440,812 - 66,470,613 (-)ENTREZGENE
CHM1_11590,169,132 - 90,199,097 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001381923   ⟹   NP_001368852
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381589,784,895 - 89,814,852 (-)NCBI
RefSeq Acc Id: NM_001381924   ⟹   NP_001368853
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381589,784,895 - 89,806,628 (-)NCBI
Reference Sequences
RefSeq Acc Id: NP_001141   ⟸   NM_001150
- Peptide Label: precursor
- UniProtKB: P15144 (UniProtKB/Swiss-Prot),   A0A024RC61 (UniProtKB/TrEMBL),   Q59E93 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001368852   ⟸   NM_001381923
RefSeq Acc Id: NP_001368853   ⟸   NM_001381924
RefSeq Acc Id: ENSP00000452934   ⟸   ENST00000559874
RefSeq Acc Id: ENSP00000453413   ⟸   ENST00000560137
RefSeq Acc Id: ENSP00000453405   ⟸   ENST00000560028
RefSeq Acc Id: ENSP00000453545   ⟸   ENST00000560030
RefSeq Acc Id: ENSP00000300060   ⟸   ENST00000300060
RefSeq Acc Id: ENSP00000502886   ⟸   ENST00000679248
Protein Domains
ERAP1_C   Peptidase_M1

Promoters
RGD ID:6810721
Promoter ID:HG_ACW:27988
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:ANPEP.JAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361588,136,206 - 88,136,706 (-)MPROMDB
RGD ID:6810747
Promoter ID:HG_ACW:27990
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:ANPEP.HAPR07,   CHARSWY.AAPR07-UNSPLICED
Position:
Human AssemblyChrPosition (strand)Source
Build 361588,143,606 - 88,145,457 (-)MPROMDB
RGD ID:6810718
Promoter ID:HG_ACW:27991
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562
Transcripts:ANPEP.FAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361588,146,631 - 88,147,131 (-)MPROMDB
RGD ID:6810720
Promoter ID:HG_ACW:27992
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:ANPEP.BAPR07,   ANPEP.CAPR07,   ANPEP.GAPR07,   ANPEP.IAPR07,   ANPEP.LAPR07
Position:
Human AssemblyChrPosition (strand)Source
Build 361588,148,106 - 88,150,507 (-)MPROMDB
RGD ID:6814553
Promoter ID:HG_XEF:2862
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:NB4
Transcripts:NM_001009252,   NM_001075144,   NM_001082326,   NM_001089325,   NM_001095122,   NM_001146034,   NM_008486,   NM_031012,   NM_204861,   NM_214277
Position:
Human AssemblyChrPosition (strand)Source
Build 361588,150,806 - 88,151,306 (-)MPROMDB
RGD ID:6792095
Promoter ID:HG_KWN:22312
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:K562,   NB4
Transcripts:OTTHUMT00000313425
Position:
Human AssemblyChrPosition (strand)Source
Build 361588,158,999 - 88,159,499 (-)MPROMDB
RGD ID:7230491
Promoter ID:EPDNEW_H20991
Type:initiation region
Name:ANPEP_2
Description:alanyl aminopeptidase, membrane
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20992  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381589,806,628 - 89,806,688EPDNEW
RGD ID:7230493
Promoter ID:EPDNEW_H20992
Type:initiation region
Name:ANPEP_1
Description:alanyl aminopeptidase, membrane
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H20991  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381589,814,852 - 89,814,912EPDNEW

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 15q26.1-26.3(chr15:89679237-101978958)x3 copy number gain See cases [RCV000052354] Chr15:89679237..101978958 [GRCh38]
Chr15:90222468..102519161 [GRCh37]
Chr15:88023472..100336684 [NCBI36]
Chr15:15q26.1-26.3
pathogenic
GRCh38/hg38 15q24.2-26.3(chr15:75307767-101723215)x3 copy number gain Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000052346]|See cases [RCV000052346] Chr15:75307767..101723215 [GRCh38]
Chr15:75600108..102263418 [GRCh37]
Chr15:73387161..100080941 [NCBI36]
Chr15:15q24.2-26.3
pathogenic
GRCh38/hg38 15q24.3-26.3(chr15:77543797-101843411)x3 copy number gain See cases [RCV000052347] Chr15:77543797..101843411 [GRCh38]
Chr15:77836139..102383614 [GRCh37]
Chr15:75623194..100201137 [NCBI36]
Chr15:15q24.3-26.3
pathogenic
GRCh38/hg38 15q25.2-26.3(chr15:84169153-101904929)x3 copy number gain See cases [RCV000052352] Chr15:84169153..101904929 [GRCh38]
Chr15:84837905..102445132 [GRCh37]
Chr15:82628909..100262655 [NCBI36]
Chr15:15q25.2-26.3
pathogenic
NM_001150.2(ANPEP):c.1252G>A (p.Glu418Lys) single nucleotide variant Malignant melanoma [RCV000070952] Chr15:89803930 [GRCh38]
Chr15:90347161 [GRCh37]
Chr15:88148165 [NCBI36]
Chr15:15q26.1
not provided
NM_001150.2(ANPEP):c.2415G>A (p.Gly805=) single nucleotide variant Malignant melanoma [RCV000062948] Chr15:89792273 [GRCh38]
Chr15:90335504 [GRCh37]
Chr15:88136508 [NCBI36]
Chr15:15q26.1
not provided
GRCh38/hg38 15q25.2-26.3(chr15:83711377-101843270)x3 copy number gain See cases [RCV000135858] Chr15:83711377..101843270 [GRCh38]
Chr15:84380129..102383473 [GRCh37]
Chr15:82171133..100200996 [NCBI36]
Chr15:15q25.2-26.3
pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:87904735-101843270)x3 copy number gain See cases [RCV000135568] Chr15:87904735..101843270 [GRCh38]
Chr15:88447966..102383473 [GRCh37]
Chr15:86248970..100200996 [NCBI36]
Chr15:15q25.3-26.3
pathogenic
GRCh38/hg38 15q25.2-26.3(chr15:82859676-101810992)x3 copy number gain See cases [RCV000136849] Chr15:82859676..101810992 [GRCh38]
Chr15:83528428..102351195 [GRCh37]
Chr15:81325482..100168718 [NCBI36]
Chr15:15q25.2-26.3
pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:85826665-101920998)x4 copy number gain See cases [RCV000137264] Chr15:85826665..101920998 [GRCh38]
Chr15:86369896..102461201 [GRCh37]
Chr15:84170900..100278724 [NCBI36]
Chr15:15q25.3-26.3
pathogenic
GRCh38/hg38 15q25.3-26.3(chr15:85397539-101888909)x3 copy number gain See cases [RCV000141899] Chr15:85397539..101888909 [GRCh38]
Chr15:85940770..102429112 [GRCh37]
Chr15:83741774..100246635 [NCBI36]
Chr15:15q25.3-26.3
pathogenic
GRCh38/hg38 15q26.1(chr15:89738724-89788051)x1 copy number loss See cases [RCV000142209] Chr15:89738724..89788051 [GRCh38]
Chr15:90281955..90331282 [GRCh37]
Chr15:88082959..88132286 [NCBI36]
Chr15:15q26.1
uncertain significance
GRCh38/hg38 15q22.2-26.3(chr15:59828460-101920998)x3 copy number gain See cases [RCV000142915] Chr15:59828460..101920998 [GRCh38]
Chr15:60120659..102461201 [GRCh37]
Chr15:57907951..100278724 [NCBI36]
Chr15:15q22.2-26.3
pathogenic
GRCh38/hg38 15q23-26.3(chr15:72154949-101920998)x3 copy number gain See cases [RCV000143019] Chr15:72154949..101920998 [GRCh38]
Chr15:72447290..102461201 [GRCh37]
Chr15:70234344..100278724 [NCBI36]
Chr15:15q23-26.3
pathogenic
GRCh38/hg38 15q26.1-26.3(chr15:88676575-98364743)x3 copy number gain See cases [RCV000142727] Chr15:88676575..98364743 [GRCh38]
Chr15:89219806..98907972 [GRCh37]
Chr15:87020810..96725495 [NCBI36]
Chr15:15q26.1-26.3
pathogenic
GRCh37/hg19 15q24.2-26.3(chr15:76061144-102429112)x3 copy number gain See cases [RCV000511332] Chr15:76061144..102429112 [GRCh37]
Chr15:15q24.2-26.3
pathogenic
GRCh37/hg19 15q22.31-26.3(chr15:64637227-102509910)x3 copy number gain See cases [RCV000240602] Chr15:64637227..102509910 [GRCh37]
Chr15:15q22.31-26.3
pathogenic
GRCh37/hg19 15q22.1-26.3(chr15:59297293-102480888)x3 copy number gain not provided [RCV000415836] Chr15:59297293..102480888 [GRCh37]
Chr15:15q22.1-26.3
likely pathogenic
GRCh37/hg19 15q25.2-26.3(chr15:85089467-102495441)x3 copy number gain See cases [RCV000449119] Chr15:85089467..102495441 [GRCh37]
Chr15:15q25.2-26.3
pathogenic
GRCh37/hg19 15q15.1-26.3(chr15:41745084-102354798)x4 copy number gain See cases [RCV000447123] Chr15:41745084..102354798 [GRCh37]
Chr15:15q15.1-26.3
pathogenic
GRCh37/hg19 15q26.1-26.3(chr15:90346994-102354798) copy number loss See cases [RCV000447603] Chr15:90346994..102354798 [GRCh37]
Chr15:15q26.1-26.3
pathogenic
GRCh37/hg19 15q26.1-26.3(chr15:89924847-102429112)x3 copy number gain See cases [RCV000445978] Chr15:89924847..102429112 [GRCh37]
Chr15:15q26.1-26.3
pathogenic
GRCh37/hg19 15q25.1-26.3(chr15:80648093-102429112)x3 copy number gain See cases [RCV000445705] Chr15:80648093..102429112 [GRCh37]
Chr15:15q25.1-26.3
pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:20733395-102511616)x4 copy number gain See cases [RCV000447765] Chr15:20733395..102511616 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q25.3-26.3(chr15:86148286-102511616)x3 copy number gain See cases [RCV000448044] Chr15:86148286..102511616 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
GRCh37/hg19 15q25.3-26.1(chr15:88295992-94215607)x1 copy number loss See cases [RCV000448680] Chr15:88295992..94215607 [GRCh37]
Chr15:15q25.3-26.1
pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112)x3 copy number gain See cases [RCV000510717] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q11.2-26.3(chr15:22770422-102429112) copy number gain See cases [RCV000512019] Chr15:22770422..102429112 [GRCh37]
Chr15:15q11.2-26.3
pathogenic
GRCh37/hg19 15q25.3-26.3(chr15:86899001-98734014)x3 copy number gain See cases [RCV000511629] Chr15:86899001..98734014 [GRCh37]
Chr15:15q25.3-26.3
likely pathogenic
Single allele duplication not provided [RCV000677926] Chr15:31115047..102354857 [GRCh37]
Chr15:15q13.2-26.3
pathogenic
GRCh37/hg19 15q23-26.3(chr15:71329220-102270758)x3 copy number gain not provided [RCV000683703] Chr15:71329220..102270758 [GRCh37]
Chr15:15q23-26.3
pathogenic
GRCh37/hg19 15q24.3-26.3(chr15:77479244-102429112)x3 copy number gain not provided [RCV000683710] Chr15:77479244..102429112 [GRCh37]
Chr15:15q24.3-26.3
pathogenic
GRCh37/hg19 15q26.1-26.3(chr15:89743929-102429112)x3 copy number gain not provided [RCV000683718] Chr15:89743929..102429112 [GRCh37]
Chr15:15q26.1-26.3
pathogenic
GRCh37/hg19 15q25.3-26.3(chr15:88385150-102461162)x3 copy number gain not provided [RCV000738864] Chr15:88385150..102461162 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
GRCh37/hg19 15q26.1-26.3(chr15:90277151-102376761)x3 copy number gain not provided [RCV000751387] Chr15:90277151..102376761 [GRCh37]
Chr15:15q26.1-26.3
pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20016811-102493540)x3 copy number gain not provided [RCV000751155] Chr15:20016811..102493540 [GRCh37]
Chr15:15q11.1-26.3
pathogenic
GRCh37/hg19 15q11.1-26.3(chr15:20071673-102461162)x3 copy number gain not provided [RCV000751156] Chr15:20071673..102461162 [GRCh37]
Chr15:15q11.1-26.3
pathogenic
NM_001150.3(ANPEP):c.894C>G (p.Val298=) single nucleotide variant not provided [RCV000936952] Chr15:89805081 [GRCh38]
Chr15:90348312 [GRCh37]
Chr15:15q26.1
likely benign
NM_001150.3(ANPEP):c.614+9C>T single nucleotide variant not provided [RCV000971634] Chr15:89805961 [GRCh38]
Chr15:90349192 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.1245C>A (p.Ser415=) single nucleotide variant not provided [RCV000922391] Chr15:89803937 [GRCh38]
Chr15:90347168 [GRCh37]
Chr15:15q26.1
likely benign
NM_001150.3(ANPEP):c.1437+10G>A single nucleotide variant not provided [RCV000926467] Chr15:89803637 [GRCh38]
Chr15:90346868 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.2808C>T (p.Ala936=) single nucleotide variant not provided [RCV000926800] Chr15:89785445 [GRCh38]
Chr15:90328676 [GRCh37]
Chr15:15q26.1
likely benign
NM_001150.3(ANPEP):c.2013C>G (p.Ala671=) single nucleotide variant not provided [RCV000894057] Chr15:89797719 [GRCh38]
Chr15:90340950 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.1437+9C>G single nucleotide variant not provided [RCV000967381] Chr15:89803638 [GRCh38]
Chr15:90346869 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.1437+8C>G single nucleotide variant not provided [RCV000967390] Chr15:89803639 [GRCh38]
Chr15:90346870 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.2310G>A (p.Glu770=) single nucleotide variant not provided [RCV000961013] Chr15:89792502 [GRCh38]
Chr15:90335733 [GRCh37]
Chr15:15q26.1
benign
GRCh37/hg19 15q25.2-26.1(chr15:83883823-92165844) copy number loss not provided [RCV000767759] Chr15:83883823..92165844 [GRCh37]
Chr15:15q25.2-26.1
pathogenic
GRCh37/hg19 15q26.1(chr15:90308996-90502529)x1 copy number loss not provided [RCV000849248] Chr15:90308996..90502529 [GRCh37]
Chr15:15q26.1
uncertain significance
GRCh37/hg19 15q25.3-26.3(chr15:87189245-102429112)x1 copy number loss not provided [RCV001006718] Chr15:87189245..102429112 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
GRCh37/hg19 15q26.1-26.3(chr15:90288175-102429112)x3 copy number gain not provided [RCV000846885] Chr15:90288175..102429112 [GRCh37]
Chr15:15q26.1-26.3
pathogenic
GRCh37/hg19 15q26.1(chr15:90111672-90671886)x3 copy number gain not provided [RCV001006720] Chr15:90111672..90671886 [GRCh37]
Chr15:15q26.1
uncertain significance
NM_001150.3(ANPEP):c.1265C>G (p.Ala422Gly) single nucleotide variant not provided [RCV000888712] Chr15:89803917 [GRCh38]
Chr15:90347148 [GRCh37]
Chr15:15q26.1
likely benign
NM_001150.3(ANPEP):c.772C>A (p.Leu258Ile) single nucleotide variant not provided [RCV000888713] Chr15:89805203 [GRCh38]
Chr15:90348434 [GRCh37]
Chr15:15q26.1
likely benign
NM_001150.3(ANPEP):c.1431C>T (p.Tyr477=) single nucleotide variant not provided [RCV000917413] Chr15:89803653 [GRCh38]
Chr15:90346884 [GRCh37]
Chr15:15q26.1
likely benign
NM_001150.3(ANPEP):c.1839C>T (p.Ser613=) single nucleotide variant not provided [RCV000958696] Chr15:89799540 [GRCh38]
Chr15:90342771 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.298C>T (p.Leu100=) single nucleotide variant not provided [RCV000961073] Chr15:89806286 [GRCh38]
Chr15:90349517 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.2433C>T (p.Phe811=) single nucleotide variant not provided [RCV000894217] Chr15:89792255 [GRCh38]
Chr15:90335486 [GRCh37]
Chr15:15q26.1
benign
NM_001150.3(ANPEP):c.192C>A (p.Thr64=) single nucleotide variant not provided [RCV000955497] Chr15:89806392 [GRCh38]
Chr15:90349623 [GRCh37]
Chr15:15q26.1
benign
GRCh37/hg19 15q25.3-26.3(chr15:86962053-102531392)x1 copy number loss See cases [RCV001263026] Chr15:86962053..102531392 [GRCh37]
Chr15:15q25.3-26.3
pathogenic
NC_000015.9:g.(?_32964879)_(91358519_?)dup duplication Bloom syndrome [RCV001343104]|Familial colorectal cancer [RCV001325176] Chr15:32964879..91358519 [GRCh37]
Chr15:15q13.3-26.1
uncertain significance

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:500 AgrOrtholog
COSMIC ANPEP COSMIC
Ensembl Genes ENSG00000166825 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000300060 ENTREZGENE, UniProtKB/Swiss-Prot
  ENSP00000452934 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSP00000453405 UniProtKB/TrEMBL
  ENSP00000453413 ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENSP00000453545 UniProtKB/TrEMBL
  ENSP00000502886 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000300060 ENTREZGENE, UniProtKB/Swiss-Prot
  ENST00000559874 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENST00000560028 UniProtKB/TrEMBL
  ENST00000560030 UniProtKB/TrEMBL
  ENST00000560137 ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ENST00000679248 UniProtKB/Swiss-Prot
Gene3D-CATH 2.60.40.1730 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000166825 GTEx
HGNC ID HGNC:500 ENTREZGENE
Human Proteome Map ANPEP Human Proteome Map
InterPro Aminopeptidase_N-like_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  ERAP1-like_C_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  M1_APN-typ UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Peptidase_M1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Peptidase_M1_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:290 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
NCBI Gene 290 ENTREZGENE
OMIM 151530 OMIM
Pfam ERAP1_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Peptidase_M1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA24815 PharmGKB
PRINTS ALADIPTASE UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE ZINC_PROTEASE UniProtKB/Swiss-Prot
Superfamily-SCOP SSF63737 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024RC61 ENTREZGENE, UniProtKB/TrEMBL
  AMPN_HUMAN UniProtKB/Swiss-Prot
  H0YKT6_HUMAN UniProtKB/TrEMBL
  H0YLZ8_HUMAN UniProtKB/TrEMBL
  H0YM04_HUMAN UniProtKB/TrEMBL
  H0YMC1_HUMAN UniProtKB/TrEMBL
  P15144 ENTREZGENE
  Q59E93 ENTREZGENE, UniProtKB/TrEMBL
UniProt Secondary Q16728 UniProtKB/Swiss-Prot
  Q6GT90 UniProtKB/Swiss-Prot
  Q8IUK3 UniProtKB/Swiss-Prot
  Q8IVH3 UniProtKB/Swiss-Prot
  Q9UCE0 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2016-01-12 ANPEP  alanyl aminopeptidase, membrane    alanyl (membrane) aminopeptidase  Symbol and/or name change 5135510 APPROVED
2011-08-16 ANPEP  alanyl (membrane) aminopeptidase  ANPEP  alanyl (membrane) aminopeptidase  Symbol and/or name change 5135510 APPROVED