DPEP2 (dipeptidase 2) - Rat Genome Database

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Gene: DPEP2 (dipeptidase 2) Homo sapiens
Analyze
Symbol: DPEP2
Name: dipeptidase 2
RGD ID: 1313962
HGNC Page HGNC:23028
Description: Enables dipeptidase activity. Involved in leukotriene D4 catabolic process. Predicted to be located in membrane.
Type: protein-coding
RefSeq Status: VALIDATED
Previously known as: MBD2
RGD Orthologs
Mouse
Rat
Bonobo
Dog
Pig
Green Monkey
Alliance Genes
More Info more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381667,987,390 - 68,000,619 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1667,987,394 - 68,000,586 (-)EnsemblGRCh38hg38GRCh38
GRCh371668,021,293 - 68,034,522 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361666,578,798 - 66,590,857 (-)NCBINCBI36Build 36hg18NCBI36
Build 341666,578,800 - 66,590,857NCBI
Celera1652,529,750 - 52,541,821 (-)NCBICelera
Cytogenetic Map16q22.1NCBI
HuRef1653,894,885 - 53,907,048 (-)NCBIHuRef
CHM1_11669,429,363 - 69,441,488 (-)NCBICHM1_1
T2T-CHM13v2.01673,783,178 - 73,796,408 (-)NCBIT2T-CHM13v2.0
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations     Click to see Annotation Detail View

Gene Ontology Annotations     Click to see Annotation Detail View

Biological Process

Cellular Component
membrane  (IEA,ISS)
side of membrane  (IEA)

Molecular Function

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. 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
Additional References at PubMed
PMID:12477932   PMID:12738806   PMID:12975309   PMID:14702039   PMID:15342556   PMID:15489334   PMID:16335952   PMID:16344560   PMID:18193043   PMID:21555454   PMID:25056061   PMID:25464930  
PMID:26186194   PMID:28514442   PMID:32325220   PMID:33961781  


Genomics

Comparative Map Data
DPEP2
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381667,987,390 - 68,000,619 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p13 Ensembl1667,987,394 - 68,000,586 (-)EnsemblGRCh38hg38GRCh38
GRCh371668,021,293 - 68,034,522 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361666,578,798 - 66,590,857 (-)NCBINCBI36Build 36hg18NCBI36
Build 341666,578,800 - 66,590,857NCBI
Celera1652,529,750 - 52,541,821 (-)NCBICelera
Cytogenetic Map16q22.1NCBI
HuRef1653,894,885 - 53,907,048 (-)NCBIHuRef
CHM1_11669,429,363 - 69,441,488 (-)NCBICHM1_1
T2T-CHM13v2.01673,783,178 - 73,796,408 (-)NCBIT2T-CHM13v2.0
Dpep2
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398106,711,577 - 106,732,658 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl8106,711,576 - 106,718,391 (-)EnsemblGRCm39 Ensembl
GRCm39 Ensembl8106,711,577 - 106,723,055 (-)EnsemblGRCm39 Ensembl
GRCm388105,984,945 - 106,006,026 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8105,984,944 - 105,991,759 (-)EnsemblGRCm38mm10GRCm38
GRCm38.p6 Ensembl8105,984,945 - 105,996,423 (-)EnsemblGRCm38mm10GRCm38
MGSCv378108,508,957 - 108,520,323 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv368108,874,186 - 108,885,552 (-)NCBIMGSCv36mm8
Celera8110,213,109 - 110,224,474 (-)NCBICelera
Cytogenetic Map8D3NCBI
Dpep2
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
mRatBN7.21933,883,557 - 33,896,487 (-)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl1933,885,478 - 33,891,954 (-)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx1940,701,008 - 40,707,443 (-)NCBIRnor_SHR
UTH_Rnor_SHRSP_BbbUtx_1.01941,354,322 - 41,360,757 (-)NCBIRnor_SHRSP
UTH_Rnor_WKY_Bbb_1.01943,653,038 - 43,659,469 (-)NCBIRnor_WKY
Rnor_6.01937,964,098 - 37,975,154 (-)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl1937,964,105 - 37,970,537 (-)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.01948,831,084 - 48,851,920 (-)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.41935,832,224 - 35,838,659 (-)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.11935,837,105 - 35,843,540 (-)NCBI
Celera1933,313,021 - 33,319,456 (-)NCBICelera
Cytogenetic Map19q12NCBI
DPEP2
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan11683,421,784 - 83,438,196 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01648,328,281 - 48,341,510 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11667,715,805 - 67,729,164 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1667,715,805 - 67,729,164 (-)Ensemblpanpan1.1panPan2
DPEP2
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1581,506,635 - 81,511,282 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl581,506,330 - 81,511,175 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha581,495,291 - 81,501,196 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0581,940,443 - 81,946,361 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl581,940,034 - 81,946,254 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1581,766,906 - 81,772,812 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0581,449,218 - 81,455,110 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0582,091,144 - 82,097,061 (+)NCBIUU_Cfam_GSD_1.0
DPEP2
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl628,593,546 - 28,599,051 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1628,593,542 - 28,599,076 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.2626,020,128 - 26,025,817 (+)NCBISscrofa10.2Sscrofa10.2susScr3
DPEP2
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1559,439,237 - 59,447,400 (+)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl559,440,951 - 59,447,698 (+)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604722,172,991 - 22,187,738 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0

Variants

.
Variants in DPEP2
18 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 16q13-22.2(chr16:56883592-71279975)x3 copy number gain See cases [RCV000052405] Chr16:56883592..71279975 [GRCh38]
Chr16:56917504..71313878 [GRCh37]
Chr16:55475005..69871379 [NCBI36]
Chr16:16q13-22.2		 pathogenic
GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3 copy number gain See cases [RCV000052408] Chr16:58456122..74708723 [GRCh38]
Chr16:58490026..74742621 [GRCh37]
Chr16:57047527..73300122 [NCBI36]
Chr16:16q21-23.1		 pathogenic
GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3 copy number gain See cases [RCV000052421] Chr16:65313395..90081985 [GRCh38]
Chr16:65347298..90148393 [GRCh37]
Chr16:63904799..88675894 [NCBI36]
Chr16:16q21-24.3		 pathogenic
GRCh38/hg38 16q21-22.1(chr16:63318997-70555249)x1 copy number loss Developmental Delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]|Developmental delay and additional significant developmental and morphological phenotypes referred for genetic testing [RCV000053334]|See cases [RCV000053334] Chr16:63318997..70555249 [GRCh38]
Chr16:63352901..70589152 [GRCh37]
Chr16:61910402..69146653 [NCBI36]
Chr16:16q21-22.1		 pathogenic
GRCh38/hg38 16q21-22.1(chr16:64311275-68062011)x1 copy number loss See cases [RCV000053335] Chr16:64311275..68062011 [GRCh38]
Chr16:64345179..68095914 [GRCh37]
Chr16:62902680..66653415 [NCBI36]
Chr16:16q21-22.1		 pathogenic
NM_022355.3(DPEP2):c.1438C>T (p.Pro480Ser) single nucleotide variant Malignant melanoma [RCV000071190] Chr16:67987529 [GRCh38]
Chr16:68021432 [GRCh37]
Chr16:66578933 [NCBI36]
Chr16:16q22.1		 not provided
GRCh38/hg38 16q21-24.1(chr16:62925929-84585795)x3 copy number gain See cases [RCV000135863] Chr16:62925929..84585795 [GRCh38]
Chr16:62959833..84619401 [GRCh37]
Chr16:61517334..83176902 [NCBI36]
Chr16:16q21-24.1		 pathogenic
GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3 copy number gain See cases [RCV000139426] Chr16:65511483..90096995 [GRCh38]
Chr16:65545386..90163403 [GRCh37]
Chr16:64102887..88690904 [NCBI36]
Chr16:16q21-24.3		 pathogenic
GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3 copy number gain See cases [RCV000142578] Chr16:64389378..90081985 [GRCh38]
Chr16:64423281..90148393 [GRCh37]
Chr16:62980782..88675894 [NCBI36]
Chr16:16q21-24.3		 pathogenic|likely pathogenic
GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3 copy number gain See cases [RCV000143425] Chr16:52899183..90088654 [GRCh38]
Chr16:52933095..90155062 [GRCh37]
Chr16:51490596..88682563 [NCBI36]
Chr16:16q12.2-24.3		 pathogenic
GRCh38/hg38 16q12.1-22.1(chr16:49685521-68401712)x3 copy number gain See cases [RCV000143752] Chr16:49685521..68401712 [GRCh38]
Chr16:49719432..68435615 [GRCh37]
Chr16:48276933..66993116 [NCBI36]
Chr16:16q12.1-22.1		 pathogenic
GRCh38/hg38 16q21-23.3(chr16:65957829-83611443)x3 copy number gain See cases [RCV000143742] Chr16:65957829..83611443 [GRCh38]
Chr16:65991732..83645048 [GRCh37]
Chr16:64549233..82202549 [NCBI36]
Chr16:16q21-23.3		 pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1 copy number loss Ductal breast carcinoma [RCV000207138] Chr16:46615804..90142285 [GRCh37]
Chr16:16q11.2-24.3		 uncertain significance
GRCh37/hg19 16q12.2-22.2(chr16:55359026-70884455)x1 copy number loss Ductal breast carcinoma [RCV000207067] Chr16:55359026..70884455 [GRCh37]
Chr16:16q12.2-22.2		 likely pathogenic|uncertain significance
Single allele complex Ductal breast carcinoma [RCV000207314] Chr16:56368689..90141355 [GRCh37]
Chr16:16q12.2-24.3		 uncertain significance
GRCh37/hg19 16q22.1(chr16:67654566-68404073)x1 copy number loss See cases [RCV000449234] Chr16:67654566..68404073 [GRCh37]
Chr16:16q22.1		 likely pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46464488-90155062)x3 copy number gain See cases [RCV000446110] Chr16:46464488..90155062 [GRCh37]
Chr16:16q11.2-24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3 copy number gain See cases [RCV000446684] Chr16:69193..90274381 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3 copy number gain See cases [RCV000511622] Chr16:9273328..89548493 [GRCh37]
Chr16:16p13.2-q24.3		 uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626429] Chr16:46497599..90354753 [GRCh37]
Chr16:16q11.2-24.3		 drug response
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3 copy number gain See cases [RCV000512138] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3 copy number gain See cases [RCV000512511] Chr16:57051473..89797669 [GRCh37]
Chr16:16q13-24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062) copy number gain See cases [RCV000511296] Chr16:85881..90155062 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1 copy number loss Poly (ADP-Ribose) polymerase inhibitor response [RCV000626435] Chr16:46455960..90354753 [GRCh37]
Chr16:16q11.2-24.3		 drug response
GRCh37/hg19 16q12.2-22.2(chr16:54416050-72453266)x3 copy number gain not provided [RCV000683820] Chr16:54416050..72453266 [GRCh37]
Chr16:16q12.2-22.2		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90274695)x3 copy number gain not provided [RCV000738918] Chr16:88165..90274695 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:61451-90294632)x3 copy number gain not provided [RCV000738915] Chr16:61451..90294632 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16p13.3-q24.3(chr16:88165-90163275)x3 copy number gain not provided [RCV000738917] Chr16:88165..90163275 [GRCh37]
Chr16:16p13.3-q24.3		 pathogenic
GRCh37/hg19 16q21-22.1(chr16:65669673-70180183)x1 copy number loss not provided [RCV001006797] Chr16:65669673..70180183 [GRCh37]
Chr16:16q21-22.1		 pathogenic
GRCh37/hg19 16q22.1(chr16:67132790-68166320) copy number loss not provided [RCV000767617] Chr16:67132790..68166320 [GRCh37]
Chr16:16q22.1		 pathogenic
GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3 copy number gain not provided [RCV001249359] Chr16:61524229..90155062 [GRCh37]
Chr16:16q21-24.3		 not provided
GRCh37/hg19 16q22.1(chr16:67765964-68246270)x1 copy number loss not provided [RCV001259860] Chr16:67765964..68246270 [GRCh37]
Chr16:16q22.1		 uncertain significance
NC_000016.9:g.(?_66545871)_(72146396_?)dup duplication Dyskeratosis congenita, autosomal dominant 6 [RCV001900384]|Immunodeficiency [RCV001900385]|not provided [RCV001900386] Chr16:66545871..72146396 [GRCh37]
Chr16:16q21-22.2		 uncertain significance
GRCh37/hg19 16q11.2-24.3(chr16:46503968-90155062)x3 copy number gain not provided [RCV002221458] Chr16:46503968..90155062 [GRCh37]
Chr16:16q11.2-24.3		 pathogenic
NC_000016.9:g.(?_65821800)_(72146396_?)del deletion Dyskeratosis congenita, autosomal dominant 6 [RCV003122496] Chr16:65821800..72146396 [GRCh37]
Chr16:16q21-22.2		 uncertain significance
NM_022355.4(DPEP2):c.892G>T (p.Asp298Tyr) single nucleotide variant Inborn genetic diseases [RCV002902691] Chr16:67990838 [GRCh38]
Chr16:68024741 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.959A>C (p.Gln320Pro) single nucleotide variant Inborn genetic diseases [RCV002785178] Chr16:67990082 [GRCh38]
Chr16:68023985 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.376C>G (p.Leu126Val) single nucleotide variant Inborn genetic diseases [RCV002978604] Chr16:67992524 [GRCh38]
Chr16:68026427 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.1162G>A (p.Val388Ile) single nucleotide variant Inborn genetic diseases [RCV002799186] Chr16:67987896 [GRCh38]
Chr16:68021799 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.470G>A (p.Arg157His) single nucleotide variant Inborn genetic diseases [RCV002821546] Chr16:67992114 [GRCh38]
Chr16:68026017 [GRCh37]
Chr16:16q22.1		 likely benign
NM_022355.4(DPEP2):c.803G>A (p.Arg268Gln) single nucleotide variant Inborn genetic diseases [RCV002929745] Chr16:67990927 [GRCh38]
Chr16:68024830 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.190C>T (p.Leu64Phe) single nucleotide variant Inborn genetic diseases [RCV002830574] Chr16:67993023 [GRCh38]
Chr16:68026926 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.158C>G (p.Thr53Ser) single nucleotide variant Inborn genetic diseases [RCV002767467] Chr16:67993055 [GRCh38]
Chr16:68026958 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.826G>A (p.Ala276Thr) single nucleotide variant Inborn genetic diseases [RCV002699439] Chr16:67990904 [GRCh38]
Chr16:68024807 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.1184G>A (p.Arg395Gln) single nucleotide variant Inborn genetic diseases [RCV002669411] Chr16:67987874 [GRCh38]
Chr16:68021777 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.814G>A (p.Glu272Lys) single nucleotide variant Inborn genetic diseases [RCV002940971] Chr16:67990916 [GRCh38]
Chr16:68024819 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.275T>C (p.Leu92Pro) single nucleotide variant Inborn genetic diseases [RCV002944581] Chr16:67992625 [GRCh38]
Chr16:68026528 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.833T>A (p.Val278Glu) single nucleotide variant Inborn genetic diseases [RCV002679610] Chr16:67990897 [GRCh38]
Chr16:68024800 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.230G>A (p.Arg77Gln) single nucleotide variant Inborn genetic diseases [RCV003192274] Chr16:67992983 [GRCh38]
Chr16:68026886 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.1285G>A (p.Asp429Asn) single nucleotide variant Inborn genetic diseases [RCV003190503] Chr16:67987682 [GRCh38]
Chr16:68021585 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_022355.4(DPEP2):c.712G>A (p.Gly238Arg) single nucleotide variant Inborn genetic diseases [RCV003188570] Chr16:67991135 [GRCh38]
Chr16:68025038 [GRCh37]
Chr16:16q22.1		 uncertain significance
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:2470
Count of miRNA genes:921
Interacting mature miRNAs:1115
Transcripts:ENST00000268795, ENST00000393847, ENST00000412757, ENST00000572624, ENST00000572888, ENST00000573808, ENST00000574316, ENST00000574865, ENST00000575203, ENST00000575510
Prediction methods:Microtar, Miranda, Rnahybrid
Result types:miRGate_prediction

The detailed report is available here: Full Report CSV TAB Printer

miRNA Target Status data imported from miRGate (http://mirgate.bioinfo.cnio.es/).
For more information about miRGate, see PMID:25858286 or access the full paper here.

Markers in Region
SHGC-60842  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371668,021,321 - 68,021,576UniSTSGRCh37
Build 361666,578,822 - 66,579,077RGDNCBI36
Celera1652,529,778 - 52,530,033RGD
Cytogenetic Map16q22.1UniSTS
HuRef1653,894,913 - 53,895,168UniSTS
GeneMap99-GB4 RH Map16406.22UniSTS
Whitehead-RH Map16306.4UniSTS
NCBI RH Map16508.6UniSTS
SHGC-60762  
Human AssemblyChrPosition (strand)SourceJBrowse
GRCh371668,021,301 - 68,021,451UniSTSGRCh37
Build 361666,578,802 - 66,578,952RGDNCBI36
Celera1652,529,758 - 52,529,908RGD
Cytogenetic Map16q22.1UniSTS
HuRef1653,894,893 - 53,895,043UniSTS
GeneMap99-GB4 RH Map16404.61UniSTS
Whitehead-RH Map16304.7UniSTS
NCBI RH Map16508.6UniSTS


Expression


RNA-SEQ Expression
High: > 1000 TPM value   Medium: Between 11 and 1000 TPM
Low: Between 0.5 and 10 TPM   Below Cutoff: < 0.5 TPM

alimentary part of gastrointestinal system circulatory system endocrine system exocrine system hemolymphoid system hepatobiliary system integumental system musculoskeletal system nervous system renal system reproductive system respiratory system sensory system visual system adipose tissue appendage entire extraembryonic component pharyngeal arch
High
Medium 96 720 29 2 1137 1 46 7 5 17 9 401 1 52 8 1
Low 2098 1739 1406 523 694 375 3290 1535 2414 315 1174 979 150 1140 2102 2
Below cutoff 157 528 268 85 98 74 788 613 1234 49 197 77 19 1 12 678 2 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001324159 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001369657 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_022355 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NR_136706 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005256090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523266 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523268 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523271 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523273 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011523274 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023542 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023543 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023545 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_017023547 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450372 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_024450376 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434459 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434460 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434461 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434463 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434464 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047434465 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313622 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313623 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313624 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313625 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313626 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313627 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313628 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313629 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313630 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313631 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313632 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313633 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313634 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313635 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313636 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313637 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313638 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313639 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054313640 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008484713 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_008484714 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_243420 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_933389 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_933390 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_933391 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XR_933392 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AA404265 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AC040162 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AJ295149 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK092884 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298003 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK315090 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358454 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC024021 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BP299049 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CB528462 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CH471092 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  CP068262 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DA677374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  DB038910 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  KC877614 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000268795
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,991,643 - 68,000,581 (-)Ensembl
RefSeq Acc Id: ENST00000393847   ⟹   ENSP00000377430
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,987,394 - 67,999,484 (-)Ensembl
RefSeq Acc Id: ENST00000572624   ⟹   ENSP00000460169
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,992,173 - 67,999,518 (-)Ensembl
RefSeq Acc Id: ENST00000572888   ⟹   ENSP00000458977
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,987,506 - 67,993,863 (-)Ensembl
RefSeq Acc Id: ENST00000573808   ⟹   ENSP00000463604
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,990,898 - 67,999,512 (-)Ensembl
RefSeq Acc Id: ENST00000574316
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,992,817 - 68,000,568 (-)Ensembl
RefSeq Acc Id: ENST00000574865   ⟹   ENSP00000461250
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,992,557 - 67,994,328 (-)Ensembl
RefSeq Acc Id: ENST00000575203   ⟹   ENSP00000459375
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,987,397 - 68,000,586 (-)Ensembl
RefSeq Acc Id: ENST00000575510   ⟹   ENSP00000462652
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p13 Ensembl1667,990,049 - 68,000,564 (-)Ensembl
RefSeq Acc Id: NM_001324159   ⟹   NP_001311088
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,394 - 67,994,291 (-)NCBI
CHM1_11669,429,363 - 69,436,264 (-)NCBI
T2T-CHM13v2.01673,783,182 - 73,790,079 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001369657   ⟹   NP_001356586
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,993,394 (-)NCBI
T2T-CHM13v2.01673,783,178 - 73,789,182 (-)NCBI
Sequence:
RefSeq Acc Id: NM_022355   ⟹   NP_071750
RefSeq Status: VALIDATED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,394 - 67,999,484 (-)NCBI
GRCh371668,021,293 - 68,034,493 (-)NCBI
Build 361666,578,798 - 66,590,857 (-)NCBI Archive
Celera1652,529,750 - 52,541,821 (-)RGD
HuRef1653,894,885 - 53,907,048 (-)NCBI
CHM1_11669,429,363 - 69,441,488 (-)NCBI
T2T-CHM13v2.01673,783,182 - 73,795,272 (-)NCBI
Sequence:
RefSeq Acc Id: NR_136706
RefSeq Status: VALIDATED
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,394 - 68,000,619 (-)NCBI
CHM1_11669,429,363 - 69,442,556 (-)NCBI
T2T-CHM13v2.01673,783,182 - 73,796,407 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005256090   ⟹   XP_005256147
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,993,394 (-)NCBI
GRCh371668,021,293 - 68,034,493 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011523266   ⟹   XP_011521568
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,999,484 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011523268   ⟹   XP_011521570
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,993,394 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011523271   ⟹   XP_011521573
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,993,394 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011523273   ⟹   XP_011521575
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 68,000,619 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011523274   ⟹   XP_011521576
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 68,000,619 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017023545   ⟹   XP_016879034
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,994,291 (-)NCBI
Sequence:
RefSeq Acc Id: XM_017023547   ⟹   XP_016879036
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 68,000,619 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024450372   ⟹   XP_024306140
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,994,291 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024450373   ⟹   XP_024306141
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 68,000,619 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024450374   ⟹   XP_024306142
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,999,484 (-)NCBI
Sequence:
RefSeq Acc Id: XM_024450376   ⟹   XP_024306144
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 68,000,619 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047434459   ⟹   XP_047290415
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,994,975 (-)NCBI
RefSeq Acc Id: XM_047434460   ⟹   XP_047290416
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,994,291 (-)NCBI
RefSeq Acc Id: XM_047434461   ⟹   XP_047290417
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,999,484 (-)NCBI
RefSeq Acc Id: XM_047434462   ⟹   XP_047290418
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,390 - 67,999,484 (-)NCBI
RefSeq Acc Id: XM_047434463   ⟹   XP_047290419
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,848 - 67,993,394 (-)NCBI
RefSeq Acc Id: XM_047434464   ⟹   XP_047290420
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,848 - 67,993,394 (-)NCBI
RefSeq Acc Id: XM_047434465   ⟹   XP_047290421
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,987,848 - 67,993,394 (-)NCBI
RefSeq Acc Id: XM_054313622   ⟹   XP_054169597
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,790,079 (-)NCBI
RefSeq Acc Id: XM_054313623   ⟹   XP_054169598
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,790,763 (-)NCBI
RefSeq Acc Id: XM_054313624   ⟹   XP_054169599
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,796,408 (-)NCBI
RefSeq Acc Id: XM_054313625   ⟹   XP_054169600
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,795,503 (-)NCBI
RefSeq Acc Id: XM_054313626   ⟹   XP_054169601
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,795,272 (-)NCBI
RefSeq Acc Id: XM_054313627   ⟹   XP_054169602
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,789,182 (-)NCBI
RefSeq Acc Id: XM_054313628   ⟹   XP_054169603
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,790,079 (-)NCBI
RefSeq Acc Id: XM_054313629   ⟹   XP_054169604
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,795,272 (-)NCBI
RefSeq Acc Id: XM_054313630   ⟹   XP_054169605
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,789,182 (-)NCBI
RefSeq Acc Id: XM_054313631   ⟹   XP_054169606
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,795,503 (-)NCBI
RefSeq Acc Id: XM_054313632   ⟹   XP_054169607
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,636 - 73,789,182 (-)NCBI
RefSeq Acc Id: XM_054313633   ⟹   XP_054169608
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,789,182 (-)NCBI
RefSeq Acc Id: XM_054313634   ⟹   XP_054169609
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,636 - 73,789,182 (-)NCBI
RefSeq Acc Id: XM_054313635   ⟹   XP_054169610
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,796,404 (-)NCBI
RefSeq Acc Id: XM_054313636   ⟹   XP_054169611
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,790,079 (-)NCBI
RefSeq Acc Id: XM_054313637   ⟹   XP_054169612
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,636 - 73,789,182 (-)NCBI
RefSeq Acc Id: XM_054313638   ⟹   XP_054169613
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,796,405 (-)NCBI
RefSeq Acc Id: XM_054313639   ⟹   XP_054169614
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,796,402 (-)NCBI
RefSeq Acc Id: XM_054313640   ⟹   XP_054169615
RefSeq Status:
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,783,178 - 73,796,404 (-)NCBI
RefSeq Acc Id: XR_008484713
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,785,835 - 73,789,182 (-)NCBI
RefSeq Acc Id: XR_008484714
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01673,785,113 - 73,789,182 (-)NCBI
RefSeq Acc Id: XR_243420
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,990,047 - 67,993,394 (-)NCBI
GRCh371668,021,293 - 68,034,493 (-)NCBI
Sequence:
RefSeq Acc Id: XR_933392
RefSeq Status:
Type: NON-CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,989,325 - 67,993,394 (-)NCBI
Sequence:
Protein Sequences
Protein RefSeqs NP_001311088 (Get FASTA)   NCBI Sequence Viewer  
  NP_001356586 (Get FASTA)   NCBI Sequence Viewer  
  NP_071750 (Get FASTA)   NCBI Sequence Viewer  
  XP_005256147 (Get FASTA)   NCBI Sequence Viewer  
  XP_011521568 (Get FASTA)   NCBI Sequence Viewer  
  XP_011521570 (Get FASTA)   NCBI Sequence Viewer  
  XP_011521573 (Get FASTA)   NCBI Sequence Viewer  
  XP_011521575 (Get FASTA)   NCBI Sequence Viewer  
  XP_011521576 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879034 (Get FASTA)   NCBI Sequence Viewer  
  XP_016879036 (Get FASTA)   NCBI Sequence Viewer  
  XP_024306140 (Get FASTA)   NCBI Sequence Viewer  
  XP_024306141 (Get FASTA)   NCBI Sequence Viewer  
  XP_024306142 (Get FASTA)   NCBI Sequence Viewer  
  XP_024306144 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290415 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290416 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290417 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290418 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290419 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290420 (Get FASTA)   NCBI Sequence Viewer  
  XP_047290421 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169597 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169598 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169599 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169600 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169601 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169602 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169603 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169604 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169605 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169606 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169607 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169608 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169609 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169610 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169611 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169612 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169613 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169614 (Get FASTA)   NCBI Sequence Viewer  
  XP_054169615 (Get FASTA)   NCBI Sequence Viewer  
GenBank Protein AAH24021 (Get FASTA)   NCBI Sequence Viewer  
  AAQ88819 (Get FASTA)   NCBI Sequence Viewer  
  BAG37555 (Get FASTA)   NCBI Sequence Viewer  
  BAG52621 (Get FASTA)   NCBI Sequence Viewer  
  BAG60309 (Get FASTA)   NCBI Sequence Viewer  
  CAC14667 (Get FASTA)   NCBI Sequence Viewer  
  EAW83200 (Get FASTA)   NCBI Sequence Viewer  
  EAW83201 (Get FASTA)   NCBI Sequence Viewer  
  EAW83202 (Get FASTA)   NCBI Sequence Viewer  
  EAW83203 (Get FASTA)   NCBI Sequence Viewer  
  EAW83204 (Get FASTA)   NCBI Sequence Viewer  
  Q9H4A9 (Get FASTA)   NCBI Sequence Viewer  
Reference Sequences
RefSeq Acc Id: NP_071750   ⟸   NM_022355
- Peptide Label: isoform 1 precursor
- UniProtKB: Q8TC95 (UniProtKB/Swiss-Prot),   Q9H4A9 (UniProtKB/Swiss-Prot),   A0A024R6Y5 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005256147   ⟸   XM_005256090
- Peptide Label: isoform X5
- Sequence:
RefSeq Acc Id: XP_011521576   ⟸   XM_011523274
- Peptide Label: isoform X12
- Sequence:
RefSeq Acc Id: XP_011521575   ⟸   XM_011523273
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: XP_011521568   ⟸   XM_011523266
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_011521573   ⟸   XM_011523271
- Peptide Label: isoform X8
- Sequence:
RefSeq Acc Id: XP_011521570   ⟸   XM_011523268
- Peptide Label: isoform X2
- Sequence:
RefSeq Acc Id: NP_001311088   ⟸   NM_001324159
- Peptide Label: isoform 2
- Sequence:
RefSeq Acc Id: XP_016879036   ⟸   XM_017023547
- Peptide Label: isoform X14
- Sequence:
RefSeq Acc Id: XP_016879034   ⟸   XM_017023545
- Peptide Label: isoform X10
- Sequence:
RefSeq Acc Id: XP_024306141   ⟸   XM_024450373
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024306144   ⟸   XM_024450376
- Peptide Label: isoform X13
- Sequence:
RefSeq Acc Id: XP_024306142   ⟸   XM_024450374
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: XP_024306140   ⟸   XM_024450372
- Peptide Label: isoform X1
- Sequence:
RefSeq Acc Id: NP_001356586   ⟸   NM_001369657
- Peptide Label: isoform 1 precursor
- UniProtKB: Q8TC95 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: ENSP00000458977   ⟸   ENST00000572888
RefSeq Acc Id: ENSP00000460169   ⟸   ENST00000572624
RefSeq Acc Id: ENSP00000463604   ⟸   ENST00000573808
RefSeq Acc Id: ENSP00000461250   ⟸   ENST00000574865
RefSeq Acc Id: ENSP00000462652   ⟸   ENST00000575510
RefSeq Acc Id: ENSP00000459375   ⟸   ENST00000575203
RefSeq Acc Id: ENSP00000377430   ⟸   ENST00000393847
RefSeq Acc Id: XP_047290418   ⟸   XM_047434462
- Peptide Label: isoform X6
RefSeq Acc Id: XP_047290417   ⟸   XM_047434461
- Peptide Label: isoform X4
RefSeq Acc Id: XP_047290415   ⟸   XM_047434459
- Peptide Label: isoform X1
RefSeq Acc Id: XP_047290416   ⟸   XM_047434460
- Peptide Label: isoform X3
- UniProtKB: Q8TC95 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_047290420   ⟸   XM_047434464
- Peptide Label: isoform X9
RefSeq Acc Id: XP_047290419   ⟸   XM_047434463
- Peptide Label: isoform X7
RefSeq Acc Id: XP_047290421   ⟸   XM_047434465
- Peptide Label: isoform X11
RefSeq Acc Id: XP_054169599   ⟸   XM_054313624
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054169613   ⟸   XM_054313638
- Peptide Label: isoform X12
RefSeq Acc Id: XP_054169615   ⟸   XM_054313640
- Peptide Label: isoform X14
RefSeq Acc Id: XP_054169610   ⟸   XM_054313635
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054169614   ⟸   XM_054313639
- Peptide Label: isoform X13
RefSeq Acc Id: XP_054169606   ⟸   XM_054313631
- Peptide Label: isoform X6
RefSeq Acc Id: XP_054169600   ⟸   XM_054313625
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054169604   ⟸   XM_054313629
- Peptide Label: isoform X4
RefSeq Acc Id: XP_054169601   ⟸   XM_054313626
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054169598   ⟸   XM_054313623
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054169611   ⟸   XM_054313636
- Peptide Label: isoform X10
RefSeq Acc Id: XP_054169603   ⟸   XM_054313628
- Peptide Label: isoform X3
- UniProtKB: Q8TC95 (UniProtKB/Swiss-Prot)
RefSeq Acc Id: XP_054169597   ⟸   XM_054313622
- Peptide Label: isoform X1
RefSeq Acc Id: XP_054169608   ⟸   XM_054313633
- Peptide Label: isoform X8
RefSeq Acc Id: XP_054169605   ⟸   XM_054313630
- Peptide Label: isoform X5
RefSeq Acc Id: XP_054169602   ⟸   XM_054313627
- Peptide Label: isoform X2
RefSeq Acc Id: XP_054169609   ⟸   XM_054313634
- Peptide Label: isoform X9
RefSeq Acc Id: XP_054169607   ⟸   XM_054313632
- Peptide Label: isoform X7
RefSeq Acc Id: XP_054169612   ⟸   XM_054313637
- Peptide Label: isoform X11

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9H4A9-F1-model_v2 AlphaFold Q9H4A9 1-486 view protein structure

Promoters
RGD ID:6793039
Promoter ID:HG_KWN:24071
Type:CpG-Island
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell,   CD4+TCell_12Hour,   HeLa_S3,   K562,   Lymphoblastoid,   NB4
Transcripts:ENST00000322384,   UC002EVD.2,   UC010CEY.1
Position:
Human AssemblyChrPosition (strand)Source
Build 361666,584,684 - 66,585,184 (-)MPROMDB
RGD ID:6792976
Promoter ID:HG_KWN:24072
Type:Non-CpG
SO ACC ID:SO:0000170
Source:MPROMDB
Tissues & Cell Lines:CD4+TCell_12Hour,   Lymphoblastoid,   NB4
Transcripts:NM_022355
Position:
Human AssemblyChrPosition (strand)Source
Build 361666,590,756 - 66,591,747 (-)MPROMDB
RGD ID:7232617
Promoter ID:EPDNEW_H22054
Type:initiation region
Name:DPEP2_3
Description:dipeptidase 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22055  EPDNEW_H22056  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,994,302 - 67,994,362EPDNEW
RGD ID:7232619
Promoter ID:EPDNEW_H22055
Type:initiation region
Name:DPEP2_1
Description:dipeptidase 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22054  EPDNEW_H22056  
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381667,999,484 - 67,999,544EPDNEW
RGD ID:7232621
Promoter ID:EPDNEW_H22056
Type:initiation region
Name:DPEP2_2
Description:dipeptidase 2
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Alternative Promoters:null; see alsoEPDNEW_H22054  EPDNEW_H22055  
Experiment Methods:Single-end sequencing.; Paired-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381668,000,586 - 68,000,646EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:23028 AgrOrtholog
COSMIC DPEP2 COSMIC
Ensembl Genes ENSG00000167261 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Protein ENSP00000377430 ENTREZGENE
  ENSP00000377430.1 UniProtKB/Swiss-Prot
  ENSP00000458977 ENTREZGENE
  ENSP00000458977.1 UniProtKB/Swiss-Prot
  ENSP00000459375.1 UniProtKB/Swiss-Prot
  ENSP00000460169.1 UniProtKB/TrEMBL
  ENSP00000461250.1 UniProtKB/TrEMBL
  ENSP00000462652.1 UniProtKB/TrEMBL
  ENSP00000463604.1 UniProtKB/TrEMBL
Ensembl Transcript ENST00000393847 ENTREZGENE
  ENST00000393847.6 UniProtKB/Swiss-Prot
  ENST00000572624.5 UniProtKB/TrEMBL
  ENST00000572888 ENTREZGENE
  ENST00000572888.5 UniProtKB/Swiss-Prot
  ENST00000573808.1 UniProtKB/TrEMBL
  ENST00000574865.1 UniProtKB/TrEMBL
  ENST00000575203 ENTREZGENE
  ENST00000575203.5 UniProtKB/Swiss-Prot
  ENST00000575510.5 UniProtKB/TrEMBL
Gene3D-CATH Metal-dependent hydrolases UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000167261 GTEx
HGNC ID HGNC:23028 ENTREZGENE
Human Proteome Map DPEP2 Human Proteome Map
InterPro Dipep_AS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Metal_Hydrolase UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Pept_M19 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:64174 UniProtKB/Swiss-Prot
NCBI Gene 64174 ENTREZGENE
OMIM 609925 OMIM
PANTHER DIPEPTIDASE 2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR10443 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Pfam Peptidase_M19 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA134985997 PharmGKB
PROSITE RENAL_DIPEPTIDASE_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  RENAL_DIPEPTIDASE_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP SSF51556 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A024R6Y5 ENTREZGENE
  DPEP2_HUMAN UniProtKB/Swiss-Prot
  I3L348_HUMAN UniProtKB/TrEMBL
  I3L4H3_HUMAN UniProtKB/TrEMBL
  J3KSU4_HUMAN UniProtKB/TrEMBL
  J3QLL2_HUMAN UniProtKB/TrEMBL
  Q8TC95 ENTREZGENE
  Q9H4A9 ENTREZGENE
UniProt Secondary A0A024R6Y5 UniProtKB/Swiss-Prot
  B2RCF8 UniProtKB/Swiss-Prot
  B3KS59 UniProtKB/Swiss-Prot
  I3L248 UniProtKB/Swiss-Prot
  Q6UX92 UniProtKB/Swiss-Prot
  Q8TC95 UniProtKB/Swiss-Prot