PCDHB11 (protocadherin beta 11) - Rat Genome Database

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Gene: PCDHB11 (protocadherin beta 11) Homo sapiens
Analyze
Symbol: PCDHB11
Name: protocadherin beta 11
RGD ID: 1346313
HGNC Page HGNC:8682
Description: Predicted to enable calcium ion binding activity. Predicted to be involved in cell adhesion. Predicted to be located in plasma membrane.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cadherin ME2; ME2; MGC138337; MGC142171; PCDH-beta-11; PCDH-BETA11; protocadherin beta-11
RGD Orthologs
Bonobo
Dog
Pig
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
GRCh385141,199,627 - 141,203,779 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5141,199,610 - 141,203,779 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,579,200 - 140,583,352 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,559,532 - 140,562,802 (+)NCBINCBI36Build 36hg18NCBI36
Build 345140,559,531 - 140,562,802NCBI
Celera5136,656,170 - 136,659,440 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,724,395 - 135,727,665 (+)NCBIHuRef
CHM1_15140,012,547 - 140,015,817 (+)NCBICHM1_1
T2T-CHM13v2.05141,724,941 - 141,729,093 (+)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
membrane  (IEA,NAS)
plasma membrane  (IEA,TAS)
synapse  (IEA)

Molecular Function

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:9182820   PMID:10380929   PMID:10716726   PMID:10817752   PMID:10835267   PMID:11230163   PMID:11322959   PMID:12231349   PMID:12477932   PMID:15489334   PMID:19054571   PMID:21873635  
PMID:27068704   PMID:28514442   PMID:33961781  


Genomics

Comparative Map Data
PCDHB11
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh385141,199,627 - 141,203,779 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl5141,199,610 - 141,203,779 (+)EnsemblGRCh38hg38GRCh38
GRCh375140,579,200 - 140,583,352 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 365140,559,532 - 140,562,802 (+)NCBINCBI36Build 36hg18NCBI36
Build 345140,559,531 - 140,562,802NCBI
Celera5136,656,170 - 136,659,440 (+)NCBICelera
Cytogenetic Map5q31.3NCBI
HuRef5135,724,395 - 135,727,665 (+)NCBIHuRef
CHM1_15140,012,547 - 140,015,817 (+)NCBICHM1_1
T2T-CHM13v2.05141,724,941 - 141,729,093 (+)NCBIT2T-CHM13v2.0
PCDHB11
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v24136,450,859 - 136,455,446 (+)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan15134,590,413 - 134,594,998 (+)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v05136,562,547 - 136,565,623 (+)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.15142,676,555 - 142,679,201 (+)NCBIpanpan1.1PanPan1.1panPan2
LOC487176
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1236,239,316 - 36,242,793 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl236,239,463 - 36,241,796 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha233,291,117 - 33,296,960 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0236,693,804 - 36,699,659 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl236,694,065 - 36,696,398 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1233,767,862 - 33,773,715 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0234,578,871 - 34,584,712 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0235,386,523 - 35,392,366 (+)NCBIUU_Cfam_GSD_1.0
LOC100737316
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.12142,891,363 - 142,895,906 (+)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
Sscrofa10.22149,089,509 - 149,094,185 (+)NCBISscrofa10.2Sscrofa10.2susScr3

Variants

.
Variants in PCDHB11
58 total Variants

Clinical Variants
Name Type Condition(s) Position(s) Clinical significance
GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3 copy number gain See cases [RCV000051193] Chr5:130860928..155321811 [GRCh38]
Chr5:130196621..154701371 [GRCh37]
Chr5:130224520..154681564 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.2-32(chr5:138871137-145812309)x1 copy number loss See cases [RCV000052142] Chr5:138871137..145812309 [GRCh38]
Chr5:138206826..145191872 [GRCh37]
Chr5:138234725..145172065 [NCBI36]
Chr5:5q31.2-32
pathogenic
GRCh38/hg38 5q31.3(chr5:141185055-141211630)x1 copy number loss See cases [RCV000052580] Chr5:141185055..141211630 [GRCh38]
Chr5:140564630..140591202 [GRCh37]
Chr5:140544814..140571386 [NCBI36]
Chr5:5q31.3
uncertain significance
GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1 copy number loss See cases [RCV000053524] Chr5:106619588..156124387 [GRCh38]
Chr5:105955289..155551397 [GRCh37]
Chr5:105983188..155483975 [NCBI36]
Chr5:5q21.3-33.2
pathogenic
NM_018931.2(PCDHB11):c.2314C>T (p.Pro772Ser) single nucleotide variant Malignant melanoma [RCV000066723] Chr5:141202088 [GRCh38]
Chr5:140581661 [GRCh37]
Chr5:140561845 [NCBI36]
Chr5:5q31.3
not provided
NM_018931.2(PCDHB11):c.8A>T (p.Asn3Ile) single nucleotide variant Malignant melanoma [RCV000061153] Chr5:141199782 [GRCh38]
Chr5:140579355 [GRCh37]
Chr5:140559539 [NCBI36]
Chr5:5q31.3
not provided
NM_018931.2(PCDHB11):c.9C>T (p.Asn3=) single nucleotide variant Malignant melanoma [RCV000061154] Chr5:141199783 [GRCh38]
Chr5:140579356 [GRCh37]
Chr5:140559540 [NCBI36]
Chr5:5q31.3
not provided
NM_018931.2(PCDHB11):c.2231C>T (p.Thr744Ile) single nucleotide variant Malignant melanoma [RCV000061155] Chr5:141202005 [GRCh38]
Chr5:140581578 [GRCh37]
Chr5:140561762 [NCBI36]
Chr5:5q31.3
not provided
NM_018930.3(PCDHB10):c.2321C>T (p.Ser774Leu) single nucleotide variant Malignant melanoma [RCV000066722] Chr5:141194873 [GRCh38]
Chr5:140574446 [GRCh37]
Chr5:140554630 [NCBI36]
Chr5:5q31.3
not provided
GRCh38/hg38 5q31.3(chr5:140963199-142322798)x1 copy number loss See cases [RCV000136949] Chr5:140963199..142322798 [GRCh38]
Chr5:140453735..141702363 [GRCh37]
Chr5:140322968..141682547 [NCBI36]
Chr5:5q31.3
uncertain significance
GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3 copy number gain See cases [RCV000138808] Chr5:129847794..153353546 [GRCh38]
Chr5:129183487..152733106 [GRCh37]
Chr5:129211386..152713299 [NCBI36]
Chr5:5q23.3-33.2
pathogenic
GRCh38/hg38 5q31.3-32(chr5:141089988-149530678)x3 copy number gain See cases [RCV000139504] Chr5:141089988..149530678 [GRCh38]
Chr5:140469572..148910241 [GRCh37]
Chr5:140449756..148890434 [NCBI36]
Chr5:5q31.3-32
pathogenic
GRCh38/hg38 5q31.2-31.3(chr5:138942857-144605017)x3 copy number gain See cases [RCV000142806] Chr5:138942857..144605017 [GRCh38]
Chr5:138278546..143984580 [GRCh37]
Chr5:138306445..143964773 [NCBI36]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3 copy number gain not provided [RCV000487658] Chr5:94844077..178830410 [GRCh37]
Chr5:5q15-35.3
likely benign
NC_000005.9:g.(?_86400000)_(154000000_?)del deletion Familial adenomatous polyposis 1 [RCV002231249]|Hereditary cancer-predisposing syndrome [RCV000554476] Chr5:86400000..154000000 [GRCh37]
Chr5:5q14.3-33.2
pathogenic
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910)x3 copy number gain See cases [RCV000449349] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
GRCh37/hg19 5q31.3(chr5:140559899-140580412)x1 copy number loss See cases [RCV000449410] Chr5:140559899..140580412 [GRCh37]
Chr5:5q31.3
likely benign
GRCh37/hg19 5q31.3(chr5:140581626-140593602)x3 copy number gain See cases [RCV000445866] Chr5:140581626..140593602 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140581626-140589370)x3 copy number gain See cases [RCV000445906] Chr5:140581626..140589370 [GRCh37]
Chr5:5q31.3
benign|likely benign
GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3 copy number gain See cases [RCV000448245] Chr5:106716357..180687338 [GRCh37]
Chr5:5q21.3-35.3
pathogenic
GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1 copy number loss See cases [RCV000511978] Chr5:17628741..176575720 [GRCh37]
Chr5:5p15.1-q35.2
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3 copy number gain See cases [RCV000512039] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789) copy number gain See cases [RCV000510723] Chr5:113577..180719789 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
NM_018931.3(PCDHB11):c.1069C>T (p.Pro357Ser) single nucleotide variant Inborn genetic diseases [RCV003250298] Chr5:141200843 [GRCh38]
Chr5:140580416 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2098C>T (p.Leu700Phe) single nucleotide variant Inborn genetic diseases [RCV003306930] Chr5:141201872 [GRCh38]
Chr5:140581445 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.911G>C (p.Arg304Thr) single nucleotide variant Inborn genetic diseases [RCV003254128] Chr5:141200685 [GRCh38]
Chr5:140580258 [GRCh37]
Chr5:5q31.3
likely benign
GRCh37/hg19 5q31.2-31.3(chr5:139147238-141540491)x1 copy number loss not provided [RCV000682600] Chr5:139147238..141540491 [GRCh37]
Chr5:5q31.2-31.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:25328-180693344)x3 copy number gain not provided [RCV000744323] Chr5:25328..180693344 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5p15.33-q35.3(chr5:13648-180905029)x3 copy number gain not provided [RCV000744317] Chr5:13648..180905029 [GRCh37]
Chr5:5p15.33-q35.3
pathogenic
GRCh37/hg19 5q31.3(chr5:140558308-140594381)x1 copy number loss not provided [RCV000745227] Chr5:140558308..140594381 [GRCh37]
Chr5:5q31.3
benign
GRCh37/hg19 5q31.3(chr5:140559849-140606802)x3 copy number gain not provided [RCV000745228] Chr5:140559849..140606802 [GRCh37]
Chr5:5q31.3
benign
Single allele deletion Neurodevelopmental disorder [RCV000787436] Chr5:14685137..149511942 [GRCh37]
Chr5:5p15.2-q32
uncertain significance
NM_018931.3(PCDHB11):c.1584C>G (p.Asp528Glu) single nucleotide variant not provided [RCV000946882] Chr5:141201358 [GRCh38]
Chr5:140580931 [GRCh37]
Chr5:5q31.3
benign
NM_018931.3(PCDHB11):c.900A>C (p.Glu300Asp) single nucleotide variant Inborn genetic diseases [RCV003247614] Chr5:141200674 [GRCh38]
Chr5:140580247 [GRCh37]
Chr5:5q31.3
likely benign
GRCh37/hg19 5q31.3-32(chr5:140424333-148985999)x3 copy number gain not provided [RCV000848228] Chr5:140424333..148985999 [GRCh37]
Chr5:5q31.3-32
uncertain significance
NM_018931.3(PCDHB11):c.1346C>G (p.Pro449Arg) single nucleotide variant Inborn genetic diseases [RCV003252714] Chr5:141201120 [GRCh38]
Chr5:140580693 [GRCh37]
Chr5:5q31.3
uncertain significance
NC_000005.9:g.(?_136633338)_(140998481_?)dup duplication PURA-related severe neonatal hypotonia-seizures-encephalopathy syndrome [RCV001339088] Chr5:136633338..140998481 [GRCh37]
Chr5:5q31.2-31.3
uncertain significance
GRCh37/hg19 5q23.3-33.3(chr5:130125085-157574910) copy number gain not specified [RCV002053526] Chr5:130125085..157574910 [GRCh37]
Chr5:5q23.3-33.3
pathogenic
NM_018931.3(PCDHB11):c.241A>G (p.Thr81Ala) single nucleotide variant Inborn genetic diseases [RCV003255060] Chr5:141200015 [GRCh38]
Chr5:140579588 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1829C>T (p.Thr610Met) single nucleotide variant Inborn genetic diseases [RCV003256806] Chr5:141201603 [GRCh38]
Chr5:140581176 [GRCh37]
Chr5:5q31.3
uncertain significance
GRCh37/hg19 5q31.3(chr5:140082762-140773954)x3 copy number gain not provided [RCV002474614] Chr5:140082762..140773954 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.547A>G (p.Arg183Gly) single nucleotide variant Inborn genetic diseases [RCV002841024] Chr5:141200321 [GRCh38]
Chr5:140579894 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.887A>G (p.Gln296Arg) single nucleotide variant Inborn genetic diseases [RCV002771798] Chr5:141200661 [GRCh38]
Chr5:140580234 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1208T>C (p.Leu403Ser) single nucleotide variant Inborn genetic diseases [RCV002968522] Chr5:141200982 [GRCh38]
Chr5:140580555 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1222C>T (p.Pro408Ser) single nucleotide variant Inborn genetic diseases [RCV002863995] Chr5:141200996 [GRCh38]
Chr5:140580569 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.104T>C (p.Val35Ala) single nucleotide variant Inborn genetic diseases [RCV002754026] Chr5:141199878 [GRCh38]
Chr5:140579451 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1264A>G (p.Thr422Ala) single nucleotide variant Inborn genetic diseases [RCV002784325] Chr5:141201038 [GRCh38]
Chr5:140580611 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1478C>T (p.Pro493Leu) single nucleotide variant Inborn genetic diseases [RCV002849115] Chr5:141201252 [GRCh38]
Chr5:140580825 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1705T>C (p.Ser569Pro) single nucleotide variant Inborn genetic diseases [RCV002980524] Chr5:141201479 [GRCh38]
Chr5:140581052 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1702G>C (p.Gly568Arg) single nucleotide variant Inborn genetic diseases [RCV002868453] Chr5:141201476 [GRCh38]
Chr5:140581049 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.566G>A (p.Arg189Lys) single nucleotide variant Inborn genetic diseases [RCV002707851] Chr5:141200340 [GRCh38]
Chr5:140579913 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.341C>A (p.Thr114Lys) single nucleotide variant Inborn genetic diseases [RCV002691675] Chr5:141200115 [GRCh38]
Chr5:140579688 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.164A>T (p.Lys55Met) single nucleotide variant Inborn genetic diseases [RCV002798486] Chr5:141199938 [GRCh38]
Chr5:140579511 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.919C>G (p.Leu307Val) single nucleotide variant Inborn genetic diseases [RCV002951596] Chr5:141200693 [GRCh38]
Chr5:140580266 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1588C>T (p.Arg530Cys) single nucleotide variant Inborn genetic diseases [RCV002782787] Chr5:141201362 [GRCh38]
Chr5:140580935 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2204A>G (p.His735Arg) single nucleotide variant Inborn genetic diseases [RCV002737974] Chr5:141201978 [GRCh38]
Chr5:140581551 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1566G>T (p.Glu522Asp) single nucleotide variant Inborn genetic diseases [RCV002713590] Chr5:141201340 [GRCh38]
Chr5:140580913 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2147G>A (p.Arg716Lys) single nucleotide variant Inborn genetic diseases [RCV002768491] Chr5:141201921 [GRCh38]
Chr5:140581494 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1583A>G (p.Asp528Gly) single nucleotide variant Inborn genetic diseases [RCV002713497] Chr5:141201357 [GRCh38]
Chr5:140580930 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.178T>C (p.Ser60Pro) single nucleotide variant Inborn genetic diseases [RCV002698894] Chr5:141199952 [GRCh38]
Chr5:140579525 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.389C>T (p.Ser130Phe) single nucleotide variant Inborn genetic diseases [RCV002742544] Chr5:141200163 [GRCh38]
Chr5:140579736 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1936G>A (p.Asp646Asn) single nucleotide variant Inborn genetic diseases [RCV002986383] Chr5:141201710 [GRCh38]
Chr5:140581283 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1355C>T (p.Thr452Ile) single nucleotide variant Inborn genetic diseases [RCV002767310] Chr5:141201129 [GRCh38]
Chr5:140580702 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.866G>T (p.Arg289Leu) single nucleotide variant Inborn genetic diseases [RCV002812210] Chr5:141200640 [GRCh38]
Chr5:140580213 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2215G>A (p.Val739Met) single nucleotide variant Inborn genetic diseases [RCV002878119] Chr5:141201989 [GRCh38]
Chr5:140581562 [GRCh37]
Chr5:5q31.3
likely benign
NM_018931.3(PCDHB11):c.235A>G (p.Ile79Val) single nucleotide variant Inborn genetic diseases [RCV002793138] Chr5:141200009 [GRCh38]
Chr5:140579582 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1670A>G (p.Asn557Ser) single nucleotide variant Inborn genetic diseases [RCV002672845] Chr5:141201444 [GRCh38]
Chr5:140581017 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2134C>T (p.Arg712Trp) single nucleotide variant Inborn genetic diseases [RCV002935460] Chr5:141201908 [GRCh38]
Chr5:140581481 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.167T>A (p.Val56Glu) single nucleotide variant Inborn genetic diseases [RCV002965018] Chr5:141199941 [GRCh38]
Chr5:140579514 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2162C>G (p.Ser721Trp) single nucleotide variant Inborn genetic diseases [RCV002807698] Chr5:141201936 [GRCh38]
Chr5:140581509 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.470C>T (p.Ala157Val) single nucleotide variant Inborn genetic diseases [RCV002936024] Chr5:141200244 [GRCh38]
Chr5:140579817 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2015C>T (p.Pro672Leu) single nucleotide variant Inborn genetic diseases [RCV002677774] Chr5:141201789 [GRCh38]
Chr5:140581362 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1431C>G (p.Asp477Glu) single nucleotide variant Inborn genetic diseases [RCV002655958] Chr5:141201205 [GRCh38]
Chr5:140580778 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1825G>C (p.Ala609Pro) single nucleotide variant Inborn genetic diseases [RCV002723746] Chr5:141201599 [GRCh38]
Chr5:140581172 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2212G>T (p.Asp738Tyr) single nucleotide variant Inborn genetic diseases [RCV002945041] Chr5:141201986 [GRCh38]
Chr5:140581559 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.49C>G (p.Leu17Val) single nucleotide variant Inborn genetic diseases [RCV003209765] Chr5:141199823 [GRCh38]
Chr5:140579396 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1139G>T (p.Arg380Ile) single nucleotide variant Inborn genetic diseases [RCV003196591] Chr5:141200913 [GRCh38]
Chr5:140580486 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2276C>T (p.Ser759Phe) single nucleotide variant Inborn genetic diseases [RCV003193920] Chr5:141202050 [GRCh38]
Chr5:140581623 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.227A>G (p.Gln76Arg) single nucleotide variant Inborn genetic diseases [RCV003183499] Chr5:141200001 [GRCh38]
Chr5:140579574 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2327C>A (p.Ala776Glu) single nucleotide variant Inborn genetic diseases [RCV003201474] Chr5:141202101 [GRCh38]
Chr5:140581674 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1329C>A (p.Asp443Glu) single nucleotide variant Inborn genetic diseases [RCV003210760] Chr5:141201103 [GRCh38]
Chr5:140580676 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1378G>A (p.Val460Ile) single nucleotide variant Inborn genetic diseases [RCV003201724] Chr5:141201152 [GRCh38]
Chr5:140580725 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.203C>T (p.Ser68Phe) single nucleotide variant Inborn genetic diseases [RCV003207114] Chr5:141199977 [GRCh38]
Chr5:140579550 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1893C>A (p.Ser631Arg) single nucleotide variant Inborn genetic diseases [RCV003304275] Chr5:141201667 [GRCh38]
Chr5:140581240 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1318T>G (p.Leu440Val) single nucleotide variant Inborn genetic diseases [RCV003213436] Chr5:141201092 [GRCh38]
Chr5:140580665 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1680C>G (p.Phe560Leu) single nucleotide variant Inborn genetic diseases [RCV003265158] Chr5:141201454 [GRCh38]
Chr5:140581027 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1664A>G (p.Asn555Ser) single nucleotide variant Inborn genetic diseases [RCV003288105] Chr5:141201438 [GRCh38]
Chr5:140581011 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.659C>T (p.Pro220Leu) single nucleotide variant Inborn genetic diseases [RCV003338278] Chr5:141200433 [GRCh38]
Chr5:140580006 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1151C>A (p.Ser384Tyr) single nucleotide variant Inborn genetic diseases [RCV003361679] Chr5:141200925 [GRCh38]
Chr5:140580498 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.2214C>G (p.Asp738Glu) single nucleotide variant Inborn genetic diseases [RCV003377358] Chr5:141201988 [GRCh38]
Chr5:140581561 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1001T>C (p.Ile334Thr) single nucleotide variant Inborn genetic diseases [RCV003352610] Chr5:141200775 [GRCh38]
Chr5:140580348 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.703A>G (p.Ile235Val) single nucleotide variant Inborn genetic diseases [RCV003378324] Chr5:141200477 [GRCh38]
Chr5:140580050 [GRCh37]
Chr5:5q31.3
likely benign
NM_018931.3(PCDHB11):c.2165T>C (p.Val722Ala) single nucleotide variant Inborn genetic diseases [RCV003384944] Chr5:141201939 [GRCh38]
Chr5:140581512 [GRCh37]
Chr5:5q31.3
uncertain significance
NM_018931.3(PCDHB11):c.1596C>A (p.Gly532=) single nucleotide variant not provided [RCV003429837] Chr5:141201370 [GRCh38]
Chr5:140580943 [GRCh37]
Chr5:5q31.3
likely benign
NM_018931.3(PCDHB11):c.1416T>C (p.Ser472=) single nucleotide variant not provided [RCV003428640] Chr5:141201190 [GRCh38]
Chr5:140580763 [GRCh37]
Chr5:5q31.3
likely benign
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:403
Count of miRNA genes:295
Interacting mature miRNAs:310
Transcripts:ENST00000354757, ENST00000536699
Prediction methods:Miranda, Rnahybrid
Result types:miRGate_prediction

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

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

Markers in Region
RH36905  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map20p13UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map1p21.2UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map5q33.3UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map7q22.1UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map9p24.3UniSTS
Cytogenetic Map10p14UniSTS
Cytogenetic Map19q13.32UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map11q12.3UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map17q21.31UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map7q36.1UniSTS
Cytogenetic Map12q13.3UniSTS
Cytogenetic Map1p12UniSTS
Cytogenetic Map10p12.33UniSTS
Cytogenetic Map12q13.12UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map18p11.3-p11.2UniSTS
Cytogenetic Map16q24.1UniSTS
Cytogenetic Map14q24.1UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map10q24.32UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11q13.5UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map3q27-q28UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map3q26.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic MapXp22.33UniSTS
Cytogenetic MapYp11.32UniSTS
Cytogenetic Map5p13.2UniSTS
Cytogenetic Map17p13.3UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map14q13.2UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map2p21UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map15q21UniSTS
Cytogenetic Map12p12UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map5q13UniSTS
Cytogenetic Map8p21.2UniSTS
Cytogenetic Map20p11.23UniSTS
Cytogenetic Map6p24.3UniSTS
Cytogenetic Map3q12.2-q12.3UniSTS
Cytogenetic Map11p15.4UniSTS
Cytogenetic Map1q21.2-q21.3UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map12q24.2-q24.31UniSTS
Cytogenetic Map7p11.2UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map17q23.3UniSTS
Cytogenetic Map16q22UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q12-q13.1UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map9q21.33UniSTS
Cytogenetic Map19q13.41UniSTS
Cytogenetic Map11p15.1UniSTS
Cytogenetic Map5q12.3UniSTS
Cytogenetic Map18p11.2UniSTS
Cytogenetic Map19q13.3-q13.4UniSTS
Cytogenetic Map9q31.1UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map8p21.1UniSTS
Cytogenetic Map1q25.3UniSTS
Cytogenetic Map6p24-p22.3UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map2p13UniSTS
Cytogenetic Map7q31.1-q31.2UniSTS
Cytogenetic Map8q22.2UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map16q21UniSTS
Cytogenetic Map10q21UniSTS
Cytogenetic Map8q24.3UniSTS
Cytogenetic Map1p36.21UniSTS
Cytogenetic Map1p34.3UniSTS
Cytogenetic Map19p13.13UniSTS
Cytogenetic Map10q26.13UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map4q25-q27UniSTS
Cytogenetic Map9q34UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map15q15.3UniSTS
Cytogenetic Map4q28-q32UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map10q24.1UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map7p14.3UniSTS
Cytogenetic Map19q13.33UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map2p14UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map17p11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map1p13.2UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map12p11.21UniSTS
Cytogenetic Map7q11.21UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map1p21.3UniSTS
Cytogenetic Map15q21.3UniSTS
Cytogenetic Map10q22.2UniSTS
Cytogenetic Map2q35UniSTS
Cytogenetic Map3q27.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map3p25.1UniSTS
Cytogenetic Map10q25-q26UniSTS
Cytogenetic Map11q13.2UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map11q13UniSTS
Cytogenetic Map17q21.2UniSTS
Cytogenetic Map5q33.1UniSTS
Cytogenetic Map7p14UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map16q22.1UniSTS
D8S2279  
Human AssemblyChrPosition (strand)SourceJBrowse
Cytogenetic Map21q22.12UniSTS
Cytogenetic Map15q13UniSTS
Cytogenetic Map9q32UniSTS
Cytogenetic Map15q22.3UniSTS
Cytogenetic Map17p12UniSTS
Cytogenetic Map21q21.3UniSTS
Cytogenetic Map3p22-p21.3UniSTS
Cytogenetic Map1q21.1UniSTS
Cytogenetic Map2q24.2UniSTS
Cytogenetic Map17q24.2UniSTS
Cytogenetic Map1q32UniSTS
Cytogenetic Map3p25.3UniSTS
Cytogenetic Map20q13.3UniSTS
Cytogenetic Map2q31.1UniSTS
Cytogenetic Map1q21UniSTS
Cytogenetic Map3p14.1UniSTS
Cytogenetic Map2q37.3UniSTS
Cytogenetic Map7p14.1UniSTS
Cytogenetic Map2q22.3UniSTS
Cytogenetic Map15q13.2UniSTS
Cytogenetic Map12q24.1UniSTS
Cytogenetic Map7p15.2UniSTS
Cytogenetic Map5q31.2UniSTS
Cytogenetic Map2p25.2UniSTS
Cytogenetic Map3p24.3UniSTS
Cytogenetic Map17q25.3UniSTS
Cytogenetic Map15q22.31UniSTS
Cytogenetic Map5q14UniSTS
Cytogenetic Map5q31UniSTS
Cytogenetic Map1p36.32UniSTS
Cytogenetic Map1q42.12UniSTS
Cytogenetic Map7q21.11UniSTS
Cytogenetic Map9q34.2UniSTS
Cytogenetic Map19q13.3UniSTS
Cytogenetic Map22q13.33UniSTS
Cytogenetic Map8q22.3UniSTS
Cytogenetic Map6p21.1-p12UniSTS
Cytogenetic Map1p36.13UniSTS
Cytogenetic Map7q36.3UniSTS
Cytogenetic Map2p25.1UniSTS
Cytogenetic Map7p21.3UniSTS
Cytogenetic Map4q12UniSTS
Cytogenetic Map22q11.22UniSTS
Cytogenetic Map11p13UniSTS
Cytogenetic Map1q12UniSTS
Cytogenetic Map8p23UniSTS
Cytogenetic Map11q13.2-q13.3UniSTS
Cytogenetic Map13q14.1-q14.3UniSTS
Cytogenetic Map3q22-q24UniSTS
Cytogenetic Map3q13.1-q13.2UniSTS
Cytogenetic Map16q24UniSTS
Cytogenetic Map5q23.3-q31.1UniSTS
Cytogenetic Map8p21.3UniSTS
Cytogenetic Map14q32.3UniSTS
Cytogenetic Map7q11.23UniSTS
Cytogenetic Map7q32UniSTS
Cytogenetic Map14q32.33UniSTS
Cytogenetic Map19p13.2UniSTS
Cytogenetic Map9q34.3UniSTS
Cytogenetic Map1p32.3UniSTS
Cytogenetic Map17q11UniSTS
Cytogenetic Map17p13.1-p12UniSTS
Cytogenetic Map18q21.33UniSTS
Cytogenetic Map19p13.12UniSTS
Cytogenetic Map5q14.1UniSTS
Cytogenetic Map14q24.3UniSTS
Cytogenetic Map1q21-q23UniSTS
Cytogenetic MapXp11.23UniSTS
Cytogenetic Map4q21.1UniSTS
Cytogenetic Map12q13.13UniSTS
Cytogenetic Map14q23.3UniSTS
Cytogenetic Map17p12-p11.2UniSTS
Cytogenetic Map6p21.1UniSTS
Cytogenetic Map1q24UniSTS
Cytogenetic Map1q43UniSTS
Cytogenetic Map9q34.13UniSTS
Cytogenetic Map19q13.4UniSTS
Cytogenetic Map2q32UniSTS
Cytogenetic MapXp22.2UniSTS
Cytogenetic Map19p13.11UniSTS
Cytogenetic Map2q33UniSTS
Cytogenetic Map10p13UniSTS
Cytogenetic Map2q11.2UniSTS
Cytogenetic Map3q27UniSTS
Cytogenetic Map17q25.1UniSTS
Cytogenetic Map4p16.1UniSTS
Cytogenetic Map14q22.3UniSTS
Cytogenetic Map10q23-q24UniSTS
Cytogenetic Map2q37.1UniSTS
Cytogenetic Map17q12UniSTS
Cytogenetic Map14q31-q32UniSTS
Cytogenetic Map5p15.33UniSTS
Cytogenetic Map1q23.2UniSTS
Cytogenetic Map16q24.3UniSTS
Cytogenetic Map4p14UniSTS
Cytogenetic Map2q32.3UniSTS
Cytogenetic Map15q21.1UniSTS
Cytogenetic Map4q32.2UniSTS
Cytogenetic Map10q23UniSTS
Cytogenetic Map5q14.2UniSTS
Cytogenetic Map4q32.1UniSTS
Cytogenetic Map1q25.1UniSTS
Cytogenetic Map11q14.1UniSTS
Cytogenetic Map4p16.3UniSTS
Cytogenetic Map1p34.2UniSTS
Cytogenetic Map11q23.1UniSTS
Cytogenetic Map3p21.1UniSTS
Cytogenetic Map16q22.2UniSTS
Cytogenetic Map14q32.31UniSTS
Cytogenetic Map16q11.2UniSTS
Cytogenetic Map6q22UniSTS
Cytogenetic Map10p15.3UniSTS
Cytogenetic Map11q23UniSTS
Cytogenetic Map22q13.2UniSTS
Cytogenetic Map12q12UniSTS
Cytogenetic Map19q13.42UniSTS
Cytogenetic Map19q13.11UniSTS
Cytogenetic Map12q24.31UniSTS
Cytogenetic Map15q15UniSTS
Cytogenetic Map2q33.1UniSTS
Cytogenetic Map22q12.3UniSTS
Cytogenetic Map20q11UniSTS
Cytogenetic Map22q11.23UniSTS
Cytogenetic Map17q25UniSTS
Cytogenetic Map1p13.3UniSTS
Cytogenetic Map3p22.1UniSTS
Cytogenetic Map8q22.1UniSTS
Cytogenetic Map16q22.1UniSTS
Cytogenetic Map18p11.31UniSTS
Cytogenetic Map19p12UniSTS
Cytogenetic Map11q13.1UniSTS
Cytogenetic Map19p13.3UniSTS
Cytogenetic Map2p22.1UniSTS
Cytogenetic Map16p13.3UniSTS
Cytogenetic Map1p35.2UniSTS
Cytogenetic MapYp11.2UniSTS
Cytogenetic Map13q13.1UniSTS
Cytogenetic Map20q11.22UniSTS
Cytogenetic Map19q13.2UniSTS
Cytogenetic Map18q12UniSTS
Cytogenetic Map17q21.33UniSTS
Cytogenetic Map15q15.1UniSTS
Cytogenetic Map3q27.2UniSTS
Cytogenetic Map3q21.3UniSTS
Cytogenetic Map5p15.2UniSTS
Cytogenetic Map20q13.12UniSTS
Cytogenetic Map17q21UniSTS
Cytogenetic Map1q42UniSTS
Cytogenetic Map14q32.11UniSTS
Cytogenetic Map17q21.2-q21.3UniSTS
Cytogenetic Map5q32-q34UniSTS
Cytogenetic Map15q14UniSTS
Cytogenetic Map16q13UniSTS
Cytogenetic Map3q21.2UniSTS
Cytogenetic Map3p21.3UniSTS
Cytogenetic Map14q24.2UniSTS
Cytogenetic Map12q24.13UniSTS
Cytogenetic Map13q14.11UniSTS
Cytogenetic Map3q27.3UniSTS
Cytogenetic Map1q32.3UniSTS
Cytogenetic Map6p22.1UniSTS
Cytogenetic Map9q34.11UniSTS
Cytogenetic Map6q21UniSTS
Cytogenetic Map6q25.3UniSTS
Cytogenetic Map2p11.2UniSTS
Cytogenetic Map13q14.3UniSTS
Cytogenetic Map17q11.2UniSTS
Cytogenetic Map10p12UniSTS
Cytogenetic Map2q33.3UniSTS
Cytogenetic Map14q21.3UniSTS
Cytogenetic Map8p22-p21UniSTS
Cytogenetic Map18q11.2UniSTS
Cytogenetic Map2p15UniSTS
Cytogenetic Map17q22UniSTS
Cytogenetic Map12q21.33UniSTS
Cytogenetic Map20q13.32UniSTS
Cytogenetic Map1p34.1UniSTS
Cytogenetic Map10q26UniSTS
Cytogenetic Map8p23.1UniSTS
Cytogenetic Map19p13UniSTS
Cytogenetic Map7q21.13UniSTS
Cytogenetic Map7q31.1UniSTS
Cytogenetic Map1p33UniSTS
Cytogenetic Map21q22.3UniSTS
Cytogenetic Map1p35.1UniSTS
Cytogenetic Map22q12.2UniSTS
Cytogenetic Map9q22.3UniSTS
Cytogenetic Map8q13.1UniSTS
Cytogenetic Map3q25UniSTS
Cytogenetic Map1p36.33UniSTS
Cytogenetic Map20q13.33UniSTS
Cytogenetic Map1p31.3UniSTS
Cytogenetic Map14q31.1UniSTS
Cytogenetic Map22q13.1UniSTS
Cytogenetic Map12q13.2UniSTS
Cytogenetic Map22q13.31-q13.33UniSTS
Cytogenetic Map20q13.31UniSTS
Cytogenetic Map11p11.2UniSTS
Cytogenetic Map1q41UniSTS
Cytogenetic Map1p36.11UniSTS
Cytogenetic Map15q25.2UniSTS
Cytogenetic Map14q11.2UniSTS
Cytogenetic Map17q23.2UniSTS
Cytogenetic Map7q32.2UniSTS
Cytogenetic Map19q13.12UniSTS
Cytogenetic Map1q32.1UniSTS
Cytogenetic Map6q25.1UniSTS
Cytogenetic Map19q13.43UniSTS
Cytogenetic Map9p13.3UniSTS
Cytogenetic Map16p11.2UniSTS
Cytogenetic Map2p13.1UniSTS
Cytogenetic Map22q11.21UniSTS
Cytogenetic Map3q29UniSTS
Cytogenetic Map7p13UniSTS
Cytogenetic Map11q23.3UniSTS
Cytogenetic Map14q31-q32.1UniSTS
Cytogenetic Map1q42.11UniSTS
Cytogenetic Map4q35.1UniSTS
Cytogenetic Map2p23.3UniSTS
Cytogenetic Map2p13.3UniSTS
Cytogenetic MapXp11.3UniSTS
Cytogenetic Map2q11.2-q12.1UniSTS
Cytogenetic Map20q13.13UniSTS
Cytogenetic Map1p22UniSTS
Cytogenetic Map6q16.2UniSTS
Cytogenetic Map18q23UniSTS
Cytogenetic Map2q14UniSTS
Cytogenetic Map20p11.23-p11.21UniSTS
Cytogenetic Map16p12.2UniSTS
Cytogenetic Map8p11.23UniSTS
Cytogenetic Map19q13.1UniSTS
Cytogenetic Map19q13UniSTS
Cytogenetic Map8p11.21UniSTS
Cytogenetic Map12q14.3UniSTS
Cytogenetic MapXq26.3UniSTS
Cytogenetic Map8q24.11UniSTS
Cytogenetic Map10q23.1UniSTS
Cytogenetic Map1q44UniSTS
Cytogenetic Map9q22.33UniSTS
Cytogenetic Map3p21.31UniSTS
Cytogenetic Map17p13.2UniSTS
Cytogenetic Map9q21.32UniSTS
Cytogenetic Map7q34UniSTS
Cytogenetic Map9q33.3UniSTS
Cytogenetic Map1p36.1UniSTS
Cytogenetic Map20q12UniSTS
Cytogenetic Map4q21.23UniSTS
Cytogenetic Map5q13.2UniSTS
Cytogenetic Map22q12.1UniSTS
Cytogenetic Map5q31.1UniSTS
Cytogenetic Map2q21.3UniSTS
Cytogenetic Map7q21.2UniSTS
Cytogenetic Map17q22.2UniSTS
Cytogenetic Map17p13UniSTS
Cytogenetic Map12q24.11UniSTS
Cytogenetic Map18q21UniSTS
Cytogenetic Map10q11.1UniSTS
Cytogenetic Map22q11.2UniSTS
Cytogenetic Map19q12UniSTS
Cytogenetic Map7q34-q35UniSTS
Cytogenetic Map15q24.1UniSTS
Cytogenetic Map18p11.21UniSTS
Cytogenetic Map1q23.1UniSTS
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Cytogenetic Map7q21.1-q22UniSTS
Cytogenetic Map15q26.1UniSTS
Cytogenetic Map3q13.13-q13.2UniSTS
Cytogenetic MapXp22.13UniSTS
Cytogenetic Map13q12.12UniSTS
Cytogenetic Map13q14.2UniSTS
Cytogenetic Map12qUniSTS
Cytogenetic Map1pUniSTS
Cytogenetic Map16pUniSTS
Cytogenetic Map15qUniSTS
Cytogenetic Map7qUniSTS
Cytogenetic Map2qUniSTS
Cytogenetic Map5q13.1UniSTS
Cytogenetic Map11p14.1UniSTS
Cytogenetic Map4q32UniSTS
Cytogenetic Map2p22UniSTS
Cytogenetic Map5q14.3UniSTS
Cytogenetic Map10p12.1UniSTS
Cytogenetic Map5q23.2UniSTS
Cytogenetic Map2p24.1UniSTS
Cytogenetic Map8q24.13UniSTS
Cytogenetic Map12p13.32UniSTS
Cytogenetic Map9p21.1UniSTS
Cytogenetic Map9q34.2-q34.3UniSTS


Expression


RNA-SEQ Expression
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 5 23 4 2 2 9 7 10 10 35 28
Low 1851 1653 1183 192 179 58 3481 1123 2570 259 1269 1455 141 1176 2101 2
Below cutoff 560 834 465 362 773 338 858 1056 1125 139 132 110 26 28 687 2

Sequence


RefSeq Acc Id: ENST00000354757   ⟹   ENSP00000346802
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5141,199,627 - 141,203,779 (+)Ensembl
RefSeq Acc Id: ENST00000624887   ⟹   ENSP00000485553
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl5141,199,610 - 141,202,279 (+)Ensembl
RefSeq Acc Id: NM_018931   ⟹   NP_061754
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh385141,199,627 - 141,203,779 (+)NCBI
GRCh375140,578,916 - 140,582,618 (+)NCBI
Build 365140,559,532 - 140,562,802 (+)NCBI Archive
Celera5136,656,170 - 136,659,440 (+)RGD
HuRef5135,724,395 - 135,727,665 (+)ENTREZGENE
CHM1_15140,012,547 - 140,015,817 (+)NCBI
T2T-CHM13v2.05141,724,941 - 141,729,093 (+)NCBI
Sequence:
RefSeq Acc Id: NP_061754   ⟸   NM_018931
- Peptide Label: precursor
- UniProtKB: B4DSF7 (UniProtKB/Swiss-Prot),   Q2M223 (UniProtKB/Swiss-Prot),   Q9Y5F2 (UniProtKB/Swiss-Prot),   B2R8M3 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000485553   ⟸   ENST00000624887
RefSeq Acc Id: ENSP00000346802   ⟸   ENST00000354757
Protein Domains
Cadherin

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-Q9Y5F2-F1-model_v2 AlphaFold Q9Y5F2 1-797 view protein structure


Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:8682 AgrOrtholog
COSMIC PCDHB11 COSMIC
Ensembl Genes ENSG00000197479 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot
  ENSG00000291690 UniProtKB/Swiss-Prot
Ensembl Transcript ENST00000354757 ENTREZGENE
  ENST00000354757.5 UniProtKB/Swiss-Prot
  ENST00000624887.1 UniProtKB/Swiss-Prot
  ENST00000708378.1 UniProtKB/Swiss-Prot
  ENST00000708379.1 UniProtKB/Swiss-Prot
Gene3D-CATH Cadherins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000197479 GTEx
  ENSG00000291690 GTEx
HGNC ID HGNC:8682 ENTREZGENE
Human Proteome Map PCDHB11 Human Proteome Map
InterPro Cadherin-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin_C UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin_N UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:56125 UniProtKB/Swiss-Prot
NCBI Gene 56125 ENTREZGENE
OMIM 606337 OMIM
PANTHER CADHERIN-87A UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PROTOCADHERIN BETA-11 UniProtKB/TrEMBL, UniProtKB/Swiss-Prot
Pfam Cadherin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin_C_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA33027 PharmGKB
PRINTS CADHERIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PROSITE CADHERIN_1 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CADHERIN_2 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
SMART SM00112 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Superfamily-SCOP Cadherin-like UniProtKB/TrEMBL, UniProtKB/Swiss-Prot
UniProt B2R8M3 ENTREZGENE, UniProtKB/TrEMBL
  B4DSF7 ENTREZGENE
  PCDBB_HUMAN UniProtKB/Swiss-Prot
  Q2M223 ENTREZGENE
  Q9Y5F2 ENTREZGENE
UniProt Secondary B4DSF7 UniProtKB/Swiss-Prot
  Q2M223 UniProtKB/Swiss-Prot