CDH16 (cadherin 16) - Rat Genome Database

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Gene: CDH16 (cadherin 16) Homo sapiens
Analyze
Symbol: CDH16
Name: cadherin 16
RGD ID: 1323200
HGNC Page HGNC:1755
Description: Predicted to enable cadherin binding activity and calcium ion binding activity. Predicted to be involved in cell adhesion. Predicted to act upstream of or within calcium-dependent cell-cell adhesion via plasma membrane cell adhesion molecules. Located in extracellular exosome. Biomarker of thyroid cancer.
Type: protein-coding
RefSeq Status: REVIEWED
Previously known as: cadherin 16, KSP-cadherin; cadherin-16; kidney-specific cadherin; KSP-cadherin
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
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381666,908,122 - 66,918,885 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1666,908,122 - 66,918,917 (-)EnsemblGRCh38hg38GRCh38
GRCh371666,942,025 - 66,952,788 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361665,499,526 - 65,510,267 (-)NCBINCBI36Build 36hg18NCBI36
Build 341665,499,525 - 65,510,267NCBI
Celera1651,450,284 - 51,461,025 (-)NCBICelera
Cytogenetic Map16q22.1NCBI
HuRef1652,816,134 - 52,826,996 (-)NCBIHuRef
CHM1_11668,349,034 - 68,359,895 (-)NCBICHM1_1
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)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

Cellular Component

Molecular Function

Phenotype Annotations     Click to see Annotation Detail View

Human Phenotype
References

References - curated
# Reference Title Reference Citation
1. CDH16/Ksp-cadherin is expressed in the developing thyroid gland and is strongly down-regulated in thyroid carcinomas. Calì G, etal., Endocrinology. 2012 Jan;153(1):522-34. doi: 10.1210/en.2011-1572. Epub 2011 Oct 25.
2. GOAs Human GO annotations GOA_HUMAN data from the GO Consortium
3. ClinVar Automated Import and Annotation Pipeline RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
4. Data Import for Chemical-Gene Interactions RGD automated import pipeline for gene-chemical interactions
Additional References at PubMed
PMID:7615566   PMID:8125298   PMID:9721215   PMID:10409308   PMID:10828602   PMID:12477932   PMID:12851251   PMID:12975309   PMID:15023525   PMID:15489334   PMID:15670782   PMID:15886705  
PMID:17895753   PMID:18343407   PMID:21873635   PMID:21988832   PMID:23533145   PMID:26355662   PMID:30021884   PMID:31753913   PMID:32814053   PMID:33845483   PMID:33961781   PMID:35606285  
PMID:37899424  


Genomics

Comparative Map Data
CDH16
(Homo sapiens - human)
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381666,908,122 - 66,918,885 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh38.p14 Ensembl1666,908,122 - 66,918,917 (-)EnsemblGRCh38hg38GRCh38
GRCh371666,942,025 - 66,952,788 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361665,499,526 - 65,510,267 (-)NCBINCBI36Build 36hg18NCBI36
Build 341665,499,525 - 65,510,267NCBI
Celera1651,450,284 - 51,461,025 (-)NCBICelera
Cytogenetic Map16q22.1NCBI
HuRef1652,816,134 - 52,826,996 (-)NCBIHuRef
CHM1_11668,349,034 - 68,359,895 (-)NCBICHM1_1
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)NCBIT2T-CHM13v2.0
Cdh16
(Mus musculus - house mouse)
Mouse AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCm398105,328,547 - 105,351,028 (-)NCBIGRCm39GRCm39mm39
GRCm39 Ensembl8105,328,543 - 105,351,028 (-)EnsemblGRCm39 Ensembl
GRCm388104,601,915 - 104,624,396 (-)NCBIGRCm38GRCm38mm10GRCm38
GRCm38.p6 Ensembl8104,601,911 - 104,624,396 (-)EnsemblGRCm38mm10GRCm38
MGSCv378107,138,047 - 107,148,161 (-)NCBIGRCm37MGSCv37mm9NCBIm37
MGSCv368107,503,276 - 107,513,390 (-)NCBIMGSCv36mm8
Celera8108,846,745 - 108,856,860 (-)NCBICelera
Cytogenetic Map8D3NCBI
cM Map853.04NCBI
Cdh16
(Rattus norvegicus - Norway rat)
Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCr819367,202 - 377,710 (+)NCBIGRCr8
mRatBN7.219360,824 - 371,008 (+)NCBImRatBN7.2mRatBN7.2
mRatBN7.2 Ensembl19360,824 - 371,007 (+)EnsemblmRatBN7.2 Ensembl
UTH_Rnor_SHR_Utx19348,915 - 359,097 (+)NCBIRnor_SHRUTH_Rnor_SHR_Utx
UTH_Rnor_SHRSP_BbbUtx_1.0191,115,720 - 1,125,902 (+)NCBIRnor_SHRSPUTH_Rnor_SHRSP_BbbUtx_1.0
UTH_Rnor_WKY_Bbb_1.019390,913 - 401,095 (+)NCBIRnor_WKYUTH_Rnor_WKY_Bbb_1.0
Rnor_6.019568,329 - 578,513 (+)NCBIRnor6.0Rnor_6.0rn6Rnor6.0
Rnor_6.0 Ensembl19568,287 - 578,520 (+)EnsemblRnor6.0rn6Rnor6.0
Rnor_5.019562,589 - 572,773 (+)NCBIRnor5.0Rnor_5.0rn5Rnor5.0
RGSC_v3.419279,359 - 289,543 (+)NCBIRGSC3.4RGSC_v3.4rn4RGSC3.4
RGSC_v3.119279,358 - 289,542 (+)NCBI
Celera19357,030 - 367,220 (+)NCBICelera
Cytogenetic Map19p14NCBI
Cdh16
(Chinchilla lanigera - long-tailed chinchilla)
Chinchilla AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChiLan1.0 EnsemblNW_00495543323,413,349 - 23,423,323 (-)EnsemblChiLan1.0
ChiLan1.0NW_00495543323,413,904 - 23,423,324 (-)NCBIChiLan1.0ChiLan1.0
CDH16
(Pan paniscus - bonobo/pygmy chimpanzee)
Bonobo AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
NHGRI_mPanPan1-v21876,408,051 - 76,418,829 (-)NCBINHGRI_mPanPan1-v2
NHGRI_mPanPan11682,320,586 - 82,331,361 (-)NCBINHGRI_mPanPan1
Mhudiblu_PPA_v01647,223,506 - 47,234,305 (-)NCBIMhudiblu_PPA_v0Mhudiblu_PPA_v0panPan3
PanPan1.11666,325,345 - 66,336,573 (-)NCBIpanpan1.1PanPan1.1panPan2
PanPan1.1 Ensembl1666,325,615 - 66,335,657 (-)Ensemblpanpan1.1panPan2
CDH16
(Canis lupus familiaris - dog)
Dog AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
CanFam3.1582,398,443 - 82,417,807 (+)NCBICanFam3.1CanFam3.1canFam3CanFam3.1
CanFam3.1 Ensembl582,398,541 - 82,408,061 (+)EnsemblCanFam3.1canFam3CanFam3.1
Dog10K_Boxer_Tasha582,387,135 - 82,406,493 (+)NCBIDog10K_Boxer_Tasha
ROS_Cfam_1.0582,835,051 - 82,854,428 (+)NCBIROS_Cfam_1.0
ROS_Cfam_1.0 Ensembl582,835,148 - 82,844,668 (+)EnsemblROS_Cfam_1.0 Ensembl
UMICH_Zoey_3.1582,658,232 - 82,677,589 (+)NCBIUMICH_Zoey_3.1
UNSW_CanFamBas_1.0582,345,049 - 82,364,362 (+)NCBIUNSW_CanFamBas_1.0
UU_Cfam_GSD_1.0582,984,014 - 83,003,379 (+)NCBIUU_Cfam_GSD_1.0
Cdh16
(Ictidomys tridecemlineatus - thirteen-lined ground squirrel)
Squirrel AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HiC_Itri_2NW_02440934942,419,995 - 42,428,117 (+)NCBIHiC_Itri_2
SpeTri2.0NW_00493647517,161,228 - 17,169,113 (-)NCBISpeTri2.0SpeTri2.0SpeTri2.0
CDH16
(Sus scrofa - pig)
Pig AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
Sscrofa11.1 Ensembl627,589,184 - 27,598,987 (-)EnsemblSscrofa11.1susScr11Sscrofa11.1
Sscrofa11.1627,589,183 - 27,599,002 (-)NCBISscrofa11.1Sscrofa11.1susScr11Sscrofa11.1
CDH16
(Chlorocebus sabaeus - green monkey)
Green Monkey AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
ChlSab1.1552,607,436 - 52,618,645 (-)NCBIChlSab1.1ChlSab1.1chlSab2
ChlSab1.1 Ensembl552,607,396 - 52,618,310 (-)EnsemblChlSab1.1ChlSab1.1 EnsemblchlSab2
Vero_WHO_p1.0NW_02366604723,295,627 - 23,306,554 (+)NCBIVero_WHO_p1.0Vero_WHO_p1.0
Cdh16
(Heterocephalus glaber - naked mole-rat)
Naked Mole-Rat AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
HetGla_female_1.0 EnsemblNW_00462474619,590,445 - 19,602,672 (+)EnsemblHetGla_female_1.0HetGla_female_1.0 EnsemblhetGla2
HetGla 1.0NW_00462474619,590,590 - 19,600,101 (+)NCBIHetGla_female_1.0HetGla 1.0hetGla2

Variants

.
Variants in CDH16
37 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(chr16:62179331-67770414)x1 copy number loss See cases [RCV000053333] Chr16:62179331..67770414 [GRCh38]
Chr16:62213235..67804317 [GRCh37]
Chr16:60770736..66361818 [NCBI36]
Chr16:16q21-22.1		 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
GRCh38/hg38 16q22.1(chr16:66694180-67865445)x1 copy number loss See cases [RCV000053336] Chr16:66694180..67865445 [GRCh38]
Chr16:66728083..67899348 [GRCh37]
Chr16:65285584..66456849 [NCBI36]
Chr16:16q22.1		 pathogenic
NM_001204744.1(CDH16):c.2105C>T (p.Ser702Phe) single nucleotide variant Malignant melanoma [RCV000071178] Chr16:66910090 [GRCh38]
Chr16:66943993 [GRCh37]
Chr16:65501494 [NCBI36]
Chr16:16q22.1		 not provided
NM_001204744.1(CDH16):c.558G>A (p.Leu186=) single nucleotide variant Malignant melanoma [RCV000071179] Chr16:66915245 [GRCh38]
Chr16:66949148 [GRCh37]
Chr16:65506649 [NCBI36]
Chr16:16q22.1		 not provided
GRCh38/hg38 16q21-22.1(chr16:66245888-67473023)x1 copy number loss See cases [RCV000134709] Chr16:66245888..67473023 [GRCh38]
Chr16:66279791..67506926 [GRCh37]
Chr16:64837292..66064427 [NCBI36]
Chr16:16q21-22.1		 pathogenic
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 16q22.1(chr16:66893204-67357178)x3 copy number gain See cases [RCV000137368] Chr16:66893204..67357178 [GRCh38]
Chr16:66927107..67391081 [GRCh37]
Chr16:65484608..65948582 [NCBI36]
Chr16:16q22.1		 likely pathogenic|uncertain significance
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 Breast ductal adenocarcinoma [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 Breast ductal adenocarcinoma [RCV000207067] Chr16:55359026..70884455 [GRCh37]
Chr16:16q12.2-22.2		 likely pathogenic|uncertain significance
Single allele complex Breast ductal adenocarcinoma [RCV000207314] Chr16:56368689..90141355 [GRCh37]
Chr16:16q12.2-24.3		 uncertain significance
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 16q21-22.1(chr16:66537021-67369281)x3 copy number gain See cases [RCV000510388] Chr16:66537021..67369281 [GRCh37]
Chr16:16q21-22.1		 uncertain significance
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 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 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 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 16q13-24.3(chr16:57051473-89797669)x3 copy number gain See cases [RCV000512511] Chr16:57051473..89797669 [GRCh37]
Chr16:16q13-24.3		 pathogenic
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 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
NM_004062.4(CDH16):c.849T>C (p.Asn283=) single nucleotide variant not provided [RCV000919498] Chr16:66913545 [GRCh38]
Chr16:66947448 [GRCh37]
Chr16:16q22.1		 likely benign
NM_004062.4(CDH16):c.2150G>A (p.Arg717His) single nucleotide variant not provided [RCV000966011] Chr16:66910277 [GRCh38]
Chr16:66944180 [GRCh37]
Chr16:16q22.1		 benign
NM_004062.4(CDH16):c.129+8G>A single nucleotide variant not provided [RCV000902116] Chr16:66917634 [GRCh38]
Chr16:66951537 [GRCh37]
Chr16:16q22.1		 benign
GRCh37/hg19 16q22.1(chr16:66797153-67109495)x3 copy number gain not provided [RCV000848721] Chr16:66797153..67109495 [GRCh37]
Chr16:16q22.1		 uncertain significance
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(chr16:66876199-67150370)x3 copy number gain not provided [RCV000846681] Chr16:66876199..67150370 [GRCh37]
Chr16:16q22.1		 uncertain significance
NC_000016.9:g.(?_65821800)_(67208957_?)del deletion Cataract 5 multiple types [RCV003107427]|not provided [RCV003122561] Chr16:65821800..67208957 [GRCh37]
Chr16:16q21-22.1		 pathogenic|no classifications from unflagged records
NM_004062.4(CDH16):c.1131C>T (p.Leu377=) single nucleotide variant not provided [RCV000894225] Chr16:66912815 [GRCh38]
Chr16:66946718 [GRCh37]
Chr16:16q22.1		 benign
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
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_004062.4(CDH16):c.1420G>A (p.Ala474Thr) single nucleotide variant Inborn genetic diseases [RCV002774509] Chr16:66912370 [GRCh38]
Chr16:66946273 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1153G>A (p.Gly385Arg) single nucleotide variant Inborn genetic diseases [RCV002879900] Chr16:66912793 [GRCh38]
Chr16:66946696 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1979C>T (p.Pro660Leu) single nucleotide variant Inborn genetic diseases [RCV002837160] Chr16:66910448 [GRCh38]
Chr16:66944351 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.986A>G (p.Glu329Gly) single nucleotide variant Inborn genetic diseases [RCV002818405] Chr16:66913199 [GRCh38]
Chr16:66947102 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1484C>G (p.Thr495Arg) single nucleotide variant Inborn genetic diseases [RCV002774224] Chr16:66912306 [GRCh38]
Chr16:66946209 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1646C>A (p.Ala549Asp) single nucleotide variant Inborn genetic diseases [RCV002777173] Chr16:66912043 [GRCh38]
Chr16:66945946 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1774A>G (p.Ile592Val) single nucleotide variant Inborn genetic diseases [RCV002752077] Chr16:66911915 [GRCh38]
Chr16:66945818 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1435C>T (p.Leu479Phe) single nucleotide variant Inborn genetic diseases [RCV002752710] Chr16:66912355 [GRCh38]
Chr16:66946258 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1438G>A (p.Glu480Lys) single nucleotide variant Inborn genetic diseases [RCV002945242] Chr16:66912352 [GRCh38]
Chr16:66946255 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.830C>T (p.Pro277Leu) single nucleotide variant Inborn genetic diseases [RCV002974061] Chr16:66913564 [GRCh38]
Chr16:66947467 [GRCh37]
Chr16:16q22.1		 likely benign
NM_004062.4(CDH16):c.1451G>A (p.Arg484His) single nucleotide variant Inborn genetic diseases [RCV002689864] Chr16:66912339 [GRCh38]
Chr16:66946242 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.161A>T (p.Gln54Leu) single nucleotide variant Inborn genetic diseases [RCV002692900] Chr16:66916398 [GRCh38]
Chr16:66950301 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.2246A>G (p.Asn749Ser) single nucleotide variant Inborn genetic diseases [RCV002950030] Chr16:66910015 [GRCh38]
Chr16:66943918 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1913C>T (p.Ala638Val) single nucleotide variant Inborn genetic diseases [RCV002844783] Chr16:66911193 [GRCh38]
Chr16:66945096 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.441C>G (p.Phe147Leu) single nucleotide variant Inborn genetic diseases [RCV002704561] Chr16:66915362 [GRCh38]
Chr16:66949265 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.2338A>G (p.Met780Val) single nucleotide variant Inborn genetic diseases [RCV002666266] Chr16:66909321 [GRCh38]
Chr16:66943224 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1166G>A (p.Arg389Lys) single nucleotide variant Inborn genetic diseases [RCV002919710] Chr16:66912780 [GRCh38]
Chr16:66946683 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.920G>C (p.Arg307Pro) single nucleotide variant Inborn genetic diseases [RCV002742573] Chr16:66913265 [GRCh38]
Chr16:66947168 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1258A>G (p.Met420Val) single nucleotide variant Inborn genetic diseases [RCV002983265] Chr16:66912688 [GRCh38]
Chr16:66946591 [GRCh37]
Chr16:16q22.1		 likely benign
NM_004062.4(CDH16):c.553C>T (p.Arg185Trp) single nucleotide variant Inborn genetic diseases [RCV002764969] Chr16:66915250 [GRCh38]
Chr16:66949153 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.451T>C (p.Ser151Pro) single nucleotide variant Inborn genetic diseases [RCV002891870] Chr16:66915352 [GRCh38]
Chr16:66949255 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1531A>G (p.Arg511Gly) single nucleotide variant Inborn genetic diseases [RCV002920795] Chr16:66912259 [GRCh38]
Chr16:66946162 [GRCh37]
Chr16:16q22.1		 likely benign
NM_004062.4(CDH16):c.56A>T (p.Lys19Met) single nucleotide variant Inborn genetic diseases [RCV002896158] Chr16:66917715 [GRCh38]
Chr16:66951618 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.2444A>G (p.Asp815Gly) single nucleotide variant Inborn genetic diseases [RCV002792530] Chr16:66908438 [GRCh38]
Chr16:66942341 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1511A>T (p.Glu504Val) single nucleotide variant Inborn genetic diseases [RCV002959279] Chr16:66912279 [GRCh38]
Chr16:66946182 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.41C>T (p.Pro14Leu) single nucleotide variant Inborn genetic diseases [RCV002723044] Chr16:66918025 [GRCh38]
Chr16:66951928 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1271G>A (p.Gly424Asp) single nucleotide variant Inborn genetic diseases [RCV002723578] Chr16:66912675 [GRCh38]
Chr16:66946578 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1328A>G (p.Asn443Ser) single nucleotide variant Inborn genetic diseases [RCV003202970] Chr16:66912535 [GRCh38]
Chr16:66946438 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1941C>A (p.Ser647Arg) single nucleotide variant Inborn genetic diseases [RCV003205190] Chr16:66910486 [GRCh38]
Chr16:66944389 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.367G>T (p.Val123Leu) single nucleotide variant Inborn genetic diseases [RCV003308847] Chr16:66916122 [GRCh38]
Chr16:66950025 [GRCh37]
Chr16:16q22.1		 uncertain significance
NM_004062.4(CDH16):c.1103C>A (p.Ser368Tyr) single nucleotide variant Inborn genetic diseases [RCV003348507] Chr16:66912843 [GRCh38]
Chr16:66946746 [GRCh37]
Chr16:16q22.1		 uncertain significance
GRCh37/hg19 16q21-22.1(chr16:66110708-67240652)x3 copy number gain not provided [RCV003485115] Chr16:66110708..67240652 [GRCh37]
Chr16:16q21-22.1		 uncertain significance
GRCh37/hg19 16q12.2-22.1(chr16:55329260-67180113)x1 copy number loss not specified [RCV003987196] Chr16:55329260..67180113 [GRCh37]
Chr16:16q12.2-22.1		 pathogenic
miRNA Target Status

Predicted Target Of
Summary Value
Count of predictions:4503
Count of miRNA genes:930
Interacting mature miRNAs:1169
Transcripts:ENST00000299752, ENST00000394055, ENST00000565235, ENST00000565796, ENST00000567009, ENST00000567269, ENST00000568632, ENST00000568698, ENST00000570262
Prediction methods:Microtar, Miranda, Rnahybrid, Targetscan
Result types:miRGate_prediction

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

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


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 24
Medium 14 669 12 7 1 2 1 316 59 665 5 1
Low 285 206 145 122 110 94 342 171 172 16 308 97 30 11 323
Below cutoff 1653 2173 662 348 729 258 3268 1724 2289 24 829 559 96 844 2244 1

Sequence

Nucleotide Sequences
RefSeq Transcripts NM_001204744 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204745 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_001204746 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  NM_004062 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_005255770 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_011522807 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_047433490 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379373 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379374 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  XM_054379375 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
GenBank Nucleotide AC009084 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AF016272 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AI733140 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK075243 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225544 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK225552 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298255 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK298334 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AK313101 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  AY358911 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BC027912 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles
  BI759247 (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
  DC361453 (Get FASTA)   NCBI Sequence Viewer   Search GEO for Microarray Profiles

Reference Sequences
RefSeq Acc Id: ENST00000299752   ⟹   ENSP00000299752
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,908,122 - 66,918,885 (-)Ensembl
RefSeq Acc Id: ENST00000394055   ⟹   ENSP00000377619
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,908,122 - 66,918,917 (-)Ensembl
RefSeq Acc Id: ENST00000565235   ⟹   ENSP00000463451
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,915,220 - 66,918,847 (-)Ensembl
RefSeq Acc Id: ENST00000565796   ⟹   ENSP00000454784
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,908,129 - 66,918,848 (-)Ensembl
RefSeq Acc Id: ENST00000567009   ⟹   ENSP00000460891
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,913,185 - 66,916,396 (-)Ensembl
RefSeq Acc Id: ENST00000567269   ⟹   ENSP00000455523
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,908,129 - 66,918,884 (-)Ensembl
RefSeq Acc Id: ENST00000568632   ⟹   ENSP00000455263
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,908,123 - 66,918,848 (-)Ensembl
RefSeq Acc Id: ENST00000568698   ⟹   ENSP00000456891
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,908,133 - 66,918,852 (-)Ensembl
RefSeq Acc Id: ENST00000570262   ⟹   ENSP00000456690
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh38.p14 Ensembl1666,908,124 - 66,918,876 (-)Ensembl
RefSeq Acc Id: NM_001204744   ⟹   NP_001191673
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,908,122 - 66,918,885 (-)NCBI
GRCh371666,942,025 - 66,952,887 (-)ENTREZGENE
HuRef1652,816,134 - 52,826,996 (-)ENTREZGENE
CHM1_11668,349,034 - 68,359,895 (-)NCBI
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001204745   ⟹   NP_001191674
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,908,122 - 66,918,885 (-)NCBI
GRCh371666,942,025 - 66,952,887 (-)ENTREZGENE
HuRef1652,816,134 - 52,826,996 (-)ENTREZGENE
CHM1_11668,349,034 - 68,359,895 (-)NCBI
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)NCBI
Sequence:
RefSeq Acc Id: NM_001204746   ⟹   NP_001191675
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,908,122 - 66,918,885 (-)NCBI
GRCh371666,942,025 - 66,952,887 (-)ENTREZGENE
HuRef1652,816,134 - 52,826,996 (-)ENTREZGENE
CHM1_11668,349,034 - 68,359,895 (-)NCBI
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)NCBI
Sequence:
RefSeq Acc Id: NM_004062   ⟹   NP_004053
RefSeq Status: REVIEWED
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,908,122 - 66,918,885 (-)NCBI
GRCh371666,942,025 - 66,952,887 (-)ENTREZGENE
Build 361665,499,526 - 65,510,267 (-)NCBI Archive
HuRef1652,816,134 - 52,826,996 (-)ENTREZGENE
CHM1_11668,349,034 - 68,359,895 (-)NCBI
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)NCBI
Sequence:
RefSeq Acc Id: XM_005255770   ⟹   XP_005255827
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,908,122 - 66,916,154 (-)NCBI
GRCh371666,942,025 - 66,952,887 (-)NCBI
Sequence:
RefSeq Acc Id: XM_011522807   ⟹   XP_011521109
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,908,122 - 66,918,885 (-)NCBI
Sequence:
RefSeq Acc Id: XM_047433490   ⟹   XP_047289446
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,908,122 - 66,918,885 (-)NCBI
RefSeq Acc Id: XM_054379373   ⟹   XP_054235348
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)NCBI
RefSeq Acc Id: XM_054379374   ⟹   XP_054235349
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01672,702,422 - 72,713,185 (-)NCBI
RefSeq Acc Id: XM_054379375   ⟹   XP_054235350
Type: CODING
Position:
Human AssemblyChrPosition (strand)Source
T2T-CHM13v2.01672,702,422 - 72,710,454 (-)NCBI
Reference Protein Sequences
RefSeq Acc Id: NP_001191675   ⟸   NM_001204746
- Peptide Label: isoform 4 precursor
- UniProtKB: B2R7S8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191674   ⟸   NM_001204745
- Peptide Label: isoform 3 precursor
- UniProtKB: B2R7S8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_001191673   ⟸   NM_001204744
- Peptide Label: isoform 2 precursor
- UniProtKB: B2R7S8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: NP_004053   ⟸   NM_004062
- Peptide Label: isoform 1 precursor
- UniProtKB: H3BPD3 (UniProtKB/Swiss-Prot),   B4DPA8 (UniProtKB/Swiss-Prot),   Q6UW93 (UniProtKB/Swiss-Prot),   O75309 (UniProtKB/Swiss-Prot),   B2R7S8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_005255827   ⟸   XM_005255770
- Peptide Label: isoform X3
- UniProtKB: H3BSG2 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: XP_011521109   ⟸   XM_011522807
- Peptide Label: isoform X1
- UniProtKB: B2R7S8 (UniProtKB/TrEMBL)
- Sequence:
RefSeq Acc Id: ENSP00000456690   ⟸   ENST00000570262
RefSeq Acc Id: ENSP00000299752   ⟸   ENST00000299752
RefSeq Acc Id: ENSP00000463451   ⟸   ENST00000565235
RefSeq Acc Id: ENSP00000454784   ⟸   ENST00000565796
RefSeq Acc Id: ENSP00000377619   ⟸   ENST00000394055
RefSeq Acc Id: ENSP00000460891   ⟸   ENST00000567009
RefSeq Acc Id: ENSP00000455523   ⟸   ENST00000567269
RefSeq Acc Id: ENSP00000456891   ⟸   ENST00000568698
RefSeq Acc Id: ENSP00000455263   ⟸   ENST00000568632
RefSeq Acc Id: XP_047289446   ⟸   XM_047433490
- Peptide Label: isoform X2
- UniProtKB: H3BSG2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054235349   ⟸   XM_054379374
- Peptide Label: isoform X2
- UniProtKB: H3BSG2 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054235348   ⟸   XM_054379373
- Peptide Label: isoform X1
- UniProtKB: B2R7S8 (UniProtKB/TrEMBL)
RefSeq Acc Id: XP_054235350   ⟸   XM_054379375
- Peptide Label: isoform X3
- UniProtKB: H3BSG2 (UniProtKB/TrEMBL)
Protein Domains
Cadherin

Protein Structures
Name Modeler Protein Id AA Range Protein Structure
AF-O75309-F1-model_v2 AlphaFold O75309 1-829 view protein structure

Promoters
RGD ID:7232455
Promoter ID:EPDNEW_H21973
Type:initiation region
Name:CDH16_1
Description:cadherin 16
SO ACC ID:SO:0000170
Source:EPDNEW (Eukaryotic Promoter Database, http://epd.vital-it.ch/)
Experiment Methods:Single-end sequencing.
Position:
Human AssemblyChrPosition (strand)Source
GRCh381666,918,885 - 66,918,945EPDNEW

Additional Information

Database Acc Id Source(s)
AGR Gene HGNC:1755 AgrOrtholog
COSMIC CDH16 COSMIC
Ensembl Genes ENSG00000166589 Ensembl, ENTREZGENE, UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
Ensembl Transcript ENST00000299752 ENTREZGENE
  ENST00000299752.9 UniProtKB/Swiss-Prot
  ENST00000394055 ENTREZGENE
  ENST00000394055.7 UniProtKB/Swiss-Prot
  ENST00000565235.2 UniProtKB/TrEMBL
  ENST00000565796 ENTREZGENE
  ENST00000565796.5 UniProtKB/Swiss-Prot
  ENST00000567009.5 UniProtKB/TrEMBL
  ENST00000567269.5 UniProtKB/TrEMBL
  ENST00000568632 ENTREZGENE
  ENST00000568632.5 UniProtKB/Swiss-Prot
  ENST00000568698.5 UniProtKB/TrEMBL
  ENST00000570262.5 UniProtKB/TrEMBL
Gene3D-CATH Cadherins UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
GTEx ENSG00000166589 GTEx
HGNC ID HGNC:1755 ENTREZGENE
Human Proteome Map CDH16 Human Proteome Map
InterPro Cadherin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin-like_dom UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin-like_sf UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  Cadherin_CS UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
KEGG Report hsa:1014 UniProtKB/Swiss-Prot
NCBI Gene 1014 ENTREZGENE
OMIM 603118 OMIM
PANTHER CADHERIN 16, KSP-CADHERIN UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  CADHERIN-23 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
  PTHR24027:SF443 UniProtKB/TrEMBL
Pfam Cadherin UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
PharmGKB PA26289 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 SSF49313 UniProtKB/Swiss-Prot, UniProtKB/TrEMBL
UniProt A0A0B4J288_HUMAN UniProtKB/TrEMBL
  B2R7S8 ENTREZGENE, UniProtKB/TrEMBL
  B4DPA8 ENTREZGENE
  CAD16_HUMAN UniProtKB/Swiss-Prot
  H3BPD3 ENTREZGENE
  H3BSG2 ENTREZGENE, UniProtKB/TrEMBL
  H3BSV3_HUMAN UniProtKB/TrEMBL
  I3L418_HUMAN UniProtKB/TrEMBL
  J3QLA1_HUMAN UniProtKB/TrEMBL
  O75309 ENTREZGENE
  Q6UW93 ENTREZGENE
UniProt Secondary B4DPA8 UniProtKB/Swiss-Prot
  H3BPD3 UniProtKB/Swiss-Prot
  Q6UW93 UniProtKB/Swiss-Prot


Nomenclature History
Date Current Symbol Current Name Previous Symbol Previous Name Description Reference Status
2015-12-08 CDH16  cadherin 16    cadherin 16, KSP-cadherin  Symbol and/or name change 5135510 APPROVED