ENSG00000213892


Homo sapiens

Features
Gene ID: ENSG00000213892
  
Biological name :CEACAM16
  
Synonyms : carcinoembryonic antigen related cell adhesion molecule 16 / CEACAM16 / Q2WEN9
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 19
Strand: 1
Band: q13.31
Gene start: 44699151
Gene end: 44710714
  
Corresponding Affymetrix probe sets:
  
Cross references: Ensembl peptide - ENSP00000385576
Ensembl peptide - ENSP00000466561
NCBI entrez gene - 388551     See in Manteia.
OMIM - 614591
RefSeq - XM_017026795
RefSeq - NM_001039213
RefSeq Peptide - NP_001034302
swissprot - Q2WEN9
Ensembl - ENSG00000213892
  
Related genetic diseases (OMIM): 614614 - Deafness, autosomal dominant 4B, 614614
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 si:dkey-11o1.7ENSDARG00000105324Danio rerio
 E9QA28ENSMUSG00000014686Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
P13688 / CEACAM1 / carcinoembryonic antigen related cell adhesion molecule 1ENSG0000007938529
P06731 / CEACAM5 / carcinoembryonic antigen related cell adhesion molecule 5ENSG0000010538829
PSG9 / Q00887 / pregnancy specific beta-1-glycoprotein 9ENSG0000018366826
PSG3 / Q16557 / pregnancy specific beta-1-glycoprotein 3ENSG0000022182625
PSG4 / Q00888 / pregnancy specific beta-1-glycoprotein 4ENSG0000024313725
PSG6 / Q00889 / pregnancy specific beta-1-glycoprotein 6ENSG0000017084825
P40199 / CEACAM6 / carcinoembryonic antigen related cell adhesion molecule 6ENSG0000008654824
PSG8 / Q9UQ74 / pregnancy specific beta-1-glycoprotein 8ENSG0000012446724
PSG11 / Q9UQ72 / pregnancy specific beta-1-glycoprotein 11ENSG0000024313024
PSG1 / P11464 / pregnancy specific beta-1-glycoprotein 1ENSG0000023192424
PSG2 / P11465 / pregnancy specific beta-1-glycoprotein 2ENSG0000024222123
P31997 / CEACAM8 / carcinoembryonic antigen related cell adhesion molecule 8ENSG0000012446922
Q3KPI0 / CEACAM21 / carcinoembryonic antigen related cell adhesion molecule 21ENSG0000000712920
A8MTB9 / CEACAM18 / carcinoembryonic antigen related cell adhesion molecule 18ENSG0000021382219
PSG5 / Q15238 / pregnancy specific beta-1-glycoprotein 5ENSG0000020494118
CEACAM20 / carcinoembryonic antigen related cell adhesion molecule 20ENSG0000027377718
Q14002 / CEACAM7 / carcinoembryonic antigen related cell adhesion molecule 7ENSG0000000730618
PSG7 / pregnancy specific beta-1-glycoprotein 7 (gene/pseudogene)ENSG0000022187815
O75871 / CEACAM4 / carcinoembryonic antigen related cell adhesion molecule 4ENSG0000010535211
AC243967.1ENSG0000026788111


Protein motifs (from Interpro)
Interpro ID Name
 IPR003598  Immunoglobulin subtype 2
 IPR003599  Immunoglobulin subtype
 IPR007110  Immunoglobulin-like domain
 IPR013783  Immunoglobulin-like fold
 IPR036179  Immunoglobulin-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0007605 sensory perception of sound IMP
 cellular_componentGO:0005576 extracellular region IEA
 cellular_componentGO:0005615 extracellular space IDA
 cellular_componentGO:0032426 stereocilium tip ISS
 molecular_functionGO:0042802 identical protein binding IDA


Pathways (from Reactome)
Pathway description
No match


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000006 Autosomal dominant inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in heterozygotes. In the context of medical genetics, an autosomal dominant disorder is caused when a single copy of the mutant allele is present. Males and females are affected equally, and can both transmit the disorder with a risk of 50% for each child of inheriting the mutant allele." [HPO:curators]
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 HP:0000365 Hearing loss 
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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