CEA cell adhesion molecule 16, tectorial membrane component (Q21132939)

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mammalian protein found in Homo sapiens

Carcinoembryonic antigen-like 2
CEACAM16
carcinoembryonic antigen-related cell adhesion molecule 16
carcinoembryonic antigen like-2 protein
carcinoembryonic antigen related cell adhesion molecule 16

Language	Label	Description	Also known as
English	CEA cell adhesion molecule 16, tectorial membrane component	mammalian protein found in Homo sapiens	Carcinoembryonic antigen-like 2 CEACAM16 carcinoembryonic antigen-related cell adhesion molecule 16 carcinoembryonic antigen like-2 protein carcinoembryonic antigen related cell adhesion molecule 16

Statements

1 reference

13 November 2019

UniProt protein ID

Immunoglobulin-like fold

1 reference

InterPro Release 71.0

http://www.ebi.ac.uk/interpro/protein/Q2WEN9

Immunoglobulin-like domain superfamily

1 reference

InterPro Release 71.0

http://www.ebi.ac.uk/interpro/protein/Q2WEN9

Immunoglobulin subtype, protein family

1 reference

based on heuristic

inferred from protein domain or family

Immunoglobulin subtype 2, protein family

1 reference

based on heuristic

inferred from protein domain or family

immunoglobulin-like domain, protein family

1 reference

based on heuristic

inferred from protein domain or family

1 reference

13 November 2019

UniProt protein ID

1 reference

13 November 2019

UniProt protein ID

molecular function

identical protein binding

determination method or standard

1 reference

8 April 2019

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

extracellular region

determination method or standard

1 reference

8 April 2019

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

extracellular space

determination method or standard

1 reference

27 March 2018

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q2WEN9&geneProductId=UniProtKB:Q2WEN9

determination method or standard

extracellular space

determination method or standard

stereocilium tip

determination method or standard

3 references

8 April 2019

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

8 April 2019

Ensembl genome database project

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

8 April 2019

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

biological process

determination method or standard

2 references

27 March 2018

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q2WEN9&geneProductId=UniProtKB:Q2WEN9

determination method or standard

27 March 2018

Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).

Mouse Genome Informatics

http://www.ebi.ac.uk/QuickGO/annotations?protein=Q2WEN9&geneProductId=UniProtKB:Q2WEN9

determination method or standard

determination method or standard

3 references

8 April 2019

Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family

UniProt protein ID

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

8 April 2019

Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).

Mouse Genome Informatics

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

8 April 2019

Phylogenetic-based propagation of functional annotations within the Gene Ontology consortium

http://www.ebi.ac.uk/QuickGO/annotations?geneProductId=UniProtKB:Q2WEN9

determination method or standard

immunoglobulin-like domain

1 reference

InterPro Release 71.0

http://www.ebi.ac.uk/interpro/protein/Q2WEN9

immunoglobulin subtype 2

1 reference

InterPro Release 71.0

http://www.ebi.ac.uk/interpro/protein/Q2WEN9

immunoglobulin subtype

1 reference

InterPro Release 71.0

http://www.ebi.ac.uk/interpro/protein/Q2WEN9

Identifiers

RefSeq protein ID

1 reference

30 May 2020

1 reference

30 May 2020

UniProt protein ID

1 reference

13 November 2019

UniProt protein ID

Ensembl protein ID

ENSP00000385576

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000385576

ENSP00000466561

1 reference

Ensembl Release 99

Ensembl protein ID

ENSP00000466561

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

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