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Grainyhead-like protein 2 homolog

Summary

UniProt ID

Q6ISB3

Gene Symbol

BOM
GRHL2
TFCP2L3

Gene ID

79977

Organism

Homo sapiens (human)

External Links

GlyGen: Q6ISB3
The O-GlcNAc Database: Q6ISB3
O-GlcNAcAtlas: Q6ISB3
Re-Glyco: Q6ISB3

Annotation

Keyword

3D-structure
Activator
Alternative splicing
Corneal dystrophy
DNA-binding
Disease variant
Dwarfism
Ectodermal dysplasia
Membrane
Non-syndromic deafness
Nucleus
Reference proteome
Transcription regulation

Gene Ontology (GO)

Displaying **all 5** entries
GO Term
chromatin
nucleus
cell-cell junction
membrane
nucleoplasm

Subcellular Location(GO Annotation)

Subcellular in which this glycoprotein is expressed are highlighted in blue.

Displaying entries **1 - 10** of 21 in total

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GO Term
regulation of transcription by RNA polymerase II
cell junction assembly
embryonic digit morphogenesis
camera-type eye development
embryonic cranial skeleton morphogenesis
lung epithelial cell differentiation
cardiac ventricle morphogenesis
multicellular organism growth
face development
bicellular tight junction assembly

Displaying **all 10** entries
GO Term
chromatin DNA binding
identical protein binding
sequence-specific DNA binding
DNA-binding transcription factor binding
intronic transcription regulatory region sequence-specific DNA binding
DNA-binding transcription activator activity
RNA polymerase II cis-regulatory region sequence-specific DNA binding
DNA-binding transcription factor activity, RNA polymerase II-specific
DNA-binding transcription activator activity, RNA polymerase II-specific
DNA-binding transcription factor activity

Annotation information from UniProt.

Sequence

MSQESDNNKRLVALVPMPSDPPFNTRRAYTSEDEAWKSYLENPLTAATKAMMSINGDEDSAAALGLLYDYYKVPRDKRLLSVSKASDSQEDQEKRNCLGTSEAQSNLSGGENRVQVLKTVPVNLSLNQDHLENSKREQYSISFPESSAIIPVSGITVVKAEDFTPVFMAPPVHYPRGDGEEQRVVIFEQTQYDVPSLATHSAYLKDDQRSTPDSTYSESFKDAATEKFRSASVGAEEYMYDQTSSGTFQYTLEATKSLRQKQGEGPMTYLNKGQFYAITLSETGDNKCFRHPISKVRSVVMVVFSEDKNRDEQLKYWKYWHSRQHTAKQRVLDIADYKESFNTIGNIEEIAYNAVSFTWDVNEEAKIFITVNCLSTDFSSQKGVKGLPLMIQIDTYSYNNRSNKPIHRAYCQIKVFCDKGAERKIRDEERKQNRKKGKGQASQTQCNSSSDGKLAAIPLQKKSDITYFKTMPDLHSQPVLFIPDVHFANLQRTGQVYYNTDDEREGGSVLVKRMFRPMEEEFGPVPSKQMKEEGTKRVLLYVRKETDDVFDALMLKSPTVKGLMEAISEKYGLPVEKIAKLYKKSKKGILVNMDDNIIEHYSNEDTFILNMESMVEGFKVTLMEI

N : N-glycosylation Site
___ : Potential Sequon

Glycosylation Sites

Displaying **all 4** entries
Position	GlyTouCan ID	Source
100	G49108TO	The O-GlcNAc Database
147	G49108TO	GlyGen
153	G49108TO	GlyGen The O-GlcNAc Database
156	G49108TO	The O-GlcNAc Database

Feature

: Glycosylation Site from GlyGen
: Glycosylation Site from UniProt

Disease

Displaying **all 2** entries
DO ID	Disease Name	Source
DOID:0080669	posterior polymorphous corneal dystrophy 4	Alliance of Genome Resources
DOID:0110557	autosomal dominant nonsyndromic deafness 28	Alliance of Genome Resources

GlyTouCan

GlyComb

GlycoPOST

UniCarb-DR

LM-GlycoRepo

All Resources

Other Information

Tools

Search Tools

Guidelines

Summary

External Links

Annotation

International Collaboration

Acknowledgements