Homo sapiens (human): 79977
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Entry
79977 CDS
T01001
Symbol
GRHL2, BOM, DFNA28, ECTDS, PPCD4, TFCP2L3
Name
(RefSeq) grainyhead-like protein 2 homolog isoform 1
KO
K09275
transcription factor CP2 and related proteins
Organism
hsa
Homo sapiens (human)
Disease
H00604
Deafness, autosomal dominant
H00961
Posterior polymorphous corneal dystrophy
H03029
Ectodermal dysplasia/short stature syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
79977 (GRHL2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
beta-Scaffold factors with minor groove contacts
Grainyhead
79977 (GRHL2)
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
CP2
GRHL1_C
Sp-DndD
Motif
Other DBs
NCBI-GeneID:
79977
NCBI-ProteinID:
NP_079191
OMIM:
608576
HGNC:
2799
Ensembl:
ENSP00000495564.1
UniProt:
Q6ISB3
Structure
PDB
PDBj
LinkDB
All DBs
Position
8:101492439..101681200
Genome browser
AA seq
625 aa
AA seq
DB search
MSQESDNNKRLVALVPMPSDPPFNTRRAYTSEDEAWKSYLENPLTAATKAMMSINGDEDS
AAALGLLYDYYKVPRDKRLLSVSKASDSQEDQEKRNCLGTSEAQSNLSGGENRVQVLKTV
PVNLSLNQDHLENSKREQYSISFPESSAIIPVSGITVVKAEDFTPVFMAPPVHYPRGDGE
EQRVVIFEQTQYDVPSLATHSAYLKDDQRSTPDSTYSESFKDAATEKFRSASVGAEEYMY
DQTSSGTFQYTLEATKSLRQKQGEGPMTYLNKGQFYAITLSETGDNKCFRHPISKVRSVV
MVVFSEDKNRDEQLKYWKYWHSRQHTAKQRVLDIADYKESFNTIGNIEEIAYNAVSFTWD
VNEEAKIFITVNCLSTDFSSQKGVKGLPLMIQIDTYSYNNRSNKPIHRAYCQIKVFCDKG
AERKIRDEERKQNRKKGKGQASQTQCNSSSDGKLAAIPLQKKSDITYFKTMPDLHSQPVL
FIPDVHFANLQRTGQVYYNTDDEREGGSVLVKRMFRPMEEEFGPVPSKQMKEEGTKRVLL
YVRKETDDVFDALMLKSPTVKGLMEAISEKYGLPVEKIAKLYKKSKKGILVNMDDNIIEH
YSNEDTFILNMESMVEGFKVTLMEI
NT seq
1878 nt
NT seq
+upstream
nt +downstream
nt
atgtcacaagagtcggacaataataaaagactagtggccttagtgcccatgcccagtgac
cctccattcaatacccgaagagcctacaccagtgaggatgaagcctggaagtcatacttg
gagaatcccctgacagcagccaccaaggccatgatgagcattaatggtgatgaggacagt
gctgctgccctcggcctgctctatgactactacaaggttcctcgagacaagaggctgctg
tctgtaagcaaagcaagtgacagccaagaagaccaggagaaaagaaactgccttggcacc
agtgaagcccagagtaatttgagtggaggagaaaaccgagtgcaagtcctaaagactgtt
ccagtgaacctttccctaaatcaagatcacctggagaattccaagcgggaacagtacagc
atcagcttccccgagagctctgccatcatcccggtgtcgggaatcacggtggtgaaagct
gaagatttcacaccagttttcatggccccacctgtgcactatccccggggagatggggaa
gagcaacgagtggttatctttgaacagactcagtatgacgtgccctcgctggccacccac
agcgcctatctcaaagacgaccagcgcagcactccggacagcacatacagcgagagcttc
aaggacgcagccacagagaaatttcggagtgcttcagttggggctgaggagtacatgtat
gatcagacatcaagtggcacatttcagtacaccctggaagccaccaaatctctccgtcag
aagcagggggagggccccatgacctacctcaacaaaggacagttctatgccataacactc
agcgagaccggagacaacaaatgcttccgacaccccatcagcaaagtcaggagtgtggtg
atggtggtcttcagtgaagacaaaaacagagatgaacagctcaaatactggaaatactgg
cactctcggcagcatacggcgaagcagagggtccttgacattgccgattacaaggagagc
tttaatacgattggaaacattgaagagattgcatataatgctgtttcctttacctgggac
gtgaatgaagaggcgaagattttcatcaccgtgaattgcttgagcacagatttctcctcc
caaaaaggggtgaaaggacttcctttgatgattcagattgacacatacagttataacaat
cgtagcaataaacccattcatagagcttattgccagatcaaggtcttctgtgacaaagga
gcagaaagaaaaatccgagatgaagagcggaagcagaacaggaagaaagggaaaggccag
gcctcccaaactcaatgcaacagctcctctgatgggaagttggctgccatacctttacag
aagaagagtgacatcacctacttcaaaaccatgcctgatctccactcacagccagttctc
ttcatacctgatgttcactttgcaaacctgcagaggaccggacaggtgtattacaacacg
gatgatgaacgagaaggtggcagtgtccttgttaaacggatgttccggcccatggaagag
gagtttggtccagtgccttcaaagcagatgaaagaagaagggacaaagcgagtgctcttg
tacgtgaggaaggagactgacgatgtgttcgatgcattgatgttgaagtctcccacagtg
aagggcctgatggaagcgatatctgagaaatatgggctgcccgtggagaagatagcaaag
ctttacaagaaaagcaaaaaaggcatcttggtgaacatggatgacaacatcatcgagcac
tactcgaacgaggacaccttcatcctcaacatggagagcatggtggagggcttcaaggtc
acgctcatggaaatctag
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