Homo sapiens (human): 9247
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Entry
9247 CDS
T01001
Symbol
GCM2, FIH2, GCMB, HRPT4, hGCMb
Name
(RefSeq) glial cells missing transcription factor 2
KO
K21598
chorion-specific transcription factor GCM
Organism
hsa
Homo sapiens (human)
Pathway
hsa04928
Parathyroid hormone synthesis, secretion and action
Network
nt06318
CaSR-PTH signaling
Element
N00293
GCM2-mediated transcription
Disease
H00246
Primary hyperparathyroidism
H01862
Hypoparathyroidism
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09152 Endocrine system
04928 Parathyroid hormone synthesis, secretion and action
9247 (GCM2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
9247 (GCM2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Other transcription factors
Others
9247 (GCM2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
GCM
Motif
Other DBs
NCBI-GeneID:
9247
NCBI-ProteinID:
NP_004743
OMIM:
603716
HGNC:
4198
Ensembl:
ENSG00000124827
UniProt:
O75603
LinkDB
All DBs
Position
6:complement(10873223..10882041)
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AA seq
506 aa
AA seq
DB search
MPAAAVQEAVGVCSYGMQLSWDINDPQMPQELALFDQFREWPDGYVRFIYSSDEKKAQRH
LSGWAMRNTNNHNGHILKKSCLGVVVCTQACTLPDGSRLQLRPAICDKARLKQQKKACPN
CHSALELIPCRGHSGYPVTNFWRLDGNAIFFQAKGVHDHPRPESKSETEARRSAIKRQMA
SFYQPQKKRIRESEAEENQDSSGHFSNIPPLENPEDFDIVTETSFPIPGQPCPSFPKSDV
YKATCDLATFQGDKMPPFQKYSSPRIYLPRPPCSYELANPGYTNSSPYPTLYKDSTSIPN
DTDWVHLNTLQCNVNSYSSYERSFDFTNKQHGWKPALGKPSLVERTNHGQFQAMATRPYY
NPELPCRYLTTPPPGAPALQTVITTTTKVSYQAYQPPAMKYSDSVREVKSLSSCNYAPED
TGMSVYPEPWGPPVTVTRAASPSGPPPMKIAGDCRAIRPTVAIPHEPVSSRTDEAETWDV
CLSGLGSAVSYSDRVGPFFTYNNEDF
NT seq
1521 nt
NT seq
+upstream
nt +downstream
nt
atgccggcggccgcggtgcaggaagcggtcggcgtgtgctcctacgggatgcagctcagc
tgggacatcaacgatccgcagatgcctcaggagctggccctctttgaccaattccgagag
tggcctgacggctatgtgcgcttcatctacagcagcgatgagaagaaggcacagcgtcac
ctgagcggctgggccatgcgcaacaccaacaaccacaatggccacatcctcaagaagtcg
tgcctgggtgtggtggtgtgtacacaggcctgcaccctgcccgacggttcccgcctgcag
ctgaggccggccatctgcgacaaggcacggctgaaacagcagaagaaggcatgccctaac
tgtcattctgctttggagttgattccttgtcgagggcacagcggataccccgtaaccaac
ttttggcggcttgatggcaacgcgatcttttttcaggccaagggagttcatgatcatcca
agaccagagagcaaatcagagacagaagctagaagaagcgccatcaagagacaaatggcc
tctttctaccaaccccagaaaaagagaattcgagaatccgaggcagaagaaaatcaagac
agcagtggtcatttcagcaacatacctcccttggaaaatccagaagactttgatatagtt
actgaaaccagcttccctattccagggcagccttgcccttccttcccaaagtctgatgtt
tacaaagctacctgtgacctagccacctttcaaggagacaaaatgccacccttccagaaa
tactcaagcccaagaatctatttgcctaggccaccttgcagctatgaattggcaaaccct
ggttatacaaattcaagcccatatcccaccctttataaggattccaccagtatccctaat
gacacagactgggttcatctgaacacactacaatgtaatgtcaattcatacagcagctat
gagagaagctttgatttcaccaacaaacagcatggctggaaaccagctcttggaaaaccc
agccttgtggaaaggactaaccatgggcagtttcaggccatggccactcgcccttattat
aacccagagcttccctgcaggtacctcacgactccaccaccaggtgcccctgccctacaa
accgtgatcaccaccaccactaaagtgtcctaccaggcctaccagccccctgctatgaaa
tacagtgacagtgtgcgagaggtgaagagcctttcgagctgtaactatgctcctgaagat
actgggatgtctgtctatccagaaccctggggtcctccggtgacagtcaccagggcagcc
tctccttcagggccacctcctatgaaaattgcaggagattgccgggccatcagacccact
gtggctattccccacgagccagtttcctctaggacagatgaagcagagacttgggatgtg
tgtctgtctgggctgggctccgcagtcagttactcagacagagtgggtcccttctttacc
tacaacaatgaggatttttga
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