Homo sapiens (human): 145258
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Entry
145258 CDS
T01001
Symbol
GSC, GSC1, SAMS
Name
(RefSeq) goosecoid homeobox
KO
K09324
homeobox protein goosecoid
Organism
hsa
Homo sapiens (human)
Disease
H02481
Syndromic disorder with short stature
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
145258 (GSC)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Homeo domain Paired-related
145258 (GSC)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Homeodomain
Homeobox_KN
Motif
Other DBs
NCBI-GeneID:
145258
NCBI-ProteinID:
NP_776248
OMIM:
138890
HGNC:
4612
Ensembl:
ENSG00000133937
UniProt:
P56915
Structure
PDB
PDBj
LinkDB
All DBs
Position
14:complement(94768223..94770113)
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AA seq
257 aa
AA seq
DB search
MPASMFSIDNILAARPRCKDSVLPVAHSAAAPVVFPALHGDSLYGASGGASSDYGAFYPR
PVAPGGAGLPAAVSGSRLGYNNYFYGQLHVQAAPVGPACCGAVPPLGAQQCSCVPTPPGY
EGPGSVLVSPVPHQMLPYMNVGTLSRTELQLLNQLHCRRKRRHRTIFTDEQLEALENLFQ
ETKYPDVGTREQLARKVHLREEKVEVWFKNRRAKWRRQKRSSSEESENAEKWNKTSSSKA
SPEKREEEGKSDLDSDS
NT seq
774 nt
NT seq
+upstream
nt +downstream
nt
atgcccgccagcatgttcagcatcgacaacatcctagccgcccggccgcgctgcaaggac
tcggtgttgccggtggcgcacagcgcggcggctcccgtcgtcttcccggccctgcacggg
gactcgctctacggcgccagcggcggcgcctcctcggactatggcgccttctacccgcgc
cccgtggcccccggcggcgcgggcctcccggccgcggtcagcggctcccgcctcggctac
aacaactacttctacgggcagctgcacgtgcaggcggcgcccgtgggcccggcctgctgc
ggggccgtgccgccgctgggcgcccagcagtgctcctgcgtcccgacgcccccaggctac
gagggccccggttcggtgctggtgtccccggtaccgcaccagatgctgccctacatgaac
gtgggcacgctgtcgcgcaccgagctgcagcttctcaaccagctgcactgtcggcggaag
cggcggcaccgcaccatcttcactgacgagcagctcgaagctctcgagaacctcttccag
gagaccaagtacccggacgtgggcacgcgcgagcagctggcccggaaagtgcacctccgc
gaggagaaagtggaggtctggtttaagaaccgccgcgccaaatggaggcggcagaagcgg
tcctcatcagaggagtcggagaacgcggagaagtggaacaagacgtcgtcgtcgaaggcg
tcaccggagaagagggaagaggaaggtaaaagcgatttggactcggacagctga
DBGET
integrated database retrieval system
