KEGG   Homo sapiens (human): 3047
Entry
3047              CDS       T01001                                 
Symbol
HBG1, HBG-T2, HBGA, HBGR, HSGGL1, PRO2979
Name
(RefSeq) hemoglobin subunit gamma 1
  KO
K13824  hemoglobin subunit gamma
Organism
hsa  Homo sapiens (human)
Disease
H00228  Thalassemia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99994 Others
    3047 (HBG1)
SSDB
Motif
Pfam: Globin
Other DBs
NCBI-GeneID: 3047
NCBI-ProteinID: NP_000550
OMIM: 142200
HGNC: 4831
Ensembl: ENSG00000213934
UniProt: P69891 D9YZU8
Structure
Position
11:complement(5248269..5249857)
AA seq 147 aa
MGHFTEEDKATITSLWGKVNVEDAGGETLGRLLVVYPWTQRFFDSFGNLSSASAIMGNPK
VKAHGKKVLTSLGDATKHLDDLKGTFAQLSELHCDKLHVDPENFKLLGNVLVTVLAIHFG
KEFTPEVQASWQKMVTAVASALSSRYH
NT seq 444 nt   +upstreamnt  +downstreamnt
atgggtcatttcacagaggaggacaaggctactatcacaagcctgtggggcaaggtgaat
gtggaagatgctggaggagaaaccctgggaaggctcctggttgtctacccatggacccag
aggttctttgacagctttggcaacctgtcctctgcctctgccatcatgggcaaccccaaa
gtcaaggcacatggcaagaaggtgctgacttccttgggagatgccacaaagcacctggat
gatctcaagggcacctttgcccagctgagtgaactgcactgtgacaagctgcatgtggat
cctgagaacttcaagctcctgggaaatgtgctggtgaccgttttggcaatccatttcggc
aaagaattcacccctgaggtgcaggcttcctggcagaagatggtgactgcagtggccagt
gccctgtcctccagataccactga

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Ontology (1)   
   KEGG BRITE (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (10)   
   KEGG ORTHOLOGY (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (4)   
   OC (1)   
Protein sequence (4)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (1)   
DNA sequence (9)   
   RefSeq(nuc) (1)   
   GenBank (4)   
   EMBL (4)   
3D Structure (2)   
   PDB (2)   
Protein domain (1)   
   Pfam (1)   
All databases (31)   

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