Homo sapiens (human): 3047 Help 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) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Globin Motif Other DBs NCBI-GeneID:  3047 NCBI-ProteinID:  NP_000550 OMIM:  142200 HGNC:  4831 Ensembl:  ENSG00000213934 UniProt:  P69891 D9YZU8 Structure PDBPDBj LinkDB All DBs Position 11:complement(5248269..5249857) Genome browser AA seq 147 aa AA seqDB search MGHFTEEDKATITSLWGKVNVEDAGGETLGRLLVVYPWTQRFFDSFGNLSSASAIMGNPK VKAHGKKVLTSLGDATKHLDDLKGTFAQLSELHCDKLHVDPENFKLLGNVLVTVLAIHFG KEFTPEVQASWQKMVTAVASALSSRYH NT seq 444 nt NT seq  +upstreamnt  +downstreamnt atgggtcatttcacagaggaggacaaggctactatcacaagcctgtggggcaaggtgaat gtggaagatgctggaggagaaaccctgggaaggctcctggttgtctacccatggacccag aggttctttgacagctttggcaacctgtcctctgcctctgccatcatgggcaaccccaaa gtcaaggcacatggcaagaaggtgctgacttccttgggagatgccacaaagcacctggat gatctcaagggcacctttgcccagctgagtgaactgcactgtgacaagctgcatgtggat cctgagaacttcaagctcctgggaaatgtgctggtgaccgttttggcaatccatttcggc aaagaattcacccctgaggtgcaggcttcctggcagaagatggtgactgcagtggccagt gccctgtcctccagataccactga

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