Homo sapiens (human): 3048 Help Entry 3048              CDS       T01001                                  Symbol HBG2, HBG-T1, TNCY Name (RefSeq) hemoglobin subunit gamma 2   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     3048 (HBG2) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Globin Motif Other DBs NCBI-GeneID:  3048 NCBI-ProteinID:  NP_000175 OMIM:  142250 HGNC:  4832 Ensembl:  ENSG00000196565 UniProt:  P69892 D9YZU9 Structure PDBPDBj LinkDB All DBs Position 11:complement(5253188..5254781) Genome browser AA seq 147 aa AA seqDB search MGHFTEEDKATITSLWGKVNVEDAGGETLGRLLVVYPWTQRFFDSFGNLSSASAIMGNPK VKAHGKKVLTSLGDAIKHLDDLKGTFAQLSELHCDKLHVDPENFKLLGNVLVTVLAIHFG KEFTPEVQASWQKMVTGVASALSSRYH NT seq 444 nt NT seq  +upstreamnt  +downstreamnt atgggtcatttcacagaggaggacaaggctactatcacaagcctgtggggcaaggtgaat gtggaagatgctggaggagaaaccctgggaaggctcctggttgtctacccatggacccag aggttctttgacagctttggcaacctgtcctctgcctctgccatcatgggcaaccccaaa gtcaaggcacatggcaagaaggtgctgacttccttgggagatgccataaagcacctggat gatctcaagggcacctttgcccagctgagtgaactgcactgtgacaagctgcatgtggat cctgagaacttcaagctcctgggaaatgtgctggtgaccgttttggcaatccatttcggc aaagaattcacccctgaggtgcaggcttcctggcagaagatggtgactggagtggccagt gccctgtcctccagataccactga

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