KEGG   Homo sapiens (human): 3188
Entry
3188              CDS       T01001                                 
Symbol
HNRNPH2, FTP3, HNRPH', HNRPH2, MRXSB, NRPH2, hnRNPH'
Name
(RefSeq) heterogeneous nuclear ribonucleoprotein H2
  KO
K12898  heterogeneous nuclear ribonucleoprotein F/H
Organism
hsa  Homo sapiens (human)
Disease
H00658  X-linked syndromic intellectual developmental disorder
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03041 Spliceosome [BR:hsa03041]
    3188 (HNRNPH2)
Spliceosome [BR:hsa03041]
 Complex C
  Other components
   hnRNP proteins
    3188 (HNRNPH2)
SSDB
Motif
Pfam: RRM_1 zf-RNPHF
Other DBs
NCBI-GeneID: 3188
NCBI-ProteinID: NP_001027565
OMIM: 300610
HGNC: 5042
Ensembl: ENSG00000126945
UniProt: P55795 A0A384MDT2
Structure
Position
X:101408222..101414133
AA seq 449 aa
MMLSTEGREGFVVKVRGLPWSCSADEVMRFFSDCKIQNGTSGIRFIYTREGRPSGEAFVE
LESEEEVKLALKKDRETMGHRYVEVFKSNSVEMDWVLKHTGPNSPDTANDGFVRLRGLPF
GCSKEEIVQFFSGLEIVPNGMTLPVDFQGRSTGEAFVQFASQEIAEKALKKHKERIGHRY
IEIFKSSRAEVRTHYDPPRKLMAMQRPGPYDRPGAGRGYNSIGRGAGFERMRRGAYGGGY
GGYDDYGGYNDGYGFGSDRFGRDLNYCFSGMSDHRYGDGGSSFQSTTGHCVHMRGLPYRA
TENDIYNFFSPLNPMRVHIEIGPDGRVTGEADVEFATHEDAVAAMAKDKANMQHRYVELF
LNSTAGTSGGAYDHSYVELFLNSTAGASGGAYGSQMMGGMGLSNQSSYGGPASQQLSGGY
GGGYGGQSSMSGYDQVLQENSSDYQSNLA
NT seq 1350 nt   +upstreamnt  +downstreamnt
atgatgctgagcacggaaggcagggaggggttcgtggtgaaggtcaggggcctaccctgg
tcctgctcagccgatgaagtgatgcgcttcttctctgattgcaagatccaaaatggcaca
tcaggtattcgtttcatctacaccagagaaggcagaccaagtggtgaagcatttgttgaa
cttgaatctgaagaggaagtgaaattggctttgaagaaggacagagaaaccatgggacac
agatacgttgaagtattcaagtctaacagtgttgaaatggattgggtgttgaagcataca
ggtccgaatagccctgatactgccaacgatggcttcgtccggcttagaggactcccattt
ggctgtagcaaggaagagattgttcagttcttttcagggttggaaattgtgccaaatggg
atgacactgccagtggactttcaggggcgaagcacaggggaagcctttgtgcagtttgct
tcacaggagatagctgagaaggccttaaagaaacacaaggaaagaatagggcacaggtac
attgagatcttcaagagtagccgagctgaagttcgaacccactatgatccccctcgaaag
ctcatggctatgcagcggccaggtccctatgataggccgggggctggcagagggtataat
agcattggcagaggagctgggtttgaaaggatgaggcgtggtgcctatggtggagggtat
ggaggctatgatgactatggtggctataatgatggatatggctttgggtctgatagattt
ggaagagacctcaattactgtttttcaggaatgtctgatcatagatacggagatggtggg
tccagtttccagagcaccacagggcactgtgtacacatgagggggttaccttacagagcc
actgagaatgatatttataatttcttctcacctcttaatcccatgagagtacatattgaa
attggacccgatggcagagttaccggtgaggcagatgttgaatttgctactcatgaagat
gctgtggcagctatggcaaaagacaaagctaatatgcaacacagatatgtggagctcttc
ttaaattctactgcaggaacaagtgggggtgcttacgatcacagctatgtagaacttttt
ttgaattctacagcaggggcaagtggtggcgcttatggtagccaaatgatgggagggatg
ggcttatccaaccagtctagttatggaggtcctgctagccagcagctgagtggtggttat
ggaggtggttatggtggtcagagcagtatgagtggatatgaccaagttctgcaggaaaac
tccagtgactatcagtcaaaccttgcttag

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