KEGG   Homo sapiens (human): 3187
Entry
3187              CDS       T01001                                 
Symbol
HNRNPH1, HNRPH, HNRPH1, NEDCDS, hnRNPH
Name
(RefSeq) heterogeneous nuclear ribonucleoprotein H1
  KO
K12898  heterogeneous nuclear ribonucleoprotein F/H
Organism
hsa  Homo sapiens (human)
Disease
H02460  Neurodevelopmental disorder with dysmorphic facies and skeletal anomalies
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03041 Spliceosome [BR:hsa03041]
    3187 (HNRNPH1)
Spliceosome [BR:hsa03041]
 Complex C
  Other components
   hnRNP proteins
    3187 (HNRNPH1)
SSDB
Motif
Pfam: RRM_1 zf-RNPHF
Other DBs
NCBI-GeneID: 3187
NCBI-ProteinID: NP_001244222
OMIM: 601035
HGNC: 5041
Ensembl: ENSG00000169045
UniProt: P31943 A0A384MEJ3
Structure
Position
5:complement(179614178..179634784)
AA seq 449 aa
MMLGTEGGEGFVVKVRGLPWSCSADEVQRFFSDCKIQNGAQGIRFIYTREGRPSGEAFVE
LESEDEVKLALKKDRETMGHRYVEVFKSNNVEMDWVLKHTGPNSPDTANDGFVRLRGLPF
GCSKEEIVQFFSGLEIVPNGITLPVDFQGRSTGEAFVQFASQEIAEKALKKHKERIGHRY
IEIFKSSRAEVRTHYDPPRKLMAMQRPGPYDRPGAGRGYNSIGRGAGFERMRRGAYGGGY
GGYDDYNGYNDGYGFGSDRFGRDLNYCFSGMSDHRYGDGGSTFQSTTGHCVHMRGLPYRA
TENDIYNFFSPLNPVRVHIEIGPDGRVTGEADVEFATHEDAVAAMSKDKANMQHRYVELF
LNSTAGASGGAYEHRYVELFLNSTAGASGGAYGSQMMGGMGLSNQSSYGGPASQQLSGGY
GGGYGGQSSMSGYDQVLQENSSDFQSNIA
NT seq 1350 nt   +upstreamnt  +downstreamnt
atgatgttgggcacggaaggtggagagggattcgtggtgaaggtccggggcttgccctgg
tcttgctcggccgatgaagtgcagaggtttttttctgactgcaaaattcaaaatggggct
caaggtattcgtttcatctacaccagagaaggcagaccaagtggcgaggcttttgttgaa
cttgaatcagaagatgaagtcaaattggccctgaaaaaagacagagaaactatgggacac
agatatgttgaagtattcaagtcaaacaacgttgaaatggattgggtgttgaagcatact
ggtccaaatagtcctgacacggccaatgatggctttgtacggcttagaggacttcccttt
ggatgtagcaaggaagaaattgttcagttcttctcagggttggaaatcgtgccaaatggg
ataacattgccggtggacttccaggggaggagtacgggggaggccttcgtgcagtttgct
tcacaggaaatagctgaaaaggctctaaagaaacacaaggaaagaatagggcacaggtat
attgaaatctttaagagcagtagagctgaagttagaactcattatgatccaccacgaaag
cttatggccatgcagcggccaggtccttatgacagacctggggctggtagagggtataac
agcattggcagaggagctggctttgagaggatgaggcgtggtgcttatggtggaggctat
ggaggctatgatgattacaatggctataatgatggctatggatttgggtcagatagattt
ggaagagacctcaattactgtttttcaggaatgtctgatcacagatacggggatggtggc
tctactttccagagcacaacaggacactgtgtacacatgcggggattaccttacagagct
actgagaatgacatttataattttttttcaccgctcaaccctgtgagagtacacattgaa
attggtcctgatggcagagtaactggtgaagcagatgtcgagttcgcaactcatgaagat
gctgtggcagctatgtcaaaagacaaagcaaatatgcaacacagatatgtagaactcttc
ttgaattctacagcaggagcaagcggtggtgcttacgaacacagatatgtagaactcttc
ttgaattctacagcaggagcaagcggtggtgcttatggtagccaaatgatgggaggcatg
ggcttgtcaaaccagtccagctacgggggcccagccagccagcagctgagtgggggttac
ggaggcggctacggtggccagagcagcatgagtggatacgaccaagttttacaggaaaac
tccagtgattttcaatcaaacattgcatag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (20)   
   KEGG ORTHOLOGY (1)   
   RefGene (9)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (55)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (52)   
DNA sequence (78)   
   RefSeq(nuc) (52)   
   GenBank (13)   
   EMBL (13)   
3D Structure (3)   
   PDB (3)   
Protein domain (2)   
   Pfam (2)   
All databases (164)   

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