KEGG   Homo sapiens (human): 9987
Entry
9987              CDS       T01001                                 
Symbol
HNRNPDL, HNRNP, HNRPDL, JKTBP, JKTBP2, LGMD1G, LGMDD3, laAUF1
Name
(RefSeq) heterogeneous nuclear ribonucleoprotein D like
  KO
K13044  heterogeneous nuclear ribonucleoprotein A/B/D
Organism
hsa  Homo sapiens (human)
Disease
H00593  Limb-girdle muscular dystrophy
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03041 Spliceosome [BR:hsa03041]
    9987 (HNRNPDL)
Spliceosome [BR:hsa03041]
 Other splicing related proteins
  Spliceosome associated proteins (SAPs)
   hnRNP proteins
    9987 (HNRNPDL)
SSDB
Motif
Pfam: RRM_1 RRM_7 RRM_3 Nup35_RRM_2 CBFNT
Other DBs
NCBI-GeneID: 9987
NCBI-ProteinID: NP_112740
OMIM: 607137
HGNC: 5037
Ensembl: ENSG00000152795
UniProt: O14979
Structure
Position
4:complement(82422564..82430462)
AA seq 420 aa
MEVPPRLSHVPPPLFPSAPATLASRSLSHWRPRPPRQLAPLLPSLAPSSARQGARRAQRH
VTAQQPSRLAGGAAIKGGRRRRPDLFRRHFKSSSIQRSAAAAAATRTARQHPPADSSVTM
EDMNEYSNIEEFAEGSKINASKNQQDDGKMFIGGLSWDTSKKDLTEYLSRFGEVVDCTIK
TDPVTGRSRGFGFVLFKDAASVDKVLELKEHKLDGKLIDPKRAKALKGKEPPKKVFVGGL
SPDTSEEQIKEYFGAFGEIENIELPMDTKTNERRGFCFITYTDEEPVKKLLESRYHQIGS
GKCEIKVAQPKEVYRQQQQQQKGGRGAAAGGRGGTRGRGRGQGQNWNQGFNNYYDQGYGN
YNSAYGGDQNYSGYGGYDYTGYNYGNYGYGQGYADYSGQQSTYGKASRGGGNHQNNYQPY
NT seq 1263 nt   +upstreamnt  +downstreamnt
atggaggtcccgcccaggctttcccatgtgccgccgccattgttcccctccgctcccgct
actttagcctcccgcagcctctcccattggcggccgcggccgccgcggcagctagccccg
ctcctcccttcgctcgctcccagctccgcccggcagggggcgcgccgggcccagcgccac
gtcaccgcccagcagccctcccgattggcgggcggggcggctataaagggagggcgcagg
cggcgcccggatctcttccgccgccattttaaatccagctccatacaacgctccgccgcc
gctgctgccgcgacccggactgcgcgccagcacccccctgccgacagctccgtcactatg
gaggatatgaacgagtacagcaatatagaggaattcgcagagggatccaagatcaacgcg
agcaagaatcagcaggatgacggtaaaatgtttattggaggcttgagctgggatacaagc
aaaaaagatctgacagagtacttgtctcgatttggggaagttgtagactgcacaattaaa
acagatccagtcactgggagatcaagaggatttggatttgtgcttttcaaagatgctgct
agtgttgataaggttttggaactgaaagaacacaaactggatggcaaattgatagatccc
aaaagggccaaagctttaaaagggaaagaacctcccaaaaaggtttttgtgggtggattg
agcccggatacttctgaagaacaaattaaagaatattttggagcctttggagagattgaa
aatattgaacttcccatggatacaaaaacaaatgaaagaagaggattttgttttatcaca
tatactgatgaagagccagtaaaaaaattgttagaaagcagataccatcaaattggttct
gggaagtgtgaaatcaaagttgcacaacccaaagaggtatataggcagcaacagcaacaa
caaaaaggtggaagaggtgctgcagctggtggacgaggtggtacgaggggtcgtggccga
ggtcagggccaaaactggaaccaaggatttaataactattatgatcaaggatatggaaat
tacaatagtgcctatggtggtgatcaaaactatagtggctatggcggatatgattatact
gggtataactatgggaactatggatatggacagggatatgcagactacagtggccaacag
agcacttatggcaaggcatctcgagggggtggcaatcaccaaaacaattaccagccatac
taa

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (29)   
   KEGG ORTHOLOGY (1)   
   RefGene (8)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (15)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (34)   
   RefSeq(nuc) (4)   
   GenBank (15)   
   EMBL (15)   
3D Structure (1)   
   PDB (1)   
Protein domain (5)   
   Pfam (5)   
All databases (79)   

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