Homo sapiens (human): 9987
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
RRM_1
RRM_7
RRM_PARP14_3
RRM_3
Nup35_RRM_2
CBFNT
Motif
Other DBs
NCBI-GeneID:
9987
NCBI-ProteinID:
NP_112740
OMIM:
607137
HGNC:
5037
Ensembl:
ENSG00000152795
UniProt:
O14979
Structure
PDB
PDBj
LinkDB
All DBs
Position
4:complement(82422564..82430462)
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AA seq
420 aa
AA seq
DB search
MEVPPRLSHVPPPLFPSAPATLASRSLSHWRPRPPRQLAPLLPSLAPSSARQGARRAQRH
VTAQQPSRLAGGAAIKGGRRRRPDLFRRHFKSSSIQRSAAAAAATRTARQHPPADSSVTM
EDMNEYSNIEEFAEGSKINASKNQQDDGKMFIGGLSWDTSKKDLTEYLSRFGEVVDCTIK
TDPVTGRSRGFGFVLFKDAASVDKVLELKEHKLDGKLIDPKRAKALKGKEPPKKVFVGGL
SPDTSEEQIKEYFGAFGEIENIELPMDTKTNERRGFCFITYTDEEPVKKLLESRYHQIGS
GKCEIKVAQPKEVYRQQQQQQKGGRGAAAGGRGGTRGRGRGQGQNWNQGFNNYYDQGYGN
YNSAYGGDQNYSGYGGYDYTGYNYGNYGYGQGYADYSGQQSTYGKASRGGGNHQNNYQPY
NT seq
1263 nt
NT seq
+upstream
nt +downstream
nt
atggaggtcccgcccaggctttcccatgtgccgccgccattgttcccctccgctcccgct
actttagcctcccgcagcctctcccattggcggccgcggccgccgcggcagctagccccg
ctcctcccttcgctcgctcccagctccgcccggcagggggcgcgccgggcccagcgccac
gtcaccgcccagcagccctcccgattggcgggcggggcggctataaagggagggcgcagg
cggcgcccggatctcttccgccgccattttaaatccagctccatacaacgctccgccgcc
gctgctgccgcgacccggactgcgcgccagcacccccctgccgacagctccgtcactatg
gaggatatgaacgagtacagcaatatagaggaattcgcagagggatccaagatcaacgcg
agcaagaatcagcaggatgacggtaaaatgtttattggaggcttgagctgggatacaagc
aaaaaagatctgacagagtacttgtctcgatttggggaagttgtagactgcacaattaaa
acagatccagtcactgggagatcaagaggatttggatttgtgcttttcaaagatgctgct
agtgttgataaggttttggaactgaaagaacacaaactggatggcaaattgatagatccc
aaaagggccaaagctttaaaagggaaagaacctcccaaaaaggtttttgtgggtggattg
agcccggatacttctgaagaacaaattaaagaatattttggagcctttggagagattgaa
aatattgaacttcccatggatacaaaaacaaatgaaagaagaggattttgttttatcaca
tatactgatgaagagccagtaaaaaaattgttagaaagcagataccatcaaattggttct
gggaagtgtgaaatcaaagttgcacaacccaaagaggtatataggcagcaacagcaacaa
caaaaaggtggaagaggtgctgcagctggtggacgaggtggtacgaggggtcgtggccga
ggtcagggccaaaactggaaccaaggatttaataactattatgatcaaggatatggaaat
tacaatagtgcctatggtggtgatcaaaactatagtggctatggcggatatgattatact
gggtataactatgggaactatggatatggacagggatatgcagactacagtggccaacag
agcacttatggcaaggcatctcgagggggtggcaatcaccaaaacaattaccagccatac
taa
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