Homo sapiens (human): 3187
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
RRM_1
zf-RNPHF
Motif
Other DBs
NCBI-GeneID:
3187
NCBI-ProteinID:
NP_001244222
OMIM:
601035
HGNC:
5041
Ensembl:
ENSG00000169045
UniProt:
P31943
A0A384MEJ3
Structure
PDB
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All DBs
Position
5:complement(179614178..179634784)
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AA seq
449 aa
AA seq
DB search
MMLGTEGGEGFVVKVRGLPWSCSADEVQRFFSDCKIQNGAQGIRFIYTREGRPSGEAFVE
LESEDEVKLALKKDRETMGHRYVEVFKSNNVEMDWVLKHTGPNSPDTANDGFVRLRGLPF
GCSKEEIVQFFSGLEIVPNGITLPVDFQGRSTGEAFVQFASQEIAEKALKKHKERIGHRY
IEIFKSSRAEVRTHYDPPRKLMAMQRPGPYDRPGAGRGYNSIGRGAGFERMRRGAYGGGY
GGYDDYNGYNDGYGFGSDRFGRDLNYCFSGMSDHRYGDGGSTFQSTTGHCVHMRGLPYRA
TENDIYNFFSPLNPVRVHIEIGPDGRVTGEADVEFATHEDAVAAMSKDKANMQHRYVELF
LNSTAGASGGAYEHRYVELFLNSTAGASGGAYGSQMMGGMGLSNQSSYGGPASQQLSGGY
GGGYGGQSSMSGYDQVLQENSSDFQSNIA
NT seq
1350 nt
NT seq
+upstream
nt +downstream
nt
atgatgttgggcacggaaggtggagagggattcgtggtgaaggtccggggcttgccctgg
tcttgctcggccgatgaagtgcagaggtttttttctgactgcaaaattcaaaatggggct
caaggtattcgtttcatctacaccagagaaggcagaccaagtggcgaggcttttgttgaa
cttgaatcagaagatgaagtcaaattggccctgaaaaaagacagagaaactatgggacac
agatatgttgaagtattcaagtcaaacaacgttgaaatggattgggtgttgaagcatact
ggtccaaatagtcctgacacggccaatgatggctttgtacggcttagaggacttcccttt
ggatgtagcaaggaagaaattgttcagttcttctcagggttggaaatcgtgccaaatggg
ataacattgccggtggacttccaggggaggagtacgggggaggccttcgtgcagtttgct
tcacaggaaatagctgaaaaggctctaaagaaacacaaggaaagaatagggcacaggtat
attgaaatctttaagagcagtagagctgaagttagaactcattatgatccaccacgaaag
cttatggccatgcagcggccaggtccttatgacagacctggggctggtagagggtataac
agcattggcagaggagctggctttgagaggatgaggcgtggtgcttatggtggaggctat
ggaggctatgatgattacaatggctataatgatggctatggatttgggtcagatagattt
ggaagagacctcaattactgtttttcaggaatgtctgatcacagatacggggatggtggc
tctactttccagagcacaacaggacactgtgtacacatgcggggattaccttacagagct
actgagaatgacatttataattttttttcaccgctcaaccctgtgagagtacacattgaa
attggtcctgatggcagagtaactggtgaagcagatgtcgagttcgcaactcatgaagat
gctgtggcagctatgtcaaaagacaaagcaaatatgcaacacagatatgtagaactcttc
ttgaattctacagcaggagcaagcggtggtgcttacgaacacagatatgtagaactcttc
ttgaattctacagcaggagcaagcggtggtgcttatggtagccaaatgatgggaggcatg
ggcttgtcaaaccagtccagctacgggggcccagccagccagcagctgagtgggggttac
ggaggcggctacggtggccagagcagcatgagtggatacgaccaagttttacaggaaaac
tccagtgattttcaatcaaacattgcatag
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