Homo sapiens (human): 3188
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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)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
RRM_1
zf-RNPHF
Motif
Other DBs
NCBI-GeneID:
3188
NCBI-ProteinID:
NP_001027565
OMIM:
300610
HGNC:
5042
Ensembl:
ENSG00000126945
UniProt:
P55795
A0A384MDT2
Structure
PDB
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All DBs
Position
X:101408222..101414133
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AA seq
449 aa
AA seq
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MMLSTEGREGFVVKVRGLPWSCSADEVMRFFSDCKIQNGTSGIRFIYTREGRPSGEAFVE
LESEEEVKLALKKDRETMGHRYVEVFKSNSVEMDWVLKHTGPNSPDTANDGFVRLRGLPF
GCSKEEIVQFFSGLEIVPNGMTLPVDFQGRSTGEAFVQFASQEIAEKALKKHKERIGHRY
IEIFKSSRAEVRTHYDPPRKLMAMQRPGPYDRPGAGRGYNSIGRGAGFERMRRGAYGGGY
GGYDDYGGYNDGYGFGSDRFGRDLNYCFSGMSDHRYGDGGSSFQSTTGHCVHMRGLPYRA
TENDIYNFFSPLNPMRVHIEIGPDGRVTGEADVEFATHEDAVAAMAKDKANMQHRYVELF
LNSTAGTSGGAYDHSYVELFLNSTAGASGGAYGSQMMGGMGLSNQSSYGGPASQQLSGGY
GGGYGGQSSMSGYDQVLQENSSDYQSNLA
NT seq
1350 nt
NT seq
+upstream
nt +downstream
nt
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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