Homo sapiens (human): 10236
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Entry
10236 CDS
T01001
Symbol
HNRNPR, HNRPR, NEDDFSB, hnRNP-R
Name
(RefSeq) heterogeneous nuclear ribonucleoprotein R
KO
K13161
heterogeneous nuclear ribonucleoprotein R
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
]
10236 (HNRNPR)
Spliceosome [BR:
hsa03041
]
Complex C
Other components
hnRNP proteins
10236 (HNRNPR)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
RRM_1
hnRNP_Q_AcD
RRM_7
RRM_5
RBD_RDR6
RRM_occluded
Motif
Other DBs
NCBI-GeneID:
10236
NCBI-ProteinID:
NP_005817
OMIM:
607201
HGNC:
5047
Ensembl:
ENSG00000125944
UniProt:
O43390
Structure
PDB
PDBj
LinkDB
All DBs
Position
1:complement(23304688..23344284)
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AA seq
633 aa
AA seq
DB search
MANQVNGNAVQLKEEEEPMDTSSVTHTEHYKTLIEAGLPQKVAERLDEIFQTGLVAYVDL
DERAIDALREFNEEGALSVLQQFKESDLSHVQNKSAFLCGVMKTYRQREKQGSKVQESTK
GPDEAKIKALLERTGYTLDVTTGQRKYGGPPPDSVYSGVQPGIGTEVFVGKIPRDLYEDE
LVPLFEKAGPIWDLRLMMDPLSGQNRGYAFITFCGKEAAQEAVKLCDSYEIRPGKHLGVC
ISVANNRLFVGSIPKNKTKENILEEFSKVTEGLVDVILYHQPDDKKKNRGFCFLEYEDHK
SAAQARRRLMSGKVKVWGNVVTVEWADPVEEPDPEVMAKVKVLFVRNLATTVTEEILEKS
FSEFGKLERVKKLKDYAFVHFEDRGAAVKAMDEMNGKEIEGEEIEIVLAKPPDKKRKERQ
AARQASRSTAYEDYYYHPPPRMPPPIRGRGRGGGRGGYGYPPDYYGYEDYYDDYYGYDYH
DYRGGYEDPYYGYDDGYAVRGRGGGRGGRGAPPPPRGRGAPPPRGRAGYSQRGAPLGPPR
GSRGGRGGPAQQQRGRGSRGSRGNRGGNVGGKRKADGYNQPDSKRRQTNNQQNWGSQPIA
QQPLQQGGDYSGNYGYNNDNQEFYQDTYGQQWK
NT seq
1902 nt
NT seq
+upstream
nt +downstream
nt
atggctaatcaggtgaatggtaatgcggtacagttaaaagaagaggaagaaccaatggat
acttccagtgtaactcacacagaacactacaagacactgatagaggcaggcctcccacag
aaggtggcagaaagacttgatgaaatatttcagacaggattggtagcttatgtcgatctt
gatgaaagagcaattgatgctctcagggaatttaatgaagaaggagctctgtctgtacta
cagcagttcaaggaaagtgacttatcacatgttcagaacaaaagtgcatttttatgtgga
gttatgaagacctacaggcagagagagaaacaggggagcaaggtgcaagagtccacaaag
ggacctgatgaagcgaagatcaaggccttgcttgagagaactggttatactctggatgta
accacaggacagaggaagtatggtggtcctccaccagacagtgtgtactctggcgtgcaa
cctggaattggaacggaggtatttgtaggcaaaataccaagggatttatatgaggatgag
ttggtgcccctttttgagaaggccggacccatttgggatctacgtcttatgatggatcca
ctgtccggtcagaatagagggtatgcatttatcaccttctgtggaaaggaagctgcacag
gaagccgtgaaactgtgtgacagctatgaaattcgccctggtaaacaccttggagtgtgc
atttctgtggcaaacaacagactttttgttggatccattccgaagaataagactaaagaa
aacattttggaagaattcagtaaagtcacagagggtttggtggacgttattctctatcat
caacccgatgacaaaaagaagaatcgggggttctgcttccttgaatatgaggatcacaag
tcagcagcacaagccagacgccggctgatgagtggaaaagtaaaagtgtggggaaatgta
gttacagttgaatgggctgaccctgtggaagaaccagatccagaagtcatggctaaggta
aaagttttgtttgtgagaaacttggctactacggtgacagaagaaatattggaaaagtca
ttttctgaatttggaaaactcgaaagagtaaagaagttgaaagattatgcatttgttcat
tttgaagacagaggagcagctgttaaggctatggatgaaatgaatggcaaagaaatagaa
ggggaagaaattgaaatagtcttagccaagccaccagacaagaaaaggaaagagcgccaa
gctgctagacaggcctccagaagcactgcgtatgaagattattactaccaccctcctcct
cgcatgccacctccaattagaggtcggggtcgtggtggggggagaggtggatatggctac
cctccagattactacggctatgaagattactatgatgattactatggttatgattatcac
gactatcgtggaggctatgaagatccctactacggctatgatgatggctatgcagtaaga
ggaagaggaggaggaaggggagggcgaggtgctccaccaccaccaagggggaggggagca
ccacctccaagaggtagagctggctattcacagaggggggcacctttgggaccaccaaga
ggctctaggggtggcagagggggtcctgctcaacagcagagaggccgtggttcccgtgga
tctcggggcaatcgtgggggcaatgtaggaggcaagagaaaggcagatgggtacaaccag
cctgattccaagcgtcgtcagaccaacaaccaacagaactggggttcccaacccatcgct
cagcagccgcttcagcaaggtggtgactattctggtaactatggttacaataatgacaac
caggaattttatcaggatacttatgggcaacagtggaagtag
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