Homo sapiens (human): 6100
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Entry
6100 CDS
T01001
Symbol
RP9, PAP-1, PAP1
Name
(RefSeq) RP9 pre-mRNA splicing factor
KO
K19604
retinitis pigmentosa 9 protein
Organism
hsa
Homo sapiens (human)
Pathway
hsa03040
Spliceosome
Disease
H00527
Retinitis pigmentosa
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09121 Transcription
03040 Spliceosome
6100 (RP9)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03041 Spliceosome [BR:
hsa03041
]
6100 (RP9)
Spliceosome [BR:
hsa03041
]
Complex A
U2 snRNP components
U2 related factors
6100 (RP9)
Complex B
6100 (RP9)
U4/U6.U5 tri-snRNP components
U4/U6.U5 tri-snRNP related factors
6100 (RP9)
Complex C
U4/U6.U5 tri-SnRNP related factors
6100 (RP9)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
AP3D1
Med19
SR-25
Motif
Other DBs
NCBI-GeneID:
6100
NCBI-ProteinID:
NP_976033
OMIM:
607331
HGNC:
10288
Ensembl:
ENSG00000164610
UniProt:
Q8TA86
A0A090N8Z0
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All DBs
Position
7:complement(33094797..33109404)
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AA seq
221 aa
AA seq
DB search
MSSRPGREDVGAAGARRPREPPEQELQRRREQKRRRHDAQQLQQLKHLESFYEKPPPGLI
KEDETKPEDCIPDVPGNEHAREFLAHAPTKGLWMPLGKEVKVMQCWRCKRYGHRTGDKEC
PFFIKGNQKLEQFRVAHEDPMYDIIRDNKRHEKDVRIQQLKQLLEDSTSDEDRSSSSSSE
GKEKHKKKKKKEKHKKRKKEKKKKKKRKHKSSKSNEGSDSE
NT seq
666 nt
NT seq
+upstream
nt +downstream
nt
atgtcgtcccggcctgggcgcgaggacgtgggggctgcgggcgcgcggcggccgcgtgag
ccgccggagcaggagctgcagcgacgtcgggagcagaagcggcggcgacacgacgcgcag
cagctgcagcagctcaagcacctggagtccttttacgaaaaacctcctcctgggcttatc
aaggaagatgagactaagccagaagattgcataccagatgtaccaggcaatgaacacgcc
agggaatttctggctcatgcaccaactaaaggactttggatgccactggggaaagaagtc
aaagttatgcagtgttggcgttgcaaacgctatggtcaccgaacgggtgacaaagaatgc
cctttctttatcaaaggcaaccaaaagttagagcagttcagagtggcacatgaagatccc
atgtatgacatcatacgagacaataaacgacatgaaaaggacgtaaggatacagcagtta
aaacagttactggaggattctacctcagatgaagataggagcagctccagttcctctgaa
ggtaaagagaaacacaagaaaaagaagaagaaagaaaagcataagaaaaggaagaaagaa
aagaaaaagaagaaaaaacggaagcacaaatcttccaagtcaaatgagggttctgactca
gagtga
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integrated database retrieval system