Homo sapiens (human): 8636
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Entry
8636 CDS
T01001
Symbol
SSNA1, N14, NA-14, NA14
Name
(RefSeq) SS nuclear autoantigen 1
KO
K16780
sjoegren syndrome nuclear autoantigen 1
Organism
hsa
Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
8636 (SSNA1)
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
8636 (SSNA1)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Other centriole associated proteins
8636 (SSNA1)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
8636 (SSNA1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
APG6_N
Bacillus_HBL
CC149
PDC10_C
TMCO5
DUF724
DUF5917
ADIP
Med11
DUF3086
ATG17_like
Prominin
Herpes_UL6
S6OS1
DUF4200
Golgin_A5
Mis12
HALZ
HAUS4
GAS
Phlebovirus_NSM
DUF1664
ERM_helical
Flagellar_rod
UPF0242
FapA
Radial_spoke_3
DUF3993
ATAD3_N
Rootletin
Baculo_PEP_C
Seryl_tRNA_N
DUF3450
PhoU
TMPIT
FmiP_Thoc5
PRD
DUF948
EXOC6_Sec15_N
V_ATPase_I
Motif
Other DBs
NCBI-GeneID:
8636
NCBI-ProteinID:
NP_003722
OMIM:
610882
HGNC:
11321
Ensembl:
ENSG00000176101
UniProt:
O43805
LinkDB
All DBs
Position
9:137188676..137190366
Genome browser
AA seq
119 aa
AA seq
DB search
MTQQGAALQNYNNELVKCIEELCQKREELCRQIQEEEDEKQRLQNEVRQLTEKLARVNEN
LARKIASRNEFDRTIAETEAAYLKILESSQTLLSVLKREAGNLTKATAPDQKSSGGRDS
NT seq
360 nt
NT seq
+upstream
nt +downstream
nt
atgacccagcagggcgcggcgctgcagaactacaacaacgagctggtcaagtgcatagag
gagctgtgccagaagcgggaggagctgtgccggcagatccaggaggaggaggacgagaag
cagcggctgcagaatgaggtgaggcagctgacagagaagctggcccgcgtcaacgagaac
ctggcacgcaagattgcctctcgcaacgagttcgaccggaccatcgcggagacggaggcc
gcctacctcaagatcctggagagctcccagactttgctcagcgttctcaagagggaagct
gggaacctgaccaaggctacagccccagaccagaaaagtagcggcggcagggacagctga
DBGET
integrated database retrieval system