Homo sapiens (human): 124906236
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Entry
124906236 CDS
T01001
Name
(RefSeq) Sjoegren syndrome nuclear autoantigen 1 homolog
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
]
124906236
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
124906236
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Other centrosome associated proteins
124906236
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
124906236
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Tropomyosin
ACBP4_C
NET2A
TMPIT
Golgin_A5
KIF21A
DUF3379
UPF0242
DUF3450
DUF1664
Mis12
YkyA
ATAD3_N
Mce4_CUP1
Lge1
UPF0227
FapA
PI3K_P85_iSH2
HAM1_C
Seryl_tRNA_N
DUF6674
DUF6115
LOH1CR12
COG4_N
Motif
Other DBs
NCBI-GeneID:
124906236
NCBI-ProteinID:
XP_047300087
LinkDB
All DBs
Position
3:complement(49316652..49319062)
Genome browser
AA seq
127 aa
AA seq
DB search
MLTQQGMALQNYDNKLVKCIEELCQKQEELCWQIQQEEDKKQRLQNEVRQLTEKLACVNE
KLARVNENLARKIASCSKFYQTIAETEATYLKMLESSQTLLSVLKREAGNLTKATASDQK
SSGGRDS
NT seq
384 nt
NT seq
+upstream
nt +downstream
nt
atgttgacccagcagggcatggcgctgcagaactacgacaacaagctggtcaaatgcata
gaggagctatgccagaagcaggaggagctgtgctggcagatccagcaggaggaggacaag
aaacagcggctgcagaatgaggtgaggcagctgacagagaagctggcctgcgtcaacgag
aagctggcccgcgtcaacgagaacctggcacgcaagattgcctcttgcagtaagttctac
cagaccatcgcggagacggaggccacctacctcaagatgctggagagctcccagactttg
ctcagtgtcctgaagagggaagctgggaacctgaccaaggctacagcctcagaccagaaa
agtagtggtggcagggacagctga
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