Homo sapiens (human): 157657
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Entry
157657 CDS
T01001
Symbol
CFAP418, BBS21, C8orf37, CORD16, FAP418, MOT25, RP64, smalltalk
Name
(RefSeq) cilia and flagella associated protein 418
KO
K25226
protein C8orf37
Organism
hsa
Homo sapiens (human)
Disease
H00418
Bardet-Biedl syndrome
H00481
Cone-rod dystrophy and cone dystrophy
H00527
Retinitis pigmentosa
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
157657 (CFAP418)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
157657 (CFAP418)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
RMP
DGCcoil
zf-C2H2_ZN142
Motif
Other DBs
NCBI-GeneID:
157657
NCBI-ProteinID:
NP_808880
OMIM:
614477
HGNC:
27232
Ensembl:
ENSG00000156172
UniProt:
Q96NL8
LinkDB
All DBs
Position
8:complement(95244913..95269201)
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AA seq
207 aa
AA seq
DB search
MAEDLDELLDEVESKFCTPDLLRRGMVEQPKGCGGGTHSSDRNQAKAKETLRSTETFKKE
DDLDSLINEILEEPNLDKKPSKLKSKSSGNTSVRASIEGLGKSCSPVYLGGSSIPCGIGT
NISWRACDHLRCIACDFLVVSYDDYMWDKSCDYLFFRNNMPEFHKLKAKLIKKKGTRAYA
CQCSWRTIEEVTDLQTDHQLRWVCGKH
NT seq
624 nt
NT seq
+upstream
nt +downstream
nt
atggcggaggacctggacgagctcttggatgaagtcgagtccaagttttgcacacctgac
cttctaagacggggtatggtcgagcagcccaaaggctgcggcggcggcacccacagtagc
gaccggaaccaagccaaggcgaaagagacgctcagatcaacagaaacatttaaaaaagaa
gatgatcttgacagtcttattaatgaaatacttgaagagcccaacttggacaaaaaaccc
tctaaattaaaatctaaatcttcaggtaacacatctgtcagagcttccattgaaggcctt
ggtaaaagttgcagtccggtgtaccttggtggaagctctattccatgtgggattggaaca
aatatttcatggagagcatgtgaccatctgcgttgtatagcctgtgatttcttggtagtc
agctatgatgactatatgtgggacaaatcgtgtgattatctgtttttcaggaacaacatg
ccagaatttcacaaattaaaagcaaagttgataaagaagaaaggaacacgggcatatgcc
tgccagtgtagctggagaactattgaagaagtgactgaccttcagacagatcatcagctt
cgctgggtttgtggtaaacattaa
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