Homo sapiens (human): 84140
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Entry
84140 CDS
T01001
Symbol
FAM161A, RP28
Name
(RefSeq) FAM161 centrosomal protein A
KO
K16772
protein FAM161A
Organism
hsa
Homo sapiens (human)
Disease
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
]
84140 (FAM161A)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
84140 (FAM161A)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
FAM161A_B
Motif
Other DBs
NCBI-GeneID:
84140
NCBI-ProteinID:
NP_115556
OMIM:
613596
HGNC:
25808
Ensembl:
ENSG00000170264
UniProt:
Q3B820
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Position
2:complement(61800240..61854060)
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AA seq
660 aa
AA seq
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MATSHRVAKLVASSLQTPVNPITGARVAQYEREDPLKALAAAEAILEDEEEEKVAQPAGA
SADLNTSFSGVDEHAPISYEDFVNFPDIHHSNEEYFKKVEELKAAHIETMAKLEKMYQDK
LHLKEVQPVVIREDSLSDSSRSVSEKNSYHPVSLMTSFSEPDLGQSSSLYVSSSEEELPN
LEKEYPRKNRMMTYAKELINNMWTDFCVEDYIRCKDTGFHAAEKRRKKRKEWVPTITVPE
PFQMMIREQKKKEESMKSKSDIEMVHKALKKQEEDPEYKKKFRANPVPASVFLPLYHDLV
KQKEERRRSLKEKSKEALLASQKPFKFIAREEQKRAAREKQLRDFLKYKKKTNRFKARPI
PRSTYGSTTNDKLKEEELYRNLRTQLRAQEHLQNSSPLPCRSACGCRNPRCPEQAVKLKC
KHKVRCPTPDFEDLPERYQKHLSEHKSPKLLTVCKPFDLHASPHASIKREKILADIEADE
ENLKETRWPYLSPRRKSPVRCAGVNPVPCNCNPPVPTVSSRGREQAVRKSEKERMREYQR
ELEEREEKLKKRPLLFERVAQKNARMAAEKHYSNTLKALGISDEFVSKKGQSGKVLEYFN
NQETKSVTEDKESFNEEEKIEERENGEENYFIDTNSQDSYKEKDEANEESEEEKSVEESH
NT seq
1983 nt
NT seq
+upstream
nt +downstream
nt
atggccacctcccaccgagtggcgaagctggtggcctccagtctccagaccccggtaaat
cccatcactggagcgcgggtcgcccagtacgaacgcgaagaccccttaaaggccctggcg
gcagcggaggcgatcttggaggacgaagaggaggagaaagtggctcagcccgctggggca
tcggctgatttgaacaccagcttttctggggtggatgaacatgcaccgataagctatgag
gactttgtgaactttcctgatattcaccactctaatgaggagtatttcaagaaagtagaa
gagttgaaggctgcccacatagaaactatggcaaaattagagaaaatgtaccaggataaa
ttacatttaaaggaagttcagccagtggtcatcagagaagactctcttagtgactcttcc
agatctgtatcagaaaagaactcctatcaccctgtctcattaatgacatcattttcagag
cctgatttaggccagtcttcctccttgtatgtgtcctcctctgaagaggagttacccaac
ctagaaaaagagtatcctaggaaaaacagaatgatgacctatgctaaggagctcatcaac
aatatgtggacagacttttgtgttgaggattatattcgctgtaaagatactggcttccat
gcagctgaaaaaagaaggaagaaacgaaaagaatgggtgcccacaattacagtaccggag
ccttttcaaatgatgataagagaacagaagaaaaaagaagagtccatgaaatctaaatca
gatatcgaaatggtacataaagcgctcaaaaaacaagaagaggatccagagtataagaag
aaattccgagccaatccagttcctgcatctgtctttctccccctttaccatgatttagtc
aagcaaaaagaagaacggagaaggtctctgaaggagaaaagcaaagaagctcttttggcc
tcacaaaagccatttaaatttatagcaagggaggaacagaagcgagcagcccgggaaaag
cagctgagagactttcttaagtataaaaagaaaacaaatcgatttaaagccagacccatt
cctcgatctacttatggttcaactaccaatgacaagttaaaagaagaagagctctatcga
aaccttaggacacagctgagagcccaggagcatttacagaactcatctcctctgccttgt
aggtcagcttgtggatgcaggaaccccaggtgtcctgaacaggctgtaaagttgaagtgt
aaacacaaggttaggtgcccaactcctgattttgaggaccttcctgagagataccagaaa
cacctctcagaacacaagtctccaaaactcttaacagtgtgtaaaccatttgatcttcat
gcatctccacatgcatctattaaaagagaaaaaattttggcagacatcgaagcagatgaa
gaaaatttaaaagaaacacgttggccttatttgtctccaaggcgtaagtcaccagtaaga
tgtgcaggtgtaaaccctgtgccttgtaactgcaaccctcccgtgcccacggtatcttcc
agaggacgagaacaagccgtaagaaagagcgaaaaggaaaggatgagagaataccaacga
gaactagaagaaagagaagaaaaattaaaaaagaggccactgctatttgaaagagttgct
cagaaaaatgcaagaatggcagcagaaaagcattattctaataccctaaaagcactagga
atatctgatgagtttgtttcaaagaaaggccaaagtggaaaagtacttgagtacttcaac
aatcaagagacgaaaagtgtcactgaagacaaagaaagctttaatgaagaagaaaaaata
gaagaaagagagaatggggaagaaaattattttattgataccaacagccaggattcttac
aaggaaaaagatgaagccaatgaggaaagtgaagaagagaaatctgttgaagaatcacac
tga
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