Homo sapiens (human): 150468
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Entry
150468 CDS
T01001
Symbol
CKAP2L
Name
(RefSeq) cytoskeleton associated protein 2 like
KO
K16769
cytoskeleton-associated protein 2
Organism
hsa
Homo sapiens (human)
Disease
H01857
Filippi syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
150468 (CKAP2L)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Centrosome formation proteins
Other centrosome associated proteins
150468 (CKAP2L)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
CKAP2_C
DBINO
DUF7726
Motif
Other DBs
NCBI-GeneID:
150468
NCBI-ProteinID:
NP_689728
OMIM:
616174
HGNC:
26877
Ensembl:
ENSG00000169607
UniProt:
Q8IYA6
LinkDB
All DBs
Position
2:complement(112736349..112764609)
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AA seq
745 aa
AA seq
DB search
MVGPGPTAAAAVEERQRKLQEYLAAKGKLKSQNTKPYLKSKNNCQNQPPSKSTIRPKNDV
TNHVVLPVKPKRSISIKLQPRPPNTAGSQKPKLEPPKLLGKRLTSECVSSNPYSKPSSKS
FQQCEAGSSTTGELSRKPVGSLNIEQLKTTKQQLTDQGNGKCIDFMNNIHVENESLDNFL
KETNKENLLDILTEPERKPDPKLYTRSKPKTDSYNQTKNSLVPKQALGKSSVNSAVLKDR
VNKQFVGETQSRTFPVKSQQLSRGADLARPGVKPSRTVPSHFIRTLSKVQSSKKPVVKNI
KDIKVNRSQYERPNETKIRSYPVTEQRVKHTKPRTYPSLLQGEYNNRHPNIKQDQKSSQV
CIPQTSCVLQKSKAISQRPNLTVGRFNSAIPSTPSIRPNGTSGNKHNNNGFQQKAQTLDS
KLKKAVPQNHFLNKTAPKTQADVTTVNGTQTNPNIKKKATAEDRRKQLEEWQKSKGKTYK
RPPMELKTKRKVIKEMNISFWKSIEKEEEEKKAQLELSSKINNTLTECLNLIEGGVPSNE
ILNILSSIPEAEKFAKFWICKAKLLASKGTFDVIGLYEEAIKNGATPIQELRKVVLNILQ
DSNRTTEGITSDSLVAETSITSVEELAKKMESVKSCLSPKEREQVTATPRIAKAEQHNYP
GIKLQIGPIPRINGMPEVQDMKFITPVRRSSRIERAVSRYPEMLQEHDLVVASLDELLEV
EETKCFIFRRNEALPVTLGFQTPES
NT seq
2238 nt
NT seq
+upstream
nt +downstream
nt
atggtggggcccgggcctaccgctgctgccgctgtcgaagagcggcagagaaagcttcag
gagtaccttgcagccaagggaaaactgaagagccaaaacaccaagccttatctaaaatcc
aagaataattgccagaatcaaccaccttctaaatctactattagacccaaaaatgatgtt
accaaccatgttgttttgcctgtcaaacctaaaaggtccatcagcattaaactccagccc
agaccacctaatactgcagggtcccagaagccgaagttggagccaccaaaacttctgggc
aaaaggctgacttcagaatgtgtttcttctaacccatactctaagccttctagcaagagt
tttcaacagtgtgaagctggatcgtccacaacaggagaactgtcaagaaaacctgtgggg
tcacttaatatagagcaattgaaaactacaaagcagcagttaacagatcaaggaaatggt
aaatgtatagactttatgaataatatccatgttgaaaacgaatctttggataactttcta
aaagaaacaaacaaagagaacttgctcgatatcttaacagaacctgagaggaagccagat
cctaaattatataccagaagtaagccaaagactgactcttataatcaaaccaagaacagt
ttagttcctaaacaagccttgggcaaaagttcagttaatagtgctgttctgaaagatagg
gttaataaacaatttgttggagaaacacaaagcaggactttcccagtaaaatcacagcaa
ctctctagaggagcagatcttgcaagaccaggagtaaaaccctcaaggacggttccctct
cactttattcggacccttagtaaagttcagtcatcaaagaaaccagtagtcaagaacatc
aaagatataaaggttaataggagtcaatatgaaagaccaaatgaaactaagatacggtca
taccctgttactgaacagagagtgaagcacaccaaacccagaacataccccagtttgctt
cagggtgaatataacaacagacatccaaacatcaagcaagatcagaagtccagccaagtt
tgtatacctcagacatcatgtgtactgcaaaagtcaaaagccataagccagaggcctaat
ttgacagttggcagatttaattcagccattccaagcacccctagcataagaccaaatgga
accagtggtaataaacataacaataatggctttcagcaaaaagcacagactttggactcc
aagttgaaaaaggctgttccccagaaccattttctgaacaagacagctcccaaaactcaa
gctgatgtcacaaccgtaaatgggacccaaacaaacccaaatattaaaaagaaggcaaca
gcagaggatcgaaggaaacaactagaagaatggcagaaatctaagggaaaaacctataaa
cggcctcctatggaacttaaaacaaaaagaaaagtaataaaggaaatgaatatttcattc
tggaagagcattgaaaaagaagaggaagaaaagaaagcacaactcgaactgtccagtaaa
attaacaacactctgacagaatgtctgaacctcatcgaagggggtgtaccttctaatgaa
atacttaacatattgtccagcattcctgaagctgaaaaatttgctaaattctggatctgc
aaagcaaagttgttggcaagtaaaggcacctttgatgttattgggctatatgaagaggcc
attaaaaatggggcaacaccaatacaagagttgcggaaagttgttcttaatatcttgcaa
gactcaaacagaaccacagaagggattacttctgactctttagttgctgaaactagtata
acatcagtggaagagctggccaagaagatggaatctgtgaagtcttgtctttctccaaaa
gagagggaacaagtcacggcgacaccccgaatagccaaggcagaacagcataattatcct
ggtatcaaattacagattggtccaatccctagaataaatgggatgccggaagtgcaagac
atgaaatttatcactcctgtacggcgttcgtcgaggattgagcgagcagtgtcccgctac
ccagaaatgctgcaggaacacgatttagtagtggcttctcttgatgaactgttagaagtg
gaagaaacaaaatgttttatattccgtagaaatgaggcgctgcctgtaacattggggttt
caaacccctgaatcataa
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