Homo sapiens (human): 79989
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Entry
79989 CDS
T01001
Symbol
IFT56, BRENS, DYF13, TTC26, dyf-13
Name
(RefSeq) intraflagellar transport 56
KO
K19685
intraflagellar transport protein 56
Organism
hsa
Homo sapiens (human)
Disease
H02547
BRENS syndrome
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
79989 (IFT56)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
79989 (IFT56)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
TPR_19
ANAPC3
TPR_14
TPR_2
TPR_16
TPR_17
TPR_9
TPR_12
TPR_8
TPR_1
Coatomer_E
TPR_6
TPR_11
Motif
Other DBs
NCBI-GeneID:
79989
NCBI-ProteinID:
NP_079202
OMIM:
617453
HGNC:
21882
Ensembl:
ENSG00000105948
UniProt:
A0AVF1
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All DBs
Position
7:139133778..139191986
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AA seq
554 aa
AA seq
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MMLSRAKPAVGRGVQHTDKRKKKGRKIPKLEELLSKRDFTGAITLLEFKRHVGEEEEDTN
LWIGYCAFHLGDYKRALEEYENATKEENCNSEVWVNLACTYFFLGMYKQAEAAGFKASKS
RLQNRLLFHLAHKFNDEKKLMSFHQNLQDVTEDQLSLASIHYMRSHYQEAIDIYKRILLD
NREYLALNVYVALCYYKLDYYDVSQEVLAVYLQQIPDSTIALNLKACNHFRLYNGRAAEA
ELKSLMDNASSSFEFAKELIRHNLVVFRGGEGALQVLPPLVDVIPEARLNLVIYYLRQDD
VQEAYNLIKDLEPTTPQEYILKGVVNAALGQEMGSRDHMKIAQQFFQLVGGSASECDTIP
GRQCMASCFFLLKQFDDVLIYLNSFKSYFYNDDIFNFNYAQAKAATGNTSEGEEAFLLIQ
SEKMKNDYIYLSWLARCYIMNKKPRLAWELYLKMETSGESFSLLQLIANDCYKMGQFYYS
AKAFDVLERLDPNPEYWEGKRGACVGIFQMIIAGREPKETLREVLHLLRSTGNTQVEYMI
RIMKKWAKENRVSI
NT seq
1665 nt
NT seq
+upstream
nt +downstream
nt
atgatgctttcaagggccaaacctgctgtaggcagaggcgtacagcacactgacaaaaga
aagaagaaaggtaggaagattccaaaactagaggagctactttcaaaaagagatttcact
ggagctattaccctgttggagttcaaacgtcatgttggggaagaagaagaggatactaat
ttgtggattggatattgtgcctttcacctgggtgactacaagagagctctggaggaatac
gaaaatgctacaaaagaggaaaattgtaattctgaagtctgggtgaacctagcttgcacc
tacttctttcttgggatgtataaacaagctgaagcagctggatttaaagcttcaaaaagc
cgactccaaaaccgcctcctcttccacttggctcacaagtttaatgatgagaaaaaattg
atgagctttcatcaaaatcttcaggatgtcacagaagatcaactcagtttggcctcaatc
cactatatgcgatctcactaccaagaagctatagatatatataagcgaatactgctagat
aacagggaataccttgcccttaatgtttatgtggccctctgctactacaagttggattac
tatgatgtgtctcaagaagttttggctgtttaccttcagcaaattcctgatagtaccatc
gcactcaatcttaaagcctgtaaccattttcgcctttacaatggcagagcagctgaggca
gaactcaaaagcttgatggacaatgcttcttcatcctttgaatttgctaaagaactcatc
aggcacaatctggttgttttccgaggaggtgaaggggctttgcaggttttacctccccta
gttgatgtcattcctgaagctaggctaaacttggtgatttactaccttcgtcaagatgat
gtacaagaagcttataacttaattaaggatctggaacctactactcctcaggagtatatt
ctcaaaggagtggtcaatgcagcccttggccaggaaatgggttcaagggatcatatgaaa
attgcccagcagttcttccagttggtgggaggatcagctagtgaatgtgatacaatacca
gggaggcagtgcatggcttcctgtttcttcctgcttaagcaatttgatgatgttttgatt
tacctcaactcatttaagagttacttctataatgatgacatctttaactttaattatgcc
caagccaaagctgcaacaggcaataccagtgagggcgaagaggcgttcctcttgatccaa
agtgagaagatgaaaaatgattacatttacctcagctggttagctcggtgctatattatg
aataagaaaccaagactagcctgggaactttatcttaagatggaaacctccggcgagtcc
ttcagtctcttacagctcattgctaatgactgctacaagatgggccagttttactattct
gccaaagcttttgatgtccttgagaggctggatcctaaccctgaatattgggaaggcaaa
cggggtgcctgtgtgggcattttccagatgatcatagctgggagagaacccaaagagacc
cttcgagaagtgctccatttactgagaagcacaggtaacacccaagtagaatacatgatc
cggatcatgaagaaatgggccaaagaaaacagagtgtccatctaa
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