Homo sapiens (human): 317662
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Entry
317662 CDS
T01001
Symbol
FAM149B1, JBTS36, KIAA0974
Name
(RefSeq) family with sequence similarity 149 member B1
KO
K24653
primary cilium assembly protein FAM149
Organism
hsa
Homo sapiens (human)
Disease
H00530
Joubert syndrome and related disorders
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
317662 (FAM149B1)
Cilium and associated proteins [BR:
hsa03037
]
Primary cilia and associated proteins
Other primary cilia associated proteins
317662 (FAM149B1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DUF3719
Motif
Other DBs
NCBI-GeneID:
317662
NCBI-ProteinID:
NP_775483
OMIM:
618413
HGNC:
29162
Ensembl:
ENSG00000138286
UniProt:
Q96BN6
LinkDB
All DBs
Position
10:73168119..73244504
Genome browser
AA seq
582 aa
AA seq
DB search
MISRYTRKAVPQSLELKGITKHALNHHPPPEKLEEISPTSDSHEKDTSSQSKSDITRESS
FTSADTGNSLSAFPSYTGAGISTEGSSDFSWGYGELDQNATEKVQTMFTAIDELLYEQKL
SVHTKSLQEECQQWTASFPHLRILGRQIITPSEGYRLYPRSPSAVSASYETTLSQERDST
IFGIRGKKLHFSSSYAHKASSIAKSSSFCSMERDEEDSIIVSEGIIEEYLAFDHIDIEEG
FHGKKSEAATEKQKLGYPPIAPFYCMKEDVLAYVFDSVWCKVVSCMEQLTRSHWEGFASD
DESNVAVTRPDSESSCVLSELHPLVLPRVPQSKVLYITSNPMSLCQASRHQPNVNDLLVH
GMPLQPRNLSLMDKLLDLDDKLLMRPGSSTILSTRNWPNRAVEFSTSSLSYTVQSTRRRN
PPPRTLHPISTSHSCAETPRSVEEILRGARVPVAPDSLSSPSPTPLSRNNLLPPIGTAEV
EHVSTVGPQRQMKPHGDSSRAQSAVVDEPNYQQPQERLLLPDFFPRPNTTQSFLLDTQYR
RSCAVEYPHQARPGRGSAGPQLHGSTKSQSGGRPVSRTRQGP
NT seq
1749 nt
NT seq
+upstream
nt +downstream
nt
atgatctccagatacactcggaaggcggtgccacagagcttggagctgaaaggaataaca
aaacatgctcttaaccatcatccccctccagagaagctggaggaaatttcccccaccagt
gacagtcatgagaaagacacaagttcccaaagcaagtctgacatcacaagagaatcatct
tttacatcagccgacactgggaattcactgtctgcttttccaagttatacaggcgcaggg
atatctactgaaggaagctcggacttctcctggggatatggtgaactcgatcaaaatgcc
actgaaaaagtccagacaatgttcacagccattgatgaactcttgtatgagcagaagttg
agtgtgcataccaagagtctacaagaagagtgccaacagtggacagctagctttcctcac
ctcaggattctaggtaggcagataatcactccaagtgaaggttatagattgtatcctaga
tccccttctgctgtttccgcttcatatgaaacaaccttgtctcaagaaagagattctact
atatttggtataaggggaaagaagttacatttttcatcttcttatgctcataaagcatct
tccattgccaaatcctccagcttttgttctatggaaagagatgaggaagactctataatc
gtctcagaaggaataattgaggaatacctagcattcgatcacatagatatagaagaggga
tttcatgggaagaaatcagaagcagctacagagaaacagaaattagggtatcctcccatt
gctccattttactgcatgaaagaagatgtccttgcttatgtgtttgacagtgtatggtgc
aaggttgtgagctgtatggagcagttgacacgtagtcactgggaaggatttgcctctgat
gatgagagtaatgttgcagttaccagacccgattcagaaagttcctgtgtgctgagtgaa
ctacatcctttggtgttaccgcgagtgccacagtctaaggtgctgtacattacctcaaat
ccgatgagtctctgtcaagcaagcagacatcagccaaatgtgaatgatctcttggttcat
ggaatgcctctacagccaagaaatctctccctaatggacaagctcctagatcttgatgac
aagctacttatgaggcctgggtccagtaccatcctttcaactcgaaattggccaaatcga
gctgtggagtttagtacatcatctctgtcatacacagtgcagtccaccaggagacgcaat
ccaccaccacgaactcttcatccgatcagcacgagccattcatgtgctgaaacaccaaga
tctgtggaagaaatcctcagaggagcccgagtcccagtggcacccgactcgctctcctct
ccctcaccgacgcccctgagtcgaaataatctgctaccacctattggcacagctgaagtg
gaacatgtgagcactgtggggccacaaagacagatgaaaccccatggcgactctagtcga
gctcaaagtgcggtggtggatgaacctaactatcagcagccacaagaaaggctccttttg
cccgactttttccccaggcccaacacaactcaatcatttttgctggatacacagtatcgt
cgctcatgtgcagttgagtatcctcatcaggcccgacctggcaggggatctgcaggtcct
cagttacatgggtctacaaaatctcaaagcggaggcagaccagtctctcgaaccaggcag
ggaccataa
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