Homo sapiens (human): 127602
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Entry
127602 CDS
T01001
Symbol
DNAH14, C1orf67, Dnahc14, HL-18, HL18
Name
(RefSeq) dynein axonemal heavy chain 14
KO
K10408
dynein axonemal heavy chain
Organism
hsa
Homo sapiens (human)
Pathway
hsa04814
Motor proteins
hsa05014
Amyotrophic lateral sclerosis
hsa05016
Huntington disease
hsa05022
Pathways of neurodegeneration - multiple diseases
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09142 Cell motility
04814 Motor proteins
127602 (DNAH14)
09160 Human Diseases
09164 Neurodegenerative disease
05014 Amyotrophic lateral sclerosis
127602 (DNAH14)
05016 Huntington disease
127602 (DNAH14)
05022 Pathways of neurodegeneration - multiple diseases
127602 (DNAH14)
09180 Brite Hierarchies
09183 Protein families: signaling and cellular processes
03037 Cilium and associated proteins [BR:
hsa03037
]
127602 (DNAH14)
04812 Cytoskeleton proteins [BR:
hsa04812
]
127602 (DNAH14)
Cilium and associated proteins [BR:
hsa03037
]
Motile cilia and associated proteins
Dynein arm
127602 (DNAH14)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Microtubules
Tubulin-binding proteins
Dyneins
127602 (DNAH14)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
DUF4168
FlgM
Motif
Other DBs
NCBI-GeneID:
127602
NCBI-ProteinID:
NP_001138626
OMIM:
603341
HGNC:
2945
Ensembl:
ENSG00000185842
UniProt:
Q0VDD8
LinkDB
All DBs
Position
1:224929654..225399286
Genome browser
AA seq
453 aa
AA seq
DB search
METFIPIDLTTENQEMDKEETKTKPRLLRYEEKKYEDVKPLETQPAEIAEKETLEYKTVR
TFSESLKSEKTEDYLRESIIQQHMVSPEPASLKEKGKSRRKKDQTHACPNVRKARPVSYD
RTEPKDDDVIRNIIRLREKLGWQTILPQHSLKYGSSKIAIQKITLKKPLEDDGEFVYCLP
RKSPKSLYNPYDLQVVSAHTAKHCKEFWVITASFISKVINIVGSVKEVELIPTLEWLSER
RHYYLLRQFKIFSDFRMNKAFVTWKLNVKRIKTEKSRSFLYHHLFLADDLFQTCLVYIRG
LCEDAINLKNYNDHENNLSAICLVKLDSSRTYSLDEFCEEQLQQATQALKQLEDIRNKAI
SEMKSTFLKVAEKNEIKEYFESKLSEDDTTHFKLPKYRRLLETFFKFVMLVDYIFQELIR
QLMNTAVTLLLELFNGSAGMPFSVEKKNENLIR
NT seq
1362 nt
NT seq
+upstream
nt +downstream
nt
atggagacgtttatacccattgatttgacaactgaaaatcaagagatggacaaggaggaa
accaagacaaaaccaagacttttaagatatgaagagaaaaaatatgaagatgtgaaacca
ttagagactcaaccagctgaaatagcagaaaaggaaacattggaatataaaacagttaga
acattctctgaatctttgaagtcagagaaaacagaagattaccttagagaaagtataatt
caacaacatatggtttctccagagccagcttcccttaaggagaaagggaagtcaaggaga
aaaaaggatcaaactcatgcttgtccaaatgttaggaaagccaggcctgtgtcctatgat
agaacagaaccaaaagatgatgatgtgataagaaatattattaggctacgagaaaagctt
ggttggcaaactatattaccgcagcacagtttgaaatacggaagctccaaaattgcaatt
cagaagattactttaaagaaacctttggaagatgatggagaatttgtttattgccttcct
cggaaaagtcctaaatccctttacaatccatatgatcttcaggtagtatcggctcatact
gctaaacattgcaaagaattttgggttattactgcttcatttatctcaaaggttattaat
atagttggtagtgtaaaggaagtagaactcatacctactttggaatggctatcagaaaga
agacattactatttattacggcaattcaagatattttctgatttccgaatgaataaagca
tttgttacctggaaattgaatgttaaaagaattaagacagagaagagcaggtcatttttg
taccaccatctttttttggctgatgacttgtttcaaacctgtttggtttatataagagga
ctttgtgaagatgcaattaatctcaaaaattataatgaccatgaaaataatctatctgcc
atatgccttgtaaagctggatagttctcgaacatattctctagatgaattttgtgaagag
cagttacagcaagctacccaggcattgaaacaacttgaggacatcaggaataaagcaatt
tcagagatgaaaagtacttttctaaaggttgcagaaaagaatgaaatcaaagagtatttt
gagtcaaaactctctgaagatgacacaacacatttcaagctgcctaaatatagacgttta
ttagaaacatttttcaagtttgtaatgctggttgactacatatttcaggaactcattcgt
caacttatgaacactgcagtcacactacttttggaattatttaatggttctgctggaatg
ccattttcagtggaaaaaaagaatgaaaatcttatcaggtaa
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