Hyaena hyaena (striped hyena): 120230892
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Entry
120230892 CDS
T07257
Symbol
SHH
Name
(RefSeq) sonic hedgehog protein isoform X1
KO
K11988
sonic hedgehog
Organism
hhv
Hyaena hyaena (striped hyena)
Pathway
hhv04340
Hedgehog signaling pathway
hhv04360
Axon guidance
hhv05200
Pathways in cancer
hhv05205
Proteoglycans in cancer
hhv05217
Basal cell carcinoma
hhv05226
Gastric cancer
Brite
KEGG Orthology (KO) [BR:
hhv00001
]
09130 Environmental Information Processing
09132 Signal transduction
04340 Hedgehog signaling pathway
120230892 (SHH)
09150 Organismal Systems
09158 Development and regeneration
04360 Axon guidance
120230892 (SHH)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
120230892 (SHH)
05205 Proteoglycans in cancer
120230892 (SHH)
09162 Cancer: specific types
05226 Gastric cancer
120230892 (SHH)
05217 Basal cell carcinoma
120230892 (SHH)
09180 Brite Hierarchies
09181 Protein families: metabolism
01002 Peptidases and inhibitors [BR:
hhv01002
]
120230892 (SHH)
09183 Protein families: signaling and cellular processes
00536 Glycosaminoglycan binding proteins [BR:
hhv00536
]
120230892 (SHH)
Peptidases and inhibitors [BR:
hhv01002
]
Cysteine peptidases
Family C46: hedgehog family
120230892 (SHH)
Glycosaminoglycan binding proteins [BR:
hhv00536
]
Heparan sulfate / Heparin
Morphogens
120230892 (SHH)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
HH_signal
Hint
Peptidase_M15_3
Vint
Ribosomal_S6e
Motif
Other DBs
NCBI-GeneID:
120230892
NCBI-ProteinID:
XP_039086599
LinkDB
All DBs
Position
Unknown
AA seq
456 aa
AA seq
DB search
MLLARGMLAVLFSALLLCPGLACGPGRGFGKRRHPKKLTPLAYKQFIPNVAEKTLGASGR
YEGKISRNSERFKELTPNYNPDIIFKDEENTGADRLMTQRCKDKLNALAISVMNQWPGVK
LRVTEGWDEDGHHSEESLHYEGRAVDITTSDRDRSKYGMLARLAVEAGFDWVYYESKAHI
HCSVKAENSVAAKSGGCFPGSATVHLEHGGTKLVKDLRPGDRVLAADDQGRLLYSDFLAF
LDRDDGARKVFYVIETREPRERLLLTAAHLLFVAPPHNGSAAAGREARAGGAPGRRALFA
SRVRPGQRVYVVAERGGGRRLLPAAVHSVTLREEATGAYAPLTAQGTILINRVLASCYAV
IEEHGWAHRAFAPFRLAHALLAALAPARTDRGGGGGGGGGGGPLSPPAPGAPDAPGAADA
PGAAGIHWYSQLLYQIGTWLLDSEALHPLGVAVKSS
NT seq
1371 nt
NT seq
+upstream
nt +downstream
nt
atgctgctggcgagaggcatgctggcggtgctcttctccgcactgctgctgtgcccgggg
ctggcgtgcggacccggcaggggctttgggaagaggcggcaccccaaaaagctgacccct
ttagcctacaagcagtttatccccaacgtggccgagaagaccctaggggccagcggaaga
tacgaagggaagatctcgagaaactcagagcggtttaaggaactcacccccaattacaac
cccgacatcatatttaaagatgaagaaaacacaggagccgaccgtctgatgactcagcgc
tgtaaggacaagctgaacgccttggccatctcggtgatgaaccagtggcccggagtgaag
cttcgggtgaccgagggctgggacgaagacggccaccactcggaggagtcgctgcactac
gagggccgtgcggtggacatcaccacgtcagaccgcgaccgcagcaagtacggcatgctg
gcgcgcctggccgtggaggccggcttcgactgggtttactacgagtccaaggcgcacatc
cactgctccgtgaaagcagagaactcggtggcggccaaatccggcggctgcttcccgggc
tcggccacggtgcacctggagcacggcggcaccaagctggtgaaggacctgcgccccggg
gaccgcgtgctggcggccgacgaccagggccggctgctctacagcgacttcctcgccttc
ctggaccgcgacgacggcgcccggaaggtcttctacgtgatcgagacgcgcgagccgcgc
gagcgcctgctgctcaccgccgcgcacctgctcttcgtggcgccgccgcacaacggctcg
gcggccgcggggcgcgaggcgcgggcggggggcgcgccggggcgccgggcgctcttcgcc
agccgcgtgcgcccgggccagcgcgtgtacgtggtggccgagcgcggcgggggccgccgg
ctgctcccggccgccgtgcacagcgtgacgctccgcgaggaggccacgggcgcgtacgcg
ccgctcacggcgcagggcaccatcctcatcaacagggtgctggcgtcgtgctacgcggtc
atcgaggagcacggctgggcgcaccgcgccttcgcgcccttccgcctggcgcacgcgctc
ctggccgcgctggcgcccgcgcgcacggaccgcggcggcggcggcggcggcggcggcggc
ggcggccccctgtccccgcccgcgccgggggcgcccgacgccccgggggcggccgacgcg
ccgggtgccgcgggcatccactggtactcgcagctgctctaccaaatcggcacctggctg
ttggacagcgaggccctgcacccgctgggcgttgcggtcaagtccagctga
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