Homo sapiens (human): 84628
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Entry
84628 CDS
T01001
Symbol
NTNG2, LHLL9381, Lmnt2, NEDBASH, NTNG1, NetrinG2, bA479K20.1
Name
(RefSeq) netrin G2
KO
K16359
netrin-G2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04360
Axon guidance
hsa04514
Cell adhesion molecule (CAM) interaction
Disease
H02397
Neurodevelopmental disorder with movement abnormalities or hypotonia
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09133 Signaling molecules and interaction
04514 Cell adhesion molecule (CAM) interaction
84628 (NTNG2)
09150 Organismal Systems
09158 Development and regeneration
04360 Axon guidance
84628 (NTNG2)
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Gene cluster
GFIT
Motif
Pfam:
Laminin_N
EGF_laminin
EGF_LMN_ATRN
EGF
EGF_2
JAG1-like_EGF2
Motif
Other DBs
NCBI-GeneID:
84628
NCBI-ProteinID:
NP_115925
OMIM:
618689
HGNC:
14288
Ensembl:
ENSG00000196358
UniProt:
Q96CW9
Structure
PDB
PDBj
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All DBs
Position
9:132161689..132244526
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AA seq
530 aa
AA seq
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MLHLLALFLHCLPLASGDYDICKSWVTTDEGPTWEFYACQPKVMRLKDYVKVKVEPSGIT
CGDPPERFCSHENPYLCSNECDASNPDLAHPPRLMFDKEEEGLATYWQSITWSRYPSPLE
ANITLSWNKTVELTDDVVMTFEYGRPTVMVLEKSLDNGRTWQPYQFYAEDCMEAFGMSAR
RARDMSSSSAHRVLCTEEYSRWAGSKKEKHVRFEVRDRFAIFAGPDLRNMDNLYTRLESA
KGLKEFFTLTDLRMRLLRPALGGTYVQRENLYKYFYAISNIEVIGRCKCNLHANLCSMRE
GSLQCECEHNTTGPDCGKCKKNFRTRSWRAGSYLPLPHGSPNACATAGSFGNCECYGHSN
RCSYIDFLNVVTCVSCKHNTRGQHCQHCRLGYYRNGSAELDDENVCIECNCNQIGSVHDR
CNETGFCECREGAAGPKCDDCLPTHYWRQGCYPNVCDDDQLLCQNGGTCLQNQRCACPRG
YTGVRCEQPRCDPADDDGGLDCDRAPGAAPRPATLLGCLLLLGLAARLGR
NT seq
1593 nt
NT seq
+upstream
nt +downstream
nt
atgctgcatctgctggcgctcttcctgcactgcctccctctggcctctggggactatgac
atctgcaaatcctgggtgaccacagatgagggccccacctgggagttctacgcctgccag
cccaaggtgatgcgcctgaaggactacgtcaaggtgaaggtggagccctcaggcatcaca
tgtggagacccccctgagaggttctgctcccatgagaatccctacctatgcagcaacgag
tgtgacgcctccaacccggacctggcccacccgcccaggctcatgttcgacaaggaggag
gagggcctggccacctactggcagagcatcacctggagccgctaccccagcccgctggaa
gccaacatcaccctttcgtggaacaagaccgtggagctgaccgacgacgtggtgatgacc
ttcgagtacggccggcccacggtcatggtcctggagaagtccctggacaacgggcgcacc
tggcagccctaccagttctacgccgaggactgcatggaggccttcggtatgtccgcccgc
cgggcccgcgacatgtcatcctccagcgcgcaccgcgtgctctgcaccgaggagtactcg
cgctgggcaggctccaagaaggagaagcacgtgcgcttcgaggtgcgggaccgcttcgcc
atctttgccggccccgacctgcgcaacatggacaacctctacacgcggctggagagcgcc
aagggcctcaaggagttcttcaccctcaccgacctgcgcatgcggctgctgcgcccggcg
ctgggcggcacctatgtgcagcgggagaacctctacaagtacttctacgccatctccaac
atcgaggtcatcggcaggtgcaagtgcaacctgcacgccaacctgtgctccatgcgcgag
ggcagcctgcagtgcgagtgcgagcacaacaccaccggccccgactgcggcaagtgcaag
aagaatttccgcacccggtcctggcgggccggctcctacctgccgctgccccatggctct
cccaacgcctgtgccactgcaggttcctttggcaactgcgaatgctacggtcactccaac
cgctgcagctacattgacttcctgaatgtggtgacctgcgtcagctgcaagcacaacacg
cgaggtcagcactgccagcactgccggctgggctactaccgcaacggctcggcagagctg
gatgatgagaacgtctgcattgagtgtaactgcaaccagataggctccgtgcacgaccgg
tgcaacgagaccggcttctgcgagtgccgcgagggcgcggcgggccccaagtgcgacgac
tgcctccccacgcactactggcgccagggctgctaccccaacgtgtgcgacgacgaccag
ctgctgtgccagaacggaggcacctgcctgcagaaccagcgctgcgcctgcccgcgcggc
tacaccggcgtgcgctgcgagcagccccgctgcgaccccgccgacgatgacggcggtctg
gactgcgaccgcgcgcccggggccgccccgcgccccgccaccctgctcggctgcctgctg
ctgctggggctggccgcccgcctgggccgctga
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