Homo sapiens (human): 163175
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Entry
163175 CDS
T01001
Symbol
LGI4, AMC1, AMCNMY, LGIL3
Name
(RefSeq) leucine rich repeat LGI family member 4
KO
K25430
leucine-rich repeat LGI family member 4
Organism
hsa
Homo sapiens (human)
Disease
H02299
Arthrogryposis multiplex congenita
H02358
Arthrogryposis multiplex congenita, neurogenic, with myelin defect
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09190 Not Included in Pathway or Brite
09193 Unclassified: signaling and cellular processes
99995 Signaling proteins
163175 (LGI4)
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EPTP
LRR_8
LRR_4
LRR_5
LRRCT
LRR_9
Motif
Other DBs
NCBI-GeneID:
163175
NCBI-ProteinID:
NP_644813
OMIM:
608303
HGNC:
18712
Ensembl:
ENSG00000153902
UniProt:
Q8N135
A5D6Y5
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All DBs
Position
19:complement(35124513..35135059)
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AA seq
537 aa
AA seq
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MGGAGILLLLLAGAGVVVAWRPPKGKCPLRCSCSKDSALCEGSPDLPVSFSPTLLSLSLV
RTGVTQLKAGSFLRIPSLHLLLFTSNSFSVIEDDAFAGLSHLQYLFIEDNEIGSISKNAL
RGLRSLTHLSLANNHLETLPRFLFRGLDTLTHVDLRGNPFQCDCRVLWLLQWMPTVNASV
GTGACAGPASLSHMQLHHLDPKTFKCRAIELSWFQTVGESALSVEPFSYQGEPHIVLAQP
FAGRCLILSWDYSLQRFRPEEELPAASVVSCKPLVLGPSLFVLAARLWGGSQLWARPSPG
LRLAPTQTLAPRRLLRPNDAELLWLEGQPCFVVADASKAGSTTLLCRDGPGFYPHQSLHA
WHRDTDAEALELDGRPHLLLASASQRPVLFHWTGGRFERRTDIPEAEDVYATRHFQAGGD
VFLCLTRYIGDSMVMRWDGSMFRLLQQLPSRGAHVFQPLLIARDQLAILGSDFAFSQVLR
LEPDKGLLEPLQELGPPALVAPRAFAHITMAGRRFLFAACFKGPTQIYQHHEIDLSA
NT seq
1614 nt
NT seq
+upstream
nt +downstream
nt
atgggaggggcaggcattctgctgctgctgctggctggggcgggggtggtggtggcctgg
agacccccaaagggaaagtgtcccctgcgctgctcctgctctaaagacagcgccctgtgt
gagggctccccggacctgcccgtcagcttctctccgaccctgctgtcactctcactcgtc
aggacgggagtcacccagctgaaggccggcagcttcctgagaattccgtctctgcacctg
ctcctcttcacctccaactccttctccgtgattgaggacgatgcatttgcgggcctgtcc
cacctgcagtacctcttcatcgaggacaatgagattggctccatctctaagaatgccctc
agaggacttcgctcgcttacacacctaagcctggccaataaccatctggagaccctcccc
agattcctgttccgaggcctggacacccttactcatgtggacctccgcgggaacccgttc
cagtgtgactgccgcgtcctctggctcctgcagtggatgcccaccgtgaatgccagcgtg
gggaccggcgcctgtgcgggccccgcctccctgagccacatgcagctccaccacctcgac
cccaagactttcaagtgcagagccatagagctgtcctggttccagacggtgggggagtcg
gcactgagcgtagagcccttctcctaccaaggggagcctcacattgtgctggcacagccc
ttcgccggccgctgcctgattctctcctgggactacagcctgcagcgcttccggcccgag
gaagagctgcccgcggcctccgtggtgtcctgcaagccactggtgctgggcccgagcctc
ttcgtgctggctgcccgcctgtgggggggctcacagctgtgggcccggcccagtcccggc
ctgcgcctggccccaacgcagaccctggccccgcggcggctgctgcggcccaatgacgcc
gagctcctgtggctggaagggcaaccctgcttcgtggtggccgatgcctccaaggcgggc
agcaccacgctgctgtgccgcgacgggcccggcttttacccgcaccagagcctgcacgcc
tggcaccgggacacggacgctgaggccctggagctggacggccggccccacctgctgctg
gcctcggcttcccagcggcccgtgctcttccactggaccggtggccgcttcgagagacgc
acagacatccccgaggccgaggatgtctatgccacacgccacttccaggctggtggggac
gtgttcctgtgcctcacacgctacattggggactccatggtcatgcgctgggacggctcc
atgtttcgtctgctgcagcaacttccctcgcgcggtgcccacgtcttccagccactgctc
atcgccagggaccagctggccatcctaggcagcgacttcgccttcagccaggtcctccgc
cttgagcctgacaaggggctcctggagccactgcaggagctggggcctccggccctggtg
gccccccgtgcctttgcccacatcactatggccggcagacgcttcctctttgctgcttgc
tttaagggccccacacagatctaccagcatcacgagatcgacctcagtgcctga
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