Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
26033
Gene name Gene Name - the full gene name approved by the HGNC.
Attractin like 1
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
ATRNL1
Synonyms (NCBI Gene) Gene synonyms aliases
ALP, bA338L11.1, bA454H24.1
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q25.3
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT026568 hsa-miR-192-5p Microarray 19074876
MIRT529317 hsa-miR-548ac PAR-CLIP 22012620
MIRT529316 hsa-miR-548bb-3p PAR-CLIP 22012620
MIRT529315 hsa-miR-548d-3p PAR-CLIP 22012620
MIRT529314 hsa-miR-548h-3p PAR-CLIP 22012620
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005112 Function Notch binding IBA
GO:0007186 Process G protein-coupled receptor signaling pathway IEA
GO:0016020 Component Membrane IEA
GO:0030246 Function Carbohydrate binding IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
612869 29063 ENSG00000107518
Protein
UniProt ID Q5VV63
Protein name Attractin-like protein 1
Protein function May play a role in melanocortin signaling pathways that regulate energy homeostasis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00431 CUB 93 206 CUB domain Domain
PF07974 EGF_2 249 280 EGF-like domain Domain
PF13854 Kelch_5 352 392 Repeat
PF13418 Kelch_4 466 518 Repeat
PF13854 Kelch_5 579 614 Repeat
PF00059 Lectin_C 765 874 Lectin C-type domain Domain
PF01437 PSI 889 939 Plexin repeat Family
PF01437 PSI 942 1012 Plexin repeat Family
Sequence
METGGRARTGTPQPAAPGVWRARPAGGGGGGASSWLLDGNSWLLCYGFLYLALYAQVSQS
KPCERTGSCFSGRCVNSTCLCDPGWVGDQCQHCQGRFKLTEPSGYLTDGPINYKYKTKCT
WLIEGYPNAVLRLRFNHFATECSWDHMYVYDGDSIYAPLIAVLSGLIVPEIRGNETVPEV
VTTSGYALLHFFSDAAYNLTGFNIFY
SINSCPNNCSGHGKCTTSVSVPSQVYCECDKYWK
GEACDIPYCKANCGSPDHGYCDLTGEKLCVCNDSWQGPDCSLNVPSTESYWILPNVKPFS
PSVGRASHKAVLHGKFMWVIGGYTFNYSSFQMVLNYNLESSIWNVGTPSRGPLQRYGHSL
ALYQENIFMYGGRIETNDGNVTDELWVFNIHS
QSWSTKTPTVLGHGQQYAVEGHSAHIME
LDSRDVVMIIIFGYSAIYGYTSSIQEYHISSNTWLVPETKGAIVQGGYGHTSVYDEITKS
IYVHGGYKALPGNKYGLVDDLYKYEVNTKTWTILKESG
FARYLHSAVLINGAMLIFGGNT
HNDTSLSNGAKCFSADFLAYDIACDEWKILPKPNLHRDVNRFGHSAVVINGSMYIFGGFS
SVLLNDILVYKPPN
CKAFRDEELCKNAGPGIKCVWNKNHCESWESGNTNNILRAKCPPKT
AASDDRCYRYADCASCTANTNGCQWCDDKKCISANSNCSMSVKNYTKCHVRNEQICNKLT
SCKSCSLNLNCQWDQRQQECQALPAHLCGEGWSHIGDACLRVNSSRENYDNAKLYCYNLS
GNLASLTTSKEVEFVLDEIQKYTQQKVSPWVGLRKINISYWGWEDMSPFTNTTLQWLPGE
PNDSGFCAYLERAAVAGLKANPCTSMANGLVCEK
PVVSPNQNARPCKKPCSLRTSCSNCT
SNGMECMWCSSTKRCVDSNAYIISFPYGQCLEWQTATCS
PQNCSGLRTCGQCLEQPGCGW
CNDPSNTGRGHCIEGSSRGPMKLIGMHHSEMVLDTNLCPKEKNYEWSFIQCP
ACQCNGHS
TCINNNVCEQCKNLTTGKQCQDCMPGYYGDPTNGGQCTACTCSGHANICHLHTGKCFCTT
KGIKGDQCQLCDSENRYVGNPLRGTCYYSLLIDYQFTFSLLQEDDRHHTAINFIANPEQS
NKNLDISINASNNFNLNITWSVGSTAGTISGEETSIVSKNNIKEYRDSFSYEKFNFRSNP
NITFYVYVSNFSWPIKIQIAFSQHNTIMDLVQFFVTFFSCFLSLLLVAAVVWKIKQTCWA
SRRREQLLRERQQMASRPFASVDVALEVGAEQTEFLRGPLEGAPKPIAIEPCAGNRAAVL
TVFLCLPRGSSGAPPPGQSGLAIASALIDISQQKASDSKDKTSGVRNRKHLSTRQGTCV
Sequence length 1379
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Huntington Disease Huntington's disease progression N/A N/A GWAS
Oligodendroglioma Oligodendroglioma N/A N/A GWAS
Restless Legs Syndrome Restless legs syndrome N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Congenital Abnormalities Associate 30623622
Developmental Disabilities Associate 30623622
Renal Insufficiency Associate 32123936