Gene Gene information from NCBI Gene database.
Entrez ID 167838
Gene name Taxilin beta
Gene symbol TXLNB
Synonyms (NCBI Gene)
C6orf198LST001MDP77dJ522B19.2
Chromosome 6
Chromosome location 6q24.1
miRNA miRNA information provided by mirtarbase database.
169
miRTarBase ID miRNA Experiments Reference
MIRT619519 hsa-miR-6892-3p HITS-CLIP 23824327
MIRT619518 hsa-miR-2276-5p HITS-CLIP 23824327
MIRT619517 hsa-miR-3183 HITS-CLIP 23824327
MIRT619516 hsa-miR-4723-3p HITS-CLIP 23824327
MIRT619515 hsa-miR-6769b-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21903422, 25416956, 28514442, 29892012, 31515488, 32296183, 33961781
GO:0005737 Component Cytoplasm IDA
GO:0019905 Function Syntaxin binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
611438 21617 ENSG00000164440
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N3L3
Protein name Beta-taxilin (Muscle-derived protein 77) (hMDP77)
Protein function Promotes motor nerve regeneration (By similarity). May be involved in intracellular vesicle traffic.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09728 Taxilin 143 450 Myosin-like coiled-coil protein Coiled-coil
Tissue specificity TISSUE SPECIFICITY: Expressed in skeletal muscle.
Sequence
MEANHSEQLSAERQSTPPGDSSSLPSHNGLEKEDGQDSPTPVQPPEKEASVHPDISEELN
RQLEDIINTYGSAASTAGKEGSARASEQPENAESPDNEDGDCEETTEEAGREPVASGEPP
TVKEPVSNKEQKLEKKILKGLGKEANLLMQNLNKLQTPEEKFDFLFKKYAELLDEHRTEQ
KKLKLLQKKQVQIQKEKDQLQGEHSRAILARSKLESLCRELQRHNKTLKEEALQRAREEE
EKRKEITSHFQSTLTDIQGQIEQQSERNMKLCQENTELAEKLKSIIDQYELREEHLDKIF
KHRELQQKLVDAKLEQAQEMMKEAEERHKREKEYLLNQAAEWKLQAKVLKEQETVLQAQL
TLYSGRFEEFQSTLTKSNEVFATFKQEMDKTTKKMKKLEKDTATWKARFENCNKALLDMI
EEKALRAKEYECFVMKIGRLENLCRALQEE
RNELHKKIRDAEISEKDDQSQHNSDEEPES
NVSVDQEIDAEEVNSVQTAVKNLATAFMIIHHPESTPHQSKETQPEIGSSQESADAALKE
PEQPPLIPSRDSESPLPPLTPQAEAEGGSDAEPPSKASNSPAGLGAETQCEGLPVGAQAD
QASWKPEAEASGQAPQAPTEASLQKMEADVPAPACAAEEHVAAMVPACEPSRQPPRAAAE
ELPVGASAGPQPRNVADTNLEGVD
Sequence length 684
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
OBESITY GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations