Gene Gene information from NCBI Gene database.
Entrez ID 343702
Gene name XK related 7
Gene symbol XKR7
Synonyms (NCBI Gene)
C20orf159dJ310O13.4
Chromosome 20
Chromosome location 20q11.21
miRNA miRNA information provided by mirtarbase database.
186
miRTarBase ID miRNA Experiments Reference
MIRT708400 hsa-miR-1207-3p HITS-CLIP 19536157
MIRT708399 hsa-miR-4267 HITS-CLIP 19536157
MIRT708398 hsa-miR-204-3p HITS-CLIP 19536157
MIRT708397 hsa-miR-4646-5p HITS-CLIP 19536157
MIRT708396 hsa-miR-6512-3p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
8
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane IEA
GO:0005886 Component Plasma membrane ISS
GO:0016020 Component Membrane IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q5GH72
Protein name XK-related protein 7
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF09815 XK-related 58 442 XK-related protein Family
Sequence
Sequence length 579
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG 
  Efferocytosis  
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Moyamoya angiopathy Likely pathogenic rs748725549 RCV004704501
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)