Gene Gene information from NCBI Gene database.
Entrez ID 137835
Gene name Transmembrane protein 71
Gene symbol TMEM71
Synonyms (NCBI Gene)
-
Chromosome 8
Chromosome location 8q24.22
miRNA miRNA information provided by mirtarbase database.
6
miRTarBase ID miRNA Experiments Reference
MIRT1439085 hsa-miR-3130-3p CLIP-seq
MIRT1439086 hsa-miR-586 CLIP-seq
MIRT1439087 hsa-miR-767-5p CLIP-seq
MIRT2131500 hsa-miR-3074-5p CLIP-seq
MIRT2131501 hsa-miR-3124-3p CLIP-seq
Transcription factors Transcription factors information provided by TRRUST V2 database.
1
Transcription factor Regulation Reference
ING2 Unknown 20676127
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 32296183
GO:0005739 Component Mitochondrion IDA
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
620287 26572 ENSG00000165071
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6P5X7
Protein name Transmembrane protein 71
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15121 TMEM71 1 150 TMEM71 protein family Family
Sequence
MYRISQLMSTPVASSSRLEREYAGELSPTCIFPSFTCDSLDGYHSFECGSIDPLTGSHYT
CRRSPRLLTNGYYIWTEDSFLCDKDGNITLNPSQTSVMYKENLVRIFRKKKRICHSFSSL
FNLSTSKSWLHGSIFGDINSSPSEDNWLKG
TRRLDTDHCNGNADDLDCSSLTDDWESGKM
NAESVITSSSSHIISQPPGGNSHSLSLQSQLTASERFQENSSDHSETRLLQEVFFQAILL
AVCLIISACARWFMGEILASVFTCSLMITVAYVKSLFLSLASYFKTTACARFVKI
Sequence length 295
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
6
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
ASTROCYTOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ATTENTION DEFICIT HYPERACTIVITY DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CONGESTIVE HEART FAILURE Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
HEART FAILURE CTD, Disgenet
CTD, Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Glioblastoma Glioblastoma BEFREE 31180187
★☆☆☆☆
Found in Text Mining only
Glioblastoma Glioblastoma Pubtator 31180187 Associate
★☆☆☆☆
Found in Text Mining only
Glioblastoma Multiforme Glioblastoma BEFREE 31180187
★☆☆☆☆
Found in Text Mining only
Glioma Glioma BEFREE 31180187
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 31180187 Associate
★☆☆☆☆
Found in Text Mining only
Hyperthyroidism Hyperthyroidism GWASCAT_DG 30367059
★★☆☆☆
Found in Text Mining + Unknown/Other Associations