Gene Gene information from NCBI Gene database.
Entrez ID 3975
Gene name LIM homeobox 1
Gene symbol LHX1
Synonyms (NCBI Gene)
LIM-1LIM1
Chromosome 17
Chromosome location 17q12
Summary This gene encodes a member of a large protein family which contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein is a transcription factor important for the development of the renal and urogenital systems. This gene is a
miRNA miRNA information provided by mirtarbase database.
75
miRTarBase ID miRNA Experiments Reference
MIRT614583 hsa-miR-141-3p HITS-CLIP 23824327
MIRT614582 hsa-miR-200a-3p HITS-CLIP 23824327
MIRT614581 hsa-miR-302c-5p HITS-CLIP 23824327
MIRT614580 hsa-miR-552-5p HITS-CLIP 23824327
MIRT614583 hsa-miR-141-3p HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
149
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin ISA
GO:0000977 Function RNA polymerase II transcription regulatory region sequence-specific DNA binding IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IBA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific IEA
GO:0000981 Function DNA-binding transcription factor activity, RNA polymerase II-specific ISA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
601999 6593 ENSG00000273706
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
P48742
Protein name LIM/homeobox protein Lhx1 (LIM homeobox protein 1) (Homeobox protein Lim-1) (hLim-1)
Protein function Potential transcription factor. May play a role in early mesoderm formation and later in lateral mesoderm differentiation and neurogenesis.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00412 LIM 4 59 LIM domain Domain
PF00412 LIM 63 122 LIM domain Domain
PF00046 Homeodomain 181 237 Homeodomain Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in the brain, thymus, and tonsils. Expressed in samples from patients with chronic myeloid leukemia (CML) and in 58% of acute myeloid leukemia (AML) cell lines. {ECO:0000269|PubMed:9212161}.
Sequence
MVHCAGCKRPILDRFLLNVLDRAWHVKCVQCCECKCNLTEKCFSREGKLYCKNDFFRCFG
TKCAGCAQGISPSDLVRRARSKVFHLNCFTCMMCNKQLSTGEELYIIDENKFVCKEDYLS
NS
SVAKENSLHSATTGSDPSLSPDSQDPSQDDAKDSESANVSDKEAGSNENDDQNLGAKR
RGPRTTIKAKQLETLKAAFAATPKPTRHIREQLAQETGLNMRVIQVWFQNRRSKERRMKQ
LSALGARRHAFFRSPRRMRPLVDRLEPGELIPNGPFSFYGDYQSEYYGPGGNYDFFPQGP
PSSQAQTPVDLPFVPSSGPSGTPLGGLEHPLPGHHPSSEAQRFTDILAHPPGDSPSPEPS
LPGPLHSMSAEVFGPSPPFSSLSVNGGASYGNHLSHPPEMNEAAVW
Sequence length 406
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
12
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Clear cell carcinoma of kidney Benign rs111571482 RCV005938687
LHX1-related disorder Benign; Likely benign rs111571482, rs35618899, rs749643400, rs75973369, rs368870359, rs377505639, rs77646323, rs376578880, rs201825686, rs145694637 RCV003921886
RCV003964481
RCV003939819
RCV003931542
RCV003914515
RCV003951523
RCV003922087
RCV003934627
RCV003972329
RCV003976549
Ovarian serous cystadenocarcinoma Benign rs111571482 RCV005938688
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Autism Spectrum Disorder Associate 36700567
Cardiovascular Abnormalities Associate 25510704
Chromosome Duplication Associate 25510704
Colorectal Neoplasms Associate 33111631
Developmental Disabilities Associate 36700567
Endometrial Neoplasms Stimulate 36116266
Glioblastoma Associate 38563293
Glioma Associate 22983390, 32857719, 35180817
Glycosuria Renal Associate 22583611
Hypoxia Stimulate 38563293