Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
3549
Gene name Gene Name - the full gene name approved by the HGNC.
Indian hedgehog signaling molecule
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
IHH
Synonyms (NCBI Gene) Gene synonyms aliases
BDA1, HHG2
Disease Acronyms (UniProt) Disease acronyms from UniProt database
BDA1
Chromosome Chromosome number
2
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
2q35
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the hedgehog family of proteins. The encoded preproprotein is proteolytically processed to generate multiple protein products, including an N-terminal fragment that is involved in signaling. Hedgehog family proteins are essen
SNPs SNP information provided by dbSNP.
SNP ID Visualize variation Clinical significance Consequence
rs121917853 C>T Pathogenic Coding sequence variant, missense variant
rs121917857 A>G Pathogenic Coding sequence variant, missense variant
rs121917861 G>A Pathogenic Coding sequence variant, missense variant
rs143959492 C>T Conflicting-interpretations-of-pathogenicity Coding sequence variant, missense variant
rs267606872 G>T Pathogenic Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT447255 hsa-miR-4433b-3p PAR-CLIP 22100165
MIRT447254 hsa-miR-518c-5p PAR-CLIP 22100165
MIRT447253 hsa-miR-326 PAR-CLIP 22100165
MIRT447252 hsa-miR-330-5p PAR-CLIP 22100165
MIRT447251 hsa-miR-6764-3p PAR-CLIP 22100165
Transcription factors
Transcription factor Regulation Reference
RUNX2 Unknown 21328448
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001501 Process Skeletal system development IMP 21537345
GO:0001569 Process Branching involved in blood vessel morphogenesis IEA
GO:0001649 Process Osteoblast differentiation IEA
GO:0001701 Process In utero embryonic development IEA
GO:0001708 Process Cell fate specification IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600726 5956 ENSG00000163501
Protein
UniProt ID Q14623
Protein name Indian hedgehog protein (IHH) (EC 3.1.-.-) (HHG-2) [Cleaved into: Indian hedgehog protein N-product]
Protein function Plays a role in embryonic morphogenesis; it is involved in the regulation of endochondral skeleton formation, and the development of retinal pigment epithelium (RPE), photoreceptors and periocular tissues (By similarity). {ECO:0000250|UniProtKB:
PDB 3K7G , 3K7H , 3K7I , 3K7J , 3N1F , 3N1M , 3N1O , 3N1P
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01085 HH_signal 28 189 Hedgehog amino-terminal signalling domain Domain
PF01079 Hint 192 397 Hint module Family
Tissue specificity TISSUE SPECIFICITY: Expressed in embryonic lung, and in adult kidney and liver.
Sequence
Sequence length 411
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  KEGG   Reactome
  Hedgehog signaling pathway
Proteoglycans in cancer
  Hedgehog ligand biogenesis
Release of Hh-Np from the secreting cell
Ligand-receptor interactions
Activation of SMO
HHAT G278V abrogates palmitoylation of Hh-Np
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Acrocapitofemoral dysplasia Acrocapitofemoral Dysplasia, Acrocapitofemoral dysplasia rs121917856, rs121917857, rs1454141074 12632327, 21167467, 25959774
Brachydactyly Brachydactyly, BRACHYDACTYLY, TYPE A1 (disorder), Brachydactyly type A1 rs121908949, rs28937580, rs121909082, rs104894122, rs863223289, rs863223290, rs104894121, rs1587657302, rs863223292, rs74315386, rs74315387, rs28936397, rs753691079, rs121909348, rs121917852
View all (22 more)
21167467, 11455389, 12384778, 25959774, 21537345, 12632327
Gastrointestinal stromal tumor Gastrointestinal Stromal Tumors, Gastrointestinal Stromal Sarcoma rs587776653, rs74315368, rs74315369, rs587776793, rs587776794, rs587776795, rs606231209, rs121908589, rs121913685, rs121913680, rs794726675, rs587776804, rs121913517, rs121913234, rs121913512
View all (59 more)
27793025
Macrocephaly Macrocephaly, Relative macrocephaly rs786204854, rs764333096, rs1557739557
Unknown
Disease term Disease name Evidence References Source
Endometriosis Endometriosis 21063030 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Acrocallosal Syndrome Associate 22234151
Acrocapitofemoral Dysplasia Associate 19277064
Anophthalmos with limb anomalies Associate 30374058
Bone Diseases Associate 21537345
Bone Neoplasms Associate 22766796
Brachydactyly Associate 19277064
Brachydactyly type A1 Associate 21537345, 22234151, 30651074, 34315464
Breast Neoplasms Associate 18636275
Carcinogenesis Associate 18405344, 24384722
Carcinoma Ductal Associate 18636275