Gene Gene information from NCBI Gene database.
Entrez ID 55084
Gene name Sine oculis binding protein homolog
Gene symbol SOBP
Synonyms (NCBI Gene)
JXC1MRAMS
Chromosome 6
Chromosome location 6q21
Summary The protein encoded by this gene is a nuclear zinc finger protein that is involved in development of the cochlea. Defects in this gene have also been linked to intellectual disability. [provided by RefSeq, Mar 2011]
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs267607078 C>T Pathogenic Coding sequence variant, stop gained
rs368271940 C>A Conflicting-interpretations-of-pathogenicity Coding sequence variant, missense variant
miRNA miRNA information provided by mirtarbase database.
197
miRTarBase ID miRNA Experiments Reference
MIRT016801 hsa-miR-335-5p Microarray 18185580
MIRT043220 hsa-miR-324-5p CLASH 23622248
MIRT723626 hsa-miR-3123 HITS-CLIP 19536157
MIRT723625 hsa-miR-8076 HITS-CLIP 19536157
MIRT723624 hsa-miR-4733-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
GO:0007605 Process Sensory perception of sound IEA
GO:0007626 Process Locomotory behavior IEA
GO:0008270 Function Zinc ion binding IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
613667 29256 ENSG00000112320
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
A7XYQ1
Protein name Sine oculis-binding protein homolog (Jackson circler protein 1)
Protein function Implicated in development of the cochlea.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15279 SOBP 224 543 Sine oculis-binding protein Family
Sequence
MAEMEKEGRPPENKRSRKPAHPVKREINEEMKNFAENTMNELLGWYGYDKVELKDGEDIE
FRSYPTDGESRQHISVLKENSLPKPKLPEDSVISPYNISTGYSGLATGNGLSDSPAGSKD
HGSVPIIVPLIPPPFIKPPAEDDVSNVQIMCAWCQKVGIKRYSLSMGSEVKSFCSEKCFA
ACRRAYFKRNKARDEDGHAENFPQQHYAKETPRLAFKNNCELLVCDWCKHIRHTKEYLDF
GDGERRLQFCSAKCLNQYKMDIFYKETQANLPAGLCSTLHPPMENKAEGTGVQLLTPDSW
NIPLTDARRKAPSPVATAGQSQGPGPSASTTVSPSDTANCSVTKIPTPVPKSIPISETPN
IPPVSVQPPASIGPPLGVPPRSPPMVMTNRGPVPLPIFMEQQIMQQIRPPFIRGPPHHAS
NPNSPLSNPMLPGIGPPPGGPRNLGPTSSPMHRPMLSPHIHPPSTPTMPGNPPGLLPPPP
PGAPLPSLPFPPVSMMPNGPMPVPQMMNFGLPSLAPLVPPPTLLVPYPVIVPLPVPIPIP
IPI
PHVSDSKPPNGFSSNGENFIPNAPGDSAAAGGKPSGHSLSPRDSKQGSSKSADSPPG
CSGQALSLAPTPAEHGRSEVVDLTRRAGSPPGPPGAGGQLGFPGVLQGPQDGVIDLTVGH
RARLHNVIHRALHAHVKAEREPSAAERRTCGGCRDGHCSPPAAGDPGPGAPAGPEAAAAC
NVIVNGTRGAAAEGAKSAEPPPEQPPPPPPPAPPKKLLSPEEPAVSELESVKENNCASNC
HLDGEAAKKLMGEEALAGGDKSDPNLNNPADEDHAYALRMLPKTGCVIQPVPKPAEKAAM
APCIISSPMLSAGPEDLEPPLKRRCLRIRNQNK
Sequence length 873
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
9
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
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ANTERIOR MAXILLARY PROTRUSION, STRABISMUS, INTELLECTUAL DISABILITY SYNDROME Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ANTERIOR MAXILLARY PROTRUSION-STRABISMUS-INTELLECTUAL DISABILITY SYNDROME Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CARCINOMA, BASAL CELL CTD
★★☆☆☆
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
Anterior maxillary protrusion-strabismus-intellectual disability syndrome Anterior Maxillary Protrusion-Strabismus-Intellectual Disability Syndrome Orphanet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
B-Cell Lymphomas B-Cell Lymphoma BEFREE 31686349
★☆☆☆☆
Found in Text Mining only
Global developmental delay Developmental Delay HPO_DG
★☆☆☆☆
Found in Text Mining only
Intellectual Disability Mental retardation BEFREE 21035105
★☆☆☆☆
Found in Text Mining only
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Mental Retardation, Anterior Maxillary Protrusion, And Strabismus BEFREE 17618476
★☆☆☆☆
Found in Text Mining only
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Mental Retardation, Anterior Maxillary Protrusion, And Strabismus GENOMICS_ENGLAND_DG 17618476, 21035105
★☆☆☆☆
Found in Text Mining only
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Mental Retardation, Anterior Maxillary Protrusion, And Strabismus CLINVAR_DG
★☆☆☆☆
Found in Text Mining only
MENTAL RETARDATION, ANTERIOR MAXILLARY PROTRUSION, AND STRABISMUS Mental Retardation, Anterior Maxillary Protrusion, And Strabismus CTD_human_DG
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 31686349
★☆☆☆☆
Found in Text Mining only
Nonorganic psychosis Nonorganic Psychosis BEFREE 21035105
★★☆☆☆
Found in Text Mining + Unknown/Other Associations