Gene Gene information from NCBI Gene database.
Entrez ID 79906
Gene name MORN repeat containing 1
Gene symbol MORN1
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1p36.32
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.
Q5T089
Protein name MORN repeat-containing protein 1
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF02493 MORN 23 35 MORN repeat Repeat
PF02493 MORN 39 61 MORN repeat Repeat
PF02493 MORN 62 83 MORN repeat Repeat
PF02493 MORN 86 108 MORN repeat Repeat
PF02493 MORN 109 131 MORN repeat Repeat
PF02493 MORN 132 154 MORN repeat Repeat
PF02493 MORN 155 177 MORN repeat Repeat
PF02493 MORN 178 200 MORN repeat Repeat
Sequence
MAAAGEGTPSSRGPRRDPPRRPPRNGYGVYVYPNSFFRYEGEWKAGRKHGHGKLLFKDGS
Y
YEGAFVDGEITGEGRRHWAWSGDTFSGQFVLGEPQGYGVMEYKAGGCYEGEVSHGMREG
HGFLVDRDGQV
YQGSFHDNKRHGPGQMLFQNGDKYDGDWVRDRRQGHGVLRCADGSTYKG
QWHSDVFSGLGSMAHCSGVT
YYGLWINGHPAEQATRIVILGPEVMEVAQGSPFSVNVQLL
QDHGEIAKSESGRVLQISAGVRYVQLSAYSEVNFFKVDRDNQETLIQTPFGFECIPYPVS
SPAAGVPGPRAAKGGAEADVPLPRGDLELHLGALHGQEDTPGGLLARGHAPHCPGACQRV
EQGCAEFTDVLLGPPPPGYHPFLFLDSLHKKAGGRSRGGLHPRGTPPTAQEPPGGSRPEG
RATEEQAAAAHLGEYVLMIRDVTTPPFLGRRLPPAFKHLRVVAKRAGQPPHVLEEGPEAS
SSWQAAHSCTPEPPAPR
Sequence length 497
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
1
Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Melanoma Uncertain significance rs772641540 RCV005939348
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Sacral defect and anterior sacral meningocele Associate 28007035