RLIM ring finger protein, LIM domain interacting

Information
Symbol
RLIM
Type
protein-coding
Description
ring finger protein, LIM domain interacting
Entrez Gene ID
51132
Genome
hg19
Position
chrX:73,802,811-73,834,459
Genome
hg38
Position
chrX:74,582,976-74,614,624
MIM
300379 OMIM
HGNC
HGNC:13429 HGNC
Ensembl
ENSG00000131263 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Pathogenic 0 12
Likely pathogenic 0 16
Benign 0 12
Likely benign 0 30
Conflicting classifications of pathogenicity 0 2
not provided 6 0
Uncertain significance 2 126
Ranking
ClinVar
0
0
20
160
10
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Variant name Gene AA change CDS Japanese
frequency		 TogoVar MGeND Genome ClinVar CIViC evidence DisGeNET entry COSMIC
occurrence		 Prediction
Entry Origin Type Annotation Entry Origin Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Size Chromosome Start Stop Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
Search Word
Target data :
MGeND data only
Category :
Search word :
Filtering :
Name MGeND Type Genome Gene symbol Chromosome Genomic start Genomic stop Strand Ref Alt ClinVar Origin Entry CIViC evidence DisGeNET entry
Entry Origin Type Annotation
TypeID
SYNONYM MRX61
SYNONYM NY-REN-43
SYNONYM RNF12
SYNONYM TOKAS
MIM 300379 OMIM
HGNC HGNC:13429 HGNC
Ensembl ENSG00000131263 Ensembl
AllianceGenome HGNC:13429
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000349225.2 hg38 chrX 74,590,118 74,614,617 24,500
ENST00000332687.11 hg38 chrX 74,582,976 74,614,624 31,649
ENST00000332687.11 hg19 chrX 73,802,811 73,834,459 31,649
ENST00000349225.2 hg19 chrX 73,809,953 73,834,452 24,500
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