FIRRM FIGNL1 interacting regulator of recombination and mitosis

Information
Symbol
FIRRM
Type
protein-coding
Description
FIGNL1 interacting regulator of recombination and mitosis
Entrez Gene ID
55732
Genome
hg19
Position
chr1:169,764,550-169,823,221
Genome
hg38
Position
chr1:169,795,409-169,854,080
HGNC
HGNC:25565 HGNC
Ensembl
ENSG00000000460 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 4
Likely benign 0 4
Uncertain significance 0 10
Ranking
ClinVar
0
0
0
16
2
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data :
MGeND data only
Category :
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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 Apolo1
SYNONYM C1orf112
SYNONYM FLIP
SYNONYM MEICA1
HGNC HGNC:25565 HGNC
Ensembl ENSG00000000460 Ensembl
AllianceGenome HGNC:25565
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000496973.5 hg38 chr1 169,795,043 169,804,347 9,305
ENST00000286031.10 hg38 chr1 169,795,409 169,854,080 58,672
ENST00000472795.5 hg38 chr1 169,794,730 169,804,386 9,657
ENST00000359326.9 hg38 chr1 169,795,040 169,854,080 59,041
ENST00000413811.3 hg38 chr1 169,795,921 169,853,037 57,117
ENST00000472795.5 hg19 chr1 169,763,871 169,773,527 9,657
ENST00000359326.9 hg19 chr1 169,764,181 169,823,221 59,041
ENST00000496973.5 hg19 chr1 169,764,184 169,773,488 9,305
ENST00000286031.10 hg19 chr1 169,764,550 169,823,221 58,672
ENST00000413811.3 hg19 chr1 169,765,062 169,822,178 57,117
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