ITGAL integrin subunit alpha L

Information
Symbol
ITGAL
Type
protein-coding
Description
integrin subunit alpha L
Entrez Gene ID
3683
Genome
hg19
Position
chr16:30,484,063-30,534,506
Genome
hg38
Position
chr16:30,472,742-30,523,185
MIM
153370 OMIM
HGNC
HGNC:6148 HGNC
Ensembl
ENSG00000005844 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 14
Likely benign 0 8
Uncertain significance 0 52
Ranking
ClinVar
0
0
0
72
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 :
Search word :
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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 CD11A
SYNONYM LFA-1
SYNONYM LFA1A
MIM 153370 OMIM
HGNC HGNC:6148 HGNC
Ensembl ENSG00000005844 Ensembl
AllianceGenome HGNC:6148
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000356798.11 hg38 chr16 30,472,742 30,523,185 50,444
ENST00000358164.9 hg38 chr16 30,472,729 30,522,968 50,240
ENST00000433423.2 hg38 chr16 30,472,751 30,521,779 49,029
ENST00000358164.9 hg19 chr16 30,484,050 30,534,289 50,240
ENST00000356798.11 hg19 chr16 30,484,063 30,534,506 50,444
ENST00000433423.2 hg19 chr16 30,484,072 30,533,100 49,029
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