The LRRFIP2 gene homepage

General information
Gene symbol LRRFIP2
Gene name leucine rich repeat (in FLII) interacting protein 2
Chromosome 3
Chromosomal band p22.1
Imprinted Unknown
Genomic reference NC_000003.11
Transcript reference NM_001134369.1, NM_006309.2, NM_017724.2, XM_005265538.1, XM_005265539.1, XM_005265540.1, XM_005265541.1, XM_005265542.1, XM_005265543.1, XM_005265544.1, XM_005265545.1, XM_005265546.1, XM_005265547.1, XM_005265548.1, XM_005265549.1, XM_005265550.1, XM_005265551.1, XM_005265552.1, XM_005265553.1, XM_005265554.1, XM_005265555.1, XM_005265556.1, XM_005265557.1, XM_005265558.1
Associated with diseases -
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 151
Unique public DNA variants reported 20
Individuals with public variants 35
Hidden variants 48
Date created October 29, 2013
Date last updated September 28, 2016
Version LRRFIP2:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:6703
Entrez Gene 9209
PubMed articles LRRFIP2
OMIM - Gene 614043
HGMD LRRFIP2
GeneCards LRRFIP2
GeneTests LRRFIP2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00004425 3 transcript variant 1 NM_006309.2 NP_006300.1 151
00004426 3 transcript variant 3 NM_001134369.1 NP_001127841.1 63
00017860 3 Manually created transcript. (removed from reference sequence) NM_017724.2 - 63
00042927 3 transcript variant X7 XM_005265544.1 XP_005265601.1 -
00042928 3 transcript variant X14 XM_005265551.1 XP_005265608.1 -
00042929 3 transcript variant X10 XM_005265547.1 XP_005265604.1 -
00042930 3 transcript variant X12 XM_005265549.1 XP_005265606.1 -
00042931 3 transcript variant X21 XM_005265558.1 XP_005265615.1 -
00042932 3 transcript variant X17 XM_005265554.1 XP_005265611.1 -
00042933 3 transcript variant X11 XM_005265548.1 XP_005265605.1 -
00042934 3 transcript variant X16 XM_005265553.1 XP_005265610.1 -
00042935 3 transcript variant X3 XM_005265540.1 XP_005265597.1 -
00042936 3 transcript variant X9 XM_005265546.1 XP_005265603.1 -
00042937 3 transcript variant X2 XM_005265539.1 XP_005265596.1 -
00042938 3 transcript variant X13 XM_005265550.1 XP_005265607.1 -
00042939 3 transcript variant X19 XM_005265556.1 XP_005265613.1 -
00042940 3 transcript variant X18 XM_005265555.1 XP_005265612.1 -
00042941 3 transcript variant X5 XM_005265542.1 XP_005265599.1 -
00042942 3 transcript variant X6 XM_005265543.1 XP_005265600.1 -
00042943 3 transcript variant X8 XM_005265545.1 XP_005265602.1 -
00042944 3 transcript variant X20 XM_005265557.1 XP_005265614.1 -
00042945 3 transcript variant X4 XM_005265541.1 XP_005265598.1 -
00042946 3 transcript variant X1 XM_005265538.1 XP_005265595.1 -
00042947 3 transcript variant X15 XM_005265552.1 XP_005265609.1 -


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