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Human (GRCh37.p13)
Description

inverted formin, FH2 and WH2 domain containing [Source:HGNC Symbol;Acc:23791]

Gene Synonyms

C14orf151, C14orf173, CMTDIE, FSGS5, MGC13251, pp9484

Location

Chromosome 14: 105,155,943-105,185,942 forward strand.

GRCh37:CM000676.1

About this gene

This gene has 8 transcripts (splice variants), 12 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000392634.4INF2-00146721249aaENSP00000376410.4
 
Protein coding
CCDS9989Q27J81 NM_022489.3Ensembl CanonicalGENCODE basic
ENST00000330634.7INF2-00346481240aaENSP00000376406.3
 
Protein coding
CCDS45173Q27J81 NM_001031714.3GENCODE basic
ENST00000252527.8INF2-0103050717aaENSP00000252527.8
 
Protein coding
--CDS 5' incomplete
ENST00000398337.4INF2-0091689234aaENSP00000381380.4
 
Protein coding
CCDS41999Q27J81 NM_032714.2GENCODE basic
ENST00000481338.1INF2-0051102No protein-
 
Processed transcript
---
ENST00000474229.1INF2-006947No protein-
 
Retained intron
---
ENST00000480763.2INF2-007581No protein-
 
Retained intron
---
ENST00000477497.1INF2-008545No protein-
 
Retained intron
---