Human (GRCh37.p13)
Description

RGD motif, leucine rich repeats, tropomodulin domain and proline-rich containing [Source:HGNC Symbol;Acc:27089]

Gene Synonyms

CARMIL2, CARMIL2b, LRRC16C

Location

Chromosome 16: 67,678,822-67,691,472 forward strand.

GRCh37:CM000678.1

About this gene

This gene has 12 transcripts (splice variants), 2 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000334583.6RLTPR-00146871435aaENSP00000334958.5
 
Protein coding
CCDS45513Q6F5E8 NM_001013838.1Ensembl CanonicalGENCODE Basic
ENST00000545661.1RLTPR-00241191372aaENSP00000441481.1
 
Protein coding
Q6F5E8 -GENCODE Basic
ENST00000602563.1RLTPR-004104855aaENSP00000473580.1
 
Nonsense mediated decay
R4GNC4 --
ENST00000602368.1RLTPR-010953124aaENSP00000473419.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000602321.1RLTPR-0034494No protein-
 
Retained intron
---
ENST00000602562.1RLTPR-007893No protein-
 
Retained intron
---
ENST00000602633.1RLTPR-008888No protein-
 
Retained intron
---
ENST00000602705.1RLTPR-012638No protein-
 
Retained intron
---
ENST00000602742.1RLTPR-006591No protein-
 
Retained intron
---
ENST00000602931.1RLTPR-009526No protein-
 
Retained intron
---
ENST00000602924.1RLTPR-013521No protein-
 
Retained intron
---
ENST00000602467.1RLTPR-005485No protein-
 
Retained intron
---