Mouse (GRCm39)
Description

cerebral cavernous malformation 2 [Source:MGI Symbol;Acc:MGI:2384924]

Location
About this transcript

This transcript has 10 exons, is annotated with 10 domains and features, is associated with 2560 variant alleles and maps to 233 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchFlags
ENSMUST00000000388.15Ccm2-2011858453aaENSMUSP00000000388.9
 
Protein coding
CCDS24422Q8K2Y9 Ensembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENSMUST00000109722.9Ccm2-2031760389aaENSMUSP00000105344.3
 
Protein coding
CCDS48751F7AVU1 GENCODE basicTSL:1
ENSMUST00000109721.3Ccm2-2021551389aaENSMUSP00000105343.3
 
Protein coding
CCDS48751F7AVU1 GENCODE basicTSL:5
ENSMUST00000160633.8Ccm2-206827243aaENSMUSP00000125072.2
 
Protein coding
E0CXR5 TSL:5CDS 3' incomplete
ENSMUST00000159007.8Ccm2-205431113aaENSMUSP00000125608.2
 
Protein coding
E0CZ84 TSL:3CDS 3' incomplete
ENSMUST00000161501.8Ccm2-207691126aaENSMUSP00000123790.2
 
Nonsense mediated decay
E0CYY2 TSL:5
ENSMUST00000144293.2Ccm2-2041182No protein-
 
Protein coding CDS not defined
-TSL:1
ENSMUST00000161667.2Ccm2-208815No protein-
 
Retained intron
-TSL:2
Statistics

Exons: 10, Coding exons: 9, Transcript length: 1,760 bps, Translation length: 389 residues

CCDS

This transcript is a member of the Mouse CCDS set: CCDS48751

Transcript Support Level (TSL)

TSL:1

Version

ENSMUST00000109722.9

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.