Mouse (GRCm39)
Description

microcephaly, primary autosomal recessive 1 [Source:MGI Symbol;Acc:MGI:2443308]

Gene Synonyms

5430437K10Rik, BRIT1, D030046N04Rik

Location
About this transcript

This transcript has 14 exons, is annotated with 35 domains and features, is associated with 10527 variant alleles and maps to 248 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchFlags
ENSMUST00000039412.15Mcph1-2014662822aaENSMUSP00000037000.9
 
Protein coding
CCDS22124Q7TT79 Ensembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENSMUST00000146819.8Mcph1-2052067600aaENSMUSP00000131616.2
 
Protein coding
E9PX19 GENCODE basicTSL:1
ENSMUST00000133417.2Mcph1-203768256aaENSMUSP00000121636.2
 
Protein coding
F6Q8J5 TSL:3CDS 5' and 3' incomplete
ENSMUST00000141244.3Mcph1-204681112aaENSMUSP00000119267.3
 
Protein coding
F6QJ89 TSL:3CDS 5' incomplete
ENSMUST00000124910.8Mcph1-2023878133aaENSMUSP00000131698.2
 
Nonsense mediated decay
G3UWE9 TSL:1
ENSMUST00000153133.2Mcph1-2062998No protein-
 
Retained intron
-TSL:1
Statistics

Exons: 14, Coding exons: 14, Transcript length: 4,662 bps, Translation length: 822 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q7TT79

CCDS

This transcript is a member of the Mouse CCDS set: CCDS22124

Transcript Support Level (TSL)

TSL:1

Version

ENSMUST00000039412.15

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

GENCODE basic gene

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