Description

keratin 33B, type I [Source:HGNC Symbol;Acc:HGNC:6451]

Synonyms

Ha-3II, KRTHA3B

Location

Chromosome 17: 41,363,494-41,397,592 reverse strand.

View alleles of this gene on alternate assemblies

INSDC coordinates

chromosome:GRCh38:CM000679.2:41363494:41397592:1

About this gene

This gene has 2 transcripts (splice variants), 1 gene allele, 183 orthologues, 23 paralogues, is a member of 1 Ensembl protein family and is associated with 76 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
KRT33B-001ENST000002516461607404aaENSP00000251646
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS11389Q14525 NM_002279
NP_002270
TSL:1

Transcript Support Level 1, when transcripts are supported by at least one non-suspect mRNA.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS P2

PRINCIPAL2 - APPRIS candidate principal isoform (CCDS).

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

KRT33B-201ENST000006204211284404aaENSP00000485008
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
-A0A087X2I6 -TSL:5

Transcript Support Level 5, for transcripts that are not supported at all by either an mRNA or an EST.

The Transcript Support Level (TSL) is a method to highlight the well-supported and poorly-supported transcript models for users. The method relies on the primary data that can support full-length transcript structure: mRNA and EST alignments supplied by UCSC and Ensembl.

GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).APPRIS ALT1

ALTERNATIVE1 - APPRIS candidate principal isoform that is conserved in at least three tested non-primate species.

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

Gene-based displays