Human (GRCh38.p14)
Description

RNA binding region (RNP1, RRM) containing 3 [Source:HGNC Symbol;Acc:HGNC:18666]

Gene Synonyms

FLJ20008, KIAA1839, RBM40, SNRNP65

Location

Chromosome 1: 103,525,691-103,555,239 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 9 transcripts (splice variants), 197 orthologues, 1 paralogue and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000423855.7RNPC3-2012144517aaENSP00000391432.1
 
Protein coding
CCDS781Q96LT9-1 NM_017619.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P4TSL:1
ENST00000533099.5RNPC3-2083641517aaENSP00000432886.1
 
Protein coding
CCDS781Q96LT9-1 -GENCODE basicAPPRIS P4TSL:5
ENST00000524631.5RNPC3-2022013516aaENSP00000437278.1
 
Protein coding
Q96LT9-2 -GENCODE basicAPPRIS ALT1TSL:2
ENST00000527062.5RNPC3-205768138aaENSP00000436315.1
 
Protein coding
E9PPV2 -TSL:5CDS 3' incomplete
ENST00000531883.5RNPC3-206686185aaENSP00000431344.1
 
Protein coding
X6RLP6 -TSL:2CDS 3' incomplete
ENST00000524641.1RNPC3-203547182aaENSP00000435440.1
 
Protein coding
H0YEB8 -TSL:4CDS 5' and 3' incomplete
ENST00000532117.1RNPC3-20723718aaENSP00000434721.1
 
Nonsense mediated decay
H0YE07 -TSL:3CDS 5' incomplete
ENST00000533834.1RNPC3-2093658No protein-
 
Retained intron
--TSL:1
ENST00000525323.1RNPC3-204432No protein-
 
Retained intron
--TSL:3