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Human (GRCh37.p13)
Description

AF4/FMR2 family, member 3 [Source:HGNC Symbol;Acc:6473]

Gene Synonyms

LAF4, MLLT2-like

Location

Chromosome 2: 100,162,323-100,759,201 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 16 transcripts (splice variants), 3 paralogues and is associated with 74 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
AFF3-001ENST00000409236.294071226aaENSP00000387207.1
 
Protein coding
CCDS42723C9J622 C9J847 C9JC67
C9JMS1 C9JZ66 P51826
-GENCODE basic
AFF3-201ENST00000317233.481351226aaENSP00000317421.4
 
Protein coding
CCDS42723C9J622 C9J847 C9JC67
C9JMS1 C9JZ66 P51826
NM_002285
NP_002276
GENCODE basic
AFF3-202ENST00000356421.281181251aaENSP00000348793.2
 
Protein coding
CCDS33258P51826 NM_001025108
NP_001020279
GENCODE basic
AFF3-002ENST00000409579.143421251aaENSP00000386834.1
 
Protein coding
CCDS33258P51826 -GENCODE basic
AFF3-003ENST00000423966.1702155aaENSP00000396582.1
 
Protein coding
-C9J847 C9JC67 C9JMS1
C9JZ66
-CDS 3' incomplete
AFF3-008ENST00000440445.1591155aaENSP00000393732.1
 
Protein coding
-C9JUC4 -CDS 3' incomplete
AFF3-009ENST00000415384.1574183aaENSP00000407448.1
 
Protein coding
-C9JUY1 -CDS 3' incomplete
AFF3-014ENST00000432037.1559161aaENSP00000406484.1
 
Protein coding
-C9J622 C9J847 C9JC67
C9JMS1 C9JZ66
-CDS 3' incomplete
AFF3-015ENST00000445815.1555185aaENSP00000416685.1
 
Protein coding
-H7C4C2 -CDS 5' and 3' incomplete
AFF3-006ENST00000424600.1551114aaENSP00000411383.1
 
Protein coding
-C9J847 C9JMS1 -CDS 3' incomplete
AFF3-005ENST00000416492.154599aaENSP00000395068.1
 
Protein coding
-C9JMS1 -CDS 3' incomplete
AFF3-007ENST00000441400.1543128aaENSP00000399795.1
 
Protein coding
-C9J847 C9JMS1 C9JZ66
-CDS 3' incomplete
AFF3-010ENST00000427118.152817aaENSP00000416131.1
 
Protein coding
---CDS 3' incomplete
AFF3-012ENST00000430789.1730179aaENSP00000414099.1
 
Nonsense mediated decay
---CDS 5' incomplete
AFF3-011ENST00000483600.1852No protein-
 
Processed transcript
----
AFF3-013ENST00000498090.11673No protein-
 
Retained intron
----

Gene-based displays