Human (GRCh37.p13)
Description

solute carrier family 44, member 4 [Source:HGNC Symbol;Acc:13941]

Gene Synonyms

C6orf29, CTL4, FLJ14491, NG22

Location

Chromosome 6: 31,830,969-31,846,823 reverse strand.

GRCh37:CM000668.1

View alleles of this gene on alternative sequences

About this gene

This gene has 9 transcripts (splice variants), 1 gene allele, 4 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000544672.1SLC44A4-2022634634aaENSP00000444109.1
 
Protein coding
CCDS54989Q53GD3 NM_001178045.1GENCODE basic
ENST00000229729.6SLC44A4-0012589710aaENSP00000229729.6
 
Protein coding
CCDS4724Q53GD3 NM_025257.2GENCODE basic
ENST00000375562.4SLC44A4-2012505668aaENSP00000364712.4
 
Protein coding
CCDS54990Q53GD3 NM_001178044.1GENCODE basic
ENST00000414427.1SLC44A4-0041233411aaENSP00000398901.1
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000465707.1SLC44A4-002681No protein-
 
Processed transcript
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ENST00000462671.1SLC44A4-003426No protein-
 
Processed transcript
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ENST00000487680.1SLC44A4-007392No protein-
 
Processed transcript
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ENST00000479777.1SLC44A4-006655No protein-
 
Retained intron
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ENST00000475563.1SLC44A4-005575No protein-
 
Retained intron
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