Human (GRCh37.p13)
Description

multiple coagulation factor deficiency 2 [Source:HGNC Symbol;Acc:18451]

Gene Synonyms

F5F8D, F5F8D2, LMAN1IP, SDNSF

Location

Chromosome 2: 47,129,009-47,168,994 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 17 transcripts (splice variants) and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000409105.1MCFD2-0024210146aaENSP00000386651.1
 
Protein coding
CCDS33192C9JTR4 Q8NI22 NM_001171506.2Ensembl CanonicalGENCODE Basic
ENST00000319466.4MCFD2-0014182146aaENSP00000317271.4
 
Protein coding
CCDS33192C9JTR4 Q8NI22 NM_139279.5GENCODE Basic
ENST00000444761.2MCFD2-2014169127aaENSP00000394647.2
 
Protein coding
CCDS54355Q8NI22 NM_001171511.2GENCODE Basic
ENST00000409913.1MCFD2-009397594aaENSP00000386941.1
 
Protein coding
CCDS54354Q8NI22 NM_001171509.2GENCODE Basic
ENST00000409800.1MCFD2-008395594aaENSP00000387202.1
 
Protein coding
CCDS54354Q8NI22 NM_001171510.2GENCODE Basic
ENST00000409207.1MCFD2-0031113146aaENSP00000386386.1
 
Protein coding
CCDS33192C9JTR4 Q8NI22 -GENCODE Basic
ENST00000409973.1MCFD2-004821146aaENSP00000386279.1
 
Protein coding
CCDS33192C9JTR4 Q8NI22 -GENCODE Basic
ENST00000409147.1MCFD2-01067194aaENSP00000387082.1
 
Protein coding
CCDS54354Q8NI22 -GENCODE Basic
ENST00000409218.1MCFD2-005648146aaENSP00000386261.1
 
Protein coding
CCDS33192C9JTR4 Q8NI22 -GENCODE Basic
ENST00000412438.1MCFD2-006588146aaENSP00000402717.1
 
Protein coding
C9JTR4 Q8NI22 -CDS 3' incomplete
ENST00000417180.1MCFD2-00756561aaENSP00000387541.1
 
Protein coding
C9JTR4 -CDS 3' incomplete
ENST00000434262.1MCFD2-01137690aaENSP00000387360.1
 
Protein coding
H7BZ18 -CDS 5' incomplete
ENST00000493804.1MCFD2-016807No protein-
 
Processed transcript
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ENST00000470873.1MCFD2-015552No protein-
 
Processed transcript
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ENST00000477791.1MCFD2-014665No protein-
 
Retained intron
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ENST00000487121.1MCFD2-013627No protein-
 
Retained intron
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ENST00000479225.1MCFD2-012568No protein-
 
Retained intron
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