NM_144966.5(FREM1):c.*2704A>C AND Oculotrichoanal syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000316343.14
Allele description [Variation Report for NM_144966.5(FREM1):c.*2704A>C]
NM_144966.5(FREM1):c.*2704A>C
Condition(s)
- Name:
- Oculotrichoanal syndrome (MOTA)
- Synonyms:
- Marles Greenberg Persaud syndrome; Unilateral upper eyelid coloboma, aberrant anterior hairline pattern, and anal anomalies; Marles syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0009560; MedGen: C1855425; OMIM: 248450
-
ubiquitin carboxyl-terminal hydrolase 48 isoform X3 [Gallus gallus]
ubiquitin carboxyl-terminal hydrolase 48 isoform X3 [Gallus gallus]gi|1390089758|ref|XP_024998322.1|Protein
-
PMC Links for GEO DataSets (Select 4248) (1)
PMC
-
PMC Links for GEO DataSets (Select 4307) (1)
PMC
-
RecName: Full=Histone-lysine N-methyltransferase 2D; Short=Lysine N-methyltransf...
RecName: Full=Histone-lysine N-methyltransferase 2D; Short=Lysine N-methyltransferase 2D; AltName: Full=ALL1-related protein; AltName: Full=Myeloid/lymphoid or mixed-lineage leukemia protein 2gi|313104132|sp|O14686.2|KMT2D_HUMAProtein
-
Homo sapiens chromosome 5 open reading frame 3 (C5orf3), mRNA
Homo sapiens chromosome 5 open reading frame 3 (C5orf3), mRNAgi|8922068|ref|NM_018691.1|Nucleotide
Your browsing activity is empty.
Activity recording is turned off.
See more...Assertion and evidence details
Last Updated: Nov 10, 2024