ZMP
mef2cb
Ensembl ID:
ZFIN ID:
Description:
myocyte-specific enhancer factor 2C [Source:RefSeq peptide;Acc:NP_001124434]
Human Orthologue:
MEF2C
Human Description:
myocyte enhancer factor 2C [Source:HGNC Symbol;Acc:6996]
Mouse Orthologue:
Mef2c
Mouse Description:
myocyte enhancer factor 2C Gene [Source:MGI Symbol;Acc:MGI:99458]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20523 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20523
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000044083 | Nonsense | 242 | 475 | 6 | 9 |
| ENSDART00000135911 | Nonsense | 233 | 474 | 6 | 10 |
The following transcripts of ENSDARG00000009418 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 49971753)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 47537451 |
| GRCz11 | 5 | 48188962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGAATGAATAAAAGCATGCAGGCGAAATCTCCTCCGCCGGTGAACT[T/A]GGGCATGAACAGTCGCAAGCCTGACCTGCGAGTGCTCATCCCGCCTGGAG
Long Flanking Sequence:
TTTGATGGAGGGTGAACGAGAGGGTGTGTTTACCAAGCGCTTGGTGCAAATGAATGAGTGGTGGCGGAGGTGAAAGTTGTGTCAAATGGTGTGGAAACATCGAATTGAAAGAGCACATTCTTGCTGAAATATGGTTGCAATACTCCAGAACGGATAAAAAAGCGGTGTTTAATGGCAGCGTGTGGTGAAGGCTCACTGGAAGCGTGTGGAGAGCTGCAGACAGGCCTGAATGGAGGCTTCACAGTAGATGACGCTGGAAATGGTGCATCCTGGTGCAGGCGAGAGACTCAAATGAAGCTTGCTTAAATAGTGTGGCACGCTGAAAGTTTGATGTACTCCATTTGGCTCTGTTGTGTCTAATGACTTTTTTTTTTCTCCTCTCCCTTTCTGTCTCTCATTAGGAAACGGCTATGGAAACCACCGCAACTCTCCAGGTCTGCTGGTGTCCTCTGGAGGAATGAATAAAAGCATGCAGGCGAAATCTCCTCCGCCGGTGAACT[T/A]GGGCATGAACAGTCGCAAGCCTGACCTGCGAGTGCTCATCCCGCCTGGAGCCAAGAACAACATGCCCTCTATCGTAAGTCCATTACTTTTGAAACAAAATATCAGATCATTTACTCACCTTCATGTCATTACAAATCCATTAAACCTTCAATCAATTTAAATGAATACATTAATACACTAACTGTAAGAGATTTCTGTCCCTCCGTTGAAAGTTACTTCACCTAAAACTATAAATATAAAACATTATTCACTAGACTTTTTTTAGGCATGCACGATATAACAGCGGCCATATCGATATCGGCCGATAAATGCTATTTTTAATGTTACCATTATCGGTTCGATATTAAAATTAAGCCGATATCTTTAGGCCAATAGATTATGTCATTGTTCAGAATTGCCTGCTTGTCATTTTGTTATTTAACCTATTATTTTTTTGCAATGGTTTTATATGAATTCGCTATGCAAAGAAAAGAATACATTTTTGGCGTGCTGATTTATGT
Associated Phenotype:
Not determined