ZMP
zgc:92066
Ensembl ID:
ZFIN ID:
Description:
ferritin heavy chain [Source:RefSeq peptide;Acc:NP_001002378]
Human Orthologue:
FTL
Human Description:
ferritin, light polypeptide [Source:HGNC Symbol;Acc:3999]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33211 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33211
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044238 | Essential Splice Site | 125 | 174 | None | 4 |
ENSDART00000109791 | Essential Splice Site | 177 | 226 | None | 5 |
The following transcripts of ENSDARG00000031776 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 3 (position 32237521)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 31968831 |
GRCz11 | 3 | 32100545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTCTGCTGGACCTGCATAAAGTCGCCTCTCAAAAGGGAGACCCTCATG[T/C]AAGTTAATAAAGTCCATAATATACATTGGTCCTTAATACTTTAATTAGGT
Long Flanking Sequence:
TTCTCTAACGTTGTATTTCACGACGCCATTAGCTGTAAAAGATCACGTTGCTCTGCGTGTTTATTAAATTTTCGCAATCCATATTTCAACCAACAGGCTTTCTACTTTGACCGGGACGATGTGGCTCTTCCTGGATTTGCCAAGTTCTTCAAGAAGAACAGTGAGGAGGAGCGCGAACATGCTGAGAAATTCATGGAGTTCCAGAACAAGAGAGGTGGACGCATTGTCCTTCAGGACATCAAGGTGAGCATATTTCTTCTTTCCTGTTTGCGTTTTAATAAGAAAAACTTTTGTATAGATGCAATCATATATAACTGCTCAAAGTGGAGGGGGGAAGGGCGTCACGTGCTCACTGACGTGTTTGTTTTTCCAGAAACCTGAGCGCGATGAGTGGGACAATGGGCTGACTGCTATGCAGTGTGCTCTTCAGCTGGAGAAGAACGTCAACCAGGCTCTGCTGGACCTGCATAAAGTCGCCTCTCAAAAGGGAGACCCTCATG[T/C]AAGTTAATAAAGTCCATAATATACATTGGTCCTTAATACTTTAATTAGGTGTCTTAACATCTTCTCTGATGTCTTGTTCATCAGCTGTGTGATTTCCTGGAGTCTCACTACCTGAATGAGCAGGTTGAGGCCATCAAGAAGCTTGGTGACCACATCACTAACCTCTCCAAGATGGATGCTGGAAATAACAGGATGGCGGAGTACCTGTTTGACAAGCACACCCTGGACAGCTAAACTCGGATCATCTGCAGCCACTAAAGCCTCCAGTTGTACTCTATGCATAAATCATGAAACCATGTTGTCCCGCAGTAAAATCTTTGAGGTTAACATTTAGAGGCTTCATGTTTAAGATCTGCCTTGTTAAATCAGTCATCTAGCTGATGCCTTGCTTGTTGAATGTGCACTGACTTGTTGGTCACCTTGTGAATCTGATGAATAAACATTTCTGGCTGAATTTACTTGTCATTTTTCTGTTTTTCAACAAACTGAAGGTGCATTCG
Associated Phenotype:
Not determined