Busch Lab

ZMP

fech

Ensembl ID:
ENSDARG00000003462
ZFIN ID:
ZDB-GENE-000928-1
Description:
ferrochelatase, mitochondrial [Source:RefSeq peptide;Acc:NP_571706]
Human Orthologue:
FECH
Human Description:
ferrochelatase [Source:HGNC Symbol;Acc:3647]
Mouse Orthologue:
Fech
Mouse Description:
ferrochelatase Gene [Source:MGI Symbol;Acc:MGI:95513]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa23835 Nonsense Available for shipment Available now
sa37199 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23835
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113389 Nonsense 66 409 3 12
Genomic Location (Zv9):
Chromosome 21 (position 1974693)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 1626121
GRCz11 21 1651945
KASP Assay ID:
2261-5090.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTACAGAAAACCCAAAACAGGCATTCTGATGCTGAATATGGGCGGTCCA[G/T]AGAAGCTGGAGGATGTTCATGATTTCCTGCTGCGCCTCTTCATGGATACA
Long Flanking Sequence:
CACACACTGCCACAAACACACTGGCAAAAATAAAGTCCAAACACATGCGCTATAGCGGAATTGATTAACTAAATTGTCCGTAGTCTATAAGTGTGTATGGGTGTTCCCCAGTACTGGGTTGCAGCTGGAAGGGCATCCACTGCAAATAACATATGCTGGAATAGTTGGCAGTTCATTCGGCTGTGGCGACCTCTGAAATAGAGACTAATCGGAAGGAAGATGAACGAATAGAAGATTTCTAAAAGTCTTCAGCTTCAACACAAAAGAAAAGCTTTAAAGTGTGGAATATTTCCTGCTGTCTGGACTTCTCATGTGCAGCATTCTCTCAGGGTTTACATTAATGCTTTTAGCTGACGGTTTTAAAAACGGGGCTTTTCTTTTCTCCACTAAGTCTGACTCTTCTGCATGACTGAACATTCACTGAGATGACTAAAGAAATACTGTGTTTTCACTACAGAAAACCCAAAACAGGCATTCTGATGCTGAATATGGGCGGTCCA[G/T]AGAAGCTGGAGGATGTTCATGATTTCCTGCTGCGCCTCTTCATGGATACAGACCTCATGCAGCTGCCCGTGCAGAAGTAAGAAAGACTATTCAACATTTATAGGTCTAATATATACACTTCCTGACAAGTTTATTTTTTATTTTTATTATTTTTATTATTTTTTTTATTAACAAGAACCAGCATGTACAGTTTTCTTATACAATACAATACAATCACTTTACATTTCTTAACAAGAATGAAATGAGTGAAAAAACATAAAGGAGAAGAGAAAGAAAAAAAAACAGAGGAGAGGGTACATAATTATCAAACTACATATAAATATGTTTCGCACATTTTCCAATTTTAGTTATTTACAAGAGTTAGTAATGCACTTTTTTTTCTTTTCTTTTTTTTTTTTACAGGAAATTCATTTATACAAACATTTTATGTAAAAATGTTAAAGGGTCACGACCAAAACAACACCAGAACACATGTGTTGAGCTGTTGACAGTCATATATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37199
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000113389 Nonsense 311 409 9 12
Genomic Location (Zv9):
Chromosome 21 (position 1988658)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 1640086
GRCz11 21 1665910
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCGTGGTTGGGGCCACAGACAGATGAGGTCATCAAGGGTCTCTGTCAG[C/T]GAGGCAAGAGGAACCTGCTGCTGGTGCCCATCGCCTTCACCAGCGACCAC
Long Flanking Sequence:
GTGTAATGAAGGTTTCTCGTGTTCCATGTGTGATTATTGTGAGAATAGTTTGCTGGGTTCCATGTGTGTTTCCTGTGTGATAAATGCACTTGACATGTATCTTGTGTACTTCAGGTGGTGAACCGGGGTGATCCATACCCACAGGAAGTGGGCGCTACAGTTCAGAGAGTGATGGACCGACTGGGCCACTGTAACCCATACAGACTCGTCTGGCAGTCAAAGGTCAGTTTATATATATATATATATATATATATATATATATATCATAATATTTACCTTTATTGATTTTAAAAGTCATTGTAATTTAGTGCTTCATACATATTATGTGCTTCACATGATAGAGTACACCACACACAGATCTCTCCGTAACATTCATATTTTCTATAGAATGATTTTTAATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGGTTGGGCCGATGGCGTGGTTGGGGCCACAGACAGATGAGGTCATCAAGGGTCTCTGTCAG[C/T]GAGGCAAGAGGAACCTGCTGCTGGTGCCCATCGCCTTCACCAGCGACCACATCGAGACGCTGCACGAGCTGGACATCGAGTACTCACAGGTCCTCGGAGAAGAGGTGTGTGTGTGTATATGTTTTTGTGACATATCAGGACAAATGTGTATCATGTCATAGGAATGACACCGGTATTAGAGACTGAATTATGAAGACACAGCTTCCTTTAAAGGGTTATGTGTAGGGTTGTGGAGGGGGACAAGGTTATAGTAGTTTTGCATTTTTCATTAGTTTTAGTTATTTTATTTTGAGTTTTTTTTTAAATGAAATTAGTTTTAACTAGTTTTAGAGGCAGATTTACTAGTTTTTATTTCTTTCTATATTTTGAAATTGCTTAGTTTTAGTTTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACATCAGAATGAACCGCCAATTATCTAGCATATGTTTTAGGCAGCAAATGCCTTTCTAGCC
Associated Phenotype:
Not determined