ZMP
zgc:63647
Ensembl ID:
ZFIN ID:
Description:
formimidoyltransferase-cyclodeaminase [Source:RefSeq peptide;Acc:NP_957371]
Human Orthologue:
FTCD
Human Description:
formiminotransferase cyclodeaminase [Source:HGNC Symbol;Acc:3974]
Mouse Orthologue:
Ftcd
Mouse Description:
formiminotransferase cyclodeaminase Gene [Source:MGI Symbol;Acc:MGI:1339962]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14646 | Nonsense | Available for shipment | Available now |
sa24106 | Essential Splice Site | Available for shipment | Available now |
sa9153 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14646
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 |
---|---|---|---|---|---|
ENSDART00000044683 | Nonsense | 211 | 550 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 22 (position 12916929)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12752859 |
GRCz11 | 22 | 12777636 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAYAACGTGAATCTGCTGAGCACGAAGGAACAGGCTCAMAGAATCGCAT[T/A]GGACATCAGAGAACAGGGCCGCAGTAAAGATCAAGTATGTCTTTGTCTGA
Long Flanking Sequence:
TTATCATCCCATGTCTAGTTGGTATTGCAAATTACAATACAAAAACCTGCTAATAAACTGATGTGATCATCTATGAATAATTTATTATACAATATATTGTTTCAAACTACTAAAATCTCTAAAAAAAAAGTCACTTTGCTAAACTGCACGATTAAATTTTCAACATCAAATGTCAACAGAGCAGAGAATAATGGTCCGATAATATAATTTTACCCATGAATAAAAAAAATAAATAAATAACTGTTAATAAAAATATACAGAACATGTAAATTAATGGATATCATTTACATTATGAGGCCTAATTTCTGAGGAACAAAGAAATATGTTAACACCTCTTTTGTTCTTTGTCCCTCAGTTGAAAAAGAGTGAATGGGCTCCTGAATTCGGCCCAGCCACCTTTGTCCCCTCATGGGGAGCAACAGTCACCGGTGCCCGAAAGTTCCTTGTCGCCTATAACGTGAATCTGCTGAGCACGAAGGAACAGGCTCACAGAATCGCAT[T/A]GGACATCAGAGAACAGGGCCGCAGTAAAGATCAAGTATGTCTTTGTCTGACGTCACTGTATTGGTTTCGGTTTTCACTGCGTGTCAAATCTAGAACTTAAGAATCAAGGCAATCTGACCTAATTATACATATCACTTCCTTGAGGGTTTTCCCTATGTTCTGATCCCTGATGATTCAATGAAAGTGTTTCTGAATGTTGCTGGAGTATAGCCCGGGCTTCTCAAGAAAGTTCAAGGGATGGGATGGTACCTGGAAGAGTCCAATCTGGCGCAAGTGTCCACTAATATCCTGGACTTTGAGCTGACGCCAATGCACACGGTGTATGAAGAGATCTGTAGAGACGCCAAGGTGAGTCAACTTCAAATCTGAATTGGCATATCAGGAATCAGTCTCATGCTCCCTGCTCCTCCATGATTGCCGCAGCATCTGCTCAGGATACAGCCTGGTCTAGCATTATGGATACCTTGGCATCATTTCTTCACAGGTCTTTGATCGCATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24106
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044683 | Essential Splice Site | 491 | 550 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 22 (position 12922112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12758042 |
GRCz11 | 22 | 12782819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAAGAGATGGTCAAATATGGAAATGTGGCATGTAAATCAGACATTCAG[G/A]TGAGAGATGTTAAACTAGACCTTTTTTTTCTAAATAAATTAATGTTTACA
Long Flanking Sequence:
CAGATGAAATCAAAAGGTAAAGTTTAACATTGCTATTGTGCTTACACAAAACAGAAGTCATCCATCAAACTAGACATAATACGTGAAGGAACATTCTGTGTCCTGTTAAACCAGTTTAAGGGTTCAGTTGATGTAAAAACACTCCATGCACCACTAAGAAATAAGAAAGACTGGCAAAGACTTGACATATATTTGCAGAGAAGCATCTGACTGATAAAACAAACACATTATGCAAGCGTTCAGTTAAACACAACACTGGTAAAAACAAATATGGATCAGTAGCTATACATTAACTCTGCTGTTTGTCAAAATCATATGAAAGTTCAGCACTGATTGGCTGTATGTTGTGTTTGTTTGTCAGGAGGGAGGAAGCCATGCAGGAGGGTCTGAAAGCAGCGGTTCGTGTTCCTCTGTCTCTGGCAGAGAGAATAAACACACTCTGGCCGCATATTAAAGAGATGGTCAAATATGGAAATGTGGCATGTAAATCAGACATTCAG[G/A]TGAGAGATGTTAAACTAGACCTTTTTTTTCTAAATAAATTAATGTTTACACTTTTTAAATAAATATATTTGAATTATCTGAAATATGTTATATACATACAGTGGGTAAAATAAGTATTGAACACAGCTTATTTCGGTGCAGTTGACTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTACGAGATGTCAGCAACAACTAAAGTAATCCATACATACAAAGAAAACAAATCTAATTAGTTTAGAATTGAAGTTATGTGTAATGAAATGAAATGACTAAGGAAAAAAGAATTGAACACATGAAGAAAGGAAGGTTTAGAAAGGCAGTGAACGCCCACCCAGCTAGAAGAGAACGTTCTCTCAACTTTAGCTAACATTCCCTACAGGTTGTGTCATTGTTATAAAGAAAACAAAACAATGAACAAGAACATTCTGGCAATATCTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9153
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044683 | Nonsense | 497 | 550 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 22 (position 12925406)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 12761336 |
GRCz11 | 22 | 12786113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATWTACTTGAATTCTTGACTCCTTGTATGATCAGGTAGCGGCTAAAGCTT[T/A]GGAAAYAGCAGTGTATGGAGCTTATTTCAACGTCATTATAAACCTGAAGG
Long Flanking Sequence:
GAAAATATTTTCCTATCTTTTACGAGAATTTTGTGGGAACTAAAACAAAACTACCCACAGAAACAGTAATGCAACATTGCTTGGTAATATTCTCAGAACATGTAGAGAACTAAACATTTCTAGCTGGGCAGACAACAGCTGAAATCTCTGAGTATTGCTTCAGCAATCCTCTGCCCTTGGTTTTTGTAAATTAATATTCGCTGCTTCAGTTCAACATCTACATAATCAGGATGATGAAGATGAATCCCGGTTGGACATTTCAGCAAGACAAGGATCCAAAACACAGCCAAAGAAACTCAAGTGATTTGAGAGAAAGAAAATAAAGCTGAAGAATGGCCCAACCAATAACCTGATCCGAATCCAATAGAAAATAAGGACTAAAGATCATAGCTGACAGAAGAAACCCACAGAAACATTAAGGTTTTTAGACTGTGTTGAAGCAATGCATGCATTTACTTGAATTCTTGACTCCTTGTATGATCAGGTAGCGGCTAAAGCTT[T/A]GGAAACAGCAGTGTATGGAGCTTATTTCAACGTCATTATAAACCTGAAGGACATCACAGACGCTTCATTCAGGGCCAGCGTGAGTATATCCGACATCTGTTCGATATCTAGGTCATGCTTCCCAAATGGTGTATTAGATATCCCACATGTTTTTTCCGCTTTAATAACCCACACGCTCAGTGATATGAAACCTCTTTTGAGGAACCAATAAATGTCAACGAGCAAATTGAGAAAATGTTTCTGGCACTCACGGTTGATTTTGTGGCTTGTTGATTTGTAGACTGAAGCAAAAGTTTCTGCGCTGTTGAAAAGCTCCAGAGAGAACGCCAACATAGCGCTGGAGACGGCAGACCAGAGGAAATGATGACACAGCCAGACTGTAACTCACAACACGTTGAATAAAGAATGAAATGAAGACATGCTAATGTGCAGTTTGTGTTATTTCTGCTACTAAACACTTTATTTTGACTTAAAGTAGCCGTGAAATCTACAGTACAAAA
Associated Phenotype:
Not determined