ZMP
fzd8a
Ensembl ID:
ZFIN ID:
Description:
frizzled homolog 8a [Source:RefSeq peptide;Acc:NP_570993]
Human Orthologue:
FZD8
Human Description:
frizzled homolog 8 (Drosophila) [Source:HGNC Symbol;Acc:4046]
Mouse Orthologue:
Fzd8
Mouse Description:
frizzled homolog 8 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:108460]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37812 | Nonsense | Available for shipment | Available now |
| sa5986 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44078 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa37811 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44077 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa44076 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa24435 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37812
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000066835 | Nonsense | 43 | 579 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 4527516)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 4418009 |
| GRCz11 | 24 | 4449796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGATCACCTGTCAGGAGATCGCCGTTCCGCTGTGCAAGGGCATCGGTTA[T/G]AACTACACCTACATGCCCAACCAGTTCAACCACGACACGCAGGATGAAGC
Long Flanking Sequence:
TGTCCGCACGACTGTCTTTTATACTCAGTGCGTCCTACTCTACAGCACTGATTTGTATGAGAAAGCCTCTCGCGAACACCACGAATGTTGAAAACGCGTTTACACCGGGAGTTTTCTTGTTGACAGAGAAGTTTTGAAGAACAAACCGCGGCTTTATTTTTTAACACATCGCCGGAGCGGGAATAAGGAGAGGAAATACGAGACGGCTGCATTTATTCCCTCAGCCATTTTGCCTGCGCCCGCCCGAGGGCTATTTATTCTCGGTATGCAACCCAACCGCGACTCCGTGCCAAACAAGTGAAGCGGAGATGGGTCTGCTCTGCAACATCTGAACTGAACTGTTCCCAGCGCCGCGTTGCTTGTGTTGACAGGATGGAGTGCTACCTGTTGGGGATTTACCTGTTCCTCGCGCTGGCTCTGCTGCCCCGATCGAGCGGTACCACGGCCAAGGAGATCACCTGTCAGGAGATCGCCGTTCCGCTGTGCAAGGGCATCGGTTA[T/G]AACTACACCTACATGCCCAACCAGTTCAACCACGACACGCAGGATGAAGCCGGCTTGGAGGTGCACCAGTTCTGGCCTCTGGTGGAGATTCAGTGCTCCCCGGATCTCAAGTTCTTCTTGTGCAGCATGTACACCCCGATATGCCTGGAGGACTATAAGAAACCCCTTCCGCCGTGCCGGAGCGTCTGCGAGAGAGCCAAGGCGGGCTGCGCCCCGCTCATGCGGCAATACGGCTTCCCTTGGCCGGATCGGATGAGGTGCGATCTACTGCCCGTGCAAGGAGCCCCAGACACGCTGTGCATGGACTACAACCGAACCGACTCCACCACAGTGTCGCCGGTGCTGTCCAAACCCACCAACTACCCCAGCAAAGCCATTAATCCGCACAAAAAGAAAAGCGGGCGGCCAGGCGTCGGACCCAATAAGAATAAGCCCTGCGAGCCGGGCTGCCAGTGTCGCGCGCCGATGGTGCCGGTGAACAGCGATCGACACCCGCTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5986
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000066835 | Nonsense | 47 | 579 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 4527504)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 4417997 |
| GRCz11 | 24 | 4449784 |
KASP Assay ID:
554-3879.1 (used for ordering genotyping assays)
KASP Sequence:
CAGGAGATCGCCGTTCCGCTGTGCAAGGGCATCGGTTATAACTACACCTA[C/A]ATGCCCAACCAGTTCAACCACGACACGCAGGATGAAGCCGGCTTGGAGGT
Long Flanking Sequence:
TGTCTTTTATACTCAGTGCGTCCTACTCTACAGCACTGATTTGTATGAGAAAGCCTCTCGCGAACACCACGAATGTTGAAAACGCGTTTACACCGGGAGTTTTCTTGTTGACAGAGAAGTTTTGAAGAACAAACCGCGGCTTTATTTTTTAACACATCGCCGGAGCGGGAATAAGGAGAGGAAATACGAGACGGCTGCATTTATTCCCTCAGCCATTTTGCCTGCGCCCGCCCGAGGGCTATTTATTCTCGGTATGCAACCCAACCGCGACTCCGTGCCAAACAAGTGAAGCGGAGATGGGTCTGCTCTGCAACATCTGAACTGAACTGTTCCCAGCGCCGCGTTGCTTGTGTTGACAGGATGGAGTGCTACCTGTTGGGGATTTACCTGTTCCTCGCGCTGGCTCTGCTGCCCCGATCGAGCGGTACCACGGCCAAGGAGATCACCTGTCAGGAGATCGCCGTTCCGCTGTGCAAGGGCATCGGTTATAACTACACCTA[C/A]ATGCCCAACCAGTTCAACCACGACACGCAGGATGAAGCCGGCTTGGAGGTGCACCAGTTCTGGCCTCTGGTGGAGATTCAGTGCTCCCCGGATCTCAAGTTCTTCTTGTGCAGCATGTACACCCCGATATGCCTGGAGGACTATAAGAAACCCCTTCCGCCGTGCCGGAGCGTCTGCGAGAGAGCCAAGGCGGGCTGCGCCCCGCTCATGCGGCAATACGGCTTCCCTTGGCCGGATCGGATGAGGTGCGATCTACTGCCCGTGCAAGGAGCCCCAGACACGCTGTGCATGGACTACAACCGAACCGACTCCACCACAGTGTCGCCGGTGCTGTCCAAACCCACCAACTACCCCAGCAAAGCCATTAATCCGCACAAAAAGAAAAGCGGGCGGCCAGGCGTCGGACCCAATAAGAATAAGCCCTGCGAGCCGGGCTGCCAGTGTCGCGCGCCGATGGTGCCGGTGAACAGCGATCGACACCCGCTCTACAACCGCGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44078
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000066835 | Nonsense | 291 | 579 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 4526774)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 4417267 |
| GRCz11 | 24 | 4449054 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTTTCCTCTCGGCGTGCTACATGTTTGTGTCGATCGGGTATATAGTG[C/T]GATTGATCGCCGGGCACGAAAAAGTGGCGTGCAATCGGGAGTATGACGTG
Long Flanking Sequence:
GGCCGGATCGGATGAGGTGCGATCTACTGCCCGTGCAAGGAGCCCCAGACACGCTGTGCATGGACTACAACCGAACCGACTCCACCACAGTGTCGCCGGTGCTGTCCAAACCCACCAACTACCCCAGCAAAGCCATTAATCCGCACAAAAAGAAAAGCGGGCGGCCAGGCGTCGGACCCAATAAGAATAAGCCCTGCGAGCCGGGCTGCCAGTGTCGCGCGCCGATGGTGCCGGTGAACAGCGATCGACACCCGCTCTACAACCGCGTTAAGACGGGTCAAATCCCAAACTGCGCCATGCCATGTCACAACCCATATTTTACGCAGGATGAGCGGACTTTTACGGCCTTCTGGATCGGACTTTGGTCCGTGTTGTGCTTCATATCCACCTTCGCCACAGTCGCCACCTTCCTAATCGACATGGAGCGGTTTAAATACCCAGAGCGCCCTATTATTTTCCTCTCGGCGTGCTACATGTTTGTGTCGATCGGGTATATAGTG[C/T]GATTGATCGCCGGGCACGAAAAAGTGGCGTGCAATCGGGAGTATGACGTGGAGCACATTCACTACGAGACCACCGGCCCCGCGTTGTGCACCGTTGTGTTCCTGCTTATCTACTTCTTCGGAATGGCCAGCTCCATATGGTGGGTCATCCTCTCGCTCACCTGGTTCCTCGCGGCGGGCATGAAGTGGGGAAACGAGGCCATCGCGGGCTACTCTCAGTACTTTCACCTGGCCGCTTGGCTCATCCCGTCCATGAAGTCTATAGCCGTCCTCGCGCTGAGCTCGGTGGACGGAGATCCGGTCGCCGGGATCTGCTACGTTGGCAACCAGAACTTGGACAATCTGCGGGGCTTCGTGCTGGCCCCCCTGGTCATATACCTATTTATAGGCACCATGTTTCTTTTGGCTGGATTTGTGTCGCTTTTTAGGATCAGGAGTGTCATTAAACAGGGGGGCACTAAAACGGACAAGCTGGAGAAGCTGATGATCCGAATTGGGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37811
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000066835 | Nonsense | 305 | 579 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 4526730)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 4417223 |
| GRCz11 | 24 | 4449010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAGTGCGATTGATCGCCGGGCACGAAAAAGTGGCGTGCAATCGGGAGTA[T/G]GACGTGGAGCACATTCACTACGAGACCACCGGCCCCGCGTTGTGCACCGT
Long Flanking Sequence:
CCAGACACGCTGTGCATGGACTACAACCGAACCGACTCCACCACAGTGTCGCCGGTGCTGTCCAAACCCACCAACTACCCCAGCAAAGCCATTAATCCGCACAAAAAGAAAAGCGGGCGGCCAGGCGTCGGACCCAATAAGAATAAGCCCTGCGAGCCGGGCTGCCAGTGTCGCGCGCCGATGGTGCCGGTGAACAGCGATCGACACCCGCTCTACAACCGCGTTAAGACGGGTCAAATCCCAAACTGCGCCATGCCATGTCACAACCCATATTTTACGCAGGATGAGCGGACTTTTACGGCCTTCTGGATCGGACTTTGGTCCGTGTTGTGCTTCATATCCACCTTCGCCACAGTCGCCACCTTCCTAATCGACATGGAGCGGTTTAAATACCCAGAGCGCCCTATTATTTTCCTCTCGGCGTGCTACATGTTTGTGTCGATCGGGTATATAGTGCGATTGATCGCCGGGCACGAAAAAGTGGCGTGCAATCGGGAGTA[T/G]GACGTGGAGCACATTCACTACGAGACCACCGGCCCCGCGTTGTGCACCGTTGTGTTCCTGCTTATCTACTTCTTCGGAATGGCCAGCTCCATATGGTGGGTCATCCTCTCGCTCACCTGGTTCCTCGCGGCGGGCATGAAGTGGGGAAACGAGGCCATCGCGGGCTACTCTCAGTACTTTCACCTGGCCGCTTGGCTCATCCCGTCCATGAAGTCTATAGCCGTCCTCGCGCTGAGCTCGGTGGACGGAGATCCGGTCGCCGGGATCTGCTACGTTGGCAACCAGAACTTGGACAATCTGCGGGGCTTCGTGCTGGCCCCCCTGGTCATATACCTATTTATAGGCACCATGTTTCTTTTGGCTGGATTTGTGTCGCTTTTTAGGATCAGGAGTGTCATTAAACAGGGGGGCACTAAAACGGACAAGCTGGAGAAGCTGATGATCCGAATTGGGATTTTCACGGTGCTCTACACGGTTCCCGCCACCATCATCGTGGCGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44077
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000066835 | Nonsense | 353 | 579 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 4526587)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 4417080 |
| GRCz11 | 24 | 4448867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTGGGTCATCCTCTCGCTCACCTGGTTCCTCGCGGCGGGCATGAAGT[G/A]GGGAAACGAGGCCATCGCGGGCTACTCTCAGTACTTTCACCTGGCCGCTT
Long Flanking Sequence:
TAAGCCCTGCGAGCCGGGCTGCCAGTGTCGCGCGCCGATGGTGCCGGTGAACAGCGATCGACACCCGCTCTACAACCGCGTTAAGACGGGTCAAATCCCAAACTGCGCCATGCCATGTCACAACCCATATTTTACGCAGGATGAGCGGACTTTTACGGCCTTCTGGATCGGACTTTGGTCCGTGTTGTGCTTCATATCCACCTTCGCCACAGTCGCCACCTTCCTAATCGACATGGAGCGGTTTAAATACCCAGAGCGCCCTATTATTTTCCTCTCGGCGTGCTACATGTTTGTGTCGATCGGGTATATAGTGCGATTGATCGCCGGGCACGAAAAAGTGGCGTGCAATCGGGAGTATGACGTGGAGCACATTCACTACGAGACCACCGGCCCCGCGTTGTGCACCGTTGTGTTCCTGCTTATCTACTTCTTCGGAATGGCCAGCTCCATATGGTGGGTCATCCTCTCGCTCACCTGGTTCCTCGCGGCGGGCATGAAGT[G/A]GGGAAACGAGGCCATCGCGGGCTACTCTCAGTACTTTCACCTGGCCGCTTGGCTCATCCCGTCCATGAAGTCTATAGCCGTCCTCGCGCTGAGCTCGGTGGACGGAGATCCGGTCGCCGGGATCTGCTACGTTGGCAACCAGAACTTGGACAATCTGCGGGGCTTCGTGCTGGCCCCCCTGGTCATATACCTATTTATAGGCACCATGTTTCTTTTGGCTGGATTTGTGTCGCTTTTTAGGATCAGGAGTGTCATTAAACAGGGGGGCACTAAAACGGACAAGCTGGAGAAGCTGATGATCCGAATTGGGATTTTCACGGTGCTCTACACGGTTCCCGCCACCATCATCGTGGCGTGTTATTTCTATGAGCAGCACAACAGACAGAGTTGGGAGATCACTCATAACTGTTCGTGTTTACTGGAGCAGGAGATCAAGAGGCCGGACTATGCCGTCTTCATGCTCAAATACTTCATGTGCCTTCTGGTGGGCATCACCTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44076
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:
G > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000066835 | Nonsense | 353 | 579 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 4526586)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 4417079 |
| GRCz11 | 24 | 4448866 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGGTCATCCTCTCGCTCACCTGGTTCCTCGCGGCGGGCATGAAGTG[G/A]GGAAACGAGGCCATCGCGGGCTACTCTCAGTACTTTCACCTGGCCGCTTG
Long Flanking Sequence:
AAGCCCTGCGAGCCGGGCTGCCAGTGTCGCGCGCCGATGGTGCCGGTGAACAGCGATCGACACCCGCTCTACAACCGCGTTAAGACGGGTCAAATCCCAAACTGCGCCATGCCATGTCACAACCCATATTTTACGCAGGATGAGCGGACTTTTACGGCCTTCTGGATCGGACTTTGGTCCGTGTTGTGCTTCATATCCACCTTCGCCACAGTCGCCACCTTCCTAATCGACATGGAGCGGTTTAAATACCCAGAGCGCCCTATTATTTTCCTCTCGGCGTGCTACATGTTTGTGTCGATCGGGTATATAGTGCGATTGATCGCCGGGCACGAAAAAGTGGCGTGCAATCGGGAGTATGACGTGGAGCACATTCACTACGAGACCACCGGCCCCGCGTTGTGCACCGTTGTGTTCCTGCTTATCTACTTCTTCGGAATGGCCAGCTCCATATGGTGGGTCATCCTCTCGCTCACCTGGTTCCTCGCGGCGGGCATGAAGTG[G/A]GGAAACGAGGCCATCGCGGGCTACTCTCAGTACTTTCACCTGGCCGCTTGGCTCATCCCGTCCATGAAGTCTATAGCCGTCCTCGCGCTGAGCTCGGTGGACGGAGATCCGGTCGCCGGGATCTGCTACGTTGGCAACCAGAACTTGGACAATCTGCGGGGCTTCGTGCTGGCCCCCCTGGTCATATACCTATTTATAGGCACCATGTTTCTTTTGGCTGGATTTGTGTCGCTTTTTAGGATCAGGAGTGTCATTAAACAGGGGGGCACTAAAACGGACAAGCTGGAGAAGCTGATGATCCGAATTGGGATTTTCACGGTGCTCTACACGGTTCCCGCCACCATCATCGTGGCGTGTTATTTCTATGAGCAGCACAACAGACAGAGTTGGGAGATCACTCATAACTGTTCGTGTTTACTGGAGCAGGAGATCAAGAGGCCGGACTATGCCGTCTTCATGCTCAAATACTTCATGTGCCTTCTGGTGGGCATCACCTCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24435
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 |
|---|---|---|---|---|---|
| ENSDART00000066835 | Nonsense | 402 | 579 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 24 (position 4526440)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 24 | 4416933 |
| GRCz11 | 24 | 4448720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGACGGAGATCCGGTCGCCGGGATCTGCTACGTTGGCAACCAGAACT[T/A]GGACAATCTGCGGGGCTTCGTGCTGGCCCCCCTGGTCATATACCTATTTA
Long Flanking Sequence:
GACTTTTACGGCCTTCTGGATCGGACTTTGGTCCGTGTTGTGCTTCATATCCACCTTCGCCACAGTCGCCACCTTCCTAATCGACATGGAGCGGTTTAAATACCCAGAGCGCCCTATTATTTTCCTCTCGGCGTGCTACATGTTTGTGTCGATCGGGTATATAGTGCGATTGATCGCCGGGCACGAAAAAGTGGCGTGCAATCGGGAGTATGACGTGGAGCACATTCACTACGAGACCACCGGCCCCGCGTTGTGCACCGTTGTGTTCCTGCTTATCTACTTCTTCGGAATGGCCAGCTCCATATGGTGGGTCATCCTCTCGCTCACCTGGTTCCTCGCGGCGGGCATGAAGTGGGGAAACGAGGCCATCGCGGGCTACTCTCAGTACTTTCACCTGGCCGCTTGGCTCATCCCGTCCATGAAGTCTATAGCCGTCCTCGCGCTGAGCTCGGTGGACGGAGATCCGGTCGCCGGGATCTGCTACGTTGGCAACCAGAACT[T/A]GGACAATCTGCGGGGCTTCGTGCTGGCCCCCCTGGTCATATACCTATTTATAGGCACCATGTTTCTTTTGGCTGGATTTGTGTCGCTTTTTAGGATCAGGAGTGTCATTAAACAGGGGGGCACTAAAACGGACAAGCTGGAGAAGCTGATGATCCGAATTGGGATTTTCACGGTGCTCTACACGGTTCCCGCCACCATCATCGTGGCGTGTTATTTCTATGAGCAGCACAACAGACAGAGTTGGGAGATCACTCATAACTGTTCGTGTTTACTGGAGCAGGAGATCAAGAGGCCGGACTATGCCGTCTTCATGCTCAAATACTTCATGTGCCTTCTGGTGGGCATCACCTCTGGAGTTTGGACCTGGTCCGGTAAGACATTGGAGTCCTGGAGGAGTTTCTGCACGCGCTGCTGTTGGGGCAGCAAGGGCTCCGGTGGCTCCATGTACAGTGACGTGAGCACGGGATTAACGTGGAGGTCCGGTACCGCCAGCTCCGTGT
Associated Phenotype:
Not determined