ZMP
march7
Ensembl ID:
ZFIN IDs:
Description:
E3 ubiquitin-protein ligase MARCH7 [Source:RefSeq peptide;Acc:NP_001108052]
Human Orthologue:
MARCH7
Human Description:
membrane-associated ring finger (C3HC4) 7 [Source:HGNC Symbol;Acc:17393]
Mouse Orthologue:
March7
Mouse Description:
membrane-associated ring finger (C3HC4) 7 Gene [Source:MGI Symbol;Acc:MGI:1931053]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30623 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40644 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa10385 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa30623
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 |
|---|---|---|---|---|---|
| ENSDART00000090366 | None | None | 179 | 5 | 15 |
| ENSDART00000126243 | Nonsense | 235 | 768 | 5 | 11 |
| ENSDART00000129198 | None | None | 179 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 11703065)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 11556691 |
| GRCz11 | 6 | 11792118 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATTTCTTTTTGTGCTTCAGATCGTTCAGAACGTGTTGCTTCTACCTA[T/A]GCACAAGGTGCTCGACCCAAAGATAGCCAGTACTCGTCCCACAGAGAGAA
Long Flanking Sequence:
GTTGTGTATTGTATGTATGGAACTTGGACATACTACATTCTCCAATTGTCATAAATGCATGACTTACCTGCGTCAGTTGCATCGTTTCTCCCATTTATAAATTCTCTCACTTTGTACCATGGGATAGCCTAGCATCCATCAGATTCACACTTCAGAATCTTGCTGGAAGTAGTAGGTTTTCCAGGTACTTCTCGCATACTTATTTTTTATTTTATTTTTTTCCGAATTCTATGAATTGGAACATACTACTTGACTCGCATACTGTTTTTAGTTTACTATATAGTATAGAAGTATGTGATTTCGGAGACAGCCCAGGTCTTTCAGTCTCGGCTAATGAGCTGATGATTTTAATCTGGTGTGTTTGGTTAAGGAGATGTGGTAAATGTGCAGAGCTGCTAGTCCTCCAAGAACGTGGTTGAGAAACACTGTTTTAGACCATCATGCTAATACTATATTTCTTTTTGTGCTTCAGATCGTTCAGAACGTGTTGCTTCTACCTA[T/A]GCACAAGGTGCTCGACCCAAAGATAGCCAGTACTCGTCCCACAGAGAGAACAGTTCATCTAGTCGCCGCATCCCATCCGAGTACATCCCCTCTCCTCTAGAGCGCAACTCCCAAAGGCTAACCTCTGATTACCAGTCTAATTTATTCCCTCGGGATACACCACGCTCCAGTTCCACTAGAACCTCCACCTCTGTATCGGACACCTCCCACCATTCATCTTGGAGTTCCACCCCTTACACAGCTCTCTCTGCCTGTACCTCCAGCCCACCTTCCATTAGCCCTGCTCCTACTCCACTGCCTGCTCAGAATACAGGAGAATCGGATGGTAGAGGAACAACCAGGCGTCTCCTATCCCGCCTTTTCTCCCGACGCTCCAGTCAGGAGTCCAACTCCACTGCCAGCACTGCCTCCGATTCAAGGTCCTACGACTCTAGCCCAGATGAAGCCCCGCCCACTGAAGCTCCTCCTCCAATTAGTAGAGAGAATTTAGAAGCGGAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40644
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 |
|---|---|---|---|---|---|
| ENSDART00000090366 | Nonsense | 27 | 179 | 5 | 15 |
| ENSDART00000126243 | Nonsense | 567 | 768 | 5 | 11 |
| ENSDART00000129198 | Nonsense | 27 | 179 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 11702071)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 11555697 |
| GRCz11 | 6 | 11791124 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGTTTGCCTGAGAATGTGTTGATTGGTGTTGGAGTCGAGGGGAGGAGT[C/T]AAGCTGATGAGCAGCCCAAAGACAAGCCTGCCCCATCCAGAGACCCAGAG
Long Flanking Sequence:
CGGAGCTGAGGAACTCTGATCCCGCTCAGGCGTTTTCGTTCCTGCGCAGACGTGGACCATCTCTTGCACCCGTCCAGGAGAGCACTGATGTAGAGCCTGAACAGGAGTCCCTCAGACCTCCAGCTGGCCTGTCCTGGCTCAACTGGAACCGATGTACCCCACTGTTCTCCCGTCGCAGGAGGGAAGGCCGTGATGAAAGCGCGCGCATGGACCCTCATCGTTCGCCCCAGTTCTCCCTGGGTGACCGAGATGGTCGTAAAACACCTGATCAGGGCACACATTGTGAAGATGATGATGATGAGGATGATGATGATGAGGATGAGTCCTCGGAGGGGGCTGCAGCAGGACCCTCTTCTGGAGCCTCTGCACTCTCTGCATCACTCCTGCAGGATGGAGCCCATTTGGCAGGACGGAGCCACGGCATGGGCAGGGGAATGAACAGCCCGCTTTTCCGTTTGCCTGAGAATGTGTTGATTGGTGTTGGAGTCGAGGGGAGGAGT[C/T]AAGCTGATGAGCAGCCCAAAGACAAGCCTGCCCCATCCAGAGACCCAGAGAGACTGCGAAAGATTCAGGAAAGGTTGGTTTTCCTTGTGGAGAATAGGGTTGTCACGATACTGGAATTCGATACCAATCGATACAGAAATTTTGAAATGTTCACATTTGAGCACATTTTTTAAACAGTGCTGATTTGCCATTGGGTTCACATGCTTAACAGAAATGACTGTGATTGGCCGTAAAGGTTTACCAAACCAGTTTACTGAGTGTTACTACAGATACCGGGACACTAAAGCTTTTCAATGTTATGTCGATCAGCTAGTTTGTCTTTAAGCTGACATATGAGCAATCCGCTGATGAATCGCAGCTTTGAAACGCTTCAGTGTCCCTGTTATCTGTGGTTACATTCAGTAAACTGGCTTCAGGGCCAATCACAGTAATTTCTGTTTAGCATGTAAAGCCAATGGCAATTCAGCACTGTTTAAAAACATTCTCAATTGCGCTCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10385
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 |
|---|---|---|---|---|---|
| ENSDART00000090366 | Nonsense | 54 | 179 | 6 | 15 |
| ENSDART00000126243 | Nonsense | 594 | 768 | 6 | 11 |
| ENSDART00000129198 | Nonsense | 54 | 179 | 6 | 9 |
Genomic Location (Zv9):
Chromosome 6 (position 11698753)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 6 | 11552379 |
| GRCz11 | 6 | 11787806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTTCTTTTGTGTATCGACCTCACATTGCTTCTTGCTTTTAGCCTGCTGT[T/A]GGAGGAATCTGATGAGGARGAGGGTGATCTGTGCCGAATCTGTCAGATGG
Long Flanking Sequence:
TCACTAAAATATAGATTATTTTGGTTCGATCTCTTTTGATCATGCAGAAATTTTATCAGATGATTCAAAGACCTTATCCCAATCTGTTCTTGCAAATCTCAGCTGGATAACCTTATCTTGATGTGTAAATTAGAAGTTTCATCCAGTTTAAACTTACTTTAAACTTTAGTACCCAAACCCACAATCACAAGATCATATAGTTCCACAAATCATCATAATCCTGCAATTTTCTGATGTGCGTCTGTGCTGACGTGCACATTATTCATTAGTTTTTTTAAACAGTTATTAATAGGCACTGTAACAAAGTTTCTAATCTTGACATCCACCTTCCAAATTAAGCCCGCTGCTACACGTCTTTCTGGAAGCATCTTGTGAAAATCTAGATTAGCTGCTTCACTTGTTTTTAAGTAAGGATGAATCTAAACTCTAGGATTTAGTACTCCTTGTTTGATTTCTTTTGTGTATCGACCTCACATTGCTTCTTGCTTTTAGCCTGCTGT[T/A]GGAGGAATCTGATGAGGAGGAGGGTGATCTGTGCCGAATCTGTCAGATGGGGGAGCAGTGGAGTTCCAACCCTCTGATCGAACCCTGCAAGTGCACAGGCAGCCTGCAGTATGTGCACCAGGACTGCATTAAGAAATGGCTCCGCTCCAAAATCAGCTCTGGTATGGTTTTTTTTTTCTCCCCTAAGGCCAGAAATTAGGTTTTTATATAGCGTGTATTCATTTGTTTGATCTGCTGTGAGAAAGGAACCACTTTCAAGTTCAGCCTGACAAAGGGGATTTAGGGTTCATTTCCTGTGCAGTGCGAGACTCTGTTGGTGCATAACGGTGTGAAATGCAGATGGATCAAATAAAAACGTTAAAGGAACATTCTACTTTTTGGGGTAGGGGGGATAGGCTGATTTTACAAGTCCCCTAGAGTTAAACAGCTTGAGTTCTGCCATTTTATTTTATTTTTTTAATTCAGCCGGTCTTTAGGTCTGGTGTGAGCACTTTTAGCTT
Associated Phenotype:
Not determined