ZMP
zgc:63599
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393645 [Source:RefSeq peptide;Acc:NP_956966]
Human Orthologue:
SWAP70
Human Description:
SWAP switching B-cell complex 70kDa subunit [Source:HGNC Symbol;Acc:17070]
Mouse Orthologue:
Swap70
Mouse Description:
SWA-70 protein Gene [Source:MGI Symbol;Acc:MGI:1298390]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa8626 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21131 | Nonsense | Available for shipment | Available now |
| sa21130 | Nonsense | Available for shipment | Available now |
| sa45301 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8626
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 |
|---|---|---|---|---|---|
| ENSDART00000061302 | None | None | 224 | None | 6 |
| ENSDART00000079899 | Nonsense | 416 | 587 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 69084157)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66962178 |
| GRCz11 | 7 | 67185826 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAATGGAGGAGCAGGTGATTGAGAARTCGAATGAAGTGGAGCAGTACTGG[C/T]AGCGKATGCAGGAACTGGAGGAAATGTACCTTCAGCTCAAACAGGCTCTG
Long Flanking Sequence:
CAGAAGGGGGAAATGCCAGAGTAAAATGAGAAAATATGATACGCCGGTGTTTTGGAATATGGAAAAACTGTGTTTATGCTGTTTTCATCTGTTGTTATATTATTTGTTTTTATTTTGTTTATACTTGTGTCTTTTATTTCTGTTTATGTAAAGCACTTTGAGTTGCCACTGTGTATGTATGTACACACATACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATACAAATATAAATGTGCTGTATAAATAAACTTGCCTTGCCTTGACTAAAGGTGTATCAAATCGTGATTTAGCACATTGCTTAGAAGATTAATTAGGATGTTGCTGTTCTGCAGTTGCAAGATTTGTTGGTGTAAAACAAATTATTAAAAATAAAACCATTGTTTCTTAGGCTCGAATGCAAATGGAGGAGCAGGTGATTGAGAAGTCGAATGAAGTGGAGCAGTACTGG[C/T]AGCGTATGCAGGAACTGGAGGAAATGTACCTTCAGCTCAAACAGGCTCTGCAGGATGAGAAGCAGGCCAAGGAGGATGAAGAAATACTGCGCAAACTGCAGGCCAGGTAACAGTACACAAACTCAGACACACAATCGCAACAGCTGCTTCCGTTCTGAACCATTGTATGTTGTCTTGTTTGCAGACTGCTACAAGAGGAGGAAAACAAGAGACTTGAATTAGAGCAGATTCACCTGCAGCAGCAACGGGTCTTATCCCAGTCCCAGAAGGAGAAGGAGGAGCTGGCGAAGGAGCGGGAAGAGAAGGAGCGAGCCCTGCAAGCGGCACAGGAGCAGCTGGAGAGCCTGAAAAGACAGAGGGAGGGAGCGGAGGAGGAATACATGGTAGCAGATTCACTTGGTCACACACACACACACACACACATACAGGGGTCAGACAATGAAACTGAAAAGCCTGGTTTTAGACCACAATAATTCACCAGCATAGTGTAGGGCCTTCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21131
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061302 | None | None | 224 | None | 6 |
| ENSDART00000079899 | Nonsense | 437 | 587 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 69084094)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66962115 |
| GRCz11 | 7 | 67185763 |
KASP Assay ID:
2259-9766.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGGAGGAAATGTACCTTCAGCTCAAACAGGCTCTGCAGGATGAGAAG[C/T]AGGCCAAGGAGGATGAAGAAATACTGCGCAAACTGCAGGCCAGGTAACAG
Long Flanking Sequence:
AAAACTGTGTTTATGCTGTTTTCATCTGTTGTTATATTATTTGTTTTTATTTTGTTTATACTTGTGTCTTTTATTTCTGTTTATGTAAAGCACTTTGAGTTGCCACTGTGTATGTATGTACACACATACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATACAAATATAAATGTGCTGTATAAATAAACTTGCCTTGCCTTGACTAAAGGTGTATCAAATCGTGATTTAGCACATTGCTTAGAAGATTAATTAGGATGTTGCTGTTCTGCAGTTGCAAGATTTGTTGGTGTAAAACAAATTATTAAAAATAAAACCATTGTTTCTTAGGCTCGAATGCAAATGGAGGAGCAGGTGATTGAGAAGTCGAATGAAGTGGAGCAGTACTGGCAGCGTATGCAGGAACTGGAGGAAATGTACCTTCAGCTCAAACAGGCTCTGCAGGATGAGAAG[C/T]AGGCCAAGGAGGATGAAGAAATACTGCGCAAACTGCAGGCCAGGTAACAGTACACAAACTCAGACACACAATCGCAACAGCTGCTTCCGTTCTGAACCATTGTATGTTGTCTTGTTTGCAGACTGCTACAAGAGGAGGAAAACAAGAGACTTGAATTAGAGCAGATTCACCTGCAGCAGCAACGGGTCTTATCCCAGTCCCAGAAGGAGAAGGAGGAGCTGGCGAAGGAGCGGGAAGAGAAGGAGCGAGCCCTGCAAGCGGCACAGGAGCAGCTGGAGAGCCTGAAAAGACAGAGGGAGGGAGCGGAGGAGGAATACATGGTAGCAGATTCACTTGGTCACACACACACACACACACACATACAGGGGTCAGACAATGAAACTGAAAAGCCTGGTTTTAGACCACAATAATTCACCAGCATAGTGTAGGGCCTTCTTTTGTGACCAACACAGCATCAGTTCATCTTGGGATTGACTGCACAGTGGCCAGAAGGCCTAACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21130
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061302 | None | None | 224 | None | 6 |
| ENSDART00000079899 | Nonsense | 442 | 587 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 69084079)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66962100 |
| GRCz11 | 7 | 67185748 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTCAGCTCAAACAGGCTCTGCAGGATGAGAAGCAGGCCAAGGAGGAT[G/T]AAGAAATACTGCGCAAACTGCAGGCCAGGTAACAGTACACAAACTCAGAC
Long Flanking Sequence:
CTGTTTTCATCTGTTGTTATATTATTTGTTTTTATTTTGTTTATACTTGTGTCTTTTATTTCTGTTTATGTAAAGCACTTTGAGTTGCCACTGTGTATGTATGTACACACATACACACACACATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATATACAAATATAAATGTGCTGTATAAATAAACTTGCCTTGCCTTGACTAAAGGTGTATCAAATCGTGATTTAGCACATTGCTTAGAAGATTAATTAGGATGTTGCTGTTCTGCAGTTGCAAGATTTGTTGGTGTAAAACAAATTATTAAAAATAAAACCATTGTTTCTTAGGCTCGAATGCAAATGGAGGAGCAGGTGATTGAGAAGTCGAATGAAGTGGAGCAGTACTGGCAGCGTATGCAGGAACTGGAGGAAATGTACCTTCAGCTCAAACAGGCTCTGCAGGATGAGAAGCAGGCCAAGGAGGAT[G/T]AAGAAATACTGCGCAAACTGCAGGCCAGGTAACAGTACACAAACTCAGACACACAATCGCAACAGCTGCTTCCGTTCTGAACCATTGTATGTTGTCTTGTTTGCAGACTGCTACAAGAGGAGGAAAACAAGAGACTTGAATTAGAGCAGATTCACCTGCAGCAGCAACGGGTCTTATCCCAGTCCCAGAAGGAGAAGGAGGAGCTGGCGAAGGAGCGGGAAGAGAAGGAGCGAGCCCTGCAAGCGGCACAGGAGCAGCTGGAGAGCCTGAAAAGACAGAGGGAGGGAGCGGAGGAGGAATACATGGTAGCAGATTCACTTGGTCACACACACACACACACACACATACAGGGGTCAGACAATGAAACTGAAAAGCCTGGTTTTAGACCACAATAATTCACCAGCATAGTGTAGGGCCTTCTTTTGTGACCAACACAGCATCAGTTCATCTTGGGATTGACTGCACAGTGGCCAGAAGGCCTAACGATATAGGTCGTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45301
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000061302 | None | None | 224 | None | 6 |
| ENSDART00000079899 | Essential Splice Site | 517 | 587 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 7 (position 69083773)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 66961794 |
| GRCz11 | 7 | 67185442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGGAGAGCCTGAAAAGACAGAGGGAGGGAGCGGAGGAGGAATACATG[G/A]TAGCAGATTCACTTGGTCACACACACACACACACACACATACAGGGGTCA
Long Flanking Sequence:
TTGCAAGATTTGTTGGTGTAAAACAAATTATTAAAAATAAAACCATTGTTTCTTAGGCTCGAATGCAAATGGAGGAGCAGGTGATTGAGAAGTCGAATGAAGTGGAGCAGTACTGGCAGCGTATGCAGGAACTGGAGGAAATGTACCTTCAGCTCAAACAGGCTCTGCAGGATGAGAAGCAGGCCAAGGAGGATGAAGAAATACTGCGCAAACTGCAGGCCAGGTAACAGTACACAAACTCAGACACACAATCGCAACAGCTGCTTCCGTTCTGAACCATTGTATGTTGTCTTGTTTGCAGACTGCTACAAGAGGAGGAAAACAAGAGACTTGAATTAGAGCAGATTCACCTGCAGCAGCAACGGGTCTTATCCCAGTCCCAGAAGGAGAAGGAGGAGCTGGCGAAGGAGCGGGAAGAGAAGGAGCGAGCCCTGCAAGCGGCACAGGAGCAGCTGGAGAGCCTGAAAAGACAGAGGGAGGGAGCGGAGGAGGAATACATG[G/A]TAGCAGATTCACTTGGTCACACACACACACACACACACATACAGGGGTCAGACAATGAAACTGAAAAGCCTGGTTTTAGACCACAATAATTCACCAGCATAGTGTAGGGCCTTCTTTTGTGACCAACACAGCATCAGTTCATCTTGGGATTGACTGCACAGTGGCCAGAAGGCCTAACGATATAGGTCGTTATGATAACATTACATGCCTTCAGTGATTTCCTGAAGATAAATACCAAAAAAATAGCACAACTAGAAGCACTACAGCAGTCGCCATCGTCTGATCTCACATGAAGCAGCTGCTCCTAGGAGATCGCGAGGACATATGATGACGTGTGCAGGTGCTGTAGTGCTGTCCTAATTCTTAGGGGTAAATTTCGAAGCCGTTCCCCTTCACCCTCGGTTGTAATGGCCAAGGGGAAGGGGTAGGGAGAGAAAAATAGAATTAGGATTGGCTTAATGCTCAGGTTTTTTCTGTCTTTTTTTCTTTTATCAGGCTGT
Associated Phenotype:
Not determined