ZMP
zswim7
Ensembl ID:
ZFIN ID:
Description:
Zinc finger SWIM domain-containing protein 7 [Source:UniProtKB/Swiss-Prot;Acc:A4FVI0]
Human Orthologue:
ZSWIM7
Human Description:
zinc finger, SWIM-type containing 7 [Source:HGNC Symbol;Acc:26993]
Mouse Orthologue:
Zswim7
Mouse Description:
zinc finger, SWIM-type containing 7 Gene [Source:MGI Symbol;Acc:MGI:1916997]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa18824 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa9071 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38520 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18824
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 |
|---|---|---|---|---|---|
| ENSDART00000097351 | Nonsense | 72 | 140 | 4 | 5 |
| ENSDART00000146879 | Nonsense | 72 | 140 | 5 | 6 |
| ENSDART00000097351 | Nonsense | 72 | 140 | 4 | 5 |
| ENSDART00000146879 | Nonsense | 72 | 140 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 65825527)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 62080435 |
| GRCz11 | 5 | 62765161 |
KASP Assay ID:
2259-6727.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCACATTTCATGTTTGTTTGTGTCTCCCTCTGTCAGGTATTAGGTGGAT[C/A]GGGTCGTCTGTACACGTGCTTCACGTCCTGTCACTACTGCCCGTGCCCGG
Long Flanking Sequence:
GCAGTTTGAAACCTACTTTCACTGTTCCATCTTGCAGTGTAAACACAGCAGCGACTGATCGCTACCCTGGATAGTCATGCAGTGTGAAAACATCTGCGACACGACTATTGTACTTTAAAAAGTATGCGGTCTGAACTCGGCAGAAGGGAGGAATTATTGTCAAAATTTTCCTTTTACTGCTCTTGATATTTTATAATAAAGCTTAATATGTATATTTTTTATATCCACAGAGCACAGTCTGTAGATTTGGAAAGTAATTCAGTTCTGAAATGTAATATTTAATGAAGAACTCAAAAGAATGTTGTTTAAAGAGTTGAACTGAGACCCACACTGCAATCTGTCCGTTTATCTGCCTGCTGTGCTAGACACTGTAAACTCAAAGTATGTATTTTTGGAAGCTGAAATCCTCAAGAGATGCAGCTGTGATGAGATGGTCAGCATAACAGCGGTCTCACATTTCATGTTTGTTTGTGTCTCCCTCTGTCAGGTATTAGGTGGAT[C/A]GGGTCGTCTGTACACGTGCTTCACGTCCTGTCACTACTGCCCGTGCCCGGCCTTCTCTTTCACTGTGCTCAGGAGAAACGAAAGTCTCATGGTGAGGTCACTTCCTCTTTCTGTTCACACATACACACACACACAGCTGCACAGATTGAACCTTAGACCTTCATCCTGTTTTTATAATTTTTTAGCTTTTTCTGCATTGCTCATAAAATTATATGTCTGTCTGTCAGTCTTTGTGTGTCTTTTTGTCTGTTTTGTTCTTTTTAAATTAACTATTAACCTTAATCATTCAAGATTTGACTGCTCCAGTGGCACATTGTCACCGGCATAACAGGATGTGCAAATGACATTCAAAACTCACGCATCCTCACCGAAATGTAAATACTAGTGGGACTGTAAAAATGAATCAATGATTAATCATTTAATAGAACCATGTTTAATGATTAAAAGTAATGACTAATATAAAGCATGTCACTATCGCCATCTCAAATGTACATATACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9071
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 |
|---|---|---|---|---|---|
| ENSDART00000097351 | Nonsense | 72 | 140 | 4 | 5 |
| ENSDART00000146879 | Nonsense | 72 | 140 | 5 | 6 |
| ENSDART00000097351 | Nonsense | 72 | 140 | 4 | 5 |
| ENSDART00000146879 | Nonsense | 72 | 140 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 65825527)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 62080435 |
| GRCz11 | 5 | 62765161 |
KASP Assay ID:
2259-6727.1 (used for ordering genotyping assays)
KASP Sequence:
CTMACATTTCATGTTTGTTTGTGTCTCCCTCTGTCAGGTATTAGGTGGAT[C/A]GGGTCGTCTGTACACGTGCTTCACGTCCTGTCACTACTGCCCGTGCCCGG
Long Flanking Sequence:
GCAGTTTGAAACCTACTTTCACTGTTCCATCTTGCAGTGTAAACACAGCAGCGACTGATCGCTACCCTGGATAGTCATGCAGTGTGAAAACATCTGCGACACGACTATTGTACTTTAAAAAGTATGCGGTCTGAACTCGGCAGAAGGGAGGAATTATTGTCAAAATTTTCCTTTTACTGCTCTTGATATTTTATAATAAAGCTTAATATGTATATTTTTTATATCCACAGAGCACAGTCTGTAGATTTGGAAAGTAATTCAGTTCTGAAATGTAATATTTAATGAAGAACTCAAAAGAATGTTGTTTAAAGAGTTGAACTGAGACCCACACTGCAATCTGTCCGTTTATCTGCCTGCTGTGCTAGACACTGTAAACTCAAAGTATGTATTTTTGGAAGCTGAAATCCTCAAGAGATGCAGCTGTGATGAGATGGTCAGCATAACAGCGGTCTCACATTTCATGTTTGTTTGTGTCTCCCTCTGTCAGGTATTAGGTGGAT[C/A]GGGTCGTCTGTACACGTGCTTCACGTCCTGTCACTACTGCCCGTGCCCGGCCTTCTCTTTCACTGTGCTCAGGAGAAACGAAAGTCTCATGGTGAGGTCACTTCCTCTTTCTGTTCACACATACACACACACACAGCTGCACAGATTGAACCTTAGACCTTCATCCTGTTTTTATAATTTTTTAGCTTTTTCTGCATTGCTCATAAAATTATATGTCTGTCTGTCAGTCTTTGTGTGTCTTTTTGTCTGTTTTGTTCTTTTTAAATTAACTATTAACCTTAATCATTCAAGATTTGACTGCTCCAGTGGCACATTGTCACCGGCATAACAGGATGTGCAAATGACATTCAAAACTCACGCATCCTCACCGAAATGTAAATACTAGTGGGACTGTAAAAATGAATCAATGATTAATCATTTAATAGAACCATGTTTAATGATTAAAAGTAATGACTAATATAAAGCATGTCACTATCGCCATCTCAAATGTACATATACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38520
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 |
|---|---|---|---|---|---|
| ENSDART00000097351 | Nonsense | 122 | 140 | 5 | 5 |
| ENSDART00000146879 | Nonsense | 122 | 140 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 5 (position 65831314)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 62086222 |
| GRCz11 | 5 | 62770948 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTTTTGGCGGTCATCCTGAGTCAGGCCATGGGTTTGTGTCAGCAGGAG[C/T]AGGTCTCAGATCAGCAGATGACCCACATTCTCTCAAGGCAACCTGAGGCC
Long Flanking Sequence:
CCAGCAACCTTCTTGCTGTAAGGCCACAGTGCTAACCTCTGAGCCACCATGCTGCCCGATTTTTCTTTGTCTTATTATTATTAGTACTATTACAGTATTCGTGTTAAACGCATCTCATCTTGAATTTGTACTCCTTCCTAATATTACCAAACATTGATATTGATATTTATTCATTTGGATAAACACCTTGAGATGTACCATCTCATTTTCAAGGGGGTCCCACAATTAATCACAATCACATAATAATAACACAAAGAGACAAAACAAAACATAACTTACACAACATACAAAAAACATAACAAAAAAAAACAAGCTAAAAAAAAGAAAGAAAGAAAAAGGGGGAGGGTGATACTTGGTACTTCAGTTGCATATTGCTTTTGTTAATCTTTATTAATAAGTGTCAGTTTATTAAAAAAAGTCTTTTCCGTATTTGTGTCCTCTAGTGTAAACACCTTTTGGCGGTCATCCTGAGTCAGGCCATGGGTTTGTGTCAGCAGGAG[C/T]AGGTCTCAGATCAGCAGATGACCCACATTCTCTCAAGGCAACCTGAGGCCAGCACATAAATAACTGATTCTGGAGTGTCGAGGGACTCTTATGTGAACATGCATGTTGGAATACAGGTATGGATTAGACTGGACTTGTCAAATGCCGTTATGACTAATTAAATTTGTCGATCAATTTTACTAGGAGATAATCAGTCGTGGAATGTAAAAGATTGCTGTAAAAGTAATTGGATAAGCAAAGCTGTAATACTAAATGATAAATGTTTATGTATGTGCTGCTCACTAAATATTTTATCTGCTGCCAGAGAATGTACATCTGTTCATTGAGCTCAATTGAGTTTATTTTTGGAGTTTCCGTTTGTTTGAAGAATCGGCAGCCGAGACTCAACAACAAACAATGAGGCCGTGAGGCTTAAATACTGTATTTAAATACTGTGTGATTTGTCTATCATAAAATAAAAAATAAAAACATTCATTAAACTTTAAGTAGATTTTGTCATC
Associated Phenotype:
Not determined