ZMP
si:ch211-269e2.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate stromal antigen 1 family [Source:UniProtKB/TrEMBL;Acc:B0S5T4]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1876 | Nonsense | Available for shipment | Available now |
sa34689 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9688 | Splice Site, Nonsense | Available for shipment | Available now |
sa18953 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9338 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa1876
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 |
---|---|---|---|---|---|
ENSDART00000112941 | Nonsense | 537 | 1174 | 15 | 31 |
ENSDART00000137416 | Nonsense | 537 | 1174 | 16 | 32 |
Genomic Location (Zv9):
Chromosome 9 (position 35421239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34640750 |
GRCz11 | 9 | 34449935 |
KASP Assay ID:
554-1866.1 (used for ordering genotyping assays)
KASP Sequence:
ACTGGACTGGTCTTACCTCACTACTCTTACCTCACACGTCCTGTCAGGAT[C/T]AAGGCTAGTACACTACACTATACATGCCAGTACACTTCTTCACCAGAAGG
Long Flanking Sequence:
CCCAATACAAAAAAAAGAATGTATTCTGACAGAATTTTAAATGACTTAATCCTGGGTTATTGTGATCCTGGTTTTTATGTTAACCCATAATTTTTAATTCTTAATATTAGCACAGCTTTTTTGCCATATTTTGAATTACTAATGTGAATTATTGCGAGTGCTGCTCTTGTAAACTTGAATTGAAAATAAGATGATATCCCTGAATTTTGGAATGTACAATGTGAAAGGTTTGAGTATGAATACCCAGGATAAATTCATAAACGATAAGTAAATAGAAAACATGATATCTCAGAGTCTTATTTGCTAGGTTTTAAAATATCCGTATTAATTGAGAGTGTGTCATTAGCTATAGGATGATGACTTCACTTCTGTCTCTTGTTTGGTAGCTGCACCAACATGTGCTATACCTGGTTGATAGCCTGTGGGACAGTGGAGGAGCTCTGCTGAAGGACTGGACTGGTCTTACCTCACTACTCTTACCTCACACGTCCTGTCAGGAT[C/T]AAGGCTAGTACACTACACTATACATGCCAGTACACTTCTTCACCAGAAGGTTGCTATTATCAGTAGCTTTTATTACAGCCCAGCAGAGATTTCCCCGCCTTAACTAATATTTACAATTATATATGCTGCTACGTTGGTTTTAATACTTGAATAACATACATTTTTGTGTTAACCGCAGCTCTGAGCAGTGCTGAGGAGGCCTTTGTGATTGAGCTCATGGTGGCGTCAGTAAGGCAGGCTGCAGAGGGTCCTCCGTTATCAGGGAGAGGAGCAGGAAAAAAGGCAAGTTTCCTTTTAATGTTTCTTTCAGGCCATGTTTTGCTCTAGTATTAACTTTCATTTTAAGCTAGCAGGTGGACAGATAAGATGTATAGCAGTTTCCACCTTGTATTAACATGTATTATACTGGACTTTTCTGACCTCTTCTGCTCAGATTTTGCCAAAACATTTAACTCTTTTTTTTTTGTCATGCTCAATGTCACTTTTGCAAAAGTGATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34689
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 |
---|---|---|---|---|---|
ENSDART00000112941 | Nonsense | 586 | 1174 | 17 | 31 |
ENSDART00000137416 | Nonsense | 586 | 1174 | 18 | 32 |
Genomic Location (Zv9):
Chromosome 9 (position 35422263)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34641774 |
GRCz11 | 9 | 34450959 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTTTTAGGTGATAAGCACTAAAGAGAAAAAATTACAAACTGATGACTG[C/A]GCCAAACTCACTGAACACTTCATTAAAGCGCTACCTGGGCTGTTATCCAA
Long Flanking Sequence:
TGAATGAACTGATATTACAAAAGCTTACAAGAGAGCAGGATAGCAAGTGATCGAAATGTGTCTGTCACTGCAACTTAGATATTGATAGCAATGCATGTGTCCATTTAAATACCTTGTTTTGGTGTGTTTTTTTACAACATGTCCCAAAATGATCACATTAGTTCAGTAGAGGGTCAGTTGTGTGGTTGTTTGAACACATTTGACTACAAGAGCATTTACATTATAAACAGAACCAATTGAATGCCTAACTCTAACCCTAACTACCTCTGGAAATGGTGGAAAATGGATAAGCTAAAAACAATTTATACCCCAGAAACCTGTGATGGGATTGACAAAATGCAAACAGGAATTAGAAATTAATTAGGCCTTCATACCCCAGCTATTCCCATTCTTGTATTTGCTTCCACATAATGAGCACTATTACTTGTTCCTAGTGTGATACCTATGTTTATTTTTTAGGTGATAAGCACTAAAGAGAAAAAATTACAAACTGATGACTG[C/A]GCCAAACTCACTGAACACTTCATTAAAGCGCTACCTGGGCTGTTATCCAAGGTAAAATTAACAATTGCATTGCAGTACCATGTCTGATTGTCAATGAATTGACCACAGTTGATTAAAGTATGTCTAATCCTCTAGTACTCAGAGGATGCTGAAAAACTGACCTCCTTTCTAAGAATACCTCGGTATTTCCAAATGGACACCTGTGATCCTGAAAACTCACAGGTGAGTGAGTGTTATTGTTTCATCTAATGCTATGATGCACTAAATATAGCAGAAAAATCCCATTTAGTAAAAAAATCCTATATATTATAATATTGCAGAATATTATGACAATTTAAAATTAACTTTTATTTTAAAATATTTTAAATGTAAACTATTCCTTAAAAAAACAATAATAATACGCTAGTGCTCAGTTTCATGTGATTCTTCAGAAATCATTGTAATAGGATGATTTGTTGCTTAAGACAAAAATCTTATTAAACATAACTTCATCAATAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9688
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112941 | Splice Site, Nonsense | 632 | 1174 | 18 | 31 |
ENSDART00000137416 | Splice Site, Nonsense | 632 | 1174 | 19 | 32 |
Genomic Location (Zv9):
Chromosome 9 (position 35422483)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34641994 |
GRCz11 | 9 | 34451179 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAAGAATACCTCRGTATTTCCAAATGGACACCTGTGAKCMTGAAAACTCA[C/T]AGGTGAGTRAGTGTTATTGTTTCATCTAATGCTATGATGCACTAAATATA
Long Flanking Sequence:
TTATAAACAGAACCAATTGAATGCCTAACTCTAACCCTAACTACCTCTGGAAATGGTGGAAAATGGATAAGCTAAAAACAATTTATACCCCAGAAACCTGTGATGGGATTGACAAAATGCAAACAGGAATTAGAAATTAATTAGGCCTTCATACCCCAGCTATTCCCATTCTTGTATTTGCTTCCACATAATGAGCACTATTACTTGTTCCTAGTGTGATACCTATGTTTATTTTTTAGGTGATAAGCACTAAAGAGAAAAAATTACAAACTGATGACTGCGCCAAACTCACTGAACACTTCATTAAAGCGCTACCTGGGCTGTTATCCAAGGTAAAATTAACAATTGCATTGCAGTACCATGTCTGATTGTCAATGAATTGACCACAGTTGATTAAAGTATGTCTAATCCTCTAGTACTCAGAGGATGCTGAAAAACTGACCTCCTTTCTAAGAATACCTCGGTATTTCCAAATGGACACCTGTGATCCTGAAAACTCA[C/T]AGGTGAGTGAGTGTTATTGTTTCATCTAATGCTATGATGCACTAAATATAGCAGAAAAATCCCATTTAGTAAAAAAATCCTATATATTATAATATTGCAGAATATTATGACAATTTAAAATTAACTTTTATTTTAAAATATTTTAAATGTAAACTATTCCTTAAAAAAACAATAATAATACGCTAGTGCTCAGTTTCATGTGATTCTTCAGAAATCATTGTAATAGGATGATTTGTTGCTTAAGACAAAAATCTTATTAAACATAACTTCATCAATAGGACGTTCAAAGTGAAGTTTCACAAACTAATTTCAAGAGGAGCATGTGAAATGATTGAGCACGACTGGCTGCTCAACTGTAATCAGTAATAATCCAATCAGAGTGATTCAAGCTTACTGTAAATAGATCGTTTCTCTCTACTGCTCTATCTTCGTTTTGAAAGAATACCCCCTTCCACCCCATCTCCTCCTATTCCACCCTTTTTTAAGGGAGAGCTCTCGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18953
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 |
---|---|---|---|---|---|
ENSDART00000112941 | Nonsense | 904 | 1174 | 25 | 31 |
ENSDART00000137416 | Nonsense | 904 | 1174 | 26 | 32 |
ENSDART00000112941 | Nonsense | 904 | 1174 | 25 | 31 |
ENSDART00000137416 | Nonsense | 904 | 1174 | 26 | 32 |
Genomic Location (Zv9):
Chromosome 9 (position 35437565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34657076 |
GRCz11 | 9 | 34466261 |
KASP Assay ID:
2260-2125.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGCAGGAATCTTCTGTCGGCGTACTGTAAGCTCATAGTGCACAGTGTGT[T/A]AGAGATGAGCATGGCTGCAGAGGTTTTCAAGCAGTACGTGAAGGTATGAC
Long Flanking Sequence:
GAGATAATGTCAGAATTTTGGGCTATTCGATTAGAAATCAAGCGCGACTCCAGCAAATCATATCAATCCTATAAATATTTCACAGAGCCGTCGATTCGTGCCGCCGCAAACTCCTCACCTCTCGAAAAAAATGCAATATAAGCTTTTGCGGATAACGTGTAATAAAAAGCAATTTAGTTATTGGATTTTCCTCACGTCACTAATGCTGTTATGAAAGCTCTCTATTAAGTGATGGCTTCGGGAGCAGGCAGGACGACGATAGACAAGAGCAGAAAATGCTGTTAACTTTAGTTCACCTCAGGAAAGCATTTCATTTATAAGATTTGAGTATCATAATTATGGCGCTCTGTTATTGAATCTGCAGCTCTCTGTTTCAATCAGTCTGTTTCTCTGTGTGTGTGCAGTCAGTGAGAGTGAGAGTGGAGAAGGACGGCTGGAGGATTTGCACCGGCGCAGGAATCTTCTGTCGGCGTACTGTAAGCTCATAGTGCACAGTGTGT[T/A]AGAGATGAGCATGGCTGCAGAGGTTTTCAAGCAGTACGTGAAGGTATGACAGTTCTCATGACTTACACTGAACTCTAGCAACCTCCTAACCAGACAGATAAGCAGAGGGCTGTGTTAATCAGATATTATTCAGATCTGTAGTTTTTTTTGTCAACATAAGATCCACAGATAACACAGCACACATTTACAGGAAATAACAGTGCTCACAGGAAATGTGAGGTTTTTGATTAAAAAAGTAGTTTTAGTATTATAATATTTAATATATAAAAGTCGTACTTGATTTGATTTGGTTAGTTAGATATATTTACCTTATTTAAATGTTTTTGTGCTTACATTATACAATACCGGTCAAAAGTTTAGAGTCAGTAGGGTTTTTAAATCTTTTAAAATAAGCTTCTCCTGCTCACCAAGGCTGCAATTATAACAGCAAAAGTACAGAACAAATTGTAAAACAGTGAAATGTTATTACACTATAAAATAACTGCTCAAAAGTAGTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9338
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 |
---|---|---|---|---|---|
ENSDART00000112941 | Nonsense | 904 | 1174 | 25 | 31 |
ENSDART00000137416 | Nonsense | 904 | 1174 | 26 | 32 |
ENSDART00000112941 | Nonsense | 904 | 1174 | 25 | 31 |
ENSDART00000137416 | Nonsense | 904 | 1174 | 26 | 32 |
Genomic Location (Zv9):
Chromosome 9 (position 35437565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34657076 |
GRCz11 | 9 | 34466261 |
KASP Assay ID:
2260-2125.1 (used for ordering genotyping assays)
KASP Sequence:
GYGCAGGAATCTTCTGTCKGCGTACTGTAAGCTCATAGTGCACAGTGTGT[T/A]AGAGATGAGCATGGCTGCAGAGGTTTTCAAGCAGTACGTGAAGGTATGAC
Long Flanking Sequence:
GAGATAATGTCAGAATTTTGGGCTATTCGATTAGAAATCAAGCGCGACTCCAGCAAATCATATCAATCCTATAAATATTTCACAGAGCCGTCGATTCGTGCCGCCGCAAACTCCTCACCTCTCGAAAAAAATGCAATATAAGCTTTTGCGGATAACGTGTAATAAAAAGCAATTTAGTTATTGGATTTTCCTCACGTCACTAATGCTGTTATGAAAGCTCTCTATTAAGTGATGGCTTCGGGAGCAGGCAGGACGACGATAGACAAGAGCAGAAAATGCTGTTAACTTTAGTTCACCTCAGGAAAGCATTTCATTTATAAGATTTGAGTATCATAATTATGGCGCTCTGTTATTGAATCTGCAGCTCTCTGTTTCAATCAGTCTGTTTCTCTGTGTGTGTGCAGTCAGTGAGAGTGAGAGTGGAGAAGGACGGCTGGAGGATTTGCACCGGCGCAGGAATCTTCTGTCGGCGTACTGTAAGCTCATAGTGCACAGTGTGT[T/A]AGAGATGAGCATGGCTGCAGAGGTTTTCAAGCAGTACGTGAAGGTATGACAGTTCTCATGACTTACACTGAACTCTAGCAACCTCCTAACCAGACAGATAAGCAGAGGGCTGTGTTAATCAGATATTATTCAGATCTGTAGTTTTTTTTGTCAACATAAGATCCACAGATAACACAGCACACATTTACAGGAAATAACAGTGCTCACAGGAAATGTGAGGTTTTTGATTAAAAAAGTAGTTTTAGTATTATAATATTTAATATATAAAAGTCGTACTTGATTTGATTTGGTTAGTTAGATATATTTACCTTATTTAAATGTTTTTGTGCTTACATTATACAATACCGGTCAAAAGTTTAGAGTCAGTAGGGTTTTTAAATCTTTTAAAATAAGCTTCTCCTGCTCACCAAGGCTGCAATTATAACAGCAAAAGTACAGAACAAATTGTAAAACAGTGAAATGTTATTACACTATAAAATAACTGCTCAAAAGTAGTTTAT
Associated Phenotype:
Not determined