ZMP
si:ch211-163l21.8
Ensembl ID:
ZFIN ID:
Description:
Novel protein (Im:7136654) [Source:UniProtKB/TrEMBL;Acc:A8Y5S9]
Human Orthologue:
KIAA1324
Human Description:
KIAA1324 [Source:HGNC Symbol;Acc:29618]
Mouse Orthologue:
5330417C22Rik
Mouse Description:
RIKEN cDNA 5330417C22 gene Gene [Source:MGI Symbol;Acc:MGI:1923930]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34396 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21284 | Essential Splice Site | Available for shipment | Available now |
sa27198 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34397 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34396
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 |
---|---|---|---|---|---|
ENSDART00000062968 | Nonsense | 243 | 906 | 7 | 21 |
ENSDART00000124686 | Nonsense | 112 | 190 | 4 | 7 |
ENSDART00000137820 | None | None | 309 | None | 8 |
ENSDART00000144229 | Nonsense | 282 | 593 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24648006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23773824 |
GRCz11 | 8 | 23795063 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTGGAGCTTGTACACAGAGACCGGCCTGCAAAACCTCTGATTACTTCTA[C/A]ACCCACACACCCTGTGATTCCAGCGCTCAGGTAACATGTAAAAACAAACA
Long Flanking Sequence:
AATTTTATCGTTATGTTTTTTTACTTAATATAATTAATAAAATTAAATATATACAGCTGATTTTAAAATAGATTTTTAAATCAATTAAAAAAACAAAATAAAAAGGCTTAGTTGTCAAATTGTTGAGGTTAAATTAACACAAATATCAATTATGTTCTAGAAACAATGGATTTCTCAAAGCATTTAAGCATGTAATGAATGGTGGTCATCCATCAAATGCTGCATGAAGGCTTTTGAACGTTACTGATCTGCATAGATGTGATCAAGCATTTAAATGTAACCACACAGAAGTAAAAAGTTGATGTAAATGACCTGCGGGATTTGCCTGCTGTGTTTTATCACTTTATCTAAATTAGTGTGTGTGTGTTTTTCCTAATGCTCCGGGCGTTTTCCTCTCTATGTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTACAGGTATTGGATCTGGAGCTTGTACACAGAGACCGGCCTGCAAAACCTCTGATTACTTCTA[C/A]ACCCACACACCCTGTGATTCCAGCGCTCAGGTAACATGTAAAAACAAACACTGATAGTCTTTGTGTCGGAAAGCACTAATTCCAGCATTTATCTTTTTTTATTTTTTTTAATTTTAATTCTGCATTAGATCCTATTCACCTGATTTAAACACAATAATAGATAAGTGGTGTGATTATATTATTTACATTTATTCTACGTTTGAGTGTGTTTAATTTAAATATAGTTCATTATTTAGCATTTAATTACATTTGTAAAAAAAAAATTATAAGCAGTCAACTGTTTTTATTTATTATATTATATTATATTATATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTAATTTACTTCTTGATTTATGGTTGATTTTCTTTTTTTATCTTTATGTATTTCTTGTTTGTTTTTAGACACAGCTACACTGTTTAAATATATATTAATTGCATAATGGGACCTTGATCTCTGCTCTGTCGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21284
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062968 | Essential Splice Site | 253 | 906 | None | 21 |
ENSDART00000124686 | Essential Splice Site | 122 | 190 | None | 7 |
ENSDART00000137820 | None | None | 309 | None | 8 |
ENSDART00000144229 | Essential Splice Site | 292 | 593 | None | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24648038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23773856 |
GRCz11 | 8 | 23795095 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTCTGATTACTTCTACACCCACACACCCTGTGATTCCAGCGCTCAGG[T/C]AACATGTAAAAACAAACACTGATAGTCTTTGTGTCGGAAAGCACTAATTC
Long Flanking Sequence:
ATTAATAAAATTAAATATATACAGCTGATTTTAAAATAGATTTTTAAATCAATTAAAAAAACAAAATAAAAAGGCTTAGTTGTCAAATTGTTGAGGTTAAATTAACACAAATATCAATTATGTTCTAGAAACAATGGATTTCTCAAAGCATTTAAGCATGTAATGAATGGTGGTCATCCATCAAATGCTGCATGAAGGCTTTTGAACGTTACTGATCTGCATAGATGTGATCAAGCATTTAAATGTAACCACACAGAAGTAAAAAGTTGATGTAAATGACCTGCGGGATTTGCCTGCTGTGTTTTATCACTTTATCTAAATTAGTGTGTGTGTGTTTTTCCTAATGCTCCGGGCGTTTTCCTCTCTATGTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTACAGGTATTGGATCTGGAGCTTGTACACAGAGACCGGCCTGCAAAACCTCTGATTACTTCTACACCCACACACCCTGTGATTCCAGCGCTCAGG[T/C]AACATGTAAAAACAAACACTGATAGTCTTTGTGTCGGAAAGCACTAATTCCAGCATTTATCTTTTTTTATTTTTTTTAATTTTAATTCTGCATTAGATCCTATTCACCTGATTTAAACACAATAATAGATAAGTGGTGTGATTATATTATTTACATTTATTCTACGTTTGAGTGTGTTTAATTTAAATATAGTTCATTATTTAGCATTTAATTACATTTGTAAAAAAAAAATTATAAGCAGTCAACTGTTTTTATTTATTATATTATATTATATTATATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTAATTTACTTCTTGATTTATGGTTGATTTTCTTTTTTTATCTTTATGTATTTCTTGTTTGTTTTTAGACACAGCTACACTGTTTAAATATATATTAATTGCATAATGGGACCTTGATCTCTGCTCTGTCGACTTTTGATGTTGAAAATTCAACTCTACAGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27198
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:
A > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062968 | Splice Site, Nonsense | 554 | 906 | 13 | 21 |
ENSDART00000124686 | None | None | 190 | None | 7 |
ENSDART00000137820 | None | None | 309 | None | 8 |
ENSDART00000144229 | Nonsense | 593 | 593 | 13 | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24653973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23779791 |
GRCz11 | 8 | 23801030 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGTCGGAAAAGAAGCCTGCATTCCTTGTGGACCTAATACATACAGCAAT[A/T]AAGTAGGCACTACCTATGATTAATTAAATGTTGATTGATTATTATACTGT
Long Flanking Sequence:
TTTATCTCTCCTCAGGGACAAAATGAAAGGAATAACATGGTTGTGGAGAGTTGGTCTGGCACTATAGGAAAGCAGTCCTACTCGTATCTTATTAAAACTAACAGCACAGTTAGCTTCAGCTGGGGGTTTCAGCGTACTGGAGCTTTTGACATGGTAAGATTAGAAACTTCACTTCTTTAATATTTTTACAGGTTATGTTTCCTTTAATAATCTAAGGCGATGTGTGTATGTCTGTGTTACAGAAGAATGAATACAGCTCTGACCTTGCTAAGATCTACTCTGTTCATCTCACTAATGTGATTGGTGGCGTAGCTTCAGAATGTCGCCAATGTGCTCTGACTGGCACTGACAGTGACTCCTGCGTCTCCTGTGCTCCAGGGCACTACATGGTCTATGGTACTGGGGTGTGCAGACACTGCCCCCCAAACACCATCATCAGACCCGAGCAGCCCGTCGGAAAAGAAGCCTGCATTCCTTGTGGACCTAATACATACAGCAAT[A/T]AAGTAGGCACTACCTATGATTAATTAAATGTTGATTGATTATTATACTGTATACTGTATATATAGAAAGTCGCTGGTTCGAGCCTCTGCCTCGCCGTTTCTGTGTGGAGTTTGCATGTTCTCCCCGCGTTCGCGTAGGTTTCCTCCAGGTGCTCCGTATTACCCCACAGTCTAAAGACATGCAGTATAGATGGATTATGTAGGCTAAATTGTCTGTAGTGTATGAGTGTGTATGGATGTTTCCTAGAGATGGGTTGCAGTTGAAAGGGAATCCGCTGTGTAAAACATATGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGCGACCCCTGATTAATAAAGGGACTAAGCCGAAAAGAAAATGGATGGATGGATTTAGGATTCAGCCAAAGCTAATGGTCTGAGTGAATGAACTGGATAAACTTTGAGCATTTAAACAAGATGTCAAGTAAATAAACCAGACACATATGAACATAAACAATGAATCAAATTGTAACCATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34397
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062968 | Nonsense | 759 | 906 | 18 | 21 |
ENSDART00000124686 | None | None | 190 | None | 7 |
ENSDART00000137820 | Nonsense | 161 | 309 | 5 | 8 |
ENSDART00000144229 | None | None | 593 | None | 13 |
Genomic Location (Zv9):
Chromosome 8 (position 24657183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 23783001 |
GRCz11 | 8 | 23804240 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCTGTGGCGCTCACAGCAGGCCTGTCCTCTCTGCTCAGAAAGTAACTAT[A/T]AGGAGATTGTCAGCGCCTGCATCCAGGGAATTCAGGTGCAGAAAACATTC
Long Flanking Sequence:
AAAAAGTAGTGTTATGAGCTTTTACAATTTTTAAACGCTGCTAATTTAGCAGCATAATTCTACACATAAATACTCATTTTCTATAGTAATAAAATATACTGAAAATAGTAAAAAACTTCACTAAAAATGCACTGAAATCTTAATAAAATTTAAAACTAATTGCAAATTTGCACAGAAATAAAACAGAAAAATATAACCACTATATATTTTTAATGATTATTTTATCTAATTAAATGCATTTTTTATTTCTAAATTGTGCAGCCTTATTTTTTTTTTTTTCAATTAAGACTGTTATAAAGTCTGTGATGTTTTGGACTGAACTTTAATGTTAGCTTAACTTTTTAATCCAACTTGGAAACAGCAGAGATGAAGTTTTTTTTAATTTTATTTCTTCTTTCGCTGTGTGTAGTAACTGCTCAGAGGGCACATGTGACGGCTGCTCTTTCCACTTCCTGTGGCGCTCACAGCAGGCCTGTCCTCTCTGCTCAGAAAGTAACTAT[A/T]AGGAGATTGTCAGCGCCTGCATCCAGGGAATTCAGGTGCAGAAAACATTCAAAAGATTTTTGAAAACATTTTTGTTGCTCTTTATCAATTCGGTTGTTTAGATTTAAATTACAATACATGTATGCTAAAAAAATAGTTTTTTTTTCTCCTGAACTGAACTATAAATCTCCACTTCATCAAGACTTTTACACAATGATTCACAGTTTTATCTGAACAGAGGGATATATTCATCCATAATGTACCTGATCATATACAATTAAAGTCAGAATTATTAGCCCCCCTTTTAATTTTTTTTCTCTTTTTAATATTTCCCAAATTATGTTTAACAGAGCAAGGATTTTTTTACAGTATGTCTGACAATATTTTTTCTTCTAGAGAAAGTCTAATTTGTTTTATTTTGGCTAGAATAAAATGTGTTTTGTTTTTTTAATAACAACAATAATTCAGAGGGGCTAATAAAAAAACAATATGATGAAAATACATAATATCCTGTTATATAC
Associated Phenotype:
Not determined