ZMP
si:ch211-79l20.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
KIAA1429
Human Description:
KIAA1429 [Source:HGNC Symbol;Acc:24500]
Mouse Orthologue:
1110037F02Rik
Mouse Description:
RIKEN cDNA 1110037F02 gene Gene [Source:MGI Symbol;Acc:MGI:1913435]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22853 | Nonsense | Available for shipment | Available now |
sa17347 | Nonsense | Available for shipment | Available now |
sa36152 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6434 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22853
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 |
---|---|---|---|---|---|
ENSDART00000113826 | Nonsense | 283 | 1835 | 8 | 23 |
ENSDART00000142215 | Nonsense | 284 | 1836 | 8 | 23 |
ENSDART00000142706 | None | None | 246 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 28941590)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26817364 |
GRCz11 | 16 | 26690806 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACAAGTGTGTGATGTGTTATGTTTTCACCTTCAGGTGATGATGGATA[T/A]GAGCAGATATCCAGTGATGAGGAGGATTTAGAGAGTGGGGCTTTCAAGCT
Long Flanking Sequence:
AAAATAAGAGTTTGTCACTTAACATTTTTAGGAACAGAAATATAATGTTTACATTCAAACAAATTATTGAAAAAAATTAGCTCCATTTTCCAGTTTATTAAAAAAGAATATTATAGAATATTTTTTTTCGAGCATGTTAATTTAGGTGTACTAAATTTTGGACTGTGGTTTTTGTTTTATTTTGTTAGATTACAGAATATTTTATTATGTATTTTGAAAATGCTCACACTTAAAATTGAGAAAATTCTTTCAAAGACTTCTAGAAGTGGTGCAGAGACCAGTTTTTCTGCACAGTTCTGACTCATACAAAAGGACCTTACAAATCTGATTTATAGTCTGATTTGCTGAGACGGCCAACTCAATTAAACACTACACGAGAATTCAAAGTCAAGACTGAACTTGCTCCATTTCTCTTCTGGTGACATGATGTTCTGTTTGCTCTTTGGAAAGGCAACAAGTGTGTGATGTGTTATGTTTTCACCTTCAGGTGATGATGGATA[T/A]GAGCAGATATCCAGTGATGAGGAGGATTTAGAGAGTGGGGCTTTCAAGCTTCCTGCTTTTGACCTGGACTATACTCCTGAAGACCTCGCCTCACTACCAACTGTGCAGTACGACCCATATGAGCGTGAACTCAGACCCCTTCAGCACTTCACCCCACCACACATCACACGCTATGAGGCAGAGCTAAAACGCCTCAAAACGGTGGACATCGAGGACTCGAGCTCCTCATGGGCAGAGTCTGCCGCTAAACTCTCAGAACTCCTGGAGGCCTGGGGGGAGGCGCAGGGGGCGGAGAGAGGTGCAGGCTGGGTAACTGCTTTAGAGGAAGTCCCTGCCTTTCTAGTAAAAGGAATGAGCTTCCTGTCTATTAAGGACCCTGATGGGCAGAGTGAAAAGTTGAAGCAATTGGTCGACTGGAGCTGTGAAGCTCTTAGTTTGGACGTTGCTCTGGCGCAGCCCATAGCACTGAACCTGCGCCAGCTTAAAGCGGGAACCAAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17347
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 |
---|---|---|---|---|---|
ENSDART00000113826 | Nonsense | 506 | 1835 | 8 | 23 |
ENSDART00000142215 | Nonsense | 507 | 1836 | 8 | 23 |
ENSDART00000142706 | None | None | 246 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 28942257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26818031 |
GRCz11 | 16 | 26691473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAACGTGCTGCGCTCCCTYGACAGCATCATCAGCGAGCCACAGGGCATC[G/T]ARGCTATGCTCAGAGACCGCCACCATCATGAKGATGATGGCACAAGCGGG
Long Flanking Sequence:
CACGCTATGAGGCAGAGCTAAAACGCCTCAAAACGGTGGACATCGAGGACTCGAGCTCCTCATGGGCAGAGTCTGCCGCTAAACTCTCAGAACTCCTGGAGGCCTGGGGGGAGGCGCAGGGGGCGGAGAGAGGTGCAGGCTGGGTAACTGCTTTAGAGGAAGTCCCTGCCTTTCTAGTAAAAGGAATGAGCTTCCTGTCTATTAAGGACCCTGATGGGCAGAGTGAAAAGTTGAAGCAATTGGTCGACTGGAGCTGTGAAGCTCTTAGTTTGGACGTTGCTCTGGCGCAGCCCATAGCACTGAACCTGCGCCAGCTTAAAGCGGGAACCAAACTGGTCTCTGCCTTGGCTGACTGTGGTGCTCAGGCTGTGCAGGATCTGCTGGAGAAGGGGATTGTTGGCAGGCTCCTAGGCCTGCTGTTTGCAGAACACGTTTCATCCACTCTGAAACTCAACGTGCTGCGCTCCCTCGACAGCATCATCAGCGAGCCACAGGGCATC[G/T]AGGCTATGCTCAGAGACCGCCACCATCATGATGATGATGGCACAAGCGGGTATCAGCGTCTGCTCGATCTGTTTCTATTGGACCAGACTGTTCGTGTCGCAACTGCAGGTGCAGCCATATTACACAAAGGACATTTATATGAGGTTTTGACTGACCTGCAGAAAACCGCCAGTGTTTGGGCTGAACGGCATCCTACTGTAGGGGAGGTGGCTGAGCGCGAGGGCAGCGAGAGCGAGGCTGGAGAGAGAGACAGAGAAAGCACTGAGAGGGAAGGGGAGGAGAGAGAGAGGGAAACCCAGGAGGCAGAGCGGGAAAGCCCAATGGACATCGATACCTTGTTGGAATCTGCCTCTTTGTCAGAGGCTGACCTGGAGAGGCTGCAGGGTCTCCTGGAGGAACTGCTCCACCTGCTGGAAACAGCACCTCACTGTATGGTGCAGCCTCCTGGGAAAGCTTTTCCCACCAATGTCCGGATCACTGGGCCACCAGAGCGAGATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36152
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113826 | Nonsense | 910 | 1835 | 11 | 23 |
ENSDART00000142215 | Nonsense | 911 | 1836 | 11 | 23 |
ENSDART00000142706 | None | None | 246 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 28947164)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26822938 |
GRCz11 | 16 | 26696380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAACATCTGACCTCAGTGATTTATATGTTTTTCAGAGCTCTCTAAGTG[G/A]TTGGAGCCACTTGAAAAATTACATTTCGATATCAGTGGCATTCCTATGCT
Long Flanking Sequence:
ACCAGGTATACTTGAAACTTCCAGGCAGGTGTGTTGAAGGAAGCTAGAGCTAAACTGTGTAGGACCGAGTTAGGACACTCCTGTCATATAATCGTTTTTAGTTAAAATAACATTTTTGTTCTGTTTAGCTTTCTGACTTGCTCTTAATCTCTCTATCAGGGACGGCAAAGCAAGGAAATCTGTAACGTATAACTATGCCTGTATGCTTGTACTGCTGGTGATTCAGACATCAAGTGATCTGCGGATGATGGAGCACTATGCCGCTCCACTTCTTCTTGTTTGCAAAGCTGATGAAAACAACGCCAAGCTTCAAGGTGAGCCTATTTAACTTTTGCAGCCCTTCAAACACTTTGATGTCAGCCAAAACATCACTTATAGAATCTTTTAAGATGCAAGTTTTATTTTATGGCCTTAAGAGCAGATTTCTAATTTTTTGCTAATGTAAAGTGCTTTAACATCTGACCTCAGTGATTTATATGTTTTTCAGAGCTCTCTAAGTG[G/A]TTGGAGCCACTTGAAAAATTACATTTCGATATCAGTGGCATTCCTATGCTTATTGACTACATAAAGCAGGTGAGCTTATCAGCCACATTCTAAACATTTACGGCATTTTGAGGGGTTTTAGATTATAGAGAATGATTTGCAACGTGTATAGCCATCTCATGTTTAATCACTGATCAAGACATTCAAGGCATTGATAGACTGTTCAGGTTTCAACATGAATGAGACACATTTTTATCCTTTTGCGATAAGCTTAAAAACATTCATTCAGTCATTGGACTAAATCACAGTGGATGACGAAGACATTTAAGAATTGTGGTATAGGAACTAAGTATTGCTGGGGGTTTTTCAGAATCTGGAGAACTTGATGACTGCAGATGGTGTGGGTCTTGTTACTGCTCTCAGAGTTCTGTGCCACATTGCCTGCCCACCAGCAACAGTGCCAGGTACATTCACACATATTACAAACCTTAATCTAAACAGGACAAAAAAAAGTGAAATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6434
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000113826 | Essential Splice Site | 965 | 1835 | 12 | 23 |
ENSDART00000142215 | Essential Splice Site | 966 | 1836 | 12 | 23 |
ENSDART00000142706 | None | None | 246 | None | 5 |
Genomic Location (Zv9):
Chromosome 16 (position 28947609)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 26823383 |
GRCz11 | 16 | 26696825 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTCAGAGTTCTGTGCCACATTGCCTGCCCACCAGCAACWGTGCCAGG[T/C]ACATTYACACATATTACAMACCTTARTCNNNNNTAAACAGGACAAAAAAAAGTGA
Long Flanking Sequence:
AGTGCTTTAACATCTGACCTCAGTGATTTATATGTTTTTCAGAGCTCTCTAAGTGGTTGGAGCCACTTGAAAAATTACATTTCGATATCAGTGGCATTCCTATGCTTATTGACTACATAAAGCAGGTGAGCTTATCAGCCACATTCTAAACATTTACGGCATTTTGAGGGGTTTTAGATTATAGAGAATGATTTGCAACGTGTATAGCCATCTCATGTTTAATCACTGATCAAGACATTCAAGGCATTGATAGACTGTTCAGGTTTCAACATGAATGAGACACATTTTTATCCTTTTGCGATAAGCTTAAAAACATTCATTCAGTCATTGGACTAAATCACAGTGGATGACGAAGACATTTAAGAATTGTGGTATAGGAACTAAGTATTGCTGGGGGTTTTTCAGAATCTGGAGAACTTGATGACTGCAGATGGTGTGGGTCTTGTTACTGCTCTCAGAGTTCTGTGCCACATTGCCTGCCCACCAGCAACAGTGCCAGG[T/C]ACATTCACACATATTACAAACCTTAATCTAAACAGGACAAAAAAAAGTGAAATGTGTCATATTATCAGATTTGTGATTACAGATTAGATATTACAGCACGGTGTCCGCTGGATCTTAAAAAGTCTTATAATGTCTTAAATCTTAAATCAAAGATTTAAGCCTTTAAAAAGTCTTAAATCTACTGAAATATTGTGTTGTAGGTCTTAAATCTTTTTTAAAATGTCTTAATTTTCCTTTGTTTAGGTATTTCTACTCAATATAGCCAAAACTTTTTTTTATTTAAAATGGTAATTTTTAACTCTGTTTGTCATAAAAAAAAATTATTTTCCTCACAATAATATTTGTTTAAAAGTGCTCCATGTATTTACTGCTAAGAACACCAACCTGCACAAATTGTTGTATATAGATTTATTTATAATTAAACTTTTAAAACATTTGTTAAATTTTTTTGTTTTATAGAAAGTTTGTTGAAAAAAAAAGTGTATGGATACAAGCAGAGC
Associated Phenotype:
Not determined