ZMP
si:dkey-18l1.1
Ensembl ID:
ZFIN ID:
Description:
Uncharacterized protein KIAA0564 homolog [Source:UniProtKB/Swiss-Prot;Acc:B0R0T1]
Human Orthologue:
KIAA0564
Human Description:
KIAA0564 [Source:HGNC Symbol;Acc:29071]
Mouse Orthologue:
1300010F03Rik
Mouse Description:
RIKEN cDNA 1300010F03 gene Gene [Source:MGI Symbol;Acc:MGI:1919008]
Alleles
There are 7 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30915 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa2515 | Nonsense | F2 line generated | Not yet available |
| sa16132 | Essential Splice Site | Available for shipment | Available now |
| sa34601 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa41388 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30915
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 |
|---|---|---|---|---|---|
| ENSDART00000111563 | Essential Splice Site | 397 | 1903 | 11 | 46 |
| ENSDART00000146706 | Essential Splice Site | 397 | 1896 | 11 | 45 |
Genomic Location (Zv9):
Chromosome 9 (position 18273834)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 17749904 |
| GRCz11 | 9 | 17757616 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCAGATCAATCTTTTTTTCCCTGTAAAGGAAATGCTGTACTTTCTCCACA[G/A]GTTCCTTCAGGGACACGGCCGATTCGCCCACCCAACAGCAGTCCCACGTT
Long Flanking Sequence:
CCATCTTATTCAAATTTGTCAACAAAATTAACAGTTGTTTTCTACTACAAATATTTCCATGTTGTATTCGTAGATTAATTAACTTTCCACCAATAGATTTTTATTTAATACTACTTTACTTATTAATTCATTAATTCACAGCAATAAGTTAAACACAATCAAATTAGTTTTTTCTACTTGTTCAAACTACTTATTAAAATGAACTGAATCAACACAATTCTTACTTTTTTTCTTTTTTTTAACGTTCAATCTATTTAAAATTGTAAAAACATTATGTTAGACAACATGAATGAATTGTGTAGAACCCAGCATTTTTTACAGTGTAACTAAGAAATTGCAATTGTGTGCTATAATATTGGGAGTTTTAGAGAAATATTACTTGAATTAGGGGTCAGCCAAGTGTCCCTGCAGCTAAGAACTATAAGATAACTCTTTATTTGGCAAAGGGGATCAGATCAATCTTTTTTTCCCTGTAAAGGAAATGCTGTACTTTCTCCACA[G/A]GTTCCTTCAGGGACACGGCCGATTCGCCCACCCAACAGCAGTCCCACGTTCATCAACACCCCCACCCACGAGCGCCTGCTGGCAGAGATGATGCAGTCCCACCTCGTCAAAGACATTTGTCTGATCGGAGCCAAGGTACACATACAACTTCCTGCGGCCACCCTCATGGAGTAAACGCACTTTTAACTAGAAAGTGAATGTGTTTTGAATTAGAACAATGGCTCATTTTTTTGTACTGCCTCTTAAGGTAATGCAGGAAGATCATCGGGGTCTTCAGTGTTTGCGTCATGAGATGTGTTCTTATTTAAGAGGTTCTGAGGCAGATTAGATCTGATGAACAATGTAAATCTAATGCTGGATCAGTAACATTGCATTGTGGTTTGGCTAATGCAGTTGTTTTGTTGTGTGTGTTTTGTATTTTAGGGTTGTGGCAAATCTGTGATTGCAAGAGAGTTCGCTGAAATGCTGGGTTACAGCATTGAACCAGTTATGCTGTATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2515
Status:
F2 line generated
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 |
|---|---|---|---|---|---|
| ENSDART00000111563 | Nonsense | 971 | 1903 | 25 | 46 |
| ENSDART00000146706 | Nonsense | 966 | 1896 | 25 | 45 |
Genomic Location (Zv9):
Chromosome 9 (position 18204360)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 17680430 |
| GRCz11 | 9 | 17688142 |
KASP Assay ID:
554-3223.1 (used for ordering genotyping assays)
KASP Sequence:
TTCGGAGAGCTTCGGGCCATGGCTGACCAGGGAACAATCACATACCCCTA[C/A]TCTACACGAGAGGTGGTAAACATCGTAAAACATCTACAGGTAATCAACTG
Long Flanking Sequence:
TTACTTGCTGTTCCTAAAGCTTGGACAAGGAACAAGATTTATATATTCTGTTTTGTTAAAATTGATTATATGTGATTTTTTTTTCTCATCAAACAACTATTTAAACAACTTTTCTTTCTTTTTTCTAAATTATAAGGGATAAAATACATTTAATGTTATGTTTGACAGACCAATTAGTGTGATTCTTTTTTTTTTTCCCCTCTTCATTTTTTTTAAATAAAAGAAGAAACGGATTGGGTTTTCATTTTTGTACTTTCCAACTCAAACATAAATAATTAAAATGAAGCTTTTGATAGGCTTATTTTCTAAATGGATTACTGATTGACTCTTTCAGGGGATATATTTAGCTGCCATGCAGTGGACAACCCCAAACCTCAGGCTGAGTTTGCCATGCTGAAGCAGTATGGGCCTGACGTTCCTGATGCCGTCCTCCAAAAACTGGTGGCGGCATTCGGAGAGCTTCGGGCCATGGCTGACCAGGGAACAATCACATACCCCTA[C/A]TCTACACGAGAGGTGGTAAACATCGTAAAACATCTACAGGTAATCAACTGAGGGTCTTAACCGCAGACTGCACACTGATAGAAAATTCACAGACAACCCAATGAGAGTTAGAGTCAAAATAGAAGCAAACATTGGTACCTTTCATTTTATCATAACGTGAATTATTGTCAAAATATTTGTTGACATGTTAACTTTGTTTCAATATATTTCAACTTGCATTGCATTACATTTACTTAATACTTCAAGCTAAATTGTGAGTAACTTAAAAGAAGTTTAAGCAAGACTAGCTTAATTTAATAAATTTAAATTAATTAAATTAATTAAATAAATAAATTAAATAAATTAATTTTCTTTTGCATTATCTTACATTTTTATATATTTCATTGGTGGCTTTCATAGTCTTGCGATCCTTCAAAAATCATTTTAATATGCTTTTTATGTTTAAGAAACAATTTTAAACAGCGTTGAAAACAGCCACAACTGATACTTGTTTGTTTTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16132
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:
A > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000111563 | Essential Splice Site | 1072 | 1903 | None | 46 |
| ENSDART00000146706 | Essential Splice Site | 1067 | 1896 | None | 45 |
Genomic Location (Zv9):
Chromosome 9 (position 18184699)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 17660769 |
| GRCz11 | 9 | 17668481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
KGCAGTTTCAGTTYATTGTTTAGTTYATTGTGCTGTTTKTGGTGCTCTTY[A/C]GGGCCCAGTGTTWCTCCGGGTTCAGAGTTAYCCTTCTRAAAGACATGART
Long Flanking Sequence:
CATGAAGTCAAACATTTCATAAATAGATAAAAATCATCATACATTTTTCATTAATGTAAATAACAGACTCAAGCTTTAAAGGTGTAGTTCACTCAAAAATTACATTTTTGTCATCATTTACACACTTTCATAGTAGGAAAAACAAATATTGTGGATGTCAAGGCTTACAGGTTTTCAGCTGTCTTTAAAATACCTTCTTTAGTGCTCAGCAGAATAAAGAAACTCATGCTTTGGCATGACCGTGGCATAAATTAAAGCTAGAGTCGTCAAAATGAGAGGTCTGTTACAGTGTTTTCATTTTTAGAGATCATAACATGCATAAAGTGTCATATTATATTGTCATTGTTAATATAATCTCAAAGTGTCACATTATATTACCATAGTCAAAGTAACATGCCAAAAATGATGTTTATATGCGTCAGACAGTTTAAAATGTACAGTGATTTGGTTTGCAGTTTCAGTTCATTGTTTAGTTTATTGTGCTGTTTGTGGTGCTCTTT[A/C]GGGCCCAGTGTTTCTCCGGGTTCAGAGTTACCCTTCTAAAAGACATGAATCCAGATCTTTAAGCTTCACTGAGGAACAGGCCCACTGGCAAATCCCTATGAACGAAGTCAACATCGTTTGTGACGTCACCACTGCTAAAGGTAAGCTTGATTTTATTTTATTTTATTTGTATAGGCCTTTTTTTCAGTTATTGAAATCGAACCCAAAAGTAGGGATCCGTTCATTCTGTTGCCCATTCACTCTAAGATAATGATCACCGTTAATTATAATAGTTTCCTGTCAGTCAATATGTATCTAACAAGTCAATTGCACATGGATGAATGAAACACTCTAAATAGCACAAAGCTTACTTATTTATCAGACATAGGTTCATTTGTTATCATGTAATATGTATAACCAAATGTTCTATGAAAACACAGCTTAAAGATTACATTCAGTAATTATTACACACTGACTGGTATTTTTGAAGTATTGTTTTTTACATAGATATTCACATTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34601
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 |
|---|---|---|---|---|---|
| ENSDART00000111563 | Nonsense | 1148 | 1903 | 29 | 46 |
| ENSDART00000146706 | Nonsense | 1141 | 1896 | 29 | 45 |
Genomic Location (Zv9):
Chromosome 9 (position 18182541)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 17658611 |
| GRCz11 | 9 | 17666323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTATGCTATGAAGGAGAAAGGAGACTCGGTACAGTGTATAGAGCTCTA[T/A]GACATCTTTCCCAGGACCATCAGTGGAGTTTGGCAGCCCTTCGTCTCTGT
Long Flanking Sequence:
GAACACCTTGGGATCCCCCTGTAGGAGCTTGAGGAAGTGTCTGATGAGAGGGAAGTCTGGGGTTCTCACCTGAGACAGCTGCCCCTGTGACCCAGCCCTGGAAAAGTGGAAGAAAATAAATGAAAGAATGAATATTAATATATTGTTATATTTCAGTTCAAAACTATGCACATTAGGCTACATATAGTATACTTGAACAAAACAGCAGCCATTTATTAAATCTGTTAAATGTGTAACTTACAAACTTGCTATTATTTTTTCTATTATAATGAATACATTATAATGAATGGCAGTCGTAGCAGTGGCAGTTTAACCAGAACGAATGACTCCCTCCTTCTGGTCTCAGTCACCATATTGTAAAATAGGCCTATTTTACAATATGGTGTAAAATAATGACTCTGTTTCTCTTTTATAGATTCCATTTATGTGGCCACGTGTAACCCTGTATCGCTGTATGCTATGAAGGAGAAAGGAGACTCGGTACAGTGTATAGAGCTCTA[T/A]GACATCTTTCCCAGGACCATCAGTGGAGTTTGGCAGCCCTTCGTCTCTGTGGCAGCGCTGGGCAACCCGCTGCAGGACCAGGTGGTGCTCCATGAAGAACAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGACCTGTAACCTACCCTACTTCATGGGTATTACACATGAAAGTGTTGCCATCTACTTGCTGCCATTACCAGTCCATTTACTGGTGTCATTCCTGCCATAATGTTATTGTGTTATTATCTGAGCCTGGAAACAGAAGATCAGATGCATCATTTCCAGCAAACTCGTGAAGGGACTAAATAATAGTGGATGGAAATGTTCAAAGATCAAAACAAATTTACGGCTGAGATGTGAGTGTATAGATTTAGTTCAGTCTGTCGAGATGGTGTTGTGTGAGGTTTTACAAAGAATATAGGATTTGGATATTTTGTTCTTTTAAAATATATGTTTCTTTAAATTCTGCTAGTCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41388
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 |
|---|---|---|---|---|---|
| ENSDART00000111563 | Essential Splice Site | 1223 | 1903 | 31 | 46 |
| ENSDART00000146706 | Essential Splice Site | 1216 | 1896 | 30 | 45 |
Genomic Location (Zv9):
Chromosome 9 (position 18176837)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 17652907 |
| GRCz11 | 9 | 17660619 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAAGCGCCACGGAAGACCTCAAACTGGTGGAACAGCAAAGAGAGTCAG[G/A]TGGAAATCTGCATCAGGACCAGTGCTTCTCAACCATATAGGAGCCTTAAG
Long Flanking Sequence:
TACCAATCAGTGCTTTCTATGAAATGGATTTAAACACTCCATTCCTCGTCAAGCTATTTTGTTTTGTGTAATGGTCATACCGCTACGATACCAACTCTGAAATTTGGAAACTAGCATCAACATATCCTTTCAACAAAATCTGAGCAAATTAGTGCAAAATAACCTTTAGGTTTCTTAAAGGGAGAGCTGTTTTTTTTAAAGCCCAGGGTCAGAGGGAGGCTGGAACATGGTTGCGTTAAACTAAATTATGAGTGTTCTTGGAGGATAAAACCTCAGCATTAACCTAACATTATAAGAGTGCTTCAGGGAATAAAACGAAATGATCTGACCTCTTTTTCAAAAAGGAACTACATGAACATTCCTGTCTCGTTTTGTAGGGCAACACAGTGCTGCATCTGGATCTGGTTACTGGTGCTGTGAGGAGGCTGATTCTGTCTCAGGACAAACAGGACGAAGCGCCACGGAAGACCTCAAACTGGTGGAACAGCAAAGAGAGTCAG[G/A]TGGAAATCTGCATCAGGACCAGTGCTTCTCAACCATATAGGAGCCTTAAGTGAAATAAAAATTATAGTTCACCCAAAAATGTTAATTCTGTCATCATTTACTCACTCTTTACTTGTTACAAACCTTTGAGTTGCTTTCTTATGTTAAAAAGAAAACATGATATTTTGAAAAATGCTGAAAATCACTAACCATTGACTTTCATAGTATTGGTTATGTCTACAATTTTTACTGGTTTCCAGCTTTCTTCCGAATATTTTCTTTTCGGTTCCATAGAAATTAAAGGTTTGTAACCAATTGAGAGTGAGTAATAGAGAGTAAACTTTCATTTTTAACTATTTCATTAAGTCCAAGGTAGTCGACTGTCTTTGATAAACTTTATGTTTAAGTAAGCCATATAAATTAATCGATTTTCGAATTCCATGGGCATTTCAAATTCATTTATTGCCCTAAATTGTTTGGTTGTGCATATACTCTGAAAGTTGTAAGAATCTCTACATTTC
Associated Phenotype:
Not determined