ZMP
zgc:152873
Ensembl ID:
ZFIN ID:
Description:
Protein KIAA0664 homolog [Source:UniProtKB/Swiss-Prot;Acc:A0JMD0]
Human Orthologue:
KIAA0664
Human Description:
KIAA0664 [Source:HGNC Symbol;Acc:29094]
Mouse Orthologue:
1300001I01Rik
Mouse Description:
RIKEN cDNA 1300001I01 gene Gene [Source:MGI Symbol;Acc:MGI:1921398]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39047 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12848 | Nonsense | Available for shipment | Available now |
sa19117 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35891 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa2783 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa39047
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 |
---|---|---|---|---|---|
ENSDART00000047471 | Essential Splice Site | 43 | 1400 | 1 | 26 |
ENSDART00000132239 | None | None | 971 | None | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 24698027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25431669 |
GRCz11 | 15 | 25366934 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCAACAGCAAAGGCACCACCAGTAAGAAGGAGGCGTCGTGTGCCTGCGG[T/C]ATGTCAGCTTTACACCGTTTCCACCTGCAGCATGTGCTTGGAAATCACGT
Long Flanking Sequence:
AGGTTTGCAACCACTCGAGGATAGGTAAAAACAGAATAAAGTAAAATATTTGGTTGAACTGTCACTTTAAAAACAAACCCATCTAAAACGCGCTTCTTCAAATGAACCTCCGGGCTTGCCGTAGCCGGTTGTTTGGTTTGGGAGGGACCAACGCAAAGGCAAGCAGGTCAAGAGGAGGAGAAACCACGTGTGACAGTCAGGCAGCCTGAGAACTGGAGCTCTGTCCTTCGCAAGTTAGCTTGTTTTTGTAATATCTTTGCATGCAACCGGACAGCCGTTCCGTCAAGCGGAGAAGGCAGGCCAATTAGCAGACTCACTAAACAGCCCACACAACGGACGTCTGCTGCTAACTCTCTCTCAACCCGAGGAACCATGGTGAGCAAGACGGATGACATCCCAGCATCAGTGCCGAACTGCAGCCCGGCTGATTTTGCCCGGGACGGAGAGACAGCCAACAGCAAAGGCACCACCAGTAAGAAGGAGGCGTCGTGTGCCTGCGG[T/C]ATGTCAGCTTTACACCGTTTCCACCTGCAGCATGTGCTTGGAAATCACGTCAATGGATGATCTTAGTGTATTTAACCTGTCAGTTTGGAGTTAATAAGTGTTCTGTGATATGATTGACTGGATAGAGGTCAAAGTGAAGCAGGTACCAAAGGACATAAACAGGCAGAGAGTCCTCCAGGGTGTCTGTTTTAGATCCTCTTAGGGTTAACAAAAGGGAAGTAGGTGCCTTACAACCTTGTACAGGCCATTCATTTCAGCTCTTCTCAACCTTCTGAACTCCAAGGCCCTCAATTGTCCTAGGATTTTGTTTATAAGTTACTGGATGAGGATAAAAAACTTGTAACATTAGTTTTAATTAGTGTTACTCAGTTTAAAGTAAGAATATAACCTTTAAATGTATTCAGCTTTGAACCTTAAATATAAATTATATGAAATGTCATTTTTTTAAAGATTGAGCTGTAGTAATCATGGTAATGTTCCTTCATAAGGATAATGTATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12848
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 |
---|---|---|---|---|---|
ENSDART00000047471 | Nonsense | 283 | 1400 | 6 | 26 |
ENSDART00000132239 | None | None | 971 | None | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 24685814)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25419456 |
GRCz11 | 15 | 25354721 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGGAACCCTCYGCCCGGCAACAGRAAAATGCACGGTGACCTCATGTA[T/A]CTGTACATYGTGACTGTTGAGGACAGACACGTCAGCATCACTGCCTCCAC
Long Flanking Sequence:
ACAGCAAATGAACTGAGCTATTCTGACACTGTGAAACAGACTATATTATAAACTACCCGTTTAAATGACACTCTTCACTCTGAAACCAGTAACATGTTTATTTAAATAAATCTCACTATTTGACAACTGCACTAGTCCACGTCCCAAGATTAATTTTGTTGTGATATATCCTGCAGTCCTATTGGTGAGCGTTTTGCTCTTTCCTCCGCAGATACTGGCAAGCGCAAAAAGAAGGGCAGTGAACTTGAGCAGATTGATTGCACACCTCCCGAACACATTCTGCCAGGCAGCAAAGAGCGTCCTTTAGTTCCCCTTCAGCCACAAAACAAAGACTGGAAGGTGAGAGTTGATAAAAGATTTTGCTATGACATCAGATGCCTTGGTTTTGATTTTGACTGCTTTCGCCTCCATCTGCAGCCTATGCAGTGCCTGAAGGTTTTGACCATGAGTAGCTGGAACCCTCCGCCCGGCAACAGAAAAATGCACGGTGACCTCATGTA[T/A]CTGTACATCGTGACTGTTGAGGACAGACACGTCAGCATCACTGCCTCCACACGCGGATTCTACCTCAATCAGTAAGAGTGTCACTTGAAATTAATTTGTAACATTAATACTAAAAAGTTCTAGTGAAACTATTATTTGTAAGTTGCAACTAAGTATTTGAAAATCATACCAAAAAAGAAATAAGGATGTCCTCTGCAACCAGTTTCCTAAATTGATTATAAGCAGGAGGTATTGTATATTTAATTGTTCATGATCACCATATTTGTGTAATTTATTTTTAGATTATAAAACTAATTAATAAATAACTTAAAAAAAATTTAAACATAAGTAAATTTGCCACAACTTGCTTTGCCCACTCGTCTTTAGCAATGAGCTCTAACTATTTCATGTTAGAGAGTCTCCTTACCATCACCCTGATCTTTAGCTCCCTCCACAGATTCTCAATTGGATTTAAGTCAGAACACTGGCTGGGACACTTTTTTTTTTTTAGAAGCCTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19117
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 |
---|---|---|---|---|---|
ENSDART00000047471 | Essential Splice Site | 1101 | 1400 | 18 | 26 |
ENSDART00000132239 | Essential Splice Site | 672 | 971 | 9 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 24673984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25407626 |
GRCz11 | 15 | 25342891 |
KASP Assay ID:
2260-8528.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGATGCCTTCCATTTCTTCCAGAGCGGACAGGCCAAGGTTCAGCAAG[G/A]TAACAAAAACAAATGATCATCGGTGCTTTGACACCTTCAACGTTTTTGCA
Long Flanking Sequence:
ATTATACTAGTAATGAAAACTGCCTTGTTCTTACTCAAGAAAGTACTTCATTGGCTAAGATTAGGTAAAAAGCAGGGTTAGGGATGGTTTTTATCAAATATATATTGGAAATATGGCAAGTACATAGTATTTTACCACACTATTACTTTAACTGAAGACTAATGGTGTGCTTTTTGCAGTGAAAGCGTGGACCAGGCAGTGGAGAAGTACGGTTTGCAGAAGATCACCCTGCTGAGGGAGATCTCAATCAAGACTGGCATTCAGGTAGTGTTTGATCCATGTGTCTCTGAGGTGCTCCGTCAGGTGTCCTGTAGTGACAAGCCTTTCCTTTGTGTCTCCCCTGCAGATCTTGATAAAGGAGTACAACTTCGACAGCCGCCACAAGCCAGCCTTCACAGAGGAGGACATCCTGAACATTTTCCCTGTTGTGAAGCACGTCAACCCCAAAGCCTCAGATGCCTTCCATTTCTTCCAGAGCGGACAGGCCAAGGTTCAGCAAG[G/A]TAACAAAAACAAATGATCATCGGTGCTTTGACACCTTCAACGTTTTTGCAGAGCTGATTGATGCGTCCTTGGTGCGCAGGCTTTCTAAAAGAGGGTTGTGAGCTCATCAACGAGGCCTTGAACCTCTTCAACAATGTGTATGGAGCCATGCATGTGGAGATCTGTGCCTGCCTGCGTCTTCTGGCTCGACTCAACTACATCATGGGCGATCACCCAGAGGTATGACCCATAAACACATGCCAGAAAACAACGTTTGGATATTGGAGACTGATTTGTTTATAATGGAGTTTTGTGGATGAATGTGCAATACTGTTTAAATCAGTTCAGGAAGGCTTTCTTTTTCATTTTTTTTATTTAAAAATTTACTAATAATACATTTTTCTTGTGCAAATGATTTAAAATACAATGAAATCTGAAGTATCATGTGACACTAAAGACTAGGGGTATGAACCTACAATGGTCTCACGGTTCAGTTACGTTTATCATGCCATTTATTCGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35891
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 |
---|---|---|---|---|---|
ENSDART00000047471 | Nonsense | 1253 | 1400 | 22 | 26 |
ENSDART00000132239 | Nonsense | 824 | 971 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 24666938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25400580 |
GRCz11 | 15 | 25335845 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTGGAGAACGCGCTGGCCATCAACACAAAATACCACGGGCCGCGATCCT[T/A]GAAAGTAGCCCTCAGGTAAATATGTATGACTGTACTCATACTCACTAGTG
Long Flanking Sequence:
GTTACTGTTTTCGGAAGTGTAAAAAAAATGGTGAACTAACAAAAATGATTTGTTAGCAAATTTAACAAAAACTAACTGTGTCAGTTATGTCTAAATGTTGTGTTTGTTTTCCGCAGATGCACTTAGCACTGTACTGCTTTGCTAACGGTCAGCTGTCCACTGCCCTGAAGCTGCTGTATCGTGCTCGCTACCTCATGCTCGTGGTCTGTGGAGAGGACCATCCTGAAATGGCTCTGCTCGATGTAAGCAGTTTATTTCAGCCTCTGCCCATCTTCTGATTCTTTTTTTGAAGTTAACCAAGGTTAACAAGAGCTAGCTGAATTCCTGTGGCCCCTTAAGTTGAGGCTTGTGGAGCAACGTCATCCTCTTACTGTGATCCTATTCTCTGATGTAGAGCAATATTGGTCTGGTGCTTCATGGTGTGATGGAGTATGACCTGTCTCTGCGTTTCCTGGAGAACGCGCTGGCCATCAACACAAAATACCACGGGCCGCGATCCT[T/A]GAAAGTAGCCCTCAGGTAAATATGTATGACTGTACTCATACTCACTAGTGACGTGTGGTAGAAATGTTTGTTAACATTTATGATGTCTGTTGTTCTGCAGTCATCACCTGGTGGCCAGAGTTTATGAGAGCAAGGCTGAGTTTCGCTCTGCACTTCAGCATGAGAAGGAGGGATATACTATATACAAGAACCAGGTACATCTAATTTCATTTGTGTATCAGTTGCGTTAAGGTGTTGTGGGGATAATTTACAGTTTGAACCCAAAAAATGACCAGTCTGTCATATGAAGAAGAGCCAGAGTTAGAGATTCAATTAGAAAAAGTTTACTAAAGATAGTTTGCAGTCTCATCAGCAGAAGCCAGCTTCAACACTCGCAATGAGTTTGTAGACCGATCTGCTTACAATCTCAGAGCATTAACAATTATACTTTTAAGTAACGTCATTAACTGCATCATACATATACAGTTGAAGTCAGAATTATTAGCCCCCTTGAATTATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2783
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047471 | Nonsense | 1383 | 1400 | 26 | 26 |
ENSDART00000132239 | Nonsense | 954 | 971 | 17 | 17 |
Genomic Location (Zv9):
Chromosome 15 (position 24654186)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 25387828 |
GRCz11 | 15 | 25323093 |
KASP Assay ID:
554-2446.1 (used for ordering genotyping assays)
KASP Sequence:
TGAAGGCTGAGGTACAGAGACGGCAGCTGATGCAGGATTCTGGGAAAATC[C/T]AGGAACAGCAGGGCAGTCATTTAGAGCTSGATGACAAGCTGCCTGTGGAT
Long Flanking Sequence:
AATGAATAATGTGAACAAATTCTATGAAGTGTGACCAATAAACTAATCGTGAACATCAGTGGAAGACTTAGTCATCTTTTAACCAGGACGCAACACAACGTTCCTTTGGCTTAAACCCTATTGTTTTAGATCTGTTTTACATCTTGTCTTGTCGAGATAAAAATAAAGAGGCTTTATTTTTTTTATTTTTTTTATTGCAAAATTGTCCGCACATTTCTGGGAATTACCACCACAAAATCAAGTCATTTTTATGGCAAATAATCACAAAACAAAGTGAAAAACTAGGGGGTCGGAATAAATTGGTAATTTTTTGGAGCTTTGGTTTTGCCGCCTTTTTGAGTGAATGTAAATGTTTTTAAAAACAAACGTAATTTCGTCCATTTTGAGATTTTTTTTTTTTTTTTTTCCATTCTCCATTTTCTCCACACAGTCAAAAGGACCTGGAGAACCTGAAGGCTGAGGTACAGAGACGGCAGCTGATGCAGGATTCTGGGAAAATC[C/T]AGGAACAGCAGGGCAGTCATTTAGAGCTCGATGACAAGCTGCCTGTGGATGATTAACAAAACCCCAAACCAACAGACCTTCTCCAGATGAGGAGGACACCATACAGCAGCCATCTGTTTCAACCTGTGGACCCGGCCACTGAGCTGTCTAATCTAACCAATTCAATTTGAGCATAACAGGGAGAGGGGGGAGGACCAGCAGCAGCCGACTAAATAAAAGTGTACAGAGAGTAGTTTATAGCTGTAAAGAAAAACGAAAGCAGATGTTTGTTTGTTTTTTCCCCTACACGTGCAATCCACTAACAAACCTCTCCCAGAGGAAGAAAAAAGAAAGTAAACCAAGCACTTCCTCTGAGAGTTTGCACCGAAGAGGATGGAGACGACCAAGGATGACCATGACATTTTATACCAGAGCCTTATCCATCCATCAATCATCTCCATCTCTAACCTTCTCATCTGAGCCCAGGATAAACCCCAATCCGTCCCAAACCGACCCACGAG
Associated Phenotype:
Not determined