ZMP
si:dkey-157l19.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8A570]
Human Orthologue:
KIAA1522
Human Description:
KIAA1522 [Source:HGNC Symbol;Acc:29301]
Mouse Orthologue:
C77080
Mouse Description:
expressed sequence C77080 Gene [Source:MGI Symbol;Acc:MGI:2140651]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa5864 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11087 | Nonsense | Available for shipment | Available now |
sa42253 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14517 | Nonsense | Available for shipment | Available now |
sa38961 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa5864
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084929 | None | None | 1390 | None | 7 |
ENSDART00000133565 | Nonsense | 14 | 221 | 1 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 36436143)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35908712 |
GRCz11 | 13 | 36034544 |
KASP Assay ID:
554-3664.1 (used for ordering genotyping assays)
KASP Sequence:
AAGCACTATTCCAGACTCACTGCTCTCTGAGGGACGACTTTGTCCGAAAA[C/T]AGTTTTGTGGAAATGCCTCACCTGAACTTTCCAGACCAGACTCACATGGT
Long Flanking Sequence:
CACAGGGAAAAGAGACTTGTTGGGTTTATATCATTCCAATATGACAGTCCACACACTGTATCTACACAGTTCTGTCCAAACAGCTAATAAAAGATGATTTTCATCATAGGTGCCCTTTATCATTTTATTATTTTTTAGTTTTTTTTTTTTGCACTTTATTTATTACTTTTTTATTATTTCGCATTTATCTTATTTAAAAATTTGTCCTGAAATGACTAAGCATCACCATAGCAATACATCCTGTAAGTCATAAATGGCATATAAATCAGCTCCACGCCCTTTAATCAGCGTGTTACGTAATGACGTCTACAGGATGTGTTTGTGGCGCGGCCGCGGGGAGGCGCCACTGAGCGGCCGAGCAGCTGAAAATGTTTGGAAACTCCCTTTAATTCTCACCTGGAGCCTCTTGAGGATTAAGCGGAGAGGAGGACCTGAAGAAGCCCAGTCTGCAAGCACTATTCCAGACTCACTGCTCTCTGAGGGACGACTTTGTCCGAAAA[C/T]AGTTTTGTGGAAATGCCTCACCTGAACTTTCCAGACCAGACTCACATGGTCCGTCCGATCTAAGGGATTTTATAGCGCTGGACGAGAGGAAACTGGGGGATCCCGACTATACAGGTAAAAACAAAAACTGCTCAAATATGAATATGAATATGACATGACAACACGTGAAGTGTGTATGAAGTAAAGTTAGAGGTAAAACTAGAACACTTTATTTACTCAGCTCTATTGTTTGCTCTGTGGGTTTAATCATTAAAGTTTGTCCGTCTCTGTGTGGTCTTAGTTTCAGTAACTTAAGTCTCTTTCACTTGATTGCATGCTTTCATTTACTGAACAAGATGGTTGTTTGAGGATGGTTAGCTTGTGTGCTGGATGATGATGCTTTTTATATGTTATTGTGTTGTGAATAATCCTGTTAAGTCCTGTTTTAGATGTGGAGGTACGGTTTGTTTTATGCATTAATCTGTATTTGTATTCTGTATACTTTTGTTTTTTAACAGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11087
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 |
---|---|---|---|---|---|
ENSDART00000084929 | Nonsense | 123 | 1390 | 2 | 7 |
ENSDART00000133565 | Nonsense | 177 | 221 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 36397229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35869798 |
GRCz11 | 13 | 35995630 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTAAATATGTGTTGGACCTCCACACAGAAGCCCAGCAGGGCCTGAAACTG[C/T]AACAGCAAGAGGGTAGGAAGACTTYAAAATCAGTCTGCTTTTGTAAAAAC
Long Flanking Sequence:
TACAATACTGTAAAGTTTATTTTAATTTAATTAAATTTTTATTATACAATTTTTCTATTATGTAGTACTATATTTTATCTATTTCTGTGTTAATTTTATTAGACTTTAACGTGTTTGTTAATTTATTTCAGCAGCAAGGATCATTACAGGAGAAAAACAAAACCTTGACTGTACAAAATGTTTTGTTAAAGCTTGGGGAAAAAATTTAAAATAAAATAAAAATATATATATATATAACAGACAGATTGCATGACAGAATTTATCTATTAGTTATTAAATTGTATTTATATTAAATATTATGTATTATTATATCATACATTATTAACATATTGTTTCATAATAAATGTACTTCTTTTTGTTTTTCTCTCTCTCCAGGCCTTAAAGAGGAGGTTGTAGGCACCGTTTCTCTTCAGCAGTTCCAAGAAAACGTGTTTGTGGAGGGTGATCGACCTAAATATGTGTTGGACCTCCACACAGAAGCCCAGCAGGGCCTGAAACTG[C/T]AACAGCAAGAGGGTAGGAAGACTTTAAAATCAGTCTGCTTTTGTAAAAACACTTACTTTTACTCAGAACCACATGTGTGCATGTTTTTGTCATACATAAGTTCATTTTAATATAAATTAGAAAGTAATGTTTTGTTTCATTAATTTGTTTGTTCCAGATGACAGGAATGGGACGGACTTCCCTGATGACCAAAGCATGATTGTAAGTATTAGTCTATGCATCATACAACACTCTGTTTCTATTTTGAATGTTTTTAACTGCTTTTATAACAACTAATTATAAATTTGATGGTTAACCGTGCTATTTGCTTTAGTCAACAGTAACTGCTCAGACTGAAGACAGCATGGCCTTCAGTGAGCTGAGAGGCTTTGAGTCTGAGAGCACAGCAGCCGATTCTGTTTCAATGCGCTCCTCCATTTCTTCACGATCAACACGCTCAGGACTAAAACGGCAAGGTGACGAAAAACACATTCTTACTAATATCCATTTTTTCCATAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42253
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084929 | Essential Splice Site | 189 | 1390 | 5 | 7 |
ENSDART00000133565 | None | None | 221 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 36396658)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35869227 |
GRCz11 | 13 | 35995059 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATTTCAAATATACAATGCCAAAGAAAAAATTCTCATTTCCTTTCTCC[A/T]GCCTCAACATTCAGGCCTCTGAAACCAGATAAGTCTGCAGAGAAGCCCAG
Long Flanking Sequence:
ACATGTGTGCATGTTTTTGTCATACATAAGTTCATTTTAATATAAATTAGAAAGTAATGTTTTGTTTCATTAATTTGTTTGTTCCAGATGACAGGAATGGGACGGACTTCCCTGATGACCAAAGCATGATTGTAAGTATTAGTCTATGCATCATACAACACTCTGTTTCTATTTTGAATGTTTTTAACTGCTTTTATAACAACTAATTATAAATTTGATGGTTAACCGTGCTATTTGCTTTAGTCAACAGTAACTGCTCAGACTGAAGACAGCATGGCCTTCAGTGAGCTGAGAGGCTTTGAGTCTGAGAGCACAGCAGCCGATTCTGTTTCAATGCGCTCCTCCATTTCTTCACGATCAACACGCTCAGGACTAAAACGGCAAGGTGACGAAAAACACATTCTTACTAATATCCATTTTTTCCATAAAAAGCAGAAAGTGCTTAAAGAATTTATTTCAAATATACAATGCCAAAGAAAAAATTCTCATTTCCTTTCTCC[A/T]GCCTCAACATTCAGGCCTCTGAAACCAGATAAGTCTGCAGAGAAGCCCAGGACTCGTAGGAAGCCTGTGAGAAATGTAGTTGGAATTCCTCGACACGTCCAGAAAGAACTGGGTATATTTTTACACTTCTACAGTGTGTTGCATGTCTTCAAGATAAACTAATTATGCTTAATATTTTTATTTTTTTTGCTTTTGTCTCTGAAGGGCTGGACAGGGCAGCATGGATCACCACCAATGCTCTTGATTACCAACTGTCCAATGGAGATGTGATCATACCCGCCATAATAACTGCTGTGGATGGTGTTTCTAGCAGCTCTGAACAAGAAAGCTTACAAGACTATCCACAGAGAGGACAGAACCTGCACATACTTTTGGAAAACAACACAGAGGTCCCCATGCTGGCAAAGCACAAAGATATCCTCCAAAGGTCCATGAACCAATTTGTAGATCCAGGCACTTTAGGTGTTCCAGAGAACCAAACTGGTGCAGTGATGTCCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14517
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 |
---|---|---|---|---|---|
ENSDART00000084929 | Nonsense | 276 | 1390 | 6 | 7 |
ENSDART00000133565 | None | None | 221 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 36396304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35868873 |
GRCz11 | 13 | 35994705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTCTAGCAGCTCTGAAMAAGAAAGCTTACAAGACTATCCACAGAGAGGA[C/T]AGAACCTGCACATACTTTTGGAAAACAACACAGAGGTCCCCATGCTGGCA
Long Flanking Sequence:
CGATCAACACGCTCAGGACTAAAACGGCAAGGTGACGAAAAACACATTCTTACTAATATCCATTTTTTCCATAAAAAGCAGAAAGTGCTTAAAGAATTTATTTCAAATATACAATGCCAAAGAAAAAATTCTCATTTCCTTTCTCCAGCCTCAACATTCAGGCCTCTGAAACCAGATAAGTCTGCAGAGAAGCCCAGGACTCGTAGGAAGCCTGTGAGAAATGTAGTTGGAATTCCTCGACACGTCCAGAAAGAACTGGGTATATTTTTACACTTCTACAGTGTGTTGCATGTCTTCAAGATAAACTAATTATGCTTAATATTTTTATTTTTTTTGCTTTTGTCTCTGAAGGGCTGGACAGGGCAGCATGGATCACCACCAATGCTCTTGATTACCAACTGTCCAATGGAGATGTGATCATACCCGCCATAATAACTGCTGTGGATGGTGTTTCTAGCAGCTCTGAACAAGAAAGCTTACAAGACTATCCACAGAGAGGA[C/T]AGAACCTGCACATACTTTTGGAAAACAACACAGAGGTCCCCATGCTGGCAAAGCACAAAGATATCCTCCAAAGGTCCATGAACCAATTTGTAGATCCAGGCACTTTAGGTGTTCCAGAGAACCAAACTGGTGCAGTGATGTCCATCTCGCCTCAGGCCACATATTTGTCTAAAATCATTCCGAATGCTGTACTTCCACCATCTGTGGATGTTGTAGAACTCAGTCGCAGCCGAAGTCGGAGCAGTGTCCGAACTGTCAGCAAGAGCAGCCTGGTGTCAGCCAGCCCAGCGTCCACCCGGGCATCCTCTAGAGTCTCTTCACATCGCTCCACTACTCGTACAGACTATTCTGGCTGGAGCAACTCAGGATCATCAGAGACGCTAGTTTCCAATTCCTCTACCATCTCCAGCAGTAGCACTCCCCGTGTGGCCAGCAGAGGGAGTCAGTTTGAACACACAAATGTGGCTGCAAAGCTAAACAATCACAGTTCCCATGTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38961
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084929 | Nonsense | 1123 | 1390 | 7 | 7 |
ENSDART00000133565 | None | None | 221 | None | 5 |
Genomic Location (Zv9):
Chromosome 13 (position 36393667)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 35866236 |
GRCz11 | 13 | 35992068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTAACTGAATCAGAGCCTCAATCAAACCACATTGACCAAACAAGAGTA[G/T]AGCCAACATGCTCATCACCTACTGAACCAAGTACCGCTTCAGCTCCTACT
Long Flanking Sequence:
TCATAGTACCTGCTCCTCCTTCACTACCCGCTGATGAAAGAATTCAGCAAGTAAATATTTCTCCTGCTGCTCCTCCTCCTCTTCCACTATCTACTGATGTAAGAAAGAAGGACAAATTGGAGACCATGGAAGTCGAGAAACGTACAAGCAGTCCCTCTCCAGCCAAAGAGGAATCCTCCAGTCCCATGGTCACTCAGTCTCTCCTGCAGATGGTTCGTCTCAGGTCAGTAAAGTCCAATCAGACTCAGGCAGCAGATCTCGATAAACCATCTCAAGCCAAACCAAAATCTGGTGCCAATCAAGAAGCACCCCCAAAGCCAATTAGACGGTCTTTGATTCTAACATCACTGCCTCCTGATCTGGAATCTCTATCCAGCACAGAACCAAAAACTGAATCTCCATCCAACACTGTACATGCAAACATAACCACCGTAACAAACACTCAGCAAGGAGTAACTGAATCAGAGCCTCAATCAAACCACATTGACCAAACAAGAGTA[G/T]AGCCAACATGCTCATCACCTACTGAACCAAGTACCGCTTCAGCTCCTACTGAATCAGTGGCTACACATCCTATTGCAGAACCACACCTCAAACCTCAAACCCTCAAGGAACAAATCCAGCCTTCAGTACCTGTCACAGAATCCTTGCCAACCAAAACAGTGCCAAAGGACCAATTAGTTAGCAAGCCATTGACTCAACTTCAGCCTCAAGGACTCCCAAAAACCCAGCATAATTCAGATAAACAATCAAGCATCATTGAAATACCTTCAAAGATTAATGTTGAACAGCCAAAAATCCAAACACCAACAACTCTTGCCACTTCCACACCTCCGGTAGGATCTTCAGCAGCTAACCCCTCCATGCGTCTCCAGGATGCAATTCGTCTGAAGGCTGCCGCTATGTCTTCAAAAGACAACCAAGCCAAGCTATTTGGTCTGCGTTCCCCTCCAGCAGCCATTGTAACCAACTCCCCTGCATCTACAGCCAGCTTCATCTTCTCC
Associated Phenotype:
Not determined