ZMP
si:dkey-3b8.4
Ensembl ID:
ZFIN IDs:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A8DZ53]
Human Orthologue:
KIAA1377
Human Description:
KIAA1377 [Source:HGNC Symbol;Acc:29264]
Mouse Orthologue:
AK129341
Mouse Description:
cDNA sequence AK129341 Gene [Source:MGI Symbol;Acc:MGI:2680221]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29070 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa29069 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36699 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43154 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29070
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 |
---|---|---|---|---|---|
ENSDART00000098911 | Nonsense | 46 | 1084 | 2 | 12 |
ENSDART00000132315 | Nonsense | 23 | 1060 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 35747003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 37426159 |
GRCz11 | 18 | 37407167 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAAACTGAAGATGAAAGGGAAGTGCTGTTACAGGAGCAGAGGTACTG[T/A]CGGGCTCGGGCTCGAAAGCTTTCTCTGGAAACTAATCGCAGAAGAAAGTA
Long Flanking Sequence:
TTGGATAAATTAAGTATCATACCAAAAGGACGTCATAAAGTCAGAGGTAGTACATGTTACCTGTTTGACGTTCCACCGGCTTTCTAGTCTTTACCTTGTTGTCATTCTTCAGTATTTTCCTTTTGAAACCTTTTGTTCCAGCTATGTTATTGCGCGATAAGATACAGTTTTGGCTATATGGATGAGATATTCGTTGTGTGGAGACCTGATATTTGGGATGTCAGTCATGGAGGACACACTTTATTACTCGTATCCTTTTTTGTGTATGAATTATATGTGGATATTGTAGTCTATTCAGCTGTAATTTACTGTAGCAAAACAACTGGCTTAGTTGATTATTTGTACAGATTTTTTTATGACTAACACTAAACAAACAAAGCACACATTATATATATATAGGAAGTACCTTCCTTAACTTTGCATCACATTAGCATCAGATCAGGTGTATATGGAGAAACTGAAGATGAAAGGGAAGTGCTGTTACAGGAGCAGAGGTACTG[T/A]CGGGCTCGGGCTCGAAAGCTTTCTCTGGAAACTAATCGCAGAAGAAAGTAAGTGTGACAAAAATGTATCTGATTTTATGTTGATTTCATTACTGCATGGGATTTTGGCTCATTTTATGGGTGGCTGATGAATTTACATCAAAGTGTATTTTATGTAAATTACATTATATTATTATATAAATTTGGTGTCAAAACATTTATCACTAAGTTAAGCAATTGCTGGAAAATTTCCACTAACTAATTTTTAAAACATTGTAGTGCAAAAATTAAAATAGCATTTTCATTAAAAATGTGCTCAATCTATTTATCTGTAAACATTTTTGTTTGTTTTTTTTTTACATTTGTGCACAATGTATGTAAACTTCAACACAAACATATTATTTTAGTTTTATTAAAAAATCTCCGGACTCATCTTTGTCAGTTAAAAGTAAATTTTCATAAAGATTTACATTTACAAAAATAACAAACATTTGCAATAGTACATTTATATGTATGTCTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29069
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 |
---|---|---|---|---|---|
ENSDART00000098911 | Essential Splice Site | 149 | 1084 | None | 12 |
ENSDART00000132315 | Essential Splice Site | 125 | 1060 | None | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 35739771)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 37418927 |
GRCz11 | 18 | 37399935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATATACTCATCCATCTCAATTTTGGTCTGGTGCCTCCCCTGTTAGCAGG[T/C]ACGACATTACTGCCATCACAATATATCATAACGGGCAGAACTATTATAGT
Long Flanking Sequence:
TAAATAGAGAGTATTTCTTTGATTTTTGAGTAAACTATCCCTTTAATAAGCTGATATATTGGCATGCATGTAAACCGTCTGGCTGTTTTTCTATTTTCAGGGCTCTAGATGAGAAAAGAAAACAGTGGGATGTTCAGGAGCAGAGACTAAGGGAGAATATTCTACAACAGCGCCATCAGCAGGTCCAGGAGGCCACAGAGAACTTCCAAAGAGCTCATCTCCCGCCTTCCCAAAGGAAAAGACCCGGTATGTTCAGTGAAAAGTCAGGTGAACACTAATCCATGTGTTTACATGCACTGTGTTAGTAGTACTATAAGGTCAGTGTGTGTGTTGTAAACAGTCCGTCTGCCATAAACAGTAAATAGGGTGATTTGTGTTCTGCAGCAGCCTTTAAGAGAAGAACACCCAACCTTGACGAAGCACTTCATCATATTCAAGGCAGTCCACTCTTATATACTCATCCATCTCAATTTTGGTCTGGTGCCTCCCCTGTTAGCAGG[T/C]ACGACATTACTGCCATCACAATATATCATAACGGGCAGAACTATTATAGTCAGCTATTACTAAAACATAAAACTAAAGCCCTTTTATTACATCAAATAAAGTAAATGTTAACTGATATGAAACATTAAAAGCATTTAGCCTATTTTATTGCTGCTACAGAATTTTCAGTGTACATTAAAGGTTCTAATTTAACTTGATAGATTTAAATAACTACTGTAAAAATGGATTCTATTTTAAAATGGTAACACTTATTTTATTCTATAAAGATCATATTTCTTCACAATAAAAAAAAACATTCACACATAAAGAATTTATTTTTCTGAAAGGGATATTTGGCCAGAATAACAAAACTTTTAAGTAGTTTCACCAAATATTGCTTTCTTTATTCTTCTTAAGTTAAAACATTAAAATTTGCTTATCTAAAAAATGTATATACAGTGCTCAGCATATATATAACAACACCCCTCACAAATCTATCTTTTAAATTCATATTTTAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36699
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 |
---|---|---|---|---|---|
ENSDART00000098911 | Nonsense | 636 | 1084 | 6 | 12 |
ENSDART00000132315 | Nonsense | 612 | 1060 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 35731174)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 37410330 |
GRCz11 | 18 | 37391338 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGGCGACCCCAACAGACATGCTAACCTGCCTCAACAAACCCATAAA[C/T]AGCTTTCTGCAGATCACTCGGACCATGTGAATTTACTCACAGGGGTATCA
Long Flanking Sequence:
GTTCTTTACAGTTGCAAAAACACAAACCATATGTAGATGAAGCCCCCAGGCTCAAAGCAGAATCCAAACCACTGTGCATAGAGGAAGCTATAGGCATAGATCCTAAAAATGAAACGGATGTCACCAAATTGGCAAAAGCCGGAATGTTGAAGTCTTCCACAGGCACAGAGGAACCTAACAGAACACCTGCAGACCCCGTGACCCATTGTGCGCCAAACAACGTCAGATTCTTGAAAGGAATTCTTAAAAACCATTTAAAATCCAAATCCGCAAACGTCAAATTCACGTACACCCCTAGCCATTTGCTTTTCACCAAGGAAGTGGCCATTTTAATCCGGGACAGCGTAGAGCTGGCAAGGGCAAAACTCAATGAGCCTGAGAAAAAACGAAATATTAAGAAGAAACTGCGTTGGTTTGATGAAGTACATAGAGTTGAGGGGGAGGAACGAGTGTTTGGCGACCCCAACAGACATGCTAACCTGCCTCAACAAACCCATAAA[C/T]AGCTTTCTGCAGATCACTCGGACCATGTGAATTTACTCACAGGGGTATCAAAGAACATCTCCAGTAAGACCTCTGCTGTCCCTGCTGGGCCCCAATCCACTAGACATGCCTGGGCAGATGTAGGGCCCCAAGAAAGCCGTGCACAGGAGCATATCAAGGAGCCCACCTCTCAAAAAAGATCCCTCTGCATTGGGGGCCCAAGGACTCCCCGGAGAGTGCGCTCAGCCAGAGTCTCCTCGTGTCCCGTTACCTCCCGGGCCAGGAAGGGCACTATCATCAGGCCCCAATCTGCCAGAGAAGCACAACATGTGGCCAAGACCCAAGGGAAAAGCTTGGTACCTCGCCCCCCTCCAAAACCTGAAGTGGCGGAGGTTGACCTAGCTGAGTGTCCCGTGTACATTTCCAAGGCCGATGAAGGTGTACAGACAATGTACAAAGATGCTCCAGATCTCCAGAATGTAGTTTCTCCGCCTGTCCTCAGAACAGATGGTATCTGTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43154
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 |
---|---|---|---|---|---|
ENSDART00000098911 | Essential Splice Site | 916 | 1084 | 7 | 12 |
ENSDART00000132315 | Essential Splice Site | 892 | 1060 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 35728378)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 37407534 |
GRCz11 | 18 | 37388542 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCAAAGGATCCTCAAGAATGGGGGGCTTTTTCTTGTCTTCCTCTAATG[G/A]TAAGGCTCTATAGGTTTATTTAATTAATGATGTCAAAGGGCATTCAGTGT
Long Flanking Sequence:
AGTTCAGCAGCTTTGTTTGAGCTATTAGAGGGATATTTTTCTAGAGTTTTTGGAATAGTGTTTTTTGGTGTTGGATCAATAGAGTGTGTTTTCTTTGGCCCTCAGCTCAGCGCTGCACCACTTGGGATTACTACTTGGTTGAAATTGATCCATTTAATGATGGACTGTTGCTCCTCAGGGGTCAATTATTTTTTTATAACATCAGGAAAAGTCGTTGTTTTGTCGACATAGACCTCAAGAACAGGAGAAGTGGCTTTCATACTTCGGGACCTTTAAGTTGAACTGTCTTCTTTCTTTTTTTGTCTTTTTTGTGTTCCTCTCTCTCTCCTTCTGAATTGATTTAGGTGACCCTCAAAGTTTTCTGGCTCACAATGGCCCGTTGTCTCCTTCGCCTCAAGTCTGTGCCAGTCTGTCCCATGTTACCATCAATGGTGATAGTCTGATCAATGGTGTCAAAGGATCCTCAAGAATGGGGGGCTTTTTCTTGTCTTCCTCTAATG[G/A]TAAGGCTCTATAGGTTTATTTAATTAATGATGTCAAAGGGCATTCAGTGTCCAAAAAGCTAGGTCATTTCCACCTGCCAGCTCATAATGTGATCAAATTGCTTATTGTTTCACTAGAGTTGTTTAAATTCACTTAAAGGAACAGTTGACCCAAAACAGAAAAGTCTGTCATCATTTACTCACCCTTCACTTGTCCCAAACCTGAGTGACTTTTTTTTCTGTTGAGCACAAAAGAAATAAATATTTTAAAGAAAGCTAGAAATTGGCAACCATTGACTTCAATAGTGTTGTTGTTTTTTTTTACTATGGATGTCAATGGTTTTTCAGCTTCAAAATAACTTCATTTTTGTTCAACTAATTAAAGAAACTTTGGGTTCTCTTGATGGTGAGTACATTTTCATTTTTGGGCGAGCTATCCTTTTAAATCCACAGAGCTTACTTATGTCCGTACCTCAAGAGGTTAAGCTTTAGATACTCTGGTGTAATAGCCTATCTTTGAGA
Associated Phenotype:
Not determined