ZMP
si:ch211-274p24.5
Ensembl ID:
ZFIN ID:
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 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37364 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43702 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa45746 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43703 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39343 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37364
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 |
|---|---|---|---|---|---|
| ENSDART00000085453 | Nonsense | 233 | 1658 | 1 | 26 |
| ENSDART00000140940 | None | None | 823 | None | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 38196599)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 39316678 |
| GRCz11 | 21 | 39361736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAACAGGACAAAAAGAAACTAAACGAAAGTGGTCCAAACAGTGCAGCA[C/T]AAGCACATCTAGATGCGATAAAGATGCAACCTGCTTATGGCATTCCAACT
Long Flanking Sequence:
TTGTGCTCAGCAGCAACCTTCACATCAGAGGAGACTCAACTGAGGCTTTGGAGCTCTTATTGGCAACAAGCGGGCAAGAGGCCAGCAGAGAAGATGGATTTGATGAAAGCAATCCACGAAATGGAGGAGAAAGAAATAGAGGGCTGGTGGGGCCGCCAAGCACAAACATCACAGGCACAAATCAATCACGCTCCATAGAGGATGAATGGCCTCTTCTGTCATCCCTCTACCAAGCACCTGCTGCTCAAAACCGAATATGCACCCATGGATTAGAAGCAGACACTTGTAAACCTGTCTTTGCTCATGGGACAGACGTTTCTTCCATGTTTGCTGCATCTTCACTAGATGTCTCAAAATGCGATTTTGACATCAGTCAGAGAGAAGATGGCACGACTCAAACAGAGCAGTACAATGAACTCAAAACCCCAAAGGAGCAATTACACGCCGAGAAGAAACAGGACAAAAAGAAACTAAACGAAAGTGGTCCAAACAGTGCAGCA[C/T]AAGCACATCTAGATGCGATAAAGATGCAACCTGCTTATGGCATTCCAACTGAATGGCCTTTGCTTCAAAAGTCGCAAAGGGAAGCACAAACTTCAGAACTCACAGCACAACCTGATGAAAAACTAGACTTCAAAATAGATGCACAGGCTTCTGAGATACTAGAGATGCGAATTATTAAACACGAGCATGCTACTGAGAAGGAAACGTCTCTTGTAGAGCAACCAGACATTGCTGACATGAGCTCTGGGCTGGAGGAGCAAGAGTTTGGGGAGATGAAGCAAAGCCCTTCACAGATAGACCAGGGTTTTGTTTGGAATAAGGAAGTAGAACAGACGCAGTGGGATTTGGAAGTGCTAAAGCAGAGCTCAGGGTTATCACTGCAGCACTCTGAGCAGACAACCCTCGCTGTGACCCAGGTAGAAAGAAAAGAGGATCAGACTGAGCGCTTCACGCTTTTTGTGGTTGATAAACTGTTCCTGGCCACTCCGAACTTTACAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43702
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 |
|---|---|---|---|---|---|
| ENSDART00000085453 | Essential Splice Site | 451 | 1658 | None | 26 |
| ENSDART00000140940 | Essential Splice Site | 47 | 823 | None | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 38200926)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 39321005 |
| GRCz11 | 21 | 39366063 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCACAGTCAAGATCCAGGCTCCTGGAACAGAACCAAGAGACTTCCAGG[T/C]AAAACCCAGGCTTGTCCCTCAGAAAAGCTTTCCACTCTTGAGCTACTGTT
Long Flanking Sequence:
AACAATTGCCACTCACAAAAGTGAAATAATTCATAAGAAATATTCTCATGGCTAAACAGACATATATGTTATCAGATTTAAGTCTGAGTTTGTTGTCATTTATTGGAAAATGATTTCACACTGCTCAGACGTCACACAATCCAACAAACAGATGTTCATTTGGGGGAGTTGGCCTTCATTGTCAACAAAATGTGCAAAAAGTACCATCAAAAATAAGTGATAACAATATTTCCTTTCCTATCATCTAATGCTTACATACAATTAATCTTCATTAACACTAATAAATGTAAACATTGCTAATTCTGTTGTGATTAATATCATTTTCGAATTGAAAATACAAGCCTCCAGCCCTGACACCATGACCAGTGGCAACGTACTAGATGGCCCAGCAGAAGGGACAGCAGAGCAGGTTTCTGCTGTTCCAGACATCGACCCTTGTGAGGATGCAGGATTCACAGTCAAGATCCAGGCTCCTGGAACAGAACCAAGAGACTTCCAGG[T/C]AAAACCCAGGCTTGTCCCTCAGAAAAGCTTTCCACTCTTGAGCTACTGTTAGTTAACTCTTGGAAGCAGAGTAGTAATTAACACTTCCAACCAATTTTGCTCCATATAGTTTTACACTCATATGCTTCCATATCTGTGTCTGTATGTCTATATTGTGTTCAAGGTGTCACCTTTAGCTACGGTGCAGGAAATTAAGCAAGTATTGATGGACCAAGAGGAGACCAGTCGGCGCACATGCTTTTCCCTGCAGCTGAATGGAGTCACTCTCGACAACTTTACCCATCTTAGATCCATACCAGATCTTCAGGAGGGCTCCGTTCTGAGTGTTGTTGAGGGTAAGACACTAAAACCTACCCAACCTCAAATCTGAGGGATTTATTTTATTGCCCCAGGAGTTCATAGTTTTGTTAGTCTACCCCAAAATGATAATTTCCTCCTAATTTAGTTACTGAAGTGGTTCTTGAGCCTAGTTTATACTTCTGCGTCAAGTGACCGGCGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45746
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 |
|---|---|---|---|---|---|
| ENSDART00000085453 | Nonsense | 617 | 1658 | 6 | 26 |
| ENSDART00000140940 | Nonsense | 213 | 823 | 5 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 38207568)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 39327647 |
| GRCz11 | 21 | 39372705 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCAGAGTGCTTGAAGGTTTTGGCCTCGAGTAGCTGGAATCCTCCGCCT[G/T]GAAACAGAAAGATGCACGGAGACCTGATGTATCTGAACGTGGTCACTATG
Long Flanking Sequence:
CGCACTTTTACAGTTGTGTAGAGAAACTTTTAAGTGGATGATGTAATGTCTAGAAGTCTGGTGATGATGACCTCTGCTGGCCAGAAAGGGGAATGACTAAGACCGAGTCGGTGACAGGTTAAAGAAATAATGATTAGCTCCTGTGATAATTTATCCGTTTTAAATATTTCCCAATTGATGTTTAACAGAGCAAAAAAAATTTCACAGTATTTCCTATATTTTTCTTCTGGAGAAAGTCTTATTTGATTTATTTCCGCTAGAATAAAAGCATTTTTTAAAATATTTTAAACAATTTTAAGGTCAGTATTATTAAGCTATATTTTTTGATTGTCTACAGAACAAAAGTCTTTCAGTTAAATAGAAATAGGGAAAAAATATATAGAGGGGGATAATAATTCAGGAGGGCTAATAAATCTGACTTCAACTGTACTTGTTCATGTTTTAAACAGTCGTCAGAGTGCTTGAAGGTTTTGGCCTCGAGTAGCTGGAATCCTCCGCCT[G/T]GAAACAGAAAGATGCACGGAGACCTGATGTATCTGAACGTGGTCACTATGGAGGACAGACACTTCAGTATAACAGCATCCACCCGTGGCTTCTTCATCAATCAGTGAGTTATGAATAGGCCCACACGGAATCTGCGCGCGCAGAATTTTGCAGATTTTCCGCAGAATTCCGCAGATTTTTAGCCCATTATTAGTTCTGTTTATTTACTTGAGTAAAATGTGTAAATCTCAATTTATTCAGTTTTTATTCAGTAATTTATAACTTTTTATTTAATATATTAAGGTTTAAGTTATGATACTTGCTGGATACTCCTAAAATAATTCCGCAGAAATCCGCAGATTTTTACCAAAAACGACGGCAGATTCCGTCTGGCCCTGGTTATGAAGTACAGTTGTCCTCCTTGTTGAACTCGAATGTATAGAAATGTATTTTTAAAAGCGTTTTAGATTATTTAAACGGCACTATTTAAACTTATAATATTAAGAATGGTCCGGAGCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43703
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 |
|---|---|---|---|---|---|
| ENSDART00000085453 | Nonsense | 769 | 1658 | 9 | 26 |
| ENSDART00000140940 | Nonsense | 365 | 823 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 38210773)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 39330852 |
| GRCz11 | 21 | 39375910 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACAAGGGAGCTTCCAAGAAAAAACGTAACAGACCGCCTGATAAGGGAT[C/T]GAGCCATTTTCAAGGTATCCTTAAACTCTTGACATGTTTAATTTACAAAA
Long Flanking Sequence:
CCACCGTTCCCTCGTGGCTGTCGGCAACATGCCTCAACCACCGCTCTCGGCTGCTTCACGAAGCAGATCTCACTTAGCTAAACTAAGCTGTGATTGATTCATGGATTCATTCATTGATGGATTGAGTGATTGGGCATTTATGTTTTATATTAAAATGTAATGTAGAATCTGCAGTAAGTTGTGTGTGTGTTCTCTTTAGAGGGTCTACTCACCCCTTCGAAAGGATTGCGACACCGTTCCAGGTGTTCAGCTGGACCGCTCCAGCTCTGGATCATACACTGGACTGTGTCCGAGCAGAGGATGTCAGCTCTTTCCGCCTGGGTTACGAAGAACACCTGCCTGTTCAGGTAAACATGTTGAATGTCTGAACAGCAGCCAGTTACACAAGCAGGACTTTACTTATTTCTCTGTGTTAAACAAAGGCCCGGGACTGGAACGAAGAACTTCAGACCACAAGGGAGCTTCCAAGAAAAAACGTAACAGACCGCCTGATAAGGGAT[C/T]GAGCCATTTTCAAGGTATCCTTAAACTCTTGACATGTTTAATTTACAAAAAAAAAGTATTTCTACAGATAAATAAGTAATGTGTGTGGCACTTTGGATAAAAGCATCTGCTAATTGTGAAAACCTAAAAATACATCTCAAAATGTTTAAGCAAAGTTTGTTTGGTACTCATTTGAGAAGTTTAAAATGAACAAAATAAGCTTTCCAATTCATACCATGGCCGAACCCATGGGAAGACCGAAGGTGCATAGCATTACAGGCCCTGCACTGTTCTCATGGCTCTCTCCTTTATGACATTCATTTTAATATCCTAATAATTTATTCAGTCATTTCAATCAAAAGTTCTGATTTATTTAAAAAAATAAAAATACACCTCAAATTTACCCACACAGTGTTGAGTCTTGTTCCCCTATAACATCTCTAGCGTTTTCCTTGCCTTGTCCTTCTGTCATTTGTTATTTTTTTAAGATTTATTTTTGGCCATTTTGCCAAAGTTTTTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39343
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085453 | Nonsense | 1120 | 1658 | 13 | 26 |
| ENSDART00000140940 | Nonsense | 716 | 823 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 21 (position 38221837)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 39341916 |
| GRCz11 | 21 | 39386974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAACAGAAACAGCAGTTAAAGGATGCAGCGAGTTTCCTCATTTCCTA[T/G]CAGATCCCTGCATTTGTAAGTATGGGGATTTCAGAAATGTGACAGATGAT
Long Flanking Sequence:
AAGACAATATAAAAGTAAACAACAAAGAAAAGATACAAAATAAACACAAAGAAAAAAAAACACACACATCAAAGTCACAAAACATACAATCAAAACTAGTGAGGGTGTATAGCTTAAACCTCAGAGGGGTCACTGGATTGCTGTGTAAATAAATTAAATAAATTAAGAAATTGACCCCAAATCCCATCTTTAAAACGTTTTCATTCTAATATGTCAGATAAATGAATTAAATAAATAAACCAACCAATTATAAATAAATCAGTAATTCAAATCAATTTTGAAAATGACTAGTGTTAGAAATGTATGCAAATTAACGCATGGTTCATAAAAAATGCCTGATTTGCATATTCTAACAAACTTTGAATTGTGGTCAGTACTTTTCACCTTATTCACCAACAGTGTCTTGTCTTAACAGGTGTACGTTTTCCCAAGGAAAGTACTGAAGAAATCCAGAAACAGAAACAGCAGTTAAAGGATGCAGCGAGTTTCCTCATTTCCTA[T/G]CAGATCCCTGCATTTGTAAGTATGGGGATTTCAGAAATGTGACAGATGATGATCTCCTGATGCCTGTTGTGCAGAATCACATCTTTGACTGTGTGTGTTTGTAGATGAAGAATTGTCTTGAGCACACATCGATGCCCACAGATGGTGTGACGCTGACAGAGGCTCTGCATCAGCATGGCATCAACATCCGCTATCTGGGCACCGTGCTGGAGTACATTGAGGAGATCCCGCTGAAAGAAAGACTCGATCATGTCTATGTAAGTGTGTGCTTTGTTCAAGCCTGAAGTCACACTGTAAAACCTCATATGTTAAGATTACTGTTAAGAAAAAACATTTGAGTAAACAAACTCATTTACTCTCCAAAGTTAATAGAACTTAATTTGATTTTGTACTGTCATACAGTTTGTGTAAAACAACTGGCACCTGTGGTTAAACCCATTTTATGTAATTAATTGCAGTGTTGGGTTTTGCAGTGCAGCTATACCTGTACACAGTCACAC
Associated Phenotype:
Not determined