ZMP
zgc:66014
Ensembl ID:
ZFIN ID:
Description:
LisH domain and HEAT repeat-containing protein KIAA1468 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6P
Human Orthologue:
KIAA1468
Human Description:
KIAA1468 [Source:HGNC Symbol;Acc:29289]
Mouse Orthologue:
2310035C23Rik
Mouse Description:
RIKEN cDNA 2310035C23 gene Gene [Source:MGI Symbol;Acc:MGI:1922832]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa609 | Nonsense | F2 line generated | Not yet available |
sa24473 | Nonsense | Available for shipment | Available now |
sa37861 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15052 | Nonsense | Available for shipment | Available now |
sa30746 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13951 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa609
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 |
---|---|---|---|---|---|
ENSDART00000055446 | Nonsense | 246 | 1189 | 5 | 29 |
Genomic Location (Zv9):
Chromosome 24 (position 19175028)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18481504 |
GRCz11 | 24 | 18625923 |
KASP Assay ID:
554-0519.1 (used for ordering genotyping assays)
KASP Sequence:
AAGAGAGCCTTAAATTTTTTAGTTAATGAATATTTATTGAAAAACGAATA[C/A]AAGTTAACGTCCATCACATTCTCCGATGAAAACGATGATCAGGTAAACTG
Long Flanking Sequence:
TGCCTATTTGTGTGTGACCCACTTCCCCCTGGTCCAGTTCTGGAGTTTGAACTGCGGAAAGCCAAGGAGACCATTCAGGCTCTTCGTGCCAACTTGACTCAGGCTGCAGGTGGCGTACTTTCATCTTTTACACACTTCAGTCCTTTCTGCCATAGGAGCTGCTCTCATTCCTGAAGGCAGTTTTGTAATGTTGATCGTAAATCAAATTTCAGCTCACTCGTTTTTTCTTTCTCTCTGTTTCTTCTTTCTCTGTAGAATGCGAGATTGCCTCTCAAGAGAGAAAGAATTACAAATCCAGTCCTGAAACCCAGGTTACCGTCATTGTTACAATTGTATTATAAACTTCAACAAACTAATAGTGAACAACTAGTTCGGAGCACAGAGCATTTACTTCATTTTTCATTTCTCCAATATTGTTTTTTCCCCCAGGAGCCTATTCGCCCCCTTGAAAAGAGAGCCTTAAATTTTTTAGTTAATGAATATTTATTGAAAAACGAATA[C/A]AAGTTAACGTCCATCACATTCTCCGATGAAAACGATGATCAGGTAAACTGCTATGCTATTATAATATGCTTTTATTTGGTTGCTTTATGCACTGTAGTGTTTTGTTGTATGTTATTTATCATTTTTGTTCCTGCAGGATTTCGAGTTGTGGGACGACGTTGGTTTAAACATTCCCAAACCTCCAGATCTGCTGCAGCTCTACAGAAACTGTGGGAACAGTCAGCCGTTGCACCGTGACAACGTAGATGTGGCGGTCAGTGTTGACCCGAGTGACTTGCCAGGAGACTATTTCACCCAGGAGCCTGTGCAGCAAACTGATGTCATACAGGTACATTTCCGAGTTAATCAATTAGTTAATTCTTTAAACACAAAGAGGTGATTCTGAAATGCCTGAAAAGAGTCTTCTAGTCTTTTTGCACAAACTTACACAGATTAAATGAAATTTGCATAATGTCAGTGTGAGGCCCTCAAATAATTTGTACCTCTGGTCTAAAAGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24473
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 |
---|---|---|---|---|---|
ENSDART00000055446 | Nonsense | 444 | 1189 | 8 | 29 |
Genomic Location (Zv9):
Chromosome 24 (position 19167433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18473909 |
GRCz11 | 24 | 18618328 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCACTACTGCTACACAACCTCACAGCAAACTGAAGGCCAATGGTCAG[C/T]AGAGTAAAAGCTCTGTCCAGTTTGACCAGCCCAACAGGTGAGACCTGCTT
Long Flanking Sequence:
CCCTTCTAGCTCAGCAGACTCTCATCATTGTGACCTTCTGCTCTCTGACATTTTTCAGCTTGGCATTTACACTTCCTAGCAAGAGATGAGCTCTACATATCTCTGTAACTAGTTTGCCTCCCGTCATATTTTATCCTCCTCATCTCGCACTGTTCTGTCCTGTATATTTCCTTCCTACATTTTCATTTTACTGCATTCTGTGGATTGGTAGATAAAAATGTCCCCAATGTGTGTGTTTGTGCAGTGATATTCAGGCACTTCAGAGAAATGTTTCATCAGAACCCACGGCTGGAGTGAAGTCAACTCCGTCTAAAGAAAACCCTAAATGTGATAAGCCCCCACTTGACAATGGACAGTATTTGGACATACGAGGGGTCACAGAAACGGACAGCTCTTCAGACACTACTAAAACCTCAACCTCTACCACTATTGCTACTGACTGCACTGAAAACTCCACTACTGCTACACAACCTCACAGCAAACTGAAGGCCAATGGTCAG[C/T]AGAGTAAAAGCTCTGTCCAGTTTGACCAGCCCAACAGGTGAGACCTGCTTTTTCTCTTTCTGGTAGACACCATTATGACTTGAGACATACAGGGATAAATAAAGGCGAAGCACACTGAATGTATTTAGAAGATGCTGAAATAGTGTTTTCTTGTAAATATATTCTTCTATTGTACTATATCTTAATGGATACAACCAATCAAAGATTTCTGTCAATATTATTCATTTATTTATAAAAAAAAGAAAAAAAGTTTGGAAAGTTATGGAAAGTACATGTGATATGTAATGGGGCACTGTAAAATAGTGTTAAGAGATTAAAACTTAATATTAGATTATCATAAATACTGTATCATATAACATATTAAACTAAAACAATGACTGTTCCTAAAATTGAATGGTAACTTGCTGCACAGCATTTTTGAGTCAACTCAACTTAAATCGAGTCAATTACGGTACTTGGGTTAAAAGTTGAGTCAACTCAATGTTAACTGTTGACTAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37861
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 |
---|---|---|---|---|---|
ENSDART00000055446 | Nonsense | 471 | 1189 | 9 | 29 |
Genomic Location (Zv9):
Chromosome 24 (position 19164648)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18471124 |
GRCz11 | 24 | 18615543 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGCAGAAAGCTGTCTCCGGCCTTCCACCAAGCACTTTTGTCCTTCTGT[C/T]GAATGTCTGCTGACAGCAGGCTGGGCTCAGAGGTGAGTGGGATCAGATTG
Long Flanking Sequence:
TGTTTATGAGCACTTATAAAGTAAGATCTTATTTTACATCCCTAATCCTACCCAACACCCAAACTAAATCTTACTAACTATAAATAAACAGCTTATTAGTAGTTTGAGCTAAAAATCTTAACTAATGGTCGTTGTTAATTGTGTAAATTGTACATTTAAAACAGTGTGAGCAATAAATGTTTTAGCCATTAGATGGCAGCACAGCACCAATCACCCTTTAGAGTGTCACTGCATTGCTGACTGGCACCATATATTCCATTCCTCATCGTTTTGCACATCTGCTCCGGATGGACTTTTGCCCCCTGAGGCCGATTCAGACAAATTACCCTTTCTTTATTTTGACTGTTCCTATATCAGCGTTTTTCCCTGTGCTGTGGAAAGCTGGCTTGATCTGTGGAGTTATTGGTAACCGGAGGTGGAGGTGGCTTGTTAATTCATGTTTTGTTTGCTTGTGCAGAAAGCTGTCTCCGGCCTTCCACCAAGCACTTTTGTCCTTCTGT[C/T]GAATGTCTGCTGACAGCAGGCTGGGCTCAGAGGTGAGTGGGATCAGATTGCAGACAGGTACAAATGCATAAGCACATGTTAAGGGTCTACCTGATGTCAAGCTAGAGGGTATAGTTAAAAAGAGATACGTCTGTTGTTATTTACTTAATCTTATGTTGGTTTAGTCCATTGTGACTTTTAATCAAAATCAGAAGATTTTCCAATTGGTTCCAGTGCAGTTACGCAGAGTAGGGCCCAGAGCTTTTAAGATGAGTTTTTAAGGATGGAAAAAGCACTATTAATGTATCATTAAATAGTCTATATGACTCATGCTCTGAATCTTCTGAAGCTATGCACTCTCAAAAATGAAATGTACAAAAGCTGTCACTGAGGAGTTACAATTATGCTTTTTGGTACTTTTATGAAAACTTTAGATAACAGCATGTAAATTTAAGGTATCAATATGAACCTTCTCACTACAAATTTCTCAACACCTGTTTTGTACCTGTTGTTTCTGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15052
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 |
---|---|---|---|---|---|
ENSDART00000055446 | Nonsense | 637 | 1189 | 14 | 29 |
Genomic Location (Zv9):
Chromosome 24 (position 19114688)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18421164 |
GRCz11 | 24 | 18565583 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTGGCAGATGATAAAGCTGATATGGTCCGAGAGGCTGTGGTRAAAAGTT[T/A]AGGAGTTATAATGGGTTAYATTGATGATCCAGACAAATACTCCCAGGTAT
Long Flanking Sequence:
ATCGCTACTCATAAAAAGACCGGTATTGCTATTAACATGACGTATGCATAATAAGGTACAGTATATGTCAAAAGCATCAGTGCAATATCAGACAGCACCCGCATATATATATATATTGCTTGTTTGTTTGATTACTGTTGATTTCAAATGCAATAAATAAGTTTGTATAAAACTTGTACCGGTGCTTACAATTGGTGGGTGCGACTAAATTTTGGCTGATGCGCCTACATTTTTAAAGTTAGGAGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTGTGTTTATATTTGACATTTGGCTAAAAATGAGACTGCTGATAAATATATACATGTATGTTTGTCTGCAGAAGGAAATCCGAAGCTCCCTGGTTTTGTCTATGCTTCAGCAAATGTTGGCAGATGATAAAGCTGATATGGTCCGAGAGGCTGTGGTGAAAAGTT[T/A]AGGAGTTATAATGGGTTATATTGATGATCCAGACAAATACTCCCAGGTATGTATATGTTTACCCACAATCTGGTGTTCTTTCATTAATAATTTCAGTATTTTCTTATGTGTCTGTGCTTTATTTTATGCATGGCTGTGTAACAGGGCTTTGAGCTGATGCTGTTGTCTCTGGGTGACCCATCGGAGCGGGTGGTCAGTGCCACCCACCAAGTGTTCATTCCTGCCTTTGCTGCCTGGTGCACAGAACTGGGCAACTTACAGTCCCAGCTCATTCCTTCCCTCCTCACACGCATCGAGAAGCTCCTCAAGGTGAAAAAACATTAGCTTACAGGATTTTAGCTTTAGTTAAGACTTTTCTTGGCTTGTCTTGGTTGTCTTTTTTAGGATGGATATTTAATATAACTCCAGTGACTATTTTTAGAAATAAAATGTAAGTTTTATATGTAGGTGTTTTTTTATATGTTCGCACAACCATATTTGAATATATAAAGAGTTTGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30746
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 |
---|---|---|---|---|---|
ENSDART00000055446 | Essential Splice Site | 652 | 1189 | 14 | 29 |
Genomic Location (Zv9):
Chromosome 24 (position 19114640)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18421116 |
GRCz11 | 24 | 18565535 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAGGAGTTATAATGGGTTATATTGATGATCCAGACAAATACTCCCAGG[T/C]ATGTATATGTTTACCCACAATCTGGTGTTCTTTCATTAATAATTTCAGTA
Long Flanking Sequence:
TAATAAGGTACAGTATATGTCAAAAGCATCAGTGCAATATCAGACAGCACCCGCATATATATATATATTGCTTGTTTGTTTGATTACTGTTGATTTCAAATGCAATAAATAAGTTTGTATAAAACTTGTACCGGTGCTTACAATTGGTGGGTGCGACTAAATTTTGGCTGATGCGCCTACATTTTTAAAGTTAGGAGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTTGTGTTTATATTTGACATTTGGCTAAAAATGAGACTGCTGATAAATATATACATGTATGTTTGTCTGCAGAAGGAAATCCGAAGCTCCCTGGTTTTGTCTATGCTTCAGCAAATGTTGGCAGATGATAAAGCTGATATGGTCCGAGAGGCTGTGGTGAAAAGTTTAGGAGTTATAATGGGTTATATTGATGATCCAGACAAATACTCCCAGG[T/C]ATGTATATGTTTACCCACAATCTGGTGTTCTTTCATTAATAATTTCAGTATTTTCTTATGTGTCTGTGCTTTATTTTATGCATGGCTGTGTAACAGGGCTTTGAGCTGATGCTGTTGTCTCTGGGTGACCCATCGGAGCGGGTGGTCAGTGCCACCCACCAAGTGTTCATTCCTGCCTTTGCTGCCTGGTGCACAGAACTGGGCAACTTACAGTCCCAGCTCATTCCTTCCCTCCTCACACGCATCGAGAAGCTCCTCAAGGTGAAAAAACATTAGCTTACAGGATTTTAGCTTTAGTTAAGACTTTTCTTGGCTTGTCTTGGTTGTCTTTTTTAGGATGGATATTTAATATAACTCCAGTGACTATTTTTAGAAATAAAATGTAAGTTTTATATGTAGGTGTTTTTTTATATGTTCGCACAACCATATTTGAATATATAAAGAGTTTGATTCCAAAACAATATACAGTAAATAATTTTGGATTCATTTGAGAAAAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13951
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000055446 | Essential Splice Site | 850 | 1189 | 18 | 29 |
Genomic Location (Zv9):
Chromosome 24 (position 19106528)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 18413004 |
GRCz11 | 24 | 18557423 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTTCTGGAGATTATGTCGGACATTTGGGAAAATCTTTACCAACACTAAG[G/A]TACAACTTGCAGGAATCTGTCTCTAKCACCTTTTCTTTTTCTTCATTGGC
Long Flanking Sequence:
AGCGTTGTTGCACTGAAAACATTTTATTTTGTACTTATTCCCTTTTATCTTTTTAGATGTTAGTCTGAATTGAATCGTTCCGTTGGTAATGAGTAAGTCTCGTACCGAACGATTCAATACAAATACACGTATTGTTACACCCTTTTTTATATATATATATATATATATATATATATATATATATATATATATACTGTATGTGTGTGTGCGCTGTTGAAATCAAAAGTTTAAAAGTGCAGAATGCTGTTGCCTTTCTTTTAAGATACAAAAATCTAATCAATGCTGGCTCAAATACGTATGCATATTACAATGTACATTGTTTCCTAAATTTGTTACATATAAATGATCTAGCTTTCTTGCTTTTTGTATACTTCAGTTTACCACAGATAATAGACATTGTCGGCCGCATTAACGTCACCTCCTCCACCTGTGTACACGAGTTTTCCAGATTCTTCTGGAGATTATGTCGGACATTTGGGAAAATCTTTACCAACACTAAG[G/A]TACAACTTGCAGGAATCTGTCTCTAGCACCTTTTCTTTTTCTTCATTGGCCAAGCAGAGTAGCTAAATCGAGCTTGTGCTTCAAATAGTCCATCTCAGTTACATCGTTCAGCAGTTCCACTCTAATTTAGGTGTTGTTTTTCCCTCATTTTTTGAAGGTAAAACCTCAATTCCAAGAAATCCTGCGGCTATCAGAGGAGAATGTGGGTAAGTGACTGTTCAGTTAACCAAAAATAACACTCCTGCTGTCAGAAGAGCGACTGGGAAGAGAAATACACACACACACACACACACACACACACACACACACGCACACACACACGCACACACACACACAAAAGCTCTGTATCTCTTTCCCATGCAGGAGACTTGTGTGTCAAATATGTGTTTTCACTCTTCATGGGATTTGAAAACGGAGCTTTTTCTTTCATACTTTGAATGTTTGTAGAGTTAAAAAAAAGTCTAGGGTTAAAGTATCTGCCAGCAAAACTGGGCATGTTG
Associated Phenotype:
Not determined