ZMP
LOC565752
Ensembl ID:
Human Orthologue:
KIAA1033
Human Description:
KIAA1033 [Source:HGNC Symbol;Acc:29174]
Mouse Orthologue:
A230046K03Rik
Mouse Description:
RIKEN cDNA A230046K03 gene Gene [Source:MGI Symbol;Acc:MGI:2441787]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9419 | Nonsense | Available for shipment | Available now |
sa19367 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38102 | Essential Splice Site | Available for shipment | Available now |
sa38101 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44330 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa9034 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38100 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9419
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 |
---|---|---|---|---|---|
ENSDART00000088315 | Nonsense | 420 | 1173 | 14 | 33 |
ENSDART00000088315 | Nonsense | 420 | 1173 | 14 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 29611995)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28302089 |
GRCz11 | 25 | 28745291 |
KASP Assay ID:
554-6234.1 (used for ordering genotyping assays)
KASP Sequence:
GTCCTACTACATATTTGTAACCTCCTGGATGATGAAGATGGAGTCGATAT[T/A]ATCAAAAGAACCAAAACCAGACAARCTGTCYGAGGATTTGAGCAACAGGT
Long Flanking Sequence:
AGACTCTTACCGCGCGAAAAAAAAAAAAAAAAACGTTAATCTGTTCTCAAAGTTGAGCTGGGTCTGTTCTACGCAAGCTATGATGACTTTCTCCTTGATATTTTAGCGCGCATGTATACCTGACCGGTGAGCCGTCTGACAAAAAAGTGCCCTTCTGAATCCAATCAGCAGGATGCCTGACTTTAACAGCAGTTCAGCAGTTTCACTTTAACTCATGAACATTTCATTCATGCCCCTCTGAAAAACTGGGGTATTAGACGCAAAGAAGGAGTAAGGACTGGTGAGAGTGTTATGGAATATAATAACGCACGCCAAACGGAAAGAAAAAATCTTGTGCATTTTGCGATGTGTGATATATATAAATTTACATATAATTTTTCAAGTGTTTTCATAAGGGATTTATATAGGGCTGATATTATAGCTAGCATTTTCTGTGTGCAGGGACATGCAGTCCTACTACATATTTGTAACCTCCTGGATGATGAAGATGGAGTCGATAT[T/A]ATCAAAAGAACCAAAACCAGACAAGCTGTCCGAGGATTTGAGCAACAGGTGTAATATTTTTGTGCAGGTATTAACTGATATTTGTTCTTCAGTTTTTACTTAATTACATTTCCAGTGCATTTCATAATCAGATGTGTTTGTATTTGAACAGGGAATACTGTATGCTTACAGCATCAGCACTATCATCAAGACCACTATGAACATGTACATGTCCATGCAGAGACCCATGACCAAGACCTCGGTGAAGGCCCTGTGCCGATTGGTCGAACTGTTAAAAGTAGGTTAATGAGTTAATCCTTTAAGTATTTCAAGCAGACTTTTCTTGCATTTTATATAAACTTTTTATAGCATAGTTTACTGTTTGTTAGCTACTAGACAGTTTTTACTGAAGGTCTAGTACAGGCTATTCAATTGGCGGCCCACAGGCCAAATCCGGCCCCCAAGACAATTTGTTCCGGTCCTCCAAAAAAGTGCGACCAAGACATCGAGAATAAATTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19367
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 |
---|---|---|---|---|---|
ENSDART00000088315 | Nonsense | 420 | 1173 | 14 | 33 |
ENSDART00000088315 | Nonsense | 420 | 1173 | 14 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 29611995)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28302089 |
GRCz11 | 25 | 28745291 |
KASP Assay ID:
554-6234.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCCTACTACATATTTGTAACCTCCTGGATGATGAAGATGGAGTCGATAT[T/A]ATCAAAAGAACCAAAACCAGACAAGCTGTCCGAGGATTTGAGCAACAGGT
Long Flanking Sequence:
AGACTCTTACCGCGCGAAAAAAAAAAAAAAAAACGTTAATCTGTTCTCAAAGTTGAGCTGGGTCTGTTCTACGCAAGCTATGATGACTTTCTCCTTGATATTTTAGCGCGCATGTATACCTGACCGGTGAGCCGTCTGACAAAAAAGTGCCCTTCTGAATCCAATCAGCAGGATGCCTGACTTTAACAGCAGTTCAGCAGTTTCACTTTAACTCATGAACATTTCATTCATGCCCCTCTGAAAAACTGGGGTATTAGACGCAAAGAAGGAGTAAGGACTGGTGAGAGTGTTATGGAATATAATAACGCACGCCAAACGGAAAGAAAAAATCTTGTGCATTTTGCGATGTGTGATATATATAAATTTACATATAATTTTTCAAGTGTTTTCATAAGGGATTTATATAGGGCTGATATTATAGCTAGCATTTTCTGTGTGCAGGGACATGCAGTCCTACTACATATTTGTAACCTCCTGGATGATGAAGATGGAGTCGATAT[T/A]ATCAAAAGAACCAAAACCAGACAAGCTGTCCGAGGATTTGAGCAACAGGTGTAATATTTTTGTGCAGGTATTAACTGATATTTGTTCTTCAGTTTTTACTTAATTACATTTCCAGTGCATTTCATAATCAGATGTGTTTGTATTTGAACAGGGAATACTGTATGCTTACAGCATCAGCACTATCATCAAGACCACTATGAACATGTACATGTCCATGCAGAGACCCATGACCAAGACCTCGGTGAAGGCCCTGTGCCGATTGGTCGAACTGTTAAAAGTAGGTTAATGAGTTAATCCTTTAAGTATTTCAAGCAGACTTTTCTTGCATTTTATATAAACTTTTTATAGCATAGTTTACTGTTTGTTAGCTACTAGACAGTTTTTACTGAAGGTCTAGTACAGGCTATTCAATTGGCGGCCCACAGGCCAAATCCGGCCCCCAAGACAATTTGTTCCGGTCCTCCAAAAAAGTGCGACCAAGACATCGAGAATAAATTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38102
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088315 | Essential Splice Site | 596 | 1173 | 18 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 29607185)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28297279 |
GRCz11 | 25 | 28740481 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGCTTGTGCTGAAAAAACTAGACTTAATCAGTGAACTAAGAGAACGG[T/G]AAGTTACATTTACTCAGCTAGCAATGCTATAAGCAACAGCAGATTTTAAT
Long Flanking Sequence:
GGTGTTTTATTAAATGTTTTTTTTGTTTGTGTGTTCTCATTAATTTTATGTTCTGTGCTGTTTTTTGTTGCTTTTTATGTTAAATGCTGTGTTCTGTTTTGTTCTTACCTGTTTCGATTGGTTACGTTCTTTTTTTTTTGTTTAAGTGTTTTTGTTTTTTTATGTCAGGGGGGCCCAAACTAGGTCCTTAAGGACCATTGTCTTGCAAGGTTTAGTTCCAACTCCAATCAGACACTACTGGGCTAGCTAATCAAGCTATAACTAGGCTTTCTAGAATATCCTTGCTGGTGTTTTGAAGCTAGTTGGAGCTTAAATCTGCAGGACATTGGCCCTCCAGGACCAAGTTTTATGTGCTGTACTGTGTGTTTCTGTTTGTTTTTTCCTGTTTTGTTAAATGTTGTTTGTTTGTTTTTACACAGAAAACCTTCAAGGATGAAGAACTCTTGCCTTTACAGCTTGTGCTGAAAAAACTAGACTTAATCAGTGAACTAAGAGAACGG[T/G]AAGTTACATTTACTCAGCTAGCAATGCTATAAGCAACAGCAGATTTTAATTTGGTTTTTACAAGTGCATGATGGGATATGCTTTCTCCTCAGAGTCAAAGTGCAATGCGACTGCAGTTTTCTGTACTGGCATCGTACTGTCTTCCCCATCTACCTGGATGACGTGTATGAAAATGCTGTGGACGCTGCCAGAATTCATGTAAAACAACCTTTCAATAATACTTACTTGATTTTTTAATAACTAAATACTTTATTCATACTTTAATATATTTTCTCTAGTACATGTTCAGTGCGCTCAGAGACTGTGTGCCCACAATGCTACATGCCAAACACATGGAGTCATGTGATCAACTGCTGGAGTGTTATGACACTGAGATCATGGAAATCCTGAATGAGGTTAACAAAATGAAGGCTGTATATATACATATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATTTTACCTGTATATTATAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38101
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088315 | Nonsense | 603 | 1173 | 19 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 29607071)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28297165 |
GRCz11 | 25 | 28740367 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCATGATGGGATATGCTTTCTCCTCAGAGTCAAAGTGCAATGCGACTG[C/A]AGTTTTCTGTACTGGCATCGTACTGTCTTCCCCATCTACCTGGATGACGT
Long Flanking Sequence:
CGATTGGTTACGTTCTTTTTTTTTTGTTTAAGTGTTTTTGTTTTTTTATGTCAGGGGGGCCCAAACTAGGTCCTTAAGGACCATTGTCTTGCAAGGTTTAGTTCCAACTCCAATCAGACACTACTGGGCTAGCTAATCAAGCTATAACTAGGCTTTCTAGAATATCCTTGCTGGTGTTTTGAAGCTAGTTGGAGCTTAAATCTGCAGGACATTGGCCCTCCAGGACCAAGTTTTATGTGCTGTACTGTGTGTTTCTGTTTGTTTTTTCCTGTTTTGTTAAATGTTGTTTGTTTGTTTTTACACAGAAAACCTTCAAGGATGAAGAACTCTTGCCTTTACAGCTTGTGCTGAAAAAACTAGACTTAATCAGTGAACTAAGAGAACGGTAAGTTACATTTACTCAGCTAGCAATGCTATAAGCAACAGCAGATTTTAATTTGGTTTTTACAAGTGCATGATGGGATATGCTTTCTCCTCAGAGTCAAAGTGCAATGCGACTG[C/A]AGTTTTCTGTACTGGCATCGTACTGTCTTCCCCATCTACCTGGATGACGTGTATGAAAATGCTGTGGACGCTGCCAGAATTCATGTAAAACAACCTTTCAATAATACTTACTTGATTTTTTAATAACTAAATACTTTATTCATACTTTAATATATTTTCTCTAGTACATGTTCAGTGCGCTCAGAGACTGTGTGCCCACAATGCTACATGCCAAACACATGGAGTCATGTGATCAACTGCTGGAGTGTTATGACACTGAGATCATGGAAATCCTGAATGAGGTTAACAAAATGAAGGCTGTATATATACATATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATTTTACCTGTATATTATACATGTATATATATATATTTTGCAATTAAATTAAATATAAATTGTAGTTTTCTGGTCTTTAGCACCTGCTAGATAAGCTGTGTAAAGAGATTGAGAAGGATCTGCGATTATCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44330
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 |
---|---|---|---|---|---|
ENSDART00000088315 | Nonsense | 660 | 1173 | 20 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 29606820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28296914 |
GRCz11 | 25 | 28740116 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTACATGCCAAACACATGGAGTCATGTGATCAACTGCTGGAGTGTTA[T/A]GACACTGAGATCATGGAAATCCTGAATGAGGTTAACAAAATGAAGGCTGT
Long Flanking Sequence:
TTTCTGTTTGTTTTTTCCTGTTTTGTTAAATGTTGTTTGTTTGTTTTTACACAGAAAACCTTCAAGGATGAAGAACTCTTGCCTTTACAGCTTGTGCTGAAAAAACTAGACTTAATCAGTGAACTAAGAGAACGGTAAGTTACATTTACTCAGCTAGCAATGCTATAAGCAACAGCAGATTTTAATTTGGTTTTTACAAGTGCATGATGGGATATGCTTTCTCCTCAGAGTCAAAGTGCAATGCGACTGCAGTTTTCTGTACTGGCATCGTACTGTCTTCCCCATCTACCTGGATGACGTGTATGAAAATGCTGTGGACGCTGCCAGAATTCATGTAAAACAACCTTTCAATAATACTTACTTGATTTTTTAATAACTAAATACTTTATTCATACTTTAATATATTTTCTCTAGTACATGTTCAGTGCGCTCAGAGACTGTGTGCCCACAATGCTACATGCCAAACACATGGAGTCATGTGATCAACTGCTGGAGTGTTA[T/A]GACACTGAGATCATGGAAATCCTGAATGAGGTTAACAAAATGAAGGCTGTATATATACATATTTTATATATATATATATATATATATATATATATATATATATATATATATATATATTTTACCTGTATATTATACATGTATATATATATATTTTGCAATTAAATTAAATATAAATTGTAGTTTTCTGGTCTTTAGCACCTGCTAGATAAGCTGTGTAAAGAGATTGAGAAGGATCTGCGATTATCTGTGCACACACACCTCAAACTGGACGACCGAAACCCTTTCAAAGTGGGCATGAAGGATCTGGCTCACTTTTTCTCTCTCAAGCCCATTCGCTTCTTCAACCGTTTCATCGACATCAAAGGTAGGGCACATGAAACACCCTTAGTAAATAATGAATATTTTAATAGGAACATATTATCAGATGTCGGCTGTTCGTCTTTGAAATTCCCTTTTAAAATGAGTGTGCAAAATTTGTTGCAAATGTTTCAATTTGCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9034
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 |
---|---|---|---|---|---|
ENSDART00000088315 | Nonsense | 879 | 1173 | 25 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 29600205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28290299 |
GRCz11 | 25 | 28733501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAATCCAGAYTCATCAAAGACATCCGATTCTTCAGGGAAACCAAGGAT[C/T]AAACCGACCAAAAGGTAGGTTGGTCTCCATTTGCGTCTTATTATTTGGTA
Long Flanking Sequence:
CTCCCGCTGGCCTGCAGATACCCACACTAGTGGATACTGCTCTCTCATTGGCTGTAGGTGATCGCCGATGTTATTTTCAATCAGATCACAATTCACACGGCATGATTTTAATAGCCAACAGGTCCAAATATTTAGCATGCCAAATATCTAAAGGGTGTCTGTGACTTATCTGCGATTCTCTCAGATTGTGTCATTGATAGTTCAGGCTGTGTAATTGTTACTCAGGTGAACGAGCACCGATTTGCCTGTGATTTCAGGCATTTGTCTGCGATTTCTCAAAATCTGTCGGCGAGGCAAAATCGGGGCTAAAATCATGCCGTCTGAACTTGACATTACTTAAAGTCTTTGTCCTGTCTAAAACCATGTTTATATCTCCTCAGGTGAACTTCACGTATCAGTTCCTCCGCAAGAAGTTCTACATTTTCAGTCAGTTCATGTACGACGAGCACATCAAATCCAGACTCATCAAAGACATCCGATTCTTCAGGGAAACCAAGGAT[C/T]AAACCGACCAAAAGGTAGGTTGGTCTCCATTTGCGTCTTATTATTTGGTAAAGTGCTATTCATTTATTTTGACATGCGTGCTGTGTTTAGTACCCATTTGAGCGAGCAGAAAAGTTCAACCGCGGTATCAGGAAGTTGGGTCTTACTCCAGATGGTCAGAGCTACCTGGACCAGTTCAGACAGCTCATCAGTCAGATCGGTAAGAGGCTTTCAAACACATCTAGTAATCTTTCCTTTTGTCTTACTGTTAACTTTATGTTGGGTTGGTTTAAGGAACACTCCACAAAAAAAATCTTTTTCTCAAGTCCCTTATAGTTAAACTGTTGAGTTTTACCATTTTTCGAATCCATTCAGTCGATCTCCAGGTCTGTCGAGAGCACTTTTAGCTTAGCTTAGCATACATTATTGAATCAGATTAGATCATTAGCATCTCCTTCATAAGTCCTTAGATTTTTCCTTTTAAAAAGCTTTACGCTTCTGTAGTGACATGGTGTATTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38100
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 |
---|---|---|---|---|---|
ENSDART00000088315 | Nonsense | 888 | 1173 | 26 | 33 |
Genomic Location (Zv9):
Chromosome 25 (position 29600102)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 28290196 |
GRCz11 | 25 | 28733398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTATTCATTTATTTTGACATGCGTGCTGTGTTTAGTACCCATTTGAG[C/T]GAGCAGAAAAGTTCAACCGCGGTATCAGGAAGTTGGGTCTTACTCCAGAT
Long Flanking Sequence:
GATTTTAATAGCCAACAGGTCCAAATATTTAGCATGCCAAATATCTAAAGGGTGTCTGTGACTTATCTGCGATTCTCTCAGATTGTGTCATTGATAGTTCAGGCTGTGTAATTGTTACTCAGGTGAACGAGCACCGATTTGCCTGTGATTTCAGGCATTTGTCTGCGATTTCTCAAAATCTGTCGGCGAGGCAAAATCGGGGCTAAAATCATGCCGTCTGAACTTGACATTACTTAAAGTCTTTGTCCTGTCTAAAACCATGTTTATATCTCCTCAGGTGAACTTCACGTATCAGTTCCTCCGCAAGAAGTTCTACATTTTCAGTCAGTTCATGTACGACGAGCACATCAAATCCAGACTCATCAAAGACATCCGATTCTTCAGGGAAACCAAGGATCAAACCGACCAAAAGGTAGGTTGGTCTCCATTTGCGTCTTATTATTTGGTAAAGTGCTATTCATTTATTTTGACATGCGTGCTGTGTTTAGTACCCATTTGAG[C/T]GAGCAGAAAAGTTCAACCGCGGTATCAGGAAGTTGGGTCTTACTCCAGATGGTCAGAGCTACCTGGACCAGTTCAGACAGCTCATCAGTCAGATCGGTAAGAGGCTTTCAAACACATCTAGTAATCTTTCCTTTTGTCTTACTGTTAACTTTATGTTGGGTTGGTTTAAGGAACACTCCACAAAAAAAATCTTTTTCTCAAGTCCCTTATAGTTAAACTGTTGAGTTTTACCATTTTTCGAATCCATTCAGTCGATCTCCAGGTCTGTCGAGAGCACTTTTAGCTTAGCTTAGCATACATTATTGAATCAGATTAGATCATTAGCATCTCCTTCATAAGTCCTTAGATTTTTCCTTTTAAAAAGCTTTACGCTTCTGTAGTGACATGGTGTATTAAGACAGACGGAAAATGAATAGTTGCAAATATGGCTAAGAAATCTACTTTCGTCCAGCGAAATTAACAAGGTACTTTGCTGCCGTGTTCATAGCTGCAACTGGTGC
Associated Phenotype:
Not determined