ZMP
si:ch211-208h7.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
KIAA0922
Human Description:
KIAA0922 [Source:HGNC Symbol;Acc:29146]
Mouse Orthologue:
D930015E06Rik
Mouse Description:
RIKEN cDNA D930015E06 gene Gene [Source:MGI Symbol;Acc:MGI:2443399]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10363 | Essential Splice Site | Available for shipment | Available now |
sa32680 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7366 | Missense | Mutation detected in F1 DNA | Not yet available |
sa31205 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10363
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111426 | Essential Splice Site | 354 | 1546 | 10 | 34 |
ENSDART00000133208 | Essential Splice Site | 353 | 1545 | 10 | 34 |
The following transcripts of ENSDARG00000079434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 24138638)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 24590409 |
GRCz11 | 1 | 25281238 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATAGGAGTGTTCATGTTGAACTCAGGTGTTAAAAAGCTCTTTGTTAAGG[T/A]ATGTGCACGTACATTGACATTGTTTTAACGTTTTTAATTATGTATGTATA
Long Flanking Sequence:
TTTTCACCTATCTTTTATGCTATATTAGGATAATCCTTAGATTTGATACATAATTGTTGAATTGAATTTTTTTCAGAATAAATAAATATAATTTATAGCCAGTTACGGAATAATTTTTGAATGATTTGACATAAGCATATACATTTTTCAAGTAAAATACATCTGTAAACGGAATTGAAAGGTAATCCATGCAAATATATATAACAAAAGTGAACCATAACTTCCTAGTACTGTACATGGGTTACACCTACCTGTATTTCTAACTTTTTGTTGACAGCATAGCCACCAACGCCCTATACGCAACTTCCTCTGATAACACAGCACCACCTTGTGGATTTAGTGGCCTTTATAGTTTCTTCTCCAAATGAAGTACAGCCACATGTTAAAAAGATAATTTTATAAAATATGTTTTGTAATGTAAATTTGTTTCTAATTCACAGCAGATCCCAAAATAGGAGTGTTCATGTTGAACTCAGGTGTTAAAAAGCTCTTTGTTAAGG[T/A]ATGTGCACGTACATTGACATTGTTTTAACGTTTTTAATTATGTATGTATATAATTAGATGACATTTAATATAGTGGGGTCACAATGCACGACTCGTCTTGTGTGTTAAAGGAGATCCAGCTTTTGTCGAGAACAGACAGCAATGTTGAACTCACTGAAGTCTTGCTCAAGCCTTCTGCTACTAACTTCACTCAAGTGGCTTCACTCTTCTGTAGACGTCAGTATTTTACTCTCCACATTTAATTTTCACATTGTACATGCTACAATGTTAGCCATGTTTATTTAATTGCCTTTGTTTTTGGTTTCAGATTCTTTGACGGCTAAAAGTAAAAGGTGTTCAAGTCAGTTCGGCCTACACATTTTAGCAAACAGAACAGTGAATTTATATCCACTGCTGCAAAGAACACACAGGTAAGGAATTCTGTGTTGACGTATATGAGTAAATTGATGTATTGAATTTATTGTAAATTAACTTTGTGTTCAGTGTTAGTATTATCTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32680
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111426 | Nonsense | 798 | 1546 | 22 | 34 |
ENSDART00000133208 | Nonsense | 797 | 1545 | 22 | 34 |
The following transcripts of ENSDARG00000079434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 24151701)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 24603472 |
GRCz11 | 1 | 25294301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCAGGCGAGTTGCCGCTGACTGTAGTGTCCATGAACATTAATGGATAT[A/T]AATGTCAGGGTTATGGTTTTGAAGTGCAGCACTGTGGATCCTTCAGAGTG
Long Flanking Sequence:
TGCTAGTTGATAGCACACAGTAATGTTGTCTGTAATCTGTTCTTTAACAGGAACAACCTGACCGTGTTTGACATGGTTCTGGTTAAAGGATTAGGAGCAAAGGAGATGTTGAGGGTGGGAGGGAAGCTTCCTGGACCTGCAGCCTCTCTGCGCTTCAATGTGCCTCAGTCCACCCTCATGGAGTGCAGAGATGGTGAGAGACATGTTGATACATCACTGTTAATTAGAGAACAAACATTTTCTCCTAGGCATTCTGTAAACATACAGCAATGAAATATTCACAATGTAGAAAATAGTTCATTTGTGCTAAAAGAATATAACTAATATTGAAAGAGGAAACAATGTTTTGTTCATTGTTCATTGACAGTATCGTTTGAATTCTATTGTTTTCCACAGGCTTACGATCAAGTAAGCCCTTATTTGCCATCCAGAAAAGCTTTAAAGTGGAGAATGCAGGCGAGTTGCCGCTGACTGTAGTGTCCATGAACATTAATGGATAT[A/T]AATGTCAGGGTTATGGTTTTGAAGTGCAGCACTGTGGATCCTTCAGAGTGGACTACAACTCCTCCTCAGAAATCACTATTGCGTAAGTTTTAAAAGTGCTGCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCATGCTGACTTTAAATATTGTGTATTAGCAGTGGGTAAAGCAGAGTGCAACTCTTGTACTGTCGCTTTATTAAATGTAAATGGGATTTGAGATGATATAAAGTCAGTTTTACCTGTAACTTCAGGTTAAGGATGGTGTAACATGACAGTATGTAGCTCAGGGTAGAAAATTAACAGGTGTTTGTGGCAAATATGTCACCAAAGTGAATAGCAAATTGTTTTCTTCAAACAAAATCCCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7366
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111426 | Missense | 1313 | 1546 | 30 | 34 |
ENSDART00000133208 | Missense | 1312 | 1545 | 30 | 34 |
The following transcripts of ENSDARG00000079434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 24168299)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 24620070 |
GRCz11 | 1 | 25310899 |
KASP Assay ID:
554-4196.1 (used for ordering genotyping assays)
KASP Sequence:
TGACAGAGAACCATACCAAAGCTCAGAAATGGGTCCWGTCCCAGCACTTC[C/A]TCACACCTTCGCWGATGTAGCTGCAGGTGTGGACAAAAACATCGGTAAGG
Long Flanking Sequence:
ACCAATCATATGAAAAAAGTCATTTAAAGGCTGATGGCTCTTCATTTGTTTCATTTGTAAATGTTTTTGTTTTTTACTATTAAAAACGACTATTTTTATCTTCTGTTGGTTATGGCTGAAATATGGTCATTCTAATAGTTGAATAAAATGTATTTGATTTTTGGAAATCACCAAGTGACCCCGCTGCCATTTGGGAACCACTGTAATGTACAACACTAATCCAGACAATCTATCACTTCAAACTATTAAAAATGTTCATAAAAGTCACATTTTCAAGGTTAAAAGTTGTTAGAAGAAAGATCAAGATCCCATAATGCAATTCAAAAGCCTAAATAAGTGAAGAAGAAAAAACATGAATCACAAAATACAGAAAATACAGATATATTCTAAAATAGAAATTGGAAATTGATTGTATGATTATGAATTTATCCACAGCATGAACAATCTTTATGACAGAGAACCATACCAAAGCTCAGAAATGGGTCCTGTCCCAGCACTTC[C/A]TCACACCTTCGCTGATGTAGCTGCAGGTGTGGACAAAAACATCGGTAAGGGCATTTTAATGCATTATTATCACAGACAGCAGCATCAAGTTATATGATGTCAGTCAGTTGGATGTGCATTATCACGCCTATTATAAGCTTCCCACATACTATTTATTTTTAAATTGGAGAACAACCTGCAATTAATCTTTAAGGTTACTGCTTAGTTCTGTTAAAAAATAGCCAAACAGATGTAAAAGAGACATTTTTAAGCATATTTCATGAGTTGGGTATGATTTGAAGCACAGCAATGATGAGAAGAGTGCTGAAAAAGTTACACGCAAGTAAAAGTAGCAATACTTGCAAAAAATTTAGTGCAAGTAGAGTAAATATATCTTTTCTATATGCTACCTAAAGTATAAGAAAGTAGCTCTTCTAAAAGTACTCCAGAGTAGTGAGTGAGCATAATGCTGTGAAAATTATTCCACTGTATACCCTGTAAATGAAAGGTGTAGCTTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31205
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111426 | Essential Splice Site | 1371 | 1546 | 31 | 34 |
ENSDART00000133208 | Essential Splice Site | 1370 | 1545 | 31 | 34 |
The following transcripts of ENSDARG00000079434 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 24170541)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 24622312 |
GRCz11 | 1 | 25313141 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGAATCTCTCCCGTTTGTCCCTCAGAATCCCTCATCCAGATATGATGGG[T/C]ACGTCTCCAGCTTCTTTCTACTTATCTAGCATTTTTTTTTCTTCACATAA
Long Flanking Sequence:
CTATTTAATATCAATTATTTAAATGTATTATGATTTCCACAAAAAATATGAAGCTAGACATTTTTTTTCAGTTTTTTTTTCAATGGTGATCAAATTGTCTTGCCCCTGCAAATAAACATAATCAAAATCATTTCTAAAGAAACCTATGACAATAAAGATGCGTAAACTTCAGTGTTTCAATGAGAAAATCACAGCAATAAATAATCTCATTCGCATATTGAAATGTTTGTAATAGGAAGCAGTTCCTTTGAATTGTGATAGTTTTTCACAGTATTGCTGTTTTTTTTACTATATTTTTCATCCAGTAAATTCAGCCTTAAATATGTCAGATTTATATGACTGTTTTAATGTGCAATTTGCTTTCCCCAGACGTAATTGGCTCCAGCATGATGGAAGAGACGTGGTCAGTCAACTCCGTTCCTCTGACCAATGAATTCAGGTACAACATGAGTGAATCTCTCCCGTTTGTCCCTCAGAATCCCTCATCCAGATATGATGGG[T/C]ACGTCTCCAGCTTCTTTCTACTTATCTAGCATTTTTTTTTCTTCACATAATTGATGCCCATCCACTATCAGATTCCAATGATTGCGTGTTATTATTGTGCAGCTTCCCTTGGAACAACATGAGCAGTCAGTGTAGCAGTCAGTATCCCTACAGTGACCGCAGCAACTACATGCCAACAGGTCAGGAGTTTGCTGAAAGCAGCTCAAGTTTGCCCTCTTTCAGAATGTGAAGAATGACAGATTTTTATTTGTTTTGTCCATGAAGGTAACGGCAATTACCAAAATGCATTCTCATGCCCTGAAAGCCAAACCATAAGCCACAGCCATCAGCCGGTGTGGGGTGAGAATGGAGCCCATGATATCAACTCTACATGGGACACTGGCAGCTGTGTGGGCAGCAAGGTGAGCTGTATATCTGTGTTTCTATTCGTATAACTCTTTTAAAGTAATATTTGTGAGTTATATTTATTGAGACAATTTGACAAATTCTGCAATATCTTG
Associated Phenotype:
Not determined