ZMP
zgc:91821
Ensembl ID:
ZFIN ID:
Description:
tubulin polyglutamylase complex subunit 2 [Source:RefSeq peptide;Acc:NP_001002208]
Human Orthologue:
C18orf10
Human Description:
chromosome 18 open reading frame 10 [Source:HGNC Symbol;Acc:24561]
Mouse Orthologue:
5730494M16Rik
Mouse Description:
RIKEN cDNA 5730494M16 gene Gene [Source:MGI Symbol;Acc:MGI:1913898]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10459 | Essential Splice Site | Available for shipment | Available now |
sa23875 | Essential Splice Site | Available for shipment | Available now |
sa23874 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10459
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 |
---|---|---|---|---|---|
ENSDART00000031658 | None | None | 290 | None | 7 |
ENSDART00000131607 | None | None | 92 | None | 6 |
ENSDART00000139145 | Essential Splice Site | None | 218 | 1 | 7 |
ENSDART00000142644 | None | None | 91 | None | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 10454622)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11937985 |
GRCz11 | 21 | 12030613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTACTGTYGGTRTGCCTCCAGGAACAGGGTTGGGAAACATAGACCRTAT[G/A]TATTTATAAATTKACATAGTCYTTGTAAARTTTGTCATTGTATTTTGCAC
Long Flanking Sequence:
CAGGCCCCAACTGAACATTGAGGATGATCTCTGAGTGGAGGTCTCCAAAAATTAAACCAAGCAAAGGCTTGTGCTGAAAACATTGTGCCCACCAGTCTCATGAGGTGAGGTTAATATTTAGAAAAAATAAAAAATTAAATCACCATAAAAATTATATGATTATTAGACTGTTGAAATTGTTTGTGTTGTCAATATGCCCGTGTTTATATAGGCCTTATTGTGTGCACAATGTTGGTATATTTATAACCACCTCAGAGGAATTTTGGGGGCCGTTAGTTTGGGAACTCATAGTCTGAACAGGTGCTTCCCAACTCTGTTTCTGAAGGCACACCGACAGTATACATTATTAACCTCTTCCTAATTAAACACACCTGAATCAAGTCTTTAGAATATTAGAAGAGAATCCAAAACCTCAAATGAATGGGTCAGATAAGGCAGACATCCAAAGTATGTACTGTTGGTGTGCCTCCAGGAACAGGGTTGGGAAACATAGACCGTAT[G/A]TATTTATAAATTGACATAGTCTTTGTAAAGTTTGTCATTGTATTTTGCACATCTAGAGGCAGCACCTAATATGTTTACTTATTATAGCACATGTGCTGCTGGTGATATTACAATAAAAGTGATCTGATTTGATTATTCCTTGGCTTATATTCCATCTGATAGAGAATCTCCCTGGTGTGCTGGATGTACGGTTTGTAGAGAAAGCCCCTGCAGAAAAGAGATGCCTTCTCTCCTGGGAGCAGGTATGGAGGTACTTTTGTATCACTGTGCATAATTTCGAATCAGAGATCTGACGAGAGTACAGCATGTGTACATCAGCTGTTTTTTTCTTTTTGTTCTCCAGAAAAACAACTGCGCTTTGCCGGAAGATCTCCGAGATTTTTATCTCACAACAGATGGCTTCATGCTTGCCTGGAACTCCAAGTTGGAAAGTGAGCAGCTTAAACATCACTTGAATATGGAAGATTGTCTCTGACACACACATACAGGCTAAAACTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23875
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 |
---|---|---|---|---|---|
ENSDART00000031658 | None | None | 290 | None | 7 |
ENSDART00000131607 | Essential Splice Site | 55 | 92 | 2 | 6 |
ENSDART00000139145 | None | None | 218 | None | 7 |
ENSDART00000142644 | Essential Splice Site | 55 | 91 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 10454371)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11937734 |
GRCz11 | 21 | 12030362 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGCCCCTGCAGAAAAGAGATGCCTTCTCTCCTGGGAGCAGGTATGGAG[G/A]TACTTTTGTATCACTGTGCATAATTTCGAATCAGAGATCTGACGAGAGTA
Long Flanking Sequence:
TCAGAGGAATTTTGGGGGCCGTTAGTTTGGGAACTCATAGTCTGAACAGGTGCTTCCCAACTCTGTTTCTGAAGGCACACCGACAGTATACATTATTAACCTCTTCCTAATTAAACACACCTGAATCAAGTCTTTAGAATATTAGAAGAGAATCCAAAACCTCAAATGAATGGGTCAGATAAGGCAGACATCCAAAGTATGTACTGTTGGTGTGCCTCCAGGAACAGGGTTGGGAAACATAGACCGTATGTATTTATAAATTGACATAGTCTTTGTAAAGTTTGTCATTGTATTTTGCACATCTAGAGGCAGCACCTAATATGTTTACTTATTATAGCACATGTGCTGCTGGTGATATTACAATAAAAGTGATCTGATTTGATTATTCCTTGGCTTATATTCCATCTGATAGAGAATCTCCCTGGTGTGCTGGATGTACGGTTTGTAGAGAAAGCCCCTGCAGAAAAGAGATGCCTTCTCTCCTGGGAGCAGGTATGGAG[G/A]TACTTTTGTATCACTGTGCATAATTTCGAATCAGAGATCTGACGAGAGTACAGCATGTGTACATCAGCTGTTTTTTTCTTTTTGTTCTCCAGAAAAACAACTGCGCTTTGCCGGAAGATCTCCGAGATTTTTATCTCACAACAGATGGCTTCATGCTTGCCTGGAACTCCAAGTTGGAAAGTGAGCAGCTTAAACATCACTTGAATATGGAAGATTGTCTCTGACACACACATACAGGCTAAAACTTTCTCATGATTCCAAATACATATAAGCAAGTAAGAAAGTAAAGGTATATTTGTATAGCACCTTTCCTAGACATTAAGTCACAAAGTGCTTTACAATAAGAGAAAACCAGAAAACAGGTAAAAGAACACATATCAATAAAAGAAAACATATTAAAATTATTTTTTTCCTTTTCTTTTATACATAGAAGTAAAATATCTTTTACCTAATATTATAATTTATTTGTATTTTAATTTAATATTATTAATATTTTTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23874
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000031658 | None | 84 | 290 | 4 | 7 |
ENSDART00000131607 | Nonsense | 87 | 92 | 4 | 6 |
ENSDART00000139145 | None | 12 | 218 | 4 | 7 |
ENSDART00000142644 | None | None | 91 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 10453290)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 11936653 |
GRCz11 | 21 | 12029281 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATAAGCTTTTACTCTAAAAATCAATGTTTTGTGTCCTACAGATGAAGT[G/A]GTTCCAGTGGGTTGCATGATGATCAACAACGTTGCTCAATTACGCCCTCT
Long Flanking Sequence:
AATTCAGGTGGTATTTCTTGCAATTTGGTTTTTAATTAGCAGAATTTTGAATTTGCATCTCAGTTCTGAAATTTTCCCTTCAGAATTGCAAGTTTATAGGCTTCCTTGGATTTTTTTTTTTGTTTGTTTGTCAGACAATTCAGATTTTACATGGCACATTTAAAAAAAATTTGTCTTTCAGAATTTCAACTTTATTTTTGCAATTGTGAGTTTATAGTTTCTCACACTTTTGATTCAAAATTAAAAGTTTATATCTCACAAAAAACATTTTCTTGGAATTTAGAAATTTTAACTCACACCTCTATTACTTTATATCTCATTAAAATCCAAATTATGAGGTTTATTCTCACAGTTGCAAGGAAGAAGTAGTCATCTTTTGTCGATCATTAATCATGGTTTGAATAAACTATAATGAAGCCTAAATGTAGCCCTATAACCTGATCAGTGATTCCATAAGCTTTTACTCTAAAAATCAATGTTTTGTGTCCTACAGATGAAGT[G/A]GTTCCAGTGGGTTGCATGATGATCAACAACGTTGCTCAATTACGCCCTCTGATTCAGTCAAATGTATATTGCCTCCCCAATGCACCAACCTTAGCTGATCTCGACTTTGACGATGACATAGACGGTGAGACTTTATTACATCTCTAAGCACTTTAAGAGTGCAGCATCATTTTGTTGCATTTGTTTCAGTTCAGTAAATTAGTACATAATTTGTATACAGTATATGGGTTGTTGATATGATGTTGCATTTTCACTGTCACACTGGACAAAATTGAATTTAATAAGCATTGTCATTATTTAAAATGCAAAAATAAAAGTGTCCAATAGTGTGACTGTCTCAAGCGTAGATCAATAAATGACAGCTCTTATAAATTAAAAAGTCATAAAATTGTTTATAAACACATCAGACCTAGACCTCATTTTTTATAAATGGCAATAATTTTTTATCCATATAGTTTTTACATTTTGTCACTAAAAACCATGTCCTCTGGTGTGACATT
Associated Phenotype:
Not determined