ZMP
si:ch211-244a17.4
Ensembl ID:
ZFIN ID:
Human Orthologue:
C21orf29
Human Description:
chromosome 21 open reading frame 29 [Source:HGNC Symbol;Acc:1268]
Mouse Orthologue:
C330046G03Rik
Mouse Description:
RIKEN cDNA C330046G03 gene Gene [Source:MGI Symbol;Acc:MGI:2671932]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41368 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa34570 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa41368
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000122558 | Essential Splice Site | 616 | 666 | None | 12 |
| ENSDART00000146535 | Essential Splice Site | 615 | 665 | None | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 12874468)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 12627033 |
| GRCz11 | 9 | 12598236 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACATTGCAATGAAGGTTTTGGAAAAAATGATGCATACATTTTTGTTTC[A/G]GATGGCAGGGTTACGAGGGCTTTGTCCCTGTCAACAGACTGAGCACCAAT
Long Flanking Sequence:
CTCCACATTTTCGTTAGCAGTTTAAGTTTCATATTACATTATCATTTTATAATCCTGGCAAGTCACGTATGCTTAGAAAGGTCTGACAGTCACAGTTTAATGGTTGCTGTCTGTGTTGTGATAAAATAAAACTGTGAGAGAAATGAATGGATTTGTGACAGGAACAACTGGACAGGAATACTGTAATTGCAAACCGAAAAAAATCTCTTGGGAACCTAATTTTTGTCAGGATTTGGAAAATAAGTTCCATTTGACATTTAGCTTTGATTTTATAGCAATTCTTAACTTCAAATCATGTTATGAGTTAATATTAGGAATATGTTTAATGCAATATTTAAAACAGTGCAGTGCAGTTTATGTGACCTATAAATGTAGCATCTTTAATTTTTTTAGATATGCTTTGACTTTGATTTGTCTCAACTTGTAAAGCAGATTTGTAGATATCTGATTGGACATTGCAATGAAGGTTTTGGAAAAAATGATGCATACATTTTTGTTTC[A/G]GATGGCAGGGTTACGAGGGCTTTGTCCCTGTCAACAGACTGAGCACCAATGGCTGCAGAGACTGGGAATTTTTCAACACAACCGACGGCTACTACCTCATCTACTCCAGTGCCAGAGCTGCTCTCTCTAAGGTCCTTAAATTAAGGACCATATAGTGGCACTGGACATATAAACAAAGACTAGCAGTAACTCTAAGCATGAACTGTAAATACGATGTTCTTGGATATAGCTGTTATCCAAAACTGAAATAATATTCATTTACCACATGCACTTAATGACATTCCTTGTAACAAGCTGAAGGATCTGTCTCACTACACTGAAAACATCCTGAACAACAACAGCACAATCGCAAAGAGACTATGGAAAAATTGAGAAAACTCACTTCAGAAGATTTCATACTCGCACTTATTTTGCACACAGTTCACCAGTACGCTTTGTTTAATAATATGTCATTATGTCCTGTGATCATCTGCACATAAAGGCAGCTAACTAGTTAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34570
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 |
|---|---|---|---|---|---|
| ENSDART00000122558 | Nonsense | 654 | 666 | 12 | 12 |
| ENSDART00000146535 | Nonsense | 653 | 665 | 12 | 12 |
Genomic Location (Zv9):
Chromosome 9 (position 12874354)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 9 | 12626919 |
| GRCz11 | 9 | 12598122 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAATTTTTCAACACAACCGACGGCTACTACCTCATCTACTCCAGTGCC[A/T]GAGCTGCTCTCTCTAAGGTCCTTAAATTAAGGACCATATAGTGGCACTGG
Long Flanking Sequence:
GTTGTGATAAAATAAAACTGTGAGAGAAATGAATGGATTTGTGACAGGAACAACTGGACAGGAATACTGTAATTGCAAACCGAAAAAAATCTCTTGGGAACCTAATTTTTGTCAGGATTTGGAAAATAAGTTCCATTTGACATTTAGCTTTGATTTTATAGCAATTCTTAACTTCAAATCATGTTATGAGTTAATATTAGGAATATGTTTAATGCAATATTTAAAACAGTGCAGTGCAGTTTATGTGACCTATAAATGTAGCATCTTTAATTTTTTTAGATATGCTTTGACTTTGATTTGTCTCAACTTGTAAAGCAGATTTGTAGATATCTGATTGGACATTGCAATGAAGGTTTTGGAAAAAATGATGCATACATTTTTGTTTCAGATGGCAGGGTTACGAGGGCTTTGTCCCTGTCAACAGACTGAGCACCAATGGCTGCAGAGACTGGGAATTTTTCAACACAACCGACGGCTACTACCTCATCTACTCCAGTGCC[A/T]GAGCTGCTCTCTCTAAGGTCCTTAAATTAAGGACCATATAGTGGCACTGGACATATAAACAAAGACTAGCAGTAACTCTAAGCATGAACTGTAAATACGATGTTCTTGGATATAGCTGTTATCCAAAACTGAAATAATATTCATTTACCACATGCACTTAATGACATTCCTTGTAACAAGCTGAAGGATCTGTCTCACTACACTGAAAACATCCTGAACAACAACAGCACAATCGCAAAGAGACTATGGAAAAATTGAGAAAACTCACTTCAGAAGATTTCATACTCGCACTTATTTTGCACACAGTTCACCAGTACGCTTTGTTTAATAATATGTCATTATGTCCTGTGATCATCTGCACATAAAGGCAGCTAACTAGTTAGTTTATAAAATGACTGGAAAAGATCGATTTATCAGCCAACAAAACACTGTATTAACTGTACTGTACTGTTTGTAAGCTACCGACTTTTACATTTGTTTTATTAGAAGGTCTTTAAATG
Associated Phenotype:
Not determined