ZMP
wu:fc43b12
Ensembl ID:
ZFIN ID:
Human Orthologue:
C10orf88
Human Description:
chromosome 10 open reading frame 88 [Source:HGNC Symbol;Acc:25822]
Mouse Orthologue:
2310057M21Rik
Mouse Description:
RIKEN cDNA 2310057M21 gene Gene [Source:MGI Symbol;Acc:MGI:1915527]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30665 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa27904 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30665
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 |
|---|---|---|---|---|---|
| ENSDART00000129495 | Essential Splice Site | 111 | 364 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 12462975)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 11318628 |
| GRCz11 | 12 | 11356931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTGCGGCACCTGCCGTGGAGAGGAAGTTCAAATATCACACACTAATGGG[T/C]ATATGTATGCGAATGCTTAAGTTTACTTTACTAAACTTACTCAATTAAAT
Long Flanking Sequence:
TGGTGACTCATTATACTTGGAATTTGTGCTCAGCCTTTAACTCATCCAAGTGCAGTGAACAGACACACCATGAACACACACCTAGAGCAGTTGGGGGTTCTGTGCCTTGCTCAAGGGACTCCTCTTAGCCATGGTATTATAAGTGGTGAGAGCACTGGTTATTCACTCTTACCACCTACCATCTCTGCCGGTGCCAGGACTCGAGCCTGTGACCTTCACAAGTCCAACTCTTTAAACATTAGGCCATGACTCTTCCCATGAAGTGTTTTTGTGACTGTATTTGCACATGCATTTCTCCTAGGAATGAAGCTGTCTGTCTGGAGAGAGCAGAAGAGGACTCACCGTGTGTCGTCACACTTCAGTGTTCACCCGGCTCTGCGTCTGCGATCAGCAGTCTTCAGGTGGTCAGTGAAGCCCGCACTATTGAAGTGTACTCGCTGTCTGGAGAATACTGCGGCACCTGCCGTGGAGAGGAAGTTCAAATATCACACACTAATGGG[T/C]ATATGTATGCGAATGCTTAAGTTTACTTTACTAAACTTACTCAATTAAATCCTAATCATGTCATGACAAACTATATATCAGTGGAAGGTCTAAGACTTTTAAATACATATTTCATCACTTTTTTGTTATGTAGGAAGAGTAATAGATTAAAAAATATATATAAGGTCAATATGGTCACCAATGGAAACTGGATGTCATCTGGTCCTGATAATTGATCTTGCAGCCAAGCCAAATAAAATCTTACTAAAAGCTTCTAATTTGAAATATGAGTGGTTCAGATAATTAGATTTTCTGCCATTTTTCAAAACATAAAATACATATTGTATGTAATGTATTCATAAACAATGAAGGCACATAACTTTTATTTTAATCGACATTTCAACTTCTGCCTTCTGTCTTCTTTAAAATAAGACCAAGCTTAAATCTATTGACCAAGGCATTGAAGACATTTAAGTTGAACGTCATTTTCATATGTGCAAAAAGTGGGGGCGACAGTTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27904
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000129495 | Essential Splice Site | 135 | 364 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 12 (position 12465304)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 12 | 11320957 |
| GRCz11 | 12 | 11359260 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGGAATAATCTGATTCTGGAAAGCCCTGCTGTGTCCTGTGAGGTGAAG[G/A]TAAGAAATGTGAGAAGTAAATCCACACTTTCATTGCAGGCATTCAAACTG
Long Flanking Sequence:
TTAACCAGGCAAGTTAGGGTAATTAGGCAAGTTACTGTATAAGGATGGTTTGTTCTGTAGACAATAGAAAAAAAAACTAGCTTAAAAGGGCTAATAATTTTGACCTTAAAATGGTGTTTAAAAAATTGAAAACTGCTTTTATTCCAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATCAGGCCTACTTTGAAAATTTCCTTTCTCTGTTAAACATCATTTGGAAAATATTTGAAAATGAAAAAATAAAAAATAAAGTGGGCTATTAATTCAGACTAGTTTTTGTTATTTTTAGTTTTTGTCAAACAAGAAAATGTAATTAATTATATTCCACCTCACAAAATGAATTTGTTTTTTGGGTTTTCTTTTAAGTTAAATGTGATTACCCTGATGGTTTGCTCTATTTTGTGGCAGTTCTGAAGAAGAGAGGCATTTCTACAGGAATAATCTGATTCTGGAAAGCCCTGCTGTGTCCTGTGAGGTGAAG[G/A]TAAGAAATGTGAGAAGTAAATCCACACTTTCATTGCAGGCATTCAAACTGATATATGATGTGTTTGTACAGCTGCTGTCTCTCGGTGGCCGCTCCTCTGTGTCTGTCGCTCATGTTTGTGTGGGACTGGAGACACTGAAGGGCAGACAAGGTGGGCCGAGAGTAGAGCCAGGCATTGACCTTCAGCAGGTGCAGGCCATGATGGAGGAGATGGGCACCACCCTTTCACCGGGAGCACAAAATCTATTGGAGCTGGTGCAGTGCCAGCAAAAGGTCTGGTCTCAGTCTCTTATTACAGCATAATCACCACTGCACTGGGCAGATTTAATAGGATTGATATTATACAGAGGAATAATAATGAAAATATATTAAATTAAATAATAAATAGTATTTTTTTATATTACTTTATTACTGTTTTCAGTAATAATTTTAGTTGAAAAAGTAAAAATAAAATTCTTTTAGTTGTAACAAATTGAAGTAATTTAGGATGATTATAGATGG
Associated Phenotype:
Not determined