ZMP
zgc:162468
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC553443 [Source:RefSeq peptide;Acc:NP_001077288]
Human Orthologue:
C10orf72
Human Description:
chromosome 10 open reading frame 72 [Source:HGNC Symbol;Acc:26470]
Mouse Orthologue:
E130203B14Rik
Mouse Description:
RIKEN cDNA E130203B14 gene Gene [Source:MGI Symbol;Acc:MGI:2444633]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa406 | Nonsense | Available for shipment | Available now |
sa38951 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12738 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa406
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057469 | Nonsense | 135 | 329 | 2 | 8 |
The following transcripts of ENSDARG00000010154 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 31177601)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30823549 |
GRCz11 | 13 | 30953999 |
KASP Assay ID:
554-0265.1 (used for ordering genotyping assays)
KASP Sequence:
ATGGGGGAAACTACACCTGTAAAGTGCAGGAAATACGGAAACACAGAAAC[A/T]AATGGAGGGCCTCGTCCAATGGAACAGGGAGCATGGAATTACGAGGTAAA
Long Flanking Sequence:
CTTTTTTTATTTGCTGGCGTTTTTTGTAATTGGCTGTGTTTCTTAAATTGCAGCACATTAAGCTCTCTCGGCCACCGTACATTGGTTTTAGTCAATATCCCTCAATTTGTAACAGAAAAAAAATTGAAGCTTCCTTCTACTTTTTCCCAGAGCTGAGTGATGCTTTAAATGTGACCGTCACACCTGGCCCAGTCAGCATGTGTATGGAGGGAGACAACATCACTTTGTCCTGCTTAGTGTCTCAGAAGAAGAGAAGCAGCAGTGTTTTAGTTCTGCGCTGGCTCTACTTCCCCACCCCTGAAGACGAGCATCTTGTGGTGAGGATGGGCATGAAGAAAGCCAAGTATTATGGCAACTACAGCAAGCTCTTTCCTCAGACCAAGTTTCTCCTTTGGGAAGAAAATGATGGGCAGCTCTACCGTCTGCTGATCAAAAATGTGTCACGGGAGGATGGGGGAAACTACACCTGTAAAGTGCAGGAAATACGGAAACACAGAAAC[A/T]AATGGAGGGCCTCGTCCAATGGAACAGGGAGCATGGAATTACGAGGTAAAGAAGAATATTTTCCTGAGCTGTATCTTAAGTGAATTAATGACTTATATTGTCTTAACTTATATTGTCTAAAATATTTTTTTCTTCTGTTGATTTAACAAATCCTCTGTGTTGATGTTAGCTTTAACATGTTAGCCATAAGCTCCTAAAATCCTGGTTTGCATTATAAATATATATATATATATATATATATATATATATATACTGTATGCATTATATATATAATCTCAAAACATAAATCACACGTTGAATTGCTAGCTTCACCACAAAAGTTTTGATAATTGACAAATCTACGATCTTGGTATATTTGCTAATCTAACATTGTGGCTTCATAGTTTTAATAGCAGATGAAAGCAAACTACTGCATACTATACATTCAATCCTAATGTGTTTAATTACAACATATTTAATCATACTACAGAACAAGCAGCCTTCAAACTATGCCCCATGTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa38951
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 |
---|---|---|---|---|---|
ENSDART00000057469 | Essential Splice Site | 204 | 329 | 5 | 8 |
The following transcripts of ENSDARG00000010154 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 31187418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30833366 |
GRCz11 | 13 | 30963816 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTACACATTTATTTATACTTTTATGTTTGTTTAACTTTGTCTCCATCTA[G/A]CCAGCTATAACCTGGTGAAGTGTCCAGAAAACAGGTAAACTTATGTAACA
Long Flanking Sequence:
GCATGTACCTATGTGTGTATGTGTGTGTGTGTGTATGTGCATGCATGTATTTATTTATTTATTTATTTATTTTTTGACTGTAAATTAGAATAAGATTCTGATGGTATGATAACCTTGGATAAAAATATCACAGTTTCACGGTATCACAGTATGATGTTTGCTGCTTAAGGTACAATTCTGTACCATTTTTTTTGAGAGTGTGTAACAGAACATCTTAGCACTTTTAAAACTAAGACTTTCCCTTGAAACCAGATATCATTCCATGCATACTGTACAAGTCTAGCATTTTTTGACTCTTTACTTAGTTTTAGCAGCTAATTAATCAGAAACCTCACTAATTAAAAAAAGAAGCTCACTTCTGTTTTGCAAAGTAAGGTGGATTTAATGTCATTAACACATAAAATGATTCTTTAATAAGCAAACTATTTTGTTATTGCCTTTTTTATTCTTGTTACACATTTATTTATACTTTTATGTTTGTTTAACTTTGTCTCCATCTA[G/A]CCAGCTATAACCTGGTGAAGTGTCCAGAAAACAGGTAAACTTATGTAACAGGATTTACCATTGCTTTTCTCTTATTTATGTTTGCCTGATTCCAAGGCTCACATTGTTATGTTTTATATCTCCAGCTCAGGAGAGACAGTAACCAGTGTGTCCAGCTGCTCTCCTGCAATGCACAGAAAAGAGAAACGACACAAAGCACAGCCCAGAGACGTCACTGAACCACCGCCACCACCACAGATACCAGCTAAAGGTAACCGAATCACATATTTTCAAATCCAAGACAACTGGGTATTGCTAGATAAAAAAAAAATAATAATAAAAACATTGGGTTTAATCAATAATTGCACTGGGTGTCAACAATGAGTGGTGGGTCTTAAGTTATGATTTGCCCTTTAAAGACTTGTGTTTCTTTTTACCCTTTTAAAACTTATTTCAGTATTTTAAACCACTTCCACCTGAAACATTAAGTAAGAGTGGAGCTTTCTTTTTACAAATCAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12738
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 |
---|---|---|---|---|---|
ENSDART00000057469 | Essential Splice Site | 215 | 329 | 6 | 8 |
The following transcripts of ENSDARG00000010154 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 31187543)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 30833491 |
GRCz11 | 13 | 30963941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTATGTTTKCCTGATTCCAAGGCTCACATTGTTATGTTTTATATCTCCA[G/A]CTCAGGAGAGACAGTAACCRGTRTGTCCAGCTGCTCTCCTGCAATGCACA
Long Flanking Sequence:
TATCACAGTTTCACGGTATCACAGTATGATGTTTGCTGCTTAAGGTACAATTCTGTACCATTTTTTTTGAGAGTGTGTAACAGAACATCTTAGCACTTTTAAAACTAAGACTTTCCCTTGAAACCAGATATCATTCCATGCATACTGTACAAGTCTAGCATTTTTTGACTCTTTACTTAGTTTTAGCAGCTAATTAATCAGAAACCTCACTAATTAAAAAAAGAAGCTCACTTCTGTTTTGCAAAGTAAGGTGGATTTAATGTCATTAACACATAAAATGATTCTTTAATAAGCAAACTATTTTGTTATTGCCTTTTTTATTCTTGTTACACATTTATTTATACTTTTATGTTTGTTTAACTTTGTCTCCATCTAGCCAGCTATAACCTGGTGAAGTGTCCAGAAAACAGGTAAACTTATGTAACAGGATTTACCATTGCTTTTCTCTTATTTATGTTTGCCTGATTCCAAGGCTCACATTGTTATGTTTTATATCTCCA[G/A]CTCAGGAGAGACAGTAACCAGTGTGTCCAGCTGCTCTCCTGCAATGCACAGAAAAGAGAAACGACACAAAGCACAGCCCAGAGACGTCACTGAACCACCGCCACCACCACAGATACCAGCTAAAGGTAACCGAATCACATATTTTCAAATCCAAGACAACTGGGTATTGCTAGATAAAAAAAAAATAATAATAAAAACATTGGGTTTAATCAATAATTGCACTGGGTGTCAACAATGAGTGGTGGGTCTTAAGTTATGATTTGCCCTTTAAAGACTTGTGTTTCTTTTTACCCTTTTAAAACTTATTTCAGTATTTTAAACCACTTCCACCTGAAACATTAAGTAAGAGTGGAGCTTTCTTTTTACAAATCAATTCCCTTAAAGCAAACTAATATAGGGACTTGGTTAAAATGATTGTAAAAAGAGACTTAAGCCACTTAAAACACAGAAGCAAATGGTTAGACTTCAAAAATTAACAAAAAAAAAATTTCTCGGTCGAT
Associated Phenotype:
Not determined