ZMP
si:ch211-223p8.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B7ZD03]
Human Orthologue:
C10orf79
Human Description:
chromosome 10 open reading frame 79 [Source:HGNC Symbol;Acc:26684]
Mouse Orthologue:
D19Ertd652e
Mouse Description:
DNA segment, Chr 19, ERATO Doi 652, expressed Gene [Source:MGI Symbol;Acc:MGI:1289258]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22296 | Nonsense | Available for shipment | Available now |
sa35482 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22297 | Nonsense | Available for shipment | Available now |
sa35483 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22296
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 |
---|---|---|---|---|---|
ENSDART00000002858 | Nonsense | 48 | 1642 | 2 | 38 |
ENSDART00000147713 | Nonsense | 57 | 1651 | 2 | 38 |
Genomic Location (Zv9):
Chromosome 13 (position 24942209)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24587869 |
GRCz11 | 13 | 24718319 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTTGCTACACCTGCGGAAACTTCATCGTTTTCCTCAATGTGGAAACT[A/T]AAGAGAGGAAGACGCTGCAGAGTCCCGGCTCTGGTATTGGAGCATTTACA
Long Flanking Sequence:
AATAATAATAATAATGTGTTAAAAGCTATGGTTAAAAGTCTAACGTTATGTGGTGTTGGTTGCTAAGGAAACGGACGCAAGCACAGATGGTGGCTGAAATGGATGTGCTGCGAAACTTCGAAGTTCAGTGAGTTACAGTCCATTGATTAAAAAGCGTGGATAATCTTTGATTAATTTACGTAACTGTTAAATAAATTGTAGCTTGTGAAGGTATCCAGTCTGTAAAACAGGATTATCTATGCTAACGCTCTACCTAGCACTAATGGTAAAATGCGTCTTCAACGTGCTAACTTTAATCCAATCTCAAAATATGTTACAAATATTGTAGTATTCGTTGCAAGGGCAATATGGCATACAAAAATACAGAAATGCTGTTTTAATGTTGATTATTATCTTCAAGATGGGTGCAAGGATTCACCAATGGCACATTTAGGTTTGTCGACAAGAAAACAGTTTGCTACACCTGCGGAAACTTCATCGTTTTCCTCAATGTGGAAACT[A/T]AAGAGAGGAAGACGCTGCAGAGTCCCGGCTCTGGTATTGGAGCATTTACAGCCAGTGGGCAACGTAGGTGTATTGCTTTCTCTGATCTCGGACTCAAGCCTTCCATCTTTATCTACAAATATCCAGAGCTTGAGCTGACAAGTGAACTAAAAGGTCAGTCAATGCTTAGTTACAGCTTTAGCACAGGGGTTGTCAAACTGGGGTCCAGGGCAGGGACACTTGGGAGGAGCAGATGTGTGTACTGGGGGTTAGTGGAAAAGTTTTGAGAAACACTGTAAAAAAAAAAGTAATTATTACAGATTAAAGTAACTAAATCAATTTAAAATTAAGGCACTACCCAACGAATGTAGTTTATTAAAAACATAAAAATACATAAATATTTAGGACATTTAGCATTTATGATATACATTTTTCACAAGTATGAATTGTGTCATTATACAGGAAACTATATCAAAGTGTGTTACATTTTAGCTGGTCATAGTGGTCATATCTGGGAGTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35482
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002858 | Essential Splice Site | 362 | 1642 | 9 | 38 |
ENSDART00000147713 | Essential Splice Site | 371 | 1651 | 9 | 38 |
Genomic Location (Zv9):
Chromosome 13 (position 24945358)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24591018 |
GRCz11 | 13 | 24721468 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGAAAGGAAATTCACGAGAATGCTTAAAATCTTTTAGTTTTCTTTCTT[A/C]GGGCTGTGTTTACAGATTCAAACCACTGCTAAAGGATAAAGCTGTCAAAG
Long Flanking Sequence:
GGGTCCTATTGTGCTTTTTACACAATTTTGGTTTTAAAATATATTTATTACATTTTAGAATATTATAGAAACAACAAAAAACGGGCAAGCGAGACAAGGGGAGAATCAAAATGCAGGAAAATGAAGAAAAAATAAATAATAAAATATTTCCCAGTACTGAGTTACAGCTGGAAGGGCATTCGATGTGTAAAACTTGCTGGATAAGTTGTCGGTTCATTCTGCTGTGGTGACCCCTAATGAATAAATTGACCAAGGGAAATGAATGAATGAATAATTAAAATATAAATAAATATTTTAAACTGAAACATCACAATCTGGGACACCTGAGATCCAAAAATGGCATAATAGATTATAATAGATAAATTATTATTATTATTTTTCAATTAAAATGTTATTAGAAAACCTGTTACAGACTTTGTATTTTTATTAAAACACAATGCAGAACTTATAAAAGAAAGGAAATTCACGAGAATGCTTAAAATCTTTTAGTTTTCTTTCTT[A/C]GGGCTGTGTTTACAGATTCAAACCACTGCTAAAGGATAAAGCTGTCAAAGTCCTGGATGTCCTTTGTGGAGATTTTGTGACTGTTGCTCCAGTTTACACTGATAGAAGCATTTGTTTGGTAATTATAATACATATATTACTTTAATATAGTAAAAAGTAGAATGCAAGGCAGATCTGGAATGAAAAGTGTTTAATTCAGTGGTTTTAAATATTAATAAGGCATGTGCATCTCCATTTATTCAGTCAGTTAGAGAAGCAGGAGTTGTACAGCTTTGGACTCTGGATGATGGACTTTGCATGGGCTCCATCTCTCTGCAAACTCACGTTAGTGCTGTATTTGAGGTTTTGTATGACACACACACTATTTTTCGTAAAACAAGTGAATCAGTACATAAATGTTTGTCATTTGGTGTGACTTTACTTCAGGTAACTAGTATGGCATGCTGTCCCATAGCGCAGTACATTGTGGTAGGGACTGCCACCGGAGATGTGCTGTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22297
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000002858 | Nonsense | 1291 | 1642 | 31 | 38 |
ENSDART00000147713 | Nonsense | 1300 | 1651 | 31 | 38 |
Genomic Location (Zv9):
Chromosome 13 (position 24961211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24606871 |
GRCz11 | 13 | 24737321 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTTTATGATGTCCCTGGACACTCAATTGACCAGCTATATAAACTTTA[C/A]AAACGCAGACCAAGGTATTATTTCAGAAGATTTGCAGCTTGTTTGTTCAT
Long Flanking Sequence:
AAGGCACGAATTAAAAAGGTGATCTTCGTTTGTATAATGAATTGCCTCTTATCTCTTATTCAGCAGTGACGTTGCATGTTTACAGTAACTCTACAACATCAGAAATTGGCAGTTCTAACTTTCAATTATAATGTTCTTGATTATGACAAAAATGTCATGCAAGAACAAACTTGTGCAGCACACTAATCCGTTTCTTTGAGAGCGACTGTTTTGCACATGTTGGAGTGTATGAGTCACCTCTCTTTACTGACAGAATGAAATTGGGGAGGAATTGAAAAAACACAAGGAGACTGTTGATGAGTTTAGAGAGGCGTATGATAACACAGTCGCTGAGGACAAAGTAAGATTACAAACATATCTTGCATATGCATATCCATAATGTTCTCGCCAAAAAAAGTCTCATCCAACCATCTTCCTAATTTATAGCTACTTGACAAAGGATTCCGCAAAGAGTTTTATGATGTCCCTGGACACTCAATTGACCAGCTATATAAACTTTA[C/A]AAACGCAGACCAAGGTATTATTTCAGAAGATTTGCAGCTTGTTTGTTCATAAGTGTTTGTCCGGTCTTAACTGAGTAAAGGTGTTGTTTGACAGGGTTCAGAGGATGAAAACACAGACTGAAAATAACCCATTTAAAGAAGGGGCAGCACCATCTGATGGACTCTCTTTGATGATGAAGGCCATGGAGGAGTTGGACGCTCCAGAGCACATGCTGGAAGGTTTAGATCCAGCTGTGTGGGAGAGGTTTTGCCTGGCAAGACGGGCCAAAGTGGAAAGTGAACAAAAGGTAAGAATAGCTAGATAAGCTAAATGTCACCCTAATCAAATTTCTAAAGAGAAAGATCACCCAAAAATGACAATTCAGACATCATTTACCCAACCTCTTGAGTTTCTTTCTTCTGTTGAACACAAAATAAAATATTTTGAAGAGTGTTGGAAAGCAACAGCCGTTAACTTTCATAGTATACTTTGATCCTGCAATGAATGTAAATGGATGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35483
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 |
---|---|---|---|---|---|
ENSDART00000002858 | Essential Splice Site | 1360 | 1642 | 32 | 38 |
ENSDART00000147713 | Essential Splice Site | 1369 | 1651 | 32 | 38 |
Genomic Location (Zv9):
Chromosome 13 (position 24961499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24607159 |
GRCz11 | 13 | 24737609 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAGAGGTTTTGCCTGGCAAGACGGGCCAAAGTGGAAAGTGAACAAAAG[G/A]TAAGAATAGCTAGATAAGCTAAATGTCACCCTAATCAAATTTCTAAAGAG
Long Flanking Sequence:
GACTGTTGATGAGTTTAGAGAGGCGTATGATAACACAGTCGCTGAGGACAAAGTAAGATTACAAACATATCTTGCATATGCATATCCATAATGTTCTCGCCAAAAAAAGTCTCATCCAACCATCTTCCTAATTTATAGCTACTTGACAAAGGATTCCGCAAAGAGTTTTATGATGTCCCTGGACACTCAATTGACCAGCTATATAAACTTTACAAACGCAGACCAAGGTATTATTTCAGAAGATTTGCAGCTTGTTTGTTCATAAGTGTTTGTCCGGTCTTAACTGAGTAAAGGTGTTGTTTGACAGGGTTCAGAGGATGAAAACACAGACTGAAAATAACCCATTTAAAGAAGGGGCAGCACCATCTGATGGACTCTCTTTGATGATGAAGGCCATGGAGGAGTTGGACGCTCCAGAGCACATGCTGGAAGGTTTAGATCCAGCTGTGTGGGAGAGGTTTTGCCTGGCAAGACGGGCCAAAGTGGAAAGTGAACAAAAG[G/A]TAAGAATAGCTAGATAAGCTAAATGTCACCCTAATCAAATTTCTAAAGAGAAAGATCACCCAAAAATGACAATTCAGACATCATTTACCCAACCTCTTGAGTTTCTTTCTTCTGTTGAACACAAAATAAAATATTTTGAAGAGTGTTGGAAAGCAACAGCCGTTAACTTTCATAGTATACTTTGATCCTGCAATGAATGTAAATGGATGCTGGTTTACAACATTCTTCAAAATATCTTCTTTTGTAATCAACAAGAAAAAAATCATAAACGTATAGAACCACTTGAGTGCTAGTAAATGGTAAGAAACTTTATTTCGAGACACGTACATCATAATTCATAAAGCGTTTTTGTTTGTTTTGTTTTTTTCGTTCAGTCAGCTATTTACGAATTTTGTTTATGTTATAGAGTGTTATAAATAGTAAATCAGTGTTTCTCAACCACGTTCCTGAAGGACCACCAGCACTGCATGTTCTAGATGTCTACATTGTCACACCAATTA
Associated Phenotype:
Not determined