ZMP
si:dkey-21k24.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A2BG06]
Human Orthologue:
C11orf41
Human Description:
chromosome 11 open reading frame 41 [Source:HGNC Symbol;Acc:24836]
Mouse Orthologue:
D430041D05Rik
Mouse Description:
RIKEN cDNA D430041D05 gene Gene [Source:MGI Symbol;Acc:MGI:2181743]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15271 | Splice Site, Nonsense | Available for shipment | Available now |
sa38030 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa18639 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15271
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 > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090397 | Splice Site, Nonsense | 178 | 1319 | 3 | 23 |
ENSDART00000143141 | None | None | 899 | None | 19 |
Genomic Location (Zv9):
Chromosome 25 (position 15765582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 15312126 |
GRCz11 | 25 | 15408526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTCCTCAATCTCACTCCCCTCACRYAAAACCTTCTCTGCTTTYAGAC[G/T]AGACTCTTAGYGAATTCCCCAGGAACCCTGATCTACCCACTGCCCCGGGC
Long Flanking Sequence:
CAGTACATTTTCAGACTGAGCCTGGGTTGGACACAAGCCTTTTACAACTGCATTTTATGATATAATAATAAATAATTTTTACACTGGATTTACACTGCTATTTTAAATGAACTCTAATTGGTTTTGTTAAGCAGTCAATGCCTTCGGACTATCAAGATGTGTTTATGTTTGTGTTTTCTAAAGTGTCTGACATACTCAATAACACTCGTCTTGTGCATTGTTAAACTTTAAATTATGATGCTCTCATAGATCACACACCCCTACACTGAATCTGCTTGTCCGAGTAATAGAAAAATAAAACTCAAAATCATGTTATATTCTGTTTTATGATGCAAGTGGTGCAAAAAATTACACACTTCAACAAGTCCTGTCACTGAATAATCCCCCAAGCTACATCCGTCCTCTCCCACATGTCCTATGTGTCATTCCTCACCATCAGCGAGCATCATGTGTGTCCTCAATCTCACTCCCCTCACACAAAACCTTCTCTGCTTTCAGAC[G/T]AGACTCTTAGTGAATTCCCCAGGAACCCTGATCTACCCACTGCCCCGGGCTCCTCTTTCACAACTCTGGCAGAGACAGACGCCACCCTCACAGACAATGTGACTACTTCAGCCTCTATTTCTGCTTCTAACGCCACTTCACCTGAAAGACCTGAAAATGGTTCATCTGCTACTACAGTACAAAGCAACTCTCACACTGTGACCAGCGACAGTCTCCAACTCACCACAGTGACCACCACGACTGTCACTCCCTTAACTGTGACATCCATGACTGTGACTCCACCCACTCCGGTCGTCATGGTGAAAGAGGTCGAAACCACCATGCCGACTACAACAACCACCCAAACCACAACAACTGAGACAGAACCACCAACAACGAGTACCACCACCACCACTACAACAACTACTACCACCACAACCACAAAAGTAGCACCAACAACTACCAAACCCCCCACAACCACGTTGGCAACTACCACCACAACGACGATGACGACTCCTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38030
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 |
---|---|---|---|---|---|
ENSDART00000090397 | Essential Splice Site | 492 | 1319 | 5 | 23 |
ENSDART00000143141 | Essential Splice Site | 86 | 899 | 2 | 19 |
Genomic Location (Zv9):
Chromosome 25 (position 15781693)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 15328237 |
GRCz11 | 25 | 15424637 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGCTTCATGGCTACCCACCCTCGGCATCCACTTGCAGCTCAAAACAG[G/A]TGAGACTCTTTTCCATCTGTCTTTTTTTTTTCTTTTTTTGATATTGCCTT
Long Flanking Sequence:
GATCAACTGGAAGTCAAGTTATTATTTGTTGTTTCTAAAACCTAAAACAATTAATAGAATGTTTTAGAAAAACAGTTTTAGTTAGATTTTTTTGGTAACATAAGTGTCTATCTGTACAATCACTTTTAATAAATGAACAAAATCGACTAAAGATATTAATTTCTTATTGAACATTTGTGTACATTCTTAAAATTTATTTATGGGACTACTCTAAAAAATTGCCAAAGATGTGATAAAAATGGTGGAAAACATTGTATGTGATCATTGTTCTCTCTAGATGGAAAAAGACATCTGCACTCCTTCTAATGTGACTGTGGGCTACTTCGTCATGAGAGGGAAGGCTGTGCTCGTGGCGTCGGTTGTAATAGACACTTTAGTTTCCTATGGCTTTGACAAGATATTGACTGATATCAGAGAGTATGTTCCTGTGGTATTGGCCATCCCCAATCCAGTGGCTTCATGGCTACCCACCCTCGGCATCCACTTGCAGCTCAAAACAG[G/A]TGAGACTCTTTTCCATCTGTCTTTTTTTTTTCTTTTTTTGATATTGCCTTTCATGTGAATAGATCAGTGAACATGATGAATAGAGTTATTGATTCCAAATAGGAAAAAAAAAACTGATTTTGTACAACAAAAAAAAACATCAACCTTTTTTGTATCCCAACATCTATTCATTTTGACGATATAATGAAAAGAATTGTGAAAGGAGGTGCGGCAGTTGCACAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTTGCTGGGTTGCTGGTTTGTACCTTGGCTCAGTTGGCGTTTCTGTGTGGAGTTTGCATGTTCTCCCTGCCTTTGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCAAAAGACATGCAGTACAGGTGAATTGGGTGGGCTAAATTGTCCGTAGTGTATGAGTGTGTGTGTGTGTAAATGTTCCCCAGTGATGGGTTGCGGCTGGAAGGGCATCCGCTGCGTAAAAACTTGATACATCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18639
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 |
---|---|---|---|---|---|
ENSDART00000090397 | Nonsense | 1294 | 1319 | 21 | 23 |
ENSDART00000143141 | Nonsense | 876 | 899 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 25 (position 15835238)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 15381782 |
GRCz11 | 25 | 15478182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCGTCCTCTCTCCACCGTCCTCGTACCGCAGCCCGTCCTGGATGTCCTA[C/A]CCTCCAGAACCAGAGGACCTTCCGCACCAGTGGAACGACACAGTAAAGGC
Long Flanking Sequence:
AATATAATATTTTATTGTGTCTTTTTTTTATATATTTTTAAGTGTATAAAATATTGTCTTTTCTCATGTATTAAACCATGGTAAAAATCATTTTATGTGGGCCATGACATGTATGATGTTTGTGATGTGTACCATATACCAATTTACTTTTTTATCCATCATGATTTTTTTACATGTACCATGGTAACAATGCTTTTTATTACATGTACCATGGTAATATAATCATCTTTGACATTGTATTATAGCAATAGCATAGGGTTTTCACATGTATAACAAAATAAAACAAACAAAAAATGCTGTGTTTTTTTTGGAACACTAATATAATGCTAATATCGCATCTTGAATGCATTTTAAACTAATATTTTTGTCTATCGTTTTTATCATGTTACAGGAAACCCAATGACAGCAGTATATGCCATATCTGCCAACCGGCCCGGGTACTCGGACTACTTCGTCCTCTCTCCACCGTCCTCGTACCGCAGCCCGTCCTGGATGTCCTA[C/A]CCTCCAGAACCAGAGGACCTTCCGCACCAGTGGAACGACACAGTAAAGGCAAGCTCTGCTTCTGTTTATAGTTCCGTCAACATGACTAAACCTACCCGATGTCTGCTAACACATCTGGTACTGTGACCTTATTATGTCTTCTGATTATGCTTTAAGAGTGAATAGTCCACCTCTGGGTTTCTGTATTGTCTCTGCTGTGTCATTTTAAACTGAAATGTTTTTGTTATGTTGATCTTTTTTCTTTTCTTTACAGAACCAGTGTCACCTGGAGACCATCTGCTGAACTGGAGTTATTTCTGATGTTGAGCAGACACAGAATTTTAACAGGGTACTGGTACTTTTAGATATTTTGGCACTTTGCTTTATGGATTTTGTAAATCATATTGTAGCTGATGAGCAACTTCTTATGGATGGTTTTAAAAATTATCTGAAATTTCATATTGCACATTAACCAAAAAAAAAAGATATAAAATATATTTTTTAATGATATATATTTTTAT
Associated Phenotype:
Not determined