ZMP
CXorf57 (2 of 2)
Ensembl ID:
Description:
chromosome X open reading frame 57 [Source:HGNC Symbol;Acc:25486]
Human Orthologue:
CXorf57
Human Description:
chromosome X open reading frame 57 [Source:HGNC Symbol;Acc:25486]
Mouse Orthologue:
D330045A20Rik
Mouse Description:
RIKEN cDNA D330045A20 gene Gene [Source:MGI Symbol;Acc:MGI:2147848]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31560 | Nonsense | Available for shipment | Available now |
sa20896 | Nonsense | Available for shipment | Available now |
sa34034 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31560
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 |
---|---|---|---|---|---|
ENSDART00000053138 | Nonsense | 396 | 809 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 20571319)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19161755 |
GRCz11 | 7 | 19413723 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGTCAGAGATGGAGGAGTATCGCTGGATCCAGATGGTGGACCGGACAT[C/A]AGACCAGCCAATCATGATCAAACTTTTCTCCACATCACAGCCTGATGTTC
Long Flanking Sequence:
GAGTGTGAAAGTGTATGGGCATTTCCCAGTACTAGAATGGCATCCACTGTGTAAAAGATATGCTGGAATAGTTGGTGGTTCATTCCGCTGTGGCTGAAAGAATAAAGAATAATTAGCTTTTGGAGTTAAAGGTATAACTTTGCAAGTCTTTTTCATGCTTAAACAATAACATTACCCACTTAAGGAAGTTTGATATGAAAAGCGTAATATTACCTTTAAATATAAATCAATTGCTTGTACAACACAGAGAAATGCATTAGTGATCATGTCTTGCAGACAGGAGATTTCTAGTTGCCCAGAAGGCCACATCTGTGATGTCATTGGTGTGGTGATCTTTGTTGGTCGTTCAGAACGAAAGGTCAAAAGGAAAGGTGAGATGCAAACAGAGAAATGATTATTACATGTATATTTAAATAACGGACTGAACAAATTTCATCTTGCAGATGGGCAGAGGTCAGAGATGGAGGAGTATCGCTGGATCCAGATGGTGGACCGGACAT[C/A]AGACCAGCCAATCATGATCAAACTTTTCTCCACATCACAGCCTGATGTTCAGAGCCGCATCTCTCCAAGTATGACAACAGACTGTTTTCTCTTTGTCTGTATTAAAGACACACTTTAATTTTTTGCTTTCTTTTCTTTAATTCAGTGGCACTGGTTGTCTGCACCAGATTAAAGCTCATCAGAAGTGCAGTTGACGGAGCTACAACTTTTGATTATCTCACCAACACCTCACTGACCCAGGTTTACTGCACAGGTAAATACCATGCTTTAACACACAGGTATCAAATCCAGTTCCTAGAGAGCCACAGCCGTGCACAGTTTAGCTTTAACCCTACTTAAAAACACCTGATCAGACTAACAGAGTCCTTAAGGCTTGTTTGAAACCTACAGGTAGGTGTGTTGAAGCATGGTCAGAACTAAACTCTGCAGAGCTGCGGCCCTCCAGGAACTAGATTTGACACCTGTGCTTAACACTTTTGTAGATCAGACATTTCATATGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20896
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000053138 | Nonsense | 398 | 809 | 6 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 20571314)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19161750 |
GRCz11 | 7 | 19413718 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAGATGGAGGAGTATCGCTGGATCCAGATGGTGGACCGGACATCAGAC[C/T]AGCCAATCATGATCAAACTTTTCTCCACATCACAGCCTGATGTTCAGAGC
Long Flanking Sequence:
TGAAAGTGTATGGGCATTTCCCAGTACTAGAATGGCATCCACTGTGTAAAAGATATGCTGGAATAGTTGGTGGTTCATTCCGCTGTGGCTGAAAGAATAAAGAATAATTAGCTTTTGGAGTTAAAGGTATAACTTTGCAAGTCTTTTTCATGCTTAAACAATAACATTACCCACTTAAGGAAGTTTGATATGAAAAGCGTAATATTACCTTTAAATATAAATCAATTGCTTGTACAACACAGAGAAATGCATTAGTGATCATGTCTTGCAGACAGGAGATTTCTAGTTGCCCAGAAGGCCACATCTGTGATGTCATTGGTGTGGTGATCTTTGTTGGTCGTTCAGAACGAAAGGTCAAAAGGAAAGGTGAGATGCAAACAGAGAAATGATTATTACATGTATATTTAAATAACGGACTGAACAAATTTCATCTTGCAGATGGGCAGAGGTCAGAGATGGAGGAGTATCGCTGGATCCAGATGGTGGACCGGACATCAGAC[C/T]AGCCAATCATGATCAAACTTTTCTCCACATCACAGCCTGATGTTCAGAGCCGCATCTCTCCAAGTATGACAACAGACTGTTTTCTCTTTGTCTGTATTAAAGACACACTTTAATTTTTTGCTTTCTTTTCTTTAATTCAGTGGCACTGGTTGTCTGCACCAGATTAAAGCTCATCAGAAGTGCAGTTGACGGAGCTACAACTTTTGATTATCTCACCAACACCTCACTGACCCAGGTTTACTGCACAGGTAAATACCATGCTTTAACACACAGGTATCAAATCCAGTTCCTAGAGAGCCACAGCCGTGCACAGTTTAGCTTTAACCCTACTTAAAAACACCTGATCAGACTAACAGAGTCCTTAAGGCTTGTTTGAAACCTACAGGTAGGTGTGTTGAAGCATGGTCAGAACTAAACTCTGCAGAGCTGCGGCCCTCCAGGAACTAGATTTGACACCTGTGCTTAACACTTTTGTAGATCAGACATTTCATATGCAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34034
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 |
---|---|---|---|---|---|
ENSDART00000053138 | Essential Splice Site | 513 | 809 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 7 (position 20568227)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 19158663 |
GRCz11 | 7 | 19410631 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCCACCTCTTCCTGTTTCACTGCATTATTTCATGGAGAGCAAACAAAG[T/C]AAGGAAGCACAGATATATACAAAAATATGTGTTTTTGGATTGAATGATGC
Long Flanking Sequence:
CAATAAATAAATATTTACACACTATTTATTCACTCTCAAGTGAATAAATTTCTCTCTCTCTAAATTTCACACTCAAATTTCTGTATTGTGTTGAACACAAAAGAAGATATTTTAAAGAAAGCTTTAACCATTGAATTTCATAGTAGGAAAAACAAGTGCTATGAAAGTCAACGGTTACACACTTCCAACTTTCTTTAATCTATTTTTTGTGTTCATAAGAAAAAATTAGGACAGACTTTGGAATAACTATCCCACACATTTACAGTATGTGGAATTAGATGAATCCAAATAATTTCCAAAAAACTATTTTCAAATATTAAAACAGGTACAGGGTCTCGCCCTGTGATGCCATACAGGGGCATACGGCCCATCCGACGGTTTCTCCACTGGCTGAGGCAGGTGGATGAGAGGAGTCTGCTGGACAGAGCTGTGGTTGGTGGATATTTCAGCTACCCACCTCTTCCTGTTTCACTGCATTATTTCATGGAGAGCAAACAAAG[T/C]AAGGAAGCACAGATATATACAAAAATATGTGTTTTTGGATTGAATGATGCATGTAGTGATGTCTGTATTTTCAATGTGCCTGTGAAGGAGAAGCTGGTCTCATCAGCGGAGGAGAGATGAAATTAGAGTGTGAGAAGTTAAATTATAGAGAAAAGCAGCGGTTTGCTATTCAGTGTGTGATCACTGCAGCCTGCTACCATCATCGAGAGGTACACGCATACAGTATATACATATATGGTGGGCCATTTATATATATATATACACCTTAATAAAATGGGAATGGTTAATGATATTAACTTCCTGTTTGTGGCACATTAGTATGTGTGAGGGGGCTTGTAAATAACTCATGAAAGAATAAAGCACATCATTGTTTTTCTTGTGAAATTTCCTATAAGTTTATTCAGGTGTATACATATAAATGGCTCACCCTGTAGATTAACAAACCACACAGACAAAAACAAAATGAACATTTAAAGGGGATAGTTTAACATTTATTCTTC
Associated Phenotype:
Not determined