Busch Lab

ZMP

CXorf57 (2 of 2)

Ensembl ID:
ENSDARG00000036575
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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
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.
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