Busch Lab

ZMP

CXorf38 (2 of 2)

Ensembl ID:
ENSDARG00000089227
Description:
chromosome X open reading frame 38 [Source:HGNC Symbol;Acc:28589]
Human Orthologue:
CXorf38
Human Description:
chromosome X open reading frame 38 [Source:HGNC Symbol;Acc:28589]
Mouse Orthologue:
1810030O07Rik
Mouse Description:
RIKEN cDNA 1810030O07 gene Gene [Source:MGI Symbol;Acc:MGI:1916405]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa44323 Nonsense Mutation detected in F1 DNA Not yet available
sa39486 Nonsense Mutation detected in F1 DNA Not yet available
sa44322 Nonsense Mutation detected in F1 DNA Not yet available
sa5108 Essential Splice Site F2 line generated Not yet available
sa38092 Nonsense Available for shipment Available now
sa44321 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44323
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123590 Nonsense 167 1162 4 20
Genomic Location (Zv9):
Chromosome 25 (position 28531530)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 27221624
GRCz11 25 27664826
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTATTAAGGTAATAAATGTACGGAACAATGTGATGCACTCCCCTGACT[T/G]AAAAATGAGCAACGAGGACATGAAAAAGCATCATAGCACAATTCTACTGC
Long Flanking Sequence:
CGTTGGTCCACAGATAAGTGGGAAGTTGCCAAGGTAAGTAATTTTCAGGAATATTACATAAGCCTAATATTATAGTGCTGCCTTTGATTGTTGTCTGTTGCGTATGGGCATGGCTATATTTAGACAAATCGTGGCAGTGCAAAAAATATTGGTCAATTACATTTTTATCTTAATTGTTTGTCTTATGTTTTTTGTAACAGGCGTACATGCCACGTGGGCACAGAGACCATTGTGAGTTTTCCCACTTTGATGTTGCTGCCATTCTGAACTTCATGAACTTCTGTAAACATTTCAGTAAAATTCAAGGGCATCATGTGAGGAATGTAAGCACATATTGCGCCACATATGTAACTTGAAATGCAAATATGTATTTTTTGGAAATCTAGTTTTCAATAATACATAATTCAGCACCAGCAGATGACACATTTTAGACTTACATCATTTCTTTTTAATTATTAAGGTAATAAATGTACGGAACAATGTGATGCACTCCCCTGACT[T/G]AAAAATGAGCAACGAGGACATGAAAAAGCATCATAGCACAATTCTACTGCTGGCCAACATGCTTCAACCTCAGGTTCCAGAACTGAATGGCTTGGAGGAGGAGATAAAACAGGTAGATGAAAAATTAATAGTAATAATAATAATATACTTGGTAATGTTCTATTTTACAATGTCTATGATACACATTCTTACAGTTAGTAAATTATGCAAAATTACATTAAATTTACACTAATTCTAACCAACAAAACCCTAACCCTAAAGTTTTTATTACAGTTTTTCTCAGTGGCTTTGGTGCATTTCTCTCAGCACTAGTTACATTTGCACAACAGTTAATGCATTTCTCAAAAAAATTTATGCAAACTGCAAAACCTGGTTAATAACCTGCAAAAGCGTGTCACTTGCTCAAAATGGATAGCTCATTTCTCAAAAGCAAGTATTCATGTCAATGAAAGTGTCAGTGTCATCAAGATGAAAAGTCCTGCCACCATTGTTTATGAACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39486
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123590 Nonsense 391 1162 8 20
Genomic Location (Zv9):
Chromosome 25 (position 28525266)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 27215360
GRCz11 25 27658562
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATGACAAAAAGGGTGCCCATCAGGAGGTAGCATGCATTGCCCTTGAA[C/T]AGATGAAATCACAGGAAGAAAGCACGAATGAACCATCCAGTTCTGTTATG
Long Flanking Sequence:
AAATCTTACAGCATGCAACTGTCACTGTAAGTGGCATTCAGTATTATTAAGTATTACACAGGTATTTGTCATGGATAAGTTTTACTCATTTTGATTCATTTTGAGTTTAAATGTTTATATGCGAGTGTACTGCAATATTAATTCCATTTAATTTCATTGCTCTTTCATCCACAGATCCATTGCTTCCTGGCATCCCACCTAGATATAAGAATCATCTTTTTGAGTTTTGTCGTGCAAAGAAATGGCTCGAGCCTGTTTTTACAGAGACTCAAGAAGCCCAGGGTATCAAGTGCACCATTTAACATTCAACATGCATATGGAAACAAATAAACATGAATTAAATTATTTATAATCATTAATTCAGGTTAGATTCAACAGTTCACATCTTCTGTACAGGTTATAGGGGTAAGGTGACAGTGAATGGGCAAAGTTTTACTGGCATAAGAGTTTTTAATGACAAAAAGGGTGCCCATCAGGAGGTAGCATGCATTGCCCTTGAA[C/T]AGATGAAATCACAGGAAGAAAGCACGAATGAACCATCCAGTTCTGTTATGCAGCCTGAGACGTCCTGCTCATCTTCCTCAGGTAAAGCAGGAATTTTGTTGACTATTTAATGCACATTGAATAATGATGCACATTCTTGCTTGAAATGAAACTATGATCAGTATGTCATTTTGAAATTTCAGGAATTTACTTTGGCAAAGTAACCGTGGATCTCAATTTAGAAGTTGAGTCAGAAAGATGCCCTTCAGCAGAGGAAGCAAGTGAAGCAGTTTATAAGATTTTATGGGAAAGTTTTCACCTCAGCGCTCCAGTACAAGGTAAATTAATCGGTCACGCTTTACATTACGGTTTCATTAGTTAATGTATTTACTAAACTGAACTAAGTATGAACAATACGTGTGCAGCGTTTATTAATCTTAGTTCAGCATTTAATGATTTCTTGTAAAATCCAGATTCATGCTTGTTAACATTATGTAATGCACCAAGAGTAATCTAACAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44322
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123590 Nonsense 553 1162 11 20
Genomic Location (Zv9):
Chromosome 25 (position 28521805)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 27211899
GRCz11 25 27655101
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTCCAATATCAGAAACGGAAAAGAACTTCAAAGGAATTCTGAAGGAGTG[T/A]CTTGAGACAAGGGGTCTCAAAAGTCCCAACTATACCACTGTGAATAATCC
Long Flanking Sequence:
ATGTTCAGACATCCCAAGTCTCCTTGAAGTTCCTGGAGTCTCTATGCATTTGCATGACTCATAATGCCTGCAAACGAGTGATAATCTCCCAGAAATCGTGCGTCTCCCTCCCGGTCCTCAAATAAGGATCCTTCTCACCCCTGAATCCCTCCTTGCTGTTTAGACACGTCACACCCCCCCATTCCCCCTGTCTTTCACATGATGACGATACCATCATCCATCTTGATGTTTCACATTAGACATCGTACGATGCCAAATTGGTTGACATCGCCCAACCCTACATCACACATTTTTCTTTTCCTTCAGCTTTGTGTGGATTTACAATCTATTGTTTGCTGATCTTTTGTTTTCATTTCTTGGATTATTTTAGATGGCTCCACCAAGAAGAAACTGGCAGATCAACAGGCAGCTAAAGTTGCCTTGCAGCATCTGTCAGGTATTTTCAACTGTGCTCCAATATCAGAAACGGAAAAGAACTTCAAAGGAATTCTGAAGGAGTG[T/A]CTTGAGACAAGGGGTCTCAAAAGTCCCAACTATACCACTGTGAATAATCCAGAGATTAGTGAAAAACAGGTGGCCATGAGCATCAGCCCAGACCTGACAAATTCTGCAGCATCTATTACTCAGGCAGCAGAGAAAGAGCATTCAGAGCTCAAGTCTGGCAACATTTGCAAATCAGCACAGCTTCCGGTATTTCAAGAGGCAGCTTGTATTCCTGTTCCTATGCTGCCAGACCCTCAAGACTCCAGTTCTCCAGCTGTAGTAAGGAAAAAGCCCAGGATTGATTGTCTAGGTAAAGCCTTCTTTATACTTTCATCTAGCATCCCACACAACTCCGCAAACTGCACACCCAGTTTGGAGATGTTTGTATTGTTTTACATTTTTTTTTTTAAACAGAACGGATTGGTCATAGTGTAGAGCAGTTTTTATTATCAACCGGTCAATGCTTGACAATTTTACCGCTACATGGGATGGGGGGAGGGGAAGTGTGAACGTAGCTTGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5108
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123590 Essential Splice Site 987 1162 None 20
Genomic Location (Zv9):
Chromosome 25 (position 28502049)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 27192143
GRCz11 25 27635345
KASP Assay ID:
554-3534.1 (used for ordering genotyping assays)
KASP Sequence:
TACTGTTCACTAAAGAACATAAATTACACAGTTGACTATGACGGAGAAGG[T/G]TAGTATTTTTGTCTGATGTCACAATAACTGGTAYTTRTTTAAAAGTTTGG
Long Flanking Sequence:
TGATCCTCCATAGTCCAGAGAGATACAAAAATGCCTCTGAACAGTCCATGTGTCTACAGTGGTTCAAACCAAAGAATTATTGTAGCTTGTTTATAATCTGACTGAACCACTGAAGGCATATGATCTGTTATAAAGATGTTTTTGATGGTCTACAGAGAGAGAGAGATCAGGGAGATGTTATCCAATATATCTTTATTTGTATTCTGAAAATGAACAAGGGTCTAAGGTGTTGACATGAAGGAGGGTGAGCAATAAATAATCTCAATTTCATTTTTGAGCCATTTAACTATTTAATGAAATGTATTTTTATGAATGACCCTTCAACTAATGCTTATTTCTTTGCCTTGAATTCAAGATGAAAAGACATCGATTGCTATGGTGAAGATGCGTTTTTCTCAGAATTCTCTTCCTCTCCCCCAGGAAGATGTTGAAGGTTCTTCAAAGTTGTTTTACTGTTCACTAAAGAACATAAATTACACAGTTGACTATGACGGAGAAGG[T/G]TAGTATTTTTGTCTGATGTCACAATAACTGGTACTTATTTAAAAGTTTGGAATACATAACGATTTAGGAAAAAATTATGAGTAATGGATCTAAATCCAGCTCTTTAATTATATAACAAACATAAAGTGCTGCATTTAGAGTAGTTTCTGCTTGTTTTTCTTGACTTGTTGTGATGCAGTACAAAACCCACTGTTAGGAATACTCTCAACACTTTTCAGAGTTGGTGGATCTTTGTCCTTTTTTGTTTCATAACTGTCTGAGGTAACATAGTGCAGTGCATTTCAAGAAGAATCTGGTCTATCATTCAACTATGTTTCAAACAGTAATAGTATAGAAAATATGATCACATAAGAAACCATAGCTCTGGATTCAGTGTGTTAATTTTTAAATTTTTTGAAAAATACTCACTAGAAGCTTGCGATTCAATTTTTGTGTACTGCAGTGGAAAAAGAAAAACGGACCATATCACTATAGCTTTAGGTCATCACATACATTTAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38092
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123590 Nonsense 1056 1162 18 20
Genomic Location (Zv9):
Chromosome 25 (position 28500009)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 27190103
GRCz11 25 27633305
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTTTCCCTGGTTGTTATGAACAAGGCCTGTGTCCAGCTGTCTTTCTG[T/A]GACTATACAATGAAGTGCACATGCCAAAGTACGAAGAAAGCAGCTCGAAA
Long Flanking Sequence:
GAAATTAAGGCAATTTAAAAGCAAAAAGAAATTGGAAAAAAACACAAGGACTGAAGAAAACAGCAAAACATCTAAATAAATGTCTATGGAACAGAAATCTGACATTGGTTTAGTAAGTATTGCAAAAGGATGCATTTTAGCCGATTAAAATTTTAATAAATCTAATTTATTTTGTTTGCAAAAAAAAAAAAAGCACATCTTTATTGCATAGCAGGCATATACTCTGTAAGTGTGCCACAAATATATAACCTTAACGCATTAACCACATTAAACATGACATGGTTCTTTTTAGGGTCCTCAGAGGATGAAGCCAAGTTGCTTGCTCTCCAGAAAGCCTTACGTTTTCTATCACCACTTTTTAATTATCCTTCCCTACCTGGAGCTGATCATCCTGAAGAGGTTCTGAATCAGTTGAGCTCTATCCTAAAGGGAGCCAGTCAGAAAGATCCTATTGTTTCCCTGGTTGTTATGAACAAGGCCTGTGTCCAGCTGTCTTTCTG[T/A]GACTATACAATGAAGTGCACATGCCAAAGTACGAAGAAAGCAGCTCGAAATCATCTCAGTGCACGAATACTGGGACTGCTAGGGATAGAAACAGGTCAGAGCAATAGAATTTCAACAAGTTTGTCTTTTTTAAAGCTTATTTTTTTATTTTAATTCAGTGATTTCAATTCTGTTCTGTAATTTATGCAGATGCAAACAACGCAAATTTGAAAAACCAATTGGATGTGTGGTTCACAAAGAATAGCCCGCCAAAACCAGTGTTTGAGGACACAGAAGTGACTGGAGCAAAGGCTACTTTCTCTGTTCAAATAACCAGCTGCAGTCCAGGTAAGCATTCTTACATGTCACGGACACTTCCAAAACAATGAATATTTAATACAATTTCATTGTATATAAATATTTAATTACTAATAAGGTACTTTTCTCAAAAAAATACATATTTATTACCATCCTCCGAAAAAAAAAGTGTTCTCACAAAATGTCTTGTGTGAACACAAAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44321
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000123590 Nonsense 1065 1162 18 20
Genomic Location (Zv9):
Chromosome 25 (position 28499984)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 27190078
GRCz11 25 27633280
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCTGTGTCCAGCTGTCTTTCTGTGACTATACAATGAAGTGCACATGC[C/T]AAAGTACGAAGAAAGCAGCTCGAAATCATCTCAGTGCACGAATACTGGGA
Long Flanking Sequence:
AAGAAATTGGAAAAAAACACAAGGACTGAAGAAAACAGCAAAACATCTAAATAAATGTCTATGGAACAGAAATCTGACATTGGTTTAGTAAGTATTGCAAAAGGATGCATTTTAGCCGATTAAAATTTTAATAAATCTAATTTATTTTGTTTGCAAAAAAAAAAAAAGCACATCTTTATTGCATAGCAGGCATATACTCTGTAAGTGTGCCACAAATATATAACCTTAACGCATTAACCACATTAAACATGACATGGTTCTTTTTAGGGTCCTCAGAGGATGAAGCCAAGTTGCTTGCTCTCCAGAAAGCCTTACGTTTTCTATCACCACTTTTTAATTATCCTTCCCTACCTGGAGCTGATCATCCTGAAGAGGTTCTGAATCAGTTGAGCTCTATCCTAAAGGGAGCCAGTCAGAAAGATCCTATTGTTTCCCTGGTTGTTATGAACAAGGCCTGTGTCCAGCTGTCTTTCTGTGACTATACAATGAAGTGCACATGC[C/T]AAAGTACGAAGAAAGCAGCTCGAAATCATCTCAGTGCACGAATACTGGGACTGCTAGGGATAGAAACAGGTCAGAGCAATAGAATTTCAACAAGTTTGTCTTTTTTAAAGCTTATTTTTTTATTTTAATTCAGTGATTTCAATTCTGTTCTGTAATTTATGCAGATGCAAACAACGCAAATTTGAAAAACCAATTGGATGTGTGGTTCACAAAGAATAGCCCGCCAAAACCAGTGTTTGAGGACACAGAAGTGACTGGAGCAAAGGCTACTTTCTCTGTTCAAATAACCAGCTGCAGTCCAGGTAAGCATTCTTACATGTCACGGACACTTCCAAAACAATGAATATTTAATACAATTTCATTGTATATAAATATTTAATTACTAATAAGGTACTTTTCTCAAAAAAATACATATTTATTACCATCCTCCGAAAAAAAAAGTGTTCTCACAAAATGTCTTGTGTGAACACAAAAATGAAGCATTACAATATACTTTATAT
Associated Phenotype:
Not determined