ZMP
CXorf38 (2 of 2)
Ensembl ID:
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.
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.
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.
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.
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
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