ZMP
ENSDARG00000078427
Ensembl ID:
Mouse Orthologues:
Gm10891, Gm10893, Gm10909, Gm13896, Gm13926, Gm13979, Gm16591, Gm16837, Gm16940, Gm17015, Gm6037, Gm6683
Mouse Descriptions:
predicted gene 10891 Gene [Source:MGI Symbol;Acc:MGI:3800299]
predicted gene 10893 Gene [Source:MGI Symbol;Acc:MGI:3704436]
predicted gene 10909 Gene [Source:MGI Symbol;Acc:MGI:3642826]
predicted gene 13896 Gene [Source:MGI Symbol;Acc:MGI:3702130]
predicted gene 13926 Gene [Source:MGI Symbol;Acc:MGI:3702147]
predicted gene 13979 Gene [Source:MGI Symbol;Acc:MGI:3651288]
predicted gene 17015 Gene [Source:MGI Symbol;Acc:MGI:4819748]
predicted gene 6037 Gene [Source:MGI Symbol;Acc:MGI:3649172]
predicted gene 6683 Gene [Source:MGI Symbol;Acc:MGI:3704133]
predicted gene, 16591 Gene [Source:MGI Symbol;Acc:MGI:4439369]
predicted gene, 16837 Gene [Source:MGI Symbol;Acc:MGI:4439761]
predicted gene, 16940 Gene [Source:MGI Symbol;Acc:MGI:4439864]
predicted gene 10893 Gene [Source:MGI Symbol;Acc:MGI:3704436]
predicted gene 10909 Gene [Source:MGI Symbol;Acc:MGI:3642826]
predicted gene 13896 Gene [Source:MGI Symbol;Acc:MGI:3702130]
predicted gene 13926 Gene [Source:MGI Symbol;Acc:MGI:3702147]
predicted gene 13979 Gene [Source:MGI Symbol;Acc:MGI:3651288]
predicted gene 17015 Gene [Source:MGI Symbol;Acc:MGI:4819748]
predicted gene 6037 Gene [Source:MGI Symbol;Acc:MGI:3649172]
predicted gene 6683 Gene [Source:MGI Symbol;Acc:MGI:3704133]
predicted gene, 16591 Gene [Source:MGI Symbol;Acc:MGI:4439369]
predicted gene, 16837 Gene [Source:MGI Symbol;Acc:MGI:4439761]
predicted gene, 16940 Gene [Source:MGI Symbol;Acc:MGI:4439864]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39878 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30824 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25116 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39878
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110378 | Essential Splice Site | 17 | 113 | 2 | 2 |
ENSDART00000110378 | Essential Splice Site | 17 | 113 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 36214973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36511683 |
GRCz11 | 2 | 36494140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCATAATAATTCATGTTAATGATATCTACTTTTTCTGTTATACTTTCC[A/G]GTGTGCAGAGGACAAGACAGAGTGGAACAGGTTGAAGGAGAAATGAGTGA
Long Flanking Sequence:
TCAATGAGGATCAATGATTTTTAATGAAACAAGATCTTATATGTGGTGATTTTATAATGGCATGACAGTTCACTAAAAGCACTTGAGCTGGTGTACTAAAAATGAAAAGTCCCTGTGCATATAGCCCATTATTAATCGCTTTCAGAAAATCATGCTTAGTCATTTCTAGTTTTCTCCAGCAGAGGTCATTGTTACTCTCTTCATATATGAGCAGATCTTGTGACAGTATTAAAACATTTAAAGTAGAGCTCAGCTCAGAAAGACAAACCTTCACAGAGTTTCAGAGAGCACAGTTGAGTCCAAATTCTGTTCTTTTACCTCAGAGATTAACTATGTGTACATGGGCTTTCATTTCCCTGTGTTTCTTTGCACATTATGACCGTAAGTACATTTAGATTTTCTGGGCACTTTAACAAAAAAAGTTTGACTGAACACTTAAGTACTGTATGCTTTCATAATAATTCATGTTAATGATATCTACTTTTTCTGTTATACTTTCC[A/G]GTGTGCAGAGGACAAGACAGAGTGGAACAGGTTGAAGGAGAAATGAGTGACAGTGAAGGAAATCATGTTATTATAAGCTGTAATTACAGCACTTCACAAACTGCATATCTCTTCTGGTACAAACAGCTGCCAAACAGATCACCAACATTCATTCTGAGTCAATACAGCGCTGAGGCTGATTTTACAAAGAGATTTTCTGCAACACTGGACTCCAAAGAAAAATCATTTCCACTGACAATCAAGAATCTGCAAGTATCAGACTCTGCTGTGTATTACTGTGCTTTGAGGCCCACAGTGACAGGAAACACAACAACACTGAACAAAAACCTGACACAACTGATTTCATTCCACAAATCTTCCTGTATTATAAACAGAATGTGAATTGTGAATAAAATAAGTATTAAACACATTATTATTTGTCCTGGTCAATATATTTCTGAAAGAGCTGAAGTCTTACTGAAGTTTCCACTCTAATTTCATCTTCATCATTCAGGTAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30824
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110378 | Essential Splice Site | 17 | 113 | 2 | 2 |
ENSDART00000110378 | Essential Splice Site | 17 | 113 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 36214973)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36511683 |
GRCz11 | 2 | 36494140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCATAATAATTCATGTTAATGATATCTACTTTTTCTGTTATACTTTCC[A/G]GTGTGCAGAGGACAAGACAGAGTGGAACAGGTTGAAGGAGAAATGAGTGA
Long Flanking Sequence:
TCAATGAGGATCAATGATTTTTAATGAAACAAGATCTTATATGTGGTGATTTTATAATGGCATGACAGTTCACTAAAAGCACTTGAGCTGGTGTACTAAAAATGAAAAGTCCCTGTGCATATAGCCCATTATTAATCGCTTTCAGAAAATCATGCTTAGTCATTTCTAGTTTTCTCCAGCAGAGGTCATTGTTACTCTCTTCATATATGAGCAGATCTTGTGACAGTATTAAAACATTTAAAGTAGAGCTCAGCTCAGAAAGACAAACCTTCACAGAGTTTCAGAGAGCACAGTTGAGTCCAAATTCTGTTCTTTTACCTCAGAGATTAACTATGTGTACATGGGCTTTCATTTCCCTGTGTTTCTTTGCACATTATGACCGTAAGTACATTTAGATTTTCTGGGCACTTTAACAAAAAAAGTTTGACTGAACACTTAAGTACTGTATGCTTTCATAATAATTCATGTTAATGATATCTACTTTTTCTGTTATACTTTCC[A/G]GTGTGCAGAGGACAAGACAGAGTGGAACAGGTTGAAGGAGAAATGAGTGACAGTGAAGGAAATCATGTTATTATAAGCTGTAATTACAGCACTTCACAAACTGCATATCTCTTCTGGTACAAACAGCTGCCAAACAGATCACCAACATTCATTCTGAGTCAATACAGCGCTGAGGCTGATTTTACAAAGAGATTTTCTGCAACACTGGACTCCAAAGAAAAATCATTTCCACTGACAATCAAGAATCTGCAAGTATCAGACTCTGCTGTGTATTACTGTGCTTTGAGGCCCACAGTGACAGGAAACACAACAACACTGAACAAAAACCTGACACAACTGATTTCATTCCACAAATCTTCCTGTATTATAAACAGAATGTGAATTGTGAATAAAATAAGTATTAAACACATTATTATTTGTCCTGGTCAATATATTTCTGAAAGAGCTGAAGTCTTACTGAAGTTTCCACTCTAATTTCATCTTCATCATTCAGGTAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25116
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 |
---|---|---|---|---|---|
ENSDART00000110378 | Nonsense | 21 | 113 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 36214960)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36511670 |
GRCz11 | 2 | 36494127 |
KASP Assay ID:
554-7837.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGTTAATGATATCTACTTTTTCTGTTATACTTTCCAGTGTGCAGAGGA[C/T]AAGACAGAGTGGAACAGGTTGAAGGAGAAATGAGTGACAGTGAAGGAAAT
Long Flanking Sequence:
ATGATTTTTAATGAAACAAGATCTTATATGTGGTGATTTTATAATGGCATGACAGTTCACTAAAAGCACTTGAGCTGGTGTACTAAAAATGAAAAGTCCCTGTGCATATAGCCCATTATTAATCGCTTTCAGAAAATCATGCTTAGTCATTTCTAGTTTTCTCCAGCAGAGGTCATTGTTACTCTCTTCATATATGAGCAGATCTTGTGACAGTATTAAAACATTTAAAGTAGAGCTCAGCTCAGAAAGACAAACCTTCACAGAGTTTCAGAGAGCACAGTTGAGTCCAAATTCTGTTCTTTTACCTCAGAGATTAACTATGTGTACATGGGCTTTCATTTCCCTGTGTTTCTTTGCACATTATGACCGTAAGTACATTTAGATTTTCTGGGCACTTTAACAAAAAAAGTTTGACTGAACACTTAAGTACTGTATGCTTTCATAATAATTCATGTTAATGATATCTACTTTTTCTGTTATACTTTCCAGTGTGCAGAGGA[C/T]AAGACAGAGTGGAACAGGTTGAAGGAGAAATGAGTGACAGTGAAGGAAATCATGTTATTATAAGCTGTAATTACAGCACTTCACAAACTGCATATCTCTTCTGGTACAAACAGCTGCCAAACAGATCACCAACATTCATTCTGAGTCAATACAGCGCTGAGGCTGATTTTACAAAGAGATTTTCTGCAACACTGGACTCCAAAGAAAAATCATTTCCACTGACAATCAAGAATCTGCAAGTATCAGACTCTGCTGTGTATTACTGTGCTTTGAGGCCCACAGTGACAGGAAACACAACAACACTGAACAAAAACCTGACACAACTGATTTCATTCCACAAATCTTCCTGTATTATAAACAGAATGTGAATTGTGAATAAAATAAGTATTAAACACATTATTATTTGTCCTGGTCAATATATTTCTGAAAGAGCTGAAGTCTTACTGAAGTTTCCACTCTAATTTCATCTTCATCATTCAGGTAATATAAGTGTTATGACT
Associated Phenotype:
Not determined