ZMP
LOC100330423
Ensembl ID:
Human Orthologue:
C12orf51
Human Description:
chromosome 12 open reading frame 51 [Source:HGNC Symbol;Acc:26611]
Mouse Orthologue:
Gm15800
Mouse Description:
predicted gene 15800 Gene [Source:MGI Symbol;Acc:MGI:3647820]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa41090 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30896 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21158 | Nonsense | Available for shipment | Available now |
sa11121 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41090
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 |
---|---|---|---|---|---|
ENSDART00000086005 | Nonsense | 578 | 1619 | 8 | 23 |
ENSDART00000086005 | Nonsense | 578 | 1619 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 75690788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72193694 |
GRCz11 | 7 | 72546060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATCAGAATGCGACAATGCTCTATTAAACATGAAGCCTGAAGACATGT[T/A]GTGGTTTCACCGGGGGTTGACCTTGCTTTTGATTTTACGGCATCTTACTA
Long Flanking Sequence:
CTCTAGCCACATCACGCTGCTTCTCAACCCCTGCCTAACAGTCCTGATGGTTCTTCAAACCGAACTACGAAAGCTTTACGACCACGAGACCCAAAGCTGGGGGTTGGTTAGCGGAGGATCCTGCACTTCCGCAACAGGCGGCAGTGGAGCGCTTGCACTTTCTGCAGAGCGGAGCCGCTTCTCTACATACTTCCACGCACTGATGGAGGTTTGCCTGGCAGTGGCGGAAGTCACTTTACCGCTGAGTTCTGGTTCTGGGACGTCAGTAATCGGCGTCCCTTCATCAACAAGCACAGCCAACTGCAGTGATTCCTCATCCTCTTCTTCGTCCTCTCCAGGCCAGACGCCGCAAAGTCCGAGTTTGCTTTCAAAGCGCAAAAAGGTGAAGCTAAAACGTGAGCGCGCTGCAGTCGGCTCAGCTTCCGCCGTCTCAGGGAAAAGTGGCTCGAGATCATCAGAATGCGACAATGCTCTATTAAACATGAAGCCTGAAGACATGT[T/A]GTGGTTTCACCGGGGGTTGACCTTGCTTTTGATTTTACGGCATCTTACTAATAAGGACCCGCAAGGTCTTGGCGTCACCGGCGACGCTGTGGCAGACGCTTGCCAAGCTTTGGTTGGCTCGACAGCTCACAGTCGCTTGCTGGTGCTCTCAGGAATCCCGACTCACCTGGAGGAGTCTGTGGTGCGCAATGCAATACGAAGAGCATGCAATGCTCATGGCGGGCTCTTCAGGGATGAGATCTTCATTCCAGTTCAGGAAGAAGACCCTAAAAAAGCCAAAGCGGAAACGACATGTGTTCCTCAAGATGTAAAGAGAGAATGCACTGCAGGAAGCCCCAACAGCAACAGTGCGGCAATGAGTGTCTCCAGCGCTTTACAGGCAGCCTTCAGAGCCTCCGGAGAGCCCTTGTCCAATCAGGAGATGGTAAACAGTCCTTCCCAGCAACAAGCACCTCTGGATCCACTCACAGTGTCCAGTCAGGAGAGTCTGGACGTGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30896
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 |
---|---|---|---|---|---|
ENSDART00000086005 | Nonsense | 578 | 1619 | 8 | 23 |
ENSDART00000086005 | Nonsense | 578 | 1619 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 75690788)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72193694 |
GRCz11 | 7 | 72546060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATCAGAATGCGACAATGCTCTATTAAACATGAAGCCTGAAGACATGT[T/A]GTGGTTTCACCGGGGGTTGACCTTGCTTTTGATTTTACGGCATCTTACTA
Long Flanking Sequence:
CTCTAGCCACATCACGCTGCTTCTCAACCCCTGCCTAACAGTCCTGATGGTTCTTCAAACCGAACTACGAAAGCTTTACGACCACGAGACCCAAAGCTGGGGGTTGGTTAGCGGAGGATCCTGCACTTCCGCAACAGGCGGCAGTGGAGCGCTTGCACTTTCTGCAGAGCGGAGCCGCTTCTCTACATACTTCCACGCACTGATGGAGGTTTGCCTGGCAGTGGCGGAAGTCACTTTACCGCTGAGTTCTGGTTCTGGGACGTCAGTAATCGGCGTCCCTTCATCAACAAGCACAGCCAACTGCAGTGATTCCTCATCCTCTTCTTCGTCCTCTCCAGGCCAGACGCCGCAAAGTCCGAGTTTGCTTTCAAAGCGCAAAAAGGTGAAGCTAAAACGTGAGCGCGCTGCAGTCGGCTCAGCTTCCGCCGTCTCAGGGAAAAGTGGCTCGAGATCATCAGAATGCGACAATGCTCTATTAAACATGAAGCCTGAAGACATGT[T/A]GTGGTTTCACCGGGGGTTGACCTTGCTTTTGATTTTACGGCATCTTACTAATAAGGACCCGCAAGGTCTTGGCGTCACCGGCGACGCTGTGGCAGACGCTTGCCAAGCTTTGGTTGGCTCGACAGCTCACAGTCGCTTGCTGGTGCTCTCAGGAATCCCGACTCACCTGGAGGAGTCTGTGGTGCGCAATGCAATACGAAGAGCATGCAATGCTCATGGCGGGCTCTTCAGGGATGAGATCTTCATTCCAGTTCAGGAAGAAGACCCTAAAAAAGCCAAAGCGGAAACGACATGTGTTCCTCAAGATGTAAAGAGAGAATGCACTGCAGGAAGCCCCAACAGCAACAGTGCGGCAATGAGTGTCTCCAGCGCTTTACAGGCAGCCTTCAGAGCCTCCGGAGAGCCCTTGTCCAATCAGGAGATGGTAAACAGTCCTTCCCAGCAACAAGCACCTCTGGATCCACTCACAGTGTCCAGTCAGGAGAGTCTGGACGTGTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21158
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 |
---|---|---|---|---|---|
ENSDART00000086005 | Nonsense | 588 | 1619 | 8 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 75690818)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72193664 |
GRCz11 | 7 | 72546090 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGAAGCCTGAAGACATGTTGTGGTTTCACCGGGGGTTGACCTTGCTTT[T/A]GATTTTACGGCATCTTACTAATAAGGACCCGCAAGGTCTTGGCGTCACCG
Long Flanking Sequence:
CTGCCTAACAGTCCTGATGGTTCTTCAAACCGAACTACGAAAGCTTTACGACCACGAGACCCAAAGCTGGGGGTTGGTTAGCGGAGGATCCTGCACTTCCGCAACAGGCGGCAGTGGAGCGCTTGCACTTTCTGCAGAGCGGAGCCGCTTCTCTACATACTTCCACGCACTGATGGAGGTTTGCCTGGCAGTGGCGGAAGTCACTTTACCGCTGAGTTCTGGTTCTGGGACGTCAGTAATCGGCGTCCCTTCATCAACAAGCACAGCCAACTGCAGTGATTCCTCATCCTCTTCTTCGTCCTCTCCAGGCCAGACGCCGCAAAGTCCGAGTTTGCTTTCAAAGCGCAAAAAGGTGAAGCTAAAACGTGAGCGCGCTGCAGTCGGCTCAGCTTCCGCCGTCTCAGGGAAAAGTGGCTCGAGATCATCAGAATGCGACAATGCTCTATTAAACATGAAGCCTGAAGACATGTTGTGGTTTCACCGGGGGTTGACCTTGCTTT[T/A]GATTTTACGGCATCTTACTAATAAGGACCCGCAAGGTCTTGGCGTCACCGGCGACGCTGTGGCAGACGCTTGCCAAGCTTTGGTTGGCTCGACAGCTCACAGTCGCTTGCTGGTGCTCTCAGGAATCCCGACTCACCTGGAGGAGTCTGTGGTGCGCAATGCAATACGAAGAGCATGCAATGCTCATGGCGGGCTCTTCAGGGATGAGATCTTCATTCCAGTTCAGGAAGAAGACCCTAAAAAAGCCAAAGCGGAAACGACATGTGTTCCTCAAGATGTAAAGAGAGAATGCACTGCAGGAAGCCCCAACAGCAACAGTGCGGCAATGAGTGTCTCCAGCGCTTTACAGGCAGCCTTCAGAGCCTCCGGAGAGCCCTTGTCCAATCAGGAGATGGTAAACAGTCCTTCCCAGCAACAAGCACCTCTGGATCCACTCACAGTGTCCAGTCAGGAGAGTCTGGACGTGTCTCTGTGTAGCACAGAAAGTCAAGGGAGTCTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11121
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 |
---|---|---|---|---|---|
ENSDART00000086005 | Nonsense | 1442 | 1619 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 75713830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 72170662 |
GRCz11 | 7 | 72569092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
NNNNTGTGTGTGTGTCTGTGTGTGTTAAGCTGGGAGAATAAGGATGTGTA[T/A]GTGCGAGCGGTGCGTGAGCTGCGTCTGCGGGAGCTGCAGAATGTGGAGTG
Long Flanking Sequence:
AAGAATGCTGGAAACCTGTAACCATTGACTTTCATACTATTTGTTTTTTTCCTACTGTGGAAGTCAATGGTTACCGGTTTTCAGCTTTCTTTATCATATCTTAGAAGAAACAAAATCTTAAAGGTTTGAAACTACTAGAGGAAGAAAAAATATTGTGTTAGTGTTTATATTTTTTGGTGAATTATCCGGGCCCTGTTCACGCCTGTTTTTAAAGGGATAGTTCACCTGAAATTGGAAAATGTTGTCATCATTTGACTTTCTTTATTCTGTTGAACACAAAAGAAGATATTTTGAAGAATGCTGGAAACCTGTAACCATTGACTTCCATTGGATTTATGTAATCATTTGGTCTTCAGCTGTAAATTACATCTTAAAGGGCATTAAAGAACCTTGTAATTGCTTTTTGAATGAGTTGCAAAGTTAATGAATGATCTCTAATATTTCTGTGTGTGTGTGTGTGTGTGTCTGTGTGTGTTAAGCTGGGAGAATAAGGATGTGTA[T/A]GTGCGAGCGGTGCGTGAGCTGCGTCTGCGGGAGCTGCAGAATGTGGAGTGTATGTCTGCGGTGCGCGCCGGTCTGGGCTCCATCATCCCACTGCAGCTGCTGACTTTACTGAGTCCCGCAGAGGTGGAGCTGCGCACCTGCGGTCTGCCGGACATCAACCTGGAGTTCCTGAAGGTCAGTTCCAACACAGAAGTAGATATTTTGAAGAATGCTGGAAACCTGTAACCATTGACTTCTATAGGGTTTGTTTTTCCTACTTTATCCCTAAATAATCATGCACTGTTGACTGTAAACTGGCTGTTTAGGCGCACACCATGTATCAGGTGGGTCTGATGGAGACGGATCAGCATATCGAGTTCTTCTGGGCGGCGCTGGAGATGTTCACGCAGGAGGAGCTCAGCAAGTTTATTAAGTTCGCCTGCAACCAGGAGAGGATTCCCTTCACCTGCCCGTGCAAAGATGGGGGTCCGGACACCGCACATGTGCCCCCCTATCCCATG
Associated Phenotype:
Not determined