ZMP
C12orf51 (1 of 3)
Ensembl ID:
Description:
chromosome 12 open reading frame 51 [Source:HGNC Symbol;Acc:26611]
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 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa14065 | Essential Splice Site | Available for shipment | Available now |
| sa41086 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa7110 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa38657 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21151 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14065
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108874 | Essential Splice Site | 450 | 1044 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 74651776)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 72238270 |
| GRCz11 | 7 | 72501484 |
KASP Assay ID:
554-7922.1 (used for ordering genotyping assays)
KASP Sequence:
TTRAAGCACWTTTTTTGGTTTATATGCAGTTGGTTTGTTTTGTGACTCAC[A/G]GAATAAAATGAAGGAGCTGGAGCTTCTCTGTTCGCTRAAGGAGGTTCCTC
Long Flanking Sequence:
GACTTTAGCTTTTAAAAAGACACGCCAGAATAAGTATATTTCTGTAAAGCACGGCAAAATAGGATTGAAACCATTATTTAAAATGCAACACATTAAGTAATGTCGTAAAGTAAAGTAAAAATTTGGTTGATAATAAAATATTTGCTAGTAGGACTCAACACTTGTGAGCACTCACTCCAATGGGTTTGCGCAGCTCTCAGTCCCGCCCACACTCGTCAGCCCTACCAAGCTGACCAATCACAAAGCTTGCGCTACGCGTCATTGCGACATGTAGTTGCATTTTTTGAGAGGTGCGCGTCAGCATCAGCGATGGCCAGGGCGAGGACTACGCAGAGGCTGTGCCTGACCATACGCGCACGCTTGATGCAGAAGTATAAATCAGCCTCAACTTAGGCACAAACTGTAAAGGCTCCGCCCTCTTCTTGAAAAGGGGTGGGGCCAGCTGCTCCTTTGAAGCACTTTTTTTGGTTTATATGCAGTTGGTTTGTTTTGTGACTCAC[A/G]GAATAAAATGAAGGAGCTGGAGCTTCTCTGTTCGCTAAAGGAGGTTCCTCTGGACTGCACTGATCCAGAAAACGCTGTGATGGCTTTGAGGTTTGAAATGCAAATGATACAAATTGAATAATTAGAATAAATCAGTTTGGGGTCAAAGAGATTAATATAATATGAAAAAAGATTTTTTTTTTTCACTCATATTTTCCAGATTACTGAACTTTTGAATATTAGTGTTTGTGTTATTGCCGTTTGAATTAATAGTAATGTGTTTTCTTATTTTTTCAGAGAGAAGTTTTTTCATGAGGTGAACTCCACGCTGCAGCAGCAGAGAAGTGTTGTTCCTCTGGCTAAAACCAAAGCGCTTGTGAAGAGTTTGATCAACCGCTCGGAGCTGCTGCTTCATGTCACCATCGCTCCGCAGTGCAAGAGTCTGTCATCAACACCCACAAGCACACCGGGTAACACACACACACACACACACACACACACACACACACACACACACAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41086
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 |
|---|---|---|---|---|---|
| ENSDART00000108874 | Nonsense | 716 | 1044 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 74645488)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 72231982 |
| GRCz11 | 7 | 72507772 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGGAGGCGTTTGGAGAGACCATGACGTCAGTGGTGTCTCTGTGTGCC[C/T]GATACCCCATCGCCTGTGCCAACAGCATCGGCCTGCTCTGCACCATCCCC
Long Flanking Sequence:
CAAACAGGCTCTGGTTCACATGCGGGAGCTGCTGACCGCTGCCGTCCGCGTCGGTGGAGTCACTCATCTGGTCGGACCCGTCACTATGGTCCTGCAGGGGGGACCCAGGTACTCTTACACCACCACAACATCACAAATCAGCATTCACTATAGGGCTCACTGTGAGGAAATGCATGCTTTTATTTGAATACAGCGCATCTAAAGTGACCCGTCTAAAGGCATGTCTAATTTCTGTTTCACATAGGTCAAATCTTTTATGATATTACTGTATTTTTTTATTAAATAAATGCAATCTAAGTGTAACTTAGAAAAACACTCATAGTCTAATCATGTGTGTGATATTTTAATGCAATACAGCTAGACTGGCAGATGCTCATATTGTCGATGCGTGCGTGTGTGTGTGTGTTTGAAGGGTGGAGGAGCTCACCTGTGGTGGGATGATGGAGCAGGTGCAGGAGGCGTTTGGAGAGACCATGACGTCAGTGGTGTCTCTGTGTGCC[C/T]GATACCCCATCGCCTGTGCCAACAGCATCGGCCTGCTCTGCACCATCCCCTACACCAGGCAAGCACAATGATGCAACACGGGAGAATTCATGAACGGGAGGGAAGAGACATAGCTGACACTGGTGCAGTGGGTCACATGATAATGACTAGTGGAAGATGGAGAACATCCCAATTCCATTCACACTACTCGCATTCATGCTATATAGCACAGGTGTCAAACTCAGTTCCAAAAGGGCCGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAGGTAAGTGTGTTGGAGCAGGGCTGGAACTAAACTGTGCAGGGCTTCGGCCCTCCAGGAATTGAGTTTGACACCCCTGCTATATAGAACCTTCATTTCTAGCAATCGTGTAGTTAGTTGAGATCCATATGTGATACATACTTGAGTGGTAGGCCATTTGTTGATTCTCATGTGTTGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7110
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 |
|---|---|---|---|---|---|
| ENSDART00000108874 | Nonsense | 748 | 1044 | 16 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 74644943)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 72231437 |
| GRCz11 | 7 | 72508317 |
KASP Assay ID:
554-5052.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTTCTCCGCAGGAGTGAGGAGCAGTGTCTGGTGCGCAGCGGTCTGGTT[C/T]AGCTCATGGATCGCCTCTGCAGTCTGAGCAGTCAGAGAGACTGCAGCTCC
Long Flanking Sequence:
ATCCCCTACACCAGGCAAGCACAATGATGCAACACGGGAGAATTCATGAACGGGAGGGAAGAGACATAGCTGACACTGGTGCAGTGGGTCACATGATAATGACTAGTGGAAGATGGAGAACATCCCAATTCCATTCACACTACTCGCATTCATGCTATATAGCACAGGTGTCAAACTCAGTTCCAAAAGGGCCGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAGGTAAGTGTGTTGGAGCAGGGCTGGAACTAAACTGTGCAGGGCTTCGGCCCTCCAGGAATTGAGTTTGACACCCCTGCTATATAGAACCTTCATTTCTAGCAATCGTGTAGTTAGTTGAGATCCATATGTGATACATACTTGAGTGGTAGGCCATTTGTTGATTCTCATGTGTTGTTCTCCGCAGGAGTGAGGAGCAGTGTCTGGTGCGCAGCGGTCTGGTT[C/T]AGCTCATGGATCGCCTCTGCAGTCTGAGCAGTCAGAGAGACTGCAGCTCCAACGAGAAGCAAACCAAAAAGCAGAAAGTGGCCACCATGGCCTGGGCTGCGTTTCAGGTGCTGGCCAACCGCTGCATTGAGTGGGAGAAAGTCGAAGGTGAGGGACGGGAAGGCCATATGCTGAAATTTCAGCTCTCCGGTGAAACTTGTACTATTTTAAAAAAATTTCTCAAGTGGTGTTTAATAGTGGGAAGGTTTTTTTTACACATAATAGTGCCAATAATGATTTTCTAATTTCATTTATGTGTATTAAATGTCTTTCTCATGATGACAGTGTGTAATATTTTACTATAATTTTGCAAGATCAGTTTAAGGGGCAATTTAAATGCTTAACTAGGCAAGTTAGGAGAATTGGTCATTGGACAACAGTGGTTTGTTCTGTAGAAATGCTCCAAAAAAAATCCTAAGGGGGCTAATAATATTGACCGTAGCAGTTTTTATATTTTTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38657
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108874 | Essential Splice Site | 797 | 1044 | 16 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 74644794)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 72231288 |
| GRCz11 | 7 | 72508466 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTTTCAGGTGCTGGCCAACCGCTGCATTGAGTGGGAGAAAGTCGAAGG[T/C]GAGGGACGGGAAGGCCATATGCTGAAATTTCAGCTCTCCGGTGAAACTTG
Long Flanking Sequence:
TCATGCTATATAGCACAGGTGTCAAACTCAGTTCCAAAAGGGCCGCAGCTCTGCACAGTTTAGTTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAGGTAAGTGTGTTGGAGCAGGGCTGGAACTAAACTGTGCAGGGCTTCGGCCCTCCAGGAATTGAGTTTGACACCCCTGCTATATAGAACCTTCATTTCTAGCAATCGTGTAGTTAGTTGAGATCCATATGTGATACATACTTGAGTGGTAGGCCATTTGTTGATTCTCATGTGTTGTTCTCCGCAGGAGTGAGGAGCAGTGTCTGGTGCGCAGCGGTCTGGTTCAGCTCATGGATCGCCTCTGCAGTCTGAGCAGTCAGAGAGACTGCAGCTCCAACGAGAAGCAAACCAAAAAGCAGAAAGTGGCCACCATGGCCTGGGCTGCGTTTCAGGTGCTGGCCAACCGCTGCATTGAGTGGGAGAAAGTCGAAGG[T/C]GAGGGACGGGAAGGCCATATGCTGAAATTTCAGCTCTCCGGTGAAACTTGTACTATTTTAAAAAAATTTCTCAAGTGGTGTTTAATAGTGGGAAGGTTTTTTTTACACATAATAGTGCCAATAATGATTTTCTAATTTCATTTATGTGTATTAAATGTCTTTCTCATGATGACAGTGTGTAATATTTTACTATAATTTTGCAAGATCAGTTTAAGGGGCAATTTAAATGCTTAACTAGGCAAGTTAGGAGAATTGGTCATTGGACAACAGTGGTTTGTTCTGTAGAAATGCTCCAAAAAAAATCCTAAGGGGGCTAATAATATTGACCGTAGCAGTTTTTATATTTTTTTAATCCAGCTAAACTAAAAGAAATAAAACTTCTTTTCCAGAAAAAAAAATAGAGTGAAATATATTGTGAAAAATGTCCTTGCTTTGTTAAACATTACTTGATAACTAGATTCTTAAAGTTTGAGCCTGATGGTAGATAGATAGATAGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21151
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000108874 | Nonsense | 996 | 1044 | 19 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 74640635)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 72227129 |
| GRCz11 | 7 | 72512625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGGACGGAAAACTCTCCATATTCATCCATAAGAGAGAAGACCAGTCGT[C/A]GCACGAGGTGCTGCAGCCTCTGCTCAGGTAAACACAGGCAATACGACCAC
Long Flanking Sequence:
AATATTAATAAATCGCCTGTGAATTAGAAAAATTCTCACAGGGGTTTTTGTTCACATATATTGTTCATATTCGTTTTGCATTTACTTGCTACTTATAAATAAACTTTATATACTTAAAAATGCGAACATATTAAATAATATGTGTTTATACAGTAGAATTGTTCAATATTAAGTGCCCCCAAGTCAATTCACATGCACTTTAATACTTCATAATGATGATTATTTATCGTACCTTTAATAATAGTGGATCAAATTGTGAACAGAATCATATCAATAACATGCTGTCTACTTAACATTTTTATTGACATGCTTTAATGTTGTATAATGTCCACTCTCAGGCTGTCAGACGTTGCTCTCTCCCAGCGCCTCTGAGCCGGACACCAGTCTGAGCCGAGCCTGTCCCAAGAGCAGCTCTAAGACCGACAGAGATGCCAGCGAGGAGGGCGAAGCGGTGGACGGAAAACTCTCCATATTCATCCATAAGAGAGAAGACCAGTCGT[C/A]GCACGAGGTGCTGCAGCCTCTGCTCAGGTAAACACAGGCAATACGACCACAGCCACATTTAGAGAGGACCTATTATGCCCCTTTATACAAGATGTAAACTAATTCTCTAAAGTCCCTAGTGTGTGTGTGTGTGAAGTTTCAGCTCAAAATACCACACAGATAATGGTAATAACTCTCTGAAACTGACCCTTTTAGGATTTGACCCTGATTGTGGCGTTTTGGTGACTGTCGCTTTAAATGCAAATGAGATTTTCAAAAGAGGGCGGAGCTACAAATGCCTCAGCATCGTGGCAAACTCAAAACCAAGACTAACATCTAATGCTAATGAGATGGTCTCTAGTGGGCGGGGCTTATTCAAGTGTGATTATAAAAAATTAAATTATAAAATAGAAGCTGTTCATATTCACACACTGTTTCTACACGGCTGTGTTTAAACCTGCATAATAGGTCCCATTTAGTGCTGTGTCTGAAGCTGCTATGGTTGATTTGTATTTTACGTC
Associated Phenotype:
Not determined