Busch Lab

ZMP

C12orf51 (1 of 3)

Ensembl ID:
ENSDARG00000079151
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
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.
Availability:
Order Allele From EZRC
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:
sa21151
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From EZRC
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