Busch Lab

ZMP

LOC571902

Ensembl ID:
ENSDARG00000088171
Human Orthologue:
C1orf51
Human Description:
chromosome 1 open reading frame 51 [Source:HGNC Symbol;Acc:25200]
Mouse Orthologue:
Gm129
Mouse Description:
predicted gene 129 Gene [Source:MGI Symbol;Acc:MGI:2684975]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa24689 Nonsense Available for shipment Available now
sa44313 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24689
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129337 Nonsense 103 379 1 5
Genomic Location (Zv9):
Chromosome 25 (position 27537112)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 26227206
GRCz11 25 26670408
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAGGATGGTGGCTATTTTCACCTGGGACAAGAGAAACAAACAAATTA[C/A]AGATGGTGCCCTGAGAGCTCTATAGACAAAAATAGACAGGCACAGAAGAG
Long Flanking Sequence:
CAATAGAGTGTGAATATCAAATTACAATTAAACAGTTTTACACAAGCACAATCTTTATTGTGTAATGTTGTTTTGTTTATTATCAACATTTCTATAAATAAATTAAGCCAAAACTATATATTGAAATTACAAAGATTTTTTTTTTTTTATAGGTCAGTGATGGTCTGTGCTGGTTAGACCTTGCATCATAAGATGTCAGCTTCAGATTCGGACTATTCCATTGACTGGCTGGCTAGTGATGATGAGGACCATGATAGCGAATTAGAATCAGATTGTACCACAACACAGGGACAAACTACCATACCAAAATTCCCCTCCCCAGGGGTTATCCAGCTGCCCCAGACTTACCAGACACTCTTAACAAGGAATGGAGATACAGGTGAGGTGATGGACAATGAAAGCTTGAGCTATCAGGAAAGTTTTTCTTCCAGCTGTGATAGTTCTTACTACATCAAGGATGGTGGCTATTTTCACCTGGGACAAGAGAAACAAACAAATTA[C/A]AGATGGTGCCCTGAGAGCTCTATAGACAAAAATAGACAGGCACAGAAGAGAACACGGAGTTACATGGTGCTGGAGCAAAGGGAGAGGCTGCTTACACCTGAACAAATGGAGAAAGACAGACTGTTTGCATGCAAGGTGAGACGTGCCACTTTTTTGGCTAACCAACATGCCAGGAAAGAGACGTGGTGTTCTGAAAGTCCCCTTATCTTCTATATAATCTATCTCACCGAGCAGAGTAAATTAAAAAAAAAAATCTAGAAACAGAAACACTTCCAGGAAGACCCCTCCTCTGTGTTCTTTCTAGGTGAAAAGTGAGTCACACAAAGCCATTTAGATTAGAGAAGATTTGTGTTTTCCCCTGCCCTGTAGAGCTGCAATAATTCTTTTTTTTTTACACAAATGTGTGACAGAGAAGATTATTTGTTTTGTTTTGCATTAGTGTTTTTGTTTTGAAGAAATTATGAACCAATCAAAGGAATGTCTTAACTTGATAATGTTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44313
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129337 Essential Splice Site 174 379 2 5
Genomic Location (Zv9):
Chromosome 25 (position 27536383)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 26226477
GRCz11 25 26669679
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTGTCCTCAATCCTTAATGGTCTCCGATCAGGCAGATACAGAGAACG[T/A]GAGTAATCTTTATATTTGTTCCTATTAGTCTTATATTTTACTGAATCTGA
Long Flanking Sequence:
GAGCAGAGTAAATTAAAAAAAAAAATCTAGAAACAGAAACACTTCCAGGAAGACCCCTCCTCTGTGTTCTTTCTAGGTGAAAAGTGAGTCACACAAAGCCATTTAGATTAGAGAAGATTTGTGTTTTCCCCTGCCCTGTAGAGCTGCAATAATTCTTTTTTTTTTACACAAATGTGTGACAGAGAAGATTATTTGTTTTGTTTTGCATTAGTGTTTTTGTTTTGAAGAAATTATGAACCAATCAAAGGAATGTCTTAACTTGATAATGTTGATTTTGTTTGTTAATGGATAATGGCAAAGTGTACTGTCAACATCCTGAAATGAAAAAAATGGAAATTGAGAAATACAAATTCTGTAAAGCTAAAATAACAAGTAATGGCGCAAAAGGAGATGGAATACCAATTGATTCTCTTTGTTTTGCAGTGCTTGGAGCTACAGTGTTACATTCACCCTCTGTCCTCAATCCTTAATGGTCTCCGATCAGGCAGATACAGAGAACG[T/A]GAGTAATCTTTATATTTGTTCCTATTAGTCTTATATTTTACTGAATCTGACTTTATTCAAAAAATTGCCTAGAAAGATGGTATGAAATCCACATAATATTTTGGTTAATTGACTGTCATTTGTCATAGCATTTTTATTTATATGTATTATTAGTTGCATTGTGACTATGAGATATGCAGAAAAGTTGCTTGATCTTAAAATGACTGTAAAGCACCACAAGATGTTATTAGCAGTATTGAGTACAAAACAGGTTTTTGGGTAAAACTCTACAAAAAAAAAAAAAAGACGTGTAGAGCTGCTCACAAGTGCTTGGACTGGTAATGCTGTCAATACAAGGACACTGGTTGACACCAGACTTCCTGGCCACAGAGACAGCAAGTCTATCTTCCCACATGCTTCACAAGAACCCATCTGCCTTGCACACATGGCACAGCCTGTCCGTTGCTTGTGAAATAAAAAGCTTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN
Associated Phenotype:
Not determined