Busch Lab

ZMP

C10orf90

Ensembl ID:
ENSDARG00000089024
Description:
chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:26563]
Human Orthologue:
C10orf90
Human Description:
chromosome 10 open reading frame 90 [Source:HGNC Symbol;Acc:26563]
Mouse Orthologue:
D7Ertd443e
Mouse Description:
DNA segment, Chr 7, ERATO Doi 443, expressed Gene [Source:MGI Symbol;Acc:MGI:1196431]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa10450 Nonsense Available for shipment Available now
sa35373 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa10450
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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126327 Nonsense 180 714 1 11
Genomic Location (Zv9):
Chromosome 12 (position 45515100)
Other Location(s):
Assembly Chromosome Position
GRCz10 12 43686389
GRCz11 12 44849921
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTGCCCAKACAAAGACATGTGATTCTGACRGACGTMCCCAACAAYCGA[C/T]ARGACAACAGCAGGGGTCAGCAGGTGAGAAAGTGCAAAAGAGACTAATTG
Long Flanking Sequence:
TTCAGCCCCATGATGCAGCTGGCAAAAACAGCATGAGCTTCCTCCGCAGGTCCTCATCATGGAGGAGGCCTGGAGAGCGAGGTTATTATGAGGGCCCCATGGCGCAGGTGAATGAGCCCCCTCGCGGAGCTCGTCCTCAGAGCTGCATTGAAGGTGGCAGAATGGACAAATGGCTTCAAACCCTGGAGAGACTTCAATCCCGTCGGCTTCAGAAACAAGTACCTGAGTTTTCCGACTGGACCGTGTCAATGCCGGCTCTCCCAAACGAGACGATGGGAAGTAACCCACATTGTCTTGATCTGAACTCTCTCCACAGAAGGAATCAGACTCCTAGTGCCTGTTCAAGTGTTTGTGAAAGCTCCCCGAGCAGCATGGAGTCTGTTCACATTAAGCCTGTTCCCAGTGCTGAAAAAGCAAATTTCTGTGCTCTCGCTCCTGTTCGATTTGGCTGGCTGCCCATACAAAGACATGTGATTCTGACAGACGTCCCCAACAACCGA[C/T]AAGACAACAGCAGGGGTCAGCAGGTGAGAAAGTGCAAAAGAGACTAATTGGAGATGCAGGCTACATTTTGAAATTATTTTTTTGAAATAGACGAGGAAACATGCATGACTGTGCTTTAACATAGTTTACTAATAGAAAGAACAGCCAGAAAGGGAAAACTGATGGATTTGTGAAGAATATTAGCATCACTGACCATAACAATGTACCGTAAGTTACCTATTACTGTCAGCATGTTTGTGTGCTCTTTATAAATTACTGAAAAACAGCTGGGGGTAAAGTATATTGATCGCAAGTGCTCATTTTGTGATCATATCTCGGTTTTGTTCTGTTGATTTGTAGTTTCAAATATTCGTAGCGTGAAACAGATGGAAATATGAAGTTTAGTAAAGTTAGCAACAGATTCATATTTTCCGGATCAATAACTCATGACCTATTCGCTATTAGTAAAGGCTTAATAATGATAACAATAATAGTTTTTATTTATATAGCCCCTTTCCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35373
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126327 Essential Splice Site 640 714 9 11
Genomic Location (Zv9):
Chromosome 12 (position 45477667)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTCTGCA[G/T]AAAGCCTTTTGAAATCTAAAGACAGAAGCATCATGGAAAAGGGGCCACAG
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTGTGTATGTGTGTGTGTGTGCGTGCGTGCGTACGTGCGTGCGTGCGTGCGTGCGTGTGTGTGTATGTATGTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTACGTGTTTTTGTGACATATCAGGACACAAATCTGCATAATGACATGGGTATGACACAGGTATTACAAAAAGGAGGTGAAATATGAGGACATTGGTGACGTCCTCATTTCTCAAAATGCTTATAAATCACACAGAATGAGTTTAATCAGAGAGTAAAGCTGCACACAGTCTCCTGTGATGGTTGGGTTCAGGGGTGGGGTGAGGGCAATACAATATACAGTTTGGACAGTATAAAATAAAATGGAAACCTAGGTAATGTCCCCACTTTTCACAAAAACAAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTCTGCA[G/T]AAAGCCTTTTGAAATCTAAAGACAGAAGCATCATGGAAAAGGGGCCACAGATGCGGTCCAGGAGGTAAAAAAAAGAGCATGCCAGCTCTTGTTTTGATAAACACCTATTCTGCTTTATTACTTTTTAACACACACACACGCACACACACACACTCACACACACACTCACAGGTGTATCAGTTCTATCTGATTTAAAGGTGTTGTGTCTGTGTGTGCGGCTGCAGGGTTTTGCTGCCCTGATTGTGCTTTTCACAGCTTGTTTGTTTTCCTGCCGCTGAATAAAAGCTCATCCGATTAGATCTGGTCTCACTGTGATTCAGAATTAAACCTCCCTGATGCACGGCTGGATGGATTCTGCACGAATGAGTGGCCATGTTCAGAAGTTTGATTTAGGCTGTGGATATGGTGTGTGACTGAATAAACGGACAGTTATGTCAGATAACAGTGTAAATACGCACTGTTTATTTATTAACTCTGATATAGTATGATGAGAATAGATC
Associated Phenotype:
Not determined