Busch Lab

ZMP

NP_001122170.1

Ensembl ID:
ENSDARG00000035963
Description:
hypothetical protein LOC559167 [Source:RefSeq peptide;Acc:NP_001122170]
Human Orthologue:
CCDC96
Human Description:
coiled-coil domain containing 96 [Source:HGNC Symbol;Acc:26900]
Mouse Orthologue:
Ccdc96
Mouse Description:
coiled-coil domain containing 96 Gene [Source:MGI Symbol;Acc:MGI:1913967]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa27009 Nonsense Mutation detected in F1 DNA Not yet available
sa14488 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa27009
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052201 Nonsense 121 479 1 2
Genomic Location (Zv9):
Chromosome 7 (position 41130681)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 39466938
GRCz11 7 39737955
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAACAGAACCATCCCTTGAAGACTCTGAGGATGAAGAAGAAGAGGAA[G/T]AAGATGAGGAGAATAGTCTTCCAGCTCCTGAGCCGGAGAATGAGAGGTCC
Long Flanking Sequence:
TGCTTGTGATTGGCTCTTGCTATAGGTGTCCATGGCAACACGTACGAACACAAAATAGTTGATGCCAGCGCTTCTTCAAGAGCTCAAGAGAAACTACATCGAACTAATCTTGATAAACGCAACCTTCTTTAAGACGTAAAATGGAAGAGGAGTCATTAGAGTACACTCACGAGGAAAGCTTTGTTTTAGAAACTGACACACTAATGGAAAACACTAAAACCCTTGAAGGTCCTGCAGACGCAGAGCAGGTCATGGAGGAAGAAACTGAGGAACCTGAAGCTCCTAATAATCCAGAAGCTGTAGAGGAAGATAAGGCCGAGCAGCTCTTAACAGAAGACACGTCTGTGCCTGAGACCAGTGAACAACAGACCGGTGAAATCCAGATTGAGCAACATTTGATAACAGAAGAGGACCCCCTTATGAATGAGACTTTGGAGGACACTGAGGGTCCTGAAACAGAACCATCCCTTGAAGACTCTGAGGATGAAGAAGAAGAGGAA[G/T]AAGATGAGGAGAATAGTCTTCCAGCTCCTGAGCCGGAGAATGAGAGGTCCATCAGCCCTCCTGAAGAACCACAGGCTCATACAGAAGATGAGGAAGTTGACCCCAGCATCATCAAGGAAAAGATGGAGCTGCTGCATAAACTACAATCAGAGAACGAAAAGCTTAACAAGATAAACCAACAACTGCAGACCAGAATAGCAGAACACTTTAGTAAGAAGAAAGGGGATCAACATGTCAAGTTAGACGAGGATATCTCAGAGCAGGAGCAGTATGAGAAGTACATGCAACTGATAGCGGACATGAAAGAGCAGCAGCTGCATTTCTCAAAGCTTCACCAGGAGCGGATGGAGGATCTCCATCTACAGAGCTCAGAGAAACTCAAGCAGGTGGAGCAAGAGCTGAGATTCTTTGCTGCACTGAAATATGAAACTGTGATGAAGGCCTCACTGACTGGTAAGGTGGGCAAACAGGAAACACTGGCAAAGGTGGAGCTGCTGAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14488
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000052201 Nonsense 321 479 1 2
Genomic Location (Zv9):
Chromosome 7 (position 41130081)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 39466338
GRCz11 7 39737355
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATATCAAGTTGAWGAATAAAATATCTAAGTATGAGAGGGCGCTCAGGTCT[A/T]AACGGGAACTGGTGGATGGGCTCCTGCTGATGGACTTTGAGCAGCTCAAA
Long Flanking Sequence:
ACCCCAGCATCATCAAGGAAAAGATGGAGCTGCTGCATAAACTACAATCAGAGAACGAAAAGCTTAACAAGATAAACCAACAACTGCAGACCAGAATAGCAGAACACTTTAGTAAGAAGAAAGGGGATCAACATGTCAAGTTAGACGAGGATATCTCAGAGCAGGAGCAGTATGAGAAGTACATGCAACTGATAGCGGACATGAAAGAGCAGCAGCTGCATTTCTCAAAGCTTCACCAGGAGCGGATGGAGGATCTCCATCTACAGAGCTCAGAGAAACTCAAGCAGGTGGAGCAAGAGCTGAGATTCTTTGCTGCACTGAAATATGAAACTGTGATGAAGGCCTCACTGACTGGTAAGGTGGGCAAACAGGAAACACTGGCAAAGGTGGAGCTGCTGAAGGCGGAGGAATTGAAGCAGGAGGATAAGTTGGTTTGTGTGCGGCTCAACAATATCAAGTTGAAGAATAAAATATCTAAGTATGAGAGGGCGCTCAGGTCT[A/T]AACGGGAACTGGTGGATGGGCTCCTGCTGATGGACTTTGAGCAGCTCAAAACAGAAAACCAGTCTTTCATGGACAAGCTGGAGGAGAGGAGTGAAGAGCTACATCGACTGAAAAAGAAGGTCGCAAGCTCTGTGCAGGTAAATCACTGTGCTTTAATTCTAAGTAAAACAGTGTATAATATATACACCACTGGTCAAAAGTTTGGCTTGGGGTCAGTTTTAAAAAAATGTTTATTTATTAAATGTAAAAAAAATTGTTAAATATTTTTTACAATTTTAAATAACTGCTTTTTTATTGTATGTAGTTTCAAATGAAATTGTTAGGCCAGTCATTATTGCTTTTATTATTATTACCATTAATAATAATGATAATGATAATTAATATTAGAGTGATTTCTGAAGGATCATGTGACTCTGAAGACTAGAGTAATGAAGCTGAAAAATCATCTTTAAAATCACATGAATAAGGGATTCAAATAAAAGATAAACTACTTTTGAACA
Associated Phenotype:
Not determined