Busch Lab

ZMP

ENSDARG00000034836

Ensembl ID:
ENSDARG00000034836
Human Orthologues:
KRT7, KRT81, KRT82, KRT83, KRT84, KRT85, KRT86
Human Descriptions:
keratin 7 [Source:HGNC Symbol;Acc:6445]
keratin 81 [Source:HGNC Symbol;Acc:6458]
keratin 82 [Source:HGNC Symbol;Acc:6459]
keratin 83 [Source:HGNC Symbol;Acc:6460]
keratin 84 [Source:HGNC Symbol;Acc:6461]
keratin 85 [Source:HGNC Symbol;Acc:6462]
keratin 86 [Source:HGNC Symbol;Acc:6463]
Mouse Orthologues:
4732456N10Rik, 5430421N21Rik, Krt7, Krt81, Krt82, Krt83, Krt84, Krt86
Mouse Descriptions:
RIKEN cDNA 4732456N10 gene Gene [Source:MGI Symbol;Acc:MGI:3045312]
RIKEN cDNA 5430421N21 gene Gene [Source:MGI Symbol;Acc:MGI:3690448]
keratin 7 Gene [Source:MGI Symbol;Acc:MGI:96704]
keratin 81 Gene [Source:MGI Symbol;Acc:MGI:1928858]
keratin 82 Gene [Source:MGI Symbol;Acc:MGI:2149248]
keratin 83 Gene [Source:MGI Symbol;Acc:MGI:3665486]
keratin 84 Gene [Source:MGI Symbol;Acc:MGI:96700]
keratin 86 Gene [Source:MGI Symbol;Acc:MGI:109362]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa9896 Essential Splice Site Available for shipment Available now
sa14026 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa9896
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000045669 Essential Splice Site 150 376 2 8
Genomic Location (Zv9):
Chromosome 8 (position 7662596)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 7049399
GRCz11 8 7092947
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATAACGAGCTCAGAAAAGCCCAYGCACAGGTCCAGGAGCAAAAGCAGAG[G/T]TATGTATAGTYGCATCTGCTGAAAACTACAGTTCAGTTTATCATCATCAG
Long Flanking Sequence:
CCGGCAGGGAAACTCTTATTTCGGCTTTGGGAACATGATGCCGGCATCTGGAGCCCCGATCAGACCTGTGTCTGTGAACAGCAGTCTGCTGGCGCCGGTGGATCTGCAGCTGGACCCAGAGCTGCAGACGGTGCGCATGCAGGAGACACAGCAGATGAAGACGCTCAACAACCGCTTCGCCTCCTTCATCGACAAGGTCTGTTAATCACACCAGACTGAAGTTGGAAATTAATTAGAATATTTTTCGACATCTGAATAAATGACAATAAACCTTCTCTGAAACACTGGCAGGTTCGCAAACTAGAGCAGGAGAACAAGCTTTTGGAGACCAAATGGCGACTACTACAGAAAGAGACTAAAGCGGAGTCTAAACTGGAGCCCATGCTGAAGAATTACAGCACTTCCTTACAGATGCAGCTGGAGAGAGTGAAGAAAGACAAAGAGCAGCTGGATAACGAGCTCAGAAAAGCCCACGCACAGGTCCAGGAGCAAAAGCAGAG[G/T]TATGTATAGTCGCATCTGCTGAAAACTACAGTTCAGTTTATCATCATCAGCAGAATAATAGTTTTAGTGTAAACGTTAAATTCAATATATCCTAATATAAATGCTAAATAATGTAAAACAACAACAATACTGTTTGCAGCTATTATCATGGTAATCAGAGCTTAAGGCATAATATTGTGCATAATTTTCAATATACAGTTGAAGTCATAATTATTAGCCCCCCTTTGAATTTTTTGTTCCTTTTTAAATATTTTACAAGTGATGTTTAACAGAGTGGGGCGAGGCAGTGGCGCAGTAGGTAGTGCTGTCGCCTCACAGCAAGAAGGTCACTGGTTCGAACCTCGGCTCAGTTGGCGTTTCTGTGTGGAGTTTCCATGTTCTCCCTGCCTTCGTGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGACATGTGGTACAGGTGAATTGGGTAGGCTAAATTGTCTGTAGTGTATGAGTGTGTGTGTGTGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14026
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
ENSDART00000045669 Nonsense 334 376 7 8
Genomic Location (Zv9):
Chromosome 8 (position 7656281)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 7043084
GRCz11 8 7086632
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CRGTGCTTGATGCCACYGAGCAAATCCGCCTGCTGGAGGAAGCACTGCAG[A/T]AAGCCAAAAAGGAAATGGCCAGACAGCTTAGAGATTACCAGGAGCTGATG
Long Flanking Sequence:
CTTACTTCAACTGTATATATAGATATTATTAATTGTGTATTTCTATCTATGTATACCTCATAATTGTGCATATACCTGTTTTCCTCCACAGTTTGACTTGGTTTCATCTCAGGCTAACCAGTGCAGCACAGAGCTGAAAAACAACAAAGGTGCAATAGACGAGTTGAAAAGGAAAATACAGCGCCTGCAAAATGACATCACCTCAGCTAAATCACAGGTAAATTTCCAGATAACACTATTCATCGGCTCGTTTATTTACAATGAAACTGATTGTATCTGTCAGTAAAAGCATGGATGCCTTTCAATACTATCTCAGAGGCGATCTCTTAATGGGCCGGGCCTGTAGATGCATGTTAGCAGCTCGATCTGTGTGATTTACATTTCTGACACCATTACAGTGTGACAACGTGGAGGAGAAAATCAAGGAGGCGGAGCGTGACGGCGAGGAGGCGGTGCTTGATGCCACTGAGCAAATCCGCCTGCTGGAGGAAGCACTGCAG[A/T]AAGCCAAAAAGGAAATGGCCAGACAGCTTAGAGATTACCAGGAGCTGATGAACCTCAAACTGGCTCTGGATATCGAGATCGCCACATACAAGAAACTACTGGAAGGAGAAGAGGACAGGTGAGACCGTGAAGCCGGAGTGCCCCACTTATGATTTTAAGTACTGGATTAACTACTAATCTTTTAATATATCTATAGAGGGAAAATAAGTATTGAATAGGCCATCATTTTTCTCAGAAAACATATTTCTAAAGGTGCTGTTGACTTGAAATTTTCTCAAGATGTTGGTAACAACCAAAGAAATCTATATATGCAAAGAAAACTAAACTGATTAGATTATAAATTAAGTTATGTGTATTAAAATGAAATTACACCTGTAAAAAGTATTGAACACATGAAGAAAGGGAGGTGTAGAAAGGCAGTGAAAGCCCAGACAGCAGCTGAAATGTCTTGGTAGTTATTCAGCAACTCTCTGCTCTTCCTCAGTGTAAATGAATATTCG
Associated Phenotype:
Not determined