Busch Lab

ZMP

LOC556118

Ensembl ID:
ENSDARG00000022334
Human Orthologues:
KRT14, KRT16, KRT20, KRT23
Human Descriptions:
keratin 14 [Source:HGNC Symbol;Acc:6416]
keratin 16 [Source:HGNC Symbol;Acc:6423]
keratin 20 [Source:HGNC Symbol;Acc:20412]
keratin 23 (histone deacetylase inducible) [Source:HGNC Symbol;Acc:6438]
Mouse Orthologues:
Krt14, Krt16, Krt20, Krt23
Mouse Descriptions:
keratin 14 Gene [Source:MGI Symbol;Acc:MGI:96688]
keratin 16 Gene [Source:MGI Symbol;Acc:MGI:96690]
keratin 20 Gene [Source:MGI Symbol;Acc:MGI:1914059]
keratin 23 Gene [Source:MGI Symbol;Acc:MGI:2148866]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa17190 Nonsense Available for shipment Available now
sa18652 Nonsense Available for shipment Available now
sa13306 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa17190
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
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Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041914 None None 365 None 7
ENSDART00000125446 Nonsense 231 741 1 7
Genomic Location (Zv9):
Chromosome 11 (position 12281480)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 12192297
GRCz11 11 12175918
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCTCCGATACATGTCCCAAGCCCTGTTCCTTTACCTGCCCTGACACCTA[T/A]CTTAAAACTTGCTCTGAGACATGCTCTGAGACCTGTCCCAAGCCCTGTTC
Long Flanking Sequence:
ACCTGTTCTACCCAAAGCTACCCAGAGACCTGCTATGAGAGCTGCCCCAAGCACTGCTACTCCACCTGCCCTGAAATCTGCCCTAAGCCTTCCTCGTTCACCTGCCCCAAGACCTGTCTGAAGACTTTCTCTGAGAGTAGCTCCATAACTTGCCCTGAGACCTGCTCCAACACCTGCACCGCACCCTGTTCTTTCACCTGCCCTGAGACCTGTCTGAAAACTTGCTCTGAGACCTGTCCCAAGCCCTGTTCCTTTACCTGCCCCGAGACCTGTCTGAAAACTTGCTCTGAGACCTGTTCCAAGCCCAGTTCCTTCACCTGCCCTGAGACGTGTATTAAAACCTCATCTGACATCTGCTCCAAGCCCTGTTCCTTCACCTGCCCTGAGACCTGTCCCAAGTCTTTTTCAATCACCTGCCCCCAAACCTGCTCCGAGACCTGTCTGAAAACTTGCTCCGATACATGTCCCAAGCCCTGTTCCTTTACCTGCCCTGACACCTA[T/A]CTTAAAACTTGCTCTGAGACATGCTCTGAGACCTGTCCCAAGCCCTGTTCCTTTACCTGCCCTGAGTCCTGTCTTAAAACGTACTCTGAGACCTGCTCTGATACACTCTCCAAGTCCTGCTCCTTCAACAACCCCAAACCCTGCCCTGACAACTGTCTGAAGACCTGCTCTGAGACCTGCTCTACAACTTGTTCTGAGACCTGCTCCAAGCCCTGTTCATTCACCTTCCCTGATACTTGTCCGAAGACTTGCCCGGAACCCTGCACCTCAAGCTGCCCAGAAACCTCATCTGAAACCTGCCCCAAGCCTTGCCCCATCTCCAACCCCAAGTCCTGCTTTAGCACCTTCTCCAATAGCTGTTCCGTGTCTTCAGTGACCGTTCCTCGTCATTGTAGAACAGTTACAACAAAAGCCCACAGTGTATATGGTTGCGGTGTTGGAGGAAGGACCCGCATCTCTTCTTGCTCCTATCGTCCAAATACTTGCTCCCCATGTCCATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18652
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041914 Nonsense 190 365 4 7
ENSDART00000125446 Nonsense 562 741 3 7
Genomic Location (Zv9):
Chromosome 11 (position 12278987)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 12194790
GRCz11 11 12178411
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGCCGACCTGGARTTGCAGATCTGCACTTTGGARGAGGAACTTGTGTA[T/A]TTGAGAAAAACTCACCARGAGGTTGGTAGCTGTTTCTCTATAGCAGAATA
Long Flanking Sequence:
TTCAATACTTGTGTTTTGCTGTGAAAATACACAAAAATAATAAAAATCTTTTTCTTTTTGATTTAAAGAATACCGTTTGACTAGACTATTAGACAAAATCCAATGACCAATAAAAAATAACTCAGACCCTAATTCTTTAGATTTACTATTTGTTAAATGCACTGCTTTCCCATGGATGGGTTGCAGCTGGAAGGGCATGCGATGCGTAAAAACTTGCTGGAAAAGTTGGGGGTTCATTCTGCTGTGGCGACCCCGGATTAATAAAAGGACTAAGCTGAAAAGAAGATGAATGAATGAATGAATAAATGCACAGATAGCTACTTTGTTCGTGTAAGTCATAGATATGTTTCATCCTCTTTGGTCAGGTATGAGAATGAGCTGTCAATACATCAGTGTGTGAAGGCTGATATTGATAACCTGCGATGCATACTTGATAAGACATGCCTGGCAAAGGCCGACCTGGAGTTGCAGATCTGCACTTTGGAGGAGGAACTTGTGTA[T/A]TTGAGAAAAACTCACCAAGAGGTTGGTAGCTGTTTCTCTATAGCAGAATAGCTATAACAACCTAAACGCTATGCTTCAAAAGCCTTAATGCTTCAGTTATGTGTGTTTACAGGATGTGGCGGCACTAATGTGTCAGTTGACAAACTCAAAGGTGTGTGTTGAAGTGGACGCCGCTCCTCAGCAAGACCTCAAAAAGGTTTTGGATGACATCCGTTGTTATTATGACACCATCATAGACAAACACTGCACAGAACAGGAGTGCTGGTTCAAAGAGAAGGTGAGACTTTGATATCTTCAACTCCTCTAACTATACCATATAACATATAGTGAAACACAAGCTTTGTTTCTCATGAGTTAAACAGCATGATGTGTGTTTGTGATCTTCTTTAAGATGGCAGGTCTATGTAAAGATACTGCAATCAACACAGAGTGCCTGGAAACCTCCATGTCACGTATTTCTGATTTACGACGCACATTGCAGAGTCTGGAGATCGAGCTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa13306
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041914 Nonsense 233 365 5 7
ENSDART00000125446 Nonsense 605 741 4 7
Genomic Location (Zv9):
Chromosome 11 (position 12278767)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 12195010
GRCz11 11 12178631
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCGCTCCTCAGCAAGACCTCAAAAAGGTTTWGGATGACATCCGWTGTTA[T/G]TATGAMACCATCATAGACAARCACTGCACAGAACAGGAGTGCTGGTTCAA
Long Flanking Sequence:
AAAAGTTGGGGGTTCATTCTGCTGTGGCGACCCCGGATTAATAAAAGGACTAAGCTGAAAAGAAGATGAATGAATGAATGAATAAATGCACAGATAGCTACTTTGTTCGTGTAAGTCATAGATATGTTTCATCCTCTTTGGTCAGGTATGAGAATGAGCTGTCAATACATCAGTGTGTGAAGGCTGATATTGATAACCTGCGATGCATACTTGATAAGACATGCCTGGCAAAGGCCGACCTGGAGTTGCAGATCTGCACTTTGGAGGAGGAACTTGTGTATTTGAGAAAAACTCACCAAGAGGTTGGTAGCTGTTTCTCTATAGCAGAATAGCTATAACAACCTAAACGCTATGCTTCAAAAGCCTTAATGCTTCAGTTATGTGTGTTTACAGGATGTGGCGGCACTAATGTGTCAGTTGACAAACTCAAAGGTGTGTGTTGAAGTGGACGCCGCTCCTCAGCAAGACCTCAAAAAGGTTTTGGATGACATCCGTTGTTA[T/G]TATGACACCATCATAGACAAACACTGCACAGAACAGGAGTGCTGGTTCAAAGAGAAGGTGAGACTTTGATATCTTCAACTCCTCTAACTATACCATATAACATATAGTGAAACACAAGCTTTGTTTCTCATGAGTTAAACAGCATGATGTGTGTTTGTGATCTTCTTTAAGATGGCAGGTCTATGTAAAGATACTGCAATCAACACAGAGTGCCTGGAAACCTCCATGTCACGTATTTCTGATTTACGACGCACATTGCAGAGTCTGGAGATCGAGCTACAGTCTCAAATCAGCCTGGTGAGTAAGAGACATAATACCGAATGTTATAAACATCCTGGTAAAAATATTATTTTGTCTTCTGCAGCAAAGTTCCTTGATTTTTATGCCAGAATGATGATATAGTTTTTAACCATTTTGACAGAAAATATCAACTTAAAAATGTTTGTCAGTCTTACCATATAACTACAGAAGAGTCAAGCTTTAAATGGTAAAATTAGTCT
Associated Phenotype:
Not determined