ZMP
LOC556118
Ensembl ID:
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]
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]
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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