ZMP
krt1-19d
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate keratin family [Source:UniProtKB/TrEMBL;Acc:Q1LXK0]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa913 | Nonsense | Available for shipment | Available now |
sa44903 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23425 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa913
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010373 | Nonsense | 141 | 423 | 2 | 8 |
ENSDART00000105042 | Nonsense | 155 | 415 | 2 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 5955282)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 5414593 |
GRCz11 | 19 | 5331079 |
KASP Assay ID:
554-0819.1 (used for ordering genotyping assays)
KASP Sequence:
AAGTMATTTTAGTTTATTTGTTTCTCCAGATCATGGCAGSCATTCATCTG[A/T]AGGGTGGACTCCATCTCAGCATCGACAACACCAGTCTGGCCATGAATGAT
Long Flanking Sequence:
ATGTCAAAATTAAGTGAGTTTTTCTCTAAACAAGCTAAATAATCTGCCAGCGGGGTTAAGAAAAATGTTCATCTTTCCTGTTTGAAATAAAACTATTATCAATTTTTAATTTTCAGACATAATATGCCAAACTGAAGTGAGTTTTCCTTAAAACAGGCTTAATATTCTGCCAGTGGGGTCAGTAAAATATTTCATGTCATGTCAAAGTTTTATTTATGAAATTATTTCTATGAAATATATTTAATTTAATTTATTCATTTCTATGGGGGGAAAAAACTAATTTTAACTAATTTTTTTGTGAAAACAAAACATTTTTTTTTCTTTTCTAGAATATGATCTTGATTCAACATTTTTTTTTTAGATATTTTGGAGTATAAACCAAAAGCACTTAGTAAGAAAATGTGTTTTTGCAGGCTATGTTATATAATATTATAAATATGGGGAGAAACAAAGTCATTTTAGTTTATTTGTTTCTCCAGATCATGGCAGCCATTCATCTG[A/T]AGGGTGGACTCCATCTCAGCATCGACAACACCAGTCTGGCCATGAATGATTTTAAAACAAAGTGAGTGTTTTTCAGTAGATTCAATGCATTTTGGATAGATGCAACATGACATTGACTCTAGTTAAAACAGCATTATTTAATTTCATAAAGTACAAAGGTTGCTTTAAGGCATAGTTCACCCCAATATTCTGCCATCATTTACTCATCCTTCTCTTGTTCCAAACCTGTTTGAGTTTCATTCTTCTGTTGAACACAAAGAAAGACTTACTGAAGAGTGTTGAACAAACAGCCATGACTTTACTTGTATTTTTTGTTCCTATACCTTGTATGTCAATGGCTGCTGTTGGTCCTCATTCATTAAACTTGTGCCTTGTGATTGGGACTGTCTGACAGATTTGAAATGGAGCACGTCATGCGTCAGTCTGTGGAAGCGGACATTGTGGGCCTGAAGAGGGTGCTGGATGAGCTCAACATGTCCAGAAAGGACATCACCATGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44903
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010373 | Nonsense | 356 | 423 | 7 | 8 |
ENSDART00000105042 | Nonsense | 370 | 415 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 5949241)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 5408552 |
GRCz11 | 19 | 5325038 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCAGATAGTGCAGCTCCGAGCTGATCTGGAGCGCCAACGTCATGATTA[T/G]CAGATGCTTCTGGACATCAAGGCCAGACTGGAGATGGAGATCGCAGAGTA
Long Flanking Sequence:
ATGTTGGATAGGTTGTCAGTTCATTCTGTTGTGGCGACCCCTGATTAACAAAGGGACTAAGCTGAAAAAAAAATGAAGAAAATATAGAACACCTATTTTGTGTATATAATTATGAGCGTGATTGATTTTAAACGTGACTGATTTTAATTTAGTTTGTCTGTAAATCTGCATCTACAGGTATTTCTCCAAATAGCCGCAGGTCTGATTTTCCACCACAGAATGAGTGCTTATTAGTTCATAAAAAATAATAATAATTTTTACTAATAATTATTTTAATTTAGTTTTTTTTTTATTTAAAAAATTGTTTTCTTTAACCAATTGTTTTAGTTGTAGTCTTTGCTTACTAAAATAACCTTGTACTTCAATACCCTCATATAAGAGCTGAAGAACAGGACCAAATCAACTCACACCTGATGAAATACTCTGTGTTTTCAGGTCACTGTCCTGGAGGAGCAGATAGTGCAGCTCCGAGCTGATCTGGAGCGCCAACGTCATGATTA[T/G]CAGATGCTTCTGGACATCAAGGCCAGACTGGAGATGGAGATCGCAGAGTACAGGAGACTGCTGGATGGAGAAGCCACGTGAGTATTGATTTCTGCACCTTCAGGCCTGTCATTCGGATCTAAATCCTACAATTAAAAGAAAATATGATACTTAAAATAACTATTGTGTTTCTTCTACAGTGTCAAAACAACCTCCAGTTCCACCTCGAGAACAAAAGTCATCACAGTCGTGGAAGAGGTTGTAGATGGAAAAGTGGTTTCCACCTCCAGCTCTTCAACCATGTCTGACAGTCGCAGATTGATCTGATATAATAATGCCTGTTTGTATTTGCAGTATATGCACAGAACTGGAAACCAAATAAAACAGCATTTACAGTGTATTCTAACTTAAGTGTTTGAGGTAATCCCCTTTTTTATTCAAGAAAATACAGTGTGAAAACAGCAGGTGGCGCTCCTCAATGTACATATTTGTTTAGGTTCTTTCAGTTCAACATGGGTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23425
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000010373 | Essential Splice Site | 382 | 423 | None | 8 |
ENSDART00000105042 | Essential Splice Site | 396 | 415 | None | 9 |
Genomic Location (Zv9):
Chromosome 19 (position 5949063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 5408374 |
GRCz11 | 19 | 5324860 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAATTAAAAGAAAATATGATACTTAAAATAACTATTGTGTTTCTTCTAC[A/T]GTGTCAAAACAACCTCCAGTTCCACCTCGAGAACAAAAGTCATCACAGTC
Long Flanking Sequence:
TATTTCTCCAAATAGCCGCAGGTCTGATTTTCCACCACAGAATGAGTGCTTATTAGTTCATAAAAAATAATAATAATTTTTACTAATAATTATTTTAATTTAGTTTTTTTTTTATTTAAAAAATTGTTTTCTTTAACCAATTGTTTTAGTTGTAGTCTTTGCTTACTAAAATAACCTTGTACTTCAATACCCTCATATAAGAGCTGAAGAACAGGACCAAATCAACTCACACCTGATGAAATACTCTGTGTTTTCAGGTCACTGTCCTGGAGGAGCAGATAGTGCAGCTCCGAGCTGATCTGGAGCGCCAACGTCATGATTATCAGATGCTTCTGGACATCAAGGCCAGACTGGAGATGGAGATCGCAGAGTACAGGAGACTGCTGGATGGAGAAGCCACGTGAGTATTGATTTCTGCACCTTCAGGCCTGTCATTCGGATCTAAATCCTACAATTAAAAGAAAATATGATACTTAAAATAACTATTGTGTTTCTTCTAC[A/T]GTGTCAAAACAACCTCCAGTTCCACCTCGAGAACAAAAGTCATCACAGTCGTGGAAGAGGTTGTAGATGGAAAAGTGGTTTCCACCTCCAGCTCTTCAACCATGTCTGACAGTCGCAGATTGATCTGATATAATAATGCCTGTTTGTATTTGCAGTATATGCACAGAACTGGAAACCAAATAAAACAGCATTTACAGTGTATTCTAACTTAAGTGTTTGAGGTAATCCCCTTTTTTATTCAAGAAAATACAGTGTGAAAACAGCAGGTGGCGCTCCTCAATGTACATATTTGTTTAGGTTCTTTCAGTTCAACATGGGTTTTACCTTTTATTTTCACCGAACTTGTTTAGTTGGCCTTTTGTTACTCTAAAACTAATTAGATAAATTAATATTAGTAGTAATGCTTGGCGAATTAGTCTTGTTTACATCAAGAGCTAGCACTAGCATCCACAACTTGTACAATAACTTATCAAAAGCGCGCGAGTTTTGTCGCTTGTCAG
Associated Phenotype:
Not determined