Busch Lab

ZMP

krt1-19d

Ensembl ID:
ENSDARG00000023082
ZFIN ID:
ZDB-GENE-060316-1
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]
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 4 alleles of this gene:

Allele Name Consequence Status Availability
sa913 Nonsense Available for shipment Available now
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.
Availability:
Order Allele From ZIRC
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:
sa23425
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
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