Busch Lab

ZMP

krt15

Ensembl ID:
ENSDARG00000036840
ZFIN ID:
ZDB-GENE-040426-2931
Description:
keratin 15 [Source:RefSeq peptide;Acc:NP_998688]
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 3 alleles of this gene:

Allele Name Consequence Status Availability
sa6196 Nonsense Mutation detected in F1 DNA Not yet available
sa35040 Nonsense Mutation detected in F1 DNA Not yet available
sa35039 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa6196
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025016 Nonsense 9 460 2 8
ENSDART00000104250 Nonsense 19 449 1 8
ENSDART00000104254 Nonsense 9 460 1 7
ENSDART00000104260 None None 361 None 8
Genomic Location (Zv9):
Chromosome 11 (position 11639743)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11534746
GRCz11 11 11518367
KASP Assay ID:
554-4985.1 (used for ordering genotyping assays)
KASP Sequence:
GAAACTCTCCTCCGCACCGCAGCAATGACRTCCTTCAGCAGCCGTAGTTA[T/A]GTGTCCTCTGGAGGGGGCTTCGGYGGAGGCTCCCTGCGGGGTGCTTCTCT
Long Flanking Sequence:
GTTGTCCTGGAGACACCGCTGGCAAGTGCAGGTCATCCTGTCAGCACACATGTTATGAAGTCAGTAACACAGCCAGCTGTAGCACAAGCTATTCTGTCGACATGCATGGGAAAATCAAGTTCACAAATCAAAACAATCACACGTCCTATATGACAAATGTTGTCAAGTGATATATGCATGCATATTTTCAGTTACTGCATGCATTTGTCATCTGTTCTGCACATATCCCTGGGCTATGAGCTCTTAAGATTTCATTTCAACAATAACCTCACCTGCCAGATCCTCTGCCTCTGGGCATGCATTGGGCGGAGAGTAAAGTTTTGTGTTCATATTCTCCCCTCACCCCCTCCTCCATCTCCACCTCCACCCACCCCTTACCTCATCTCACAAACATATAAAAATCAATCAGCCTGGTCTGTGCGCCGCATTCCCTCTCCCTCCAGCAAAAAAGAAACTCTCCTCCGCACCGCAGCAATGACATCCTTCAGCAGCCGTAGTTA[T/A]GTGTCCTCTGGAGGGGGCTTCGGTGGAGGCTCCCTGCGGGGTGCTTCTCTTGGAGGCATGTCTTCCTCTTCAATGATGGGTGGAGGAAGCCGTATTAGCTCCATGCGTGCTGGTAGTGTATATGGGGGTGCAGGAGGCCGTGGGGTCCGTATCTCCTCTGCAGCTGGCGGTGGCGGAGGAGCAGGTTTTGGCTTTGGTGGAGGTGCTGGTGGTGGAGGAGGTTTCGGGTTCGGTGGTGGTGCTGGAGGAGGCTTCGGAGGAGGTGATATGGACCTCAACGTGACCGTCAATGAGAAAGCAACCATGCAGAACCTGAACGACCGTCTAGCAACTTACCTTGACAAGGTGCGCTCGCTGGAGAAGGCCAACGCAGATCTCGAGCTGAAGATCAGACAGTTTCTGGAGAGCAAAACCTCCCCTGCTGCGAGAGATTACTCTGCCTACCAGGCCACAATCAAGGACCTGCAGGACAAGGTAATGCTACTTTAAAACATCTCTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35040
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025016 Nonsense 230 460 4 8
ENSDART00000104250 Nonsense 219 449 4 8
ENSDART00000104254 Nonsense 230 460 3 7
ENSDART00000104260 Nonsense 170 361 4 8
Genomic Location (Zv9):
Chromosome 11 (position 11638786)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11533789
GRCz11 11 11517410
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGAGACTACTGGATGAGCTGACGCTGGCCAGATCTGACCTGGAGATG[C/T]AGATTGAGGGCTTAAAGGAGGAGCTTATCTTCCTCAAGAAGAACCATGAG
Long Flanking Sequence:
AAGGACCTGCAGGACAAGGTAATGCTACTTTAAAACATCTCTTGCACAAGGCATTGTTTTCATAGCTGCAGGATTATGGGTGTGGTCCTGTCCTCATTGTGTGTGCACTTTTGTTGATGTTCAGTGGTTGCATGTGACAAAAATAAGACAATATTTGAATATGTACTGCATGATTTAAAATTTGACAGATTTGTTTAAAAAAAGTCTCATTATCTTTGACAGATCCAAGATGCCACCCGTGTGAACGGAGGAGTCTACTTGGCAGTTGATAATGCGAAACTGGCTGCAGATGACTTCAAGACCAAGTAAATAAAAACATACTTTGTTGAAAATGATTTTTGTGTCTCACAATGGAGGTAAATGTCACAGATAAACCGTTCTGTTTTGCTTCGTTCAGGTACGAGAATGAGTTGACCATGCGTCAATCTGTCGAAGCAGACATTGCAGGGCTGAAGAGACTACTGGATGAGCTGACGCTGGCCAGATCTGACCTGGAGATG[C/T]AGATTGAGGGCTTAAAGGAGGAGCTTATCTTCCTCAAGAAGAACCATGAGGAGGTAAAATCTCTCAGCTGAGAAGGTAGTCGAACGTAAGGCACTATTATCCTCAGAAGCATGTCATCCTAAAATTCTATTCTCTGTAGGAACTGGCAGCCATGCGCTCTCAGATGTCAGGATCAGTGAATGTAGAGGTGGATGCAGCTCCACAGGTAGATCTGAATCATGTGATGGCTGAGATCCGTGAGCAGTATGAGAATGTTGCTGCCAAAAACCAGCGTGACCTAGAGAACTGGTTCCAAACCAAGGTAGATAAGGGCAAATAAATCTGTGTTCTTTGAACAAAACTGGAACAATCCATCCTTCAAACTGTGACCATAAGTGATGGCTGACTAATGTATAAATGTTCTTTATTTGCAGTCAGAAACATTGACTAAGGAGGTTGCTGCCAGTACAGAAACAATTCAAGTGTCCAAAACTGAGCTCACTGAGCTCAGACGCACCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35039
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000025016 Essential Splice Site 417 460 7 8
ENSDART00000104250 Essential Splice Site 406 449 7 8
ENSDART00000104254 Essential Splice Site 417 460 6 7
ENSDART00000104260 Essential Splice Site 357 361 7 8
Genomic Location (Zv9):
Chromosome 11 (position 11637459)
Other Location(s):
Assembly Chromosome Position
GRCz10 11 11532462
GRCz11 11 11516083
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGATGGAGATTGCGGAGTACAGAAGACTGCTGGATGGGGGAGCAAGCAGG[T/C]AGGAGATGTTGGAAGATGGATATTTATGTGAGTGTGCTTGTGCGAAACAT
Long Flanking Sequence:
AAATTCGCAGGTCTTCACTTATTCAAGTTGATTCCCCTTGTTTGCGTGCATTTTCAAACATCACATAAGAAACAAATAACACAAAGGCCATATTTTGGATATATAATTGAAGATAATCTTAATCAATTGACCTGATAGAAGCAGCAGAGCCATCTCAGACTGATTTAAGCTGTTTATTTACCAGCTGATTGATTGAACATGTACAACTTCCACTAAATATGGTCACTATCTCTCACTTTACAGTAATACATACCTGCCACCTCCTTTCTATTCTACAGAAAGCATCTCTGGAGGGAACTCTTGCAGACACTGAAGCGCGGTTCTCCAGGCAGCTGATGAACCTGCAGACTCAAGTAACAAATCTGGAGGAGCAGATTGTTCAGCTCAGAGCCGACATGGACAGACAGGGCCAAGAGTACAAAATGCTGCTGGATATCAAGACCCGACTGGAGATGGAGATTGCGGAGTACAGAAGACTGCTGGATGGGGGAGCAAGCAGG[T/C]AGGAGATGTTGGAAGATGGATATTTATGTGAGTGTGCTTGTGCGAAACATACAATAACAGATTTTTTTTTTTTTTTTCATTTTCAGCATGATAAGTACTGGTGGAGGTGGTGGTGGTGGCAGCAGCAGCACCAGCAGCAGCTCTACCAAAAGCATCACTGTGAAGACCATAGTGGAAGATATTGTCGATGGACAAGTGGTGTCAAGTAGTAAAAAATAAACACCAAATCAAACACTGCTCTTCACCTGTCTCACCAGTCTTCAGGGACTGATGTTGAGAATAAAATCAGTGATGGCACAAAAAAATGGTTGTGGGTGTTTTTACTGCTTTAAGCCAGTATGAACATTCTTGATTCACATTTCTTGAATACAAATTGTGATGCAATACATTTCATTTGACATATTATCGCCCTGGAATCATAAGGTTCTGTCTGCATTCTAAATGATTTTAAGATGTTGACCTTCAAGTTTTACATTCCATACAGCAAACAATATGCGTCC
Associated Phenotype:
Not determined