Busch Lab

ZMP

zgc:92533

Ensembl ID:
ENSDARG00000036830
ZFIN ID:
ZDB-GENE-040801-181
Description:
keratin 12 [Source:RefSeq peptide;Acc:NP_001003445]
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 5 alleles of this gene:

Allele Name Consequence Status Availability
sa16968 Nonsense Available for shipment Available now
sa36767 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa16968
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000000221 None None 466 None 7
ENSDART00000104995 None None 351 None 10
ENSDART00000105803 Nonsense 691 844 10 13
ENSDART00000146890 None None 463 None 7

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 5987597)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 5446908
GRCz11 19 5363394
KASP Assay ID:
2261-2858.1 (used for ordering genotyping assays)
KASP Sequence:
AGGCAGTTTCTGCCAAGAACCGTAAAGWTCTTGAGAGTTGGTTCCAGGCC[A/T]AGGTAAAAATCTGWTTTAACATGTCAAATTTGTTTAGCAAGATGGAAATC
Long Flanking Sequence:
TTCAGAGTCAAGTAAGTCCACCGTTGTAAGACTTTAAAAATTGCTTACAAAATCTATAATAGATCCAAAACATTTATATTGACTTTATTTATGTGCAGGTATGAGAATGAGCTGAGCATGAGGCAGTCTGTGGAAGCAGACATTGTTGGCTTGAGGAAGGTGCTGGATGAGCTCACAATGACCAGATCTGACCTGGAGTTGCAGATCGAGGGTCTGAAAGAAGAACTGATCTTCCTCAAGAAGAACCACGAGGAGGTAAATTCATTAATAGTTCACATTCAATAGTTTCTGTAAGTATATTAGTCAAGCAAATGCTCAGTATATTGTCTTTGTCTCTTCAGGAGCTCTTGGCAGCACGCACCCAGATGAGTGGACAAGTCAATGTAGAGGTCGATGCAGCACCACAGGAAGACCTGACAAAGATCTTGGCTGATATCCGTGAGCACTACGAGGCAGTTTCTGCCAAGAACCGTAAAGATCTTGAGAGTTGGTTCCAGGCC[A/T]AGGTAAAAATCTGTTTTAACATGTCAAATTTGTTTAGCAAGATGGAAATCAAAACCAACAGATGACTTATCTAGCTGCTTTTCTGTTGCATTTCCTCTCACAGAGTGAGTCCCTCAACAAGGAAGTTGCTGTAAGCACAGAAACTCTCCAAACCTCCCGCTCTGAAATCACAGAGGTTAAGCGCACACTCCAGAGTCTTGAAATCGAACTACAGTCACAACTCAGCATGGTGAGCAACAACAGATAAATAGAGGAGTCTGTGATTGATGTGTTTTGTTGTCATCAGCATAGTGTTTACTAATAATAATGACTTTTCCCCCAACAGAAAGCGTCATTGGAAGGCACTCTGGCAGACACACAGGCCCGCTACACCAACATGTTGAATGGTTACCAGTTCCAGGTGAGCAGCCTGGAAGAGCAACTGATACAGCTCCGTGCTGATCTGGAGCGCCAAGGTCAAGAGTACCAGATGCTTCTGGACATCAAGACCAGACTGGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36767
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
ENSDART00000000221 None None 466 None 7
ENSDART00000104995 None None 351 None 10
ENSDART00000105803 Nonsense 817 844 13 13
ENSDART00000146890 None None 463 None 7

The following genes are also affected by this mutation:

Genomic Location (Zv9):
Chromosome 19 (position 5986922)
Other Location(s):
Assembly Chromosome Position
GRCz10 19 5446233
GRCz11 19 5362719
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCATATTTCTATTTCTCCAGTGTTTCCACAAGCTCAAGCACTACACGC[A/T]AAGTGGTAACCATTGTGGAAGAGGTGGTGGATGGAAAAGTGGTCAGCTCA
Long Flanking Sequence:
GGTTAAGCGCACACTCCAGAGTCTTGAAATCGAACTACAGTCACAACTCAGCATGGTGAGCAACAACAGATAAATAGAGGAGTCTGTGATTGATGTGTTTTGTTGTCATCAGCATAGTGTTTACTAATAATAATGACTTTTCCCCCAACAGAAAGCGTCATTGGAAGGCACTCTGGCAGACACACAGGCCCGCTACACCAACATGTTGAATGGTTACCAGTTCCAGGTGAGCAGCCTGGAAGAGCAACTGATACAGCTCCGTGCTGATCTGGAGCGCCAAGGTCAAGAGTACCAGATGCTTCTGGACATCAAGACCAGACTGGAGATGGAGATTGCAGAGTACAGAAGACTGCTGGATGGAGAGGCTACTACGTGAGACACAACTACTACCCAAAATCTTTAGCTAACAATGTAAATAATAATATTAAAAAATTTAAATAATGTAACATGCTTCATATTTCTATTTCTCCAGTGTTTCCACAAGCTCAAGCACTACACGC[A/T]AAGTGGTAACCATTGTGGAAGAGGTGGTGGATGGAAAAGTGGTCAGCTCATCCTCCAAGGCCACAACCGAGACTAAAACCACTTAAAAGAAATCTTGACAAAAAGAGTTCTCAATCAGTGTGATAAGAAAACCAATAAACTGGTCTCACTGTGAATTTTTGTACTGGTCTTGTTTTGGGGAACATGATTTATACCATGTATAAAAGCAACCCATATTATAATAAATATGAAAATTAGTTTATTAATAGCAGAGTAAGTTTGCCAATTAGAAGCATAATAGAAACAAATGATTTGTAAAACTGCATGACACAACGTAGGCGTAATAGGCAGAAAACTTTTAAAACAAAGCAAATAACGTCTAGCCATAAAAAACATCTAGTATTAGTATTGATTCATTTGAATAAAGCATAAGACAGCCAATTACTGAATACCAATTACTAAACACACAATTACAAAGATTGTTTTCATGCATATTTTGTTCATTAAGATGCATTACTAAA
Associated Phenotype:
Not determined