ZMP
krt8
Ensembl ID:
ZFIN ID:
Description:
Keratin, type II cytoskeletal 8 [Source:UniProtKB/Swiss-Prot;Acc:Q6NWF6]
Human Orthologues:
KRT8, KRT8P11
Human Descriptions:
keratin 8 [Source:HGNC Symbol;Acc:6446]
keratin 8 pseudogene 11 [Source:HGNC Symbol;Acc:31058]
keratin 8 pseudogene 11 [Source:HGNC Symbol;Acc:31058]
Mouse Orthologue:
Krt8
Mouse Description:
keratin 8 Gene [Source:MGI Symbol;Acc:MGI:96705]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa1629 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1629
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 |
|---|---|---|---|---|---|
| ENSDART00000081215 | Nonsense | 6 | 520 | 1 | 9 |
The following transcripts of ENSDARG00000058358 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 10360380)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 23 | 10319182 |
| GRCz11 | 23 | 10254152 |
KASP Assay ID:
554-1570.1 (used for ordering genotyping assays)
KASP Sequence:
TCATTCTCTACAAGACAGAAAACACACAAGGCAGGATGTCCACCTACAGC[A/T]AGAAAACCAGCTACACCGTCAAGTCTTCTTCCTCTGGATCTATCCCACGC
Long Flanking Sequence:
GCCTTGCATTGAAGGATTTCAATACTAATGTTTAATTTTACTGACATACAACGTTTTAAAATGTTGGTATTTTGGCTTTTATTGAAAGTGTGATTCATTTTGTACAAAATAAAACAAGGTATATTAACTTGAACAAACTGAGGGAGGGTCACTAGTTTTTCAAGCACTTAATTATCCCAGAAAATGTCTGTTTCTGGTCATATTGAATTACAAAAAAGATCCATGTACTGGTTAGACTAGGAATGCAGGACAATGTTGGATTGAATTTCAGCCACACCCACCTTCTACACCTAAACACCGACCAATCAGACCCCTCCTTTGGCTCCACCCACTCCGTGTCCAGCGCATAAAGAGCAAGACAGAGTCAGCCGTTCTCTCTATCTGCTCGAGTTTCTCCAGCACAGCAGACAAGGCTCATATCTGCTGCTCTCGCTCCCCCTTTGCTCCAGGTCATTCTCTACAAGACAGAAAACACACAAGGCAGGATGTCCACCTACAGC[A/T]AGAAAACCAGCTACACCGTCAAGTCTTCTTCCTCTGGATCTATCCCACGCAACTTCAGCAGTTTGTCTTATTCCGGCCCCAGCATGAGCCGGCAGAGCTACAGTGCACGCAGCTCCTATGGAGGTGTCAATCGTGGCATGGGAGCTGGAATGGGAGGTGGTAGTGGCTTCATCTCTAGCTCTTCAGCCTACGGTCTTGGCATGGGCATGGGTACCGGAATGGGTGCAGGAGTCGTGGCACCAATTCAAGCAGTCACCGTCAACAAGAGCCTCCTGGCACCTCTGAATCTGGAGATCGACCCCAACATCCAAATTGTCCGCACCCAGGAGAAAGAGCAAATCAAGACCCTCAACAACCGCTTCGCTTCCTTCATTGACAAGGTAGGTTTGACATTTCTTTTTTTGGAGTTTTTTGGAGCAGAAAAGTGGAAAAACTGACTGCGTTCTTGCTTAAAAAGTCTGTAAAAGTTAGTCTAGAGTGGAACAGAAACTATATATTGG
Associated Phenotype:
Not determined