ZMP
si:ch73-78i5.3
Ensembl ID:
ZFIN ID:
Description:
Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:B5RHZ2]
Human Orthologue:
KRT222
Human Description:
keratin 222 [Source:HGNC Symbol;Acc:28695]
Mouse Orthologue:
Krt222
Mouse Description:
keratin 222 Gene [Source:MGI Symbol;Acc:MGI:2442728]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24098 | Essential Splice Site | Available for shipment | Available now |
| sa15999 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24098
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105813 | Essential Splice Site | 358 | 428 | None | 8 |
| ENSDART00000129343 | Essential Splice Site | 432 | 502 | None | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 11830332)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 11690500 |
| GRCz11 | 22 | 11720182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAATTTGTTTATGGAAAACTATCTTATGCTTTGCATTCTGTTTGCTAT[A/G]GGACAGAGAAGATAGACAAGGTCATCAGGCAATGGGAAGGGTCATTCTTT
Long Flanking Sequence:
GGGCATCGCTGATCCGTTCTTCACGGAGAAAACTCCAAAAAGAAGCCCATCCCTTCAGCGTCAGCGCAGTCTTGTCATCCTGACAGGTGAGGATAATGTAAAACACCTTAAAATAAAACCGCAGTGCACCTTGTTTGGACTTTCCACAGTAATTCTCAACAACTCTTTCCCTATACAACTCCCAGCACTTTGAGCTACTGTGCAAGTCTGCGTTTTGTTTGTGTTTCTCACCCAGAACCAGTCAGAAACAAAGATGGGGACATCTGTACTGTGAAGACTCAGGAGTATCTGGAAGGAAATGTAGTGAGGGAGAGTGCGGAGGGTCACGGAAACGTGGAGTGAGTTTGCATAGACTTATTTTTAAGCATCTCGCACTTGGCATGCTTGACCTTGCATGTGGCTTTACAAGCACTAAAATTATGGCAGAGCTTGTAGGTCAATTTTTTATTCTTCAATTTGTTTATGGAAAACTATCTTATGCTTTGCATTCTGTTTGCTAT[A/G]GGACAGAGAAGATAGACAAGGTCATCAGGCAATGGGAAGGGTCATTCTTTAAAGGAAATCCCAAGCTAAGGAAGAAGTCCGTGTCTCTGCGTTTTGACCTTCACATGGCAGTGGCGGACGAGGGCTGCAGCCAGATAAAACAGGACAGTCTCCCAAATGTGGAGGTCCGTCTTGTCATGAGACGGTCTCGCAGCATACCCACCTTCGCGCAGTGATGTCACAATGCTAGTACATCACATTTGTGACTTCACCATGCTACTACTACATCACAACTGTGACCTCACAATGCTACTGCATCACAATTAAGTAGTGGTGACCTTGTCTCAATGTCCCAGTGACTAAGGAAAGCCGATCACTTTAGTGACATGCCATTTGAGAGGAAAAAAATTTCAATAATCAGCATTCGAAAGCCCAAATTACTCTTATGATTGTAATGAACTCACTGCTACTTCTTTATCAGAAATATTGACTTAATTTTATTCAAACTTTGGTCTTTGGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15999
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105813 | Nonsense | 402 | 428 | 8 | 8 |
| ENSDART00000129343 | Nonsense | 476 | 502 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 11830200)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 11690368 |
| GRCz11 | 22 | 11720050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTCTCTGCKTTTTGACCTTCACATGGCAGTRGCGGACGAGGGCTGCAGC[C/T]AGATAAAACAGGACAGTCTCCCRAATGTGGAGGTCCGTCTTGTCATGAGA
Long Flanking Sequence:
GTTTGGACTTTCCACAGTAATTCTCAACAACTCTTTCCCTATACAACTCCCAGCACTTTGAGCTACTGTGCAAGTCTGCGTTTTGTTTGTGTTTCTCACCCAGAACCAGTCAGAAACAAAGATGGGGACATCTGTACTGTGAAGACTCAGGAGTATCTGGAAGGAAATGTAGTGAGGGAGAGTGCGGAGGGTCACGGAAACGTGGAGTGAGTTTGCATAGACTTATTTTTAAGCATCTCGCACTTGGCATGCTTGACCTTGCATGTGGCTTTACAAGCACTAAAATTATGGCAGAGCTTGTAGGTCAATTTTTTATTCTTCAATTTGTTTATGGAAAACTATCTTATGCTTTGCATTCTGTTTGCTATAGGACAGAGAAGATAGACAAGGTCATCAGGCAATGGGAAGGGTCATTCTTTAAAGGAAATCCCAAGCTAAGGAAGAAGTCCGTGTCTCTGCGTTTTGACCTTCACATGGCAGTGGCGGACGAGGGCTGCAGC[C/T]AGATAAAACAGGACAGTCTCCCAAATGTGGAGGTCCGTCTTGTCATGAGACGGTCTCGCAGCATACCCACCTTCGCGCAGTGATGTCACAATGCTAGTACATCACATTTGTGACTTCACCATGCTACTACTACATCACAACTGTGACCTCACAATGCTACTGCATCACAATTAAGTAGTGGTGACCTTGTCTCAATGTCCCAGTGACTAAGGAAAGCCGATCACTTTAGTGACATGCCATTTGAGAGGAAAAAAATTTCAATAATCAGCATTCGAAAGCCCAAATTACTCTTATGATTGTAATGAACTCACTGCTACTTCTTTATCAGAAATATTGACTTAATTTTATTCAAACTTTGGTCTTTGGATTTTAATGGAGAGTACGTATGTCTTGCGGTGTTTAAAATTTCGTAAATTGTGGCTCTAGAGTGTGTTGCTTTCGGTGGACGCTCTACTGTCATTATTTTTGATTATTACCATATATTACGTTACTGAGAAATC
Associated Phenotype:
Not determined