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 |
|---|---|---|---|
| sa37449 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa3176 | Nonsense | F2 line generated | Not yet available |
| sa24098 | Essential Splice Site | Available for shipment | Available now |
| sa15999 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37449
Status:
Mutation detected in F1 DNA
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105813 | Nonsense | 154 | 428 | 3 | 8 |
| ENSDART00000129343 | Nonsense | 228 | 502 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 11834554)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 11694722 |
| GRCz11 | 22 | 11724404 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGAAGGCCTCGAAAGGATGCAGTCAGTCCCACAGTTGTGTTTCCGCCA[C/T]AGGTACGAATATCCAGCCTCTCTCTATTCATACTCTCTATGGTCTGTTGG
Long Flanking Sequence:
TATTACAAAATGAAAACATCTATCCTGTTTGTATAGCCTTACCCTGTCTGGATAGATCAAATAATCAATAGCAGGTAAATATAGGCTAATATGTTTTGATGATATAGGAATATCCTGTTTGGGAAGAATATAGCATGCTTGCCTTAGATTGAAAGGAAGAAGGACATTTAGATTCCTCATGTGAGGAGCCCTTTAAATCCTCCTCTTCCTCCCTCTGGTTTTACACCCCCTCTCTCTCCCTCGTTGGCTGACAGAGAGAGCTGGATCAGCACCAGCAGCGAACAGCAGAGGAGTGTGATAGAGTGCTAGCGCAGGTTGCTGCAGGAGAGGATGGCAGAGGAATGGATCTCTCCCGGACCAGCACCCAGTGCGACCACTCCAGCCCAGCCCAGAGCAGCCCTGACTCAGCCACACCACCAACTCAAGCCTCAGGCTCCGGCCCAGCTCCAAAGAGAAGGCCTCGAAAGGATGCAGTCAGTCCCACAGTTGTGTTTCCGCCA[C/T]AGGTACGAATATCCAGCCTCTCTCTATTCATACTCTCTATGGTCTGTTGGCCAGGGCACTGCAGAGTGGTGAGTGTGTGTGTGTGCGTGTGTATGTGTGAGCGAGTGAAAAGACTGCTAAGCATCCATTATTATTCAAAACATAATCAAGAATGTCAGTCCCATTGAGGATATCCATCGCCTTTTTTTTCCGCTCTCATCAGTAGGTAATGATTTATTTGTCTCCCTGTGTGTTCGAGTAGAATTTATACCCTCGCACAAAAGCATGGGCCATTTGCCTTGTAGATCTCCTTGAAAAACAACAACACACTGCAGCCGTTTTTACAAAAATGTACTGTAGTATGTTGGTACCTTGGTAAATTGAGGGTATTTATGCAGTCTATAGTACTTGGTAGGTGTCCAAAAACTCCAATGAACAAAAAACAAGGTTTTACCATATGTGACGTATGTCCCAAAACATAAGGTATTTTCATTGAACATTATATCTTAACCAATTACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa3176
Status:
F2 line generated
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:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000105813 | Nonsense | 180 | 428 | 4 | 8 |
| ENSDART00000129343 | Nonsense | 254 | 502 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 22 (position 11833399)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 11693567 |
| GRCz11 | 22 | 11723249 |
KASP Assay ID:
554-3023.1 (used for ordering genotyping assays)
KASP Sequence:
AGGAGGCACGAGCCGAGCTCGCCGAGGCCCGAAAGCGATGGCACCGTCTA[C/T]AAGTGGAGATAGAATCGCTACATGCCTTGGTGTGTTTAACTCCCAAACRC
Long Flanking Sequence:
TGCTTTAAGAACAAGTACATTAGAAGAAATGAAGGCAGTGTTCAATTTCTGTGGAACTGTGCAGTTGTTCTTATCAGATGGAGACTGAACTGATTCCTAGACTGTGATATACATCAGCTCAGACCACAAGAGCATCATTTCAGTTTTCTATAATGTGAGCTATCATGTTTCCAGTGCTCACTGATGTCCCTTTTTGCATGTAGTTGTATATTGAGACATAAATCATAGATAATTAAAACAATAAGCTACCAAGGTTATGCTTTACAGTCATTTTGCTATGAGTAATAGGTGTCCTCAGGCAAGTGTGATGAAGCCTCCGTAAACCTTAGTAAGCAATATAAAACAAGCTCAAAAGTGCATCAGGTTTATTGTATTCTGCGGTGTTTTTATGTATACGTAATTTACGTGGTGGTTTTTGTGTGTAGGTGAAAGCAAGTGATGGGGCCCTGAAGGAGGCACGAGCCGAGCTCGCCGAGGCCCGAAAGCGATGGCACCGTCTA[C/T]AAGTGGAGATAGAATCGCTACATGCCTTGGTGTGTTTAACTCCCAAACGCATGCCCACAGACACACCCGGACACGCACACTCCCATTCAGGAACATGTAGACACACCTAAACACAAACTCTTATGAACCTATTGTACTTTAATGCATGACACATAAATTATAACATCACTTACTGCAATACTGAACGTTGTGGCAGAACAAGCCAGATCTGAATCCAGCACCTCCGGAATTGGTTTGAACCTTTGTTTTAGTGGACCAGACAATTTGTTTGCAGTAAAGATTAAGTGTTAAACGACATAAACTCTTCACCCAGAGAGAACAGATGCCAGGTTAGTGGTTGTCAAATATTATCGGTATTTTCAAACCAAGTACCGTTCATTGCCTAAGCGTATTTTGGCTAGTTACCTGAAGGTTGAGGGTTGCAACCCCAGAGACCAAAGCTCATTGCAGGCCCCATGTTATACAATTTAAACACTTGGAATCTAGGCTAACCCATATCC
Associated Phenotype:
Not determined
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