ZMP
shisa7
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q1LUE0]
Human Orthologue:
SHISA7
Human Description:
shisa homolog 7 (Xenopus laevis) [Source:HGNC Symbol;Acc:35409]
Mouse Orthologue:
Shisa7
Mouse Description:
shisa homolog 7 (Xenopus laevis) Gene [Source:MGI Symbol;Acc:MGI:3605641]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36791 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23454 | Nonsense | Available for shipment | Available now |
sa15345 | Nonsense | Available for shipment | Available now |
sa10850 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36791
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 |
---|---|---|---|---|---|
ENSDART00000092006 | Nonsense | 95 | 501 | 1 | 9 |
ENSDART00000148073 | Nonsense | 172 | 620 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 10858272)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10316811 |
GRCz11 | 19 | 10235736 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCACCCAGCCCCCGGTCCGGCACGACCCAGATTTTGACCCGCTGCAA[C/T]AACAGAGCAACAACACCGCTTACGTCATTGGGGGAGTCATCTCTTTCACC
Long Flanking Sequence:
CCGCAGTGACTCTTACCTCTGAACGCTCCTCAGTGAATGGGGGGCCGGTGCTGCTTCTGTTGCGAGGACGTGGCCGTAAGGCCCCTCCGCCTGATGTGCAGGGCAAACAGGCCGCCGCAATGGCGGCAGAGCCAGAGGCAGCCGAGATCCCTCCAAGGCCCCTGCCGCAAATTATGCTTCCCCTCAATGTGACAGACTATGCCCTGAAGCCCCCGCTGGGAGCCGCACAGGTGGCACCTCCTCCTCAGCGACTGGTGGACGTGGATGTGTGTCAGGGCTACTATGACGTGATGGGACAGTTTGACAATACTTTTAACTGCACCAAGGGCACCTACGTCTACTGCTGCGGCACCTGCCACTATCGCTTCTGCTGCGAGCACCAACGGCAACGTCTAGACCAAGACTCCTGCACTAATTACCGCTCACCTGACTGGGCCGTCACGGCGGGACCCATCACCCAGCCCCCGGTCCGGCACGACCCAGATTTTGACCCGCTGCAA[C/T]AACAGAGCAACAACACCGCTTACGTCATTGGGGGAGTCATCTCTTTCACCATGGCCGTAGCCATTGGGGTTAAAGTGGCCTTCCATAAACTGTCTCGACGGCCGAGGAACAGAGACATCAACATGCCTAGGTGAGTGACAGGGAAGGGGACAATGCTGTACACATCTGAGTCTGCATCAGTGAATGCCATCTGAAGAGATCCGTAGTGATCTTGATGTCAGACTCTTTCAGCTTTGGCCTTTTGATTCCTTCATACACTCATCCTTCCTTTTTCTATCGTTCGTCTATCTCTCTGTGTTGTTCTTCAGAGCTCTGGTGGACATTCTGCGTCACCAGTCCAGTCCGGTCCAGCAAGGAGAGAGAAACAACAGCACGGTCCTCACAACCGCCACCTCCAGCGAGGGCACCCTAGGGCGCCAGGCGAAAAACTTCTACGCTCCTGTCCTCCAGAGCAAAGACAACCGGAGTGAGTCTCACATGCACTTAAAAGTTATACAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23454
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 |
---|---|---|---|---|---|
ENSDART00000092006 | Nonsense | 127 | 501 | 1 | 9 |
ENSDART00000148073 | Nonsense | 204 | 620 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 10858176)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10316715 |
GRCz11 | 19 | 10235640 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACCATGGCCGTAGCCATTGGGGTTAAAGTGGCCTTCCATAAACTGTCT[C/T]GACGGCCGAGGAACAGAGACATCAACATGCCTAGGTGAGTGACAGGGAAG
Long Flanking Sequence:
TGCAGGGCAAACAGGCCGCCGCAATGGCGGCAGAGCCAGAGGCAGCCGAGATCCCTCCAAGGCCCCTGCCGCAAATTATGCTTCCCCTCAATGTGACAGACTATGCCCTGAAGCCCCCGCTGGGAGCCGCACAGGTGGCACCTCCTCCTCAGCGACTGGTGGACGTGGATGTGTGTCAGGGCTACTATGACGTGATGGGACAGTTTGACAATACTTTTAACTGCACCAAGGGCACCTACGTCTACTGCTGCGGCACCTGCCACTATCGCTTCTGCTGCGAGCACCAACGGCAACGTCTAGACCAAGACTCCTGCACTAATTACCGCTCACCTGACTGGGCCGTCACGGCGGGACCCATCACCCAGCCCCCGGTCCGGCACGACCCAGATTTTGACCCGCTGCAACAACAGAGCAACAACACCGCTTACGTCATTGGGGGAGTCATCTCTTTCACCATGGCCGTAGCCATTGGGGTTAAAGTGGCCTTCCATAAACTGTCT[C/T]GACGGCCGAGGAACAGAGACATCAACATGCCTAGGTGAGTGACAGGGAAGGGGACAATGCTGTACACATCTGAGTCTGCATCAGTGAATGCCATCTGAAGAGATCCGTAGTGATCTTGATGTCAGACTCTTTCAGCTTTGGCCTTTTGATTCCTTCATACACTCATCCTTCCTTTTTCTATCGTTCGTCTATCTCTCTGTGTTGTTCTTCAGAGCTCTGGTGGACATTCTGCGTCACCAGTCCAGTCCGGTCCAGCAAGGAGAGAGAAACAACAGCACGGTCCTCACAACCGCCACCTCCAGCGAGGGCACCCTAGGGCGCCAGGCGAAAAACTTCTACGCTCCTGTCCTCCAGAGCAAAGACAACCGGAGTGAGTCTCACATGCACTTAAAAGTTATACAATGGCACGAAAAGTAAGGGAATAATTAAATGAGAGGACATAGAGAATGCAGTGTTTGAACTGTAGAATCAAGAGCATAGAAAATAAGTCTGAAGGCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15345
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 |
---|---|---|---|---|---|
ENSDART00000092006 | Nonsense | 147 | 501 | 2 | 9 |
ENSDART00000148073 | Nonsense | 224 | 620 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 10857938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10316477 |
GRCz11 | 19 | 10235402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTWTYTCTCTRTGTTGTTCTTCAGAGCTCTGGTGGACATTCTGCGTCAC[C/T]AGTCCAGTCCGGTCCAGCAAGGAGAGAGRAACAACAGCACGGTCCTCRCA
Long Flanking Sequence:
CGTCTACTGCTGCGGCACCTGCCACTATCGCTTCTGCTGCGAGCACCAACGGCAACGTCTAGACCAAGACTCCTGCACTAATTACCGCTCACCTGACTGGGCCGTCACGGCGGGACCCATCACCCAGCCCCCGGTCCGGCACGACCCAGATTTTGACCCGCTGCAACAACAGAGCAACAACACCGCTTACGTCATTGGGGGAGTCATCTCTTTCACCATGGCCGTAGCCATTGGGGTTAAAGTGGCCTTCCATAAACTGTCTCGACGGCCGAGGAACAGAGACATCAACATGCCTAGGTGAGTGACAGGGAAGGGGACAATGCTGTACACATCTGAGTCTGCATCAGTGAATGCCATCTGAAGAGATCCGTAGTGATCTTGATGTCAGACTCTTTCAGCTTTGGCCTTTTGATTCCTTCATACACTCATCCTTCCTTTTTCTATCGTTCGTCTATCTCTCTGTGTTGTTCTTCAGAGCTCTGGTGGACATTCTGCGTCAC[C/T]AGTCCAGTCCGGTCCAGCAAGGAGAGAGAAACAACAGCACGGTCCTCACAACCGCCACCTCCAGCGAGGGCACCCTAGGGCGCCAGGCGAAAAACTTCTACGCTCCTGTCCTCCAGAGCAAAGACAACCGGAGTGAGTCTCACATGCACTTAAAAGTTATACAATGGCACGAAAAGTAAGGGAATAATTAAATGAGAGGACATAGAGAATGCAGTGTTTGAACTGTAGAATCAAGAGCATAGAAAATAAGTCTGAAGGCCTGATTTTAGTCGACAGATTGACAAGCCTGAGTGTATGTGGTAATGTAGAACAGACGATGTGTCAGAAATGAGTCAGATTACTTCTGCTTCAGAGGCAGAAGCTGCTATGTAACCACATGGAACTAGGGCAGCAAATTAAGAAAGAGGTGCTTTCATCAAGGCTAAAACATTAACGACTAACTTCTAGGACAGGGGTATTCCAAGTATACAGCTCAGGGGCAATTTATAGACTTTATTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10850
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000092006 | Essential Splice Site | 252 | 501 | 6 | 9 |
ENSDART00000148073 | Essential Splice Site | 348 | 620 | 5 | 6 |
ENSDART00000092006 | Essential Splice Site | 252 | 501 | 6 | 9 |
ENSDART00000148073 | Essential Splice Site | 348 | 620 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 19 (position 10847683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 10306222 |
GRCz11 | 19 | 10225147 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACGGTGATGAAACCAGAGCTTAACCGCTACAGCTCCCTCAAGAGACTGG[G/A]TAAGTGAGTGTGCNTGGTTTTGGTGGTTTACGAGGACACCAATTTATATA
Long Flanking Sequence:
CAGGGGGAAAATCCCTGAAGTGTGTGTAGTGAAAATTACTTTGAATATAAAAAGTGCCTGTGGAGCATTATTATCGTTATTTAAGGACGTATTACATTCAGTGGGAAAGCGAGAACAAGACATTACACTAGTTATGTTCCACTCTCATTGCATTCATAGCTCTTTTTAGACATCTGCCTTTGTCATTTAGAGAATCTGGACGCATCTTCAGTGTTCCAGTCACCCACATTTCTTTAGACCCACATTGCACATTCGACCTGGGTAGATGTGCCTTGTCGGTCTTTGTCTTACTTTCTTTTGTTCTCCTCTCTCAGAGCGAGTTCCACGCATGAACAACACCCAGCTGGCCTCCACAGGAACACTGCTGTCCAGCAAGCACAATAATTCCGGTTTCCACCCCTCCTTCTCTCACTCCTTCCACAACCTGGCCCAGCTACCTCCATCATACGAGACGGTGATGAAACCAGAGCTTAACCGCTACAGCTCCCTCAAGAGACTGG[G/A]TAAGTGAGTGTGCCTGGTTTTGGTGGTTTACGAGGACACCAATTTATATAATGACATTAATATAATTAAAGTAGTTTATGAGGACATGCAAAACTCGTAATAAAAAATGATTAAACACTCACCTGCCACTTTATTAAGTACACCTTACTGATACCGGGTTAGACACCATTTTGCCTTCAGAACTGCAGTAATCCTTCATGGCATAGATTCAACAAGGTACGGGAAATATTCCTCAGAGATTTTGGTTTACATTGACATGATAGCATCATGCAGGTTGCTTCAGATTTGTCGGCTGCACATCCATGATGTGAATCTACATCCCAAAGTTGCTTTATTGGATTGAGGTCTGGTGACTGTGGAGGCCATTTGAGTACAGTGAACTCATTGTCATGTTCAAGAAACCAGTCTGAGATGATTCGTGCTTTAAGACATGGCGTAGCCATCAGATGATAGGTACACTGTGGTCATAAAGGGATGGACATGGTCAGCAACAATACTCA
Associated Phenotype:
Not determined