ZMP
invs
Ensembl ID:
ZFIN ID:
Description:
Inversin [Source:UniProtKB/Swiss-Prot;Acc:Q8UVC1]
Human Orthologue:
INVS
Human Description:
inversin [Source:HGNC Symbol;Acc:17870]
Mouse Orthologue:
Invs
Mouse Description:
inversin Gene [Source:MGI Symbol;Acc:MGI:1335082]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12246 | Nonsense | Available for shipment | Available now |
sa14224 | Nonsense | Available for shipment | Available now |
sa12856 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12246
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015688 | Nonsense | 494 | 1025 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 29713574)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27550712 |
GRCz11 | 16 | 27485335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTATGTGTTAAGGGGAGAACCGCACTCCACTGGTCCTGTAATAATGGTTA[T/A]CTGGATGCTGTGAAGCTGTTGCTGGGGTGTGGGGCATTTCCCAATCACAT
Long Flanking Sequence:
AACATGACAAACCTATGTGACTACATTAGTACAAAAATTCCTAGATATCTCAATTTTAATTGTAACAGTTTCTAGTGTTCACAGCAAATCTAACCCTGTTATATATATATATATAGGAGGTGCTCGTGTTGATCTAGTAGACATAGATGGGCACTCTGCACTGCACTGGGCAGCTCTGGGTGGTAATGCAGAGGTGTGTGAGGTGCTAATGGAGAATGGGATCAGTCCTAACCTGCAGGACCAAGCTGGACGGACACCCTTACAGTGTGCAGCGTATGCTGGCTACATAAACTGCATGGCCTTGCTCATTCAGCACGATGCAGACCCTAATATTCAGGACAAGGAGGTATGAGTGTGCAGCATGCCTGAGAACATGTATTGGCCATTACCTCTGAGTGGCCTGCTATTGAAAGCTCGAAGAATAGCACTATGTATGACTTTGGTGTGTGTTTATGTGTTAAGGGGAGAACCGCACTCCACTGGTCCTGTAATAATGGTTA[T/A]CTGGATGCTGTGAAGCTGTTGCTGGGGTGTGGGGCATTTCCCAATCACATGGAGCACACTGAAGAGAGGTAACAAAGAGACAAACACTCTTGAATGGTTGGCCTGGTGGTTATGGTTCTGAAAGAGTGTCGACTCATGGCACAGATTCACTTTCTAGAACCTTCTTAAGTTTGTGTGTGTATTTTCAGGGGGAATCCAGCTGTTCACTTCAGCAAGGATGCAATAAACAACTCCTTCAGGAGTGTTCAATTATTTTGGAAATAAAAAAGACACATTTTACAAAAAATCGTTGTATTAAGACAGCAAAACACAAGAATTGAAGAATATAATGCCATTCGCTTTGAGAAAAGTCATCTCAACTTTTAGGCTGCAAATATAAAATAAAAATGTACCTGCAAAATCTTGTAGCAACTTAATAAATAAAAAAAAAGACAATGGCGATTTTTGGTTTTCAAAAAAAATTTAATAAAAAATTCTGAACTTTCGTTTATCCAAAGATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14224
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 |
---|---|---|---|---|---|
ENSDART00000015688 | Nonsense | 763 | 1025 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 29721928)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27559066 |
GRCz11 | 16 | 27493689 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACYACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCC[A/T]AAAATGCCTCCCAGGACACAYCACAACACAATGAGACACAGACAAYGTCC
Long Flanking Sequence:
CCAGCCAATCACCTAACTTGATTCCAATATAATATACCTAAATCTGGTTCAATTCCATATCAACCGCTTCTTTAGAAATATAATTCCTAGGAAAAACATGACATGTTCAATACTTATTTCCCCTGCTGTATATGGCACCATGTTACAACATGTATTGTTAATACACTTCCATAACCATAATTCTTTTCTTTTCTTCAGAGCGCAGAACAAGAGAACCTGAAACATCAGATGCTCCCTCCATCAGATCTCTCCCTCCAGTGACGCCAATGAGCACCAAGAAGTGTCCAGTCACCAGAGAGGAGGTGTGTGTGAGAGAAACATTTGGTCCAGACACGGGCATATCATTGAATTGTGGATCTGCAAATGAGCGCCGATCCCCCGCTGGCTCCAGTCGACCAGGCAGTGCCAAACCAGTCCACACAGGGGCCCATGTAGCACCAGGCCACATGGAGACTACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCC[A/T]AAAATGCCTCCCAGGACACACCACAACACAATGAGACACAGACAATGTCCAAAGGAAACAAACCCATATCAGAACACAAACCTACAGGAAGCCAGCCATCCAACAACACTTCTGTCACAAGGCAAAAAGAGAAACGACAAGAAAAAGAGACACACAGAGAAAAGGATAAAAGATCAAGGACTGAAGGAGATAAACAGACTGTCAGAGAGAAACAGAAAGGCACGGGGATTGAGAGAGACAAAGAGAGATTGATGGGCAGGACGAGAAAAAAACTAGCGGAGAAAGAGAAGGAAAAGAGGAGAGACGGCACTTGTAGTAAAAACCAGGCTGCTGTTGTGATACAGAGAGCATGGAGAAGGTACTTATGTCCTTTTACTACAAGAAGTACTTCATTCTGAGAAGCTTCAACAGTTGTGTATAATCATATACTTTTGTGTAATGACATTTAAACTTTGTGTTAGAGAGTTGATGCTGGAAGCCAGTCTACATTACATCTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12856
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000015688 | Essential Splice Site | 882 | 1025 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 16 (position 29722288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 27559426 |
GRCz11 | 16 | 27494049 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGTAGTAAAAACCAGGCTGCTGTTGTGATACAGAGRGCATGGAGAAGG[T/A]ACTTATGTCCTTTTACTACAAGAAGTACTTCATTCTGAGAAGCTTCAAYA
Long Flanking Sequence:
CAAATGAGCGCCGATCCCCCGCTGGCTCCAGTCGACCAGGCAGTGCCAAACCAGTCCACACAGGGGCCCATGTAGCACCAGGCCACATGGAGACTACCCCAACCCCTAAACCAAGACCTAGTACTACAGGTGCCCACTCCAAAAATGCCTCCCAGGACACACCACAACACAATGAGACACAGACAATGTCCAAAGGAAACAAACCCATATCAGAACACAAACCTACAGGAAGCCAGCCATCCAACAACACTTCTGTCACAAGGCAAAAAGAGAAACGACAAGAAAAAGAGACACACAGAGAAAAGGATAAAAGATCAAGGACTGAAGGAGATAAACAGACTGTCAGAGAGAAACAGAAAGGCACGGGGATTGAGAGAGACAAAGAGAGATTGATGGGCAGGACGAGAAAAAAACTAGCGGAGAAAGAGAAGGAAAAGAGGAGAGACGGCACTTGTAGTAAAAACCAGGCTGCTGTTGTGATACAGAGAGCATGGAGAAGG[T/A]ACTTATGTCCTTTTACTACAAGAAGTACTTCATTCTGAGAAGCTTCAACAGTTGTGTATAATCATATACTTTTGTGTAATGACATTTAAACTTTGTGTTAGAGAGTTGATGCTGGAAGCCAGTCTACATTACATCTACATTACGGTTACATTACATTAGATATGCACGGTGGCTCAGTGGTTTGCACGGTTGCCTCACAGCAAGAACGTCACTGGTTCAGATCCCGGTTGGGCCAGTTGGCATTTCTGTGCGGAGTTTCCCCGTTTTCGTGGGTTTCCTTCCAGGTGCTCTGGTTTCCCCCGCAATCTAAGGCATGCGCTATTAGTGAACTGGATGAACTAAATTGGCCATAGTGTATGAGTGTGTCTGTGAATATGAGTGTGTATCGGTATTTCCCAGTACTGGGTTACAGCTGTAAGGGCATCCGCTGTCCTTCATATGCTGGAATATTTGGCAGTTCATTCCACTGTGGTGAAGTCTGATAAATCAGAGACTAAGCT
Associated Phenotype:
Not determined