ZMP
si:dkey-266k12.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human and mouse intersectin 2 (ITSN2) [Source:UniProtKB/TrEMBL;Acc:Q5RI29]
Human Orthologue:
ITSN2
Human Description:
intersectin 2 [Source:HGNC Symbol;Acc:6184]
Mouse Orthologue:
Itsn2
Mouse Description:
intersectin 2 Gene [Source:MGI Symbol;Acc:MGI:1338049]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23703 | Nonsense | Available for shipment | Available now |
sa11816 | Essential Splice Site | Available for shipment | Available now |
sa23702 | Nonsense | Available for shipment | Available now |
sa17221 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23703
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000170 | Nonsense | 48 | 1418 | 1 | 30 |
ENSDART00000062780 | Nonsense | 239 | 1639 | 7 | 38 |
ENSDART00000143558 | None | None | 173 | None | 5 |
The following transcripts of ENSDARG00000000161 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 25422889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 25494192 |
GRCz11 | 20 | 25393282 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAGTACCGACAACTGTTTAACAGCCTGGACAAGCTAATGAGTGGATA[C/A]CTGTCAGGTGAGTTTATGTGTGTGTAGATCGCAGGAAGAAGAGGGGATGG
Long Flanking Sequence:
TGAGTCATTGTAGAGATGTATGGATGCAGTCGTTCAAGCTCATGGGAATCAAACACAATATTAATTCTTTTTCCACTATTGTTTATTTAACATTTTATACAGTACATTATTTCTGTTAAGTGACAAGACTTTTGCCTAAGCGAAGTCAGGTCTTACTGTCTTATTGAAATAATTTAAAATCAAGACATGATCATATTTTAAACAGTAAAATAAATGTAATATAGAGGCTTTTGCCTGTCATATAAGCCACTTTGAAACCAAATTATCAATACTAATTTGTTGTGTCTAAAACTTGGATAGGCGACGAGACTGTTGTCAGGCAGTGTATATACACTAATATAATATATATTTCTAAATGTCCACAGTTCTAACTCGTCCTCCACCACCTCCCTTGCGAGTAACTCCCCGAAAACGAGTAGTTCTGATTGGGCAGTGCCTCAGTCATCCCGTCTGAAGTACCGACAACTGTTTAACAGCCTGGACAAGCTAATGAGTGGATA[C/A]CTGTCAGGTGAGTTTATGTGTGTGTAGATCGCAGGAAGAAGAGGGGATGGCAATGTTTGCTTATGATCATGTGTGAGCATCTCTCGTTTGCCATATGCATTAACTTGCTAGTCTGTATGTTTGAAGGTCCCCAGGTCAGAAATGCCCTCACAGCTTCAAACCTCACACAAACACAGCTTGCCACTATATGGTGAGTTCACACAACACTGCTTTCACTATTGATAAAACACAACATGATGCCTTTAATGTATGATGGTTTTGATAAATTAATATCTAAAAATTAAATGTATCTTATTTTGGGAAGCCCTAAACTGCTGTTTTGTTTGTGTGACAGTGATCTATAAGGGTCTGTCAGTTTACTTTAGCTTTGTTCTTACAAAAAAATTACATGATTGCCTCCTTCTTCCCTTAACATTTAACTTTGTTACATGGTTTTATCATTTTTTTTTTTATAAATGCAAATGGAGAAGTATGTACATGTTTGTGTGTGTATGTTTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11816
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000000170 | Essential Splice Site | 118 | 1418 | 4 | 30 |
ENSDART00000062780 | Essential Splice Site | 309 | 1639 | 10 | 38 |
ENSDART00000143558 | None | None | 173 | None | 5 |
The following transcripts of ENSDARG00000000161 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 25421617)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 25492920 |
GRCz11 | 20 | 25392010 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAACAAGWTATGAAGGAGACTGTGTTTATTCTGTGCCTATAWTTGTTTTC[A/T]GAACAACTAAGTCATGTGACCTGCTAAACGGACCTGTTCCTCTGATTAGC
Long Flanking Sequence:
TTGGTTTTTGTATGTTAAATAAAATAAAACAAAATAAACTAAAATTAAATTAAATTAAATTAACATGTTGAAGACCTCTGAATTAATCACTTCCACACATTAAACTGTGGGTTCAACCTTATTTCTTTAAGCAGTGTGTTAAACATCTACTTCCACAGTCTTGCGTCTGCAGTTTAGCTGCCAGTTGTGTAATTATGAACTGTGATTCAGCTATTAAACATTTGAAATGCTTCCAGGATAATCCCAGAAGTATATATATATATATATAAAATGTCTTTCTACAGGTTTCTGGCTGATGTGGATCGTGATGGGCAGTTGAGAGCAGAAGAGTTTATTTTAGCGATGCATCTGGTTGAAATGGCCAAGACAGGGCGGCCTTTACCTCTCACTTTACCTCCCGACCTTGTGCCTCCTTCACTCAGGTAAACACACACACAGGTCTGCTGGCATTAACAAGATATGAAGGAGACTGTGTTTATTCTGTGCCTATATTTGTTTTC[A/T]GAACAACTAAGTCATGTGACCTGCTAAACGGACCTGTTCCTCTGATTAGCACTGAGCTGATTGAGCCAGAACTGCCACAGAAAAACAAGAGCAATGGTATTTGGATATGCACACACACACTTGTATATCTACTTTATGAAGACTGTCCATAGGCATAATGGGTTTTTATACCGGGGTTAAATTTATATAAATAAATAGATACAGTGTATTATGTATATGATTGATGCTAAGCTAAGCTAAAAGTGCTCTCGGCAAATCTGGAGATCATCTAAGTGGATTCAAAATGGTCAAACTCAGCTTTTTAACTTATGGGTAAAAATAGAGTATTCCTTTAAGGAAGAAATGCCGCTTATTTTGAAAAAAGCCATCCCAGTTTCAGTTAATTTAGGCCACAAAAATCTGATAAATAGCTACAAAATCCTGAAAGAACTGGAAAAAACAATTCACTTCTGATTTTGAGTTAAAAGCATTAAACTGTCATTTTTTAAATATGCAGTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23702
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 |
---|---|---|---|---|---|
ENSDART00000000170 | Nonsense | 235 | 1418 | 5 | 30 |
ENSDART00000062780 | Nonsense | 426 | 1639 | 11 | 38 |
ENSDART00000143558 | None | None | 173 | None | 5 |
The following transcripts of ENSDARG00000000161 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 25420828)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 25492131 |
GRCz11 | 20 | 25391221 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAGAGAGAGGAGGAGCGCAGGATGGAGAGACAGAGAGAGCTGGAGCGA[C/T]AGAGAGAGGAGGAACGACTGAAAGAATTAGAGCGGCGAGAGGCAAGTAGA
Long Flanking Sequence:
CAAACTCAGCTTTTTAACTTATGGGTAAAAATAGAGTATTCCTTTAAGGAAGAAATGCCGCTTATTTTGAAAAAAGCCATCCCAGTTTCAGTTAATTTAGGCCACAAAAATCTGATAAATAGCTACAAAATCCTGAAAGAACTGGAAAAAACAATTCACTTCTGATTTTGAGTTAAAAGCATTAAACTGTCATTTTTTAAATATGCAGTTTCTGTGCAAACTAATACTGTTTTCTGTCTTTCTCAGTTTCATATGAAGACAAACTGAGGGAAAATTTCCAGAGGGGAAACGCAGAGCTGGAGAAGCGTCGCCTGGCTCTTCAGGAGCAGCAGAGGAGAGAGGAGGAGCGCAGGAGAGAAGAGGAGAGGCGAGAGGAGGAGAAGAGACAGCAGAAGGAAAGAGAGGAGCGAGAGAGGAGAGAGAGAGAAGCGCGAGAAATGGAGATCAGGAGACAGAGAGAGGAGGAGCGCAGGATGGAGAGACAGAGAGAGCTGGAGCGA[C/T]AGAGAGAGGAGGAACGACTGAAAGAATTAGAGCGGCGAGAGGCAAGTAGAGCAAGCAAGGACATACAGAGGGTGAACCACCAGCAGAAAAACACAGCAGAGCCCCACGCTTTAACACAAACACGCAGGCCTTTTATACCGATACATTTGTTCTAGAAAATATGCTAATATTAATCATGGTTTGAAATACAGTTTTGTAATACTAAATAATTGACATATAGTAGTTTATTCATTCATTCATTTTCAGCTTAGTCCCTTTGTTTGCCACAGCAGAATGAACTGCCAACTTATCCAGCATATGTTTTACATAGCGGATGCCCTTCCAGATGCAACCCATCACTAGGAAGCACCCATACACACTCATGCACACACATACACTGCGGATAATTTAGCCATTTCACCTGTACAGCATGTTTTTGGACTGTGAGGGGAAACCGGAGCACCATGAGGAAACTCACCCAAACATAGGGAGAACATGCAAACTCCACACAGAAATGCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17221
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 |
---|---|---|---|---|---|
ENSDART00000000170 | Nonsense | 591 | 1418 | 12 | 30 |
ENSDART00000062780 | Nonsense | 772 | 1639 | 18 | 38 |
ENSDART00000143558 | None | None | 173 | None | 5 |
The following transcripts of ENSDARG00000000161 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 25405193)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 25476496 |
GRCz11 | 20 | 25375586 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATCCCTTCACTGCACGCAACTCAGACGAGCTCACGCTGGAGGCAGACTG[T/A]TTCATCCAGGTGCATATGGCACTCRTGCGGTTTTAAAGTGGACCTATTAT
Long Flanking Sequence:
CAGTCAGAACAACTGACAGAATCTTTCTTTGGTTGATGTATAAGGAGAGTGATGAATTGTCCAGCATGAGAAAAAGCAATGGGTCACATTGGATCTGAGTTTCCATTAGTTCTGATTGTATCTTGGTCCAGAATAATGCAATTTGGGGACATTCCCAGAACATATGTATATAACTACCTTGAGTAGAGTTGTTACATAAGTGACAAAAAGGGTCTAAAATTGGGCATTATTTAGGAAAAAACTAACAAATAAACACACACATTTACACTTTTGGTATTATATCAAGTAAAAAAGTTATCTTCCATTCCTAACACATGCAGTTACTTTGCTGATTGGCTGTGTGATTGTCATTACATGTTTTTGTTGTTTTTTATGTGTGTTTTTTCAGTTTTGCAGCCAGTAGTGATCCCTGAAGTCACGTGTAGTTCTCTGACCACCTACAGAGCTCTCTATCCCTTCACTGCACGCAACTCAGACGAGCTCACGCTGGAGGCAGACTG[T/A]TTCATCCAGGTGCATATGGCACTCATGCGGTTTTAAAGTGGACCTATTATGCAAAAATCTATAAGGGGTTTAAACACAGTTGTGTGGCAACAGTCTGAGAATCTCATTAGCTTCTATTAGTAAAAATGCATTAGTTTTATTTTTTTAGAATCACACTTCATAAAAACAGTGTGCAGAAACATTGAACATCAGAGTGTGAAAGCCCCGCCCATTAGTGATAATCTCTCTCTAATTAGCATAAGAGGTTAGTCTTGTTTTTTAATCTGCCACTATGCTGACACATAGGCATTTGTAGCTCCACCCTCTTTTGAAATGAGAGCTGGGAGCACAATCTCATTTTAATTTAAAGCGTCAGTCACCAAAATGACACATTTAGGATCAAAGCAAAAAAACAGCTGTTTCAAAGTGTTATAAATTATTATTTTGAGCTGAAACGTCACATATACACATAGGGACATCAGAGACTTCTTGCAAAAAGGAGCATAATAGCTCTCATTTAG
Associated Phenotype:
Not determined