ZMP
itsn1
Ensembl ID:
ZFIN ID:
Description:
intersectin-1 [Source:RefSeq peptide;Acc:NP_997065]
Human Orthologue:
ITSN1
Human Description:
intersectin 1 (SH3 domain protein) [Source:HGNC Symbol;Acc:6183]
Mouse Orthologue:
Itsn1
Mouse Description:
intersectin 1 (SH3 domain protein 1A) Gene [Source:MGI Symbol;Acc:MGI:1338069]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15350 | Essential Splice Site | Available for shipment | Available now |
| sa32751 | Nonsense | Available for shipment | Available now |
| sa25652 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15350
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000000087 | Essential Splice Site | 264 | 1746 | 8 | 38 |
| ENSDART00000132378 | Essential Splice Site | 240 | 1722 | 8 | 38 |
| ENSDART00000139573 | Essential Splice Site | 240 | 1221 | 8 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 47552390)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46364051 |
| GRCz11 | 1 | 47055283 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTATTCTRATGCAGTCCAGTCTACCACAAGCCCAGCTGGCCACCATCTGG[T/C]GCGGATCCAACCTGTTTTTTCTTRCTCTGTCTCYGTCTCGCATTAAAAAC
Long Flanking Sequence:
TGAGTAATAATGATGCTGAAATTTCAGCATTGCCATCAAAGAAATCAATTACATTTTAAAATAAATGAAAATCGAACAGTTTTGTTAAAATTGTGTCAAAAGTAATTTACAAATATTACAGTGTTTACTATATATTTGTCATTAAATAAATGCAGCCTTGATACAGGTGAGACTTCAATTCATTTACTTTAATCAATCAGTTGATTCAGCATATTTTAATTTAATTTCAGTTTTGCACCATCCATATTTTTTTATGAAAATGGAGCTATATGATTTGCAGGTTTGCAAAAATGACTATGGTTTGCAGAATTCAGAGTTCTTGTCATGAGTGAAAGTGGTTAGTCAGAGCAGCTTAGAGGAAAGAGAGCTTTGCTGATTCAACACAACCAGCTTTGTTTCCCCCTTTCATTCTCTTTTTCTCCCTTTCTGCCTCAGGTCCACAAGCCAGAACTATTCTGATGCAGTCCAGTCTACCACAAGCCCAGCTGGCCACCATCTGG[T/C]GCGGATCCAACCTGTTTTTTCTTACTCTGTCTCCGTCTCGCATTAAAAACTCAAACAAATCTCTGAGTTCGGAGATTCGTATCAGTGTAAACACACGGATTGGTATCTGGTTATTGTTATGAGTAAATCCATCAGTTGTTTTGATTTCTTTTAACATGCTGTTCTCAGATCTGTGTATGGCCTAAGGCTTTGTTTACTCTTGATGTTAACACAGCTGAACTGCTCACACGTGGACCAGCATAATAAATCGCTGTTTTGCCGTCTACCTGTTTCTCCCTGTAGGAATCTGTCAGATATAGATCAGGATGGGAAGTTGACCGCTGAAGAGTTTATTTTGGCCATGCACTTGATCGACATGGCCATGTCTGGTCTCCCTCTTCCCCCTTTGCTGCCGCCTGACCTTATACCTCCAACATTCAGGTGAGAGACTTCGACCAAACAAAACTAAAGTTACTCTGTTAGGCCTTGATCACACCAAACACACTTTTTGCATTGAGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32751
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 |
|---|---|---|---|---|---|
| ENSDART00000000087 | Nonsense | 546 | 1746 | 14 | 38 |
| ENSDART00000132378 | Nonsense | 522 | 1722 | 14 | 38 |
| ENSDART00000139573 | Nonsense | 522 | 1221 | 14 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 47540995)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46352656 |
| GRCz11 | 1 | 47043888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTAGGAGTCTCAGCAGTGGTTGAGTCGCTTGATTCCTGATAAACAGTG[T/A]CTGAATGACCAGCTGAAGCAGGTTCAGCAGAACAGTCTGCACAGTAAGAG
Long Flanking Sequence:
TCCTGCTGGAAGTAGCCATCAGAAGATGAGTACACTGTGGTCATAAAGGGATGGACATGGTCAGCAATGATACACAGGTAGGCTGTAGCAGAGACATGATGCTCAATTGTTAATAATGGGACAAAAGTGTGCCAAGAAAATGTATCCCCGTGTCATTACACCACTCCACCACCAGCCTGAACTGTTGATACAAGGCAGGATGGATCTAAATTCTGACCCTACCATCTGAATGTTGCAGCAGAAATCGAGACCAAGCAAAGATTTTCCAATCTTCTATTGTCTAATTTGTACAAACTTTTATTTTGGATGCAATTAATTGTTGCCGAGCACTTGTATGCATGTAGGTCTGTGTGTATATGTGCGAATAGATAACAGGATTCAAATTGTTCTGTGTATAAATGTTTCCAAGTAATCAGAGAATTTTATAAGTTTTCTCTCTTTTTTTTTCCTCATTAGGAGTCTCAGCAGTGGTTGAGTCGCTTGATTCCTGATAAACAGTG[T/A]CTGAATGACCAGCTGAAGCAGGTTCAGCAGAACAGTCTGCACAGTAAGAGCATTTTCCTCAGTGCAGTTTTCAGTTCATGTCTAGCTCAGTGTAAAAAAAAGCTACTTAAAAGAGCTTGGAAAGCTGTAAGCATTATGGGGCAAAGCAGGAGTAAAAAAAGGAAAACTGCTATCTGTCAGTGGCCCATACTGACTTGAGTATCTAAAGTAAATTGAGTAGAAATGCAAGATGTTTATATTTAAGGAGTGCTTATTTTAAATTTAGGCACACAACGGGATTAGGCTCGGGAACTAGAGCATTTGAAATTTGTATTTTTATCAGTGTTTGAGTGCTGTGTCAATCTGCTAACGGATCCGCTGATAGACTCTGCTTTCAAATGCTTCAGTGTCTAAGTGCTCTTGTAAACTGGTGATTATTAAAGCCAATCACAGTCATATCTGCTTTGTTTGTAAACACAATGGCCATTTAGCAGTGTTTGTAGATCAAATAAAAAAATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25652
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000000087 | Nonsense | 1217 | 1746 | 27 | 38 |
| ENSDART00000132378 | Nonsense | 1193 | 1722 | 27 | 38 |
| ENSDART00000139573 | Nonsense | 1193 | 1221 | 27 | 28 |
Genomic Location (Zv9):
Chromosome 1 (position 47517055)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 46328716 |
| GRCz11 | 1 | 47019948 |
KASP Assay ID:
2259-1008.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGGGAAGGGCCAAATCATCAATGTGTTGAGCAGAGAGGATCCCGATTG[G/A]TGGAAAGGAGAGTTGAATGGATCCGTCGGCCTCTTCCCCTCGAACTACGT
Long Flanking Sequence:
CCACGTTATTGGAAATAGCCTCATTTTATGACTTCCCTAGAGTTAAACAGTTTTACCATTTTTTTAATACACTCAGCTGATCTCCACGTCCAGTGGGAGCAAAAATAAAAATATAAAAATAAACAAAAAAAAGGTTTTGATAATAATTTCTATACAAGCTTGACTCTTCTGTAGTTACATCGTGTTCTAAAGTCGATCTACTCATACAGAAGTCCAATTCAACACAAACCCACATTTGCATGTTTTGCTTGTTTGTCTTCAATTGCATCAAATAAATGACCTGGGAATCAAATATTTTAGATAAAAATAGCGTGACCTACTGTATATAGCTTGGAAAATATGCTTGAGCATTACAATACATTTATACATATGCATTTGTGTTTCCTCTTTGCAGTGTGCCAGGTGATTGGCATGTATGATTACACTGCTCAGAATGATGACGAGCTGCCTTTCGGGAAGGGCCAAATCATCAATGTGTTGAGCAGAGAGGATCCCGATTG[G/A]TGGAAAGGAGAGTTGAATGGATCCGTCGGCCTCTTCCCCTCGAACTACGTCAAGCTGACCACCGACACAGACCCCAGCCAACAATGTGAGTCCAAAATGCTCTCCTGTATCTTACACACACACAGTTACACTGATCTTTCATCTATCTTGCTCAAAAGAGATGTAGATCAATTTCTCTTTAAAGAGACAATTGGCTTGCGTCACCAATAGCATCCGATTAAATGAACCGTGCCACTCTGATCCAAAGCTACTACTTTCAAATCTTTGAGGACCTTCTTCGATTTAGTTTAGCCATGTCCTCACAGTGTGGTGAGGTTTAAAACGTCCAATGTCCAATCCTTATCCTCTGCCACAATGAAGCCCCTCCTCTTCCTGTTTCCAAGCAACCTCTCACCTCATGTTGTAGAGCATTAAGTAGAACCTCACCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTGCCT
Associated Phenotype:
Not determined