ZMP
slit1a
Ensembl ID:
ZFIN ID:
Description:
slit homolog 1 protein [Source:RefSeq peptide;Acc:NP_001030140]
Human Orthologue:
SLIT1
Human Description:
slit homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:11085]
Mouse Orthologue:
Slit1
Mouse Description:
slit homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:1315203]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11050 | Nonsense | Available for shipment | Available now |
sa12013 | Nonsense | Available for shipment | Available now |
sa1497 | Essential Splice Site | Available for shipment | Available now |
sa16176 | Essential Splice Site | Available for shipment | Available now |
sa22189 | Essential Splice Site | Available for shipment | Available now |
sa35388 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11050
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 |
---|---|---|---|---|---|
ENSDART00000066080 | Nonsense | 8 | 1524 | 1 | 38 |
ENSDART00000128969 | Nonsense | 8 | 1524 | 1 | 37 |
Genomic Location (Zv9):
Chromosome 13 (position 510049)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 508032 |
GRCz11 | 13 | 638323 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTTTNCTCGGGGAGTCTTAGGAAGATCATGCCTGCGAGAGGAGGATGTTG[T/A]CTGCTGGAGGTGTGTGTGTKGGTTTTGCTGCTGGTGTGTAAGACTGRCAG
Long Flanking Sequence:
ACATGATTATACGCTGCTCTTTTAGGGAGGGGAGTGGGTTGGTGGGGGGTCTGAGTGTGTTTGGGACCCCTCCCGGGCGCTGGAGGGCCCGCCGCGGCTCCTGCGTCTGTCTGTCGGGGCTCCGGAGGATCCGCACGGGTGGGGGAGAAAAAAGGAGGAGTGTAGGGGCTGGGAGGAGTCCGGGAACTGCTATTTGTAGATCCTTGTGATGGATTACTGCCGTGTGTGTGCGTGCGTGTGTGTGTGAGAGTGTGAGTGTGTGTGTGTGTGTAGGAGAGCACAGATTTTTTGTTCCCTTTCTTTTCACGCTGCTGAGCAAACAGTGTTGCATTGAAAAGCGCTGGAGCAACTCTAGTAGAGAGAGAGAGAGAGAGAGGGAGAGTTTTTTTGTGTGTGTGTGTGTGCGCGCATGTGTGTGTGTGTGCGCGCATTGGATTTGGAAGCGCTGTAGTTTTCTCGGGGAGTCTTAGGAAGATCATGCCTGCGAGAGGAGGATGTTG[T/A]CTGCTGGAGGTGTGTGTGTGGGTTTTGCTGCTGGTGTGTAAGACTGGCAGCGGGTGCCCGGCGCTCTGCACATGCAGCGGCACCACTGTGGACTGCCACGGGCTCGGACTCAAAAACATACCCAGGAACATTCCCAGAAACACCGAGAGGCTGTGAGTTTATTTCGTTATGTGCGTTTGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGGGTGTGTGTGTTTGCAAAAGCAATTGAATGAGAACAATAGCTGAATGAGGCTGTGCCGTGATAACCTCTGGACAGGTACAATGTAATCTCATTTAATTGATATTTTATTAGTCGCATATGTGTTCACACACATGCCGTGAGATGCTTATGTATGATTGGCTGTGATCGTTATGAGTAGAAATTAATTATAGATTCAAATGAGAAATTGAGAAAAACTTTGGATATGTAGGTGTAATCATGTGCGCACTTGTGCGTACGTGTGTGTGTGTGTGTGTGTGTGTTGACATGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12013
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066080 | Nonsense | 717 | 1524 | 21 | 38 |
ENSDART00000128969 | Nonsense | 717 | 1524 | 21 | 37 |
Genomic Location (Zv9):
Chromosome 13 (position 446882)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 444865 |
GRCz11 | 13 | 575156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCATACTGATGTTGATGTTGGTGTGGTGGTGTTTTCTGTCTCAGATCAT[G/T]AGGACRTGAGCTGTGCGCCGCCGGTCCACTGTCCTGCTGACTGCAYCTGT
Long Flanking Sequence:
TGAGTCCTAATGCCCCAGTATAGTGAAGGGCACACTATACTGTCAGTGAGCGCCGTCTTTCAGATGAGACGTTAAGCTTAGGTCCTGACTCTCTGTGCTCATTAATAACCCCATGGCACTTTTGTAACCCTGGTGTCCTGGCCAAACTCTCTCCATCGGCCCTTACCCATCATCCCCATCCACCGAATTGACTCTATCACAGTATCTGGTGTGTGGTGAAGCGCTGGCGCTGTTGTCCTGTTGCTGCCGCTGCATCATCCAAGTGGAGCTGCACACTGGTTGTGATGTGGAGAGACCCCCCTCATGACTGTGAAGTGCTTTGGGTGTACGGCCATGCACAATGAATGTGCTATAGACATACACACATTACATTACACTCAGGAAGTGATTAAGTATTGATGGAACAAGAGTTTACGGATGTTTTGTGAAGTTTGGCAGGTCATTCCAGCTTCCATACTGATGTTGATGTTGGTGTGGTGGTGTTTTCTGTCTCAGATCAT[G/T]AGGACGTGAGCTGTGCGCCGCCGGTCCACTGTCCTGCTGACTGCACCTGTCTGGAGTCTGTGGTTCGCTGCAGCAACAAACACCTGCAAGCTTTACCCAAAGGCATCCCACGCAACATCACCGAACTGTGAGTGACAGCGAGTATTCTCAAAGGCCGTGTCTGAAATCACACACCTCCATGCTATATACTACACTATATAGTACGCAAAAGACAGTATGCCAGCTGAATAGTGTGTCTGAAATCAGAGTAATGTAAAAACAGATTCTGTAGTGCGCATACAATGGATGCTACACTATCCCATAATGCACCATGAGAATATTAAATAACGGGAGTGAAGTGAGGCGACTGATGTGGGTATGACAAATGGCGGATGTAGACCGTCCCAATTCCATTCACACTATCTAGAACACTCTTTTCTAAGGGTCTTGTAGTAAATTTAAATTCTGATGTAGTACATACTCGAATAGTAAGCGATTTCAGACGCAGCCAAAGTCTCGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1497
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 |
---|---|---|---|---|---|
ENSDART00000066080 | Essential Splice Site | 854 | 1524 | 25 | 38 |
ENSDART00000128969 | Essential Splice Site | 854 | 1524 | 25 | 37 |
Genomic Location (Zv9):
Chromosome 13 (position 441559)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 439542 |
GRCz11 | 13 | 569833 |
KASP Assay ID:
554-1422.1 (used for ordering genotyping assays)
KASP Sequence:
TCTGAGCTGCCGGACGGGATCTTCTCTGACGCTCAGTCACTGTCACATCT[G/A]TGAGTACAGCGAACACATCTTTCTGTGTTTGCATAGGAATAAGATTTATT
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGATGCTGTAGTATGAGAAACACGATGCCCTCAACGAACATATGTAGGCTAGCGTATGTACTTATATTTTATACATTGGGGCTGCTGAATGCTTGATTCTGATTGGCTGATGAGCAAACTAAGGTATGCTGTTATTATCAGATAAACACACAGATAAAGTAGTTCCGGCCGGTTCTGAGCACATTAGAGATCAAAACCTGCCGGAACTACTTTTATGTGTTTTTCCCAGTCAAACGTAAAGAATTAAGACTTGCTCCAGAAGTAAAAATATAATGGGAAACACTGCGAACATTTTAACATCACATGGAAACGATTGGAAAAAGATGAAACATTTCTGTTTAACATTTGCTGTTGTCTGTCATGTTTCTGACGCTTCTCAGATCTCTGCATGGGAATGATATCTCTGAGCTGCCGGACGGGATCTTCTCTGACGCTCAGTCACTGTCACATCT[G/A]TGAGTACAGCGAACACATCTTTCTGTGTTTGCATAGGAATAAGATTTATTGATCTGAATTGGCTTAATTCATGTGTTTATGTAGTTGCTAGGGTATCTAAATGGTTGCTCCAGTTTAATAAGTGAAAACAACAGAGATTTGATCATCTTGAATGAAAATAGCTCGAACCCAGTTATCTGCAATGTTCCAGGACTGAGATATGACGGGTTAATGTTGTTATATGGTTGCTAGGGTGCTATAAGTGGTTGCTAGAGAGTGGTTTTAAGTTTGTTATATCTCTATATAATACCTGCTTGATAGTCCGAGTAAAACCAGCCCACCCACAATACTCTGTGACTGTCTAAACGAGGGTGTCCAAACTCCATCCTGGAGGGCCGGTGTCCTGGAGAATATATCTCCAACCCTAATCAAACACACCTGAACCAGCTAATCAAGCTCGCACTAGATATACTAGAAACTTCCAGGCAGGTGTGTTGAAGCAAGTTGGAGCTGAACTCAGC
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa16176
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066080 | Essential Splice Site | 1107 | 1524 | 31 | 38 |
ENSDART00000128969 | Essential Splice Site | 1107 | 1524 | 31 | 37 |
Genomic Location (Zv9):
Chromosome 13 (position 435402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 433385 |
GRCz11 | 13 | 563676 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTGGACGAGCTTAACGGATACTCCTGYRTCTGCCAGAAGGGATACAGG[T/G]CTGTTCTGCACARCAAATTAATATCAAACAACACAGAATATAATACAAGA
Long Flanking Sequence:
AATATTATTATTATTGTTGTTATTGTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATGTGTTTATGAAGAGCCTACTTCTAATTTAGCACAAAACACTTGAACTAGGAGTTTACTAACTGCTTTAATTTTAAAAAATTTAATTAATAAATGCTTTAATTTAAGAATTACACTGGTAATAAGACAGAAACTCTTCAGAAAAAGATTTTCTTTTTAATTTAAAGGAGAAATTACAATTTTCTTTGATTGTTTTTCTTTTTCAACAACAATGTAATAATAAGCATGTGTGTGTGTGTCTGTCTGCCTCTCTCTCTCTCTCTGTCTGTGTATGCGTGTGTGTGTGCAGGTGTATCTGCGCTGCTGGTTATGTGGGTGAGGACTGCAGTGTGAATTATGATGACTGTAAGGATCACCGCTGTCAGAACGGAGCTCAGTGTGTGGACGAGCTTAACGGATACTCCTGCGTCTGCCAGAAGGGATACAGG[T/G]CTGTTCTGCACAGCAAATTAATATCAAACAACACAGAATATAATACAAGAAAACACTGAAGGTAGAGTCAAAAACCTTTAACCATGCACTTCAGCAGTTTCCTAACAGTGATGTTGTGGTGATTCTACAGTTGCTATGGAAACTTAACTACAGTAATTGATGTTGTGGTGATTCTACAGTTGCTATGGAAACTTAACTACAGTAATTGATGTTGTGGTGATTCTACAGTCGCTATGGAAACTTAACTACAGTAATTGATGTTGTGGTGATTCTACAGTCGCTATGGAAACTTAACTACAGTAAATGATGTTGTGGTGATTCTACAGTTGCTATGGAAACTTAACTACAGTAATTGATGTTGTAGTAATTCAACCAGTTGCTATGGCAACGCAACGACTTCAATAGTAATAATAAGCCAGTGTTTATAACCGTGACCTAAACTGAAGTGATACCCGGATCTCTGTGTGAGTGAGCTTTGAGGTGATCTGCGGTTGTTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22189
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 |
---|---|---|---|---|---|
ENSDART00000066080 | Essential Splice Site | 1227 | 1524 | 34 | 38 |
ENSDART00000128969 | Essential Splice Site | 1227 | 1524 | 34 | 37 |
Genomic Location (Zv9):
Chromosome 13 (position 433453)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 431436 |
GRCz11 | 13 | 561727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATCTCCGTATATATAATCTGACGGTCCTCTGCTGTGTGTTTTGTGCGC[A/T]GCACTGAGACGGTCAATGATGGTCAGTTCCACACCGTAGAGCTGGTGACC
Long Flanking Sequence:
GTAAAAATATGTTACTCCATATTAATAGGCTACATGCATAGGGACTTTTAATTTGTACTTAAATTATATTGCAGCATATTAATAGGGTATATGCTAAGGGACTTTTAATTTGTACTTACAAACACACTACTGCATATTAATAGGCTAAACGCACAAAAAACGGACTTTTATTTTGTAAAATGGGTTTCTTGTGTTCTGTTGATCTGCTCTTCAGGTGTCCACAGCTGAAGATAATGGCATTCTTCTGTACAATGGAGACAACGATCATATTGCAGTGGAGATTCATGAAGGTCATGTTAAAGTCAGCTACGACCCCGGCAGCCAACAAAGCCACGCCATCTACAGGTGAACACTGAACACTGCTGTCTATAATGAGCACCTATTCACTATTGAGCTGTGTGATTAGAGATCATGAGTTTTTCTGTTCAGCATTTCCCCCTCACACCTGTAGAATCTCCGTATATATAATCTGACGGTCCTCTGCTGTGTGTTTTGTGCGC[A/T]GCACTGAGACGGTCAATGATGGTCAGTTCCACACCGTAGAGCTGGTGACCTTTGACCAGATGGTGAATCTGTCTATAGACGGCGGCAGCCCCACGACCATGGACAGCTTCGGGAAGGTGCAGCCGCTGAGGGGAGAAGCTCCGCTGTATGTAGGAGGTAAGAGGGAACAACACATCTCTGCATCTGTTTATATACAACACATACTTTACAGTGAGCGTGCATCAGTCAATGCATTAGTGAACAGTGAACAGCACATCTGTTAGAGGTGAGATCAGTCCATGGTGTCTCCAGAATGTGTCTGTAAAGTTTCAGCTTAAAATATCCATCAGATCTTTTACTTTACATGCAGAACATGCCTATTTCACACGCAATCATTCATTTAATCAGTGTAAATCTACAACTGAGCTCTAAATAATCCTCCATAAACATGTTCTCTGTGGTTTACACATGTTTAATCAGATTAAATCCACAATTCAGCTGTAAATAATCCAAATAATAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35388
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000066080 | Essential Splice Site | 1279 | 1524 | 34 | 38 |
ENSDART00000128969 | Essential Splice Site | 1279 | 1524 | 34 | 37 |
Genomic Location (Zv9):
Chromosome 13 (position 433295)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 431278 |
GRCz11 | 13 | 561569 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGGGAAGGTGCAGCCGCTGAGGGGAGAAGCTCCGCTGTATGTAGGAGG[T/G]AAGAGGGAACAACACATCTCTGCATCTGTTTATATACAACACATACTTTA
Long Flanking Sequence:
AACGGACTTTTATTTTGTAAAATGGGTTTCTTGTGTTCTGTTGATCTGCTCTTCAGGTGTCCACAGCTGAAGATAATGGCATTCTTCTGTACAATGGAGACAACGATCATATTGCAGTGGAGATTCATGAAGGTCATGTTAAAGTCAGCTACGACCCCGGCAGCCAACAAAGCCACGCCATCTACAGGTGAACACTGAACACTGCTGTCTATAATGAGCACCTATTCACTATTGAGCTGTGTGATTAGAGATCATGAGTTTTTCTGTTCAGCATTTCCCCCTCACACCTGTAGAATCTCCGTATATATAATCTGACGGTCCTCTGCTGTGTGTTTTGTGCGCAGCACTGAGACGGTCAATGATGGTCAGTTCCACACCGTAGAGCTGGTGACCTTTGACCAGATGGTGAATCTGTCTATAGACGGCGGCAGCCCCACGACCATGGACAGCTTCGGGAAGGTGCAGCCGCTGAGGGGAGAAGCTCCGCTGTATGTAGGAGG[T/G]AAGAGGGAACAACACATCTCTGCATCTGTTTATATACAACACATACTTTACAGTGAGCGTGCATCAGTCAATGCATTAGTGAACAGTGAACAGCACATCTGTTAGAGGTGAGATCAGTCCATGGTGTCTCCAGAATGTGTCTGTAAAGTTTCAGCTTAAAATATCCATCAGATCTTTTACTTTACATGCAGAACATGCCTATTTCACACGCAATCATTCATTTAATCAGTGTAAATCTACAACTGAGCTCTAAATAATCCTCCATAAACATGTTCTCTGTGGTTTACACATGTTTAATCAGATTAAATCCACAATTCAGCTGTAAATAATCCAAATAATAAGTCATCTAAATTGTAAATGATAATCTGAGTGAAGTGTTGTGTGTGTGTGTTCAGGCATGCCGGTGAGCGTTCACCCCACAGCGCCGCGGGTCTGGCAGATCCAGAACAGCTCCAGCTTCCACGGCTGCATCCAGAATCTGTACATCAACAATGAGCTGC
Associated Phenotype:
Not determined