ZMP
si:ch211-238a12.4
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens SRGAP1, SLIT-ROBO Rho GTPase activating protein 1 (SRGAP1) [Sourc
Human Orthologue:
SRGAP1
Human Description:
SLIT-ROBO Rho GTPase activating protein 1 [Source:HGNC Symbol;Acc:17382]
Mouse Orthologue:
Srgap1
Mouse Description:
SLIT-ROBO Rho GTPase activating protein 1 Gene [Source:MGI Symbol;Acc:MGI:2152936]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43065 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25055 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23247 | Nonsense | Available for shipment | Available now |
sa16150 | Nonsense | Available for shipment | Available now |
sa36592 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa32190 | Essential Splice Site | Available for shipment | Available now |
sa43064 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43065
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088908 | Essential Splice Site | 167 | 1073 | 4 | 22 |
ENSDART00000140403 | None | None | 929 | None | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 12411385)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12994014 |
GRCz11 | 18 | 12962732 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCAGCTGCAAGAAGATTTGATGAAAGTCCTCAACGAGCTCTACACGG[T/C]AAGTACTGTAACACTTATCACATTTGTCGAATTCTAGAAAGTTCCTCATT
Long Flanking Sequence:
AAACCATTTTGAATGCGCCTCTGATTGACTGGGCCTCTTGCAAAAAATGACACAGTTGGACCGACACTGTCATAACCTTTTATATCACTGTTTTTAAGTGCTGAAGAAGCCTTTGTGAGCTGAAATATTAAATATGGTAATGGACATTTCAAATATGCCAATCATTGTAAGCAGTAGACCAATCACAATAGACTCTCTCTGACCAATCATAGCAGAGTAGGCTCGTTTAAATGAGAGTAGATCCTTGAATGAACCATTTCTGATGACGATAATGCCATTTATACTATGAGAAAAAAGTGTTTCGTGATCTTTAATGGATGTAAGGACATTATGGGACCATCAGAATCAAATTTAGAGCCTTTAAAATGCCATAATAATGGGACTTTTTATCAGTGAGATACCTGATGCCACCTTTTCTTTTTCCCTCTCTCATCAGAGTAAAGAAATCACCTTTCAGCTGCAAGAAGATTTGATGAAAGTCCTCAACGAGCTCTACACGG[T/C]AAGTACTGTAACACTTATCACATTTGTCGAATTCTAGAAAGTTCCTCATTAATAAAAAAAATATATATATTTAATTTCCATATTCATTAGAATTTCATTCCCATAGTTTCCGGCTGCACTCAGGAGTGCGCCATAGGAAAAGACCCATAAAAGTGCCCATACTCCACGCATACCCTCCACATCTCTGACCTCGCTAGATTACTGTGTTTACACCAATAATCAATAGTTAATTCTCACACTTTAATTGCAGCTGTCAGGTCCATCGCAGTTGCTTACAAGATTCATGTCTCTTTTGCTTCCCTTGCAGTTTTAATAAGATGCTAATATATTCTCAGGCCTTAAAAAACATCTGTGGATAGACTTGTCCTCTGTGTGTCTGTTTGGAAAATATCGTGTCGTGTGTGTTTTTCCTTTACACCTCTGTTCGCTTTTGTTGCTTTGTCTTTTATTGGTGCGACTGAACTAAAAAATACTATATAACTGCTCATTAATGCTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25055
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088908 | Nonsense | 175 | 1073 | 5 | 22 |
ENSDART00000140403 | Nonsense | 8 | 929 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 12405981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12988710 |
GRCz11 | 18 | 12957428 |
KASP Assay ID:
554-7419.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGATCTCTGATCTGTGTCCCGCAGGTGATGAAGACCTATCATATGTA[T/A]CACACAGAGAGCATCAGTGCTGAGGGTAAACTGAAGGAGGCTGAGAAGCA
Long Flanking Sequence:
TAGGCATAATCAGTTTGTTAGTACAGGCTCATACACTCTAATTCACATCCTAATGCCTGTTTTTAAATTCATCTGCATATGACTAATAACTACCCAACCAAAACATTGACTCAATTCGAAACAATGACTCAAACTAAAAAAAAAATGACTCAAACAACTGAAGTACCATTATTTTTTTACATGTATATCTCTTACTTTACAATGCGTATCAAGAATTCAGAGTCGATATATGTATAAGCTAAATATAAACATTTGTATCTTAACATATCTTCACATATATATGTATATTTTGACGTTTAAATGCAAATTAGTGTGTATGAAGAAATTTCTGAACATTAGATGTTGTTTTTTCCACTTTTATTGTATTTTTTTAGTTTGTTTATATTCAGGAATCTACTGTTAATTGATTTGTGTAAAGTGTAAAGATTAACTTGCAAGGTAAACTTTAACCTTTGATCTCTGATCTGTGTCCCGCAGGTGATGAAGACCTATCATATGTA[T/A]CACACAGAGAGCATCAGTGCTGAGGGTAAACTGAAGGAGGCTGAGAAGCAGGAGGAGAAGCAGATCGGCCGCGTTGGAGATCCAGTTTTCCACATCCGGCTGGAGGACAGACACCAGAGACGCAGCTCCGTCAAGAAGATCGAGAAGATGAAGGAGAAGGTTTGTAGGAAATCATCTTCAGTACGTTTGTAACTAGCAAGTGAACCATCCATTGGTTCAAAGAGTGTCAGGCACAGAGAGTTTATATATACATTTGATTCTTAAAATTATTAGTTGATTATTAAAATATAAACTATTAGTATTATTTTTTTATTTTTCAATTATTTATCAAATGATATTTAACAGAGCAGAAAGGAGATCAGTATTTTTACTAATATTTTTTTCTTCTGGAGAAAATCTTATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTAAATTAAAAAAAAAAGTTCTCCCCATTAAACAGAAATTGGTTAAAAAAAAAAAAAAAAAATATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23247
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 |
---|---|---|---|---|---|
ENSDART00000088908 | Nonsense | 339 | 1073 | 7 | 22 |
ENSDART00000140403 | Nonsense | 172 | 929 | 3 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 12398361)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12981090 |
GRCz11 | 18 | 12949808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGGAAATGTACCCGACCGCCTTCTGCCCTCCCGTCAAATTTGAGTTT[C/T]AGGCACATATGGGAGACGAGGTCAGTTTTAATTATAATTTTGGATTAAAC
Long Flanking Sequence:
ATTTTATAATGCAGCGAATATTACTTACAGATTTGAGAAACCCATTTGCAGTGCTGTTTTAGTATAACTAATGCTTTATTTTGTCAGCATGCATTAAATCTGGTTTTGTTTTAATTTTATATTTAATTTTACTTTTTTATTTAGTCATCAATAATAACACCGCATTCTTTTTAATTGATGAAATACAGATACAGATAAAAGAAGAATCATTTTAAATCACTCTTGAAATCTCATAACCTACATCGTTAATTAGTGACTTTTTATTCTCTTTTTTTTGCCCTCCCTTTCTTCCTGTACAGTGTTGTGATCTGGGATATCATGCCTCTCTGAACCGGGCATTGCGGACCTACCTCTCAGCCGAATATAACCTGGAGACGTCCCGTCACGAGGGCCTGGACATCATAGAGAATGCAGTGGACAGTCTGGACCCCCGTAGTGACCGCCAGCGCTTCATGGAAATGTACCCGACCGCCTTCTGCCCTCCCGTCAAATTTGAGTTT[C/T]AGGCACATATGGGAGACGAGGTCAGTTTTAATTATAATTTTGGATTAAACCAATGTAAACTCAAAGTGAGAATGTAAATATAGTTGTTATTTTTTTCAGTTTAAGACATTAATGATATGTCATACTATATTTTATACTATAATGTTTGGCTTATTTATTTTAAATTGCCAGGCATGTCAACTTTTAGATCTCAGCTTAGTTCCCTTATTCCACAGCGGAATGAACCGCCAACTAATCCAGCATATGTTTATGCAGCCGATGCCCTTTTAGCAGCAACCCAGTACTGGGAAACACTGTACACTCTTATTTATTCATACACATACAGTACACTACGGACAGCTTACCCAATTCACCTATAGCGCATGTCTTCGGACTGGAAATCGAAGCATCCGGAGGAAACCCATGCAAACAGGGAGAACATGCAAACTCCTACCAGAAATGCCAACTGACCCAGCTGAGGCTCAAACTAGCAACCTTCTTGCTGTGAGGCAATCGTGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16150
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 |
---|---|---|---|---|---|
ENSDART00000088908 | Nonsense | 400 | 1073 | 9 | 22 |
ENSDART00000140403 | Nonsense | 233 | 929 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 12379956)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12962685 |
GRCz11 | 18 | 12931403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGAGGCRACACTTACTACCATCCAGGACATGGTGACGGTTGAGGATTA[T/A]GACGTATCTGAAWRTTTCCATCATAGCCGCTCAACTGAATCAGTTAAATC
Long Flanking Sequence:
AAGATGAGAATGAAATTGGTCACTTACACGAAAGCACAGACTCAATATTTGAGTCAACAGACAACAAAACCACAAAAAACATTAGAATTACACAAAGTTTTTATTTTAAAGCGGAGAAATGGACTCTGTTTTACTATTGTAGATTATAATCCGTAATGATGAATATGCACTTCAGCTCAATAATTATGACTAAGCTGCAATTTAATGAAACCCTATTGACTATTTTTAAAAGGGGGAGGAGCTACATATTTAATTTTCACAAAGTTTTGTATTCCAGAGCACTTTAGGCGACCTATAATGTATTTTTCTAGCACTTTTGACACACCTTTTTATTAATCAATGTTGCAGCTATGTACTGGACTAAAGTAGCCATTAGTGGTCATTGATATTCTGTATGTGAACTTTGTCATTCCAGCTAAAAATGACTTTATATTTCAGATCAAGAAGACGTCTGAGGCGACACTTACTACCATCCAGGACATGGTGACGGTTGAGGATTA[T/A]GACGTATCTGAATGTTTCCATCATAGCCGCTCAACTGAATCAGTTAAATCTACCGTGTCTGAAACCTACCTCAGCAAGCCGAGCATCGCCAAGAGACGCGCCAACCAGCAGGAGACTGAGCAGTTCTATTTTATGGTCAGTATGCTTCAATCTGTTGTTGTTTTAGAATGTTTTTTTTTTTTTTTTGACTTTTAAAAATAGTTCAACAAATGTCAATATATATCAATATGTATCAATATTTCCAGTATATATATATAATAATATATTATATATTAAATATATTATATATATAACAATAATAAATAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTATTTATTATTGTTATATATTTAATATATTTATTATTATTATTATTAAACCCATATGTATTGGGTTTTACTGTGCTCAAATTGGTTTGGTTACTCAAATTAAGTTCACAGTTCATTAGTTTTTGAATTTAAATGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36592
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088908 | Essential Splice Site | 723 | 1073 | 18 | 22 |
ENSDART00000140403 | Essential Splice Site | 579 | 929 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 12351444)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12934173 |
GRCz11 | 18 | 12902891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAGGTTGATCAGGATGGAGGAGCAGAGACCCACACCAGTGAGGATGG[T/A]AAGCTTGTTTTTGTTGTTGTTTTTGTTGTACATCCTGTAGGGATATGTAT
Long Flanking Sequence:
GTTACGCAGCACCTGAAAATAGTCCCCAGCCAAGTAACTACCTAACAATGCTGTGTAATATCATTGTGCCTGCTGCAGCCATGATACTGCAGCAAATTCCCTTTACTATTACGCCAGAATGAGAGTATACAGTAGTTCCTATCCATATCACTGTAGGCACATGATGACTTAATGCATTGAAGTCTTTTTTGATTCATAGATCTTTTATGAAAAGTTGTATTGTAATTAATGTCAATGAATACTCTATATATAAAGTTACCTCAAGCCTTTAGGCTGAAATGTTTTTAAGCTCATGAGAAACATTGAGTTACTTTCTAGTTTTACAGAAAAATCAGATACAGAAATGTTAAGTGTTTCAACTACAGTAGTTTCTATATTGTTTGATGAGTTAATGAATTGATGTCCTCTGTTTTCTGCAGTGAGAGTCCATACAGTGAACATGGAGCTCTTGAAGAGGTTGATCAGGATGGAGGAGCAGAGACCCACACCAGTGAGGATGG[T/A]AAGCTTGTTTTTGTTGTTGTTTTTGTTGTACATCCTGTAGGGATATGTATAGTATGATACACTGTACCATGCCAGTGAATGTAGGCTATACACTAAATCTAGAATTACAGAGGCAGTCATTTTGACCATTTTCCAGTTTCGGTAAAATAAAACCCATATAACTATAGTGCCATGACTTTTCCTATGTGTGTATATTTAATTCGGTCACACTTTGTTTTACTGTACAATTCACACTATTAACAAACCATTAACTAAGACTTTTCTCAATAACTCAATAAAATACTAGCTGCTTATAAATAGGTAGTAACGTAGTAGTTAGGTTTAGGTATTGGGTAGAATTAGGATGTAAAATAACATCATAATTTAAAAGTGCTTATAAATGCTGTGAATTGATCATTAAAGTAAAGTGTTATCTTTCATTCTAACTCACTAAAATCACGAGAGTTCTGAGCATTTTTACTTTGAATGATGATAGCAGTCAAATTAACCACAAGCATCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32190
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 |
---|---|---|---|---|---|
ENSDART00000088908 | Essential Splice Site | 783 | 1073 | 19 | 22 |
ENSDART00000140403 | Essential Splice Site | 639 | 929 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 12337595)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12920324 |
GRCz11 | 18 | 12889042 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGGCATAGATGGACTCGTGCCTCACCAGTACATTGTTGTTCAGGATAT[G/A]TGAGTATCTGAACTGTTTAGTCAGCAAAATAAAACTTCACTGTAATGACT
Long Flanking Sequence:
GGATATATTTTTCTTCTTTCTACATTATATTACTTCAAACTACTAAAATGTCAATAAAATTAACAAAAATTAAAAGTCGACAGAGCTACAATCAAGCACCCATAATGCAATTCACAACCGTAAATAAACAGAAAACACAAAATACAGAAACTGTCAATTTACAGATATTTTTTTTACAGTGTACAAGCAAGAGTCAAAATCCAGAATGCTTTCATTTGCAGCACGGAGCTGATTTTTCAAAGACACATTCTGGGGACACCAAAGATAAAATTGTTATTTATTTATTTTAAACGATGCTTTGTGTTTGTGTGTTTTACAGAGGGAGAGCCCATTGAAGCCATCGCCAAGTTCGATTACGTGGGCCGCTCTGCGCGGGAGCTGTCATTTAAGAAGGGGGCATCTCTGCTGCTGTACCAGAGAGCATCCGACGATTGGTGGGAGGGCAGACACAATGGCATAGATGGACTCGTGCCTCACCAGTACATTGTTGTTCAGGATAT[G/A]TGAGTATCTGAACTGTTTAGTCAGCAAAATAAAACTTCACTGTAATGACTGTAATGATTCATATCTCAAGGAATGAAATGAAGGAACTAAAATGAATTTAAATCATGTTTGATACACTTTTACATTTAATACAATATACAATTAAATTTACATTGAATACAATATAACATATCTTCATCACTTTTTAAATTTGGTATTATTAACATTTTTAAACATTTTAAGCAAAATTTCAATTAATATTTTTTGAAATCTAAAAAATCACCTAATTTTTTTTCTAACTCAGGGCTTTGTTGAAGCAGTTTTGAGCTTATTAAATTATTAAATGTAAAAAATAGGGAAAAATGTAAATATGAAGAGTACAGATACAAAAACCTTCAAGTACCATCTGAAATTTTCTTTAAAATGAGCATTTTTCTCACTGCAGTTCTATTCATCTTAATTTCTATAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTAACATAGAAGTCCTAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43064
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088908 | Nonsense | 840 | 1073 | 21 | 22 |
ENSDART00000140403 | Nonsense | 696 | 929 | 17 | 18 |
Genomic Location (Zv9):
Chromosome 18 (position 12320244)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 12902973 |
GRCz11 | 18 | 12871691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTCTCTCCATTTACCAGGCACAGAAAGAGAAGTGACCCTCCAACCCGC[A/T]GACCTCCGGCTCGCCCAACTGACACCCACTGCCTCGTCCACCCATCTCAT
Long Flanking Sequence:
TCAGCTGCGCCTCTAGCTCCGCCTTTTGGCACCCTTTTGCTGTGCTAGGTACCTTTTGCAAAGGGTACCCAAAAAGTGGTACGGTACGATTCACTTTTAGGTACCTTTTAACAGTGGAAACGGCCATAAACGCATATCGAACCGATCCAAACCGTACCACTCAGTGGAAATGGGCCATAATATTGACCCTAAAATGTTTTTTTTTTTTTTTTAAAGAAAACTTCTTTAATTCTAGCCAAAGAAAAAAACTATATTATAGGAAATACTGTGTTAATTCCTTGCTCTGTTAAACATCATATGGGAAATATTTGAAAAAGAAAACAAAATTAACAGGATGGTTAATAATTTTGACTTCAACTGAAAACGTCATATTGCTTTACACCCAAATCACTCTCCAATCACATGACCCTGTTGAACAGGATGAGATGGCTGTTGAATTACTCCTTACATATTTCTCTCCATTTACCAGGCACAGAAAGAGAAGTGACCCTCCAACCCGC[A/T]GACCTCCGGCTCGCCCAACTGACACCCACTGCCTCGTCCACCCATCTCATCACAGCAGCCATACCAACCCAGATCTGGGCTCTCCGGTGATGGGCCACTACAGCCCGCGGGACATGCTGAGGGGCCGAGGACACATGCCCATGGACAGTCCAGAGAGACGACGGCGAACAGGCCATGGCAGCCTGACCAACATCAGCCGCCACGAGTCCATTAAGAAGATGGAGAGTCCACCCATCCGCCGGTCCACCTCTTCAGGACAGTACAGCAGCTTCAACGAGCCTCATGTCAAGAGTCTGGACCCCGAGAGCATCGCACAGGTCAGCGGGAGGCGAGCGACGACGCCACTCACACCATGCGCTGCAGGCCCTGCCCTGTAACATAGTCAGTTACTGCCTCCTGGTACTAATGACTAATAACATCTGCAACACACACACATACTCACACACTGGGCCTCATTAATGAAGCACAGGCAGAGACTACTTGGTTAATTAGTCAACATT
Associated Phenotype:
Not determined