Busch Lab

ZMP

svopl

Ensembl ID:
ENSDARG00000057983
ZFIN ID:
ZDB-GENE-041114-109
Description:
Putative transporter SVOPL [Source:UniProtKB/Swiss-Prot;Acc:Q1LVS8]
Human Orthologue:
SVOPL
Human Description:
SVOP-like [Source:HGNC Symbol;Acc:27034]
Mouse Orthologue:
Svopl
Mouse Description:
SV2 related protein homolog (rat)-like Gene [Source:MGI Symbol;Acc:MGI:2444335]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa25275 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33395 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa1011 Nonsense Available for shipment Available now
sa33394 Nonsense Mutation detected in F1 DNA Not yet available
sa18140 Nonsense Available for shipment Available now
sa6048 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa25275
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080744 Essential Splice Site 108 506 5 17
ENSDART00000129271 Essential Splice Site 85 483 4 16

The following transcripts of ENSDARG00000057983 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 8840359)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9777207
GRCz11 4 9778123
KASP Assay ID:
554-7640.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCGCTGCGAATGGCATCTGGAGGATTGGCAAGTGGCCCTTGTCTCCACG[G/A]TGAGGAGCTCGTCCAATCAGAGCCCTGTATTTCGTGAAGTTTTGACAGGA
Long Flanking Sequence:
AAAATAAAGATGGCATTAAAGCGATCGTCTTCCATGAAGACCCAGCTAGTGGATGCCATCCAGCTCGAAGAAGTGGAGATGGAGGAAGAGATCACCACCACAAGCAACAATAACAATCCTGTTGAACCTGCTCAGGTCAAAGGTGAGAAAACAACATGCGCAAACCAGCCTATTAACTACCTGCAGCCAGTCGTTTATTCTTTTCAATCTTTAACCCATACAGAGCCGAAATGCTACACCGTGGAGGAGGCTGTGGAGAGCATTGGTTTCGGATGTTTCCATATTCTGCTTTTTGTCATCATGGGCAGTGCCAATGTAAGACAACTGCATGCGTTTCTGTAATTCATTAACCTGCAATTAGTGTACTTGCTGTTTACATTTTTCATTGCTGGTGTGTGTAGATAGTGGAAGCGATGGAGATCATGTTGTTGGCTGTGGTTTCTCCTGAGATCCGCTGCGAATGGCATCTGGAGGATTGGCAAGTGGCCCTTGTCTCCACG[G/A]TGAGGAGCTCGTCCAATCAGAGCCCTGTATTTCGTGAAGTTTTGACAGGAATGTCGCAATACAAGATGTACATGTTTTGCTTTTGTGCTTATCTAAACATTCTGGTTTATCTATTGTATCTTTTTAGAAGTGATGCCGTTTATTTATGGATAAACCTACTAATCTACTTCCTTCTGTCCTAGATTAATGTGCAATCTAAGTGAAGTTTGCTGTGAGGTGCTATCAAATGCAGAAGTAGTCAGTTTAAGTGCTTTCTGCTGTGCTATTTTAACAGTTCCTAATTGTTTTTTGTTAGGTTTTACCTCCAACCAAGATAGAAAAATACTATATAAGATATAAATTGAAGCATCGGCTCTTTTCTCATCAGTTCTGAGGCTGCAAAAAGATAACACAGGTCCATGATAACCACTGAAATTATTCATGCCAGGACATGGCGATGTCACTTTGTACAGAAACATGATGCACATGCATTATATTTCATTTAAAGCTAACAAACTGCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33395
Status:
Mutation detected in F1 DNA
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
ENSDART00000080744 Essential Splice Site 132 506 6 17
ENSDART00000129271 Essential Splice Site 109 483 5 16

The following transcripts of ENSDARG00000057983 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 8839575)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9776423
GRCz11 4 9777339
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTGGGGTCCTCTGTGGTTACATTGCTGACAAATACGGACGCTGGAAGG[T/A]GAGATGACATTTCTTTCGATTTTAGTATAACATGTTTTTATTAAGTTTTA
Long Flanking Sequence:
GTTTTTTGTTAGGTTTTACCTCCAACCAAGATAGAAAAATACTATATAAGATATAAATTGAAGCATCGGCTCTTTTCTCATCAGTTCTGAGGCTGCAAAAAGATAACACAGGTCCATGATAACCACTGAAATTATTCATGCCAGGACATGGCGATGTCACTTTGTACAGAAACATGATGCACATGCATTATATTTCATTTAAAGCTAACAAACTGCACAAATGGAGAACACATGTTTTAACTTCTATTGTGGGTTGCAATGATTTATTTATTGGGGTTTATAGATTTAACTATCAATATTGATTATATATAGGTGTTTATTTTCATTTAAAGGCTTCCTCTCACTCGTTTCAGGTTCAGTAATGGTTTTTAATTCAGGAGACGGTACATGAGACTTATTCTATTGGTGTGTGTGTGTTTTGTTTTAGATGGTGTTTTTTGGTTTCATGGTTTGTGGGGTCCTCTGTGGTTACATTGCTGACAAATACGGACGCTGGAAGG[T/A]GAGATGACATTTCTTTCGATTTTAGTATAACATGTTTTTATTAAGTTTTACAGTAAATCAAACCCCATTACCCAAAACGTATAATAAAAATCACATCAAACTCCAATTTACACATTCCACAGCTTTACGTTTCTAAAGCTTCTTCAAAATTTCCATCACAAAGTACATAAACAGCTCCCAGATATGGCAACAATCAAAGGTTTCTTTCTTATAACATATGTGAGCTTTTTCAAGAGCCAATTATGTTGAGTTATTACGTTTATTTAACTATAGTCTATTGGAAGGGCAACTAACATTTATCCAGCACAAAAGCAATAGTTTGTATTAAACATTAATGAATCTTTTTTTTATTTATTTTGTATTAGTAGACAAAGAACAAGTTCATACATATTTAGCGTACAGTGCTCAGCATAATTGAGTACACCCCATTTAAAAAATGAATATCTTTATCTGTTTCTCAGTGAATGAAGATCATATATTTTGGTGTGTTTAAACAAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1011
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080744 Nonsense 140 506 7 17
ENSDART00000129271 Nonsense 117 483 6 16

The following transcripts of ENSDARG00000057983 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 8838581)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9775429
GRCz11 4 9776345
KASP Assay ID:
554-0915.1 (used for ordering genotyping assays)
KASP Sequence:
TGTCCAATTAAAATGTTTGTGYCCACAGGTGGTGTTTGGTGGTTTTGTAT[G/A]GGCGTCATATTTTTCTTTTCTCACTTCGTTCTCTACATCATACGGCTGGT
Long Flanking Sequence:
ACAAAACAGATTTATTAAACTGACATAATTATTAAAGGGATATTTTAGTTGCGGAACATCTTTAGAAATGAAAAGATAATACATTTAAATTTATGCAAAATATTGCAAAATAAACTACAAATTGGCAACAAAATTATATATTTTTTTGTTTTTCTTGATTTGTTTTTCTTCTTTTTATTAAAAGGTTAAAAAAAAAAAGGTAAATATTTTTACATAAGAAAGATTTGGGCTACTACAAATTTTTGAACTGTTTTTGTAAGTTATTCTGTTAGATTAGCTCCAGATTTGGCTTCAGTACTGACTAATTTAATGCATTTGCACAAATATAATATTGTAAAGCTTTCTATAGTAAATGTTAATTTAAAAGAGAGATTTTTGAGGGGTGTGCGCCTGTATATATGTATCTTTGAGTGTGATGTTTAGTGTAATTAGATCCAATAAAATGTGTTGTGTCCAATTAAAATGTTTGTGTCCACAGGTGGTGTTTGGTGGTTTTGTAT[G/A]GGCGTCATATTTTTCTTTTCTCACTTCGTTCTCTACATCATACGGCTGGTTCATCTTTCTGAGATGTATGGTGGGCTGCGGAGTGGCAGCAACATCTCAAGGGTGGGATTTCGCAAATGCACAGTATTTTGCTCATGCTTTCCATACAGTTTATAAATGATTGTAAATTTATAAATGTTTATGTTTCAAAGATGACAATGGGTTTTCTGGTATTAAACGGTAAATCACTAGGTTTTAACCATTTTTCAGTAAAAGTTTTAAATATAAACAATTAAATTGATCACATATTCTTTGAACTATTTTAATAACTATAAATTAAAAATAAGTATGTTGTTTTTTTTCTTTCATAAATATCTTTACACAGAATGACACAAATTTTTACTTTTTTTTCTCTCAAAAGTAACTTGAATCTTTTTAAAGAATCTTTTTAGGACTTTTTTTAATTGCATTTTTTTCTATGTACTATATTTAAAGGCACTTTTGTGAGTTTAATGTAATGC
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:
sa33394
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080744 Nonsense 302 506 11 17
ENSDART00000129271 Nonsense 279 483 10 16

The following transcripts of ENSDARG00000057983 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 8835750)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9772598
GRCz11 4 9773514
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCGTCACCCTGATCAGCTCGGCCTTCAGGAGAACATCGCTCCTGCTGTG[G/A]TATTCATGGTAAAGTCTACCACACTTCTCCTCTTTTGTCTATTATGTGTG
Long Flanking Sequence:
ACCAGTATTAATCTCCTAAAATAAATAAATAAACGGGTAAAATATTAACTGTTTAAAAGCCAAAACTGAATATTTCCATCAAAACAAATTAATTAGTCAATGATACGTCTCAGATAAAATATTTTTAAAGTGTGTGTATATTATGTCAGTGTGTGTGTATATTATATGCTGTGTTATTGATATAATAGTATATTGGAAATCATTGTATATGAAATTAAGCATTTATCCAAAAATATAAATGAAAAATAATGAAAAAATAAACATTTATTCTCTTTAAAAGGGTGAGTTCACACACAAATTTAAATGAGCTGATAATTAACTTTGGATATTCATATTTAGGTGTACTGGAACTTTAAATATTGCTGCACACATGCTATTTAAAGCATTTCCTTGAGTGTAAACAGCCTGAACTGACAGAAGTGTGTTCATATCCAGACAGAAAGAGGAAATGCCGTCACCCTGATCAGCTCGGCCTTCAGGAGAACATCGCTCCTGCTGTG[G/A]TATTCATGGTAAAGTCTACCACACTTCTCCTCTTTTGTCTATTATGTGTGTGTTTCTGTGTGCCAGATCATGTGTGATGTTCTGCATTGTTCATCCGTCAGGTTTGTGGCCTCGTTTTCTTATTACGGCTCCGTCCTGAGCAGCTCTGAGTTACTGGAGAAGAATCTTCTGTGCGTGACGGATCCTGATCTGGAGCATCAGATTAAACACATCCAGGAGGAGACGCTGTGTTACTGCATCCCCTTCAACTCGGACGATTACCAAACGCTCCTCATTAGCTGTTTAGGGGAGGTGGCACGTCAGTAACCTTTGAAATCTTGCTCACTTTAATTATTCTGCTTGGTTTGAATGCTAAATGCTGATGTTTGTTTGTGTGTTTTGTCTGCAGTCATTCCTCTTAATATCATCCTGTTGAATATAGTAGGACGGAAGTACAGCATGGTCATTCTGCTGCTGCTGTCGGCCTTTTTCTTCATGCTTGTTAATATTTGCACGACTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18140
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080744 Nonsense 437 506 15 17
ENSDART00000129271 Nonsense 414 483 14 16

The following transcripts of ENSDARG00000057983 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 8833359)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9770207
GRCz11 4 9771123
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGYCACCAAATTTAAACTKTTTATCATTGGCGTGTGTGTNNNNNNNNNNNNTTGCAGGTTTA[T/A]CCTACATCTGTGCGYTCAATCGGAATGGGCTTTTGCACATCGTTCAGTCG
Long Flanking Sequence:
AATATTAATAATATTAAAATAACAACAGATTTTCACTGGTTAAAATATTTATTTACTACTATATGTTAATAAAGTGTATGCAGCTAATATTTCATTATAATTAGTATCAGCTTTAACCTACATTCACATAACATTTACAGCTATTAATATTCTTGCTAAAGTAATAATTAAAATACCACACATATCAATTTTCACTGTTTACAATACAAATACTCACTGTTTATAATGTCTAGGTGTTTAATGTAATTTCCACATGGCCTTTTACTCGCAGTTCATATGTTAAAAGTGCTAATAAAGTGAATAATGTGTGCAGGTTAGGCTTCACAATCCTGCTCTTCCTCCTCCGCTCTGTGGTTTCAATGAATTTTAATGTGGTTTACATCTACACGGCAGAGGTGAGAGCTGATAAATGAACACTCCATTCAATCTCTGTGCCTTTAAAGAAGAGTTTGCCACCAAATTTAAACTGTTTATCATTGGCGTGTGTGTTTGCAGGTTTA[T/A]CCTACATCTGTGCGCTCAATCGGAATGGGCTTTTGCACATCGTTCAGTCGAATCGGAGGAATGATCGCACCTTTTATTGCACAGGTGCTCTATGTGTTTTGACTTTTTTAGAGCCAGGGTTCATCCGGTCATGGAATTTTGACTTGGCAATTTGCAGGCCTGGCAAAAATTTAGGAAAAACAAAAAAACTCACCAAATTTTGGAAAGTTTAGTTTAACAAATATCTCTATTCTTGAATATATAGTTTAGTTTTCTTTACTTTTTTTCTGTCCGAAAACATGCTCTCACATTATTAGTGCTGTGTAAGCATTATCTAAATTAGTTTTACATAGTTGCAAAAATACATTTAATCTAAATAGATTGTTGCATATTTAATTATATGCTGTCTTAAATTTGAACGTGTATAGTTTTTCTTATTATTTACTACATACACGTAGACATTACATGAAACATTAGGTCATAAAAGTTTACTTAATTTGTGGAATTTTAGCTGTAAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6048
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000080744 Nonsense 500 506 16 17
ENSDART00000129271 Nonsense 477 483 15 16

The following transcripts of ENSDARG00000057983 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 4 (position 8831654)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 9768502
GRCz11 4 9769418
KASP Assay ID:
554-3969.1 (used for ordering genotyping assays)
KASP Sequence:
GCATCATTTGTGCCATAGGAGTTTTTTTCCTGCCCATTGAGACCAGAGGA[C/T]GAGCATTATTGGTAAACATCTACCTACTGTACTATRCAGTCAAGCCTAAA
Long Flanking Sequence:
TAATGTTTTAAATCTTTAAAAACATTAAATATTAACATCACCAATGAATAATAATGCTTAACAAGAAGTGTTCATTGTCAGTTTAGTTTAATTACCTCATTTAAAGGATTAACAAACAATAGGCCTATAAAGGATCTGAATATTCTCAATCAGAATCTCATTCATGTCATATACTGTAGGCCCGATTTACATTAAAGTGATGGTGTCTTGAAAATAAATGTAAATAAACATTTTCATAATTTTGAGCAGTGATGATGCCATTGTTAAAAAATATTCTAAAGGTTTAAATAAATTATTTATTGCATTTGGATCACACATTATAAATATAGGTTTTTGAAGATTGGCAGCAAAGCAGTTACACATTCTGATTTCTTCTAAGGTTATGTTTCGTGTTCTAGGTGTTGATGTCCAAATCTGTGATTCTGGCTTTATCACCGTTCGCCACAGCGTGCATCATTTGTGCCATAGGAGTTTTTTTCCTGCCCATTGAGACCAGAGGA[C/T]GAGCATTATTGGTAAACATCTACCTACTGTACTATACAGTCAAGCCTAAAATTATTCAGTCATTAAAAAAACTTGCTTATTGATTAAAATTAACTTCAAGTCAGAATTTGCCAGGGGTATGAATAATTTTTTAATCTGTCAAACTAAATAGTTCGCTTTCCTAGAGTTTCACAACTTTGTGTTTTGCTTTCTTCCACCATTTCAGCAAGATGCCTGAAGTTCACCAAACAGAGATGAAGGACAATTGCACTTTTCTAACAAAACATGAACTCATATTAAAGCTGGATCCATTTTTTTAAGAATTTCAATGCTGCCTGTGATACGTTCTTCATTATTTATAACAATTAAAGAATATATATATTGTCAAATCTTTGTTCCTGTGTTGACATATTTCTTCTTGCAATGACATCGCAAAACTCACCAAAACCAAGATATGGCTAGATAGTGGGAGACTAGTATTAGAAGAGGACACAATCTCATTACTTAGCATTTATTTGATA
Associated Phenotype:
Not determined