Busch Lab

ZMP

si:dkey-39n1.3

Ensembl ID:
ENSDARG00000058000
ZFIN ID:
ZDB-GENE-030131-6975
Description:
Novel protein similar to vertebrate centrosomal protein 350kDa (CEP350) [Source:UniProtKB/TrEMBL;Acc
Human Orthologue:
CEP350
Human Description:
centrosomal protein 350kDa [Source:HGNC Symbol;Acc:24238]
Mouse Orthologue:
Cep350
Mouse Description:
centrosomal protein 350 Gene [Source:MGI Symbol;Acc:MGI:1921331]

Alleles

There are 14 alleles of this gene:

Allele Name Consequence Status Availability
sa41151 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa1172 Nonsense Confirmed mutation in F2 line Not yet available
sa9175 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa38676 Nonsense Mutation detected in F1 DNA Not yet available
sa15445 Nonsense Available for shipment Available now
sa31635 Essential Splice Site Available for shipment Available now
sa41150 Nonsense Mutation detected in F1 DNA Not yet available
sa34350 Nonsense Mutation detected in F1 DNA Not yet available
sa21227 Nonsense Available for shipment Available now
sa41149 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa41151
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Essential Splice Site 29 3018 None 37
ENSDART00000132327 Essential Splice Site 29 1078 None 15
ENSDART00000146175 None None 1836 None 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15121471)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14566815
GRCz11 8 14604520
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCTGTCCCTTCCCAGCCTCCCTTTGCTGGGCAAGACAACAGGAGAGG[T/C]TTGTACAGCTGTGTCACTCTATCAGTCCCTCCAAAAGTTTGCGAGTCCAA
Long Flanking Sequence:
ACATACAAGGACAGGGACTCCATGTTATAATGGTATTGCCTTTTAAATGAAAAGCTCTGAGGCCATCATATGTCTGGCTTCAGGCATTCTAGCAAATTGTACACAATTTTTTTAGACCACATTGAAGGGACAACCGAGGCCTCTGGGTGAGACTTGGAAAATAAAAGTGATACGCTTTGATCAATCTATCTCAGGATCTATTGGTTGAATTTGTGGTTTGGTCAAATTTAGAGCCTCCATTTGCACAAAGCGTACTGGGAATGAAGTCATGTGTGTTAGTGCCACTTAAGGCCAAAATCTAAGCAACAAGTCATTGCCAATGAAAGCAATGTTTGACAGCAGATAATGACAAGATAATTGCTTCTCTCACATTGTTTGCCTGTTTTCCCCCTTTCCTCTTAGGTTGGCATAGCGATGTGGAGTCGCTTGCGAAGTGAGGCGGGGCCACCAGCCTCTGTCCCTTCCCAGCCTCCCTTTGCTGGGCAAGACAACAGGAGAGG[T/C]TTGTACAGCTGTGTCACTCTATCAGTCCCTCCAAAAGTTTGCGAGTCCAATAGTTCTTGAAATCGCAAGAATTGAAGTCAAGTCCTCTTTAATTCTGTAGCGCTTGTTACAATGCAGATTCTGTCAAAGCAGCTTACCATACATGGAGAAAAGAGAATGAAAAGCCACAACAATATTTCAGATTGTGGAACATTCCAGCATATCAGGCAAACAGGAGAGTAGATGTAGAATGCTACCTCTAGTTAAATTAAAACCGATTCAGTTCAAATTAATACATCAGCACAGTTAAAACCAAACAAACTAGTGGTGATGATTACAAGGAACCAAAACTCCACGATTTGACAGAGATGAAGAACAACCGTTGGGAGAAACCACAAATAATGACTTAAGGTTTGAGAAAGCCATCACAAAATCAGTCATTTTAGGCCCAAATATAAAAATAAAAATCTTCCTTGCAAAATCCTGGTGGAACTGGTGTATACTTTAAACATCCATGTGAG
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa626
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Nonsense 245 3018 5 37
ENSDART00000132327 Nonsense 245 1078 7 15
ENSDART00000146175 None None 1836 None 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15118791)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14564135
GRCz11 8 14601840
KASP Assay ID:
554-0536.1 (used for ordering genotyping assays)
KASP Sequence:
TAACACATCTCAGACGTCCAGTCCGGGCTCAATTGCTTCTGCACAACGGT[T/G]AGAGAGCCTGCGGCAGCGTGTGCCTGATGAAAAGATAGAGAAGCTGAAAG
Long Flanking Sequence:
CACAATTTCTGCTTGGATAACTTCCAAAACACAATATACCCTTTCTCAAACCAGCTTTTTTCTCTTGTCAGTTGTGTTGCTGTATAGATGACTACCAGTAAATCTTTTTCCTATGCTCTTTAGTTTAAGCTTAATCGTGTTTTTTTTTTTTTTTCTTTCTTCAAACAGGGAAGCATCTCCGCTGCCAGTATCCCTCACCCAATCTGAACCAGAAGCCCTTTTGTTACCGACAGAGGTGGATATCCTTCAGCCTGATTTTACTCTAAGCCAGCTGGTGTATCAGCGTGACACCCGAGACATGCAGACCGCAGACCTGGACAGCCTGCACTCCTCAGCTGTAGACAGCACATCAGTACACTACCTCAATGATCTGTCTGCTCTTAACGCCATCCAGCAGCCTGACCAACCCATATTAGAGTCAGAGGGCAGGCCCAGAACACAATTACAGGCTAACACATCTCAGACGTCCAGTCCGGGCTCAATTGCTTCTGCACAACGGT[T/G]AGAGAGCCTGCGGCAGCGTGTGCCTGATGAAAAGATAGAGAAGCTGAAAGAGAAAATCCGCAGACAGAAGAAACATCTGGAGGAAACGGAGGAGAGAAGCAAGCTTTTGGGATACCTGGAGCAACCTGTGGGTATTGGGACAACCGGATACAATACCGCAGTACCCACTGCTAAAGTTCGGAAGGTGGCCCCAGCCCCTCCTGCACCCATTTATAAAGGTAAACCCTGGAAAGAAATGATGTGGTAGTGAAAGGTAGTGGGTTCAATCCCCATTAGGACTATAACCACTGAGCTTGAATGAGGCACTTAACTTCAGGTTGCTCTAGGAATACTGGGTTAAAGGTGTATTCTGAGATGCTTAATATAGAAGCTTCTGCTGAATGTTTTATTAGGTTGTTGAGTGAGAGGAAGCTGACTTCTGCGATTTCTTGTTTTTTAGGCTTCAACACCAGTGAGACTAAGATTCGCACATCTGATGGGAAAGTGTGGGCAGAGGAGGA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5471
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Nonsense 595 3018 9 37
ENSDART00000132327 Nonsense 595 1078 11 15
ENSDART00000146175 None None 1836 None 23
ENSDART00000090254 Nonsense 595 3018 9 37
ENSDART00000132327 Nonsense 595 1078 11 15
ENSDART00000146175 None None 1836 None 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15108766)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14554110
GRCz11 8 14591815
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAGGAGGAAGAGAACAAGAATAAACGCCTACAAGAGCTCTACAGGAAA[C/T]AACGAGCAGGGGCCAATAAGGGCCCGGTTGCACCTGAAGTTCCRATAAAA
Long Flanking Sequence:
CTTTGTCTTCATATTTTCCTGCAGGCCCTGTTCCACGTTCCAGCTCTGATCCTCGTCTGGAGCATAACCGGCGCCCAAGGCACAGCAGCTCAGAAAGATCTCGCAATAACGTTCCTCCAGATGAAACTGCTGGACCCTCCATGTCAGCCGGCAGTGATAGAAGAAAGTCTCCCGTCACAGACCTCCTCTCAGCTGACATCCGTGGCATCCTAGATGACCTGCAATTGGAGGAGGACGACAGCAGGAGGGAGGCAGTGCCCACCTCCAGAGTCCGTGCCTCGACCCGCACCTCCCGCAGTGCCAGCCCTGCCAAAACTACCAAGAGAGCAGAGCCCCCCGAGCAGCCTGTGCCAAAGAAACGGCACTATGATGCTGAAGCGGTGCGGCTTTATATCGTGCAAAAGCAGGAAGAAAGGAAAAAACGGCAAGCAGAGGCGAGGAGAGCTCAGAGAGAGGAGGAAGAGAACAAGAATAAACGCCTACAAGAGCTCTACAGGAAA[C/T]AACGAGCAGGGGCCAATAAGGGCCCGGTTGCACCTGAAGTTCCGATAAAAAAGCGGCTCCAGGAAACATACACCAAGCTACTGTTGGAGCACACTCAGCTCCGAGAAGAGATCAATGGAGAGGCTGTAGCAAACGGAAGCCAGCAGGTAAAGTGCTTTTATTTTATTTTTTATTTTTTGAAGATATCATGATTTTATTACTGTTATATTATAAATGCACGTACATGTTAAGTGAGCTTTACATTTTTATCAAAAGAAGTTATTTTTAATTAACTAAAATGTATTGAATTGTTTAAATTCTTCTGTTCATCAAATAATTCTTAAAGGGATAGTTCAGCACAATATACAAATTTGCTAGCCCTCAATTGGTTACAGACTTTTAGCACTTTCTGTTTTCTGCTGAACTTCAAAGAATATATTTTGAAGAATGCTGGAAATCTGTAATCAATGACTTCCATATTGGGAAAAACAAAAACTGTGGAAGCCAGTGGTTACAGTTTT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa8369
Status:
Allele not cryopreserved
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Nonsense 595 3018 9 37
ENSDART00000132327 Nonsense 595 1078 11 15
ENSDART00000146175 None None 1836 None 23
ENSDART00000090254 Nonsense 595 3018 9 37
ENSDART00000132327 Nonsense 595 1078 11 15
ENSDART00000146175 None None 1836 None 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15108766)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14554110
GRCz11 8 14591815
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGAGGAGGAAGAGAACAAGAATAAACGCCTACAAGAGCTCTACAGGAAA[C/T]AACGAGCAGGGGCCAATAAGGGCCCGGTTGCACCTGAAGTTCCRATAAAA
Long Flanking Sequence:
CTTTGTCTTCATATTTTCCTGCAGGCCCTGTTCCACGTTCCAGCTCTGATCCTCGTCTGGAGCATAACCGGCGCCCAAGGCACAGCAGCTCAGAAAGATCTCGCAATAACGTTCCTCCAGATGAAACTGCTGGACCCTCCATGTCAGCCGGCAGTGATAGAAGAAAGTCTCCCGTCACAGACCTCCTCTCAGCTGACATCCGTGGCATCCTAGATGACCTGCAATTGGAGGAGGACGACAGCAGGAGGGAGGCAGTGCCCACCTCCAGAGTCCGTGCCTCGACCCGCACCTCCCGCAGTGCCAGCCCTGCCAAAACTACCAAGAGAGCAGAGCCCCCCGAGCAGCCTGTGCCAAAGAAACGGCACTATGATGCTGAAGCGGTGCGGCTTTATATCGTGCAAAAGCAGGAAGAAAGGAAAAAACGGCAAGCAGAGGCGAGGAGAGCTCAGAGAGAGGAGGAAGAGAACAAGAATAAACGCCTACAAGAGCTCTACAGGAAA[C/T]AACGAGCAGGGGCCAATAAGGGCCCGGTTGCACCTGAAGTTCCGATAAAAAAGCGGCTCCAGGAAACATACACCAAGCTACTGTTGGAGCACACTCAGCTCCGAGAAGAGATCAATGGAGAGGCTGTAGCAAACGGAAGCCAGCAGGTAAAGTGCTTTTATTTTATTTTTTATTTTTTGAAGATATCATGATTTTATTACTGTTATATTATAAATGCACGTACATGTTAAGTGAGCTTTACATTTTTATCAAAAGAAGTTATTTTTAATTAACTAAAATGTATTGAATTGTTTAAATTCTTCTGTTCATCAAATAATTCTTAAAGGGATAGTTCAGCACAATATACAAATTTGCTAGCCCTCAATTGGTTACAGACTTTTAGCACTTTCTGTTTTCTGCTGAACTTCAAAGAATATATTTTGAAGAATGCTGGAAATCTGTAATCAATGACTTCCATATTGGGAAAAACAAAAACTGTGGAAGCCAGTGGTTACAGTTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa1172
Status:
Confirmed mutation in F2 line
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
ENSDART00000090254 Nonsense 1354 3018 18 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Nonsense 173 1836 4 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15098525)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14543869
GRCz11 8 14581574
KASP Assay ID:
554-1082.1 (used for ordering genotyping assays)
KASP Sequence:
AGATGATCAACCAGCAGGCTGAGGCCGCACGACACACAGCTGAAACAGCA[C/T]GACACATTAAAGAAGTGAGACGTTATTACTCTTAAAACATTTGTATTAAT
Long Flanking Sequence:
AACAAATAGTATCGATGTCAGTGGTTACAGGCTTTTAGCTTTCTTCAAAATATCTTATTTTTTGTTTAACAGAAGAAAGAAACTCAAACAGATTTGGAACAAGTGAATGAAGAGTAAATGATGACAGTTTTCATTTTGGATGAACTGTCCCTTTAATATTTAAAAACCTTTTGGTGACTAATCAAGTCAGTTTGATGTCAGACTTTGGTTTGTTTAGTATGAAGCCTGTTTGTTTAACTTTGTAAAGTACATCCTGGGATACATTTGAAACTTTGTTCAAGAAGTTTATTTGTTACAAAAAGAAAGATCTGCAGGATTTTTTAGTTAAACTTGAAGTTAAATGATTAAATTTAATGATATTTGGTTGATTCAAGGTTCATGCAGAGCTGCAGGAGAGTTTGCTTCAGTCTCAACAGCAGGCGTTAGGAGGTTTGCATGAGGCCACAAACAAGATGATCAACCAGCAGGCTGAGGCCGCACGACACACAGCTGAAACAGCA[C/T]GACACATTAAAGAAGTGAGACGTTATTACTCTTAAAACATTTGTATTAATTTTTTTAGGCTGAATAAAATGTATGTTTAAAAAAAGCTTTGAATGAAATTAACAAATGTGTTCTTGACAACCAAGTGAATTTAGCTGAAGTTACTTAAATTACAAACTAGAAACAAAACAAAAAAAAATCAACTAAAACTTTAAATAAAATAAATGAAAGTAATGTGTAGTTACAAACTCTTGGGTTCTTTATTGTAGAAAAAAAAACTACATTTTAGAAACAAGATTACATGCTTATTTGCTCAGTGTAAATTACACTTTTTCAAGGATTATACGTTTTGTTAATTCTCTCTCTCTCTGTCTCTACACCCCCCCCCCCCCCCCCCCTCTCCCCGTAGATGACTGAGCTGGCGCGTTCACAGATTGTAGGAGCACTAAGTGTTCCTGGACCCTCCATTACAGCCCTGCATGACCAGCAGAGACAGCACAGCCGCAGTTCAAAACCGCACC
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa27152
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Essential Splice Site 1495 3018 21 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Essential Splice Site 313 1836 7 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15097279)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14542623
GRCz11 8 14580328
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGACTCTCTTTGCTCAAACAGTGTGCTTGGCCCTCTTGAAGAGAAAGG[T/C]AAAGCTTGTATTGAGTGATATTCATGTGTATACAGTGCTGCAGACTGCTT
Long Flanking Sequence:
TTTTTGGATGAACTATCCTTTAAACCGTGCCTTGCATTTACTAAAGTGAAATGTTTTTTCTAATTTGTCATAGTAGTGAATGCAATATATACATCAGTAATGTTACTGTTTTGGATCTTCTCCAGTAGTTGGAAAAGCGAAATGTCTCCTGAGAGACATCAGAGTCCATCAGAGGTCGAGACGCCACCAGACAGCCTCTCAGAGTCCATCCCTTCCAGAAGACCCACCATCAGGTAACACATTTCATTTTAGCTGATTTCTTTCATTTACAGATTATAAATAATTGGTCTTATAGAACAGTCTGTTAATGCTCATTTCTGTCTGTTTTAAAGTGGGGGTGGCAGTAGTAGTACCCAATTGAGTCCACCTCATTCTGGTCAAACGGAAAGGAGGACACCTGGTAAAGACAGAAGCAGTAGTTCAGTGGAGGACCAGGCTCACACTGCTGCCGATGACTCTCTTTGCTCAAACAGTGTGCTTGGCCCTCTTGAAGAGAAAGG[T/C]AAAGCTTGTATTGAGTGATATTCATGTGTATACAGTGCTGCAGACTGCTTTATTTCCTTTTGCTGCACGATATTGGGAGAATGTTGAATATTGCAATATTGATAAAGAAATTAGTTAAAAATCATATACGTGTAATGATCAAACGAAAATATTTGAAGCATATAAAAATATTAAACGTACTCTAATTCTCTTTAATCTAATTCAGGCTAAAAAAACTTTCAAGGAAGGTGCAAAGACTTTGACTTTAAAATACAATGTATTGTCAAAAACCTCAGTAGACATTCTGATTTCTGGTTTGGTTTTATCATAGACATATAAACACTAAATGCATTACTCTCAAACATTATTTTTATTCCCATAAGCAACACAGCATCTTAAACTAGTCCGTATTTTAAGCAAAACGCTTCCTTGCCTGTTTTTATAAATAAAGTATACAGTCCTTAAATAATTGGTATGAAGTGGAAATACTAACATCTTGTCCACATAATTTTTCGATATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9175
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Essential Splice Site 1625 3018 None 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Essential Splice Site 443 1836 None 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15095223)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14540567
GRCz11 8 14578272
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAGAGAGAAGACCAAGGCTGAAGTGGCCTGGCTGGAGCACCAGAAGAGG[C/T]AGGCCAAATCATTCATTTTATGAGTTCTCTTTGACTATATGAACCAAAAA
Long Flanking Sequence:
ATGACATCGAAGAAAGATCGTTCCGCTCTCTTTTACCATCTGAGGCTCACCGTCGCGAATCACTGGACAAGAAGCCTGAAGCTCATCTCGAATCTGATGAAGACCACAACCATGACCAATCCAGCCCTAGAGCCAGTACAAAGGTAGCATCTCTGATTCCAGCTTTGTTCTGTATGAAACAGACTGTTGTGTTTGCTTCTGTTTGGTTGTCATAGTTGGTTTGTTTGTGTTTTGCTGGAGGGTTGATAAGAAGCTCTTTTGTGTGGAATTGATAAGTGACTCAGCTATTGTTTGTTTTCCCCATATCACAGCAGGATGGCAGCATGCCCTTCTCCAGCGGCCAGGACAGCTTCTCCAAGTTCACCATGGACTTGGTGCGCCAGTACATGAAGGAGGAGGAGGTTCGTGCTCAGCATCAGAGTTCTCTGCTGCGTCTGCGTGAAAAAGCCCTCAGAGAGAAGACCAAGGCTGAAGTGGCCTGGCTGGAGCACCAGAAGAGG[C/T]AGGCCAAATCATTCATTTTATGAGTTCTCTTTGACTATATGAACCAAAAAAAATTTTAATAATGACCCCAAGTGCTTTTGAATAATTGCATGGTCTGACTGAGACAATTCGTTCTCTTTAAACTGATTTCTTTACATAAACTTTCATTAAAATCCAAGAACATTTACTGCCACTGAAATGTATGACTTTTCATTTAACCAGGGCTGCATCCATGGCCTGGTTTATTCCAGTCAAATGAATACAATGAAGTCTCATGCTACTTTTTACACTTAATATTCAGTTTCACTCAGTATGTAAACTGGCATTAAAATGTTTGTGGTAAGAAGCATTTAAAACAAAGTCTTGTATGCTAAACTACTTTCATTTGATCAAAACTCTTATCAGACAGTAATAATGTGAAAATATTAACACTATAAACTCATTCTTAATATTATTAAAATATTACAGTCTGTATTATAAACGTATTCATGTGATGGCAAAGCAGATTTTCAGCATCTATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38676
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Nonsense 1670 3018 25 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Nonsense 488 1836 11 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15093023)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14538367
GRCz11 8 14576072
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGGCGGAGATTAAACGACTCCAGGAGGCCAATAAAGCAGCGAGAAGA[G/T]AGAGACAGCTGCTCCTCAAACAGCAGGAGGAGATTGAGAGAATGAGACAC
Long Flanking Sequence:
GGTTGTTTTTTAATGTAACTTTTACCTATGCTATGCATAAAATATGGTATTTCTAATAGTTTAATAAAATACATTAGAATTTTGGAAATCACCAAGCGACCACCCCCCAGCTACACTGCTTTAAGATACACTCAGAAATAAATGATATTACAATTTTCACAACGTCTTAAATTACACACAATGCCTATAGAAAATCATCATACCCTGTGATCCCTATTCTCATTATACCCTGCTTTCAAAAGACCTTCAGGATAAAGTTGTAGAAAGGCAGAAATTAGGAGAAGGCTACAAAAACATTTCAAAGGCTGGAAAAGTTATTTGTAATATGATTCGATTTTAGGCTGAATGGCAAATAAAGTAATTATTTTAAAAGGGTATGATGATTTTCTGTAGGCACTGTAAATTATGTCATACAGGGGGAAAAAATTAAAACATTGCCGTTATTTCTCCTACAGGCGGAGATTAAACGACTCCAGGAGGCCAATAAAGCAGCGAGAAGA[G/T]AGAGACAGCTGCTCCTCAAACAGCAGGAGGAGATTGAGAGAATGAGACACACAACCCTCAAACTCAAAGAGCGACTCAAGACTGCTGGAGACACAAAGATGGTCAGTCGTGCCTTTTGAAAACTGTACTTGTGCTTAAGTGAACGTTACAACCCCTAATATATTTTTCTCCCCCAAATGGTCTGCAGGAGTCACCTGTGTCAGGTGTGGCAGAGTCGTCGGCTCCGCCCAGTGTAATTGTGACAGATGCAGACACCCGAAGCCCCTCCCCCATGTCTGTGTCAGGCAGTGAAACCAGCAGCATCATGCAGAAACTGAAGAAGATGCGCTCTCACATGGATGAGAAGTAAATAACGCTCACACACGTTACTCTATTCTTCAATCTTATCTCTCCTTTGTCCAATAAAGTGGTGCATTAGTTTAAGTTGTAATCAGAACTTTGCACATTTGATTATATTAACCAAAACTAAATGCAAACCTCTTCCAGCTGATCAAACACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15445
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Nonsense 1677 3018 25 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Nonsense 495 1836 11 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15093002)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14538346
GRCz11 8 14576051
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAGGAGGCCAATAAAGCAGCGAGAAGAGAGAGACAGCTGCTSCTCAAA[C/T]AGCAGSAGGAGATTGAGAGAATGAGACACACAACCCTCAAACTCAAAGAR
Long Flanking Sequence:
TTACCTATGCTATGCATAAAATATGGTATTTCTAATAGTTTAATAAAATACATTAGAATTTTGGAAATCACCAAGCGACCACCCCCCAGCTACACTGCTTTAAGATACACTCAGAAATAAATGATATTACAATTTTCACAACGTCTTAAATTACACACAATGCCTATAGAAAATCATCATACCCTGTGATCCCTATTCTCATTATACCCTGCTTTCAAAAGACCTTCAGGATAAAGTTGTAGAAAGGCAGAAATTAGGAGAAGGCTACAAAAACATTTCAAAGGCTGGAAAAGTTATTTGTAATATGATTCGATTTTAGGCTGAATGGCAAATAAAGTAATTATTTTAAAAGGGTATGATGATTTTCTGTAGGCACTGTAAATTATGTCATACAGGGGGAAAAAATTAAAACATTGCCGTTATTTCTCCTACAGGCGGAGATTAAACGACTCCAGGAGGCCAATAAAGCAGCGAGAAGAGAGAGACAGCTGCTCCTCAAA[C/T]AGCAGGAGGAGATTGAGAGAATGAGACACACAACCCTCAAACTCAAAGAGCGACTCAAGACTGCTGGAGACACAAAGATGGTCAGTCGTGCCTTTTGAAAACTGTACTTGTGCTTAAGTGAACGTTACAACCCCTAATATATTTTTCTCCCCCAAATGGTCTGCAGGAGTCACCTGTGTCAGGTGTGGCAGAGTCGTCGGCTCCGCCCAGTGTAATTGTGACAGATGCAGACACCCGAAGCCCCTCCCCCATGTCTGTGTCAGGCAGTGAAACCAGCAGCATCATGCAGAAACTGAAGAAGATGCGCTCTCACATGGATGAGAAGTAAATAACGCTCACACACGTTACTCTATTCTTCAATCTTATCTCTCCTTTGTCCAATAAAGTGGTGCATTAGTTTAAGTTGTAATCAGAACTTTGCACATTTGATTATATTAACCAAAACTAAATGCAAACCTCTTCCAGCTGATCAAACACTGTTTGGTGTGCTTAAGGGGCGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31635
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:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Essential Splice Site 1999 3018 30 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Essential Splice Site 817 1836 16 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15083510)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14528854
GRCz11 8 14566559
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAAGAGCGACTAAAGGCACAGGAAGCAAGTTTGCTGAAACAATTGGAG[G/A]TCAGCAACCTGCGCTTTACATATTCACTTGTTTCTGTGCAGCAATATTCT
Long Flanking Sequence:
GGACAAAGCAGAACAACCTACTCTAATATACAGCACACAATGATGAATAAGGTATTTAAAATAATTTATAAATCTTAGTGCACCATGGTTAACAGTATCCAATGCATGCAGACTCTGAGATGAAGCATGCATATAGATAACATCTCATAGTCCAATTTCGAAATAAATGTTGCATTAACCAGCTTCTGTTTAGCATCAAAAAAGGCAGTTCTTAATTCTAAAATAGAATCCGATAACCTTAAAAAATAGGCATGTGAATGTGCACATTAATTGACAAAGTTTTAACATGCATTTCTTTGTAGAGATATTTTATAATATTTTTTTGTGTTCCTACCATAGAGACCACATCTGATCAGAGTGATATTGAGAGCCGCATTCACGCTCTCAAGGATGAGCTCCGCAAGCGCAAATCAGTGGTATACCAGCTAAAGAAGGAGCAAAAGAAAAGGCAAAAAGAGCGACTAAAGGCACAGGAAGCAAGTTTGCTGAAACAATTGGAG[G/A]TCAGCAACCTGCGCTTTACATATTCACTTGTTTCTGTGCAGCAATATTCTGATTATCTTAAAATGCTTGTTACTATATATTAATTTACTGTAATGAATCCTACTTAGTATTCTGTATGTTAATATTTGTTGCCGTTTCTGATTCTCTACTAGTCATATAATGACTTTATTCAGAAGACTAAGGCTGAGTTGAGTAAAGGGCCTGACGGCACTCCAGCTACTAAACCCCAGATTAAAACTCCCACGTCAGCCAGTGAAAAACCTCGAATAAAACCCCCTCCACTTCAGAGGTCAGCCTTGCCATTTAACACTCATTATTAATATACTCTCCAATCTGTTTCATGTCCTTGTATACTTACTATACCATGCACATTTACCTTTACAGACCAGAGACTAGCAAGAACTGGAAAATCGTCACAGAATCTGAGAAATCAGAGATTGTTCCCTCTGAGACATCAGGAGATAAAGGTGAAATACCTTTTAGACCAAAACACAAGAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41150
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Nonsense 2356 3018 33 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Nonsense 1174 1836 19 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15082093)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14527437
GRCz11 8 14565142
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACCAATGGCAACTTCCAAACTGAAAGTCGACCAGACCTCAATAGCCTT[G/T]GAAGAGGCTCTAAAGACGTCATCGGCCCTTCACCACAGCCACAAGTGCCA
Long Flanking Sequence:
TTGGGCTTCAGATGCCATCTCTGAAGGATGTGAATGCTAAATCTGACAAGGAAAGATTGTCTGAGAAGGATACTGCTGACAAGCCAGCATTTCAAGACTCTGCTGATGTTGGAGAAAGCATGAGATTAACTGAATCAAATTTGTCTCCTGTAGAGGTGTCCAAACATATAGACTACCCTTCAGCTAGGAAGACCATTTCAGTCATAGATCATTCCTATACTTCTGACTTCTCATTAGCCAAGAGGGAGGATTCCACAAGGATGAAAAAAACCCAGTCACCCACAGGCGATGGCTATAATGATGACTTTGAGTCTTCCTTTGAGTCATCATTAAACCATGAATCAAAGCCAACATCACCTACTGCTCCACAGCCCAAAGAAAAATCTTTTAAGTCTCCAATCTACAGTAGTGAGGAGGAAATTGAAGAAGAACTAAGCGTCCAATCTGGAAGTACCAATGGCAACTTCCAAACTGAAAGTCGACCAGACCTCAATAGCCTT[G/T]GAAGAGGCTCTAAAGACGTCATCGGCCCTTCACCACAGCCACAAGTGCCAATCTTGCCAATAAAGGACGAATTGCCAAGCTTCTGCATTGGAGACAGGGTTTTAGTGAGTAACGTACAACCAGGGACACTGAGATTCAAAGGACAAACTAACTTTGCCAATGGATTCTGGGCTGGGGTTGAACTGGACAACCCTGAGGGAAGTAACAATGGAACTTACGATGGAGTGGCGTACTTTGAGTGCCGGGAAAAACATGGTATATTTGCCCCGCCAGACAAGATTTCACGTCTTCCAGAGAAGTTTGAGGCCAGTGCAGATACAGAGGATGACGATTCTTCGTGTGATGACCAGCCAAACAGAGAAAACAAAGCCTCTGAGGAGCAGTTGGAAAAAAGAAATCTGCTAAACAAAATAAAAGAAGAAAAATCTGACCTAGATTTATATCCTGAGGCCAGAGAGCCTTTGCGTGAGCAAGGCAAGCCATTGGAACTCAACATCAAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34350
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
ENSDART00000090254 Nonsense 2368 3018 33 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Nonsense 1186 1836 19 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15082057)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14527401
GRCz11 8 14565106
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTCAATAGCCTTGGAAGAGGCTCTAAAGACGTCATCGGCCCTTCACCA[C/T]AGCCACAAGTGCCAATCTTGCCAATAAAGGACGAATTGCCAAGCTTCTGC
Long Flanking Sequence:
CTAAATCTGACAAGGAAAGATTGTCTGAGAAGGATACTGCTGACAAGCCAGCATTTCAAGACTCTGCTGATGTTGGAGAAAGCATGAGATTAACTGAATCAAATTTGTCTCCTGTAGAGGTGTCCAAACATATAGACTACCCTTCAGCTAGGAAGACCATTTCAGTCATAGATCATTCCTATACTTCTGACTTCTCATTAGCCAAGAGGGAGGATTCCACAAGGATGAAAAAAACCCAGTCACCCACAGGCGATGGCTATAATGATGACTTTGAGTCTTCCTTTGAGTCATCATTAAACCATGAATCAAAGCCAACATCACCTACTGCTCCACAGCCCAAAGAAAAATCTTTTAAGTCTCCAATCTACAGTAGTGAGGAGGAAATTGAAGAAGAACTAAGCGTCCAATCTGGAAGTACCAATGGCAACTTCCAAACTGAAAGTCGACCAGACCTCAATAGCCTTGGAAGAGGCTCTAAAGACGTCATCGGCCCTTCACCA[C/T]AGCCACAAGTGCCAATCTTGCCAATAAAGGACGAATTGCCAAGCTTCTGCATTGGAGACAGGGTTTTAGTGAGTAACGTACAACCAGGGACACTGAGATTCAAAGGACAAACTAACTTTGCCAATGGATTCTGGGCTGGGGTTGAACTGGACAACCCTGAGGGAAGTAACAATGGAACTTACGATGGAGTGGCGTACTTTGAGTGCCGGGAAAAACATGGTATATTTGCCCCGCCAGACAAGATTTCACGTCTTCCAGAGAAGTTTGAGGCCAGTGCAGATACAGAGGATGACGATTCTTCGTGTGATGACCAGCCAAACAGAGAAAACAAAGCCTCTGAGGAGCAGTTGGAAAAAAGAAATCTGCTAAACAAAATAAAAGAAGAAAAATCTGACCTAGATTTATATCCTGAGGCCAGAGAGCCTTTGCGTGAGCAAGGCAAGCCATTGGAACTCAACATCAAGCAGCTTTCTACTGGGCAAAGCACCTTTATTAAATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21227
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000090254 Nonsense 2513 3018 33 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Nonsense 1331 1836 19 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15081622)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14526966
GRCz11 8 14564671
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAATCTGACCTAGATTTATATCCTGAGGCCAGAGAGCCTTTGCGTGAG[C/T]AAGGCAAGCCATTGGAACTCAACATCAAGCAGCTTTCTACTGGGCAAAGC
Long Flanking Sequence:
CTGAAAGTCGACCAGACCTCAATAGCCTTGGAAGAGGCTCTAAAGACGTCATCGGCCCTTCACCACAGCCACAAGTGCCAATCTTGCCAATAAAGGACGAATTGCCAAGCTTCTGCATTGGAGACAGGGTTTTAGTGAGTAACGTACAACCAGGGACACTGAGATTCAAAGGACAAACTAACTTTGCCAATGGATTCTGGGCTGGGGTTGAACTGGACAACCCTGAGGGAAGTAACAATGGAACTTACGATGGAGTGGCGTACTTTGAGTGCCGGGAAAAACATGGTATATTTGCCCCGCCAGACAAGATTTCACGTCTTCCAGAGAAGTTTGAGGCCAGTGCAGATACAGAGGATGACGATTCTTCGTGTGATGACCAGCCAAACAGAGAAAACAAAGCCTCTGAGGAGCAGTTGGAAAAAAGAAATCTGCTAAACAAAATAAAAGAAGAAAAATCTGACCTAGATTTATATCCTGAGGCCAGAGAGCCTTTGCGTGAG[C/T]AAGGCAAGCCATTGGAACTCAACATCAAGCAGCTTTCTACTGGGCAAAGCACCTTTATTAAATCTCAGCATAACCTGGATTTTAACGATATTGACTGCAATATCATTAACGAGTGTGACAAAGGTCCGCACACAGTGCCTAACGGCGGAGACAGGGACATTATTCTCAAACTCGAGGATGCATCTGTTGATAACGCTGTGCCATTGCTCAATAATTTGGATAAAGGTACATCTAAAAAACAAAAGCAGGAAGACGAACCACCAGCAGTCATTTTGGACCTCTTGTTAGAGGGGGAGAAATCCAGAGTTGATGGTCTTCAGAAATCTACTGATATTTCAATTGAGGAGGCCAGTCTAGATAACAAAAGAGCTTTGACTACTCTTGCAGATAAACTTGTGGAAAACTTCTTAAGTGATGCAGTGAAGCAATTTCAGAAGATCAAAAAAGACAAAGAGGAGAAGTTATCTGCTGCTAATCAATTGAAACGAGACTTCATCAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa41149
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
ENSDART00000090254 Nonsense 2960 3018 36 37
ENSDART00000132327 None None 1078 None 15
ENSDART00000146175 Nonsense 1778 1836 22 23

The following transcripts of ENSDARG00000058000 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 8 (position 15078475)
Other Location(s):
Assembly Chromosome Position
GRCz10 8 14523819
GRCz11 8 14561524
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAACAGACTGGCAAAAAATGATCAAATTTGGACGGAAAAAGCGAGAC[C/T]GAGTAGACCACATCCTAGTAAGTGAACTTCACATTATTATCTTCATCCAT
Long Flanking Sequence:
GGTTTGATAATGGCAAGAATTGCCCTTAAAATACAGTATGACCATGGTTAAAGATGAAGTGTTTTCAGAAGTCAAGCAATAAACTGTAATACTGCTTTAAAACGCTATCATATATTAATCCGGGCTTTACAGAAATCTCTTAATAAAATGTCATCCAATATAACAGTTGTTTATACAGCAAAACATATTTAATATTTTAGTCATTTAAACTGTAGGAATTTATTATAATTCTTTTATTTAAATTTATTATATTATTACTATATATTTTCATATTCACATATTATGCTGAATGACTTTTTCCCATATTTTGACTGATTATTTGCAGCTTTTGATGATATTTATATACATATGCATATTTTTAAGTATTTTTTGAAAAAGGTTTTTGTTTATTTCAGGAATTTGTCACCACTGAGGTCTTGAAATTGTGTGGTCTAAAGAAAGAGCAGAACCAGAAAACAGACTGGCAAAAAATGATCAAATTTGGACGGAAAAAGCGAGAC[C/T]GAGTAGACCACATCCTAGTAAGTGAACTTCACATTATTATCTTCATCCATAACATTGAGTATTTCCATTTTTGTCCTCCTGATAGTATGCAGTTTAGGCTTACTAAATGCATAATTCCACAATCCCTCTTCCTCTTCTAGGTCCAGGAGTTGCATGAAGAGGAATCCCAGTGGGTCAACTATGATGAGGATGAACTTTTTGTAAAGATGCAGCTAGCTGATGGGATTTTTGATGCCTTGCTAAAAGACACCGCTGACGTTCTGACCCAAATCCAAGAGAAGAAATTTAAAACAACTCTTTGATGATGCTCTTGTTTGTACAGAAAAAATGTTTTAGGTACTTTCTGATTTAAAAAAAAAAAAAAAAAAAAAAAGAGAGGTTTCATTGTTGGCATAAAGGACATTCAGTGCGGAGTTCTCTTTGAGTCTACATGTGCTGTCCACGACCTGTTGTGGGTTCAGGATTCAAGGCCATAACACCTTGCCTAGAAGTCTGACCTG
Associated Phenotype:
Not determined