Busch Lab

ZMP

NR_027750.1

Ensembl ID:
ENSDARG00000089722
Description:
wu:fb63d09 (wu:fb63d09), non-coding RNA [Source:RefSeq DNA;Acc:NR_027750]
Human Orthologue:
C1S
Human Description:
complement component 1, s subcomponent [Source:HGNC Symbol;Acc:1247]
Mouse Orthologues:
C1s, Gm5077
Mouse Descriptions:
complement component 1, s subcomponent Gene [Source:MGI Symbol;Acc:MGI:1355312]
predicted gene 5077 Gene [Source:MGI Symbol;Acc:MGI:3644269]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa36186 Nonsense Mutation detected in F1 DNA Not yet available
sa28692 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa17835 Nonsense Available for shipment Available now
sa42761 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa45581 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa10018 Nonsense Available for shipment Available now
sa36185 Nonsense Available for shipment Available now
sa39111 Nonsense Mutation detected in F1 DNA Not yet available
sa18410 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa36186
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122049 Nonsense 43 673 2 11
Genomic Location (Zv9):
Chromosome 16 (position 34192333)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31730303
GRCz11 16 31685863
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACATCCACTAGGTTATGAACCTTATTCCAATATGACTTGGAAAGAGTG[T/A]GCTCCGGCTGGACACAGAATCACACTCACTCTCACACATGTAGACCTGGA
Long Flanking Sequence:
AGACAACAATGGTTTATCTGAAACAGCCATTAAATTGAGGAATCTCTGCTCACCAAATTATTCAGTCTAGAGTAAACGCCCACTAACAGATGTTGACAAACACTCAGTTAGAAGTACTTCCATGTTTTTTTTTTTAGGAGAAAAGGGGTTGGACATTATGATCCACACAGAGCATGAAAGTGAAAGTTCAGAAAGAGGAGGGATCCAGTTATGTTTCAACACTTCGCATCATGATTGCTTTCTGGTATGTGTTTTTCTCTATCTGTTGCAATTTATCAAGCAAAATGTTCCATTGATTATCTATCTGTCTGTCTGTCTGTCTGTCTATCTATCCTTGTTTTCGATAATGAAGTTGCTTCCTGCTGATGTTTCTTCTTTCTGTCCAGTGTGATTTCCCTTTTCTTTCCCCTGTGTGGGTCAGTGCCATTGTCTGGATGGATTCAGTCCCCTGGACATCCACTAGGTTATGAACCTTATTCCAATATGACTTGGAAAGAGTG[T/A]GCTCCGGCTGGACACAGAATCACACTCACTCTCACACATGTAGACCTGGAGGAAAGCTTTAACTGTGAGGATGACGCCTTGAAGGTGTGTGTGTTAGAAAAAGTTTTTTTTTTTTTTCTTCACACATGGTTTGTACGTAGGTGTTATAAACTTTTTAAATACGCAGTTTTATGTGAAAGTGTTGTAAAAATAAATGTACGCACTGTGAAAAAAAGTGTTTTGCACTTTTCCAGATTACAATTTTTCTCAATTGCTTATGCTCAATTCTCGATTGAATTTTTTTGTTCTTCAAAACAGTAAGTTTAGATGCTCATTGTTCCCTTCAGAGTGGCATTTCTTATTGATTTAAGCAACTTGCAAATGTCTTGGCACATGTCTGCAAACAGTAAGTACAGTTGTCTGTAGATTGGACAAAAACCAATTGCATAAGCCTTGTTAATCAAAACTGATGAAGCCATTCTCATTTAAACTCTTAATCATGTGTCAATATGTAAGCCATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa28692
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
ENSDART00000122049 Essential Splice Site 237 673 5 11
Genomic Location (Zv9):
Chromosome 16 (position 34184631)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31722601
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGACGTGGAAAAGGCAGACAATGGACGGTGCATTGACTCATTAACCG[T/A]AGGTAACATGTAAAGTCTTGTCTCTTTCTCTTTGTATTTCGCCTCAATGA
Long Flanking Sequence:
ATTCCACTGTGGCAACCCCTGATAAATAAAGGGACTAAGCCGAAGGAAAATTAATGAATGAATGAAAATACATATACTGCAGCATCATATTCTGCATCTCTATCCAATACTTAAACTTGCCACAAAACAAGTAACAGTAATAAGCTACAAATTAGGAGTCTATTAAAGCAAAAGATGTAGTTATTGTTTGATTGAAAGCGAGAACTGAACTTTAAAACAATTGGTATTTTCATTTCTTATTGACAGCCGTAATGCATAATCCATAATCCTGACACCAGTGACACTGTTCTCTCTCTGTATGTCAGTTAGCTGTAGTAAAAATTACACAGGCTCTTTAGAAGGTGAGCTGAAGTCGCCACACTGGCCCAGTCCATATCCAGAAAACTCTGTGTGCTCTTACATACTGGCTGTAGAAGAAGGCCTGCAGTTTGAGCTGACGTTCACAGGGACGTTTGACGTGGAAAAGGCAGACAATGGACGGTGCATTGACTCATTAACCG[T/A]AGGTAACATGTAAAGTCTTGTCTCTTTCTCTTTGTATTTCGCCTCAATGACCTGTTCTCTCTTTCTCTATGCATTCCTTCTAGATAAAACCTCTCATTGGTGAAGCTAAAACATATTGTGGAAAAGATCTTCCTTCTTCCTTTCTCACAAGGTCTGAGAGTGTTGAGATTACTTTTAGGACTGACCATAAAGGAACAAACCGAGGGTTTCGCCTTAGTTATAAAACTAAAGGTTTGTTTTTCCTATCATTAAAACTAAACACTTCATATGCTGCATAAAAAGGATTGGTGGGACTACAGTATATATAAGAATGTTCCATTAATAATAAACTAATTTCATTGGTCCACTCATCTCAACTTATTTATTATTATTATTATTTATTTATTTATATTTATGTATAACCAGCGTTTATTTAGATGTTATGGTGGTGATTATTTCCTACCTTACAGAGATGAAATGTATTGGACCTGTGACGCCAACATCTAGTTTGTTGCCACAGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa17835
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122049 Nonsense 283 673 6 11
Genomic Location (Zv9):
Chromosome 16 (position 34184410)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31722380
GRCz11 16 31679378
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTTTTAGGACWRACCATAAAGGAACAAACCGAGGGTTTCGCCTTAGWTA[T/G]AAAACTAAAGGTTTGTYTTTCCTATCATTAAAASTAAASACTTCATATRC
Long Flanking Sequence:
TGGTATTTTCATTTCTTATTGACAGCCGTAATGCATAATCCATAATCCTGACACCAGTGACACTGTTCTCTCTCTGTATGTCAGTTAGCTGTAGTAAAAATTACACAGGCTCTTTAGAAGGTGAGCTGAAGTCGCCACACTGGCCCAGTCCATATCCAGAAAACTCTGTGTGCTCTTACATACTGGCTGTAGAAGAAGGCCTGCAGTTTGAGCTGACGTTCACAGGGACGTTTGACGTGGAAAAGGCAGACAATGGACGGTGCATTGACTCATTAACCGTAGGTAACATGTAAAGTCTTGTCTCTTTCTCTTTGTATTTCGCCTCAATGACCTGTTCTCTCTTTCTCTATGCATTCCTTCTAGATAAAACCTCTCATTGGTGAAGCTAAAACATATTGTGGAAAAGATCTTCCTTCTTCCTTTCTCACAAGGTCTGAGAGTGTTGAGATTACTTTTAGGACTGACCATAAAGGAACAAACCGAGGGTTTCGCCTTAGTTA[T/G]AAAACTAAAGGTTTGTTTTTCCTATCATTAAAACTAAACACTTCATATGCTGCATAAAAAGGATTGGTGGGACTACAGTATATATAAGAATGTTCCATTAATAATAAACTAATTTCATTGGTCCACTCATCTCAACTTATTTATTATTATTATTATTTATTTATTTATATTTATGTATAACCAGCGTTTATTTAGATGTTATGGTGGTGATTATTTCCTACCTTACAGAGATGAAATGTATTGGACCTGTGACGCCAACATCTAGTTTGTTGCCACAGCTTCATGAATATCCCACATATGGCAAAGTTACAGTGACATGTGACAAAGGACATGTATTAATAGTAAGTATTTCAGTATTTCAAACATTTCGGACTTAATGATTTTAAATTCAGTTTGCTGGAGAGCCATAGCTGAATTTTATGGATTTGTTGAGGTTCATTGTGTTTTAAAAAGTGTGTTTTAGATAACTTGAATTTGTAATAGAATTAACATTATTATTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa42761
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122049 Essential Splice Site 394 673 9 11
Genomic Location (Zv9):
Chromosome 16 (position 34183274)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31721244
GRCz11 16 31678241
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATCAGTCTCAAGTGCAAATCTAAATTTTATCAACTGGATACAAATGG[T/G]GAGACTTGTATGGTTTATGTGAATTACAGTAATTCTAAACAAACAAATAT
Long Flanking Sequence:
CTTCAGAACATCTGAAGTGTATTTTAGTTTCTGTGGCTAATGCTTAATCAGCGATCCGTGGGTGTGACATTTGAGACTGAAACTAGATGATAGCCTTTAGCATGTAGTTTAAGAGTCAAATCTTTAATAATCACTGCAAGTCACACTTTGTTTCACAGAGTGAATTAGCTGAGGTTAAGAACCTGTATGAATCCACATGCCAGAAAAATGGACAGTGGAGTCCGGTTATCCCCTGTGAACGTAAGAAAATGTTTTAAAACCTTTTCTTTAAAAAATTTATTTCTGTTTTCTGCCCTCTTTCTGTGATTCCTAGAATTCCTTATATATGACTTCACAATATTAAAAAACAACACTTTTCTTGTTTCCTCCTCAGCTGTAGATTGTGGTGTTCCAGAACATTTTGAATTATTGGAGCTCTCAGAAAATGATCCTCAAACAACTTTTATGAAACAAATCAGTCTCAAGTGCAAATCTAAATTTTATCAACTGGATACAAATGG[T/G]GAGACTTGTATGGTTTATGTGAATTACAGTAATTCTAAACAAACAAATATGTAATTCTGCATCCTTGTCTTTTATCATTGTTTTAATTCTATTTTATTGTTTTCCTTTCATTAGCTATTTTTACATGCAACGCCGAAGGTAACTGGGTGTCTGAGAATGGTGACATTTTAACAAAAGATTTTCCTAAATGTGAACCAGGTAGTCGTTTATCCTGAATGTACCTATAAACCCAAATATATTTGGAGATGTTTTGTATGTTTCTCTCTTCCTTAATATCTCTCTTTCTCTATCTTTTAGTATGTGGAATGAACACAGAGGACTCTTTTGGTGGAAGAGTCTTTGGCGGGAAGCGAGCACAACCAGGACAGATTCCATGGCAGCTCTTACATAAGTTCAACCCTAGAGGTGGTGCATCTCTGATCAGTGATTACTGGGCTCTGACAGCTGCTCATGTAGTGGATGGATATGAAAGCAAAACCATGAGTTGGTTAGGGGGAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa45581
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
ENSDART00000122049 Essential Splice Site 422 673 11 11
Genomic Location (Zv9):
Chromosome 16 (position 34182977)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31720947
GRCz11 16 31677946
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTTGTATGTTTCTCTCTTCCTTAATATCTCTCTTTCTCTATCTTTTA[G/A]TATGTGGAATGAACACAGAGGACTCTTTTGGTGGAAGAGTCTTTGGCGGG
Long Flanking Sequence:
TTTCTGTGATTCCTAGAATTCCTTATATATGACTTCACAATATTAAAAAACAACACTTTTCTTGTTTCCTCCTCAGCTGTAGATTGTGGTGTTCCAGAACATTTTGAATTATTGGAGCTCTCAGAAAATGATCCTCAAACAACTTTTATGAAACAAATCAGTCTCAAGTGCAAATCTAAATTTTATCAACTGGATACAAATGGTGAGACTTGTATGGTTTATGTGAATTACAGTAATTCTAAACAAACAAATATGTAATTCTGCATCCTTGTCTTTTATCATTGTTTTAATTCTATTTTATTGTTTTCCTTTCATTAGCTATTTTTACATGCAACGCCGAAGGTAACTGGGTGTCTGAGAATGGTGACATTTTAACAAAAGATTTTCCTAAATGTGAACCAGGTAGTCGTTTATCCTGAATGTACCTATAAACCCAAATATATTTGGAGATGTTTTGTATGTTTCTCTCTTCCTTAATATCTCTCTTTCTCTATCTTTTA[G/A]TATGTGGAATGAACACAGAGGACTCTTTTGGTGGAAGAGTCTTTGGCGGGAAGCGAGCACAACCAGGACAGATTCCATGGCAGCTCTTACATAAGTTCAACCCTAGAGGTGGTGCATCTCTGATCAGTGATTACTGGGCTCTGACAGCTGCTCATGTAGTGGATGGATATGAAAGCAAAACCATGAGTTGGTTAGGGGGAATAACTGATGGTCTGGACGAAAAACAAGTCGCTATGGTGACTGAAAAAATAATCATTCATCCAAAATATAATAAAGTTGGGCTTGAATTGGGAAAAAACCAAACAAACTTTGATAATGACATTGCTCTGATGAAAATGTCTGCCAGGGTGCCTCTAGGTACAAACATCAGGCCGGTGTGCTTGCCAAACAAAAGAGACGAAGCTGTGATGGAGGGCACAGTCTCAGGTTTTGGAGGACTAGAAAGAAAGAATTTGAGTCGATATCTGCTTTATGGTCCAGTCCAGATATATCCACTTGTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10018
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
ENSDART00000122049 Nonsense 445 673 11 11
Genomic Location (Zv9):
Chromosome 16 (position 34182908)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31720878
GRCz11 16 31677877
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGACTCTTTTGGTGGAAGAGTCTTTGGCGGGAAGCRAGCACAACCAGGA[C/T]ARATTCCATGGCAGCTCTTACATAAGTTCAACCCTAGAGGTGGTGCATCT
Long Flanking Sequence:
TCCTCAGCTGTAGATTGTGGTGTTCCAGAACATTTTGAATTATTGGAGCTCTCAGAAAATGATCCTCAAACAACTTTTATGAAACAAATCAGTCTCAAGTGCAAATCTAAATTTTATCAACTGGATACAAATGGTGAGACTTGTATGGTTTATGTGAATTACAGTAATTCTAAACAAACAAATATGTAATTCTGCATCCTTGTCTTTTATCATTGTTTTAATTCTATTTTATTGTTTTCCTTTCATTAGCTATTTTTACATGCAACGCCGAAGGTAACTGGGTGTCTGAGAATGGTGACATTTTAACAAAAGATTTTCCTAAATGTGAACCAGGTAGTCGTTTATCCTGAATGTACCTATAAACCCAAATATATTTGGAGATGTTTTGTATGTTTCTCTCTTCCTTAATATCTCTCTTTCTCTATCTTTTAGTATGTGGAATGAACACAGAGGACTCTTTTGGTGGAAGAGTCTTTGGCGGGAAGCGAGCACAACCAGGA[C/T]AGATTCCATGGCAGCTCTTACATAAGTTCAACCCTAGAGGTGGTGCATCTCTGATCAGTGATTACTGGGCTCTGACAGCTGCTCATGTAGTGGATGGATATGAAAGCAAAACCATGAGTTGGTTAGGGGGAATAACTGATGGTCTGGACGAAAAACAAGTCGCTATGGTGACTGAAAAAATAATCATTCATCCAAAATATAATAAAGTTGGGCTTGAATTGGGAAAAAACCAAACAAACTTTGATAATGACATTGCTCTGATGAAAATGTCTGCCAGGGTGCCTCTAGGTACAAACATCAGGCCGGTGTGCTTGCCAAACAAAAGAGACGAAGCTGTGATGGAGGGCACAGTCTCAGGTTTTGGAGGACTAGAAAGAAAGAATTTGAGTCGATATCTGCTTTATGGTCCAGTCCAGATATATCCACTTGTTGAATGTAAATCGGGAGGTTCAAAAGTCACCAATAACATGATCTGTGCTGGAGGAGACAGAGTAGACAGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36185
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122049 Nonsense 481 673 11 11
Genomic Location (Zv9):
Chromosome 16 (position 34182800)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31720770
GRCz11 16 31677769
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATTACTGGGCTCTGACAGCTGCTCATGTAGTGGATGGATATGAAAGC[A/T]AAACCATGAGTTGGTTAGGGGGAATAACTGATGGTCTGGACGAAAAACAA
Long Flanking Sequence:
AAATTTTATCAACTGGATACAAATGGTGAGACTTGTATGGTTTATGTGAATTACAGTAATTCTAAACAAACAAATATGTAATTCTGCATCCTTGTCTTTTATCATTGTTTTAATTCTATTTTATTGTTTTCCTTTCATTAGCTATTTTTACATGCAACGCCGAAGGTAACTGGGTGTCTGAGAATGGTGACATTTTAACAAAAGATTTTCCTAAATGTGAACCAGGTAGTCGTTTATCCTGAATGTACCTATAAACCCAAATATATTTGGAGATGTTTTGTATGTTTCTCTCTTCCTTAATATCTCTCTTTCTCTATCTTTTAGTATGTGGAATGAACACAGAGGACTCTTTTGGTGGAAGAGTCTTTGGCGGGAAGCGAGCACAACCAGGACAGATTCCATGGCAGCTCTTACATAAGTTCAACCCTAGAGGTGGTGCATCTCTGATCAGTGATTACTGGGCTCTGACAGCTGCTCATGTAGTGGATGGATATGAAAGC[A/T]AAACCATGAGTTGGTTAGGGGGAATAACTGATGGTCTGGACGAAAAACAAGTCGCTATGGTGACTGAAAAAATAATCATTCATCCAAAATATAATAAAGTTGGGCTTGAATTGGGAAAAAACCAAACAAACTTTGATAATGACATTGCTCTGATGAAAATGTCTGCCAGGGTGCCTCTAGGTACAAACATCAGGCCGGTGTGCTTGCCAAACAAAAGAGACGAAGCTGTGATGGAGGGCACAGTCTCAGGTTTTGGAGGACTAGAAAGAAAGAATTTGAGTCGATATCTGCTTTATGGTCCAGTCCAGATATATCCACTTGTTGAATGTAAATCGGGAGGTTCAAAAGTCACCAATAACATGATCTGTGCTGGAGGAGACAGAGTAGACAGTTGTAAAGGTGACAGTGGAGGTCCTTTGTTTTTCCCTCCTCTGGGAAATGGGTCCCCAGACCAGCCTTATCGTCTTACAGGCATAGTATCCTGGGGTCCTCCTAATTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39111
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
ENSDART00000122049 Nonsense 497 673 11 11
Genomic Location (Zv9):
Chromosome 16 (position 34182752)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31720722
GRCz11 16 31677721
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAAACCATGAGTTGGTTAGGGGGAATAACTGATGGTCTGGACGAAAAA[C/T]AAGTCGCTATGGTGACTGAAAAAATAATCATTCATCCAAAATATAATAAA
Long Flanking Sequence:
AATTACAGTAATTCTAAACAAACAAATATGTAATTCTGCATCCTTGTCTTTTATCATTGTTTTAATTCTATTTTATTGTTTTCCTTTCATTAGCTATTTTTACATGCAACGCCGAAGGTAACTGGGTGTCTGAGAATGGTGACATTTTAACAAAAGATTTTCCTAAATGTGAACCAGGTAGTCGTTTATCCTGAATGTACCTATAAACCCAAATATATTTGGAGATGTTTTGTATGTTTCTCTCTTCCTTAATATCTCTCTTTCTCTATCTTTTAGTATGTGGAATGAACACAGAGGACTCTTTTGGTGGAAGAGTCTTTGGCGGGAAGCGAGCACAACCAGGACAGATTCCATGGCAGCTCTTACATAAGTTCAACCCTAGAGGTGGTGCATCTCTGATCAGTGATTACTGGGCTCTGACAGCTGCTCATGTAGTGGATGGATATGAAAGCAAAACCATGAGTTGGTTAGGGGGAATAACTGATGGTCTGGACGAAAAA[C/T]AAGTCGCTATGGTGACTGAAAAAATAATCATTCATCCAAAATATAATAAAGTTGGGCTTGAATTGGGAAAAAACCAAACAAACTTTGATAATGACATTGCTCTGATGAAAATGTCTGCCAGGGTGCCTCTAGGTACAAACATCAGGCCGGTGTGCTTGCCAAACAAAAGAGACGAAGCTGTGATGGAGGGCACAGTCTCAGGTTTTGGAGGACTAGAAAGAAAGAATTTGAGTCGATATCTGCTTTATGGTCCAGTCCAGATATATCCACTTGTTGAATGTAAATCGGGAGGTTCAAAAGTCACCAATAACATGATCTGTGCTGGAGGAGACAGAGTAGACAGTTGTAAAGGTGACAGTGGAGGTCCTTTGTTTTTCCCTCCTCTGGGAAATGGGTCCCCAGACCAGCCTTATCGTCTTACAGGCATAGTATCCTGGGGTCCTCCTAATTGTGGAGATGAAAGCTTTAAAGGTTACTATACGAAAGTCCAAAACTACCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18410
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000122049 Nonsense 511 673 11 11
Genomic Location (Zv9):
Chromosome 16 (position 34182708)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 31720678
GRCz11 16 31677677
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
RAAAAACAAGTCGCTATRGTGACTGAAAAAATAATCATTCATCCAAAATA[T/G]AATAAAGTTGGGCTTGAATTGGGAAAMAAMCAAACAAACTTTGATAATGA
Long Flanking Sequence:
TGTCTTTTATCATTGTTTTAATTCTATTTTATTGTTTTCCTTTCATTAGCTATTTTTACATGCAACGCCGAAGGTAACTGGGTGTCTGAGAATGGTGACATTTTAACAAAAGATTTTCCTAAATGTGAACCAGGTAGTCGTTTATCCTGAATGTACCTATAAACCCAAATATATTTGGAGATGTTTTGTATGTTTCTCTCTTCCTTAATATCTCTCTTTCTCTATCTTTTAGTATGTGGAATGAACACAGAGGACTCTTTTGGTGGAAGAGTCTTTGGCGGGAAGCGAGCACAACCAGGACAGATTCCATGGCAGCTCTTACATAAGTTCAACCCTAGAGGTGGTGCATCTCTGATCAGTGATTACTGGGCTCTGACAGCTGCTCATGTAGTGGATGGATATGAAAGCAAAACCATGAGTTGGTTAGGGGGAATAACTGATGGTCTGGACGAAAAACAAGTCGCTATGGTGACTGAAAAAATAATCATTCATCCAAAATA[T/G]AATAAAGTTGGGCTTGAATTGGGAAAAAACCAAACAAACTTTGATAATGACATTGCTCTGATGAAAATGTCTGCCAGGGTGCCTCTAGGTACAAACATCAGGCCGGTGTGCTTGCCAAACAAAAGAGACGAAGCTGTGATGGAGGGCACAGTCTCAGGTTTTGGAGGACTAGAAAGAAAGAATTTGAGTCGATATCTGCTTTATGGTCCAGTCCAGATATATCCACTTGTTGAATGTAAATCGGGAGGTTCAAAAGTCACCAATAACATGATCTGTGCTGGAGGAGACAGAGTAGACAGTTGTAAAGGTGACAGTGGAGGTCCTTTGTTTTTCCCTCCTCTGGGAAATGGGTCCCCAGACCAGCCTTATCGTCTTACAGGCATAGTATCCTGGGGTCCTCCTAATTGTGGAGATGAAAGCTTTAAAGGTTACTATACGAAAGTCCAAAACTACCTGGACTGGATTAAACAAACCATGGAAATTAACTAACATCAGCATGC
Associated Phenotype:
Not determined