Busch Lab

ZMP

ADAMTS16

Ensembl ID:
ENSDARG00000074646
Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 16 [Source:HGNC Symbol;Acc:17108]
Human Orthologue:
ADAMTS16
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 16 [Source:HGNC Symbol;Acc:17108]
Mouse Orthologue:
Adamts16
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 16 Gene

Alleles

There are 10 alleles of this gene:

Allele Name Consequence Status Availability
sa36010 Nonsense Available for shipment Available now
sa18552 Splice Site, Nonsense Available for shipment Available now
sa9951 Nonsense Available for shipment Available now
sa39072 Splice Site, Nonsense Mutation detected in F1 DNA Not yet available
sa4631 Essential Splice Site F2 line generated Not yet available
sa22737 Nonsense Available for shipment Available now
sa39073 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa36010
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
ENSDART00000092657 Nonsense 152 1224 3 23
Genomic Location (Zv9):
Chromosome 16 (position 1129364)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1078571
GRCz11 16 1105666
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACGCTGGATGGAGAGATGATGTGTTTCTATCAGGGGGAGCTGAGGATG[C/T]AGGAACACTCCTCTGTGGCTCTGTCCACATGCATGGGGATGGTGAGTGAG
Long Flanking Sequence:
GCTAACGCTTTGGATCCCTCTAATTGTAGATTGAGTTGTGTAAATGTGCAAACATGTCAACAATTCTGGGTGCTGTGTGGGCATTATTGAGGGAAAAATTAACTTGATTGCATCAAATGGCTGCAATATAACTGAGTGAGATGTTTAAGGGGGTCTGAATGCTGTCCATACCCGCTGTATATCGTCACATTTGCCAGTATTAACCCTGAGTGTGTCCTCCATCAGAATATGAGCTGGTGTCCCCATATGAGGTGGATCCTGAGGGCCAGTATATCTCCCACGCCGTGTCTCATCAGCACCGCAGTAAACGCTCCACAGACGCCTCCACTGTGCACTTCAGACTACAGGGATTGGGACGGGAATTCCAGCTGGACCTGCGGCCGTCCCGGGGCCTGATCGCGGCCGAGTTCACTGTGCAGACGCTGGGCAGGAGCGGGACCCGGAGTCTGCAGACGCTGGATGGAGAGATGATGTGTTTCTATCAGGGGGAGCTGAGGATG[C/T]AGGAACACTCCTCTGTGGCTCTGTCCACATGCATGGGGATGGTGAGTGAGTAAGGGCACTTACTAGTGCTTAATATGTTTTGTAAAAGCCATGAATGTGAGAAAAAACAAACTGAGGAAAAAAGATTATTTTTAAGTGTTATTATTATTATTACTATTATTATTATCATTAGTAGTAGTACTTTAGTATTATTAAGTAAAATACAAAAAAAATGCTAATGTGCAATAATTATAAAAATAATAATAATCATCACTATCATCATGATTGTTGTTGTTGTTGTTGTTGTTTTATTATTATTATTATTATTATTATTATAAATGTATTAAATATTTAAATAAATGAATGCAAGGTAATTTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATCATTATTATTAATATAAATGTATTAAATATTTAAATAAATGAATGCAAGGTCATTTTATTATTATTATAATTATTATTATTATTATTATT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28560
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092657 Nonsense 176 1224 4 23
Genomic Location (Zv9):
Chromosome 16 (position 1147302)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1096509
GRCz11 16 1123679
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTGTGTTTTCCATCTAGTCAGGTTTGATCAGGACTCGGGACGCAGATTA[T/A]TTTCTGAAGCCGCTGCATCCACATCAGGCACTATTGGAGAACTTCTCGGC
Long Flanking Sequence:
TTTTGTGTCCTGCAGCACATTAATGTTATGACAGTGCTTGCAAAACACTGTTCCTCAGTCAGTCTCCGGCATTAAATATTAAACGTCTGCAGTCAATTTAGACTCAACTGCTGAATCTGCAGACTCCACACTGTAAAAAGGGTTTAGTTGACTTTAATTGAAATAAAAGTGAGTAAGCTGGTGGCTCAGTGGTTAGCAGTAGGAAGGTTGCTGGTTCGAGTCCCGGATGACTCAGTTTGCATGTTCTCTAAATGTTGGTGTGGGTTTCCTCCGGGTGCTTCCCCAAAGTCCAAACACATGCTAAACTAAATCGGCCGTAGTTTATGGGTGTGAATGAGGGTGTATGGGTGTTTCCCAGCACTTGGTTGCGGCTGGAAGGGCATCCGCTGTGTAAAACAGCAGTGAATGATGCATGAAGTGTCTCTGGATCGGATTTCTGCATCACTGACCCGTGTGTTTTCCATCTAGTCAGGTTTGATCAGGACTCGGGACGCAGATTA[T/A]TTTCTGAAGCCGCTGCATCCACATCAGGCACTATTGGAGAACTTCTCGGCTCCATCACCAGACCACCAGCCACACATTCTCTACAAGAGACCCGCACCGACAAACACACGCAGAACCAGGAGATCGTCTGAACCAAGGCCTGGAGATCCTGCAATCCCAAACAGATGGAGAACCAGCAGACAAGCTGAGAAAAACACACACACGCTGATTAATCCAGAGGAGATGCAGAAAACAACACACAAGAACAGCACACGGCGGAGACAGCACTACTGCGGGAGACGCAAGAAATGTATGTACACTGCGAACAAATGCTATCTATTTTGTCTTGATTCTAGTCTGATCTAAAAACTCTTAAAGGGCAGCAGCTCTGATGAAAGCTGTTTGGACAGAACTGTGTGTAGTATAGTGTCTCCACAGTCATGTTGGGGTAATAGAAACACAATAAGTCTCTCCCTGATGTTAAAATAGCATCCAAATACCTCCCATCATGAGGCTGACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18552
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092657 Splice Site, Nonsense 273 1224 5 23
Genomic Location (Zv9):
Chromosome 16 (position 1150247)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1099454
GRCz11 16 1126607
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWMGTTAAATGCYTGASCGGGTGTTGATAWTGTCTTGATCCTGTTTCAGA[T/A]ATGCCCAAGCCTCCCGAGGAAGACATCTATATTTTTCCAGATGAATATAA
Long Flanking Sequence:
GTTTGGCCAGGCGAAATCAGATTGTATCTTTGTAAGATTATATGACATTGGAGAAATCCCAAAAATGGCAAACAGTAGGCAAAGGGGACCCAAAGAAAAAGCTTCTTGATTTATGAATTGTTCGATATCTGGACTAGAAACCAAGCAAAATCTCTAAGTAAGAAAAGCGTTTTGTATTGTTGTTTGTTATAGTCACGGCTGCTCCGGGGTCAGCTTGAACATGTCTTCATGACATCATCTCACCTGTATGATGTTTGGTCAGAAACTAATTATCTTCACCTTCTCTAAACACATCCTCACCCTGCGCTTGAACCCGGAGTAATATTGTACACACCGAGTAACCAAATCTGATGTGGGATGTGAGGTCACAGCTGATACAGTTTGACACACATGGCGTGCATTAATATCTCGTATGAACTTCAGGTTTCCAGAGCTCTTCTTTGGGGAAACATCGTTAAATGCTTGAGCGGGTGTTGATATTGTCTTGATCCTGTTTCAGA[T/A]ATGCCCAAGCCTCCCGAGGAAGACATCTATATTTTTCCAGATGAATATAAGTTGATGCCCAGGGGGAAGCGAGACGTCGTTTTTAAACCTGAGACGCAGCCGAGTCTGAATGTGGAGACGCTGGTGGTGGTGGACCGCAAGATGATGGATAATCACGGACATGAAAATATAACCACGTATGTGCTGACTGTGCTGAACATGGTAAGTCACTGAGCATCTTACTTGCTCATCCATCTGTCCTTATACAATCTATACAGTCTATTCAATCATGCATTCATCAGATTTCCGTCTATGCATCTATCAATTTATCCGTCCATTCATCCATCTCTCTATCCAATCATGCATCCATCTATGCACGACTGTATCTATCATCTGTCCATGCATCATCCAACCATTTATCTTCCCTTGCATCTATCTCACTATCCATCAAATGATGCATCAAATGATGTCTTTCCATCCATCCATCCATCCATGCATCTAATTTATCTATCTATCCAGTA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa7774
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
ENSDART00000092657 Nonsense 388 1224 7 23
Genomic Location (Zv9):
Chromosome 16 (position 1158029)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1107236
GRCz11 16 1134398
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGTGATAAACCATCACGCTGACCACACGCTCAACAGTTTCTGTCAGTGG[C/T]AGTCGGGTTTATCAGGCCGAGAAGGACGCCGGCATGATCAYGCTATCCTG
Long Flanking Sequence:
TATACTGATGTAGGGTCAGCAGAGGCAACGAGAAGCCAGATACGCCTGTTTTACTTTAAGTTTTTGTCTTGTTTCTTGTTCAAATGTCTAATAATTCCTAAATCAAAAAGCAATTGCTTAAGAAGTGAAACAGAAATGTTTTCAGAAATATTGAGTCAAAATTAAGTGAGAAAAAGCTAAATAATCAGGCAATGGGGTGAGCAATAAATACCCCACCGGCTGATTATTTTGCCTTTTTTAAGTAAAAACTCTCTTAATTTTGACTCATTATTTCTGAAAACAAGACAATATGCTTGTCTAGAAAACGCTTCTTGATTTACGACTTTATAGAGATTTGGACTACAAACAAGAGAAAACCTGAGTAAGAAAAGCTTTATTTGTGGTCTAGTCCACGTCCCTTGTTCACGTTACTCCTGTCTTTATTTTACTCTTTTGTCCTTTAGGATGGGCTAGTGATAAACCATCACGCTGACCACACGCTCAACAGTTTCTGTCAGTGG[C/T]AGTCGGGTTTATCAGGCCGAGAAGGACGCCGGCATGATCATGCTATCCTGCTGACCGGTCTGGACATCTGCTCCTGGAAGAATGAGCCGTGTGACACTCTGGGTGAGGAAAACACATGCAGAATATTGTGAAATTATGGATTGAACTATCCGCTCCCTCAACTTTTACCTGTTTATCATATTTTAGAGAGATTGTCTTGCTAGAGGCAGGGCCGGCGCATCCATAGAGGTGACCTAGGTGGCGTCAGCGACACCTCCTTCACCACCCGCGTCTTCAGTTATGTCCGCGACACCACCCTTACCACCCGCGTCCTCAGTTCTTTACTTTGATAACCGGTCACTTTCAATTTTACTTTCGGGGTGAGGGCGGCGTTATCGTCTTTTGCCTAGAGCAGCATTTCAGCTTGCTCTGGTCCTGGCTGGAGGGTACAACCATCCAGCTTAACGGTGCAAAAGACAATACTGTGTGGTTCAATTGGTGCTTTTGAAAACACTGTCGGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9951
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
ENSDART00000092657 Nonsense 564 1224 11 23
Genomic Location (Zv9):
Chromosome 16 (position 1175822)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1125029
GRCz11 16 1154315
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGTTCTGTTGTGTGTCRCGCAGGACATCTGTAAAGCACTGTGGTGCCAT[C/T]GATTCGGGAGAAAATGTGAGACCAAGTTCATGCCGGCAGCCGAAGGTTCA
Long Flanking Sequence:
AACAAATGTTAAAAAAATAATGATAGCAATTACTCTGGCTATTTTTAATTTCTTTATTTGCAAACATTTAACCATTACATAGTGTATTTTGTTTAGAGAAACAAAGATGAGGTTAAAAGTAGAGGAATTCTTGCATGCAATAAAAATAATAATAAATAAATAAATAAATTAAAGATGCACAAAATATTTAATGCTGGAATGACTTTTATTACTTAAAAATAAATAAATCTAAAAAGTTACAGATTCACCCACATACGGAGAGTTTAACATGTGATGCTAAACCGAAGCAGACAGGTCATTATTACATCCAGAGCTCATAAACTGTGTGATTATTCTGCAGGCTTGTGTTTTGGACTCATACAGTGTTCAAAGAGCATTTCTGTATTTTAAAGTGTTTTGCAATCCCTCATTTGTTGTGTGTAATGGCTCAGATTGACATGCATATAACAGCGGTTCTGTTGTGTGTCGCGCAGGACATCTGTAAAGCACTGTGGTGCCAT[C/T]GATTCGGGAGAAAATGTGAGACCAAGTTCATGCCGGCAGCCGAAGGTTCAGCCTGCGGGCCAGAGATGGTGAGTCTCAGACCCAATCCCAATAACACCTGTCACAGTCACCAAGTTGAGTGAGCACCAGACACACTACTCACCAGGGCACTCTACACATCACATCTGCAACTGAACTGGACTACAAATCCCATCATGCACCTTACACACACACCAGTTTCAGATCACAGCTGATTACAAACACACAGGTGAAGCTCATGAGGACTGATTACCAGGACTATAAATACACTCACAAACTTTGCTGAGTCTTGTGAGCTGTAAGTGACCTGGGTGTTTCAAATCACTTTAGTCACGTGACCTGGGTGTTTCAAATCACTTTAGTCACGTGACCTGGGTGTTTCGAATCACTTTTGTCACGTGACCTGGGTGTTTCGAATCACTTAAGTCCCATTACCTGGGTGTTTTGAATCACTTTAGTCACGTGACCTGGGTGTTTCGAAT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa28561
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092657 Essential Splice Site 636 1224 12 23
Genomic Location (Zv9):
Chromosome 16 (position 1176792)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1125999
GRCz11 16 1155285
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCTGTGAGAGCGGAGTGACCCACAGAGAGAGAGTCTGCAGCAGCCCCAG[G/T]TACAGCAGTGTGTGTGCGTGTGTGTGCGTGTGAGCGCGTGTGTGCGTGCG
Long Flanking Sequence:
ACTTTAGTCACGTGACCTGGGTGTTTCGAATCACTTTAGTCACATGACCTAGGTGTTTTGAATCACTGTAGTCATGTGACCTGGGTGTTTTCAAAACACTTTAGTCACGTGACCTGGGTGTTTCGAATCACTTTAGTCACATGACCTGGGTGTTTCGAATCACTTAAGTCCCGTTACCTGGGTGTTTCGAATCTCTTTAGTCACATGACCTGGCATTTCGAATTACTTTAGTCACGTGACCTGGCGTTTTTAATTCCCGTTGGCCGGTGAGAGCGCTCTGATTGGTTATTCTGATTGTGTGCATGTCTTTTTGTGTTTGCATGTCTCTATGTGTGTGTGTGTGTGTGTCAGTGGTGTCGTGGTGGTCAGTGTGTGAAGCAGGCTGATGCGGGTCCTAAAGCGGTTGATGGTCAGTGGTCCTCGTGGTCCGGCTGGTCCTCCTGCTCAAGGAGCTGTGAGAGCGGAGTGACCCACAGAGAGAGAGTCTGCAGCAGCCCCAG[G/T]TACAGCAGTGTGTGTGCGTGTGTGTGCGTGTGAGCGCGTGTGTGCGTGCGTGTGTGTGTATGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCATTGCATCCATTTTGCAGCAGTCTAGAAGGGATACAGCTACGGATACTGACATATACTGTATAAAGCATAGTTTTTGTGACATTACATTAATTCATACATTACTGTAAGGGTTGGGGTAGAGGTAGACATAAATGAATGGGTAAATTATTAAATAATGTAAACAATTGGGGTTATAATTCTGGTTTTTACATTACTGTGATGGGTAGGTTTAGGGTCGGGGTAGTGGTAGACGTTAAGAAAATATGATTTAATGGGAAATTAAATTAATAATATGAACAATACTCTGTATAATTACTGTTTTTACATTACTGTGGGGATTGGGGTGGCGGTAGATGTTATTAAATTACAATAAATTCATAATTTAATAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39072
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:
Splice Site, Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092657 Splice Site, Nonsense 737 1224 14 23
Genomic Location (Zv9):
Chromosome 16 (position 1179964)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1129171
GRCz11 16 1158457
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACGCTCTGCGCACAGGACAGCACCGACGTCTGCATCGACGGCATTTGT[G/T]AGGTATTGTGCACTATTCACATAGTTCACTCGGACACAAAGCAGACAGAT
Long Flanking Sequence:
TCGACAGCGGCCTCTGGTGGATTTATGTGAGTAGTATGTGATCACTCAAAAGAGAAATCTGAGATCTAAAAAGGTGTAAACAGCGCCCTCTGGTGGAGTCGCGAAAAACAAAACTGCAAACAAAAAATCATAGCACCTGGGACGTATTTTGCTCTCTCCAGAACTGTATATAGGGGTACATAATCAGAATGAGCCTGGATTGACAGTAAAGCATCCATACAATCACTAACAATCCATCTCAATAGAACTTAAACATTTTATTTTTGACTATTTTATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCAGATCAGGACGTGTGTAAGCTGTACTGTTTGGCTGAGGGTTATGACTTCTTCTTCGCTCTCTCCAGTAAAGTCCGTGACGGGACGCTCTGCGCACAGGACAGCACCGACGTCTGCATCGACGGCATTTGT[G/T]AGGTATTGTGCACTATTCACATAGTTCACTCGGACACAAAGCAGACAGATGTTGTTGGAGTATGCTTTAGGAGAAAATACCATCCCAGTGTTTCTACTTAAAGATTTAATGCATGCAAATGCATCTTCTGTGCGCTTCAGATTGTGTTTGTGTTTGCATGGACGGAGCCAAACACAACTCTGTTTCAGCTCACATCACAAATCTCCTGTAATATCTGAAGGGAAAGGGTGTTAGTAGAGCGGTGACACTTTGCAGTGGAGCAGAACCATTGTCAATCAGTGGGTTCAGTTTAAATAAGCAGTAATGATGGATCCTCTGAGGCATGTTTTAGATTATACATGATGCCATAATGAGTTCAGAGTGAAAACATTACAGAATAGTTATATTTGCAAAATGCACATGGACATACTGGAGGACTGTTTAAATGAGACTGTCGTTTCTGTGTGTCTTATATATGCGTGATGAAATCATCATTTTCTTGTTGCTTAAATATTTATATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa4631
Status:
F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000092657 Essential Splice Site 861 1224 17 23
Genomic Location (Zv9):
Chromosome 16 (position 1183921)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1133128
GRCz11 16 1162414
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATGTGGTRTGGAGGAGTTATATATGCTAATTAGTGTGTTTCTCCTGCGC[A/T]GGTACTCCTGCAGGGCTGGAATCCAGGTGTGCAGTGGGAATATACACTGA
Long Flanking Sequence:
TGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTGTAGAGTATTACCGTGTGGTGACAATTCCGGCTGGAGCTCGCAGTATCCGTGTTTCAGAGCTGAACTCCTCCAGCTCTTATCTGGCCCTCAGGAACCTGCAGAGGAAATATTACCTCAACGGCGCCTGGACAGTGGACTGGCCCGGACGGCACTCCATCGCTGGGGCTATTTTTGACTATAAGAGACCCTACAACCGTCCCGAGAGCCTGAGCTCCAGCGGACCCACCAACCAGACCCTCGTCATCGAGGTACAGCCACTGCTTCATCAACACATCTACACTACCTGCCAAAAGTCTTGTCATCGATCCCAGATGTAATTGCAGGGATTGTTTTGTCAAGCGCACTCACCTGTGTGAGGCACACTCAGAATTGCATCATTGTTTGAGGTTGTCATGTGGTGTGGAGGAGTTATATATGCTAATTAGTGTGTTTCTCCTGCGC[A/T]GGTACTCCTGCAGGGCTGGAATCCAGGTGTGCAGTGGGAATATACACTGAACCGAGAGCAGAAACACAACTACAGCTGGGCTGTGGTGCGCTCGCAGTGCTCATCCAGCTGTGCCGGAGGTGCTGCGTCCACCATAACACACAACATCCACTATGACACACTGTTTTTCCTGTCCTTAAAGGGGAGTTATTATGCAAAACTCACTATTATAAAGGGTTTAAACACAGTTGTGTGTCAGCAGTGTGTGAATATCTCCAGCCTCTAATGGTCAACATGAAATAATTGTGTTTGTTCTAATCAGACTTGATAGACAAAAACACTTTGATTGGCATTCTCCCTTTGTACGTGTCATCAGACGAGGAAAGCCCCGCCCATTAGTCTCCCTACTTAGCATGTCCAGCAGCCCTGAGTGAGAAGCAGCCGTCTGTCCATTAGCCATTAGAGTGTTTGAGCTGCTGAAGATAATGTCAGCGTAGACTCAGAGGATTATACATGTGGAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa22737
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
ENSDART00000092657 Nonsense 1064 1224 20 23
Genomic Location (Zv9):
Chromosome 16 (position 1198059)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1147266
GRCz11 16 1174835
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGAGATCTGCTTCATCAAACACTGCAGAAAACAGCGCAAGGCTCAGTG[G/A]TTCGTCTCCACATGGACACCGGTGAGAAAGACACACACAACGCACCGCAA
Long Flanking Sequence:
CGCCTCCGTTTTTAGACGTCTCCGTTTTCCCTCATCCACACTGAGACAGAGCAGCAGCGCTTCACAATGAAAACAGCCTCTCCAGTGTTTCCAAAACGCTCCGTTTTCAGCGCTCGAAAACTCCGGCGTAGTGTTGATGGATGGCGTAATCGTAGCAAAACTTGTTTTTGTTTTAAACGCATTAGTGTAAACAGAGCCTGAATTTCATTGGCTGACGCTGTTATGATGATCGCGTCAGCCCCAACTTCAAACACGCCTTCAGTCAAGCGTTGACGCTGAAGCCCCGTGTGAATGGGGCGTTAATGTAAATGAATGTTGTTGATGTGTGTGTGTCTGCAGTGTTCTCGTAAGTGTGGTAAGGGTGTGATGAAGCGTCCGGTGCTGTGTGTGCTCAGTAATGGAGTTGTTCTGCCGGACTCGTCCTGCGCTGATCTGCTCAAACCCAGCGTTCAGGAGATCTGCTTCATCAAACACTGCAGAAAACAGCGCAAGGCTCAGTG[G/A]TTCGTCTCCACATGGACACCGGTGAGAAAGACACACACAACGCACCGCAAAACACTGCATGCTTCTCTTAAGGCTGATTTATACTTCTGCGTCAAACACCGGCGTATGCTATGGCGCTGACGCATAGCCCTTCGCTGTGGCCGTCGCCGTCGCTGACGTGCACCTCTCAAAAAATGTAACTACACGTAGCAGTGACGAGTCGGGGTGGGACCGAGAGCCACGCGAATGGCGCGAACCCAATGGAGCGATTGTTTACAAGTGTGGAGTCCCGTGAAGGACTCCGGATGGAAAGTTTTGTTTTGTGTTTTCCTCATAGTTAAAGTTGTTGCACTTCCGCCGGTTCCTGCCTCAAAATGAGCAAGTCTGAGCCACTTGTACATCCTGGAAGTGTCCAGAAGTGTTTATACTGGAAACTCGACACAGAGGAACATTTACACCTCACTGCCAACTAGTGTTTCGGAAGTGTTAATGCAGGCCGACAGAAACAGCAGCAGAAGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39073
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
ENSDART00000092657 Nonsense 1198 1224 23 23
Genomic Location (Zv9):
Chromosome 16 (position 1199646)
Other Location(s):
Assembly Chromosome Position
GRCz10 16 1148853
GRCz11 16 1176422
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGTATGTGTGTGCAGATGTGGTGTGTAAGGATCACTTCAGCTGGTGTTA[T/A]CTGGTGCCGCAGCACAGCGTCTGCAACCACAAGTTCTACGGGAAGCAGTG
Long Flanking Sequence:
TAACACTTCTCAAATCAAAAGGAGCCTTAAAACGGTTTGATTTTAAGAACTCTTAGTGATCAGATTGAATTTTTTGTAAATGATGTTAACCATGGTGTGTGTGTGTGTGTGCAGTGTACAGTGTCGTGTGGTGGAGGTGTGCAGATACGCTCGGTGCAGTGTCTCTCTCTGGGACGTCCCGCCTCTGGATGTGTCCTGCAGATGAAGCCGCTCATGTCTCAGGCCTGCAACACAGCCTTCTGCCCCCAGCCGGAGCTCAATGGTCTGTACACACTGATATATAATGCTTTTTACACAGAGCTTTGGTCGAGTTTCTAGTCCAAATATCTAGAAACTCTTAAATCAAGAAGCATTTTCTGGAAAAGTACAAAATATAGTCTTGTGTTCAGAAAAATAATGAGCGAGTTTTTCCTTAAAACATGTGTCTCTGCTGTGAGTGTGTGACCCAGTGTGTATGTGTGTGCAGATGTGGTGTGTAAGGATCACTTCAGCTGGTGTTA[T/A]CTGGTGCCGCAGCACAGCGTCTGCAACCACAAGTTCTACGGGAAGCAGTGCTGCAAATCCTGCCGGCAGAGCAAACCTTGAGCAGCTCAGATGGAGAAACTCACAGACAGAACACACTTTCACATGCACGAACTTTCTGTAAAGAGATCATGTGTGAACAGACCGCGTTTTTAAATACTGGTAAGTTCGTTCTGGTGATGGACATGTTTGTGTGGGACGGCTCTCGAGACTGCAGGACATGAAGCCCACAGAGCAAAAGACTCCTTTCGTTGTGTTTGCCAGAGCTTCAGACATTACAGAAGAGAAAACATCATCATCATCCTCTGGAAATATAGACTAGACTCAGTTCATGTGGGTAAATGGATGGACAAGTGTTTTGTTGTTCCTTGAACGTGCCTCAATAATCTCATGTGTAACACAGGGCTTAAAGGGACAGTTCACGCAAGACTGAAAGTGATCCAGTGGTTTACTCACACTCAATGCATTCTAAGTGTGTTTGA
Associated Phenotype:
Not determined