Busch Lab

ZMP

si:dkey-92f12.2

Ensembl ID:
ENSDARG00000086490
ZFIN ID:
ZDB-GENE-091204-379
Human Orthologue:
SUN2
Human Description:
Sad1 and UNC84 domain containing 2 [Source:HGNC Symbol;Acc:14210]
Mouse Orthologue:
Sun2
Mouse Description:
Sad1 and UNC84 domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:2443011]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa20810 Nonsense Available for shipment Available now
sa30877 Nonsense Mutation detected in F1 DNA Not yet available
sa40788 Nonsense Mutation detected in F1 DNA Not yet available
sa16555 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa20810
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
ENSDART00000129701 Nonsense 4 577 1 17
ENSDART00000140086 Nonsense 4 577 2 18

The following transcripts of ENSDARG00000086490 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 47986075)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 48046727
GRCz11 6 48045486
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTACTTTTACACAGTCTATGTTTGTATGTGTTCTGCAGAGATGTCAAGA[C/T]GAAGCACAAGATCAGTGACCAAACCGACGTCCTTTCCTGACGATGACGCT
Long Flanking Sequence:
ATAAATAAAGTAGAGCAAACATACAAATGAAGTAGTCTTAACAGTATACAGGTACAGAAATAACATCAACACTTTAATGAACAATAAAGCTGTATGTTTTTCATTGTGTAAATAGTTAAATACAATTATTCTTTGTTGAAGCTATAAACATGATAATTTCCTATAGCTCCTAACTGCCAACATGCTTTAAAATCGCCTCTGAGGTTTACACGGGCCTTAAAAAAACAATAAAAATTGATAAACTTTCACTTTATTATGGTTGAACTGAAATGACTCTGAAATTCTCATGTGTTCTGATCTGTTGTACCTGGTCAACTATAGTCCTGACTCCACACTGCATGTTCTGCGATGTGACTATTATGTATTCACACATAGCAATATATCGATGCTAAAAGATATATTGTGCAGCCCTATTAGTGATATTCAGTCACCTTAAAAAGAAAAAAGAAAGGTACTTTTACACAGTCTATGTTTGTATGTGTTCTGCAGAGATGTCAAGA[C/T]GAAGCACAAGATCAGTGACCAAACCGACGTCCTTTCCTGACGATGACGCTGCCAGCACCAGTTCCACTGGATCCACTGGCCACATCTCTTACAAAGAGAGTCCAACCAGGTGCGTTTGTACATGCTGGAGCCCTCAGTGTATTGTGTACATAGTTTGAATGTTCATTTAAAGTAGCCATACATGTTGATGCATGCTTTCCTGTAGGATTTTTCAGAAGAGGACCAGCCGCAAGGGCACTGGCAGCGTTTCACGCAATTCAAGTCGTGCGAGCAGCGTGAGTCTAATACTGCCACCGCGCATCGACTTCAACCCCACTGAGAATGAGAATGGTCAGTAATTTTAAATAATTAAATATTTCATATAATATGTAGATAAACAAATATAAATATGTATCTATCACTGAGTAATCAACATTTGAAGCATCAAAAGTTTTTAGATTTGCCCAAATAGTTTGATTCACTTCACATGTTTAGAAACATGTATGAATGCATGTACAGCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa30877
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
ENSDART00000129701 Nonsense 101 577 3 17
ENSDART00000140086 Nonsense 101 577 4 18
ENSDART00000129701 Nonsense 101 577 3 17
ENSDART00000140086 Nonsense 101 577 4 18

The following transcripts of ENSDARG00000086490 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 47986764)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 48047416
GRCz11 6 48046175
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACTCAAGGATTTTCCTCTGGATATTCCTCAGCTGAGGATCATTATGAA[C/T]AACCCATAAAGTCAAACCCTAGTAAGTGTTCGTTATTCAATTTCATACGT
Long Flanking Sequence:
TGCATGCTTTCCTGTAGGATTTTTCAGAAGAGGACCAGCCGCAAGGGCACTGGCAGCGTTTCACGCAATTCAAGTCGTGCGAGCAGCGTGAGTCTAATACTGCCACCGCGCATCGACTTCAACCCCACTGAGAATGAGAATGGTCAGTAATTTTAAATAATTAAATATTTCATATAATATGTAGATAAACAAATATAAATATGTATCTATCACTGAGTAATCAACATTTGAAGCATCAAAAGTTTTTAGATTTGCCCAAATAGTTTGATTCACTTCACATGTTTAGAAACATGTATGAATGCATGTACAGCTATTAATATAGATGTTGATTTTCTGTATAAATAACAGATTTACTGTACATACAGTGTAGATTAAAACAGTATTGCTTTACTAAATTTAGTTCTTGTAATATATGCACTTATTCCCATTGTCAACGCATTTCAGGCATTCCTACTCAAGGATTTTCCTCTGGATATTCCTCAGCTGAGGATCATTATGAA[C/T]AACCCATAAAGTCAAACCCTAGTAAGTGTTCGTTATTCAATTTCATACGTGCAAAAAACTATTTCTAACTGGTTGGTTGATTAAAAGTTTACTCAAAAATGAAGCATTTATTTTATTTTACCCTTCACCTTTCTTTTATTCTGCTTAACATTCACACACAGGGCTTTTTGTAAATTGTGGGGACATAACATATGCTTCTATTGTTTTTATTTTGTACAAACTGTATTTTCTTTGGCCTTACTCCTAAACCCAACCCTCACAGCAAACTAAACTCATTCTGTGTGATTTCTAAGCTTCTTGAGAAATGAGGTAATCAGCAATATCCTCATAATTCACCACCTTCTTGTAATACCCATATCATTATACAGATTTGTGTCCTGATGCGTCACAAAAACATGTACACACACACACACACACACACACACACACACACGCACACACACACACACACACACACGTATAAAATTAGTTTGGAAAAAGGTTTGTCACCAAACATCTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40788
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
ENSDART00000129701 Nonsense 101 577 3 17
ENSDART00000140086 Nonsense 101 577 4 18
ENSDART00000129701 Nonsense 101 577 3 17
ENSDART00000140086 Nonsense 101 577 4 18

The following transcripts of ENSDARG00000086490 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 47986764)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 48047416
GRCz11 6 48046175
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACTCAAGGATTTTCCTCTGGATATTCCTCAGCTGAGGATCATTATGAA[C/T]AACCCATAAAGTCAAACCCTAGTAAGTGTTCGTTATTCAATTTCATACGT
Long Flanking Sequence:
TGCATGCTTTCCTGTAGGATTTTTCAGAAGAGGACCAGCCGCAAGGGCACTGGCAGCGTTTCACGCAATTCAAGTCGTGCGAGCAGCGTGAGTCTAATACTGCCACCGCGCATCGACTTCAACCCCACTGAGAATGAGAATGGTCAGTAATTTTAAATAATTAAATATTTCATATAATATGTAGATAAACAAATATAAATATGTATCTATCACTGAGTAATCAACATTTGAAGCATCAAAAGTTTTTAGATTTGCCCAAATAGTTTGATTCACTTCACATGTTTAGAAACATGTATGAATGCATGTACAGCTATTAATATAGATGTTGATTTTCTGTATAAATAACAGATTTACTGTACATACAGTGTAGATTAAAACAGTATTGCTTTACTAAATTTAGTTCTTGTAATATATGCACTTATTCCCATTGTCAACGCATTTCAGGCATTCCTACTCAAGGATTTTCCTCTGGATATTCCTCAGCTGAGGATCATTATGAA[C/T]AACCCATAAAGTCAAACCCTAGTAAGTGTTCGTTATTCAATTTCATACGTGCAAAAAACTATTTCTAACTGGTTGGTTGATTAAAAGTTTACTCAAAAATGAAGCATTTATTTTATTTTACCCTTCACCTTTCTTTTATTCTGCTTAACATTCACACACAGGGCTTTTTGTAAATTGTGGGGACATAACATATGCTTCTATTGTTTTTATTTTGTACAAACTGTATTTTCTTTGGCCTTACTCCTAAACCCAACCCTCACAGCAAACTAAACTCATTCTGTGTGATTTCTAAGCTTCTTGAGAAATGAGGTAATCAGCAATATCCTCATAATTCACCACCTTCTTGTAATACCCATATCATTATACAGATTTGTGTCCTGATGCGTCACAAAAACATGTACACACACACACACACACACACACACACACACACGCACACACACACACACACACACACGTATAAAATTAGTTTGGAAAAAGGTTTGTCACCAAACATCTGA
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa5385
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129701 Essential Splice Site 159 577 5 17
ENSDART00000140086 Essential Splice Site 159 577 6 18

The following transcripts of ENSDARG00000086490 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 47987633)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 48048285
GRCz11 6 48047044
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAGCCTCACCTCTCGACTGTCTTTCATCAACRTTTTTCTGCTCAGCCGG[T/C]ACAGTGCTCTCTGTGTGTTTGTCTGTTTCTGCATAATTACAATTGTATGA
Long Flanking Sequence:
ATTTGTGTCCTGATGCGTCACAAAAACATGTACACACACACACACACACACACACACACACACACGCACACACACACACACACACACACGTATAAAATTAGTTTGGAAAAAGGTTTGTCACCAAACATCTGATCAAACAAATATCATTATTCCTACTATTGAAGACAGTGGTTACTATCAACTATTGACCAACTCTTGGAGTTGAACAATCCCTCCATGTAAAGAGTCGCTTTTTTTCCCCATTCAGGTTCTACCCAGTCTGCTGCTGAACCAGGCTTTGGCGTGTGGGACGTGTTTCAATCTCCAGGTATTACATGTATAAAGCCTGTGTTCAGCCCTCAACATGAACAATCAGTCTTTTTCTCCTGCAGTAGTCATGTGCTCATGTGTGTGTGTGCCTTACAGCTCAAGCTCTGGTTCTGCTGTACTGGTGGCTGGGCACTGCATGGTACAGCCTCACCTCTCGACTGTCTTTCATCAACGTTTTTCTGCTCAGCCGG[T/C]ACAGTGCTCTCTGTGTGTTTGTCTGTTTCTGCATAATTACAATTGTATGAACATGAGAAAAAAAAAAATTATTTGATAAGAATCTTTTTATATGATCAACTCAAATCATTTTATTGCAGCATTATGAAATCAGAATTATTCATTCCCGTTTAATGAACATAAAAGTATTTATTTTAAATGATTTATCTGTGCACAAAATTTCAAATTGATGTGCCATTGTACTTTTTTATTATTAATAAAAATAATAATAATAAATAAGAATAATAATTAGGGCTGTGCGATTAATCAAAATCGAATCACAATCGTGATTTGAAACATTGCGATTAGCTAAAAATCGCAAGAGGCTGCGAAATGTAATTTATGTATTATATAATGTCCCCCACCCAGAGCAAATGCGTGACTGCCGTCTGTGTGTGACATTCTTATTAGCCAATTGAGTGACCACACTTTCATTCTGCCCAATCAGAATTGCACAATTGAACTATGTAGAATGCCCACAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16555
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
ENSDART00000129701 Nonsense 344 577 12 17
ENSDART00000140086 Nonsense 344 577 13 18

The following transcripts of ENSDARG00000086490 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 6 (position 47993108)
Other Location(s):
Assembly Chromosome Position
GRCz10 6 48053760
GRCz11 6 48052519
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAAAGATCCAAGCTCWCTGGAWTCAAGTATAGTGCTGCGCCCGGAGCTG[C/T]AGAGGGCGCTACAGGATCTGGAGAAGCAGATACTAGAGAAACTAGCACAT
Long Flanking Sequence:
CGCCTCTGTTTGTTCTGTCATGGCAACACAGCACAAAACAGGAAATGATGTCATCCATCTAATTGTTTATTTGTCTGTTTGTCTCCTAGATGATGCAAACCGATGTGAGGACTATGAATGATCACATGAGGAAGTGAGTCCCTTTGCAGCGTTTAATCTGCTTTTGCAGACGTTGCATCATAGTTTAATCCAACTGATGACATGTTTTACTTTTCCCAGCGCTGAATCTGAACGTGGTCAGCAGATCTCTGAGCTGAAGTCCAGCATCTCAAACCTTCATTCAACCCAAGACCTCCTTACGAGAAGAGTCGATGCACTTGAAGCTCATAACAACAATGTAAGGGCATGTTTTTGGCTCATTTTAAACAATGGAGCATCAATGTTTGCAACTAATGATGTCATTTACTGTGCAGCTGAGAGCAGAGCTGTCTGATTGGCTAATAAAACACCTGAAAGATCCAAGCTCACTGGATTCAAGTATAGTGCTGCGCCCGGAGCTG[C/T]AGAGGGCGCTACAGGATCTGGAGAAGCAGATACTAGAGAAACTAGCACATGAGAAAGGGAGCAGCAGAGATGTCTGGAGGACTGTTGGAGAGACACTGCAGCAGGAAGGAGCCGGAGCCGCTACTATACAAGTGCGTGTCTGACAGGAGACTTTTTTCTTTTTGAGAGAGTGTGACTTTATCTGAGAATCAGGGTGTTTTTTATGTGTGTGTTTAATAACAGGATGTGAAAGAAATCGTCCACAGGGCTATTAGTCTGTACAGAGCGGATGGGATTGGATTGGCAGACTATGCTTTGGAATCTTCAGGTATTGTACCAGTTTTCTGCTTGATAACTGAATTTATTAATTTACATATATATATATATACACACACACACACACACACACACACACATACTAACATACATCCATGGATTAAATTTAGGGATCACCATTTTTCTTACTTTAAACAATAAATGTAACTAGGCTGTATATGGTTAATCAAAATTTCAGGAAAAAG
Associated Phenotype:
Not determined