ZMP
si:dkey-92f12.2
Ensembl ID:
ZFIN ID:
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 |
sa40788 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30877 | 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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa40788
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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:
sa30877
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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:
sa16555
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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