ZMP
sdad1
Ensembl ID:
ZFIN ID:
Description:
Protein SDA1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6NV26]
Human Orthologue:
SDAD1
Human Description:
SDA1 domain containing 1 [Source:HGNC Symbol;Acc:25537]
Mouse Orthologue:
Sdad1
Mouse Description:
SDA1 domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2140779]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29527 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14966 | Essential Splice Site | Available for shipment | Available now |
sa13304 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa29527
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099795 | Essential Splice Site | 394 | 682 | 14 | 22 |
ENSDART00000142986 | None | None | 212 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 8923782)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9280376 |
GRCz11 | 21 | 9373109 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAATAACTTTGTTACAGACAGAAATTCAGGGGAGGTCATGACAGTTGGG[T/C]ATGTGCTATGTAAATATGAGTAACATACAATAAGGTTTAAATGTCTAATA
Long Flanking Sequence:
TAAAAGTACCCTTTTATAGTAAAATCATAAAAGTTATTTTACTTTTATTCATCAAGGACACATTCAATTGTTCAAAAGTCAGTAAAGACATTTATAATTACAGTTATTATTTTCTATTTTAAATAAATATTGGTTTTCGAACTAAAAAAAAAAAAAAAAAAAAACTAAAATATTAAGCTGTACAGCCATTTTCTGCATTTATGAGTAGACGTCTTTGAGCACCAAATCAGCATAATAGAAATATTTCTGAAGGATTATGGACTGAATTCTTGATAAAACGCAATCAAATTGAAAATGTTTGTGTGAAATTATAGCGATATTTAAGAATATTAATGTGTCTATTACATTTTTGGTCAAATAAATGCAGCTTCGAACATGGGGATCTACAAATAGAGTGTGCTAACTTCTTGTTATATTTACAGATCATTGAGCCAGTCATCATGACCATTGCCAATAACTTTGTTACAGACAGAAATTCAGGGGAGGTCATGACAGTTGGG[T/C]ATGTGCTATGTAAATATGAGTAACATACAATAAGGTTTAAATGTCTAATACAAAGTAATAATGCATCCCCCCCCCACTTATATCTCAGAATCAACGCCATAAAGGAAGTGGTTGCCCGTTGTCCTCTTTCTATGTCAGAAGATCTGCTTCAGGATCTCACACAGTACAAATCCCACAAAGATAAAAGTATGAAGTGGATCATTATTTATCATAATCTTTATATCAGATGCAACTTTTTATAGTAGACTGTTGAATGTATTGTTTGACTTGTTGTCTTCCAGATGTTGTGATGTCTGCTAGGGGTCTTATCCAGCTCTTCAGAGACCTCAATCCAAAGATGCTAACCAGAAAAGACAGGGTGAGAAGTGTTTGCAGTTTTATATCATATTAAAATTGATCAAATCATTCTCAAAATCTATTCAGTCTATATTAAGGATTTCTAACCATGGTCTCCTTTGACCTCAAATATACAAAAACATAGTAGTATTTCAATAAATTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14966
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099795 | Essential Splice Site | 452 | 682 | 16 | 22 |
ENSDART00000142986 | None | None | 212 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 8924142)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9280016 |
GRCz11 | 21 | 9372749 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGCTCTTCAGAGACCTCAATCCAAAGATGCTAACCAGAAAAGACAGGG[T/C]GAGAAGTGTTTGCAGTTTTATATYATATTAAAATTGATCAAATCATTCTC
Long Flanking Sequence:
AATGCAGCTTCGAACATGGGGATCTACAAATAGAGTGTGCTAACTTCTTGTTATATTTACAGATCATTGAGCCAGTCATCATGACCATTGCCAATAACTTTGTTACAGACAGAAATTCAGGGGAGGTCATGACAGTTGGGTATGTGCTATGTAAATATGAGTAACATACAATAAGGTTTAAATGTCTAATACAAAGTAATAATGCATCCCCCCCCCACTTATATCTCAGAATCAACGCCATAAAGGAAGTGGTTGCCCGTTGTCCTCTTTCTATGTCAGAAGATCTGCTTCAGGATCTCACACAGTACAAATCCCACAAAGATAAAAGTATGAAGTGGATCATTATTTATCATAATCTTTATATCAGATGCAACTTTTTATAGTAGACTGTTGAATGTATTGTTTGACTTGTTGTCTTCCAGATGTTGTGATGTCTGCTAGGGGTCTTATCCAGCTCTTCAGAGACCTCAATCCAAAGATGCTAACCAGAAAAGACAGGG[T/C]GAGAAGTGTTTGCAGTTTTATATCATATTAAAATTGATCAAATCATTCTCAAAATCTATTCAGTCTATATTAAGGATTTCTAACCATGGTCTCCTTTGACCTCAAATATACAAAAACATAGTAGTATTTCAATAAATTAACAATTTTCTTGTTTTACAGTTTCTGATATTTCCCTGAAATATGTTTATGGATTTGCTATATTGTCAGTTAGTCATGCTAGTTTTATTTTATTATATTTGTTATTGATTTTTAAGTATACACATTCACAAACCCCACAGCCCTTACCCAGAATAGAAGATACAATAGTTTTCTAGCTGTCAGTTACTTCAGTCTGAAATTACTGCTGTTTGGAGAGACATAATGATAATAATAAAAGAAATAAATACATACATAAAAAAGGGAAACATAAAAAAATAATTAAGTGTATAAAAACTCATGTAGACACTTTCCAACAGAGAAAAGATCAGGGTTCATGCGGTCATGAAAAACCTGGAAAAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13304
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099795 | Nonsense | 633 | 682 | 21 | 22 |
ENSDART00000142986 | None | None | 212 | None | 7 |
Genomic Location (Zv9):
Chromosome 21 (position 8929544)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 9274614 |
GRCz11 | 21 | 9367347 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGACTGACAGGAAGGAGTTTACCAAAAAGAGAGGTAAACTAAACCCGTA[T/A]GCCAGCACCAGTAACAAGGAGAAGAAACGGAAGAAGAACTTCATGATGAT
Long Flanking Sequence:
ACTGATTTTAAAGTTTAGGGTTAGTGAAAAAAAAAAAAAAAAAAATTAGCCAGGATGGATTTTTTTCATAAGTGATTTTCCAAATGATTCCCATTACAACTAAATACTTTAAACTCATCAATAGTCTTAATTATAATGTATCATTATTTTCCACAAATATATGAACTTTCAACCATTATAATAGTAAATAATTGTTTAAAACAACATCAAAACAGTATATTACAATTATTTTAAAGATAATGTGAGATTCGGCTTTGCAACACTGGAATAAATTACAATTTAAAATATATTTAATTAGTTTTAGTAGCAAGATTTGACTATGCGCATAACTATCTTTCAGTAACTAACTAGGTTTTTAATGGATGTCTTTGTTACAAAATAGAAAAAAAAGTGCCATAAATATCAGTATAAAATTGTTGTTATTATTATATATTTTTTTCTCAGGCTGGACGGACTGACAGGAAGGAGTTTACCAAAAAGAGAGGTAAACTAAACCCGTA[T/A]GCCAGCACCAGTAACAAGGAGAAGAAACGGAAGAAGAACTTCATGATGATGAGACACAGTCAGAATGTTAGAACTAAAGGCAAACGCTCCTTCAGAGAGAAACAGGTGAGCCGTTTACACTCCTTTAACGCTTTTAGGTGCCATAAATATGTGTGTGCTTTATGTAGATTGGTTGTTTTTACTCATCATGATTTGTCTCCCTCAGATCGCATTAAGAGATTCACTCTTGAAGAAGAGAAAGTTCAAGTAGTTCCCACTTTTAATGGACTGGAACTAATTTATGCTTCGTGATCTGTGTGGACCATTGTGTAAAGGAAGACAGTGAACAGACTTGGCTGTGTGGGTTTTCTTGTTGCCTTTTAATAAAAACATTTAAACAGTTGACGTTTTGATTTGAATTTAAAGGGCACATAATTTCCCCCTTTTTATGATTTAATATTAATATTATGGTTCTTCTGAGTGTGCCAGTTTAGGTTCAGTTCAAAGCACAGTTTAGATTT
Associated Phenotype:
Not determined