ZMP
abhd11
Ensembl ID:
ZFIN ID:
Description:
Abhydrolase domain-containing protein 11 [Source:UniProtKB/Swiss-Prot;Acc:Q6DRD9]
Human Orthologue:
ABHD11
Human Description:
abhydrolase domain containing 11 [Source:HGNC Symbol;Acc:16407]
Mouse Orthologue:
Abhd11
Mouse Description:
abhydrolase domain containing 11 Gene [Source:MGI Symbol;Acc:MGI:1916008]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43653 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa37320 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43653
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 |
---|---|---|---|---|---|
ENSDART00000101208 | Essential Splice Site | 52 | 317 | None | 6 |
The following transcripts of ENSDARG00000069501 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 25102623)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25685960 |
GRCz11 | 21 | 25722565 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTCTCGCGGCTGGACCGCGCTGGCAGTGACAGCATGAGAACCGCCAGG[T/C]GTTGCATCTTTAATCTTCCGGATGAAATATTGTTAATTGCACAGAACTTC
Long Flanking Sequence:
AAAGTTTAGTTAAATGAATAAATATTAACTAGATTTAAAAATAAGTATAATAATGTCAATGTGATGTCCACAATTTTGAAAATCCCAGATTTAGACAGTCAGTCGTAAATGTGAAACATTTATATTTTTTAAAAAACTAAAAAATGGAAGTGTTTAGTTGTATCTGCTTTCATTTGCATTTAAACAGTTCTACATTTGTTGCGGTTTTATTTTGTTTTTCTAGCGAGATCTGGCAACCCTGTCGTGCGGGAAGGGTTTCCCTAGTGTTAGCTAAACAACATCACGACGACCTTTGAAGTCGCCAACCCCGGTCGAATGAATGAAGTCCGGACGCACGTTTTAGCATGTCAAATTTTGCCATGAGTGCCCTGTGCCGTGTTTTCACAAGAGGAGCGCCTTGCGGCCTGTCGTCATGTTCATCTGTAACGGGACTTCGGGATTTTTGCAGCGGAGTCTCGCGGCTGGACCGCGCTGGCAGTGACAGCATGAGAACCGCCAGG[T/C]GTTGCATCTTTAATCTTCCGGATGAAATATTGTTAATTGCACAGAACTTCATGTGTGAGAGATTATTGTTACTTTAAAAAGTTATTTGTAGTTTATTTTAACGTTATTATTCGTGCATTTACTGTCACCTTAGAAAATTAGCCAGTAGTAGATGGGTTTTAATCAGAAATAGAGTAAAAAGAGTAAAACCAGTCAAAATTACCTACACGTTATCTTTTGTTGTGGCTAATAACGGGTAATGGTTACATTAATTAAGTTATAAATTAGATATTACTATATTGGTATGATTTTGTAAACAAGGCCATGTTTCCACTTTCCAGTCATCACCATATCTTATCTTTAAGTAAAACATCAATAAAAACTCATACTTATGAGTCTTGTGAAAGGCAATATACTGAAATGCTATTCAGATTTAAAGTTAATATTCTCCTGAGACTAAAATTCATAGAGCTTTAAAGCTACAACTTAAACCAAGGTCATATTCAGATTTGATTTGTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37320
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 |
---|---|---|---|---|---|
ENSDART00000101208 | Nonsense | 104 | 317 | 3 | 6 |
The following transcripts of ENSDARG00000069501 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 21 (position 25095889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25679226 |
GRCz11 | 21 | 25715831 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCACTGTCCTGACTGTACTTTGTCTAGTTAGGTGCTGACAATCGATGCT[C/T]GAAACCACGGCAAAAGCCCACACAGCCCTGTCTTGACCTACGACACAATG
Long Flanking Sequence:
TTTTCCTTTTATGTCTACACAGTAAAAAAGGATTAGCAACTTATTTTAAAAATGGATAAACCTACTGTTGTAACTTGGAACTCTTAAGCTGACTTAACTTATTTTTTTATAATTATACATTTGTTCATTTACTTAAGAATTTTGAGGCAATGGGTTTAAAGTGGCAGTGTGGCGATTTTATTTGTACTTTTTCCGCAATTGATTTGCTCTCTTTTTTTAAGTAAACCCAACTAACCACTTTTTACAATGTACTCTTCTCTCTCTTAGCCCTGTAAACCTGACCTATGATGTGTTTGATGGGAAAGGTGACAGCACGCCACTGGTGTTTCTTCATGGCTTGTTTGGGAGCAAATCAAACTTTCACTCCATTGCCAAGTCTCTGGTTCAACGGACCGGCAGGAAGGTACGCCTCCAGTTTCACCAGTACTTTGGGCTGTTCAGAGGAGTCTGTTCACTGTCCTGACTGTACTTTGTCTAGTTAGGTGCTGACAATCGATGCT[C/T]GAAACCACGGCAAAAGCCCACACAGCCCTGTCTTGACCTACGACACAATGACTAGTGATCTGACACATCTGCTGGGACAGCTGCACATTGGGAAGTGTGTCCTGATTGGACACAGCATGGGCGGAAAGGTTGCAATGACTACAGCCTTATCACAGGTACATTGCTTCATTTATACTGTTGAAATGATGATGAAGTTAAAAAGTTAATTTTGATCATTTTAGGGGTTATGTAGGATGAAATGTTAGGAATGACCTGGTATCATAATGAAGGTGGAAACAAAATAAATATGCATTATTTTTGATAAAATATTATGAATAGCAAGAGAGGGTTGACCCTAAACTAAACTTATGTGGTGCGACTGTCATGCAGAAAAACATGAAGTATGAAATTGTTTCAAAGTAAAATGTCCCTCTTGATTTTGTGCCGATGTCTGATTATAAAAGATCTAATAATTAGATTTTTTATTACAAGACAGGTGGTAATAAAATATTTAGGTGGTA
Associated Phenotype:
Not determined