ZMP
alkbh3
Ensembl ID:
ZFIN ID:
Description:
alkB, alkylation repair homolog 3 [Source:RefSeq peptide;Acc:NP_001003511]
Human Orthologue:
ALKBH3
Human Description:
alkB, alkylation repair homolog 3 (E. coli) [Source:HGNC Symbol;Acc:30141]
Mouse Orthologue:
Alkbh3
Mouse Description:
alkB, alkylation repair homolog 3 (E. coli) Gene [Source:MGI Symbol;Acc:MGI:1916363]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16257 | Essential Splice Site | Available for shipment | Available now |
sa25232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16257
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067057 | Essential Splice Site | 26 | 282 | 3 | 10 |
ENSDART00000123220 | Essential Splice Site | 26 | 282 | 2 | 9 |
ENSDART00000145924 | Essential Splice Site | 26 | 181 | 3 | 8 |
ENSDART00000147327 | Essential Splice Site | 26 | 115 | 4 | 7 |
ENSDART00000148250 | Essential Splice Site | 26 | 91 | 4 | 7 |
Genomic Location (Zv9):
Chromosome 25 (position 31230288)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 29797649 |
GRCz11 | 25 | 30240656 |
KASP Assay ID:
554-7145.1 (used for ordering genotyping assays)
KASP Sequence:
RTAGAAAAAAAGGTRAATTGAATTGAAYTGAATATATTTGCGTTCTTTCA[G/A]YTCAAGATGTCCANNNNNNATCAGCATCAGGATCATGGAAATCTGGACCA
Long Flanking Sequence:
ACTACCAAAATGTATTATTTTCAGAATTCTTTTTTCCCTTAAAAGCAAATTTGTGGAAAAGTGAATAACAAACAAAGTAATAATTATGGAAATTATTTGTGAAACACACAGACACATGAAAGAAAAAACCTATGATTAAATATCTACATACCCATTCAGTATATTCAGATAAATTGTACATGTATGATTCACAGGTACAATAGAGGGGCATGTAAAAAATTAGGTTGTGTAAAAAATGAAATTACCTATTTTGCAAATGGGGAAACTTCATTGGCGAAATCATGATAGTATTTAATCATATCATTTTTTTCTTTATTTAATTATGATTCTGTGGTTATATTATATAAACTAAACTGAACTTAAACTCTGAAAACTGCACTGACACTGTTTCAAATCACTATAATTTTCTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTGTAGAAAAAAAGGTAAATTGAATTGAATTGAATATATTTGCGTTCTTTCA[G/A]TTCAAGATGTCCAATCAGCATCAGCATCAGGATCATGGAAATCTGGACCACAATCTTTTGAGTTCCACCAGCCAGCTGACGTAAGAAACATTTCTTTCTCAACAAGTGCCACATTTGAGTTTCTCCGATTTATCCTGTGTCTTTTTTTTCCAGCCCATCAGAAAGGTTCCTGCAGAGAAAGTGATTGAGTGAGTAACTTGGGCATTTTTAAGCAATAAAAGCTGTTGATTGACAATACATGTACTGGATCCAGCGTGTTGTTTTTCTTCTCTTTCTCAGAAATGCTGGTGACTATGAGATTAGTCAGGGGCCTTCTGGAGTATCCCGGTAAGAATAATGAATTTTAATGTGGCAGAAAACCTAAAAATTAAATATTAGGTTAATTAATTCATTTTATTTTCAGCTTTGTGCCTTTATTAATCTGGGGTGATTAGCAGCAGAATGAACACCAACAGTATATGTTTTACGCAGTGGATGCCCTTCCAGCAGCAACCCATCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25232
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067057 | Nonsense | 69 | 282 | 5 | 10 |
ENSDART00000123220 | Nonsense | 69 | 282 | 4 | 9 |
ENSDART00000145924 | Nonsense | 69 | 181 | 5 | 8 |
ENSDART00000147327 | Nonsense | 69 | 115 | 6 | 7 |
ENSDART00000148250 | Nonsense | 69 | 91 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 25 (position 31230583)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 29797944 |
GRCz11 | 25 | 30240951 |
KASP Assay ID:
554-7719.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATCCAGCGTGTTGTTTTTCTTCTCTTTCTCAGAAATGCTGGTGACTA[T/A]GAGATTAGTCAGGGGCCTTCTGGAGTATCCCGGTAAGAATAATGAATTTT
Long Flanking Sequence:
TCATATCATTTTTTTCTTTATTTAATTATGATTCTGTGGTTATATTATATAAACTAAACTGAACTTAAACTCTGAAAACTGCACTGACACTGTTTCAAATCACTATAATTTTCTATGTGAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTGTAGAAAAAAAGGTAAATTGAATTGAATTGAATATATTTGCGTTCTTTCAGTTCAAGATGTCCAATCAGCATCAGCATCAGGATCATGGAAATCTGGACCACAATCTTTTGAGTTCCACCAGCCAGCTGACGTAAGAAACATTTCTTTCTCAACAAGTGCCACATTTGAGTTTCTCCGATTTATCCTGTGTCTTTTTTTTCCAGCCCATCAGAAAGGTTCCTGCAGAGAAAGTGATTGAGTGAGTAACTTGGGCATTTTTAAGCAATAAAAGCTGTTGATTGACAATACATGTACTGGATCCAGCGTGTTGTTTTTCTTCTCTTTCTCAGAAATGCTGGTGACTA[T/A]GAGATTAGTCAGGGGCCTTCTGGAGTATCCCGGTAAGAATAATGAATTTTAATGTGGCAGAAAACCTAAAAATTAAATATTAGGTTAATTAATTCATTTTATTTTCAGCTTTGTGCCTTTATTAATCTGGGGTGATTAGCAGCAGAATGAACACCAACAGTATATGTTTTACGCAGTGGATGCCCTTCCAGCAGCAACCCATCTCTAGGAAACATCCATATACACTCATTCACACACATAGGGCCCTATCATACACCTGGCGCAAGACGCGATGCAATTGTTGTTTGCTAGTTTCAGCTTTTGGCGCAAGAGTCATTTTGACGTTTTGCACCACGCTGTTTAAATAGCAAATGCATCTGCGCTCATATGTGAGCCCATAGGCGTTCTGGTCTAAAAAAGGATGTGTTGAGGTGCATTGCTGGCGCATTGCTATTTTGAGGAACTATAATAGATCGTTCAAGAGACCAAAACAAAGCCAGTCTAAAGTCCAGCGCAGAGCG
Associated Phenotype:
Not determined