ZMP
mboat2b
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC692278 [Source:RefSeq peptide;Acc:NP_001038716]
Human Orthologue:
MBOAT2
Human Description:
membrane bound O-acyltransferase domain containing 2 [Source:HGNC Symbol;Acc:25193]
Mouse Orthologue:
Mboat2
Mouse Description:
membrane bound O-acyltransferase domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1914466]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13923 | Essential Splice Site, Missense | Available for shipment | Available now |
sa23729 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13923
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:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062405 | Essential Splice Site | 127 | 169 | 6 | 8 |
ENSDART00000142669 | Missense | 351 | 395 | 10 | 11 |
The following transcripts of ENSDARG00000042551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 29763684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29834897 |
GRCz11 | 20 | 29737776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAACGCTGTCCTTACAATCCCACTGCTGCCACCTTCCTGCTGTCAGCCA[T/A]GTGGCATGGGGCTTATCCAGGCTACTACCTCACCTTCCTCACGGGCATCG
Long Flanking Sequence:
GAGAGAAAAAACTAATTTGAATAAACCATGCTAGTTTGATTTCATATACCATTATGTTCTGTCTGTGTGCAAAAATGCAACATGCTGTTTTCCCAAACACAAAACTTGTACAGTACATTTTAGTCTAATGAATTGTTTATCATCAGCAGTAATAATTTTCAAAAGTGGAATTATAAACAATATTACTTTATAACAAAAATGTTATTTTTGACATATTGTTGCAATAATATGGTACATTTAAAACATGACCCTTATAATGTAAAAACAAATATATACTATGTCTTAAAGAAATTGTTGTCCCTGTCATCAAGGAATACTAAGAATAAAGGCATTAGTTGAAAAGATTTTCTTTCCTCTAATTTCCATCCTTTATTCATTTATATGCAAGCATAATAATTGCATACTGGTTTATTATGTGTGACACGATGTGTTGTCCTGTAGGGTGTGTTATGAACGCTGTCCTTACAATCCCACTGCTGCCACCTTCCTGCTGTCAGCCA[T/A]GTGGCATGGGGCTTATCCAGGCTACTACCTCACCTTCCTCACGGGCATCGTCATCACTCTCGCAGCCAGAGCCGTGAGTTTTACCATATTGATACCAAACATGCAGTGCACTTCACAATATTCCTTTCATTTTTGTCTGAGGGAGCTATTTGCTTGACCATAAGGAGCACAAGGAGTAGAATTATAGTTACCTTTAGGGTCACCTGCTGTATTATTGTTATCAGGGGGAACCAAGTGTGCCGCAAGCCTACGTTTGAGTGAAGGTTTCGGCCGTTAGATCGCCCCCTGGGGGCTGGCTGCAGTACAAGTCATAAAGCCCGCCTCCTCCGTGTTAATGAAGGAGACTTGAGCCCAAATAAAAAAAAATATTACACTTGCAATAAAATGTCCCGAAAGATAGTTCTGGTCGATTAAGGCACTGGTTATTGTGCTGAAATAGGTGCAGATCTTCATTTTTGTGAACAGTTTGTTTTTAGCAGTAATTTAATGCTGGGCATGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23729
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062405 | Nonsense | 165 | 169 | 7 | 8 |
ENSDART00000142669 | Nonsense | 391 | 395 | 11 | 11 |
The following transcripts of ENSDARG00000042551 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 29767663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 29838876 |
GRCz11 | 20 | 29741755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTTAGGTGAGGCACAATGTAAGACCACATTTCTTGGGTTCCCCAAGT[C/A]ACAAATTTGTGTATGACGTCATCACATGGGCAGCTACACAGATCGCCATT
Long Flanking Sequence:
GAATCATATGAAGTTCCAAGAACACCTGGCAATACAATGTATTGTCCATATACATATAGTACGAGTCAGCTGCACAACACACAAGCGTTGTATTAAAACTGCACACCCTAATATGGCGCAAAATACATCGATGAACAAAGTTGTTTTTGTAGTTTTTTGGCACACAAAAGGGTACTTGGAGCTTTGCATGATTACAACTGGACCATTGAATTGAAATGATTTAATGTTTCATGTTGCTTTTCTTGAGTTTGAACGTCTCTAGAGTCTAGACCATTGCTGTCTATGGAAGACGAGAGCATGTTCATTTGTGTTCCCGAGATGAACAAAGGTCTCGGGATTGGATCAACATGCTTGATTAAACAGCAAATTATCTCTTTTGGGGTGAACCAACTGCATATTTTAGTTTTTGGTTGATCTATCTCTTTAAGGATGATGATCATTGTCCCTTTTTCTTTTAGGTGAGGCACAATGTAAGACCACATTTCTTGGGTTCCCCAAGT[C/A]ACAAATTTGTGTATGACGTCATCACATGGGCAGCTACACAGATCGCCATTTGTTACACAGTAGTTCCCTTTGTGCTGCTTTCTGTGGGCCCCTCGCTCAAGTTCTACAGGTGGGCCTGACAAACCACAACACATTCAAAAACATTCTTTCTCGATCAACAGGTTGACATTCTGCTTTCTCTATATCTCTGCAGGTCATGGTACTTCTGCCTCCACATAGGCTGTATACTGCTGGCCATCGCTCTGCCGGTCAAACCACGGCATCTACGGCTGAAGGAGCAGCTATCCGCCGCACAGCCAAGCCTGGAGAGCACAGACAGCAACCAGAAACAAAAAGCCACATGAGTCCTGGAACAACTTACCAAACGTCTTTACACTCACAGACTGGGCAAATGTACCTATTCTCCAGCCACACTTGAAGAGAGTCAGATCAACTAAAGCTCACAAATAAACCAACCAACCAGCGTCTGCCTGGACTGATAGAGTAACGTCATCCCTTGG
Associated Phenotype:
Not determined