ZMP
metap1d
Ensembl ID:
ZFIN ID:
Description:
Methionine aminopeptidase 1D, mitochondrial [Source:UniProtKB/Swiss-Prot;Acc:Q4VBS4]
Human Orthologue:
METAP1D
Human Description:
methionyl aminopeptidase type 1D (mitochondrial) [Source:HGNC Symbol;Acc:32583]
Mouse Orthologue:
Metap1d
Mouse Description:
methionyl aminopeptidase type 1D (mitochondrial) Gene [Source:MGI Symbol;Acc:MGI:1913809]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39628 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa38270 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19517 | Essential Splice Site | Available for shipment | Available now |
sa39629 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39628
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022841 | Nonsense | 95 | 338 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 30012433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 30152245 |
GRCz11 | 1 | 30956176 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCCAGCAAAGTGCCTGAATGGCCAGATTACATTGAGATTAAAGATGAA[G/T]AGCAGATCCAGGGATTAAGACGAGCGTGTCAACTAGCCAGACACATACTG
Long Flanking Sequence:
TCCTATTTAGGCTGTCAGAGATTAAAGATACTCATAAAGGTTGGGAACCACTCGAGCGTAAGTAAATTGGGAGTACACTTTCTATTTGTTGTAAAGGATCCCTTTAAGATCACAGAGGGCTCCAGAAGTTCCCTCCTCAGAGCATTATCACCCCTTTCCTGATATTTTTCCCTTTGTGCAGGTGGCTTAAGGCTGCTACAGAGAATTTCAAGGCTACCTCACTGCCACAAAGATGCATCTTTGGCCCACCAGTGCCAATTTCACCGATCTTTCTTCTGGAGGAAGCCAAAAACTTCCCACAGTGTAGTCCGGCCTGCCATAGTGCGCCCAGCTTATCCCGTACCCAAGGTAACTTCCACTTCATCAAGTGACACTAAAAATGTAATGTCGATTAAATCTAAAAAAAAAATTCTACTTTGTCATAGCACATTCAGAGGCCTGACTACGTGTCATCCAGCAAAGTGCCTGAATGGCCAGATTACATTGAGATTAAAGATGAA[G/T]AGCAGATCCAGGGATTAAGACGAGCGTGTCAACTAGCCAGACACATACTGCTGCTGACAGGAAACAGTTTGAAGGTAAACTCTACACTTAGCTGAAATCCGAGACCGTAATGTTGAATGAGCTTGATGTGACTTGTCTTTTGAATTGTTATTTGCAGACACTGTCACTATATTGTTTGTTTCTCAGGTTGGTATGACGACAGATGAAATAGACTTTATAGTCCATCAAGAAGCGATTCGTCACAATGGCTACCCTTCTCCCTTACATTATGGGGGCTTTCCGAAGTCGGTCTGTACCTCTGTGAACAATGTTGTATGTCACGGCATTCCAGACAGGTAACTCAGTGCTATTAAACATAAGTGCTTTGTTTTGACTGAATCTGTATACATTTGTTTGTTAGTATGTAGTTGAATGACATAAAATAGAAGTGCTCAATTCTGGTGCTGGAGTGACCTTTAGAGTTTAACCACTACATAAAAGCATTGTTAGCCAAATATCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38270
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022841 | Nonsense | 153 | 338 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 30012720)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 30152532 |
GRCz11 | 1 | 30956463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTCACAATGGCTACCCTTCTCCCTTACATTATGGGGGCTTTCCGAAGT[C/A]GGTCTGTACCTCTGTGAACAATGTTGTATGTCACGGCATTCCAGACAGGT
Long Flanking Sequence:
AAAAACTTCCCACAGTGTAGTCCGGCCTGCCATAGTGCGCCCAGCTTATCCCGTACCCAAGGTAACTTCCACTTCATCAAGTGACACTAAAAATGTAATGTCGATTAAATCTAAAAAAAAAATTCTACTTTGTCATAGCACATTCAGAGGCCTGACTACGTGTCATCCAGCAAAGTGCCTGAATGGCCAGATTACATTGAGATTAAAGATGAAGAGCAGATCCAGGGATTAAGACGAGCGTGTCAACTAGCCAGACACATACTGCTGCTGACAGGAAACAGTTTGAAGGTAAACTCTACACTTAGCTGAAATCCGAGACCGTAATGTTGAATGAGCTTGATGTGACTTGTCTTTTGAATTGTTATTTGCAGACACTGTCACTATATTGTTTGTTTCTCAGGTTGGTATGACGACAGATGAAATAGACTTTATAGTCCATCAAGAAGCGATTCGTCACAATGGCTACCCTTCTCCCTTACATTATGGGGGCTTTCCGAAGT[C/A]GGTCTGTACCTCTGTGAACAATGTTGTATGTCACGGCATTCCAGACAGGTAACTCAGTGCTATTAAACATAAGTGCTTTGTTTTGACTGAATCTGTATACATTTGTTTGTTAGTATGTAGTTGAATGACATAAAATAGAAGTGCTCAATTCTGGTGCTGGAGTGACCTTTAGAGTTTAACCACTACATAAAAGCATTGTTAGCCAAATATCCTTGCAAATTAGTATTAATTTCATAGTTTCCCAAAATCATAATTCCAATGGACATTGCCAAACAGCATCGAATAATTGAGTGATTGTAGTTATCATATTGTCCCATAAAGGTCTAGTCCTTTATTATTTCCTTCATTTAGCCAGAAGATCACATTGAGACAGTACTGTCTCTTCTTCCAGTGAGACCTGGTCAAGACGGCAGACAGCACACTACTCAGAAAGTTGGAAGTGGGTCAAAATTAAGCTGATTTTGCAGATCATTCCAAGCCGTAGGAGCATAAATGATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19517
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022841 | Essential Splice Site | 169 | 338 | 4 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 30012770)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 30152582 |
GRCz11 | 1 | 30956513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTCTGTACCTCTGTGAACAATGTTGTATGTCACGGCATTCCAGACAGG[T/G]AACTCAGTGCTATTAAACATAAGTGCTTTGTTTTGACTGAATCTGTATAC
Long Flanking Sequence:
CCGTACCCAAGGTAACTTCCACTTCATCAAGTGACACTAAAAATGTAATGTCGATTAAATCTAAAAAAAAAATTCTACTTTGTCATAGCACATTCAGAGGCCTGACTACGTGTCATCCAGCAAAGTGCCTGAATGGCCAGATTACATTGAGATTAAAGATGAAGAGCAGATCCAGGGATTAAGACGAGCGTGTCAACTAGCCAGACACATACTGCTGCTGACAGGAAACAGTTTGAAGGTAAACTCTACACTTAGCTGAAATCCGAGACCGTAATGTTGAATGAGCTTGATGTGACTTGTCTTTTGAATTGTTATTTGCAGACACTGTCACTATATTGTTTGTTTCTCAGGTTGGTATGACGACAGATGAAATAGACTTTATAGTCCATCAAGAAGCGATTCGTCACAATGGCTACCCTTCTCCCTTACATTATGGGGGCTTTCCGAAGTCGGTCTGTACCTCTGTGAACAATGTTGTATGTCACGGCATTCCAGACAGG[T/G]AACTCAGTGCTATTAAACATAAGTGCTTTGTTTTGACTGAATCTGTATACATTTGTTTGTTAGTATGTAGTTGAATGACATAAAATAGAAGTGCTCAATTCTGGTGCTGGAGTGACCTTTAGAGTTTAACCACTACATAAAAGCATTGTTAGCCAAATATCCTTGCAAATTAGTATTAATTTCATAGTTTCCCAAAATCATAATTCCAATGGACATTGCCAAACAGCATCGAATAATTGAGTGATTGTAGTTATCATATTGTCCCATAAAGGTCTAGTCCTTTATTATTTCCTTCATTTAGCCAGAAGATCACATTGAGACAGTACTGTCTCTTCTTCCAGTGAGACCTGGTCAAGACGGCAGACAGCACACTACTCAGAAAGTTGGAAGTGGGTCAAAATTAAGCTGATTTTGCAGATCATTCCAAGCCGTAGGAGCATAAATGATAAAGCACGTTGTCCAAGTTCTGACAATATCCTTGGGACTGTTAAACAAATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39629
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000022841 | Nonsense | 336 | 338 | 10 | 10 |
Genomic Location (Zv9):
Chromosome 1 (position 30030328)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 30170140 |
GRCz11 | 1 | 30974071 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACGGTTGTCATCACTAGCGATGGTGTAGAGATTCTGACTAAGCTACCT[G/T]AGGAAGATTGACAGGAATGACGGGACATCTTGTGACGTGTGAGATGGATC
Long Flanking Sequence:
ACTGTGTGTATGTGTATATATATATATGTGTATATATATATATATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACATACACTCAAATGAATAACTTTTGCTAATTTAAAAAGGCAACTAAATTTTTGAGTTTTTCGGGCCATAACTTAATTGTTTTATGTTCACTCGCTTTAAATTTGTAAAAATAAATAAATAAATAAATAAATAAACGATTTAGTTAACGTAATAGATTTGTGTTGGGTCAACATGAAGAAATTGTGTAGAACCCAGCATTTTGTAAAGTGTATTTTTACATCACAATTTCAGATGTAGGCTTGAAAATCACTGAATGGCTGTTTGTTTGTGTGTGTGTGCGTGCGTGTGTGTGTGTGTGTGTTCTTATTGATCCTCAGGTCGGCACAGTTTGAACACACGGTTGTCATCACTAGCGATGGTGTAGAGATTCTGACTAAGCTACCT[G/T]AGGAAGATTGACAGGAATGACGGGACATCTTGTGACGTGTGAGATGGATCTGTTGTTTAGAATTTGCTATTTAAATAAAATTTTCTAAACTTTTCTCCAATTTTTAATCGTATTTTTTTTTTTACCTGTCTTAATCAAATTTCTTTTTGAAACAGCTGCACGACTCCACTGGGTTTTTACATTTCGAATTAATGGAGTTCTAATTATTTAATGCGTGTTATTTTGTAGCCTAATGAGTTTCAATATCTCTTTACTGTTACAAACTCTTGCTTTATGATATCATCTCCGACTTAAGCATGAACACACAGGGAATGAAATGTCATTATGTCTTATTATTATGTCGGGGTTTCTCCATACATCATATTACTCCGAAGTAATGTAGTTAGCTCTGTATCTCTCCAGAGGTGATTATATTTATGGGCCATGGGTTGCAGTATGAACCATGTGTAGCGTATTAAGAATACCCTGTAATCATATCTTGCTACACGACATCATTTGTA
Associated Phenotype:
Not determined