ZMP
LOC568975
Ensembl ID:
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15074 | Nonsense | Available for shipment | Available now |
sa38908 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa42095 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38907 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15074
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000145643 | Nonsense | 62 | 1106 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 47429079)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 46435358 |
GRCz11 | 12 | 46310453 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGACACCATGGTTGAATGGAGCGGCTGGTATCGGCTGTATCTGAMT[G/T]GACAAAGTGCCCAGATGTCTGAGTGGTGTATGAGTTCAATGGGCTGTGGT
Long Flanking Sequence:
CTAACAATGTCTTATTTACGATGGCTGAGAGAGCTTAACCCGCGCTGCAATTTAAGAAAGCACATGCAATTACAAAAAACACCAGCAAATACAGAAACAATCTTCATCAATTTGACAGCAAACAACTGAAGAAACTCACAGCAAATTGGTCACAACACTTGCAAATATGCACGTAACACAATGGAAATGTTTTTAGGGGATCCAAACACATGATGGACCCTGCTGAGATATGGAAGTGTTGTCATTTATGGATACAGTATTTGCAACTTATTACTTTACACCACTGCAGACTGTACAGTACATCACACTCTATCATACAGAGGTGTTTAACATCTACCTTTTTTCTCTTGATTGTCTCAGTGCATACTACTTCCAGCTTTGATCCATGTCATCAATATAACACTCTTGATGAATACTGGCGAAACATAAGAATAAGGCAATACCTTGACCATGATGACACCATGGTTGAATGGAGCGGCTGGTATCGGCTGTATCTGACT[G/T]GACAAAGTGCCCAGATGTCTGAGTGGTGTATGAGTTCAATGGGCTGTGGTGGGCACACTGGACTGTATCTCAACGGTTCTCATCCAACACTTGAGGATGGAGTGGTGACCCGTGATGTCGTGGGAAGGAACATGTGGTCCAATCAGTGTGGAAAATACAGATCCTCATCCATCCAAGTCAAAGCCTGTCCAGGAGATTATTACGTCTATAAACTCGTCAAGCCAGATCTGTCGATCCCCAAACCTTCATACTGTGCAGGTGCACTTCTCAACTTTCAAAACTTTTGATGAATGATTTTTTATTAAGCTGATTATAGGAATATTTAAGCTGCTGTCTGTAAACCATCAATAATTCAGCAGAGGTCCTCACAGACCTATACAGCATTTACTTAACACTCACAACTATAAACTTTTTAACAGTTTATGCACACTGTCTGTATATGACCATGCTGAATTATCATCACACAGTGCTTTTGGATTTAAAATGAATTATTTACCCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38908
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000145643 | Nonsense | 548 | 1106 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 47426825)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 46433104 |
GRCz11 | 12 | 46328510 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTACTTTCACATCCCACCCTATAAGAGTCAAAGCCTGTCCTGGAGATTA[T/G]TATGTGTATGAGTTTGTACAGCCGAGAACTCACTCAGCTTACTGTGTTGG
Long Flanking Sequence:
TGTGCAGGTATATTCATCTTTATACAGTGTCTGACATGCTTTGTCAGAGTATTTTTTAGACTTTACAGACCAATACAGACCTTTTAAACATGATCCATTATCTTATATTTGGAAATTGAATCTTCAGTATTTTCTGCTTGTTTTCTTTTTCTAATAGTGTCTTTCCCCACCCCAAGTGTCGACCCCTGCTACAACTATACCAGTCTGGATGAACCTTGGAGATCCACTGATAACCCTGCTAACTACTATGGCAATCATTTTGATTGGAGTGTAGCATGGAATGGCTGGTACAGGCTGTTCTACAACAATCAGAGTGCTCAGATGCCAGATTCATGTGTAAATGAAGGCATGTGTGGCACTTATTATCCACTGTGGCTCAATGGATCTCACCCAGAGCTGGAAGATGGAGTGGTCCTTCGTCAGGTCTGTGTTTCTGCATGGAGCGGCTGCTGTACTTTCACATCCCACCCTATAAGAGTCAAAGCCTGTCCTGGAGATTA[T/G]TATGTGTATGAGTTTGTACAGCCGAGAACTCACTCAGCTTACTGTGTTGGTGAGTATTTACTCATGTGCACTTTGGTCTTGTATTTTTCTGGATTTTGTTTGAAAATATCTTATAATGACATAAAATTGTTCTTTAAACCAACAGCTACAAACCAGTCCAGCACAGCAGTGACAACAACCCAGCCAATCACATCTGAAGAGTTCATTAATCCACCAACCACTGGTAAATCTTTCTTTCTTATTACATAATGATGTAGAATATGGATTGCTACAATACTCCATATAATAGTTGTTATGACCTCCATGGTTCAGTATACATATGGAAACAGTTTTTTTTTTGTGGTTTTGCCTTTAAATTATTCATTCATTCATTCATTCATTCATTCATTTTCTTGTCGGCTTAGTCCCTTTATTAATCCGGGGTCGCCACAGCGGAATGAACCACCAATTTATCCAGCAAGTTTTTACGCAGCAGATGCCCTTCCAGCCGCAACCCATCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42095
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000145643 | Essential Splice Site | 719 | 1106 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 47422364)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 46337259 |
GRCz10 | 12 | 46428643 |
GRCz11 | 12 | 46098824 |
GRCz11 | 12 | 46156241 |
GRCz11 | 12 | 46192137 |
GRCz11 | 12 | 46304027 |
GRCz11 | 12 | 46324714 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTCTATGAGTTTGTGAGGCCGACCACCTGCAATTTAGCATACTGTGCAG[G/A]TACTGGACACACATTTAACTCTGCCTTCTGTTTATGTTAGAGATGATGGC
Long Flanking Sequence:
GTAATCAGTCTGCTGTCCAAATCAGTGAGAATAAAATTTAATGCTGCTTATTTAGTGCTCCATCATGAGATTATAAACAGGAAAACTACCATGACTAATAATAAATTTGCTTCCAACAGATCCCCCTGTTGACCCCTGCAATAACTACATCATCCTGGATGAGCCATGGAGAGCCACCAGCAATCAAAACTCCTCTCAGTTAATGTGTGACAGAGCGGTGAGCTGGAGCGGCTGGTACCGTCTCTTCATTAATGGTCAGAGTGTTCAGATGCCAGACACATGTGTTGATGAGAATAGCTGCGGCACTAATGCTCCACTGTGGCTGAGCGGAGGACATCCAACACTTGAGGATGGAGTGGTCTCTCGAGATGTCTGCGGACACTGGAGCAACAACTGCTGCTATTTCCAGTCCAATCCCATTCAAGTCAAAGCCTGTCCTGGAGGTTTTTATGTCTATGAGTTTGTGAGGCCGACCACCTGCAATTTAGCATACTGTGCAG[G/A]TACTGGACACACATTTAACTCTGCCTTCTGTTTATGTTAGAGATGATGGCTTTCTGTCTGACATTTATTTGTGTTTATAGATGTGAGGTTTAACACTAGCTATACAACTGACACGCCAGAGACGACCACAACAGAAACAACAAATATAATATCTGGTAATGTAATGTACTGTAACACAATCTGCAGGATTATTGCTCAGATTAAAGTGCTTTGAGTGTCAGAATTTGTTGCTATTTTTCAAATGATTACATTAGTAATAAAAAAGAGGTGATGTGTGTATGTTTATGTGCTTAGTAGTAACTTGTAAAATGTTAGTGATTGCACTAGGTATAGGAAACAGACTGCAAGTTTGTGTTTAATTTTAGTTAAACATTGTGCTATGGAGCTGATTTGCTAATACTTTTATATGTGAGGTGCTTAGAATGCATTTAAACGTAGTAAAAGTACAGTAAAAAAACAAGATGGTTTAACTAAATTTATGTCAAGTGTATATGTATTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38907
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 |
---|---|---|---|---|---|
ENSDART00000145643 | Nonsense | 888 | 1106 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 47420412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 46426691 |
GRCz11 | 12 | 46154598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGAGTGAGAATCCTGAAGCTTTCTTTCAGCTGTGTTTATCCTCAAACA[C/T]AAACACTTTCCATGAACGTGGAGATCAACCCAGTGCAGAGGTGCCACAAC
Long Flanking Sequence:
TTGGCTACATTACCACTTCAGCTGTACATTATTTTCAAAAGAATCCACACCATCAAAACAATATTGACAGAAAAAAACAACAACCCATTTTTTACAACCTTGACCATGTTTAGTCTCCAGGCAGGTCAGTAAAGGTTATGAAAATTAGCCAAATAATAGAAACGGCCCAAACAGACTTGCGTAAAAAACTTCTCAAAGTGTTTCTTTCAGTGATGAAGAGTGGAGAACAACATGCTACCAAACACTCTGACACTTTTGCCTGCATTCTCCACTAATAATATATAACACCCCATTATTGCACTTGACAACTGGTGTCATTCCTTGAGAAATAAATACTCAATTCAAGTAAAATACCAAATAAAATGTCTATGTGTTGTCTGCAGGCCAACGGCAGCCACTTCATCTACAGTAACTATATTGTGGGGACGCCGGGAACAGAAGGTCTCATCAGCAGAGTGAGAATCCTGAAGCTTTCTTTCAGCTGTGTTTATCCTCAAACA[C/T]AAACACTTTCCATGAACGTGGAGATCAACCCAGTGCAGAGGTGCCACAACACACTCATTCTGCTTTCAGTTTGACTGCTTTATTATCGGTGTAGTTGCCAAATTAGACAATTTTACACATTTTAGTTGATCAATATATGTTTTATGCCTACTATAATACATATATGATTTAAACAGCACTGTGCACAAGGTCCTCCCCTCTGGTGAAGGGGTTTATCAGGTGCGGATGGTCCCGTATGTGGATGAAGAGTTCACTCAGCCCTTCACTGGTAGAGTGGATGCAGAGCTGAACCAGGAGATGCATGTGGAGGTTGGTGTTGAGGGGGTCGACAGCCGCCAGTTTGCCCTGGTGATGGACACGTGTTGGGCTACACCTGTGAATGACCCTGATTACAGTCTCCGCTGGGACCTCATTACTGATGAGTAAAGACTTCTTTGTTCATTAAAGATTAGTGTTAACTCACAACAATTTTTAAAATCAACTTTTGAATAAATTATAAT
Associated Phenotype:
Not determined