ZMP
LOC100334148
Ensembl ID:
Human Orthologue:
RP11-723O4.6
Human Description:
Uncharacterized protein FLJ43738 [Source:UniProtKB/Swiss-Prot;Acc:Q6ZUG5]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21926 | Nonsense | Available for shipment | Available now |
sa16331 | Nonsense | Available for shipment | Available now |
sa41849 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21926
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074853 | Nonsense | 110 | 749 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 11 (position 27610257)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 26439083 |
GRCz11 | 11 | 26676699 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCATAGCAAAACTAGATCTTTCTGATCTCCTCCAAGGATGCAGATATT[T/A]GAAGCTGACCTTGCCTATTAAGTGTTCTGCCTCTAAGCACATTGAACAGA
Long Flanking Sequence:
GTAATTCTATTTCAGAGATGATTTGTAGCATTATTTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATAATAATCCTATTCATCTTTCAATAGGCAAAATGTCTTCCTGTCTACTGTCAGTACAAGTTCGACAACATGCCAATTCACAGAAGCAAAGGCTACGATCATAGTGCTAATATTTGCTTCAGGGATGTGAATGTGATTTTTACTGGACTAATGAGCCATGGAAAGCTGGTTGAGTTTCTTAGAGGTCCACCAATAGAGATTGAAGTCCATGATCGGGATAGAAAGAATGAAAAACGCTTTACTAAACCAACTGTATTTGGGACAGATCCCAATGATGCCCGAATAGCTACCGTGGACCTGTGGACTACTGCTTTCAATCTAGACACTGAACATGATGATCATCCACATGGCATAGCAAAACTAGATCTTTCTGATCTCCTCCAAGGATGCAGATATT[T/A]GAAGCTGACCTTGCCTATTAAGTGTTCTGCCTCTAAGCACATTGAACAGAAAGTGATTAACTCAGATACCGCAATTCCAGTAGGTCATTATCTTGAAGCTAACGCCCAACTGAAAGTCCAGGTGGAGATAGCATATCCCCTCCATTCTGAAGATGAAAATGACTGTGAAGACTGTCCATTTGGTCGCATCATTTATGTCTTTAGGTACAATAATACTCCTATCTTATTCAAACTGACTTCTGAAATTCTGCAAATCAATGCAGAAGCCTTTCAGCTACATCATTATCCTGAAGAAACAATCCAAAGGGTCCTGTCAGGTCATATTATAAGCACCAAAGAAAGAGAAAACAAAAGGATGAATGTCCTCACTGGATTTCATCTGATGGATAAGGCTCTGCACCTTTTTGTTTTGGAAGGACTGAAGGATCAAGCAGTCAAAAGACTGTGGAGTGCAGTGCCTATGAAGTAAGAAAACGCTCCCACATGTGCAGAACATTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16331
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000074853 | Nonsense | 336 | 749 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 11 (position 27611578)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 26440404 |
GRCz11 | 11 | 26678020 |
KASP Assay ID:
2260-4366.1 (used for ordering genotyping assays)
KASP Sequence:
AACTCACTAAATGTYTCTTACTCACNTTTTTTTAGTWTAAGCCACATTAGG[C/T]AGGCCAAAAYACTTCAAGAAGYGGTGCACARCAATCTTTTCCCTTTAGCC
Long Flanking Sequence:
TGGTGTACTTTGATGCATCATTTAGGTGTCATTTTTTAAACTAGAAGGAAAAAATGAGGAGAAATGCTTAAACGACTGTTCACACTTGCAGACTGATTATCCTGGCTTGTTTGGTGTGGACAAAAAAAAGAAAGAAAATAATACATTAGGTCCTGTTTTGCATAGTGTTCAAGTGAGTGTAATTTTTTCCACCAAACCTAATGATACAAAAGTCAACAGGACCAAAGGTTTCCTTTTTTCTTTAAAAAAAGTCATTAATTAATAAAGTCATTAATTGTTAGTTCATGTTAACTCACAGTGCATTAAGCAATGTAAACAAGACTGAATGTGAATTTTGATAATGCATTCGTAAACGTTGCATTATGAACAGGTATTATCCATTATTAGTTCATGCCAGTAATTACACTACGTTAACTAATAAAACCTCATTGTAAAATGTGACTGTGTAAAAACTCACTAAATGTCTCTTACTCACTTTTTTTAGTATAAGCCACATTAGG[C/T]AGGCCAAAACACTTCAAGAAGCGGTGCACAACAATCTTTTCCCTTTAGCCAACATGGTTCTCAGTTTAAACAAGGAGTTTGGAGTGGATGTTGGGAGAAAGGAACTGTGGTTGGCTGCAGAGACCCAGGAATCTCAGGATATATCAGATCATCATAACATAAGGAAGAGAATGTACACACCTCTAGACAACTTCAACAGACAATATTTCCAGTGGAAACGAAACAAGTGTAAAAATGGGAAAAACTTCATTCAGGTAATGAGTTGCTTTTACAGTTTTAGAGCATGTCCCAAATCATGCAGTCGAGTAGTACGAGTAGGTAATACATTTCAATTAAACTTACATTCCACAAAATACCATTCTGTATAGTAAGAACTTTTTATTTTTTTAGGTAATTTAATAAGTTACTTATGAATGTGCCTTACTGTACAGTATTGTGTGAACTGTTTTATTTTTTTTTGTTAAACAAATATGTTTAGCAAAATAATTCAATTTTTTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41849
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 |
---|---|---|---|---|---|
ENSDART00000074853 | Essential Splice Site | 474 | 749 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 11 (position 27613655)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 26442481 |
GRCz11 | 11 | 26680097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAATTCTACAATTCGGAGTGGAGAACAACTCTACAGGGAACTATCAAAG[G/A]TTGGCACAAATTTCCATTAAGAACATCTAAGACATACCAAAAAAACCGTA
Long Flanking Sequence:
CCCAGCATTTTATTAGTTTATGATGCTATTGATGTTTGAAAAAGTTTTTGTTTTGAAGCATTAAATAAAAACTAAAAAGTCCTGTGGATACAAATTTAAAGAATTTAGAGTTTAACTTTGTCAGTACAATAAGTTTTACATGTATTTTAAGCAGTATTGAGTCAAGTAAAATACTTATAACTCAAACTAAATAAAAAAAGTAATTTAAACACATTTTTAATGATGTAATTACTAATCAAGTACTTTTTTTAACACTGACACACTGCATGTTTCCCATAGAAAGTGGGAAATTGAGTTAGCATTTTAGTGAATGAATGTTATTTTTGTTTTTAATTTAGGCAAACATTGAAGACGTCTACAGGGCTAGTAATGACTTAAAGAAGTCAAAATCTTATGTGGTTTTGGATACCATAACTGACAGTCAGACCATCAATTACCATAATAATGAAACAAATTCTACAATTCGGAGTGGAGAACAACTCTACAGGGAACTATCAAAG[G/A]TTGGCACAAATTTCCATTAAGAACATCTAAGACATACCAAAAAAACCGTAATAGTTCAACTGTTGTTTAGCATTTTTTATATTATATTTTTTCTTCCATTAGTGCTACCAAACTAAATAACGTGACTGATTATTCTCTTTCTAGAACTCCACTGCTATTGGCATCTTTTGCCCAGGTTTTAGAAGCAGCATAGAGTCAAACCAGCACCCAAAGCGGCCAGACGATGCTCGGATAGAAGAGCTAAGAAAGGTGCTGTTAAGGTCACGTTTCTCTCTCAGTGCAATGTCAACTTTATGGGAATTCCTAAGAGCTTAAGCAAGAAGATAGAGTTTTACTGATGTTTGCCTACCTTGCCCACCTCTTTACGGATCCCCAGAGTTTAAGACAGTATTATGTTGCAAGTAGGGTGACAGGACTAATGCTGATTGACTCATGGGACACAGAGCATCGTCATGAAGCATGTGTTTGCATGAAATTGATTTATCCACCTTTCAGAGTCT
Associated Phenotype:
Not determined