ZMP
zgc:174622
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC567635 [Source:RefSeq peptide;Acc:NP_001103504]
Human Orthologue:
TMEM130
Human Description:
transmembrane protein 130 [Source:HGNC Symbol;Acc:25429]
Mouse Orthologue:
Tmem130
Mouse Description:
transmembrane protein 130 Gene [Source:MGI Symbol;Acc:MGI:3607706]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38882 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2652 | Nonsense | F2 line generated | Not yet available |
sa16730 | Nonsense | Available for shipment | Available now |
sa35252 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa38882
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109132 | Essential Splice Site | 34 | 318 | 2 | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 18894985)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 17744490 |
GRCz11 | 12 | 17866364 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTGCCTTTGGGATACCAGAAGAAACCCCTCATCATCAGTTATCTGG[T/G]AAGCTGCTCCTTTTAAGGTTTTGGCTTTGTTTTTACTGGTGAAGATTCTG
Long Flanking Sequence:
TAACAGTCTGGGATTTAATGTAGCCATTTCTTGCACGTCCTCTTGGAAAGCCATTCAGAAGCCTTTAGCGAAATGGGTTTGTGAATTAGTCACATCTCTGCATGAATTATATTTGCCGTGACAGCACAACACATATCATTATTCATATGAGCATAAGGTTTCAACACGTGAACATGATTTCAAGCCTTTACCAAACAACATGAAAGACTTAAAATGCTCACTCAGTCACACTCGAGTCACAAGCTGTTTATTTGGAGATCTGTGCTGAAGAGTCCACATGGACTGGTAAATATCAAATATTGCTCTGAATATAGATGTATACTTGTTTTTCTATGATGACTAATCATGTAGTCTTCAGATTTTTTGTTAAATGTTTATGTATGAAGTTGCAAACCGATTTCCACCAGGATCCGGAGTGTTCTGGTTCACACCTTTCTCTCACTGATTTCCTCTCTTGCCTTTGGGATACCAGAAGAAACCCCTCATCATCAGTTATCTGG[T/G]AAGCTGCTCCTTTTAAGGTTTTGGCTTTGTTTTTACTGGTGAAGATTCTGATGATTAAATGTGTTTTACCAAAGGAAATGTCAAAGGAAAGCTTATTTTCCATCAGATGGAAGGGAATTCAACACTCTTGCGCAAAACAGGAAATCTGGCATCTTACACTAAAACAGTGGTTTCATTTGAACTCTATGACCCGAGGCATATCCTGCGCTCTGTCTCTTTTACATACACATGGGATTTGGGCAATGGGTAATTCATATTTCAATACATTTAATTTTCTCGTATCTCTAAAAAATGATGTTATTTACAGCTGTCATTGTTTTTAGGGAAGTGCATAAAGGCCCAGAGCCTTTTGTGAAGTTTTACTACGCCTTACCAGGGAACTACACGTTAAAACTGAGCATTGAAACAGATGCACCTCAGCATTCCAGGATGACTGGCCTGTACTCGGTAGATCTGACTGTATTAGGTGAGGGCAGATTCTGAATCACTTATTATCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2652
Status:
F2 line generated
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109132 | Nonsense | 175 | 318 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 18896026)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 17745533 |
GRCz11 | 12 | 17867407 |
KASP Assay ID:
554-3191.1 (used for ordering genotyping assays)
KASP Sequence:
TTTTTTCTCTATTGCATGTGACGNNTATAGCCCTCCGGTTTGGCTGTGCTGG[A/T]GAGTTTTGCCTGATTGCCACACACCCAATCCAGCTTCCTGCAGTTTAGTC
Long Flanking Sequence:
AGTCAAAGATTATGTTGTTTTATAGATGCTATTAGATACGTTGATCTGATAGGACCTGTGATTTATAACGTCGACCAAAACAGCAGACTGTCCTTTGAGGTTGGAGGAAGGTAAAGCATATTTCCAAACATATATATTTAGTCCTACACTGTAAATTACACAGTATTTTACTGTAATGTGAACTGTATTTTACATTTGGACATTTATGAAGTGTTACTGTATTTTATAGATGTATTGTGAACATTATAGTATTTTTTACCGTTAAGATATACAATACTGTTAATACACATAGAGCAAGATAAATGGTCATTTAAATGTAAATAAAGTATTTTTGTTGTAATTGATTTACAGTAAGTTACTGGCGAACTACTGCCAGTAAGTTATTGTAGAGGGAATTGTTCATTGTGTAACTTTTGATTAAATAAAAAGTCATCAGACTTTGATCATTGTTTTTTTCTCTATTGCATGTGACGTATAGCCCTCCGGTTTGGCTGTGCTGG[A/T]GAGTTTTGCCTGATTGCCACACACCCAATCCAGCTTCCTGCAGTTTAGTCCAGATCTATGAAAACACCTTCTGTCTGAACTACACTTTCACATCTGTAGGAACGCACTGCTTAGACCTGAGTGTGAAAAATAACATCAGCAGCCTCCAGACATTCTACAGCGTCTATGTGCAAAGTGGTCGTAAGTATAATTCTTTTATACATACTGTATATAAAACAAGTTTTATTTTATTAATTGAAAGAGACACTGGGTAACACGATGGCTCAGTGGTTAGCACTGTCGCCTCACAGCAAGAAGGTTGCTAGTTTAAGTCCTGACTGGGTCAGTTGGCTGTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTCGTAGAGAAGGGTATAAGCAGATGTCGGAGTCAGCTCCAAGTGGGTGGGACTTGAGCTCCAAGTGACCTGTACAAATCTGGAGTTTTTATTTATTTATTGTGTTGTACATGACACAGAGTCCAATATTGTGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16730
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 |
---|---|---|---|---|---|
ENSDART00000109132 | Nonsense | 230 | 318 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 18896193)
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGAGTGTGAAAAATAACATCAGCAGCCTCCAGACAKTCTACAGCRTCTA[T/A]GTGCAAAGYGGTCGTAAGTATAATWCTTTTAWACATACTGTATATAMAAC
Long Flanking Sequence:
TTACTGTAATGTGAACTGTATTTTACATTTGGACATTTATGAAGTGTTACTGTATTTTATAGATGTATTGTGAACATTATAGTATTTTTTACCGTTAAGATATACAATACTGTTAATACACATAGAGCAAGATAAATGGTCATTTAAATGTAAATAAAGTATTTTTGTTGTAATTGATTTACAGTAAGTTACTGGCGAACTACTGCCAGTAAGTTATTGTAGAGGGAATTGTTCATTGTGTAACTTTTGATTAAATAAAAAGTCATCAGACTTTGATCATTGTTTTTTTCTCTATTGCATGTGACGTATAGCCCTCCGGTTTGGCTGTGCTGGAGAGTTTTGCCTGATTGCCACACACCCAATCCAGCTTCCTGCAGTTTAGTCCAGATCTATGAAAACACCTTCTGTCTGAACTACACTTTCACATCTGTAGGAACGCACTGCTTAGACCTGAGTGTGAAAAATAACATCAGCAGCCTCCAGACATTCTACAGCGTCTA[T/A]GTGCAAAGTGGTCGTAAGTATAATTCTTTTATACATACTGTATATAAAACAAGTTTTATTTTATTAATTGAAAGAGACACTGGGTAACACGATGGCTCAGTGGTTAGCACTGTCGCCTCACAGCAAGAAGGTTGCTAGTTTAAGTCCTGACTGGGTCAGTTGGCTGTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTCGTAGAGAAGGGTATAAGCAGATGTCGGAGTCAGCTCCAAGTGGGTGGGACTTGAGCTCCAAGTGACCTGTACAAATCTGGAGTTTTTATTTATTTATTGTGTTGTACATGACACAGAGTCCAATATTGTGCTTTATGAATGTCTACACCTCAACCCTAAACCCAACCTCACAGTAACCTGATGTGTTTTATTAATATCTGCTCCACCTACATCACCTAAGCCCAAGGTTTAAGTCCCTCCCACTTGGAGGTCACCCAATCTACTCGCGGTGTAATTCCTCCCACTTGGAGGTCTCAGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35252
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109132 | Essential Splice Site | 234 | 318 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 12 (position 18896207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 17745714 |
GRCz11 | 12 | 17867588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACATCAGCAGCCTCCAGACATTCTACAGCGTCTATGTGCAAAGTGGTC[G/T]TAAGTATAATTCTTTTATACATACTGTATATAAAACAAGTTTTATTTTAT
Long Flanking Sequence:
ACTGTATTTTACATTTGGACATTTATGAAGTGTTACTGTATTTTATAGATGTATTGTGAACATTATAGTATTTTTTACCGTTAAGATATACAATACTGTTAATACACATAGAGCAAGATAAATGGTCATTTAAATGTAAATAAAGTATTTTTGTTGTAATTGATTTACAGTAAGTTACTGGCGAACTACTGCCAGTAAGTTATTGTAGAGGGAATTGTTCATTGTGTAACTTTTGATTAAATAAAAAGTCATCAGACTTTGATCATTGTTTTTTTCTCTATTGCATGTGACGTATAGCCCTCCGGTTTGGCTGTGCTGGAGAGTTTTGCCTGATTGCCACACACCCAATCCAGCTTCCTGCAGTTTAGTCCAGATCTATGAAAACACCTTCTGTCTGAACTACACTTTCACATCTGTAGGAACGCACTGCTTAGACCTGAGTGTGAAAAATAACATCAGCAGCCTCCAGACATTCTACAGCGTCTATGTGCAAAGTGGTC[G/T]TAAGTATAATTCTTTTATACATACTGTATATAAAACAAGTTTTATTTTATTAATTGAAAGAGACACTGGGTAACACGATGGCTCAGTGGTTAGCACTGTCGCCTCACAGCAAGAAGGTTGCTAGTTTAAGTCCTGACTGGGTCAGTTGGCTGTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTCGTAGAGAAGGGTATAAGCAGATGTCGGAGTCAGCTCCAAGTGGGTGGGACTTGAGCTCCAAGTGACCTGTACAAATCTGGAGTTTTTATTTATTTATTGTGTTGTACATGACACAGAGTCCAATATTGTGCTTTATGAATGTCTACACCTCAACCCTAAACCCAACCTCACAGTAACCTGATGTGTTTTATTAATATCTGCTCCACCTACATCACCTAAGCCCAAGGTTTAAGTCCCTCCCACTTGGAGGTCACCCAATCTACTCGCGGTGTAATTCCTCCCACTTGGAGGTCTCAGGGCTGCAGTGATACCTA
Associated Phenotype:
Not determined