ZMP
si:dkey-265o13.4
Ensembl ID:
ZFIN ID:
Description:
Genetic suppressor element 1 [Source:UniProtKB/Swiss-Prot;Acc:Q1LWL6]
Human Orthologues:
AC011317.1, KIAA0182
Human Description:
KIAA0182 [Source:HGNC Symbol;Acc:28979]
Mouse Orthologues:
Gm11027, Gse1
Mouse Descriptions:
genetic suppressor element 1 Gene [Source:MGI Symbol;Acc:MGI:1098275]
predicted gene 11027 Gene [Source:MGI Symbol;Acc:MGI:3779250]
predicted gene 11027 Gene [Source:MGI Symbol;Acc:MGI:3779250]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23322 | Essential Splice Site | Available for shipment | Available now |
sa32211 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23322
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089150 | Essential Splice Site | 936 | 1239 | 11 | 15 |
ENSDART00000140908 | Essential Splice Site | 900 | 1203 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 30414772)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 30492240 |
GRCz11 | 18 | 30470494 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACACAACCCTCACCCGCTTTGCAGAAGTCCTGCAGCCCATAGCTCAG[G/T]TTAGTTTGCATTGCTCTTCATCATGTGAATGCATGTACATTTGTTTGTCC
Long Flanking Sequence:
TTCTGTGTGCCGTTTGCTACCTTAATGTACAAGTAGCTAAAACTCGCTCATTCTGAGACGGGAACCGGTAGACATGCAACAAATTTAATCATAAGGTAAACACAAAACAGAACTTTCTGCCTGGAGCTTCTTCACAGGACTCTACACTTGTAAACACATGCTAAACTGCCCACACTCATCAGTGCTACCAAGCCGACCAATCACAGAGCTTTTGCTGCACGTCGTTGTGACATGTAGTTAAATTTTTTGAAAGGTGTGCTTCAGTGTCAGTCATGGTGAGGGCGAAGGCTGTGCGTTTGACGCAGAAGCATAAATCAGTCTTTGGAGATGTCGACAGCACACAACCAAAACTACCGCTAATGTCTTGTTCTTTTACTTTGTTTTAGATAACGAGAGGGTTGAGGAGTTGTTGCAGGCCATAAAACAGAAGAGTGTGACTCTAGACACCATCAGACACAACCCTCACCCGCTTTGCAGAAGTCCTGCAGCCCATAGCTCAG[G/T]TTAGTTTGCATTGCTCTTCATCATGTGAATGCATGTACATTTGTTTGTCCCTCCAGTGACTTGTGTTTTCAGCACACTTTCTGGTTTATCTTAAGTAATACAATGCTTGGCAACTTACTAACTTACTAGAACTACACCAGCATTCTACCACTATTCTGCTTCTTGCCTGATATATTGAATATGTTCTACAAAAATGAAATATTGTCATATCCTTACCTTTTTTATCCTTGTACAATCTATATTGTATAGAGTGCTATAGAAATGAAGGTGGCTTGACTTAGTAGCTGATGGTAACACATGTTTTGCTTTCTCAGCTAATTGTCATGACACATACTGAACCTGTCATTAAAATTGTTTTTTGCAGACCAGTCATCTCAGTCTCCAGTCCAGTCTGAAGAACTGCTGAATGGATGGCCGCTCAGTCCATCGCCGTCTGTGTCTATTCCACAGCCTTCAGCAGACCCTCTCTCCATCTCAGATCAGCACAGACCTCTCTCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32211
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 |
---|---|---|---|---|---|
ENSDART00000089150 | Nonsense | 1114 | 1239 | 13 | 15 |
ENSDART00000140908 | Nonsense | 1078 | 1203 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 30417758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 30495226 |
GRCz11 | 18 | 30473480 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCACCCACACCCTCCCTCATCTCAGCCCAACGGACAGCACTGCCCCCCA[C/T]AGCCCTCTCGTCAAGAGCTTTCTGCAGAGGAATCTGAGGAAGAAGAAGAG
Long Flanking Sequence:
AAATACTGGTTGTAAGAAACTAAACAAAAACATTATTCATATACTGAATAAAAATGCTAATACACAAGATGGCGTCTACAGAACTGCAGGAATAACATTGTTGTCTTTGTTACAGCAGTAAACAAAGCAGTGCGATGTCAAATCTAGCAGGATTTTAATATTCAGATAAAATCAGGCAAACTTTAGCATACTGCTATACATTGTAGAATCAAACATGATACAAAAATGAATATCTTGTAGAAAAGCATTTAAGACTTTTTAATACGTTTCCTAAATCTCTCTAAATTAAATTGTCAACATTTAAAACTTTTTAAGACCCCGTGAACACCCTGTAAATGTCTCCTCTTTTATCAGGTGGTGCATTGGTCGTATTGGAACAAAACCATGCGGTGGACTCATCCGTGCATTATAACATTCCTGAGCTCCAGAGCACACCAGGCCGCTCCAAACCCCACCCACACCCTCCCTCATCTCAGCCCAACGGACAGCACTGCCCCCCA[C/T]AGCCCTCTCGTCAAGAGCTTTCTGCAGAGGAATCTGAGGAAGAAGAAGAGGAAGACGACACTGAGGAGGATGAGCCCTCGACGTCCAGATGGCAGGGCATTGAAGCCATCTTTGAAGCTTATCAAGAGTATGCAGAAGGTACGACGTGTGGTCTATCTGCTTCTGTTGCATTTCATAGTTCTGAAAAACAACATGTATAGTATACAGTAGGAGCTGCTCCACACACACCTAAATTGTGTTGTGCTGGTGTATGTGATGTCAGGAGGCTTCTTGACACAGCTGTTTATCACAAGGAAACTGCATATGGAGGTCCCTGCATTTGGCAATACAGGACACTATCTCAGGCTTACCTCTTTCTCTTTCTGTCTCCAGAGCAAAGCATTGAACGCCAGGTTCTTCACAGTCAGTGCAGACGACTGGAAGCACATCACTATAATCTCAGTCTAACCGCTGAACAGCTCTCACACTCAATGGGGGTAAGGAACACATACACACTCTTA
Associated Phenotype:
Not determined