ZMP
pom121
Ensembl ID:
ZFIN ID:
Description:
Pom121 protein [Source:UniProtKB/TrEMBL;Acc:A9JR74]
Human Orthologues:
POM121, POM121C, POM121L2
Human Descriptions:
POM121 membrane glycoprotein C [Source:HGNC Symbol;Acc:34005]
POM121 membrane glycoprotein [Source:HGNC Symbol;Acc:19702]
POM121 membrane glycoprotein-like 2 [Source:HGNC Symbol;Acc:13973]
POM121 membrane glycoprotein [Source:HGNC Symbol;Acc:19702]
POM121 membrane glycoprotein-like 2 [Source:HGNC Symbol;Acc:13973]
Mouse Orthologues:
Pom121, Pom121l2
Mouse Descriptions:
POM121 membrane glycoprotein-like 2 (rat) Gene [Source:MGI Symbol;Acc:MGI:2684870]
nuclear pore membrane protein 121 Gene [Source:MGI Symbol;Acc:MGI:2137624]
nuclear pore membrane protein 121 Gene [Source:MGI Symbol;Acc:MGI:2137624]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27646 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16901 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27646
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 |
---|---|---|---|---|---|
ENSDART00000077426 | None | None | 136 | None | 2 |
ENSDART00000127805 | Essential Splice Site | 453 | 1201 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 10 (position 36204569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 35237271 |
GRCz11 | 10 | 35181131 |
KASP Assay ID:
2260-3491.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTAAAACGGATAAGGTGGCAGCTGATCCTGACCCTTCTCCAAATACAA[G/A]TGAGAAAGAAAATTGAACAAGTCTACAAAATAATATAGTAGTATAATTAA
Long Flanking Sequence:
TTACATATTGTGTGCAAAGCCAAAACAACTTGTTGACCTGTGGTTTAAATGGATTGAGTACATTAATCCAATTAAACCTAATGTCTTTTTTCTATAGAATCTAAGATTAATTTTACTGATAATATTGTCCCTTCCCTTTTTTTCTGTATATAGTTTTGATAAGAGTTATGTAAAATAAGGCAAAGGGGTATGTTGTTCTGTCACTGTCATGAAGAGATTCGTGTCTCCTCTTTGATCCCGGAATGGCGAATTTGAACTGGAAAAGCTGTAAAAGTGACATGTCTACTGATGCTGTGAATTGTATCTCTCTGCAATAAAAACTTAAATAAAAAAATGTGTTTTTAAAAATTGGCCTTGATATAAAATGTGAACACACAACTACTCTAATTAATAAACTATTGCTAAACTCTGTAGGGAGGAAGATGCTACCTCACCAAGTTCAACATCCTTCGCTAAAACGGATAAGGTGGCAGCTGATCCTGACCCTTCTCCAAATACAA[G/A]TGAGAAAGAAAATTGAACAAGTCTACAAAATAATATAGTAGTATAATTAAAATGTTGGTTTTCCTCTTTAATACCAAGGCTTAACTTTTGTTTTTGTTTATGCTAGCTAAACTTACCCCAAAATCTGAGGCACCTGTTGCGACATCAACGTCAGACTCTGGAAGCAGCGGTGGCAAACGTAAACGCAAAATTCAGCTGGTCACCACAAACAGAGGAGATCAGATTTCTTTGGTAATGATCAAAGCTGCTTTAGATTAGCATTCATGGCACTTTTGCATTATGGTTATTTATCACTGTAATTGTGTCTGCAGCCACCACCTCCTGAGGTTGGATATACAATCACAGTGAAAGATCTAGATATGGAGAAGAAAGCCGCTCTCAGCAAGATACAGAAAGTCCTGGAGGAGCCTGGTGAGATCTTTTAAATCCAGTTTGAATGGTTAGAGTTGCAACAAAATGAAATGCTTGCAGCTAAATCCATTAATATTTTTTTTTCCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16901
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 |
---|---|---|---|---|---|
ENSDART00000077426 | None | None | 136 | None | 2 |
ENSDART00000127805 | Nonsense | 812 | 1201 | 11 | 13 |
Genomic Location (Zv9):
Chromosome 10 (position 36201549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 35234251 |
GRCz11 | 10 | 35178111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTGCTTCAACACCCGAGGTCAAACCCACCCAGCCCACCTTCAAGCCTT[T/A]ATTTGGCAGCACCACAATTAGTRGCRTTAGTGCATTCGGGCAGACCAYCA
Long Flanking Sequence:
CGTAATATTGATGTTGTTTTTCTGTTTTATACTTGATCATGTTTATGTTCTTCTGTATTCAGCTCCAGCAGTGCCTGTATCCAGTCTTTCTGCTCCTGCTGCATCCATAATCCCAAGCAGTGGAGTTGTCAAGTCTGAATCGGGTCCCACTGCTCTGCAATCCTCATTCTCTGCCCCATCCTCCATATCATCACCTGCTTTCAAACCAGCCACCTCCATGCCCTCCACCTTTGCTCAGATCCTGGCCCAACCTCTTCAGCCCCCATCAACCATTTCATCGCTGGGTGGAGGCAGCAGCCTGTTTAGCTTGATCAAACCTGTGGCCACACCTGCATCTGAGCCTCCCAAGTCTACAGTTGCCGCACCTACAAACACAGCTGCATCAGTCAACAGCATTAGCAATCCTCTCTCATCTGGGTTTAAGCCCATTTTCAGTGCAGCAAGCACCACCCCTGCTTCAACACCCGAGGTCAAACCCACCCAGCCCACCTTCAAGCCTT[T/A]ATTTGGCAGCACCACAATTAGTGGCGTTAGTGCATTCGGGCAGACCATCACACCGACAACATCAACCCCTGCAGCTCCAGCCTCACAGAACAGTGCGATGTTATTTGGTGGATTAACCAGTACCCAGCCAACAACAGTGCCCTCTTCTGCCGCCCCGGCCACACAGACTCCCTCCCAGTCTCTGTTTGGAAAATGGTCCACACCAACCACATCTGCTCCTGCCACAAACCCCACGTTCCAGTTTGGAGCTACATCAACTACTACGGCAACACCTGCGCTGAACACCAACACTGCTAGCGTTGGCAGCGCTAACTCCGCTTTTCAATTTGGTGCAGCAAAACCAGCTGCCGCCCCACAGGCCCAAAACACGTTCACATTTGGCCAGCAGTCCACGAACCAGAACTCCACAACAACTCCATTTGGTGGATTCGGTGTGACCAGCAATGCCACCACGTCCTCAGAAGCGCCCACAACACAAACCACATTTGGAAGCTCGACTT
Associated Phenotype:
Not determined