ZMP
prom1b
Ensembl ID:
ZFIN ID:
Description:
prominin 1 b [Source:RefSeq peptide;Acc:NP_932337]
Human Orthologue:
PROM1
Human Description:
prominin 1 [Source:HGNC Symbol;Acc:9454]
Mouse Orthologue:
Prom1
Mouse Description:
prominin 1 Gene [Source:MGI Symbol;Acc:MGI:1100886]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13905 | Nonsense | Available for shipment | Available now |
| sa32663 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa13905
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045368 | Nonsense | 13 | 853 | 1 | 25 |
| ENSDART00000102768 | Nonsense | 13 | 851 | 1 | 26 |
| ENSDART00000134719 | Nonsense | 15 | 853 | 1 | 26 |
| ENSDART00000134831 | None | None | 182 | None | 7 |
| ENSDART00000140920 | None | None | 124 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 21530954)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22066121 |
| GRCz11 | 1 | 22756860 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACTGATGGACATGWGGTGGAAAGTGGGRCTCGTGCTGGTGATKTTTTG[G/A]GGTCTCACAAGCAGCGAAGACCGCGAGGAGCACCGGGAGTCCCCGCCGCG
Long Flanking Sequence:
TTATTATTATTATTATTATTATTTTATAACTCCTTCTAGGCAACGGTTATATAAAACTATTTTAATTTTGGCTTGACTCAACTAGACGTGAATTCCCTCGAAAAGCCACCTCGAGTGCGCGTGCACAGAGCCTCCGCGTGCCGGCGGACAGAAGAGGAGCGCGCAGCGGGAGGCGCAGGTCACACAAACACTCAGCTCATCCTGAGCGGCGCAGACCGAAGAGAAAGATGTTTACCATGATGCCGTCAGAAGGATACGGGGAATAAACGAATCACTTGGAATACCTTTTTACTTTTGTTTGTTTTCTATCTTTTATTATTATGTGTCCCGGATTAATTTTGTGTCATTTTTAATTTTTCATGTCGAGGACTAGAGAGCGACCCAAACAAATATACTTTTCTCACACCTAATCCGTCCTCCCCTTTTTTCCCTATCAAAATCCTCCGGCAGAGACTGATGGACATGTGGTGGAAAGTGGGACTCGTGCTGGTGATGTTTTG[G/A]GGTCTCACAAGCAGCGAAGACCGCGAGGAGCACCGGGAGTCCCCGCCGCGCACAGCGATGCTCCGAGCGCCCGTGGAAACGCTGGACTTTGGCTTTGTGCCGTCGGTGGTGTACGAGACACACGCGTATTATGAACCAGGTCCCATGGGGATTCTTTTCCACATGGTCCACGCGTTTCTTTACGTGGTTCAGCCAAACCCCTTCCCCAAAGGTGAGATGCACACTGGCTTTGGGAGCGCGCAAAAAGTTTCCCACATGTTTACGGTCTGACAAAAAATCACATATGCTTGCAGAATCATAGACTACAGACATATACATATTTAAGTCAATATCACATGGAAGACTGTTTATCCATCTTTGAGAATAGGTTTGGAGATTTATATTATGGCAAGCCATTTTCACATTCATTTCGTTCAACTAGTATTGTTGGGTACACATTTTTAGTTATTTAGGATATTTAGGATTGTATGAGGAAATCTGAATTAACAACATATCTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32663
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045368 | Essential Splice Site | 451 | 853 | None | 25 |
| ENSDART00000102768 | Essential Splice Site | 449 | 851 | None | 26 |
| ENSDART00000134719 | Essential Splice Site | 451 | 853 | None | 26 |
| ENSDART00000134831 | None | None | 182 | None | 7 |
| ENSDART00000140920 | None | None | 124 | None | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 21504394)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 22039561 |
| GRCz11 | 1 | 22730300 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATATTGAAGCATACTATCCACAGATCGACCAGCTGGACTTCTACAGG[T/C]ACTTCTGCAGAGTTCACCAATATAAAACTAACACCATACACACACTACAA
Long Flanking Sequence:
CGGTGTCCCTTCAGGTTTTAGCTCCAACTTACCTCAACACACCTGCCTGGGTGTTTTAAGTATACCTAGTAAGACCTTGATTAACTTGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAAATCTGCAGGACACCGGCCCTCCAGGAACAAGTTTGGTGACCCCTGGTCTAATCCAATTTAATGATTTATGCTAAGCTAAGCTAAATGAGGGAAATGGATATAAAAATAAAATTCAACTGTTTAAATCTAGAAGAATCATAAAATAAGCATTTTTTTAAATGGTAGTAGTGTTCCTATAATCTCCATAAAATCATATTTCTCTATCTCTGTCTCCTAAAGAAGTGAAAGGGCTGCTGGATAAATCAGGTGCAGAGATTATTGGTTTCACAAAGATGTTCCCGGTTGAGCCAGCACTTCAAAACTTCTCAAAGTTCCTGACAGACAGCCAGAAGAATATTGAAGCATACTATCCACAGATCGACCAGCTGGACTTCTACAGG[T/C]ACTTCTGCAGAGTTCACCAATATAAAACTAACACCATACACACACTACAAATAAATTCTGCTCTCACTATTTAAAAAAAAAATGTAGAAAAAAATTAAGGAGGATGGTGTGGCAAATAAGGACTTTGATGGGGCAAGGGGTCTATACTACTTGCTTCTTATCGAAATGTTGTGATAAATACAACAATATGTATTGGTGAATTATTTACTTAATCATTCATTCAAATGATTAAAAAAAATGCAGATTTATTTACAATAGAAGCAAGTGAATGTTTTAATGACTGGATCTATTAAATCGATTAATTTGATTACTAAACAGGGACTTTTGTGGAAAACCTGTTGTCTTAAGCCACACAGGGTTTTTACACATGGTGAAACAAAATAGCCCTTGTTGAATTAAACGTAAATGGAAGCTTAAGCTATATGTTAATTCAACTAGAGCTGTTTAGTTTCTCCGTTTGCCAAAACTTCAGAGGTTTTAGGATTTCCACACACTTTTCT
Associated Phenotype:
Not determined