Busch Lab

ZMP

prom1a

Ensembl ID:
ENSDARG00000039966
ZFIN ID:
ZDB-GENE-030131-1577
Description:
Prominin-1-A [Source:UniProtKB/Swiss-Prot;Acc:Q9W735]
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 8 alleles of this gene:

Allele Name Consequence Status Availability
sa11176 Essential Splice Site Available for shipment Available now
sa35759 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa11176
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105417 Essential Splice Site 430 856 10 26
ENSDART00000105418 Essential Splice Site 430 832 10 24
ENSDART00000105417 Essential Splice Site 430 856 10 26
ENSDART00000105418 Essential Splice Site 430 832 10 24

The following transcripts of ENSDARG00000039966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 49434044)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 47511282
GRCz11 14 46498363
KASP Assay ID:
554-5191.1 (used for ordering genotyping assays)
KASP Sequence:
CRCAGATYGAGGACATCTACCCGCAGATYGATCAGATGGATTTCTACAGG[T/C]ACTTCTTCCGTTTATAAAAATGTAAYGTTTYTATAGCATATTWACTGCAT
Long Flanking Sequence:
TGGCAATTACATTGTTTTACCAATAGGTGGCGACAACAAATCATCAAAATTGTATGTAACTGAATGATTCTTTTGAAAGTTTTCATTAGTGAGTTATTGAATCATTAATTGAAAATGAACATTTAAAAAATAAATATAATGCTTTTTATTTATCTTATTGTTTTTTGTTTACAAGATTATAACGTTAAATTTGTACATTTGTAGCATTATCAGCAACAGTAATGAGAGCTCAGCACCCGTAGGTGTGGAAACTTACAACTGCTCCTGTTTTGCTTCCTTGATGTTAATTGCATTACTCTGTAAAAGACTGAACTGTTGTATCTGGTGTGTCTCCTGTAGGGGTGAAGGTGTTGCTTGATGACATTGGAAATAACATCACCTCTTTCAGCAAGATGTTGCCAGTTCACAGCTCTCTGGCCAACTTCACCAGAATGATCTCTCACACACACTCGCAGATCGAGGACATCTACCCGCAGATTGATCAGATGGATTTCTACAGG[T/C]ACTTCTTCCGTTTATAAAAATGTAACGTTTTTATAGCATATTAACTGCATTGTTTCTCATACGTTGTTATGGTAAGTTCGTTTTTTGATTCCTTTCACGCTTAATAACTCACTTAATGGTCAATTAAAGGAATAGTTCACCCAAAAATAAACATTTCAAGGTCAATTACTCATCCACACAGGCCCGTGCAGAGACTGTCCAAAGGGCATGTGCAGGATAAATGTGGGGGGGGGGATGCTGCAGATCTGCAGAGTGGATGCGCGCGTACTGAAGAAGAGCGGTGTTATTGCGTGCGTACTGATCAGCTGTGTTGTCGCGCGCCTACTGAAGGGCGGGACCAAAGGTGTGCCGCATCGCGGGGGCCCTTTTGATCTTTTTGGAAGGGCACTTTCTATCCAAGACTAAAAAGGGCATGTGCACTGCACAGGTTGAGCCCTATGTGTGCACGTGCCTGCATTCACATTTAGGGCTGGGTGATATGGCCTTTAAAATAAAATAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35759
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000105417 Essential Splice Site 690 856 18 26
ENSDART00000105418 Essential Splice Site 690 832 18 24

The following transcripts of ENSDARG00000039966 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 14 (position 49413787)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 47491025
GRCz11 14 46478106
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTGATCATTTGATGAGATTCTTGATTTTTTGTGTCTGTTTTTATTAA[A/T]GAGCACACTTAATCAGAGCATCAGACTTCTGGAAAGGACGTCCTCAGATC
Long Flanking Sequence:
TCTGAGGAGTCTCGATTTTTGCTGCGATATTCGGATGGTCGGGTCAGAATTTGGCATCAGCAACATGAAAGCATGGGGTGGAACGGGAGATTCACATCATGGAAGTGGAGCTGACAAATCTGCAGCAACTGCGTGATGCTATCATGTCTATGTGGACCAAAATCTCTGAGGAATATTTCTAGTATCTTGAAGAAGGCAAAAGGGGGTCCAACCCGGTACTAGTAAGGTGTACCTAAAAAAGTGGCCGGTGAGGGTAGTTGTTTTCTGGTTAGATGTGATATTAAGTTCATCAATTTTTGACTTGTTCTCCTAAATAATGAGCATGCGATGCACGCACTTTATGCAACTTCAGTTTGCATGGCCCTTTGTCACCCCGCTGGTTCCCTAACATTTTCATTTTTATGTCTTTTACAGTAAAACAATACTATACCATTTTATAAGCATTTTAGATTATTGATCATTTGATGAGATTCTTGATTTTTTGTGTCTGTTTTTATTAA[A/T]GAGCACACTTAATCAGAGCATCAGACTTCTGGAAAGGACGTCCTCAGATCTGCCTGTAAGCTGCTCATTTTAAAGTCCCCGGTATACTTCAAACGAAAACGAAGAACCAACATTTTCCCTTGTTTTAAAGGCAAAAAGAAATTCTAAAAGGCTGAATAAAGGTATATTGTTTTTGAACATTCAGACACTCCTGTGCTGCAGGAGGCAGAGTTGTACATTGCTATTGTGTACATATAATTGCTATTGCTATTGAGCACATATAATTGTCTCAAACAAACAATTCAGACAGCATACACTAACTAAAATTCATGAAAAACAGCAAAAATGCAAAAAAAATGCATCCACAGCCATATCACCCTGCAGCCCAAGACCGGTTACTCAATGAAGCTAAGCAGGGCTGAGCCTGGTCAGTACCTGGATGGGAGACCACTAGGGAACACTAGGTTGCTGTTGGAAGTGGTGTTAGTGAGGCCAGCAGGGGGCGCTCAACCTGTGGTCTG
Associated Phenotype:
Not determined