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
sa24967 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa6357 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa11176 Essential Splice Site Available for shipment Available now
sa2762 Essential Splice Site F2 line generated Not yet available
sa5611 Essential Splice Site F2 line generated Not yet available
sa35759 Essential Splice Site Available for shipment Available now
sa42449 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35758 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24967
Status:
Mutation detected in F1 DNA
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
ENSDART00000105417 Essential Splice Site 377 856 9 26
ENSDART00000105418 Essential Splice Site 377 832 9 24

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

Genomic Location (Zv9):
Chromosome 14 (position 49434849)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 47512087
GRCz11 14 46499168
KASP Assay ID:
554-7745.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGACACTCCTGCTATGGTAACCGCTCAAACTCGAAATATTGTTGAAGG[T/C]AAGCTCACAGATTTAATTCTTTAAGCATATTTTGCTTCAGGGGCAGTTCT
Long Flanking Sequence:
GTCAGAAGTTTGGAGGCTGTAATTTATTTTTAGAAATGAATACGTTTATTCAGCAAAACTAGAGCAAATTGATAAAACAACAATAAAGACATGTGGCAAAACATTACCTAAATAATACAGTTTTTACAAAAAAAAAACTGTTTTTAACATTAATGATTGATTAATAATTCAGCTTTATGACATAAATAAATATCATTTTAATATTAAACAAACTGTTTTAAATTGTAAAATATTTGTTTCATTTTATTAGTTATTTTTTACAATTCTTTAAATCGGTTAAATGCTGTTCAATACTTTCTTAAAAAGCATAAAAATGTACTAAACCCTAGACTTATAAACAGTAGTCAATATTTCTAAAAAATAATTCATTCAGTTTTGTCTTTTAATGTGCATACCTGCGTTGTATATGCTTACGATTTTTCATCTGTCACACAGGGGATTGCATCTTTTAATGACACTCCTGCTATGGTAACCGCTCAAACTCGAAATATTGTTGAAGG[T/C]AAGCTCACAGATTTAATTCTTTAAGCATATTTTGCTTCAGGGGCAGTTCTAGATGCTTTTGGTGAGCTAAAGCCTGTCATTTCAGCCACAGTAAAACTTAACTGTTTAATAATCCTTTGATAATCTCAACAGTGCATTCAAATCTGTGTTCAGTATTTAGTCTTTTCAACCTGTATTATAATTTCTACCAGTATTAAAATCACATAATCACAGACCTACTGAAATAACAGGTTATAGTTCAGAGAAAAACACTGATCTTTATGGTAAAGATTAAAATTTCGGTTCAAAAGCAACTTTAAGCATGTGGCAATTACATTGTTTTACCAATAGGTGGCGACAACAAATCATCAAAATTGTATGTAACTGAATGATTCTTTTGAAAGTTTTCATTAGTGAGTTATTGAATCATTAATTGAAAATGAACATTTAAAAAATAAATATAATGCTTTTTATTTATCTTATTGTTTTTTGTTTACAAGATTATAACGTTAAATTTGTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6357
Status:
Mutation detected in F1 DNA
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
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:
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:
sa2762
Status:
F2 line generated
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
ENSDART00000105417 Essential Splice Site 634 856 15 26
ENSDART00000105418 Essential Splice Site 634 832 15 24
ENSDART00000105417 Essential Splice Site 634 856 15 26
ENSDART00000105418 Essential Splice Site 634 832 15 24

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

Genomic Location (Zv9):
Chromosome 14 (position 49419722)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 47496960
GRCz11 14 46484041
KASP Assay ID:
554-3100.1 (used for ordering genotyping assays)
KASP Sequence:
CWCTGAAACTGGCATTAATGAGATCGACTTTGCTGCCTATTTAGAGGAGG[T/C]ACAGTACATAACCTGCATAAACACACGCTCAGATTAAAACCTGGCACYAT
Long Flanking Sequence:
ATCCGTTATTAGAGAGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAATCTTCTCTCCATTAAACAGAAATTAGGGAAAAAATAAACAAGCGGTCTAATAATTCAGGGGAGCTATTAATTCTGACTTCAACAGTATATATATGTATGTATGTATTTACATTTACATTTAGTAATTTAGCAGACGCTTTTATCCAAAGTATGTACATACATTGTACATATATACATATATGTATGTATGTATGTATGTATGTATGGATGTATGTATGTATGTATTGTATGACAGTCCATAATAATTTCCCAGACTAATATCAGAAGCACATCCTCATCATCATGTCTTCCCGCAGTACTCCAAGGATGTGTCCAGGAAGTTTGAAGGACTGAAGGTGGATTTACGGGGCATCATTCTTCTTGAGTCTGAAGGCAAAGTCAACCTCAACAACTTCTCTGAAACTGGCATTAATGAGATCGACTTTGCTGCCTATTTAGAGGAGG[T/C]ACAGTACATAACCTGCATAAACACACGCTCAGATTAAAACCTGGCACTATGGGCATTAAATCATTAACAGTCTGGTGTGAAACTGCACATTGTTGTTTTTCATGTTTCTGTTCATCCTTCAGGTTAATAAAGGAGTGACTCGAATAGATCTCATTGATTTCGCCAATCAACTCGATGCTCAAGCTGATCAGTTGGTAAGGTTTATTTTTGGTTCAGTTCAAAAAGTAAAACGAGTCTAAAAATTTAGGAGCAAAAAAAAAAGGCTAGATCGAGTCCCGGCTCGGCCAGTTGGCATCTCTTTGTGGAGTTTGCATGCTCTCCCTGTGTTGGTGTAGGTTTCCTCTAGGTGCTCCGGTTTCCCCTACAGTCCAAAGACATGCACTATAGATGAATTGAATAAACTAATTTGGCCATAGTGAATGAGTGTGTGTGGATGTTTCCCAGTACTGGGTTGCAGCCAGAAGGGCATCCACTGCATAAAACATTTGCTGGAATACATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5611
Status:
F2 line generated
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
ENSDART00000105417 Essential Splice Site 634 856 15 26
ENSDART00000105418 Essential Splice Site 634 832 15 24
ENSDART00000105417 Essential Splice Site 634 856 15 26
ENSDART00000105418 Essential Splice Site 634 832 15 24

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

Genomic Location (Zv9):
Chromosome 14 (position 49419722)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 47496960
GRCz11 14 46484041
KASP Assay ID:
554-3100.1 (used for ordering genotyping assays)
KASP Sequence:
CWCTGAAACTGGCATTAATGAGATCGACTTTGCTGCCTATTTAGAGGAGG[T/C]ACAGTACATAACCTGCATAAACACACGCTCAGATTAAAACCTGGCACYAT
Long Flanking Sequence:
ATCCGTTATTAGAGAGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAATCTTCTCTCCATTAAACAGAAATTAGGGAAAAAATAAACAAGCGGTCTAATAATTCAGGGGAGCTATTAATTCTGACTTCAACAGTATATATATGTATGTATGTATTTACATTTACATTTAGTAATTTAGCAGACGCTTTTATCCAAAGTATGTACATACATTGTACATATATACATATATGTATGTATGTATGTATGTATGTATGGATGTATGTATGTATGTATTGTATGACAGTCCATAATAATTTCCCAGACTAATATCAGAAGCACATCCTCATCATCATGTCTTCCCGCAGTACTCCAAGGATGTGTCCAGGAAGTTTGAAGGACTGAAGGTGGATTTACGGGGCATCATTCTTCTTGAGTCTGAAGGCAAAGTCAACCTCAACAACTTCTCTGAAACTGGCATTAATGAGATCGACTTTGCTGCCTATTTAGAGGAGG[T/C]ACAGTACATAACCTGCATAAACACACGCTCAGATTAAAACCTGGCACTATGGGCATTAAATCATTAACAGTCTGGTGTGAAACTGCACATTGTTGTTTTTCATGTTTCTGTTCATCCTTCAGGTTAATAAAGGAGTGACTCGAATAGATCTCATTGATTTCGCCAATCAACTCGATGCTCAAGCTGATCAGTTGGTAAGGTTTATTTTTGGTTCAGTTCAAAAAGTAAAACGAGTCTAAAAATTTAGGAGCAAAAAAAAAAGGCTAGATCGAGTCCCGGCTCGGCCAGTTGGCATCTCTTTGTGGAGTTTGCATGCTCTCCCTGTGTTGGTGTAGGTTTCCTCTAGGTGCTCCGGTTTCCCCTACAGTCCAAAGACATGCACTATAGATGAATTGAATAAACTAATTTGGCCATAGTGAATGAGTGTGTGTGGATGTTTCCCAGTACTGGGTTGCAGCCAGAAGGGCATCCACTGCATAAAACATTTGCTGGAATACATG
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

Mutation Details

Allele Name:
sa42449
Status:
Mutation detected in F1 DNA
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
ENSDART00000105417 Essential Splice Site None 856 24 26
ENSDART00000105418 None None 832 None 24

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

Genomic Location (Zv9):
Chromosome 14 (position 49397718)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 47474956
GRCz11 14 46462037
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGCCGACTGGTGACTCTCAGGACCACCATCTGCTTTTAACTACTGAAAG[G/A]TACCAAGAGCTGAAGATGAGCGCAAGCGGGTTTGATTCTCTCTAACCAGC
Long Flanking Sequence:
GTAATTTGTGTGTAACTTATGGGTAAAACAAACACCTTGCAGGTCAGGTAGTTGAAACGGTAGGCCACAGATAATGAATTCGTTATGAACTTATTAATTATTCATAAATAATTAATTCACTACTCCCTACGACAACGATGCCATCGTCCATCGTATGTTTCACATTAGACATTGTACGATGCCAAATTGGTCATTTTGAGCTAAATTCACTTACAGCACCTTTATTGTGTAATAATGCTACATGTGTCATTCTCAAAGCCCCGTCCTGCTCCTCTGTAGGAATGATGTGCTATAGATGATGGAGAGATGACAGAGGTCAACCTACTGTAAGAATGTGTGTGTGCGTTTGCATTTGTACACTGTTGGTCTGACAGTTTTCCCTTTGTGCCTCAAGCATCCCTACCTATGACACTATGACCCGCTTCCCACGGGCCTCTGCGCCCCCGCGCCACGCCGACTGGTGACTCTCAGGACCACCATCTGCTTTTAACTACTGAAAG[G/A]TACCAAGAGCTGAAGATGAGCGCAAGCGGGTTTGATTCTCTCTAACCAGCATCCTCCCATTCAACTGAACACATCTGTGTGTGTTTTAACATTCCCCATCCTCCATATTAACACAAACCTCATTTTGATTGAGCTTTTCTGTCACTGCACCAACAGCATGCTTGGTTTTTGCATCTTCCACTTGGATAACAGCTGACGATTCTGCAAAGCTTTGTGTGAATTTATTTGTTTTTTAGGGTCCATTACTAACCACTGGCCCATATCCTTCCAATGTTTGACTTCAAACATTCCTGACAGCTCTGCAAACAGATAGATGCCAGCGCTCGCTGTGTGTTTTGTTTCTTTACCTTGGTCTAAAACTCTCATCTCCCATCTCACATCTCCTCATCCGAGTCTCTCTTTGCCGTTTATTGTGCATTTTGAAGCAGCGCAGCAGGTTTAATTCTGCAATGTTTGTTTCTTTACTCACGCAGCGATATTGGACACTGGAATTGAATCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35758
Status:
Mutation detected in F1 DNA
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
ENSDART00000105417 Essential Splice Site None 856 25 26
ENSDART00000105418 Essential Splice Site 826 832 23 24

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

Genomic Location (Zv9):
Chromosome 14 (position 49397245)
Other Location(s):
Assembly Chromosome Position
GRCz10 14 47474483
GRCz11 14 46461564
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAGCGCAGCAGGTTTAATTCTGCAATGTTTGTTTCTTTACTCACGCA[G/A]CGATATTGGACACTGGAATTGAATCTTTGTGGAATGTAAGTTGCTTCAAT
Long Flanking Sequence:
CCACCATCTGCTTTTAACTACTGAAAGGTACCAAGAGCTGAAGATGAGCGCAAGCGGGTTTGATTCTCTCTAACCAGCATCCTCCCATTCAACTGAACACATCTGTGTGTGTTTTAACATTCCCCATCCTCCATATTAACACAAACCTCATTTTGATTGAGCTTTTCTGTCACTGCACCAACAGCATGCTTGGTTTTTGCATCTTCCACTTGGATAACAGCTGACGATTCTGCAAAGCTTTGTGTGAATTTATTTGTTTTTTAGGGTCCATTACTAACCACTGGCCCATATCCTTCCAATGTTTGACTTCAAACATTCCTGACAGCTCTGCAAACAGATAGATGCCAGCGCTCGCTGTGTGTTTTGTTTCTTTACCTTGGTCTAAAACTCTCATCTCCCATCTCACATCTCCTCATCCGAGTCTCTCTTTGCCGTTTATTGTGCATTTTGAAGCAGCGCAGCAGGTTTAATTCTGCAATGTTTGTTTCTTTACTCACGCA[G/A]CGATATTGGACACTGGAATTGAATCTTTGTGGAATGTAAGTTGCTTCAATTGGCCTTGTTTTACTTTAAAGTAGTGCTTCTCAAACCTGTGTACTCCACAAACCCTGTGATTTGATATATTATTGATTTGCAAAAATACATATAAAATGCATAACCATGATCTTTATAACAGGAAAATATAATTGTTGTTTTAATTAGGGCTGTATATGTTTTGATATTGGCAATAACCATCATATTTGAAACAGTTCAAGTTCACTTCAAGCCTCCTTTGATCATTCATTTATTTTCCTTTCGACTTAGCACTTTTATTAATTTGGGGTTGCCACAGCGGAATGAACCGCCAACTTATCCAGCACATGTTTTATGCAGTGGATGGCCTTCTAGCTGCAACCCATCACTGGGAAACACCCATACACACTCATTCACACACATACACTACGCCCAATTTAGCCTATCAATTCACCTATACCACATGTCTTTGGACATGTGGGGGAAACCGG
Associated Phenotype:
Not determined