Busch Lab

ZMP

kri1l

Ensembl ID:
ENSDARG00000075380
ZFIN ID:
ZDB-GENE-040915-3
Description:
Protein KRI1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6DRJ4]
Human Orthologue:
KRI1
Human Description:
KRI1 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:25769]
Mouse Orthologue:
Kri1
Mouse Description:
KRI1 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:2384899]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa30604 Nonsense Mutation detected in F1 DNA Not yet available
sa10565 Nonsense Available for shipment Available now
sa33139 Nonsense Mutation detected in F1 DNA Not yet available
sa6032 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa40037 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30604
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000043883 Nonsense 14 765 1 24
ENSDART00000111528 Nonsense 14 765 1 19

The following transcripts of ENSDARG00000075380 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 19158538)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 19186900
GRCz11 3 19336640
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACGACAACATGTCGGATCTCAAGATTAACAAGAAGTTTGCAGAGAAGTA[T/A]GAGAAATATCGCCAGAAAGAGGAACTGCAGAGACGTAAGTTGTACTAGCA
Long Flanking Sequence:
GGTGCTTCGGCCCACTAGCCTCGATCAAGTTTGCCTTTTAGCTTTTTATAGGAAAAAGTTTGGGCACCCCTGATTAGGTGGAGACTGCGTGGCTTATGAGTTATACAACATCCCGCCACTAGGGAGCGATGAAATGTTTTGGCTTCACTTTTCAGGACATGTGTTACTCACTCGCGGCAACAAAAGCTGCTTGTTTTTATCACAGACTCCAAAAAAAAAATCGTTCTAAATATATGACAGAAAGGACCGGTTTAATTTCTAACAAGGAGTAAAATGTTAGTAGAAAAACAATCGACGAAAGGAGGCGATAGTTGAACCCTGAACTATATGACGTAGGAGAGGGTCGTAGGTCACGTGCCCATGCCGTACAGCAGAGCAACATGTCCAACGTGAGAGTTTGAATTATCGAGATATTAATCTGATCTCAAATCAGAAGATACCGCACAGTTATACGACAACATGTCGGATCTCAAGATTAACAAGAAGTTTGCAGAGAAGTA[T/A]GAGAAATATCGCCAGAAAGAGGAACTGCAGAGACGTAAGTTGTACTAGCATGCGTTATTTACTACATGTTGAATACGAAAGTGTATATTTATATCAACAATAAGTGTGGTTTTCTTGAGTTTTGTTGTAGAAATGCTTTAGTTACATTTATAAACATCAATAATCTTTTATCTACGTTTATGTCCAAGTGAAGTGAAGTGAAGTGATGTGAAAATAAATACAAATACCATAGTAACTATAACAGTTTAAACAATATGGTTACTGCAGTAAAATTGTGGTATTATTTGCCTCTTCCTTAAAAATATGACTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTATATATATATATATATATATATATATATATGAGGTTAAAAACTCACCCCAAACAAAACAACTGGTACTATAAATCTCTTCCAAAGCACTGTGGTATTAATATCAAAGCTATTGAGAAATTCTATCTATCTATC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10565
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000043883 Nonsense 95 765 4 24
ENSDART00000111528 Nonsense 95 765 4 19

The following transcripts of ENSDARG00000075380 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 19160432)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 19188794
GRCz11 3 19338534
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTACTGTACTTTTTGTTTTAATCAGCRTCTGGGTCAGGCAGCGATGAG[C/T]AACCGTCCACTTCGAAACAGTCAGAGAAACCCATGTTCCTTAAGGACTAT
Long Flanking Sequence:
TCATTAATAATATAATTTCAGAAAAGTATTTTTTTTTTTTGCAAATTCTAACTAAGGAAATCATATTAGCAGCCAATGACTATCAAAGTGCAGCACTGTCCACAGTCAATTAAACAGTGCTAGTGTTGTTTTGAAGTCTAACTTACATGTGATTTCAGACCGATTATTCAAAATAATGTGGTAAAGCATATAAGGATTGTTAAAATGAATGAATGTGTGAATATAAACTTAACTCTACCTCAGTCTATGTTTCCATGTCTAATACTCTTATATACTGTACATACAGGAGCTGGATCCAAAGCTAGACAGAGATTTTTACAGAACTCTCTCGCTTCTGAAGAAAAAGGATCCAAAGATCTATCAGAAAGATGCCAAATTCTACACAGAAGAAAGTATGTAAAGATCTTTATAGTACAATGTCTGCTCCAATTTATGATTTGTATTAAGATGCTGTACTGTACTTTTTGTTTTAATCAGCATCTGGGTCAGGCAGCGATGAG[C/T]AACCGTCCACTTCGAAACAGTCAGAGAAACCCATGTTCCTTAAGGACTATGAGAGGAAAGTCATCCTGGAGAGAGGAGGGTAAGAAATCATCGGTTTAGAAATGATGGACTTGGCTGAAACTTTTCACTGTAATATATCTACTTTTGTATTAATCAGACAGTAAATTGTCATTGTTACTTCGCTTGCATGGTTGGGAGGTTAATGAAAATAATTGGCAGATTAATTTATTTATTCACATTTCTAATGGTTCTCATTCACTCAAAGTGTTTGTATAATGTAACCGAGTGTGCTTCATTGCAGAAAATATGAAGACGATGACAGTGCTGATGAAGAAATCTCCGCAAAGATGCAGGAGGTAAACATACTTAAGATATTAGAAATCAGCGTAGAACAAAAATGATCATTTATTTTATGCCACATTTTTGCTCTGTCTTGCAGTTTATATAAATAAAAAAACTTGGAATATTATTAAAATGATAATCATAATTTTAAAGGGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33139
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000043883 Nonsense 274 765 10 24
ENSDART00000111528 Nonsense 274 765 10 19

The following transcripts of ENSDARG00000075380 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 19162678)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 19191040
GRCz11 3 19340780
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGATGATGTGGATGATTCTGAGGATGAAGGAGAATCATTTCTGCATAAA[C/T]AGGAAGACTTTGAGAGGCATTACAACTTCCGCTTTGAGGAGCCTGATGCT
Long Flanking Sequence:
GACTACTGGAACAATCCTCAGTTAGATGAGAAAGAGTCTTTCCTGCGGGACTTCATGCTCAACAAGGGCTACATGGAGGAGGAGGATGAAGAGAGGTAGGTTCTGACTCAAGTATTGCACTCATACAACAAAACCAGTAAAAAAGATGTTTTGGATCCGTTTGTTTGTCCCAGCATGGCTGCATTGTTTTATATGCAATATTTTGTAAAAACAGTAAAAATGTAATTTATTTCTTTAAATCAAAGCTGATTTTTCAGAATCACAATATACTATAATCTCTACAGTGTCAACTAGCTATAGATAAAAATCTCTCCTTTTGAACAATTAATTAATTCCTTGTCTGGTAAACATTTTAATTTCTTAAAAAATATCCTTAGCCCTTGAATGATTTTATAAGTTTCTCTGAATCTGTGAATGGTTTTAGGATCCCCACATATAATGAGCTCATGCAGGATGATGTGGATGATTCTGAGGATGAAGGAGAATCATTTCTGCATAAA[C/T]AGGAAGACTTTGAGAGGCATTACAACTTCCGCTTTGAGGAGCCTGATGCTGGAAAAGTAGGAAGAGTTCATGATCAGACTGATTTGTATTTGTGTTCTGTTCATTTCCTCAAATGAGCTCTTTTTTTTTCAAGCATTACCCATCAACCCACTGTTTCTCCACAGGTCAAAACATATCCCCGCAACATTGCAACTTCTGTCCGCAGCAAAGACGACAGGAGAAAGAGGAAGAGAGAAGAGGTTAAAGAAAGGAAGAAGAAGGTAAACATGATTTTTAATCATTTCTTTAAAGGGCCATGAAACCCCCTCGTTTCAGCAGGGTGTTTTCACACCTCTACTTTGAAAAAAGTCAGAAAAGTGGGCGTGTCCAGCTCTGTTTAGGGGGGAGTGTCGGAGGAAGAAAAGTGGGATGGTGTGGGAGTGTCTATTTGGGCACGCGGGAGTTTCAGAGTCAAAATACACACACTCACACACACACACACACACATGAGAAAGTGATGC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6032
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
ENSDART00000043883 Essential Splice Site 446 765 14 24
ENSDART00000111528 Essential Splice Site 446 765 14 19

The following transcripts of ENSDARG00000075380 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 19168145)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 19196507
GRCz11 3 19346247
KASP Assay ID:
554-3794.1 (used for ordering genotyping assays)
KASP Sequence:
TACTGCGGAGGAACACTACCAGCCCAACTGTGATGATCCTGACTTTATCG[T/C]AAGAGTAGACTTTTTAGCATGCTTTCTTATTCTTAACACGCAATATAAAT
Long Flanking Sequence:
TAGACAAAAAAGATTGATTATATTATTACAGTTTTAGGTTTTTTAAATGAATGATGTTTTATTGAATCTATTATAGTCTCATTTTATTTAGAAAAATATTTGCCAAACAACTATGTTTTACTGTTTTTGATATTAATAAGGAACATTTGATACATCTCCATATATATATATATATATATATATATATATATATATATATATATATATATATATACTTATATACTGTATATATATATATATATATATATATATATATATCAAAGCAGAAAACATTTTTAAAGAATGTTTTATCAAATATATGCAAATATATGGCTTAAATTATTGTTACTTTTTAATAAATGTATAAATAATGAATTTTTTTTCTTTTTTTTTTTTTAAAGAAAATTGGAACTGGGATACATGGGTGGGAAAACAGCAGAATGAGGAAGAGTATGACCACAAGGAAGACTATACTGCGGAGGAACACTACCAGCCCAACTGTGATGATCCTGACTTTATCG[T/C]AAGAGTAGACTTTTTAGCATGCTTTCTTATTCTTAACACGCAATATAAATGCTGCACCGAACTGATTTGTTCATTGTGTATGGCTATTAATCATACCTTAAATCTCTTGAATAGATGGATGCTGATTACGACCCAAGCCAACAGGCCGTTTCTAAAAAGAAAAGAAAAAAAGAGAGAGAGGAGAAGAAAAAGAAGAGCAAAGAGGACGTCCCACTCATGGGAAAGAAGAGGAAAAAGTCCCACTTTGCAGAGATCATCAGCAAAAGCAAGCCTGTCTTTGATCCAAGTGAGTGATAGCTGTTAACACAGATTGTTCAGACAAAATGAATATTGTAATCATTTACTCATCCTCCAGTTGTTCCAAACCAGGTTGAGTGTCTTTAGTTTGTTGAAAACAAAACAAGATACACTGAAGAATGTTGTTTACTATAGTGAGTTTTGTTCTTAACAAAGATGGCATTAGCTTCTATTTTCCAACATTTTTCAGTAGATCCTGTTTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40037
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000043883 Nonsense 529 765 16 24
ENSDART00000111528 Nonsense 529 765 16 19

The following transcripts of ENSDARG00000075380 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 3 (position 19171507)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 19199869
GRCz11 3 19349609
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACGAGTACTATAAACTGGACTTTGAGGACATCATTGATGACCTGCCGTG[C/A]AGATTTCGCTACCGAGAAGTGGTAGCCAATGACTTTGGGCTGAGCACTGA
Long Flanking Sequence:
GTCCCGGAACGACTTAAGTTTCTGCAGATTTTGTGTGATTCGAACATTTAGAAATTAAACTAAAGAGACAGTTATTGTTTAATTTTATTGGTGATTCCTAATATGAAATGTAATCATAAGCTTGGCAAGCAATTTTGGAGAATTTGTTTCCCATTTGAACAGAATGCCTGCGCATACTGGCCGAGTAACGTGTGCGCTAAAATTGTGTATTGCACATGTGGTTCCAGTCAGTTTTGATCACAGTTAGAAATAAATGCGCTGCCCTCAAGCATTCGCATCAGTAATCCCTTGATTATCCCTTACATATCTGCTTATCGGATATCAGCAAAGGCCAGTATCATGCGTCTCTACACTGTCTGTCATCGGTCGAACATACAGAAAATGTTTCAGCCTACACAAACCCCATTTGTTCCCCTGTTTCCAGACGAGAAGAGCTTCGAGCAGTACTTGGACGAGTACTATAAACTGGACTTTGAGGACATCATTGATGACCTGCCGTG[C/A]AGATTTCGCTACCGAGAAGTGGTAGCCAATGACTTTGGGCTGAGCACTGATGAGGTGAGGAGCTTCAGGCATATCCACACGAATTTAATGTGTTTAATGAAAATAAGTTCTGTGCTGATGAGCTGTGATTGTGTCTGACCTGGTATTGCTGTTCCTCCGGGAGTAACTCTGACCAGGGTCTGAAGACTGTAATCTTCTCTCTGAGCAGAGCTGCGTTGATAACCACCAGTGCAGATTAGCTTTAGGCTCACATTTTAGAGGATTTGATTTAAGAAGATTTTACATGCACTGCCATTTCAGGTAAATCTTTTATTGGAGATGCTGGAAGTTAATATAGATTTATAAATGATGTACAGTAAATCCTGTTAGATTTTTTTTGTTATTGCTTTTAGTGTTTTATTACTGTCAATTGTTTTATGTTAATTACTATCTTATTATATTTTCACTCGTACTTCTTTTTAGCATGGGCACAATACATTGATCATAAATTACAGTGAACC
Associated Phenotype:
Not determined