Busch Lab

ZMP

recql

Ensembl ID:
ENSDARG00000007175
ZFIN ID:
ZDB-GENE-050809-134
Description:
ATP-dependent DNA helicase Q1 [Source:RefSeq peptide;Acc:NP_001038561]
Human Orthologue:
RECQL
Human Description:
RecQ protein-like (DNA helicase Q1-like) [Source:HGNC Symbol;Acc:9948]
Mouse Orthologue:
Recql
Mouse Description:
RecQ protein-like Gene [Source:MGI Symbol;Acc:MGI:103021]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa40266 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa33444 Nonsense Mutation detected in F1 DNA Not yet available
sa33445 Nonsense Mutation detected in F1 DNA Not yet available
sa33446 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40266
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
ENSDART00000021610 Essential Splice Site None 639 1 16
ENSDART00000101198 Essential Splice Site None 640 1 16
Genomic Location (Zv9):
Chromosome 4 (position 16592794)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 17535634
GRCz11 4 17524610
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGGCAAACAAGAGAAAGTGGAAGGAAGCTGGTTTAGGATCATTCAGCG[G/A]TGAGTTTGCTGAATTGCGTTTTCATACAATTCATTCGATATTCATAAATG
Long Flanking Sequence:
AACCAAAAATATAATAATTATAAAATTAATAAACTTAAAAAATAGGTCTTTAAACAAGAACAAATGCCATTACATTTTAAGCTAGTTTTTGATATTTAAATATGGCAGCCAAATGCGTGTTTGAATGTTTAGTGTTTTAGGTGTTTTCCCAAATTTATAGTTATAGTGACTTTTATTTTGGAAAAAGAATCAACACTTCCTGGTCGCCCGCACTTTTAGCACTAGGAAGGTGTGTGGAGTTATATTACATTTTTCTTTACTTCTCATCACGACTACAGGTCAATCACGATTAAATGTAGTCAATAATGCATTTCTAGGACGATGCAATGTGAGTAGTACAGTTATTTTTCTTTATTTTCCCATTGAACAAGACTCTTGTCTAGTCTGGACTCCATGCAGTGATTGGTCAACTTCTCGTTAATGGTCGCGTGGGGCAACGAGGACTTCATCTGGGGCAAACAAGAGAAAGTGGAAGGAAGCTGGTTTAGGATCATTCAGCG[G/A]TGAGTTTGCTGAATTGCGTTTTCATACAATTCATTCGATATTCATAAATGTTGAACATGACTTATAAACACTTTAGACGATGCTTGAGTCGTCCAGAAATATGTCATCTGTGTTTCATTGTTTACATGTATTATTATTAACCTCAGTATCACCAAGCAAAACACAATAAAGACGGGCTGTGTATGCAATAAAGTCTAGTATCTTGTTAAAATACACTTTAATGTAAGGATAAGTGTCTTTGAGTTAAAAAACATTAAAATAATCTATAGTAATAGTTTGTTTCTTTAAGTAATAATGTTACTAATTAACTCTCTCTTACAGTCCTCCTTATCTGTAACCTTCAAGAAGAGCTGCATAAAATGGCTAATGTTGGTGAGTATATTTCCTTGAGCACCCATTATGTGCACTGGTATACATGGTAAATGTAAAATCTGTATGTATTAAAAATGAAAAAAGAAAAGTATTCATATGAGAGTATGCATACGACTGTCAGGATATTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33444
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
ENSDART00000021610 Nonsense 46 639 3 16
ENSDART00000101198 Nonsense 46 640 3 16
Genomic Location (Zv9):
Chromosome 4 (position 16594027)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 17536867
GRCz11 4 17525843
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAGAAACAGACGAGGCTAAACTCCAGGAAGAACAAACTACTGAAGGTCT[T/A]GGAGGGAGCATGCAGCTCAGCCCAGCCTTCCGGATCCGGCAAAACTCCCA
Long Flanking Sequence:
CATCCTTTCTTCAACAATGAACTTCATATAGACTTGAACAGAATCATCATTGAACTAACAAAAACAAAACTAGCTTTCCTTGGACCTAATGAGCTGAACTTGTTTCACACTTCATACCTGATTTTTGATTATTTCTTTGTAATGCTGCTTTGACAAAGTTTGCATTGTATAAAGCGCTATTGATATAAATGTGACTTGATTTGACAATATAAAGTCTATCCAGGATTTTCTTGTGAATTTTTTATGTATTTGCAGCTTAAAATCACTGATTTTGTGATGACTTTTATCAAAGCTTATGATGTGATTTGTTAAATTGTTTATTTTTGGTGCGAAAATACAAACGGATCTTCTACATTTTTCTTCTGTCTTTTTTGCAGATGATGCTCGGGAAGAGTTGGACTCGGTGGAGGCAGAGCTGGAGATGGTGGAATTGCAGATCTCTGAGTTACTGGAGAAACAGACGAGGCTAAACTCCAGGAAGAACAAACTACTGAAGGTCT[T/A]GGAGGGAGCATGCAGCTCAGCCCAGCCTTCCGGATCCGGCAAAACTCCCAAATCTTCATTCAGCAAACAGGACCTTCAACACTATGAAGACTCTGGTATTACTCATTTTCCAGAAGTTAGTTATTAAGTGTATAGTGCTCCAAAATAGCTTAAACCCAAAGGTGACTAGCAAAGATAAAGGTATTTGAGGTTTTGTAGAATAATCTGAGCTGAACCATTTTAAAGTAATGGATGCAGTATCTTTTAAATACCAGGAGTCAGTAAGTCTTTCTTATTGTTGTTGTTATTATTATTTTTATTCTTTTTTTGTTTATGAAGGTAATAATGTTGAGCAAATGTCAGTTTATATAGCTCTCTTAAAAATTCTTTTCAGAAGGATCATGTTACATTGATGCCTAAAAATAAATTATAAATAGGTACTGTATATCTGAATAACTGTTTAAAAGGTGTAATAATGTTTCAAAATATTGCTACTTTACTGTAATTTTTATGTAAACAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33445
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
ENSDART00000021610 Nonsense 103 639 4 16
ENSDART00000101198 Nonsense 103 640 4 16
Genomic Location (Zv9):
Chromosome 4 (position 16594977)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 17537817
GRCz11 4 17526793
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGAATCTATGTAACATATTCCAGCTTTCCAAATTTCGCCCTCTGCAA[C/T]GAGCGGCCATCAATCTGAGCATGTCAGGGAAAGATCTTTTCCTGGTAATG
Long Flanking Sequence:
TAATAATGTTTCAAAATATTGCTACTTTACTGTAATTTTTATGTAAACAGACCTTAAAACAGACTTTATAAATAAATATCGTCACCTTAGAATCATAAGGTTCTATCTGACATTTTTGTCAAAATTGAGTTATAACATATTCTTATTAAATGACAACTTTTTTACATTATTGGATTTTTTTTTATACGTTGTTTACATTTTTAGGCTTTTTATTTAAAAAACAAATGTTGCACACATACTGTTTGCTATAGAATGCAAAAACTTTGAAGCTCAATATCTCAAAATCATTCAGAACGCAGATAGAACCTTATAATTCCTAGGTGACGATATTTTTATTTATTTATTTATTTATTATTATTATTTTTTTTAAATCTAGCCACATAATAAAGGTTTTCAATATGATTATGTCTGTTTCTCTATCATCAGATTTCTCTTGGTCTAAAGAAGTTCAGGTGAATCTATGTAACATATTCCAGCTTTCCAAATTTCGCCCTCTGCAA[C/T]GAGCGGCCATCAATCTGAGCATGTCAGGGAAAGATCTTTTCCTGGTAATGCCCACCGGTCGAGGAAAAAGCTTATGTTACCAGCTGCCAGCCCTCTGCTCTAAAGGTATGGGCTTGAATACTTCTATGTTGTTAAATTAGACATACTTTGAATGCTCTTGCACTTGTGTTAATTCCTGTTTTAATCAGGTTTCACATTAGTTATCGCCCCACTGGTGTCTCTGATGGAGGATCAGCTGATGTATCTGCAGTCCGTTAATGTACCAGCAGTGACTCTCAATGCCTCCAGTTCAAAGGTACAGTATAACAGATGAGGTGGACAGTGTACACTCCACATTTTTTGGAAATAGTCTAATTTTACAAGTCCTCTTTTACAAGTTTTACAATTTTATAATGCATTCAGCTGGGCTCCAGGTCTGGTAAAAGCACATTTATCTTAGCTTAGCATAAATCATTGAATTTATTAGACCATTAGCATCTTACTCAAAATGCTTAACTCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa33446
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000021610 Essential Splice Site 137 639 4 16
ENSDART00000101198 Essential Splice Site 137 640 4 16
Genomic Location (Zv9):
Chromosome 4 (position 16595083)
Other Location(s):
Assembly Chromosome Position
GRCz10 4 17537923
GRCz11 4 17526899
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTCGAGGAAAAAGCTTATGTTACCAGCTGCCAGCCCTCTGCTCTAAAG[G/T]TATGGGCTTGAATACTTCTATGTTGTTAAATTAGACATACTTTGAATGCT
Long Flanking Sequence:
CTGACATTTTTGTCAAAATTGAGTTATAACATATTCTTATTAAATGACAACTTTTTTACATTATTGGATTTTTTTTTATACGTTGTTTACATTTTTAGGCTTTTTATTTAAAAAACAAATGTTGCACACATACTGTTTGCTATAGAATGCAAAAACTTTGAAGCTCAATATCTCAAAATCATTCAGAACGCAGATAGAACCTTATAATTCCTAGGTGACGATATTTTTATTTATTTATTTATTTATTATTATTATTTTTTTTAAATCTAGCCACATAATAAAGGTTTTCAATATGATTATGTCTGTTTCTCTATCATCAGATTTCTCTTGGTCTAAAGAAGTTCAGGTGAATCTATGTAACATATTCCAGCTTTCCAAATTTCGCCCTCTGCAACGAGCGGCCATCAATCTGAGCATGTCAGGGAAAGATCTTTTCCTGGTAATGCCCACCGGTCGAGGAAAAAGCTTATGTTACCAGCTGCCAGCCCTCTGCTCTAAAG[G/T]TATGGGCTTGAATACTTCTATGTTGTTAAATTAGACATACTTTGAATGCTCTTGCACTTGTGTTAATTCCTGTTTTAATCAGGTTTCACATTAGTTATCGCCCCACTGGTGTCTCTGATGGAGGATCAGCTGATGTATCTGCAGTCCGTTAATGTACCAGCAGTGACTCTCAATGCCTCCAGTTCAAAGGTACAGTATAACAGATGAGGTGGACAGTGTACACTCCACATTTTTTGGAAATAGTCTAATTTTACAAGTCCTCTTTTACAAGTTTTACAATTTTATAATGCATTCAGCTGGGCTCCAGGTCTGGTAAAAGCACATTTATCTTAGCTTAGCATAAATCATTGAATTTATTAGACCATTAGCATCTTACTCAAAATGCTTAACTCTCGTCTCTATTTAGATTGTGTACTTGGACTCTGTGAAAATGTTTGAAGTTGTTACTTTAAATGGTAAAATATGCATTTCAAGTGAGATGCTAATGGACTAATATGGTT
Associated Phenotype:
Not determined