Busch Lab

ZMP

lama4

Ensembl ID:
ENSDARG00000020785
ZFIN ID:
ZDB-GENE-040724-213
Description:
laminin subunit alpha-4 [Source:RefSeq peptide;Acc:NP_001034154]
Human Orthologue:
LAMA4
Human Description:
laminin, alpha 4 [Source:HGNC Symbol;Acc:6484]
Mouse Orthologue:
Lama4
Mouse Description:
laminin, alpha 4 Gene [Source:MGI Symbol;Acc:MGI:109321]

Alleles

There are 12 alleles of this gene:

Allele Name Consequence Status Availability
sa36927 Nonsense Mutation detected in F1 DNA Not yet available
sa23614 Nonsense Available for shipment Available now
sa43357 Nonsense Mutation detected in F1 DNA Not yet available
sa43358 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa32265 Essential Splice Site Available for shipment Available now
sa15496 Nonsense Available for shipment Available now
sa36928 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa10261 Nonsense Available for shipment Available now
sa15046 Essential Splice Site Available for shipment Available now
sa36929 Nonsense Mutation detected in F1 DNA Not yet available
sa44927 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa36927
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
ENSDART00000002661 Nonsense 323 1871 8 40
ENSDART00000133785 Nonsense 188 374 4 8
ENSDART00000138931 None None 955 None 20
Genomic Location (Zv9):
Chromosome 20 (position 249713)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 240308
GRCz11 20 228943
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAGAGAACTGTGACCTGCACACAGGAGAGTGTCTGCCTGAGCTCTCG[C/T]AAATCAGCGAGTGTAATATCAGTGAGTTCAGTCACAAAAACAAACCAGGT
Long Flanking Sequence:
TACACATGTGTGTCAAATAGGAAATGTGAAAGTAATGAGAGCTATTTTACTTGTGTTACACTATGAGCACATTGAAGAGCACATAGCTTAGCTCGTCTGTCAATAGACAGGATATACAATATTCACAGATACTCACGTCAGCTCCTGCTGTCGATTGCTATTGGCTGTCTTTGTCTTATGACCAATTGCGTCACAAAAATCGAATTAAAATCTCTTAAATGACTCTGTTCTTCATATAACAACATTTAATACGACATTTTTTGTGTGCATTAAATTCATGTGACCACTATTATTTGGCTAACGCTTGTGTTTTTCAGAAGTGAGCAGGTGCTGCAAAATCTTTCTGAAACTCTGCATTTTTAGTAGTGTGTGTATAAATGTGTACACATGTGCTTTTTCATGTAAATGTCCATTAATCTGAATGTTTGTCTTTGTCAGAATGCGACTGTCCAGAAGAGAACTGTGACCTGCACACAGGAGAGTGTCTGCCTGAGCTCTCG[C/T]AAATCAGCGAGTGTAATATCAGTGAGTTCAGTCACAAAAACAAACCAGGTCAATTAATTCAGCGAGACATACAAAGCAGTTCAAATAATTCCAACATTTTAAGGGGATCCAAAGATGTCCACAACCACAAAATCTGGCGGTTTTGTTTAGAAAATATAATAGATTTACACTCTAAGAAAATGCTGGTTGTTGTAACCCAACACTGGCTCGAATAAAACTCAGCCGTTGCATTAAAAAGTGTCATTTAAATTAAATAGAAAATAAAAGAATTACGCCATGCTTGATTTGCCATATTCAACCAAACGTTGGGTCAACACATTTCTGCACATAATAGTGTGAATAACTCATCTCTAATCACTGATTTATTTCCTCTTCTCCATGATGACAGTAAATAATATTAGACTAGATATTCTTCAAGACACTAGTGTTCAGCTTACAGTGACATGTAAAGGCTTCACTAGGGTAAAGTTAGGGTAATTAGGCAAGTCATTGTATAACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa23614
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
ENSDART00000002661 Nonsense 438 1871 11 40
ENSDART00000133785 Nonsense 303 374 7 8
ENSDART00000138931 None None 955 None 20
Genomic Location (Zv9):
Chromosome 20 (position 251716)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 242311
GRCz11 20 230946
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGAATTTGGGAAACCAAGTGGATCAAGAGACACTGAACAGCTCCACA[C/T]GAGCAAAGACCCTCACTGCTAACCTGTCATCGCTCAATGTCCTCATTGAA
Long Flanking Sequence:
TCTGGTGTTTCGTAACATCTAATTTTTTTTGAGGTGGGTCATTAGCCCAACGCTCAACCCCCAACCTGGAGGACCAGGACTAACACAGATACACTGCAGACAATTAGGCCTACCCAATTCCCCTATCGCGCATGTGTTTGGACTGTGGGGGAAACCGGAGCACCCGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGACCCAGCTGAGGGCGACAGCGTGACCCACTGCACCACCGTGCCGCCATTCACAAATGTGTAATGAAAAAAAGAAAGCATAATCATGTCAGTGTGTTCACGTCACGACTCTTCAACTGCACCAGTGCTACAACAGCACGTTCTCATTCTGTGTTCACATGGAGTCTGCATTAACATGAACAGCTTCCCTTGTGTTCATTAGAGATGACACTGAAATGATGGTTATTTTGTTTTGTCAGGAGAATGAAGTGCAGAATTTGGGAAACCAAGTGGATCAAGAGACACTGAACAGCTCCACA[C/T]GAGCAAAGACCCTCACTGCTAACCTGTCATCGCTCAATGTCCTCATTGAAGGTATCGAGACCTTCTGACTCTGTATTTGTGTGTGATGCTGTGCTGGATTAAGTGAAGCATGTCTGTGGTACCTGGAGAAAGGGCTGCCTGGTAACTGATATGTATTTGATGTACCTGCTCAGATTTACCTCAGGATGTTTCTGCCAAACCTTCAACCGTTTGTAAAGCTTTATAGTCTATCTGTAATGCCCTCTTAAACAGAAACCAACGCTTGTGTGTGCATTTCAGATATGATCAGGGACTGGGAATTATACGGTGTCTATCAGGAGTTGGATCCTCAGGTGAAGTTGCAGAAACTGGCTGAAGCTGAACGGATCTTGGGCTGGATGAGAAAACTGAACCTGTCACCCAAAGAACCGCTTGCTACAGATGAGTCCTCCGAGGCGCATGAGTGTACGATTGTTTGATTTCGCTCATGTCTAACTGCATTATCTGTGTGCTTTCCTTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43357
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
ENSDART00000002661 Nonsense 558 1871 13 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 None None 955 None 20
Genomic Location (Zv9):
Chromosome 20 (position 252388)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 242983
GRCz11 20 231618
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTCCTTCAAGCTCAGGATCTCCTTAGCAAAGCTGAAGACGCACTGAAA[C/T]AGGCCATCAACAAATACAAGAGCAACCAGCTCAAACTACAGAGGAGAGAG
Long Flanking Sequence:
AGATTTACCTCAGGATGTTTCTGCCAAACCTTCAACCGTTTGTAAAGCTTTATAGTCTATCTGTAATGCCCTCTTAAACAGAAACCAACGCTTGTGTGTGCATTTCAGATATGATCAGGGACTGGGAATTATACGGTGTCTATCAGGAGTTGGATCCTCAGGTGAAGTTGCAGAAACTGGCTGAAGCTGAACGGATCTTGGGCTGGATGAGAAAACTGAACCTGTCACCCAAAGAACCGCTTGCTACAGATGAGTCCTCCGAGGCGCATGAGTGTACGATTGTTTGATTTCGCTCATGTCTAACTGCATTATCTGTGTGCTTTCCTTCACTTTCTCTCTCTATATGTCTGATTGTAGTGCTCAGACGGGTGCGCAGCTTTGACAGAAATCTGATGACTACACAGGGCCGTCTGCCACCTATGCAGGAAGTTCTGGGTCGGTTTACTTCTAAACTCCTTCAAGCTCAGGATCTCCTTAGCAAAGCTGAAGACGCACTGAAA[C/T]AGGCCATCAACAAATACAAGAGCAACCAGCTCAAACTACAGAGGAGAGAGGTGCCTTTTTATTTATGATGCATTTTCTTTCATGAACTGATGACTAATAAGGTGTTAAAGTGGAACTGTAGACTTTATTTTCACAATCTCTCATCATCAGTTCCAGCCGCAACCCATGTCTGGGAAACACTGAGTTAACTGTTGAAATAGTATTGCTGTATTTTACGTTTAAAATGTGAGTAAATGATAGTACTTCAGATAGTAAATGACGTTAATTTAAGGCTGGCCTTGGGGCAAACATGCTGTCAACATTTTCTCTTAGAATACTGTACTATAGTACTGCAAAATACTACAATAAATACAACCCCAAATCAGCTGGGACAGTATGGAAAACGCAAATAAAAGAAAGAAGTAGTGTTTATTAATTGTCCTTGCATTTGATTGCAGACAATATGACACAGAATATTTCATGCTTTGTCTTGTCAGCTTCATTACATTTGTAAATCTCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa43358
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
ENSDART00000002661 Essential Splice Site 574 1871 13 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 None None 955 None 20
Genomic Location (Zv9):
Chromosome 20 (position 252439)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 243034
GRCz11 20 231669
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCCATCAACAAATACAAGAGCAACCAGCTCAAACTACAGAGGAGAGAG[G/A]TGCCTTTTTATTTATGATGCATTTTCTTTCATGAACTGATGACTAATAAG
Long Flanking Sequence:
ATAGTCTATCTGTAATGCCCTCTTAAACAGAAACCAACGCTTGTGTGTGCATTTCAGATATGATCAGGGACTGGGAATTATACGGTGTCTATCAGGAGTTGGATCCTCAGGTGAAGTTGCAGAAACTGGCTGAAGCTGAACGGATCTTGGGCTGGATGAGAAAACTGAACCTGTCACCCAAAGAACCGCTTGCTACAGATGAGTCCTCCGAGGCGCATGAGTGTACGATTGTTTGATTTCGCTCATGTCTAACTGCATTATCTGTGTGCTTTCCTTCACTTTCTCTCTCTATATGTCTGATTGTAGTGCTCAGACGGGTGCGCAGCTTTGACAGAAATCTGATGACTACACAGGGCCGTCTGCCACCTATGCAGGAAGTTCTGGGTCGGTTTACTTCTAAACTCCTTCAAGCTCAGGATCTCCTTAGCAAAGCTGAAGACGCACTGAAACAGGCCATCAACAAATACAAGAGCAACCAGCTCAAACTACAGAGGAGAGAG[G/A]TGCCTTTTTATTTATGATGCATTTTCTTTCATGAACTGATGACTAATAAGGTGTTAAAGTGGAACTGTAGACTTTATTTTCACAATCTCTCATCATCAGTTCCAGCCGCAACCCATGTCTGGGAAACACTGAGTTAACTGTTGAAATAGTATTGCTGTATTTTACGTTTAAAATGTGAGTAAATGATAGTACTTCAGATAGTAAATGACGTTAATTTAAGGCTGGCCTTGGGGCAAACATGCTGTCAACATTTTCTCTTAGAATACTGTACTATAGTACTGCAAAATACTACAATAAATACAACCCCAAATCAGCTGGGACAGTATGGAAAACGCAAATAAAAGAAAGAAGTAGTGTTTATTAATTGTCCTTGCATTTGATTGCAGACAATATGACACAGAATATTTCATGCTTTGTCTTGTCAGCTTCATTACATTTGTAAATCTCCATCCGACCTGCAGCACACTCCAAAATAAAAGTTGGGACTGGAGCAGTGTAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32265
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002661 Essential Splice Site 741 1871 17 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 None None 955 None 20
Genomic Location (Zv9):
Chromosome 20 (position 255318)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 245913
GRCz11 20 234548
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGCAAAAGTGTTGAATGAAGCATCGTCCCTACACTTTCAGCAGCAAG[G/A]TACAGCAGAGAGAGCTCTTTCCATGCTTTTCTACTGTTTGTTTTTCAGCA
Long Flanking Sequence:
GCCCTATGCACTCTGTCACACTTGCTGTGCCCGTGCCCTAAGATGCTTGAGCTCCTCCACCTTGGGTAAAGACTCTCCTACAACCTGGAGATGGCAAATCACCTTTTCCCACTCAGCAATGTGATCTCAGACATGGAGTTGCTGGATTTCATTCCTGCCACATCATAGACCACCCCAGTCTACATTATACCACAGCGCTAAATGACTAGCAGATTCATTTGAGTGTGGTACTCCAGAGTACTCCCAGAATATAGTGACATTTCACACGTCTGAGGTCACCTCAGTTAAGATAGAAACTGATTACTCTTTTTTTAATGTCCTGACTGCGTGAAATGATTTTTAAGAGTTTTTATAGAGCATTGTACTGTATCTCTGTTAATGTGCTCTCTTCCCATGTTTCTCTCAGGCGGTCGATAAGCTAAGCTCTCAGCTGAACCTCATGCGCTCTCAGAGTGCAAAAGTGTTGAATGAAGCATCGTCCCTACACTTTCAGCAGCAAG[G/A]TACAGCAGAGAGAGCTCTTTCCATGCTTTTCTACTGTTTGTTTTTCAGCATTTCCATATTAAATACATTAACATTACTTTTACTGTAAAAACTGCAACCCAAGCTCATTCTGAAAACGTAGCCCCGCGGACGTTTCTGGAGACCGCGATTTACGTGGCCGGAGGTAGGTATGGCCGCATTTGTTATGGGGCGGTGTGACGCCGCTCCTCTTCTTCGTACTCTCCGGCTGTGTCGGCTCACCTCCGTGTGGAGGGCTTTCCCGCCGCAACCAGTTTGTCCGCTTAGCTCGTAGTGTTATGTCGGCGGAGCGGAGGCCTGGAGGAGGAGGAGCCGGCCGCGGCATCAAACAGGTTCGACTCCGGGAAAGAGCGGTTCCCGAAATCAGGTAAGATGAAAAACAGAATCCAAAAAATAAAAGTGATGGAGTTCATGACGGGGCGAGAATGCGGCAAAATCTGAAAAACGTGGTCAAAATCGGACGAGGGCTTTTGCTTTTCTTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15496
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002661 Nonsense 795 1871 19 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 None None 955 None 20
Genomic Location (Zv9):
Chromosome 20 (position 258076)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 248671
GRCz11 20 237306
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTRAAGATCGTACCCCGAAGCGTCTGCAGTTCACTCAGGAAGTRGCT[G/T]AGGGCACTCTGAACCGCTCCGCTGAGGTGTTGGAGAAAGTGACTCCCATT
Long Flanking Sequence:
TCTTCTGGAGAAAGTCTGATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTTTAAATTTTTTTAAACACCATTTTAGGCTCAATATTATTAGCTTCTTCAAGCTATACTTATATTTGATAGTCTCCAGAACAAACCACTGTTATACAATGACTTGCCTAATTACCCTAACTTTACCCTAATTACCCTAGTGAAGCCTTTACATGTCACTGTAAGCTGAACACTAGTGTCTTGAAGAATATCTAGTCTAATATTATTTACTGGCATCATGACAAAGAGAAAATAAATCAGTTATTAGAGATGAGTTATTAACACTATTATGATTAGAGATGTGTTGGAGAAATCTGCTCTCCGTTAAACAGAAACTGGGGGTAAAATAAACAGGGGGGTGAATAATTCTGACTTGAACTGAATACATGTATATGCACATTTTGTAGTGATTTTGCATGTCTCTGTTGAAGATCGTACCCCGAAGCGTCTGCAGTTCACTCAGGAAGTGGCT[G/T]AGGGCACTCTGAACCGCTCCGCTGAGGTGTTGGAGAAAGTGACTCCCATTCTGAAGAGAGTGGAGCAGTGGGACGGCAACATGAAGAGTGAAGCCTATTCTGCTGCAGCGTTCGACCGCACTGTTCTGTCTGCTGGCGAGGCGGGTACGGCGGATCGTCTAATTCCACACAGCTGAAAATAACACGTGCACTGGCTTCTGCTCATGCTGTTAGCTAGTTTCATAAAATGATTCAGAAACACCCAGCAACTGCTGCCTTCTTGCTTTGACTACAGCAGTTCTAGTTTTTAGACATTTTTAATTGTTGAATATTTATTAGATATTATAACACAAATAAGAAAAAAACAGGTAACACTTTAGTTTAGATCATAATTGAGCATTAACTAACACTGCTAGCTTAATAAACTACTAATTAGCTGCTTATTAATAGCAATACTACTACTAATACTACTATATATTGTTTTTTTAAAGTCGTTTGGCTTCAAAATAGATCATAAATCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36928
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
ENSDART00000002661 Essential Splice Site 944 1871 21 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 Essential Splice Site 55 955 1 20
Genomic Location (Zv9):
Chromosome 20 (position 259478)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 250073
GRCz11 20 238708
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAAGACCCCATAGAGGATCGCTTCTTGCTTTACCTCGGAGACAAACAAG[T/C]GAGCACCGGCGAGGGGGAAGTGGGCCTGAGCATGTGTTATTAACACCATA
Long Flanking Sequence:
TGTCTACCATAACTAATGATGTCTGTCCTTGTGTTTGCTTAGTGAAGGACCTGTCAGCCATTGTGCCAGAGCTGCTCAGCAAGCTGCGTGTGGTTGAGGAGAAAAAACCTGTGAATAACGTCACCACGAACATCATGAAAATCAGAGAGCTCATCGCACAGGCCCGAAGCGTTGCAAAGAAGGTAAATCAGCTTGTAGAGCGCAACACATGCAGAGTCTCCATCGGGACTTTCCATTCCTCTAAAACATACAGACACTGAACATCGATGAGGATCACATTACGTCCAGGATTACTTTGCATCTTAGTAAGTTGACTTTTCGTCTATAATTGCAGGTGCAAGTGTCCATGAAGTTTGATGGCCAGTCTGCTGTAGAAGTTCATCCCCACACCAACCTGGATGAGCTGAAGACGGTGACGTCCATCAGTTTCTACATCCGAGTAGACCCAGATAAAGACCCCATAGAGGATCGCTTCTTGCTTTACCTCGGAGACAAACAAG[T/C]GAGCACCGGCGAGGGGGAAGTGGGCCTGAGCATGTGTTATTAACACCATAGCTGTGTGTTAACGGAGACATGAAATGGTTTAATTAGCACAGCAGAATTGAACAGGAGTTAGTCATTCCTGAGTGTAAGATGTAAGTTACCTAATGTCTTGATTATTGATCTGTTGTATGAGAATGATATGGTTAATGGAGGTGCTCGTGCTTCCACAATCTAGATCTCCTATAATCCTATAACCATCCCTGCCCCCTCAAAACACCTGTACTTCACTTGATGCCTTTAGGTTGGGGCTATCAGGGCATGTCTTGCTTCTGCCCTTAATCAGGTCTTAATTTTGCTTTGTCCAGGTAAAGCTACTCAATTTGGGCTGATTTCCATCCAATGACCAACAATACATCTTAATAAAATCTTATCTTTTATATTTAGGTTTTTAATTAGACACAGTTCACAGTATCTGTTAGACATTTTACAGCAAATTCCCCAAATTATGTTCCCTAATCAGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10261
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002661 Nonsense 1105 1871 25 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 Nonsense 216 955 5 20
Genomic Location (Zv9):
Chromosome 20 (position 264363)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 254958
GRCz11 20 243593
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTGTTTTCMGGCACAAGCTGGCTTTCTCTCAGAGTCGTGTCACCAGTTA[T/A]TTGTTTGACGGCACCGGCTACGCTTTAGTCAACAACATTGAGAGGCGAGG
Long Flanking Sequence:
GGCCCTATCATAAACATATGGGCCCTATCATAAACATATGGGCCATATCAAACCCCCGGCGCAATAAGGGGCAAGACGTGTTTAGTGTGTTTTTGTTTTAGAGCAGCGCAATAGTTATTTTGACATTTCCGGCACGTTGTTTACGTCCTTAACAGCGCTCAAATGTTATTAGGAAATGTACGTTTGTGAAATTTCAGTATTGATTAGTACCAAATTCCAGTGTTGTGACAATCCTACTACTGACTAAAGTGTCCTCAAACTACCAAAATGTGTGTCTAACAACTGTTTCAATGTGATCGTGAAGTGTGAATGCTTGGTTATGATCAACTCTTTTTCATGGTTTGTCTGTGCTTGTAAAGATCTGTATTTATATGATCAGTCCTGCTTTATTATGTGTTGTGTGGCTTTTTATTTCCACATGCTGTGTGTGTTTAAGAATGACAATCTCTCTGTGTTTTCAGGCACAAGCTGGCTTTCTCTCAGAGTCGTGTCACCAGTTA[T/A]TTGTTTGACGGCACCGGCTACGCTTTAGTCAACAACATTGAGAGGCGAGGAAAGATTGGCGTCGTCACTCGATTTGATATTGAAGTTCGAACTGTTGCTAACAACGGCATCCTCTTCCTCATGGTGAATGAGGTAAATGTAGATTCATTCCAAAGGTTTTCCTTTGTTTATATTCTTGCATTCTAGCACAAAACAAACATGTAATTCTGAAGATAATTCTTAAAACATTAGTAAAAAACTTAAAACATCATACATTTGAATCTCAAAGTAAAGTGTGTCAGTGTCTCAGTGGTCAGCATTGTGGCCTCACAGCAGGAAGGTCACTGGTTCATGAAACTGTAAATGAAAGACTGCAACTTAGAACAACACATACACAGAAACCCCTGGATATCATTTAAGATTGCTTAAAAAGGGCTTTATACTTTTGTCATGTGCATACTGTAAATATATGAGCAATATCACATGAGTAGCAGTGCGATATGGCATGTATATTGACACTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15046
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000002661 Essential Splice Site 1193 1871 26 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 Essential Splice Site 304 955 6 20
Genomic Location (Zv9):
Chromosome 20 (position 266259)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 256854
GRCz11 20 245489
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGAGACTAACTTAGCCAAACTGCAGATCAATGACGCTCGCTATCACGAG[G/A]TAATGTTTTCCAGCAGTACATCACGTTATATCTTTAAACACAGCGTGGAC
Long Flanking Sequence:
GCTCAGTTGGGGTTTTTGTGTGGAGTTTGCATGTTCTCCCTGCATTCGCGTGGGTTTCCTCCAGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCAGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTATGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCCTAAAACCTTGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGTGACCCCAGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGAATGAATATATATATATATATATACGCATTTTCCTAAATGAATGTGCAAAATAAATAAATGTATGCATTTGTGTTGGACTTTTGCAGACCAATTTCTTTGTGCTGGAGCTGAAAAATGGCTTTCTCCGTCTGATGTACGACTTTGGTTTCGCTAACGGTCCTGTCATCATAGAGACTAACTTAGCCAAACTGCAGATCAATGACGCTCGCTATCACGAG[G/A]TAATGTTTTCCAGCAGTACATCACGTTATATCTTTAAACACAGCGTGGACACTCTTTGTAACACCCTGTCATTTTCCCCTCAGGTGTCTGTGATCTATCATCATTCAAAGAAGATCATTTTGTTGGTGGACAGAAGCCATGTCAAGTCCTTTGAAAGTGAAAAGAAACCCCTACCCTTTTCTGATATCTATATAGGAGGAGCTCCTTCGAGAATTCTGCAGTCTAGGTAAGATCATATGCTCCAAATAAAGCGCAGAGAAATCAACTACCATTACTGATTTCTTACTTTTAACCAAGATAATTGGATGTCCAACAGGCCAGAGCTGACATCCTTGATTGGATTGAAGGGTTGTGTAAAAGGCTTCCAGTTCCAGAAAAAGGATTTCAACCTCTTGGAGGAGCAAGGAACCATTGGTATCAGCAGCGGCTGTCCTGAGGAATCGTTTGTAAGTTGCACACCTTCATGATGGCAGTGCTGATTATTTGATTACCCAGCAATT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36929
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
ENSDART00000002661 Nonsense 1198 1871 27 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 None None 955 None 20
Genomic Location (Zv9):
Chromosome 20 (position 266357)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 256952
GRCz11 20 245587
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACACTCTTTGTAACACCCTGTCATTTTCCCCTCAGGTGTCTGTGATCTA[T/A]CATCATTCAAAGAAGATCATTTTGTTGGTGGACAGAAGCCATGTCAAGTC
Long Flanking Sequence:
AGTACAGGTGAATTGGGTAGGCTAAATTGTCCGTAGTATGTGTGGATGTTTCCCAGAGATGGGTTGCGGCTGGAAGGGCATCCGCTGCCTAAAACCTTGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGTGACCCCAGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATGAATGAATATATATATATATATATACGCATTTTCCTAAATGAATGTGCAAAATAAATAAATGTATGCATTTGTGTTGGACTTTTGCAGACCAATTTCTTTGTGCTGGAGCTGAAAAATGGCTTTCTCCGTCTGATGTACGACTTTGGTTTCGCTAACGGTCCTGTCATCATAGAGACTAACTTAGCCAAACTGCAGATCAATGACGCTCGCTATCACGAGGTAATGTTTTCCAGCAGTACATCACGTTATATCTTTAAACACAGCGTGGACACTCTTTGTAACACCCTGTCATTTTCCCCTCAGGTGTCTGTGATCTA[T/A]CATCATTCAAAGAAGATCATTTTGTTGGTGGACAGAAGCCATGTCAAGTCCTTTGAAAGTGAAAAGAAACCCCTACCCTTTTCTGATATCTATATAGGAGGAGCTCCTTCGAGAATTCTGCAGTCTAGGTAAGATCATATGCTCCAAATAAAGCGCAGAGAAATCAACTACCATTACTGATTTCTTACTTTTAACCAAGATAATTGGATGTCCAACAGGCCAGAGCTGACATCCTTGATTGGATTGAAGGGTTGTGTAAAAGGCTTCCAGTTCCAGAAAAAGGATTTCAACCTCTTGGAGGAGCAAGGAACCATTGGTATCAGCAGCGGCTGTCCTGAGGAATCGTTTGTAAGTTGCACACCTTCATGATGGCAGTGCTGATTATTTGATTACCCAGCAATTGTATGTAATTCTGTATTTAATTACTCACCTCTAGTTCATTCCAAACCTGTAAGACCATATTCTGATTAGAACATTTTGGATGCAGTTTGAGATATCGG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44927
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
ENSDART00000002661 Essential Splice Site 1708 1871 36 40
ENSDART00000133785 None None 374 None 8
ENSDART00000138931 Essential Splice Site 792 955 16 20
Genomic Location (Zv9):
Chromosome 20 (position 275430)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 266025
GRCz11 20 254660
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCGGAACCGGGGACGTACTTCGCTGAGGAGGGAGGATATGTGCTGCTGG[G/A]TAATGTACTTCATTACTCTTGACTCAGACGTCCTTAAGTAAATGTTTGGG
Long Flanking Sequence:
TCATCAGGCCATGAAAAACATTCAGGTATTGTGCTCTCAGGTTATTCATTCATTCAGCTTTCTTCAGTCCCGTACTTATCAGAGGTTGCCACAGTGGAATGAACCACCAACTATTTTATGTGTTTTACATGGCGGGTGCCCGTCCAGCAGCAACCCAGTACTGGAAACATTAGTATTGTATTCTATGTCTCTCCATTTATGTGTTTGGTAAATATCATTCATAAATCTGCTTGTGTTCTGTTGTGATCAGCCCTCTCAAGTATATTTCGAGATGTTGTTGAGGAGGAAAGGGTGTAATGGAAAGTGTGAGGTTCAACAACTCTTTCTTCTCCTACTTTAGAGGACATCTGTGTCGAGTTTCACTGGCTGTGTGCGGAGTCTCCAGCTGAATGGCCGCTCGCTCACCTCTGCCTCCCACAGTTTTGGGGTCACCCCCTGCTACGAGGGCCCCTCGGAACCGGGGACGTACTTCGCTGAGGAGGGAGGATATGTGCTGCTGG[G/A]TAATGTACTTCATTACTCTTGACTCAGACGTCCTTAAGTAAATGTTTGGGAGAACGAGGAGCACAGTGTATATTTCCACCATGGCTCAGTGATTTGTCTGTCCACAGGAATTTACTTACTTTAATGTTGTTGTATGGACTTCTTTCTCAGATATTCACTGCAAAAAAAAAAAAAAAATGCTGTTTTACTTAATTACTTGGATTTTCTGTCTTGCTTCTAGTCCAAACATCTTAAAGAACACTCCTATAATATCCAGCTGCAGACCCACACACGTTTCAGGACACTCCATCTAGTGTTAGGTTAGGTTTTCCAGTGCTGGGTTGCTGATGGAAGGGCATCCACTGTGTAAAATGCATGGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGACCCAGCCAGGACTCGAACCAGTCACCTCCTTGCTGTGAAGCAATTGTGCTACCCACTGCACCACCCTGACACCCTTTTAATAAATAATGTACACATAAATCATGT
Associated Phenotype:
Not determined