Busch Lab

ZMP

ar

Ensembl ID:
ENSDARG00000067976
ZFIN ID:
ZDB-GENE-060131-1
Description:
androgen receptor [Source:RefSeq peptide;Acc:NP_001076592]
Human Orthologue:
AR
Human Description:
androgen receptor [Source:HGNC Symbol;Acc:644]
Mouse Orthologue:
Ar
Mouse Description:
androgen receptor Gene [Source:MGI Symbol;Acc:MGI:88064]

Alleles

There are 4 alleles of this gene:

Allele Name Consequence Status Availability
sa20471 Essential Splice Site, Missense Available for shipment Available now
sa40491 Nonsense Mutation detected in F1 DNA Not yet available
sa20472 Nonsense Available for shipment Available now
sa44611 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa20471
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:
C > G
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098022 Missense 177 868 1 8
ENSDART00000125329 Essential Splice Site 170 860 None 9
Genomic Location (Zv9):
Chromosome 5 (position 37180130)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 34962079
GRCz11 5 35562232
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGTGCGTGCACCACCGCCACCATCACCTCCAGCAGCAGCAGCAGCAGCA[C/G]CACTACCAGCTGCACCATATCAGAGACAGCGCGAGAGTTGTGCAAAGCCG
Long Flanking Sequence:
CTGCGAGTCCCCAGACGCAGTTTTTCACGGACCTTACCAAAGCGTTTTTCAAAACGTGCGCGTCGCGAGAGCGAGCAACCCCGAGAGTTTGGATATTTCTAGCTCCAAGAAGTGCGGCTGCCTACAGGAGGGCTCGTCGAGGGAAATGCGCTTAAGTGAGCTGTCCTCATTCAGAAGAATAATATGCTGCCCCGAAAAAGAGTACGAGAGTGCGAGTTCGGTGATACAGGCGGCGGCGAGCCGAATTCATTTTCTCAAGAGTTCATCAGGAAGCAAAAGCGACTCGTCTCTGTCATCTAGCGGCTCGGGCCGCACAGACGCCACCGAAAGCAGCGGTAGTCGCGCAGGCTTCCTTCGGGTCGTCGAGAGTGGACAGAAGGGCTGCGGTGCTGTTGAAGTTCACACACGAGAGTTGGGCTCGGGCCGTGACGCAAGTGTGGCGAGTAGTAGTCGTGCGTGCACCACCGCCACCATCACCTCCAGCAGCAGCAGCAGCAGCA[C/G]CACTACCAGCTGCACCATATCAGAGACAGCGCGAGAGTTGTGCAAAGCCGTGTCCGTATCTTTGGGCTTAGCTATGGAGTCCAGCGAACTGGGCGAGGTGGGACAGCACCATGCACCGCCGCCACCGCCCCTGACCACTGAAAGTAGTGAGGAGATCTATTTGTACGGAATGCCTTTGCTCGACTGCTCAGTGAGCGAACGAGAGGCAGGAAGGAAAGACCGAGAGTACGCTCTCGCGGCGGGACGAGACAGAGGCGAAGAGCTCCGAGGCAGGGACAAAGTGCTCGGGATGCTTAAAAGTGGCGACCTGGAACAGCTAGCTGGTGAGGTGACGACCTTGCAGTGCAGCAACGCTTCTCGAGCGAACTTGACCGCGGATGTGCATGAGTTCGGCAGCCTGTCCGGGGACATTGCCAACCTGAGTTCAGAAGGTACAGCAGCGCAGACAGCACCGGATATGGACGGACCGCGAGCGGCTTCGTGCCAGTTTGAACAACTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa40491
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
ENSDART00000098022 Nonsense 230 868 1 8
ENSDART00000125329 Nonsense 222 860 2 9
Genomic Location (Zv9):
Chromosome 5 (position 37180290)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 34962239
GRCz11 5 35562392
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCACCGCCGCCACCGCCCCTGACCACTGAAAGTAGTGAGGAGATCTA[T/A]TTGTACGGAATGCCTTTGCTCGACTGCTCAGTGAGCGAACGAGAGGCAGG
Long Flanking Sequence:
CTGTCCTCATTCAGAAGAATAATATGCTGCCCCGAAAAAGAGTACGAGAGTGCGAGTTCGGTGATACAGGCGGCGGCGAGCCGAATTCATTTTCTCAAGAGTTCATCAGGAAGCAAAAGCGACTCGTCTCTGTCATCTAGCGGCTCGGGCCGCACAGACGCCACCGAAAGCAGCGGTAGTCGCGCAGGCTTCCTTCGGGTCGTCGAGAGTGGACAGAAGGGCTGCGGTGCTGTTGAAGTTCACACACGAGAGTTGGGCTCGGGCCGTGACGCAAGTGTGGCGAGTAGTAGTCGTGCGTGCACCACCGCCACCATCACCTCCAGCAGCAGCAGCAGCAGCACCACTACCAGCTGCACCATATCAGAGACAGCGCGAGAGTTGTGCAAAGCCGTGTCCGTATCTTTGGGCTTAGCTATGGAGTCCAGCGAACTGGGCGAGGTGGGACAGCACCATGCACCGCCGCCACCGCCCCTGACCACTGAAAGTAGTGAGGAGATCTA[T/A]TTGTACGGAATGCCTTTGCTCGACTGCTCAGTGAGCGAACGAGAGGCAGGAAGGAAAGACCGAGAGTACGCTCTCGCGGCGGGACGAGACAGAGGCGAAGAGCTCCGAGGCAGGGACAAAGTGCTCGGGATGCTTAAAAGTGGCGACCTGGAACAGCTAGCTGGTGAGGTGACGACCTTGCAGTGCAGCAACGCTTCTCGAGCGAACTTGACCGCGGATGTGCATGAGTTCGGCAGCCTGTCCGGGGACATTGCCAACCTGAGTTCAGAAGGTACAGCAGCGCAGACAGCACCGGATATGGACGGACCGCGAGCGGCTTCGTGCCAGTTTGAACAACTGTTGCCCGCGAGCATGACCCATTATGCCCACCCGGAGCTCGAAAACGGACCGAGCCATAGCTTCGTAAAATCCACATCAATGTCTGGAGAGTTTGCTGGTCCCATGGAGGATTACACGAATCTCTATAATGTCAGAATCAAGACCGAGATGATGCCCCGTGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa20472
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000098022 Nonsense 509 868 2 8
ENSDART00000125329 Nonsense 501 860 3 9
Genomic Location (Zv9):
Chromosome 5 (position 37225825)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 35007774
GRCz11 5 35607927
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGACGGAGGGAGGAGTGACATTTTCCCAATGGAGTTTTTCCTTCCTCCA[C/T]AAAGGACCTGCCTAATCTGCTCTGATGAAGCATCTGGGTGTCACTACGGA
Long Flanking Sequence:
TGTCACCTCTACTTACCACCGTCATTTGACCACTGACGCACACAAGCTTTCAATTGAGCATTTCCACAGGGAATGTCACCTGTTATCTCTGAGTGCTGAACCCGCAAATGACATTTCCAATTTAGCAGCCACACACCGGACAATTGATGCAAAACTTCTGAGAATTTTAGCTGCCGGCCACACTATTTTTATTCTGTTCAATCGTCTCTACGTACCAGTGTGCACCCATTACTCGTATATTTTCCGTGCTCGAGAGCTGCTATGCGTGTTCCGTTCAAATTACTGCTAATGGACTTCATATTTTTGCTCACAATTGGCATTTCGATGTAAAAAACGAGTTCCACATTTGCAGTATATTTGTTTTCTTCTGCTGATATAACAGAGAACAGAACTTTTATGCCAGTGTTTTGTCATGCCATTAGTTTATGCTGTTGTTTTTATTTTCTAGGTTTGACGGAGGGAGGAGTGACATTTTCCCAATGGAGTTTTTCCTTCCTCCA[C/T]AAAGGACCTGCCTAATCTGCTCTGATGAAGCATCTGGGTGTCACTACGGAGCCCTCACTTGCGGAAGCTGCAAAGTGTTCTTTAAGAGAGCTGCTGAGGGTAATATAAACACACCTATTATAACTGAAGTCGGCCTTTTGGATTGTATTAGTGGCTAAATATATTCACCAAATGTGAGGAGTGTATGTGCTTTAATTAGAATTTTTAATAACAGCTATAAACTGTCATTAAAGCTGCATTAAAAGCTGCCATAGCCTTTTTGTGAATTAATATACGTTTGACCATGTGTCCAGTGCAGCTTTTATTGTTTTTCATGATTTCGATTTAAATGAGAATAGTTGGCACTTCACACACAGGCATTCAGTCAAAGAGAGAAAGAAGGCAACACTTTGCATCTTGTGTTGGTGCTTGAGTTAAAGTGCACATACACTAATAAAATATTACTCCAGTAAAAGTATAAAGTCCTCACTCTGTTTTACTTGATTCAAAGTACAAAAGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44611
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
ENSDART00000098022 Nonsense 589 868 4 8
ENSDART00000125329 Nonsense 581 860 5 9
Genomic Location (Zv9):
Chromosome 5 (position 37289113)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 35071062
GRCz11 5 35671215
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATATTGTTTTTGTTCTGTGCCACAGCCCGCAAGCTGAGGAAGATTGGA[C/T]AGATGAAAGGTCCGGATGAGGTCGGAGCAGTTCAGGGCCCGTCGGAGACT
Long Flanking Sequence:
GAGTGTTTCAGGTGGCAAAATGCACATCCGCTGCAAGTATTAGGCAAATGACGCATGTTTTGCATACTAGAACGACTGTACTTCTGCTCCACGTTACTCAAATACATCAATGCAGATACGCTAATCCTGTCAGGTCCTTTGTTGTAGTGGCAGCCGAGGGAAAAGTACATCGTCTCAGGTGTGTTTTGCGGCCAGTAATCATTCTTTGTGCTGACTGGCAGGAGATAATGTAGAGGACAGACTACCCGTCGCACTGCAGGTTTTATCCTCTGTTGTGTAATAGAGATATTCAAGAGCAGAAATAAGATCATGCCAACCTCATTACTCACAGACCACCCGCTTCATTGGTTTCTAAATAATAAAAAAAAATGAAGATGTGTTCCAGATTAATAATGTGTTTTCGGTGCAGCTTAAATTTACAAAGCAATACTTCCAGCTCTGTTTATTACATTATATTGTTTTTGTTCTGTGCCACAGCCCGCAAGCTGAGGAAGATTGGA[C/T]AGATGAAAGGTCCGGATGAGGTCGGAGCAGTTCAGGGCCCGTCGGAGACTGTCCAGTGCTTGTCGCCCAAGCCCAACCTGACTTTCCACTCGCAGTTGATCTTCCTGAACATTCTGGAGGCCATTGAGCCCGAGGTGGTGAACGCCGGCCATGATCATGGTCAGCCTGACTCAGCGGCTGCTCTTCTCACCAGCCTTAACGAGTTAGGAGAGCGGCAACTTGTCAAAGTAGTGAAATGGGCCAAAGGACTTCCAGGTAATTAAAGCCTGCCAAACTGTCACTCACTTTAGATGAAGGTGTTGACTTTTAAAAGGGGTCATTCATAGTTTTTTATCCATTAATGTACTTCAAAAATACAAGTAATTTGACTTTGCAATACACCTCCTTAGGGATCAAATTTCATCTGTCTGTCGTTTAAAAATATATTTTAATTAACAAAAGCACACTCATTTACACTACAGACAATTTAGCTTATTCAATTCACCTGCAGCATGTCTTTG
Associated Phenotype:
Not determined