Busch Lab

ZMP

ENSDARG00000089205

Ensembl ID:
ENSDARG00000089205
Human Orthologues:
RDH11, RDH12
Human Descriptions:
retinol dehydrogenase 11 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:17964]
retinol dehydrogenase 12 (all-trans/9-cis/11-cis) [Source:HGNC Symbol;Acc:19977]
Mouse Orthologues:
Rdh11, Rdh12
Mouse Descriptions:
retinol dehydrogenase 11 Gene [Source:MGI Symbol;Acc:MGI:102581]
retinol dehydrogenase 12 Gene [Source:MGI Symbol;Acc:MGI:1925224]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa37860 Nonsense Mutation detected in F1 DNA Not yet available
sa25212 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa37860
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126928 Nonsense 53 314 3 8
Genomic Location (Zv9):
Chromosome 24 (position 19025114)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 18331590
GRCz11 24 18476009
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGATGGAAAAACTGCTATAGTGACTGGAGCAAACACTGGGATTGGGAAA[G/T]AAACAGCGAAGGACCTTGCAAATCGGGGTAGGTAACGTAGCCAAACATTA
Long Flanking Sequence:
ATATACTATGGAAAATTTTTGTTTATTCAATTTATTCAATTAAACTGCATGTCTTTAGACTGTGGTGGAAACCGGAGCACCTGGAGGAAACCCACTCAAACACTAGAAGAACATGCAAACTTCACACAGAAATGCCAACTGACTTACCCATGGCTCAAACCAATGACCGTGCTACCCACTGCGCCACCATAATGCCATACCACATATTAATATTCATTAATTATTCTCAGTTATTATTTTAATAAGTTGATTAAAACTATACACATTATATTCAATTTCTATTTTAATATGCATATTGTATATGATTATAAACTGAAGTCTCTCTATTTTAAGCGTTACTTTAGCACTGTTCAACTGCTCTTATCAGCAAAATGCTATTTAAATGTTTAATAAACGAATAAACTCCTTTCAGGGGACTCATTATCAAAAGATGGTCATCTGATGTTCGCCTAGATGGAAAAACTGCTATAGTGACTGGAGCAAACACTGGGATTGGGAAA[G/T]AAACAGCGAAGGACCTTGCAAATCGGGGTAGGTAACGTAGCCAAACATTAACACACACTGGAAATAACGCATCAAGGCTTATTTTCTTTGAGGAACAGATGCGCTATATTATTTTTGACTGCGTGTCACAGTTTGATCTGATATTTAAATTTGTGCTGTACTGTATATGTCTTTACTAGTTTTTTTAACTTATAGAACAAAACTTGTTATTAATCCTAGGTGCTCGAGTGATCCTCGCCTGCAGAGACCTGGTCAAGGCTGAACAGGCGGCCAGTGACATCAGCAGAGACGTAGAGAACGCCAATGTGGTCGTTCGCAAACTAGACCTGGCTGACACGAAATCCATCTGTGAATTTGCTGAACTCATTTATAACAGTGAGTTAGGAATAATTGAAGCAGGTTTACACAGTGGCCTAAAAATAATTAAATAGATGATTAAAAAGTAATTGTACGCTTTAATCTAAATAAAAAAAATTAAATCTTTTCAATTAATTCTGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25212
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
ENSDART00000126928 Nonsense 225 314 7 8
Genomic Location (Zv9):
Chromosome 24 (position 19019993)
Other Location(s):
Assembly Chromosome Position
GRCz10 24 18326469
GRCz11 24 18470888
KASP Assay ID:
554-7881.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCAAGATTATTATAATTTTTTCTGTGGTAGAGCTGGGAGTGAGGGTTTA[T/A]GCTGTGGATCCAGGCCTGGTGAATACAGATATCACCAGACATTTGATGAA
Long Flanking Sequence:
ATTATCTAACAAATAAGCACGAGTATCATTTAATGGGACAGTTCATCCAAAATTGACAATCCTGTCATCATTTACTCATGTTTAAAAGCTATTTGAGGTTCTTTCTTGTTGAAAACAAAAGATGATAGTTTGATAAATGCTGGTTGCCATTGACTTCCATAGTCATTTTACTGGGTGCCAGCAAGCAGCATTCTTTACAAGCAATATCTTCTTTAGTGTTCAGCAGAAGAAAGAACCTCATAAAGGTTTAAAAGCACCCGAGGGAGAGCAAATGATGAGGTGATTTTCATTTTTGGATTAAAACAGCTTGCCATATTAGGAGTGCTCTTTAAACTGGAAAACCTGCTGTGTAATGCATTGCTAATTCATAAGCATGCTGTTCCAGTGTGACTGTCTCATGTTTTACCCACAAATATTCTCTTAATAATGATTGTAACTGCAGTGTAGTTCATCAAGATTATTATAATTTTTTCTGTGGTAGAGCTGGGAGTGAGGGTTTA[T/A]GCTGTGGATCCAGGCCTGGTGAATACAGATATCACCAGACATTTGATGAAGCCTGTGCAGTTCTTCGTGAAGACATTCGGTTTCATGATAAAAACCCCTGCTGAGGGTGCATATACCACGCTTTACTGTGCTCTTACTCCAGATTTACCAACTGGATCCTACTACAGGTTTGTTTGAACTTCATCTGTACACACTGTGAAATATTATGTAAAAGTATGTGCTCACAACATGTATTTTTGTTAATTTCACATATTTTAAAAGCTATACAAACTGTTTTTGTTAAAGTTGAGTGATTCAACCTAAAAATGTAGGGTAACTACAAATAATCTTGATGATCATCTTTTCCATTCACATGCTCTTTCTTTTGCTCTTGTGAGGCTAAAATTGGCTCCAACCTAATGAACTGCTCTAAATTTCCTCATGCTGAGGTTTAATAAAGTAGTTCCTCTCATGATCTCTCACAGTAACTGTGCGGTGGCCTCGTGCTCAAGGGCTGCTAA
Associated Phenotype:
Not determined