ZMP
ENSDARG00000089205
Ensembl ID:
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]
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]
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.
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.
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