ZMP

rdh10b

Ensembl ID:

ENSDARG00000012369

ZFIN ID:

ZDB-GENE-030909-7

Description:

Retinol dehydrogenase 10-B [Source:UniProtKB/Swiss-Prot;Acc:Q7T2D1]

Human Orthologue:

RDH10

Human Description:

retinol dehydrogenase 10 (all-trans) [Source:HGNC Symbol;Acc:19975]

Mouse Orthologue:

Rdh10

Mouse Description:

retinol dehydrogenase 10 (all-trans) Gene [Source:MGI Symbol;Acc:MGI:1924238]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38337	Nonsense	Mutation detected in F1 DNA	Not yet available
sa25824	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38337

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000004903	Nonsense	108	336	2	6
ENSDART00000129759	Nonsense	113	342	3	7

Genomic Location (Zv9):

Chromosome 2 (position 29898544)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	30200179
GRCz11	2	30183712

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGGTCTTCAGATAGTGTTCAGGAATTGCCTCTTCTCCAGCCGAAGGTTTA[C/A]ACGTATATGTGTGATGTCAGTAAACGTGAGAGTGTGTATTTGACTGCAGA

Long Flanking Sequence:

TTTGTTTTGTGCTACTTTTGTTTTTTCACATATGTCTTATTAAATTGTTTTGAATGTCTTTCAAAATTGTCTTTGTTGTTGTTTATGTAAGTGTGTGTTTTAATCCGTTTGGTCACATTTTAGTCTTTTCAATTGAATATTAGTAAATTAATTACCTGTTTTATTAGTTATTTTAATCTTGTATTTATTGACTTATTTTATATATTTTTGCAGTTACTTTTTATATATAATTAAGGTGATTTGTTAATTGTATGTTACTTTTCGTTTTTAATATCACTGCATTAGGCAATGCAGGTGTATTAGCTAGTTGTTGAAATGTTTCATGAAACCATTAAAATATGACATGACCCTAAATTAAGGTAGGATAAAAACCAGGTATGTGTGCAGTTTTTTTTTTTTTTTTTCCCTCCAAATATTTTTGCCTTATGTCTGTGTTATGTTTGTGTTACAGGGTCTTCAGATAGTGTTCAGGAATTGCCTCTTCTCCAGCCGAAGGTTTA[C/A]ACGTATATGTGTGATGTCAGTAAACGTGAGAGTGTGTATTTGACTGCAGAGAAGGTTCGCAGTGAGGTGGGAGACATTGACCTGCTTATCAACAATGCTGGAGTCGTGTCAGGACGACATCTTCTTGACTGCCCAGATGAGCTTATCGAAAGGACAATGATGGTCAACTGCCATGCTCACTTCTGGGTCAGTAAATCAGCACCGTTCCTGTCCAGTCTTCATGCTTGACATTCATTTTTAGATTCGGAATAAGATTTGAGTCCTAATGTCGGAAGTAGTTCATAAAGTTGATGAACTGGCCACTCCAGGATAACTTTTAATACTAGGTGAAGATTCACCAATGTTCTGTTTATCAAAACTCTTTATCACAGAGACATTACTTTATTAGATTGTACTGGTTTTAACCCAGTAAGAAACCTCCTTTTTTTAACCCTCATATTTGAACTAATCTTTAACAAAAAGTTACACCAAATTTAATTTGAAATATTATATAAATTATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa25824

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
ENSDART00000004903	Nonsense	270	336	5	6
ENSDART00000129759	Nonsense	276	342	6	7

Genomic Location (Zv9):

Chromosome 2 (position 29900098)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	30201733
GRCz11	2	30185266

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAGAAATGGCTCCATTTTTCCCTCCACTGAAGCCAGAGTACTGTGTAAAA[C/T]AGGCTATGAGAGCCATACTAACAGACCAGCCAATGATCTGCACCCCTCGG

Long Flanking Sequence:

ATAATCTAGTTTAATTACAAACACTTAATTCTTGCAATGTGATCACATAATCATCTTCTACCCAGGGGTTCATTTTTTTTTGTACTACTCAAGATATAAAATGATTAAAAAATAATAATAATAATAAATAAATAAATAAACTTTGGTCAACAATTAAATGTAGTTTTTCTCTTTTTTTATTTTTGTTGTAGGACTATTGCGCTAGCAAGTTTGGAGCCATAGGCTTTCATGAGTCTTTGAGCCATGAGCTGAAAGCAGCTGATAAGGATGGGATAAAGATGACTCTCGTCTGTCCTTTTTTAGTTGACACTGGCATGTTTGAAGGCTGCAAAATTAGGTTTGTGCTTTTCACCGCATGCCCAGAATTTACTTCTGTTGACAAAAAACTAATTTGATTATTTATATATATATTTTTTTTATATATACTGTTTTTTTTTTTTTTTAACAGGAAAGAAATGGCTCCATTTTTCCCTCCACTGAAGCCAGAGTACTGTGTAAAA[C/T]AGGCTATGAGAGCCATACTAACAGACCAGCCAATGATCTGCACCCCTCGGGTCATGTACATGGTCACCTTCATGAAAACGTAAGTATAAAGCATTATAAGTGATGATAAAAGGAAATATTAGCCCTTCTGTGAAATTAACCTAAGGTGATGTTTACGGACAAGGAAAATTTCACAGTATTTCCTCAGTTTTTTTTTTTACTTATTTTCCGTCTGGCTGGAATAAAAGCCATTTCTTAATTTAATGTTTTAAATAATAATAACCCATTAATTTTTTAACACTGTCCAATGTCTTTCCTATTTGCCTACTTGACCTATTAAAAATGCTCTAAGCTATATCTTGTAAATATTATGTACTGTCATGGCAAAGACAAAAATGAGCTATTAGAAACTGGTTATTAAACCTATAGTTTGAAATGGTGTTTCTGTTCATTGATTTTTGAAGGTCACAAATTATAGTGTATTCTTGGTTTTGTGTAAAACTTGGTTTGTTCTGTTGTCT

Associated Phenotype:

Not determined