ZMP
nr1h5
Ensembl ID:
ZFIN ID:
Description:
nuclear receptor subfamily 1, group H, member 5 [Source:RefSeq peptide;Acc:NP_001116713]
Mouse Orthologue:
Nr1h5
Mouse Description:
nuclear receptor subfamily 1, group H, member 5 Gene [Source:MGI Symbol;Acc:MGI:3026618]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15588 | Nonsense | Available for shipment | Available now |
sa21210 | Essential Splice Site, Missense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15588
Status:
Available for shipment
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:
Mutation:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064040 | Nonsense | 113 | 490 | 2 | 10 |
ENSDART00000124313 | Nonsense | 113 | 486 | 3 | 11 |
The following transcripts of ENSDARG00000031046 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 11790564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 10878560 |
GRCz11 | 8 | 10916265 |
KASP Assay ID:
2260-0212.1 (used for ordering genotyping assays)
KASP Sequence:
AGGTCCAAAGCTCAACAGCCAGAGCCAGCATTGTTGGTCTTCCAGTGCTG[A/T]AAAGACCCAGAATGGGCYATGGAGCTCGAGTGAAGGGCCAGGATGAGCTG
Long Flanking Sequence:
AACATCAGGAAGGCTCCGTTCTGTATGGTTATAAAAACCCCATAAGCTACAAAGCAAATAACAACCATAAACAAAACTGTAACCTCTTCAGCTGCATCCTGTTTCCAGAGACAGAAAAGATTCAAAAGGTCTTGCTCTTGGGCTTTTTTTATTACATCCCAACGGCCTCATAAAGTCATTAGGTAATTCAAGAATCATGTGAACGTGTTGCCTTGTGAAACATTTTCACTGGTTTCATTCATGTTCTTCTATTACCGGCAGATGTTCTTGTGGATCCTCTGAGCTGCTCTTACCAGGAACCGGATCTACAAAGCCCTCTCTATGGCCAACAACCATTTAGTCCTGTCAACGTGCAGTTCTCCATGTATGGGGCGCAGAATGTTCCAGCATGCAACCCGCCGTACCCCTACAGCCATCAGTGCTCTGAATACACCTGTGAGCCTGATATGGAGGTCCAAAGCTCAACAGCCAGAGCCAGCATTGTTGGTCTTCCAGTGCTG[A/T]AAAGACCCAGAATGGGCCATGGAGCTCGAGTGAAGGGCCAGGATGAGCTGTGTGTGGTGTGTGGAGATAAAGCCTCAGGATATCACTACAATGCCCTCACCTGTGAGGGATGCAAAGGTTGGACGCTAACAAAACACTAGTGCTGAGTTTTAGGACAACATGAATGCATGATGCACTTCTTGAGAAGAAGTAAAACATAGTATTTAGGAAGACCAGCATGGATTTCCCTTTTACATAAGCAGGAGGTTGGATAGATTCATTCATTCATTGTCCTTCAGCTTAGTCCCTTTATTCATCAGGTGTCGCTACAACGGAATAAATCGATAACTTATCCAGCATATGTTTATGCAGCGGATGCCCTTCCAGCTGCAACCTAGTACTGGGAAAAACCCATACAAACTCATTCACACACACACACACACACACACACACTGTGGCCAATTTATTCAATTCACCTATAGCGCATGTCTTTGGACTGTGGCGGAAACCGACCTTGCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21210
Status:
Available for shipment
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:
Mutation:
G > A
Consequence:
Essential Splice Site, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064040 | Missense | 386 | 490 | 9 | 10 |
ENSDART00000124313 | Essential Splice Site | 378 | 486 | 10 | 11 |
The following transcripts of ENSDARG00000031046 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 11800703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 10868421 |
GRCz11 | 8 | 10906126 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACTGACTTAATGTTTTGTTGTCTTTGCTTGTGCTTTATATCTTTGTTCA[G/A]GGTTGAATGATGAGCTCTTGAGATCTGTGGTAAATTTCCTTCATAGCATG
Long Flanking Sequence:
TGGAAGTGAATGAGACCGGAAGTCTCGTGCCAAAAAAGGTTTAAATGGCAGCGCCCGCTCGTCCGCGGAGAATAAGGTCAATAGAGTATGGAAAATGTGCTGGTATTTTATAGCTAAACAAAAAGTGTCTGACTTAAAAGTGACGGCAAACTAAGCAAAACTTCACTTCATTTTTTTCGTTGTGTTGTACCCATGTAAATGTTTTTACGTTTTTGTTTTATGTTAACTTTAGAAGCAGACGTTTTCTTTTAGCCGCATAATTTGATGTCGCGGTTATATTGCCATCTATTACAATTTTGTTTAAAGGCAGCACTGTCCTGATTGGGCCAGTAATGATTCTGTCCACTGTCCCGAGCATCTCTCACCCTGGCCTAGGGCCATCAGGCATTCCTTATTGTTGAGCCCTGCATAGCGAGTGAAAATTCAGTTGTATGCAAAAGTGAACTGATACACTGACTTAATGTTTTGTTGTCTTTGCTTGTGCTTTATATCTTTGTTCA[G/A]GGTTGAATGATGAGCTCTTGAGATCTGTGGTAAATTTCCTTCATAGCATGGTGACGATTGCAGTGACCGAGGCTGAGTATGCACTTCTAACAGCGACTGCAGTTTTGTGTTCAGGTTTGTAGATTATGATTAACACATCTGTGACTCATTTCCATGTCAATCTTCACGACAACACTTTTTCAGACTATTTGTTTGAAGGTTGAACAGTAAATTACATCATAAAAATTTTGATTACACACCTTATATTTGACCTGTTTCCTGAATTGCAAGGCTTCTGGTGTCATTACGTTTATGCTGTTGTCATGCTACTTTGTATTAAAAACTAACATTTGTTTTCTTGATGTTCTAATTAAATTTAGCACATTTTATTGCAACGTGTAAACAACTTGTGATAAAACCTCCTGGGTTCTCTAAGAAAGCATATACAGTAGACAAGGGCTGCGCAATATATCGTTTCAGCATCGATGTTGAACAACTAAATAAATACTTAGCTCTGTTTA
Associated Phenotype:
Not determined