ZMP
prlra
Ensembl ID:
ZFIN ID:
Description:
prolactin receptor a [Source:RefSeq peptide;Acc:NP_001122149]
Human Orthologue:
PRLR
Human Description:
prolactin receptor [Source:HGNC Symbol;Acc:9446]
Mouse Orthologue:
Prlr
Mouse Description:
prolactin receptor Gene [Source:MGI Symbol;Acc:MGI:97763]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa44958 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa43590 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44958
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039549 | Nonsense | 369 | 605 | 8 | 8 |
| ENSDART00000127866 | Nonsense | 369 | 605 | 9 | 9 |
| ENSDART00000128859 | Nonsense | 370 | 606 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 9666274)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 11038325 |
| GRCz11 | 21 | 11130953 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTTTTAGACAAGTGCATGGAAGGAAGTGGAAATGACCAACACAACTA[C/A]AGCCAGCACGGAGAAACAAGCTGGGCTTCTTCCAGCGAATGTAGCGAAAG
Long Flanking Sequence:
TTGCAAAATGACTAGTGCAATATTATGTACTGTCATCGTGCCACAGACGAAAAAAAGGGTTATCAACACCATCATGTATAAAAGTGTTTGATGAAAAGCCTGCGTTTAAAATAACTTTGGAAATAATGTCACGGTTATTTTTGCCTTCAACTGTACATTATATATTCATGTATGGCTATATATCAGATTTTCGAAAGTTTTACACATTCATCTCACTTGTTTGTCTTTGTTTTACAGAGCGGGAAATCAGAGGAAGTTTTCAATTCTCTGGTAATCCCAGGTTTCCCTCCAACCACTGATTACGACGATCTACTAGTGGAGTACCTCGAGGTGTACGACAACGAGGAGCAAGAGCTGGTCCTGGATGGTAAAGATCTATCAGAGGACAGCATGAAATCCAAAAGCCCATCTGACAGCGACTCGGGCAGGGGCAGCTGCGACAGTCGTACCCTGCTTTTAGACAAGTGCATGGAAGGAAGTGGAAATGACCAACACAACTA[C/A]AGCCAGCACGGAGAAACAAGCTGGGCTTCTTCCAGCGAATGTAGCGAAAGCCAAGGTTCACCTGGTTCTCCAGAGTCCACCGATGGACGCATGAAAACCTGGCCTGTTGTGTTTTCCTCACCCCAACCGCATCACCACTACCAAGTCGGAGCGACAAAACCGGCCTACCACAGCGTCCCGGAGATCCTAAAACATTCACCATCACACGCAATCCCAAGCAACTACCACCAGCTTTACCTTCAGGACATCCCGCCGCAGGAAGGGCGCTTTACTAAACCTCCCTGCCGGCATTCCCAAAGCTACAACCAGTTCAACATGGACAACGTTGACATTTCCGAAGCCGGTGTTCCTCCATCTCGCTCCTTGGAGTATGTAGAGGTGCAGAGGGTCAACCCGGAAAACATACTACTGCTTAGGCCACTTTCAGACCCAAACCGTGAACCTGAAGGGTCAGATCGCATCGATGAGGACTACAGCAAGGTCAAAGAAGTGACGTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43590
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000039549 | Nonsense | 437 | 605 | 8 | 8 |
| ENSDART00000127866 | Nonsense | 437 | 605 | 9 | 9 |
| ENSDART00000128859 | Nonsense | 438 | 606 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 21 (position 9666477)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 11038528 |
| GRCz11 | 21 | 11131156 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACAAAACCGGCCTACCACAGCGTCCCGGAGATCCTAAAACATTCACCAT[C/A]ACACGCAATCCCAAGCAACTACCACCAGCTTTACCTTCAGGACATCCCGC
Long Flanking Sequence:
ACATTCATCTCACTTGTTTGTCTTTGTTTTACAGAGCGGGAAATCAGAGGAAGTTTTCAATTCTCTGGTAATCCCAGGTTTCCCTCCAACCACTGATTACGACGATCTACTAGTGGAGTACCTCGAGGTGTACGACAACGAGGAGCAAGAGCTGGTCCTGGATGGTAAAGATCTATCAGAGGACAGCATGAAATCCAAAAGCCCATCTGACAGCGACTCGGGCAGGGGCAGCTGCGACAGTCGTACCCTGCTTTTAGACAAGTGCATGGAAGGAAGTGGAAATGACCAACACAACTACAGCCAGCACGGAGAAACAAGCTGGGCTTCTTCCAGCGAATGTAGCGAAAGCCAAGGTTCACCTGGTTCTCCAGAGTCCACCGATGGACGCATGAAAACCTGGCCTGTTGTGTTTTCCTCACCCCAACCGCATCACCACTACCAAGTCGGAGCGACAAAACCGGCCTACCACAGCGTCCCGGAGATCCTAAAACATTCACCAT[C/A]ACACGCAATCCCAAGCAACTACCACCAGCTTTACCTTCAGGACATCCCGCCGCAGGAAGGGCGCTTTACTAAACCTCCCTGCCGGCATTCCCAAAGCTACAACCAGTTCAACATGGACAACGTTGACATTTCCGAAGCCGGTGTTCCTCCATCTCGCTCCTTGGAGTATGTAGAGGTGCAGAGGGTCAACCCGGAAAACATACTACTGCTTAGGCCACTTTCAGACCCAAACCGTGAACCTGAAGGGTCAGATCGCATCGATGAGGACTACAGCAAGGTCAAAGAAGTGACGTCAAACAATACTCTCCTTCTCCAAAGAGAAACGTCTCATCAGGTTGTCAATGATTACAGCCAGGACTTTGAAAGCTATGCTGATCAATGCACAGCCCAGCAAACTCCTCACCCATGCAAACCTGTCATGACACAGTTGCACAGTCAAGACATGAGGGTGATGGGAAACGGTTACGTGGACACAACAGTCCTGATGCCATTATACAAGC
Associated Phenotype:
Not determined