ZMP
nrip1a
Ensembl ID:
ZFIN ID:
Description:
RIP140-A [Source:UniProtKB/TrEMBL;Acc:Q1L666]
Human Orthologue:
NRIP1
Human Description:
nuclear receptor interacting protein 1 [Source:HGNC Symbol;Acc:8001]
Mouse Orthologue:
Nrip1
Mouse Description:
nuclear receptor interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1315213]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22669 | Nonsense | Available for shipment | Available now |
sa22670 | Nonsense | Available for shipment | Available now |
sa6382 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32041 | Nonsense | Available for shipment | Available now |
sa5882 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6383 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa22669
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099956 | Nonsense | 286 | 1044 | 1 | 1 |
ENSDART00000135540 | Nonsense | 286 | 1080 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 29059331)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29777361 |
GRCz11 | 15 | 29710237 |
KASP Assay ID:
2260-8650.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCAACAGTATTCTCGAGAGCATGCCCTGAAAGCCAAACTTTCTGGA[C/T]GATCAGCCAGTGAAAGACTATCTGCCATGGCCACACAACAGACACCAGAT
Long Flanking Sequence:
AGGATAAAGGAGAGAGCACACTTCTAGCCAGTTTGCTACAGTCTTTTAGTTCTCGACTTCAAAATGTGAGCCTGCCACAGCAGATTATTCAAGGCTTGAGGCCACCAGACACCTCCTGCCAGATAAGCAAACCTGCACAAGAGGAAAAGGCAGATGTGCCTTGCCACAGACCTGCCTCGAGTCACCTCCAAGAGTTAGTGAGCAAGAGCAAACTTCAGAATCACAGCAACAGTGTGCCTTATCAACAGAGACGGTCTAGCCATGAAAGTTTTTCACAATCTCCTAAGGCACTGCAAAGTAGCACTCCTTCCCCATCTCCTGAGTCTCTATCTTGTACTGAGCGCCTAAAAGCAGTGGCAAGCTTGGTAAACATCAGATCAAGCCCTGCTCCATCTCCCAAACCAAGTGTTGCCTGCAGTCAACTGGCCCTTCTGCTTTCCAGTGAGGCCCACCTGCAACAGTATTCTCGAGAGCATGCCCTGAAAGCCAAACTTTCTGGA[C/T]GATCAGCCAGTGAAAGACTATCTGCCATGGCCACACAACAGACACCAGATAAACAACCTACAACTTCTAGCCAAACTCATGGACTAAGCCTCTTACAAACCAAGAATGGAATATCTTCACAAATGTCAACAAGCTCCAGTAGAAAGAGTCCCAGCCAAATTTCAGGGCAAAGAAGGACAGAAAGTTCAATGAGGACAGGACATCGCTTCAGAGAGCGTCGACCTTTCGAAAAACAAGGCAGACCATCACAGAATTGTAGCAGTCTTCTTCTTCAGCTTCTTAACAGTCACAACACCTCACAGCGAATTAATGGACAGGGTCACTTGAAAGATGACTTCATTACCTTTGGCCCTCTGGCCTCTCCACTTTTTTCAGACAGTGAACACTCAAACCCTGACAGCAGTCTCACAAAAGACAGCAGTGATGCTGAGAGCAGTTACTCTAGTTGCTCTCCTATTGACCTTTCTCTGAAGGGCAGAACAAATGTACAAACACCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22670
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099956 | Nonsense | 371 | 1044 | 1 | 1 |
ENSDART00000135540 | Nonsense | 371 | 1080 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 29059588)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29777618 |
GRCz11 | 15 | 29710494 |
KASP Assay ID:
2260-8651.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGAGAGCGTCGACCTTTCGAAAAACAAGGCAGACCATCACAGAATTG[T/A]AGCAGTCTTCTTCTTCAGCTTCTTAACAGTCACAACACCTCACAGCGAAT
Long Flanking Sequence:
AGCCATGAAAGTTTTTCACAATCTCCTAAGGCACTGCAAAGTAGCACTCCTTCCCCATCTCCTGAGTCTCTATCTTGTACTGAGCGCCTAAAAGCAGTGGCAAGCTTGGTAAACATCAGATCAAGCCCTGCTCCATCTCCCAAACCAAGTGTTGCCTGCAGTCAACTGGCCCTTCTGCTTTCCAGTGAGGCCCACCTGCAACAGTATTCTCGAGAGCATGCCCTGAAAGCCAAACTTTCTGGACGATCAGCCAGTGAAAGACTATCTGCCATGGCCACACAACAGACACCAGATAAACAACCTACAACTTCTAGCCAAACTCATGGACTAAGCCTCTTACAAACCAAGAATGGAATATCTTCACAAATGTCAACAAGCTCCAGTAGAAAGAGTCCCAGCCAAATTTCAGGGCAAAGAAGGACAGAAAGTTCAATGAGGACAGGACATCGCTTCAGAGAGCGTCGACCTTTCGAAAAACAAGGCAGACCATCACAGAATTG[T/A]AGCAGTCTTCTTCTTCAGCTTCTTAACAGTCACAACACCTCACAGCGAATTAATGGACAGGGTCACTTGAAAGATGACTTCATTACCTTTGGCCCTCTGGCCTCTCCACTTTTTTCAGACAGTGAACACTCAAACCCTGACAGCAGTCTCACAAAAGACAGCAGTGATGCTGAGAGCAGTTACTCTAGTTGCTCTCCTATTGACCTTTCTCTGAAGGGCAGAACAAATGTACAAACACCAGTGTCTACTTCATCCTCACCTGTACTAGACAGACTCCCAGAGTCCTCATTTAACATGTGGAAGCCTGAGAGTTCCCCTCTCAAAGTATCAGCAGATCACAGAGAGATGGACTCCTGTTCAGAGATGAAGCCTCATCACAAGGTCACACTATTACAGTTGCTCTTGGATCACAAAAATAACGAGAGAGTAAACAAAAGTCTGGATAATCCAGATTTGCTGCGAGCTGTAATCCCTAAGGTCACTAGTGCATCTACAAGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6382
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099956 | Nonsense | 889 | 1044 | 1 | 1 |
ENSDART00000135540 | Nonsense | 889 | 1080 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 29061140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29779170 |
GRCz11 | 15 | 29712046 |
KASP Assay ID:
554-5282.1 (used for ordering genotyping assays)
KASP Sequence:
GCATAAAAGAAGACAATGGTAGTTATTTTGCCACTGAAGGTCTAGAGACT[A/T]GAGAAGCMAGAGACCCAYCTAGCCCCCCTGAGGCAGACAGTCCACCAGCT
Long Flanking Sequence:
GAAAAAGAGAACACAGTAAGACTAATTCTGGAGAAAAACCAATGCATCAAACAACAACCCAAGCAAATGGTCCTCCGTTGGATGTTACAATCAAAACTGAGCCAACTGAAGAGGGTCAAACTAATGACTACAACAAAATGTCACAGCAATGCCAGAATTCAGTTTTGGAGCAAAGAAGCTCCAGCGCCAGTTATCTTTTTCAAGAAAACATCAAACAAGAACCACTTTCCCCAGAGGCTTCCACCAGAGATGGCCTTCTCTGTCATCTCCTTAAAAAACGACCCAAGGCACTACAGCGAAACAAGTTAGAGGACCTAAATAAGAGTTGTGTCAAAGAAGATTCAGCTGAAACCCAGGGACCAACAATCCCAAAGAAGCGAAAGTTTTCGATAGAACAAGAACATCAAAACTCTTTAATTCAGCCGACCAGCAAATTGGAACATTCTTGCAGCATAAAAGAAGACAATGGTAGTTATTTTGCCACTGAAGGTCTAGAGACT[A/T]GAGAAGCCAGAGACCCATCTAGCCCCCCTGAGGCAGACAGTCCACCAGCTAGGTTTCCACCGTATGAGTCTAACGAAAACCGAAGTTTCAATGTTTTAAAGCAGCTGCTTCTTTCAGACAACTGCTTGAAGGAATTGTCTCAACCAAGGAGTACATTCAGTTCGCCTTCACATACTGTGTTGAATGGAAATACAATCAAGCAACCATGCAATGGAGGTGAGCATCAAAACCTTCACAGAAGTCTGAGCCCCAGCAGTGCTTCTTCTAAAAAAACAAGCGGTCACAGACCAGAATCACCCCAAGTTACACAGCAAGAACCCGCAAAGTCAAAAATCGATTACAGCACCATGAAGGATTTGAAGGTCCCTACAAGGATGCTTAATGGAGATGATCAAACACAAAAATATGGGCTCGACTCACCTCGGTTTACCAAGACAAACCCTATTTTGTACTACATGCTCCAAAGGAGCAATGCACAACTGGTTAAAGAGGGGGAGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32041
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099956 | Nonsense | 910 | 1044 | 1 | 1 |
ENSDART00000135540 | Nonsense | 910 | 1080 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 29061205)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29779235 |
GRCz11 | 15 | 29712111 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCATCTAGCCCCCCTGAGGCAGACAGTCCACCAGCTAGGTTTCCACCGTA[T/A]GAGTCTAACGAAAACCGAAGTTTCAATGTTTTAAAGCAGCTGCTTCTTTC
Long Flanking Sequence:
AATGGTCCTCCGTTGGATGTTACAATCAAAACTGAGCCAACTGAAGAGGGTCAAACTAATGACTACAACAAAATGTCACAGCAATGCCAGAATTCAGTTTTGGAGCAAAGAAGCTCCAGCGCCAGTTATCTTTTTCAAGAAAACATCAAACAAGAACCACTTTCCCCAGAGGCTTCCACCAGAGATGGCCTTCTCTGTCATCTCCTTAAAAAACGACCCAAGGCACTACAGCGAAACAAGTTAGAGGACCTAAATAAGAGTTGTGTCAAAGAAGATTCAGCTGAAACCCAGGGACCAACAATCCCAAAGAAGCGAAAGTTTTCGATAGAACAAGAACATCAAAACTCTTTAATTCAGCCGACCAGCAAATTGGAACATTCTTGCAGCATAAAAGAAGACAATGGTAGTTATTTTGCCACTGAAGGTCTAGAGACTAGAGAAGCCAGAGACCCATCTAGCCCCCCTGAGGCAGACAGTCCACCAGCTAGGTTTCCACCGTA[T/A]GAGTCTAACGAAAACCGAAGTTTCAATGTTTTAAAGCAGCTGCTTCTTTCAGACAACTGCTTGAAGGAATTGTCTCAACCAAGGAGTACATTCAGTTCGCCTTCACATACTGTGTTGAATGGAAATACAATCAAGCAACCATGCAATGGAGGTGAGCATCAAAACCTTCACAGAAGTCTGAGCCCCAGCAGTGCTTCTTCTAAAAAAACAAGCGGTCACAGACCAGAATCACCCCAAGTTACACAGCAAGAACCCGCAAAGTCAAAAATCGATTACAGCACCATGAAGGATTTGAAGGTCCCTACAAGGATGCTTAATGGAGATGATCAAACACAAAAATATGGGCTCGACTCACCTCGGTTTACCAAGACAAACCCTATTTTGTACTACATGCTCCAAAGGAGCAATGCACAACTGGTTAAAGAGGGGGAGGGACTAGAGGTAGGCTTGGGACAAATGCAGACAAAGGTCAAAAATGAGTCATCAGGTGATACTGAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5882
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099956 | Nonsense | 964 | 1044 | 1 | 1 |
ENSDART00000135540 | Nonsense | 964 | 1080 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 29061365)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29779395 |
GRCz11 | 15 | 29712271 |
KASP Assay ID:
554-3682.1 (used for ordering genotyping assays)
KASP Sequence:
CTGTGTTGAATGGAAATACAATCAAGCAACCATGCAATGGAGGTGAGCAT[C/T]AAAACCTTCAMAGAAGTCTGAGCCCCAGCAGTGCTTCTTCTAAAAAAACA
Long Flanking Sequence:
TTTCCCCAGAGGCTTCCACCAGAGATGGCCTTCTCTGTCATCTCCTTAAAAAACGACCCAAGGCACTACAGCGAAACAAGTTAGAGGACCTAAATAAGAGTTGTGTCAAAGAAGATTCAGCTGAAACCCAGGGACCAACAATCCCAAAGAAGCGAAAGTTTTCGATAGAACAAGAACATCAAAACTCTTTAATTCAGCCGACCAGCAAATTGGAACATTCTTGCAGCATAAAAGAAGACAATGGTAGTTATTTTGCCACTGAAGGTCTAGAGACTAGAGAAGCCAGAGACCCATCTAGCCCCCCTGAGGCAGACAGTCCACCAGCTAGGTTTCCACCGTATGAGTCTAACGAAAACCGAAGTTTCAATGTTTTAAAGCAGCTGCTTCTTTCAGACAACTGCTTGAAGGAATTGTCTCAACCAAGGAGTACATTCAGTTCGCCTTCACATACTGTGTTGAATGGAAATACAATCAAGCAACCATGCAATGGAGGTGAGCAT[C/T]AAAACCTTCACAGAAGTCTGAGCCCCAGCAGTGCTTCTTCTAAAAAAACAAGCGGTCACAGACCAGAATCACCCCAAGTTACACAGCAAGAACCCGCAAAGTCAAAAATCGATTACAGCACCATGAAGGATTTGAAGGTCCCTACAAGGATGCTTAATGGAGATGATCAAACACAAAAATATGGGCTCGACTCACCTCGGTTTACCAAGACAAACCCTATTTTGTACTACATGCTCCAAAGGAGCAATGCACAACTGGTTAAAGAGGGGGAGGGACTAGAGGTAGGCTTGGGACAAATGCAGACAAAGGTCAAAAATGAGTCATCAGGTGATACTGAGGCCTTTGAACTTTGAAACAAAATTCACAGAATTACAATGGAACACTTAGTTGTGACTCACCACGGCTAAACGGGTCATAGAAGAAATACTAGTTTTGAGACTGTGAACCAGCTTCTGTGCTTGAACTAGAAATGTGCAACTTTTTACTCTCTTCTACTTATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6383
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000099956 | None | None | 1044 | None | 1 |
ENSDART00000135540 | Nonsense | 1062 | 1080 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 15 (position 29061659)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 29779689 |
GRCz11 | 15 | 29712565 |
KASP Assay ID:
554-4408.1 (used for ordering genotyping assays)
KASP Sequence:
GCAATGCACAACTGGTTAAAGAGGGGGAGGGACTAGAGGTAGGCTYGGGA[C/T]AAATGCAGACAAAGGTCAAAAATGAGTCATCAGGTGATACTGAGGCCTTT
Long Flanking Sequence:
CTAGCCCCCCTGAGGCAGACAGTCCACCAGCTAGGTTTCCACCGTATGAGTCTAACGAAAACCGAAGTTTCAATGTTTTAAAGCAGCTGCTTCTTTCAGACAACTGCTTGAAGGAATTGTCTCAACCAAGGAGTACATTCAGTTCGCCTTCACATACTGTGTTGAATGGAAATACAATCAAGCAACCATGCAATGGAGGTGAGCATCAAAACCTTCACAGAAGTCTGAGCCCCAGCAGTGCTTCTTCTAAAAAAACAAGCGGTCACAGACCAGAATCACCCCAAGTTACACAGCAAGAACCCGCAAAGTCAAAAATCGATTACAGCACCATGAAGGATTTGAAGGTCCCTACAAGGATGCTTAATGGAGATGATCAAACACAAAAATATGGGCTCGACTCACCTCGGTTTACCAAGACAAACCCTATTTTGTACTACATGCTCCAAAGGAGCAATGCACAACTGGTTAAAGAGGGGGAGGGACTAGAGGTAGGCTTGGGA[C/T]AAATGCAGACAAAGGTCAAAAATGAGTCATCAGGTGATACTGAGGCCTTTGAACTTTGAAACAAAATTCACAGAATTACAATGGAACACTTAGTTGTGACTCACCACGGCTAAACGGGTCATAGAAGAAATACTAGTTTTGAGACTGTGAACCAGCTTCTGTGCTTGAACTAGAAATGTGCAACTTTTTACTCTCTTCTACTTATCTGATTGCTACAGTACTTTCTATCGAGGCATCTCACATTTTTCACTTGAATTACATGTCATTCAGTTCACAAGAAGACCATGAAACCAAAGTTCATTTTGAATATTTACAATCACAACTTTGGCTGATTTCTTTCTTACTTTTTAAGTGGCAAAGGAAATAAAGTTTTCTACAATACAAAAGATGTGTGAAAGATTTGCCCTCATGTATTTGTAACAATATCAGTTCCCACTCCGTTTTCCACACAATGGTAGAGTTGGCCTGAGGCAGTAAGTTATGATGCACCAATGCACATG
Associated Phenotype:
Not determined