ZMP
rspry1
Ensembl ID:
ZFIN ID:
Description:
RING finger and SPRY domain-containing protein 1 [Source:RefSeq peptide;Acc:NP_001038537]
Human Orthologues:
RNF123, RSPRY1
Human Descriptions:
ring finger and SPRY domain containing 1 [Source:HGNC Symbol;Acc:29420]
ring finger protein 123 [Source:HGNC Symbol;Acc:21148]
ring finger protein 123 [Source:HGNC Symbol;Acc:21148]
Mouse Orthologues:
Rnf123, Rspry1
Mouse Descriptions:
ring finger and SPRY domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:1914860]
ring finger protein 123 Gene [Source:MGI Symbol;Acc:MGI:2148796]
ring finger protein 123 Gene [Source:MGI Symbol;Acc:MGI:2148796]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43079 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16314 | Nonsense | Available for shipment | Available now |
sa32199 | Essential Splice Site | Available for shipment | Available now |
sa23276 | Essential Splice Site | Available for shipment | Available now |
sa23277 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43079
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 |
---|---|---|---|---|---|
ENSDART00000090608 | Nonsense | 271 | 580 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 17398215)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17749981 |
GRCz11 | 18 | 17739047 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATTCATTATTCGTTTCAGGTGAGAACAAGTTAACGGTGTCAGAGTCATG[T/A]ATCAGTGACCGTTTGTCTGTTCTGGAATCCTGGGCAGATAACTTAGATTA
Long Flanking Sequence:
TGCATTATAATGCTTGAAGTATCAGAAGTATCGACCGATCACCATAACTTGGACTTTGTATTTGCTATTGGATGCAAAAATCTCTAGTATTTGTGTATTATTATTCTGTTTTCCTCGGATGGTTGATTGGATGTTACAGAAATTAGCACATACATTACATATAACATTAATAATTATTAATGTATAATTATTATTATATTGATTAGAGTAAGAAATGCTTTTAAATCTTCAAAGTTGTAAATCTATAGTTTTGCTTGCATATTTGACATAAGTAATTTTTTCAACTGTTTAATTCAGTTCTTTTGGTTTTCCTCAGAGTTCTGAAGCCCACCCCACTGTTATGCTGTTTGCTCTTATTGCTTTAGAGAAGTTCTCACAAACCAGTAAGTCTAACTGATGTCAGATCAATATTTCTATCAGGAATCTTTCCGAAAATGGTGCGTTTGATATGATTCATTATTCGTTTCAGGTGAGAACAAGTTAACGGTGTCAGAGTCATG[T/A]ATCAGTGACCGTTTGTCTGTTCTGGAATCCTGGGCAGATAACTTAGATTACCTAAAGCGCCAAGTGGGCTTCTGCGCTCAGTGGAGTCTTGATAACCTCTGTGAGTACGTTTTGATGGGTAATCAGGACTTTTAGTATTTGTAATTGCTATTGATACAAAGAAAATAAATGTTTCTCAGGACATCTGAAGTCTTTTTAATATAAATGATTTTTAGTAATAACTGTTTGCATTTTATAATTGTATTGTAGATTGAAGTCTTGTGGCATGTTTGACTGATGTTATCTTTGTCTCTCTTTGGCTCATAGTCATTAAAGAGGGGCGCCAGTTTACCTATGAGAAAGTCAACTTAAGCAACATCAACGCCATGCTGAACAGTAATGACGTCAGTGAATATCTCAAGATCTCTCCTACTGGACTGGAGGTGAGAGACAAACCAATATTGTTAATTATGTGAAAATTCTTCATTTAGGTAATGCATGGTGTGTTAAAGGGTCACGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16314
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 |
---|---|---|---|---|---|
ENSDART00000090608 | Nonsense | 359 | 580 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 17402320)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17754086 |
GRCz11 | 18 | 17743152 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGGCCCGTTGTGAYGCATCATCATTTGAGAGCGTCCGCTGCACGTTCTG[T/A]GTGGWTTCGGGGGTTTGGTACTATGAGGTCACGGTTATCACCTCTGGCGT
Long Flanking Sequence:
TCCCATACCAAGCCGCTTTTTTTCCTCCGACACTCCCCCCTAAACAGAGCTGGACACGCCCACTTTTCTGACTTTTTCCAAAGTAGAGGTGTGAAAACACCCTGCTGAAACGAGGGGGTTTCATGGCCCTTTAAGAATTGAAAATGTTCACTTAGTGACAGATAAAAGACAAAGTCTTTCAAAATGAAAATAAAATAAATCAACTGCGTGTACAGGGCATCAGGAATGTTCTAGAGTAGTGATTTTGTGGCAGATAGGATTCTGTTTAAACCAGGAATGAGATCGCATTCATTTCGGGTTTATCATAAACAAACAGCATTTTTTTTATTAAACTACTGAATGGTTCAGATACCGAATCAATCAGAATCCCCATGTTCATCTATTGTGCAAGAGTAGCTGTTTATATTCATAATATAATGTCTCTAATGAGATCAATGTCATCTTTGTCTTTAGGCCCGTTGTGACGCATCATCATTTGAGAGCGTCCGCTGCACGTTCTG[T/A]GTGGATTCGGGGGTTTGGTACTATGAGGTCACGGTTATCACCTCTGGCGTCATGCAAATTGGCTGGGCAACCAAGGACAGCAAGTTTCTCAACCATGTGTGTTTTAATTAAGCTCCTTTATTTCTGATTTCTCCCTTAGCTTCATGTTTTAATATTCTTATAAAAGCACAAATATTTTTATGAACACTTAAGGTACAGTGGAAGTCAGAATTAGTAGCCCCTCTTTGATTTTTTTTCTAGAGAAACATTTCACAAATGAAATTTTTACAGTATGTCGAATTTTTTTTTTTTTTAACAAGATTTGTTTTAATTCTGCTGGAATAAAATAAGTTTTTCATTTTTTAAAAACCATTTTAAAGTCAAAATTATCTGCCCATTTAAGCTATTTTTTCCGATATTCTACAGAATAAACTATCGTTATACAATAACTTGCCTAATTATTCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32199
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090608 | Essential Splice Site | 391 | 580 | 10 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 17402418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17754184 |
GRCz11 | 18 | 17743250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTCATGCAAATTGGCTGGGCAACCAAGGACAGCAAGTTTCTCAACCATG[T/C]GTGTTTTAATTAAGCTCCTTTATTTCTGATTTCTCCCTTAGCTTCATGTT
Long Flanking Sequence:
ACCCTGCTGAAACGAGGGGGTTTCATGGCCCTTTAAGAATTGAAAATGTTCACTTAGTGACAGATAAAAGACAAAGTCTTTCAAAATGAAAATAAAATAAATCAACTGCGTGTACAGGGCATCAGGAATGTTCTAGAGTAGTGATTTTGTGGCAGATAGGATTCTGTTTAAACCAGGAATGAGATCGCATTCATTTCGGGTTTATCATAAACAAACAGCATTTTTTTTATTAAACTACTGAATGGTTCAGATACCGAATCAATCAGAATCCCCATGTTCATCTATTGTGCAAGAGTAGCTGTTTATATTCATAATATAATGTCTCTAATGAGATCAATGTCATCTTTGTCTTTAGGCCCGTTGTGACGCATCATCATTTGAGAGCGTCCGCTGCACGTTCTGTGTGGATTCGGGGGTTTGGTACTATGAGGTCACGGTTATCACCTCTGGCGTCATGCAAATTGGCTGGGCAACCAAGGACAGCAAGTTTCTCAACCATG[T/C]GTGTTTTAATTAAGCTCCTTTATTTCTGATTTCTCCCTTAGCTTCATGTTTTAATATTCTTATAAAAGCACAAATATTTTTATGAACACTTAAGGTACAGTGGAAGTCAGAATTAGTAGCCCCTCTTTGATTTTTTTTCTAGAGAAACATTTCACAAATGAAATTTTTACAGTATGTCGAATTTTTTTTTTTTTTAACAAGATTTGTTTTAATTCTGCTGGAATAAAATAAGTTTTTCATTTTTTAAAAACCATTTTAAAGTCAAAATTATCTGCCCATTTAAGCTATTTTTTCCGATATTCTACAGAATAAACTATCGTTATACAATAACTTGCCTAATTATTCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCACTTTAAGCTGTATAAAAGTGTCTTGAAAAATATCTATTAAAATATTATTTACTGTCATCATTGCAAAGATAAAATAAATCATCTAAACTATTATGTTTAGAAATGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23276
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
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090608 | Essential Splice Site | 463 | 580 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 17404708)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17756474 |
GRCz11 | 18 | 17745540 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAACGGACACCAGCTGCCTCCTGAGAAGCAGGTGTTCTTCTCTGCCAC[G/A]TAAGCGAAGATCACTTCCTTAACCTTAAAACGAGCATGATGGAACTTTTT
Long Flanking Sequence:
TGTAATAATTTGAATCATAACTAATAACAAACTAAAATTGTCTGGGTGTTTCAGCTTATTTTAAATGACCAGTTTCCTGTTATATACACTTATGTATTCTAAAAATGAAATAATTGTTCTGTAGTAAGAAAACACATCTCTGTGTTTATACAGGAGGGTTATGGGATTGGAGATGATGAGTACTCGTGTGCGTATGACGGCTGCAGGCAGCTGATCTGGTACAACGCTCGCAGTAAACCTCACTCCCACCCCTGCTGGAAAGAAGGTTTGTAGAGCATCCTGTTCAGCTCCCAACATCTGCATGTGATGATTACCTATTTACAATTGCCTACATTTATTCCATATCATCATTTTGTTATTACAACGTTGTGTGATCAGTGTTCTCTGGTCTTTCTAGGTGATGCCATAGGCTTCCTGCTGGACCTCAGTAAGAAGCAGATGATTTTCTACCTTAACGGACACCAGCTGCCTCCTGAGAAGCAGGTGTTCTTCTCTGCCAC[G/A]TAAGCGAAGATCACTTCCTTAACCTTAAAACGAGCATGATGGAACTTTTTGAACACTTGGCTTTCTTTGTTTCAGGTCTGGCTTCTTTGCTGCAGCCAGTTTTATGTCCTATCAACAGTGTGAGTTCAACTTCGGAGCCAAACCCTTCCGCCATCCCCCCTCCATCAAATTCAACACCTTTAATGAGTTTGCCTCGCTCGCATCAGACGAGAAAATCATTCTGCCCAGGTTTGCACCATTTATTAGATTGCTGTACAAAGGGTGAAGTATCAATGGCCGTTATAGATGTGAATGATGCACTGGTTATTATCTAAAGTAGGTGACTCATGCAGTGAGTATCTGAAATTGCTCTTCCTTTGTTTTATTTCAGACACAGACGCCTAGCATTGCTCAAGCAGGTTAGCATCAGAGATAACTGCTGCACCCTCTGCTGCGACCAGATGGCGGACACTGAACTGAGACCCTGTTCGCACAGGTACAAAGATCAGCTTATAGAATCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23277
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000090608 | Essential Splice Site | 514 | 580 | 13 | 15 |
Genomic Location (Zv9):
Chromosome 18 (position 17404938)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 17756704 |
GRCz11 | 18 | 17745770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAATGAGTTTGCCTCGCTCGCATCAGACGAGAAAATCATTCTGCCCAGG[T/C]TTGCACCATTTATTAGATTGCTGTACAAAGGGTGAAGTATCAATGGCCGT
Long Flanking Sequence:
CAGTAAACCTCACTCCCACCCCTGCTGGAAAGAAGGTTTGTAGAGCATCCTGTTCAGCTCCCAACATCTGCATGTGATGATTACCTATTTACAATTGCCTACATTTATTCCATATCATCATTTTGTTATTACAACGTTGTGTGATCAGTGTTCTCTGGTCTTTCTAGGTGATGCCATAGGCTTCCTGCTGGACCTCAGTAAGAAGCAGATGATTTTCTACCTTAACGGACACCAGCTGCCTCCTGAGAAGCAGGTGTTCTTCTCTGCCACGTAAGCGAAGATCACTTCCTTAACCTTAAAACGAGCATGATGGAACTTTTTGAACACTTGGCTTTCTTTGTTTCAGGTCTGGCTTCTTTGCTGCAGCCAGTTTTATGTCCTATCAACAGTGTGAGTTCAACTTCGGAGCCAAACCCTTCCGCCATCCCCCCTCCATCAAATTCAACACCTTTAATGAGTTTGCCTCGCTCGCATCAGACGAGAAAATCATTCTGCCCAGG[T/C]TTGCACCATTTATTAGATTGCTGTACAAAGGGTGAAGTATCAATGGCCGTTATAGATGTGAATGATGCACTGGTTATTATCTAAAGTAGGTGACTCATGCAGTGAGTATCTGAAATTGCTCTTCCTTTGTTTTATTTCAGACACAGACGCCTAGCATTGCTCAAGCAGGTTAGCATCAGAGATAACTGCTGCACCCTCTGCTGCGACCAGATGGCGGACACTGAACTGAGACCCTGTTCGCACAGGTACAAAGATCAGCTTATAGAATCAGTGTTTACACAACTGGCTTTATGGGGACAGGGGCTTGGTTGAGGTGGAGTAGAAAAGAACAACTGTTGTTTGGGGAATTGGGACATTTGGAACACATTCAGCCTTTTGTAACCCATATCCCTGCATTAAGCCTGTTAAGAATTTTAGGGTGCACTCACACTATGCCATTTGAACTGTGTCAATGCGTGTTTCCTGGTTTGTTTGACAAGTTTGAGGGCGAGGTTCAGTTG
Associated Phenotype:
Not determined