ZMP
si:dkey-191g9.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate RAP1, GTP-GDP dissociation stimulator 1 (RAP1GDS1) [Source:UniPr
Human Orthologue:
RAP1GDS1
Human Description:
RAP1, GTP-GDP dissociation stimulator 1 [Source:HGNC Symbol;Acc:9859]
Mouse Orthologue:
Rap1gds1
Mouse Description:
RAP1, GTP-GDP dissociation stimulator 1 Gene [Source:MGI Symbol;Acc:MGI:2385189]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35465 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31921 | Nonsense | Available for shipment | Available now |
sa38934 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22277 | Nonsense | Available for shipment | Available now |
sa1446 | Essential Splice Site | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa35465
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078460 | Essential Splice Site | 80 | 560 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 21871560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21600898 |
GRCz11 | 13 | 21731348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCCACTCACCTCTCAGGTCACTTTACTGGTGGCAGAGATGGCCAGAGAAG[G/A]TAAAAACAACTATTATTATTGTTATTATTCATTTATTAATTCATTCATTT
Long Flanking Sequence:
TATAAACTGCATTTTGTCATCATTAAGCAAAAACAAACTGAAAACAAAAGCAAAATAAATGAAAATGACAAATGTGGTGGCACCCTTTGGCTTCAAATATACACATTTTTCATTACAAATTTTCACATAGGTGGTGTCATTTTGAGTACCCAGGCTTTTCATTAGAAAACTGAAGAGTTAAACCGACAGAGCTTTAAACAACAGTTGATCAATAATAAAAAACTCAACCAAACTGAATGTGATTGTTGATTTCATACAACAAATTTTGTACAGTGTGGTTAAAAAAAAAAAAGAAAAAGAAAAGAGTCTAAATGTATAAAAGCATAAAAACAAATGTGAAGGAAAAAAAAAATAATGAAGTGTATTTCTGTGTCCAGAGAAAGGAACAGCTGAGAAAATAGTGTCCAGTGGTGTTCTGCCTATCCTGACTCAAGTCCTGAGGAAGAAGAGTCCACTCACCTCTCAGGTCACTTTACTGGTGGCAGAGATGGCCAGAGAAG[G/A]TAAAAACAACTATTATTATTGTTATTATTCATTTATTAATTCATTCATTTTCTTTTTGGCTTAGTCTCTAAATTAATCTGGGTTTGCCACAGCATAATGAACCGCCAACTTATCAAGCATATGTTTTACGCGAACACGGGGAGAACATGAAACCAGCGACCTTCTTGCTGTGAGACGAGAGCACTACGCACTGCACCACCGTGCTGCCCCTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAGTAGTAGTAGTAGTAGTAGTAGTATTAAAAAAGAAGCTTCACAGTGCAAACATAAGGTGAAATGTGTGAAGCAAACAAAAAGAAATCAATGTTTTTGTGGTATTTCAAACATAATTTTTTTTTCATTTATATAACAATTATACAAACAATTTATAAACAATATTGTTAGAATAATATTAGGGTTACATGAAAAGGTAGTTTAATTTATTTACAAAAATCATTTAATGACAGCGCGGTGGCGCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31921
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 |
---|---|---|---|---|---|
ENSDART00000078460 | Nonsense | 193 | 560 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 21865683)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21595021 |
GRCz11 | 13 | 21725471 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGGCTGAGGTTTTGACCCATCAGCTGAAACGGGCTCCAGATGCAGAA[C/T]GACGGCATCTCATACTAGAGGTTCTTGGTTCACTGGGAGAAAGTGGTGAG
Long Flanking Sequence:
ACACAAAGTTTAGAGTTCTGTAGCTATTGATGCTCTGACCCTGCTCTGTGGTTTCACCTAGCCTACCCTTTATAGCTTAATTCATGTTACATTTGCATTTAATCATTTAGCAGATGTTTTTATTTAAGACGACGGCCAAATGAAGATAATAGGAGCACTTGAAAAGTCATGAAAAGTCTAAATTGGTTTAGTTTCATGTTGTTATAGCGTACCACTAACAATTGACCGCACAATATTAAGTAGGGAGTAAATTTCAGGAAAGGACTTATTGCAATAGTGGCAAAGAGTGTTTGTAGAAGCTGTCTGCATGCCTAGGTGATTGATGTTATACACCTGTGGCAATGAAGTCCTGAAACTTTGGGTAATAAAGTGCTTCTATATAATGTCTGGTGATTGATTCTGATGAGTATCTGTGTTCAGATGCTGCACGGGAGGCTCTGACAGAAGTGGATGTGGCTGAGGTTTTGACCCATCAGCTGAAACGGGCTCCAGATGCAGAA[C/T]GACGGCATCTCATACTAGAGGTTCTTGGTTCACTGGGAGAAAGTGGTGAGCTCTAATTCCAGATAGGGTTCATATGTGTTCTTGGATCACACAACCTCATTTTTACAGCATAAATTTTTTTTGAAATATGATGTCTTAAATGTGAGTACTCTTCTGTGGGATGATGATGTCTTTAAATAGCTACCTTGTAAATGTAAACGTAAATGTAAGTGTCCTTGTAAATCCCTCTGCAAATTCATGTTTGTGTCACTCAGATGCCCTGAAACTGCAGTTTGTGGAGTCAGGCGTACCTGAGGCTCTTTCCGAAATGATTCGAACTCTTCAGGGTGGCTCTGACACACATGACCTCTGCAGCATCAAAGTGGCCTCAAACCTCATAGTGACTCTCCTACTGGGAGGTATGTCTCTCTCCATTACTTTTTTTACAGTGGTTACTGTTGTAATTAATTTCACTGCTTTTATTCGAATAATTTATATCCATTGTTAGTCTATAACCAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38934
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 |
---|---|---|---|---|---|
ENSDART00000078460 | Nonsense | 258 | 560 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 21863820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21593158 |
GRCz11 | 13 | 21723608 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGCAGATTATTTGTTTTGAGCTTGATCTGCATTTCATTACAGATGAAT[C/A]AATGCAGAAATGTTTTGGAGAAGGGACGGGGATGGTGTATCAGGATGTTC
Long Flanking Sequence:
TACTAGGGATGTCCTTTGAAAGACTAGGAATGATCTGTAAGAATGTTTTCTTGTGAGAGAGTAGTGATGTCTATGAGGGACTAGTGATAAGGAGAGAGACTAGTCTGGTGGTTGCAGATGTGCAAGTAAAAAAAAAAAAAAAACAAGAGCTTCTACACCTACTACTCATTTTATGTCTGCTACAACCTTCTGAAATTTTATTGTCATGTTCTTTGTGACAGTCATTGCAAATGCTCTAATTTTGATTACTGTGTTTTCCAGAAAAAAAAAAAACTTTTTAAAAAAGTTTTGTTGAAGTTATTTTGTAAAACGATGTTTAACTAGCTTGCTACTGTAAGTATCCACAACTAAAATCCCAAATAATTTTAAAACTACTGTAAAAGATGTATACAAATAATTGTTCTATCTCAACTCTATATCGAATTTGCTTAATTGAGCAATCATTCATTTAATGCAGATTATTTGTTTTGAGCTTGATCTGCATTTCATTACAGATGAAT[C/A]AATGCAGAAATGTTTTGGAGAAGGGACGGGGATGGTGTATCAGGATGTTCTCGCTTGGCTGCAGTCATCAAACACTGAGCTGCAGCTGTCAGGCGCTCTTGCCATTGCTAATTTTGCCAGAAATGGTGAGCAAATGAACATACAGTACAGCAGCTTTCTTGCAGTTAGTGATAAAGATTTGGATTCTTTCTCACTCAAACTTTATTTAATTAAAAACATTTTTATTCCATAGACAGCAACTGTGTGAAGATGCTGGAATTAGGAGTTGTTCCTCGTATTCTGGACCTGCTGGAGCAGCACGTAGCAGAGGGAGATGTTTCTGTGCAGCATGCTGGCCTCAGTGCACTTCGAAATCTCGCCATACCAGGTACTACTGCTTTTTGAAATGCAGTTAGGGTGTGGACTATTATGTTTTATTTGAAGAGATATTGTAATTTAAAATATATATATATATTCTGTTTTATAAATGTTTGAAACATTATTTATTTCTTTGATTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22277
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 |
---|---|---|---|---|---|
ENSDART00000078460 | Nonsense | 271 | 560 | 8 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 21863780)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21593118 |
GRCz11 | 13 | 21723568 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGATGAATCAATGCAGAAATGTTTTGGAGAAGGGACGGGGATGGTGTA[T/A]CAGGATGTTCTCGCTTGGCTGCAGTCATCAAACACTGAGCTGCAGCTGTC
Long Flanking Sequence:
GAATGTTTTCTTGTGAGAGAGTAGTGATGTCTATGAGGGACTAGTGATAAGGAGAGAGACTAGTCTGGTGGTTGCAGATGTGCAAGTAAAAAAAAAAAAAAAACAAGAGCTTCTACACCTACTACTCATTTTATGTCTGCTACAACCTTCTGAAATTTTATTGTCATGTTCTTTGTGACAGTCATTGCAAATGCTCTAATTTTGATTACTGTGTTTTCCAGAAAAAAAAAAAACTTTTTAAAAAAGTTTTGTTGAAGTTATTTTGTAAAACGATGTTTAACTAGCTTGCTACTGTAAGTATCCACAACTAAAATCCCAAATAATTTTAAAACTACTGTAAAAGATGTATACAAATAATTGTTCTATCTCAACTCTATATCGAATTTGCTTAATTGAGCAATCATTCATTTAATGCAGATTATTTGTTTTGAGCTTGATCTGCATTTCATTACAGATGAATCAATGCAGAAATGTTTTGGAGAAGGGACGGGGATGGTGTA[T/A]CAGGATGTTCTCGCTTGGCTGCAGTCATCAAACACTGAGCTGCAGCTGTCAGGCGCTCTTGCCATTGCTAATTTTGCCAGAAATGGTGAGCAAATGAACATACAGTACAGCAGCTTTCTTGCAGTTAGTGATAAAGATTTGGATTCTTTCTCACTCAAACTTTATTTAATTAAAAACATTTTTATTCCATAGACAGCAACTGTGTGAAGATGCTGGAATTAGGAGTTGTTCCTCGTATTCTGGACCTGCTGGAGCAGCACGTAGCAGAGGGAGATGTTTCTGTGCAGCATGCTGGCCTCAGTGCACTTCGAAATCTCGCCATACCAGGTACTACTGCTTTTTGAAATGCAGTTAGGGTGTGGACTATTATGTTTTATTTGAAGAGATATTGTAATTTAAAATATATATATATATTCTGTTTTATAAATGTTTGAAACATTATTTATTTCTTTGATTGCAAAGCTTATTTTATTTTGTGCCAGATGATATTTTTAGAGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1446
Status:
F2 line generated
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000078460 | Essential Splice Site | 519 | 560 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 13 (position 21852797)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 21582135 |
GRCz11 | 13 | 21712585 |
KASP Assay ID:
554-1372.1 (used for ordering genotyping assays)
KASP Sequence:
ACCCAAAACTAATTTATAACCTCCTAATTACATTTCTGTTCTCTCCTACA[G/A]CCATACTAAGGGAGCAGATAACATCTCTAAACCTGAGGGACACCCTGTCC
Long Flanking Sequence:
ACATTGTAAGTCTCAGTTTCTAAAAATTGACTGTTATGGCAGGTTTTGCGTGTCCAGGTTCACATATAGCACTGAACATGAAAAGCCCGACATTATATTTACAGTTTACAGATTACATTCTACAATTTTATTGATAGATTTGTTAACAAGCTTGATATTTCTGCTTTGAGCACTACCAAATATTGTATAAAAGCGATATCTCTCCTTCCATTTTCTGTTCTGTGCAGAGGCAGTTCAAGAACCATTTCGAGATGCAGACCTTCTTCCCACCTTGCAAAAGATGCTAGATGACCCTGACGTGGCTGTGGAGGTCAAATTCAGTGCTTTAGGCCTGATCTGCAGTCTTGTCAACTCCAGTCAGTACTGCAAAATGATCAAACAGCTAAACGCACTTTCAGATATCTCTATTAGATGTTTAACTAATTACAAAGTTCTGTGAATATTAAAAAAACCCAAAACTAATTTATAACCTCCTAATTACATTTCTGTTCTCTCCTACA[G/A]CCATACTAAGGGAGCAGATAACATCTCTAAACCTGAGGGACACCCTGTCCAAACTGTCCAATCACACCAGCACAAAGCTGGCAAAGCAGGCCGACACGGTGATGGCTGTTCTTTCGGAGACCGCCTAGACTGACACGTCTTGCATAGTAATAATCCAGACACACATACAGACATCCTTGTGGGGGTATTTTCTGACAATTAATTCCCAAAAGGATAGTAAAACACTCGCACAGTTACCCCTTCTAGCTTGGCATATAGTCAGACCAAAGCAATATAAATTTACTCCACCAACTCTGGAGAAAGAGGGTGCGATTTCATCATCTAACATAGGAAGAAGTCAGCTTGTCCATGAATATTTGTTGTCAGCTGTCCCAGGAACAGGACGACACGGGAGACAGACCATCCATCAGATATCAGTAATGAACCTGCTGGCATCCCAAACAGAAACAGCTGTATAAATTCATGAGGAGTGTTCCGTGGCAAATAACTTAGTAAATAAC
Associated Phenotype:
Not determined