ZMP
NR_023320.1
Ensembl ID:
Description:
im:7138264 (im:7138264), non-coding RNA [Source:RefSeq DNA;Acc:NR_023320]
Human Orthologue:
SRCAP
Human Description:
Snf2-related CREBBP activator protein [Source:HGNC Symbol;Acc:16974]
Mouse Orthologues:
AC122417.1, Srcap
Mouse Descriptions:
Putative uncharacterized protein [Source:UniProtKB/TrEMBL;Acc:Q8BKT0]
Snf2-related CREBBP activator protein Gene [Source:MGI Symbol;Acc:MGI:2444036]
Snf2-related CREBBP activator protein Gene [Source:MGI Symbol;Acc:MGI:2444036]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17300 | Nonsense | Available for shipment | Available now |
sa15343 | Essential Splice Site | Available for shipment | Available now |
sa8992 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22109 | Essential Splice Site | Available for shipment | Available now |
sa22110 | Nonsense | Available for shipment | Available now |
sa38898 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16953 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17300
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 |
---|---|---|---|---|---|
ENSDART00000003080 | Nonsense | 1036 | 3917 | 5 | 32 |
Genomic Location (Zv9):
Chromosome 12 (position 28643081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26980690 |
GRCz11 | 12 | 27072050 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTGCAGGGYGCCCCTGTACAGAGTTCAGACAYTGCAGCTGCCTCCAAA[C/T]AGTCACAGCCTAATCCTGTTGATGAGGATGGTGAGGATTGGCATTTGGTT
Long Flanking Sequence:
GCCTATTGTAAAAGAAACACCTCAATTAAATACTCTAAAATGTAATCTAGAGTTTCAGGACTCTCGAAATGAAAATCTCAACATGTTTTCAGGTAGTCCGAATGGTCATGCGACACCATGAGGAGTTGAGGCAGAAGGAAGAGAGAGCAAAACGTGAGGAGCAAGCCAAACTGAGAAGAGTTGCTTCTTCTATTGCCAAGGAGGTCCGTGCCTTCTGGAGCAGCGTTGAAAAGGTGCTCTTTTATAGGAATCCCTATTGCCATCTCTATGAAATCTGTTGCTATAAGAACGGTGATTCACGCTTTCATCTGATTCCTGCTTATTGCTGTACACAGGTGGTCCAATATAAACAACAGTCCAGACTGGAGGAGAAGCGGAAGAAGGCTCTAGATCTTCAGCTGGATTTCATTGTGGGTCAGACAGAGCGTTACTCAGACTTGTTAAGTCAGTCCCTGCAGGGCGCCCCTGTACAGAGTTCAGACATTGCAGCTGCCTCCAAA[C/T]AGTCACAGCCTAATCCTGTTGATGAGGATGGTGAGGATTGGCATTTGGTTTATTGTCAGTGTTCAGATAAAGTTACTGTAATAAAATTGAACTGAAAATCTGAACTAGAAATGGTGTGTTTTTGATCACATTAAACAAGTCTTGTTCTTACTGAGCTTATATTGTGGCTTTTTGTCCTGCAGATAGAGACTTTGAGCCCCCTTGTGAGGAAGAGGATGACGAAGAGACTATAGAAGTTGAGGAGCAACAAGAGGGGAATGATGCAGAAACACAGAAGCGAGAGATTGAGTTACTGAGGGAGGAGAGCACACTGCCTCTTGACCAGCTACTCAGTACTTTAACTCTTCCCCAGGTATAGCCATCTTCAAGGGTCAACTCCATCACAGCAGTCATATGCTTTGTTTTCAGCATTATTGTTTGGGTAGCCTTGTTACACAGTCTCTGATTAAAGCGATCTATCACTTTATTTTTTTTAGTTCACATATATTAAATATTTTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15343
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 |
---|---|---|---|---|---|
ENSDART00000003080 | Essential Splice Site | 1454 | 3917 | 13 | 32 |
Genomic Location (Zv9):
Chromosome 12 (position 28645385)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26982994 |
GRCz11 | 12 | 27074354 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCAAGAACTTTAAGTCCCAGCGCTGGCAAAGCCTGCTCAATTTTAACAGG[T/C]ACTTGAATACAACAATATCTGTTAAGGGCTTGATCATTTATTAWCAGTGG
Long Flanking Sequence:
ATACTTTATAATCTGTGTTGAGCTCAAAGTGGATGTACACCTTTTTATGACAGGCTTGCTTTTATAGGTAACTGGGGTCCACATCTGATCATTGTGCCAACTAGTGTAATGCTCAATTGGGAGATGGAATTGAAGCGCTGGTGCCCAGGATTCAAAATCCTCACCTATTATGGCAGCCAGAAGGAGCGCAAGCTGAAGAGACAAGTAATTATTACAATAATGAGAATATAAATACAACATGAATTACAAAATAAAATGAACTCTGTGTTTTAATGTAGTTTTTCAGTCATCTTGATTTTAGATTTTTTTCATTTTTCCTTTCTTGTCAGGGCTGGACCAAACCCAATGCTTTCCATGTGTGCATCACCTCATATAAGCTAGTACTGCAAGATCATCAGGCTTTTAGACGCAAGTCTTGGAGGTACCTCATTTTGGATGAAGCCCAGAACATCAAGAACTTTAAGTCCCAGCGCTGGCAAAGCCTGCTCAATTTTAACAGG[T/C]ACTTGAATACAACAATATCTGTTAAGGGCTTGATCATTTATTAACAGTGGCCTGTTGAACAAAACTCAGAGCCAAATGGCACACTATGCACTTACACACTCATCAGCATAGTATATGAATGTAGCGTTGTCCCAAATGGAACACTACTGTTTTTTTACTGAGCGGAAATTCCCTGATGATGGTTAGAACAATCGCCTCACAGCAAGAAGGTTGCTGGTTCGAGCCCTTGCTGGATCAGTTGGTATTTCTGTGTGGAATTTGCATGTTCTTCCCGCGTTCACATGGGTTTCCTCCAGGTGCTTCGATTTCCCCCATAAGTCTAAAGACATGTGGTACAGGTGAATTGGGCTCTGGTGACCCCAGAATAATTAAGGGACGAAGCCAAAAACAAAATGAATGAATGAATGTTTGATTGACGGTTGGCAACTCAGTACCTAATAATACCTGTTTTTATTGTAAATGCACTACTTGCACTATTTATACTACTAAATGGCATAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8992
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 |
---|---|---|---|---|---|
ENSDART00000003080 | Nonsense | 2304 | 3917 | 26 | 32 |
Genomic Location (Zv9):
Chromosome 12 (position 28656248)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26993857 |
GRCz11 | 12 | 27085217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTACCATGGACACATCTATCTGAGGTTGGATGGAAGTACACGAGTGGAA[C/T]AGAGACAGGTGAAATACTAGTTCTAGTACTTTGGTAGTGTTTGCGATTGA
Long Flanking Sequence:
AATTAAAATTTAAAAAATTATGTGCATATTAACACCATGGTAAAAATGTGCCACTTTTCCACAGGTTCGTTTTTGTTATTCCTCCAGTGGAGGCAAGACCTGTCACCATGCACAGCTGCCACCCACCACCCTCCCTCAGACACCAGCAAGCTGTTTTCTCCTCTGATCTATCCTCTTATGTCTCTCCACTTACACACACACTCCATCGAATCCAGAGCAACATGAGGACATACTTCCCTGACTTGAGGCTTATTCAGTATGACTCTGGTATGTACTGTGTTTTGTATAATATACAAAACAAAATAACTATGAGACAATGAATATTTTATAACTGTTTAGGTAAGCTGCAGACACTCCACCTCCTGCTTAGAAGGTTGAAAGCAGAAGGGCACAGAGTCCTCATATTTACTCAGATGACACGTATGCTAGATGTACTTGAGCAGTTCTTGAACTACCATGGACACATCTATCTGAGGTTGGATGGAAGTACACGAGTGGAA[C/T]AGAGACAGGTGAAATACTAGTTCTAGTACTTTGGTAGTGTTTGCGATTGAACCCATTTTTCACAACATCTCTTGATTTAAGCAATCGGAACAAAGTATGTTTGACTTTATTTGAACGTTTGTCTAACTTTCAGGCTCTGATGGACCGCTTCAATGCAGACCGTCGAATTTTTTGCTTCATCCTTTCCACCCGCAGTGGAGGTGTAGGTGTTAACCTGACTGGGGCAGATACTGTTGTGTTCTATGACAGTGATTGGAACCCAACCATGGATGCCCAAGCTCAGGACCGGTGCCACAGAATTGGACAGACGAGAGATGTCCACATCTATAGGTAAAGACTAAACCTTTATATAAAAATAAATGATTAACATGGCACATATTATTGCAGCACATTTAACATCTAACATTTTTATTTAGACTGATCAGCGAACGCACAGTGGAAGAAAATATTCTTAAAAAAGCCAATCAAAAGAGGATGCTGGGAGATATGGCTATTGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22109
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 |
---|---|---|---|---|---|
ENSDART00000003080 | Essential Splice Site | 2450 | 3917 | 29 | 32 |
Genomic Location (Zv9):
Chromosome 12 (position 28656993)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26994602 |
GRCz11 | 12 | 27085962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGATGATGAGGAGTCCATCAATAAACAAAAAACCACCATTTTGGAACAG[G/A]TAAATTAAATGTATCTATTTGGGGTATTGAATTTGTTTTTCTTGCAAGAT
Long Flanking Sequence:
GACAGTGATTGGAACCCAACCATGGATGCCCAAGCTCAGGACCGGTGCCACAGAATTGGACAGACGAGAGATGTCCACATCTATAGGTAAAGACTAAACCTTTATATAAAAATAAATGATTAACATGGCACATATTATTGCAGCACATTTAACATCTAACATTTTTATTTAGACTGATCAGCGAACGCACAGTGGAAGAAAATATTCTTAAAAAAGCCAATCAAAAGAGGATGCTGGGAGATATGGCTATTGAAGGCGGAAACTTTACCACTGCCTTTTTCAAGCAGGTATGATTCAATTTAAAATATTTTTTTACAGAGAAATCATAGCCTTGATTAAAATTTAGATGAATTGATGATTCAACTCTTTCTTTCCCACAGCAAACTATTAGAGAGTTGTTTGATGTGACAGAGGGAGAAAAGAAAGAAGCTGAACAGAGTGTGCCTCAGTCAGATGATGAGGAGTCCATCAATAAACAAAAAACCACCATTTTGGAACAG[G/A]TAAATTAAATGTATCTATTTGGGGTATTGAATTTGTTTTTCTTGCAAGATGTTTATAACAAATGAGATGAGATTTTATGTTTTATTTTTATTCCAGGCCCTGTGTCGTGCTGAAGATGAAGAGGACATAGTGGCTGCATCTCAAGCAAAGGCAGAGCAGGTGGCTGAGCTTGCAGAGTTTAACGAGAATATACCTCTAGATGACGGTGACAGTAGAGACCAAGAAGAGGAAGAGCTTTCCAAGGCGGAGCAGGAAATTGCTGCCCTAGTTGAACAGGTAGGTATTTAATACATATTTACTCTTTTTAATTTTAGAAAGTAGTATTATTTACAGTGGATTTATGATTTTTTTATTGTCCATCCTTTTTTTAACAGCTCACTCCCATTGAGCGTTATGCCATGAATTTTCTTGAGGCTTCCCTCGAAGATATTTGCAAAGAGGAGTTGAAGCAGGCAGAGGTAAAAGCTTAAATAAAACAGTAACCAAGCTTTGATCTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22110
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 |
---|---|---|---|---|---|
ENSDART00000003080 | Nonsense | 2816 | 3917 | 32 | 32 |
Genomic Location (Zv9):
Chromosome 12 (position 28658389)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26995998 |
GRCz11 | 12 | 27087358 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAAATTCTCAAGGGACTTCCAGAAGATTCTCCCTCAGCCAAGGTCCTT[C/T]GAAAGCTTCCAGGTCGTCTGGTCACTGTGGTGGAGGAGAAAGAGCCAAAG
Long Flanking Sequence:
AGCTTCGCAGTGGCCCACGAGGGCGATGTACAACCAAAGAATCTGCGTCATTAGAGAACCAGACTATCCCAACCAACCAGCAGCTTATAGATTCAACAACCTTGTCCCCTGCTATGCGGGATTCATACCCAAAAATTAGTGTGCCATCCCCTCACCAACAGTCCATCTCCCCATCAAGCTCTGTGCCTTCAGCTGCTGCATCTCCCTCATTGGACAGAAACTCTTGTGGCCATCTGTCTTCCTCTACTGTTGCATGCAGAGAGGACAGTGAAGACCAAAAGGGAGAAGCACGGTCTGAAAATGTACAGAGCAGAGATCGGAGAGCCTCTGCATCATCAGACTCCATCTGTTCTCCAGAACATCACTCTGAACAGGAGTGTCAGCTCTCTCTTTCTCCCACTCTAGCATCACCTAACTCTCGCTCACCACGAAAGCGGCAGTCTGCTGAATGGGAAATTCTCAAGGGACTTCCAGAAGATTCTCCCTCAGCCAAGGTCCTT[C/T]GAAAGCTTCCAGGTCGTCTGGTCACTGTGGTGGAGGAGAAAGAGCCAAAGCGGAGACGGAGAGGTGTGAGTGGGAGTGGAGGATTGCATGAAGGTTCATCAGAGGAGCCTGAAAAGACTGAGCCAGTTCAAGACACAGTCCCTCATTCATCTGATGGATCAACTCAAACTTTTAAAGTCTCTCCTCCCAAATCTGTTCTCACATCCTTACAATCTTCCCCACCACCAACACCACGAGAGCAGGAACAGACCTCTTCGCCATTACCTTATAGTTGTATAGGTCGAGGACACAACCCCTGTTCTCCAACACATCATTCCCCAGATATGCCTGTCTTGCGGAACTTACCAGTACGCCGAAGGCTAGAAACAGAGTCCCGATTGGCTGCACAGTTAGGAGAGCAATTTTTAGGGAGAGGTAGAGGAGTGGATCGAAAATCTGCATCAACTCAGAAAAGAATAGAAACAAGCACTGACAAGGACGGTTCTGCTCCATGTGACTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38898
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 |
---|---|---|---|---|---|
ENSDART00000003080 | Nonsense | 3161 | 3917 | 32 | 32 |
Genomic Location (Zv9):
Chromosome 12 (position 28659426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26997035 |
GRCz11 | 12 | 27088395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTGTATCTTTACCACACAGCACCTCTACAGCAGCACCATATGAAACTTG[T/A]ACTGATTCTTCTCCTACACTACAGTTTACATATTCTTTCAGAGAGCCTCC
Long Flanking Sequence:
AAAACACCCCCAAGAGCACTGGAGTTGTCAGAAGAAAACACACCTGTAATTGAGAAAACAAGTCCTGAGCGGAGCCCCCCTCACTCACCAAAACGGAAAAGGGGACGTCCTCGTAAAGATTCCACCACAACTACAGGCTCACCCCCATCTTCACCCTCTGCTGGTGCTCCTTCATCCCAAGAGCCTAATTTGTCAAGGTCTAATGTCATGCCTGAGACTTTGCCTACTGACAGTAAAATTTCACCAATAAGCTCTCCAACACTCTGCCCCACTTCACCCTTAAATGCTGCTGAAGTGTCCTCACTTCCAAAACCAGATTCTGAAATAATTCAGACCACTACATCGGTTTTACTGTCCACATCTCCATCAGAAACTGGTGTAGACTCGCATGGTGATACTTACGCCAGTCTGAACACCATAAGTTCATGCAATGACTCTGACAACAGTACACTTGTATCTTTACCACACAGCACCTCTACAGCAGCACCATATGAAACTTG[T/A]ACTGATTCTTCTCCTACACTACAGTTTACATATTCTTTCAGAGAGCCTCCAGTTACTACTGTTTCAATCTGTGCTGAGGAAATTGCCCACACGTCTGTACTTTCTGATGCCAGTGAAATCACTGCTTATTCAGAATCTTTAACTGTCTCAACGGCTGCAGTAGAAGCCGAGGAAAATTCAGTCACGGATAATCAGCAAGTAAATAATTTGCAGCCTTCAAATACATCGACTCAAGTCACTTCACAATGCGTAGATGAAACCGATCCAACTACAGACCTGCCACAAACCACTTTAGAGCCAATATACAGTGTAGCTGAATCTTCTACTCCCACTGATCAGCCATCCATCCAACCTAGTTCTCCACCTGCTTTGACTTCTGAAATTGAACCTGAAGCATCTTCATCTATATTGGAGGCACCAGAAACATCTGCTGTACAGACTGTGTCAACAGTTCAAAGATCTTTACCTCAGTCTGAGCAAATTTCTCCTCCGTCACAACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16953
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 |
---|---|---|---|---|---|
ENSDART00000003080 | Nonsense | 3169 | 3917 | 32 | 32 |
Genomic Location (Zv9):
Chromosome 12 (position 28659448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 26997057 |
GRCz11 | 12 | 27088417 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCTACAGCAGCACCMTATGAAACTTGTACTGATTCTTCTCCTACACTA[C/T]AGTTTACATATTCTTTCAGAGAGCCTCCAGTTACTACTGTTTCAATCTGT
Long Flanking Sequence:
AGTTGTCAGAAGAAAACACACCTGTAATTGAGAAAACAAGTCCTGAGCGGAGCCCCCCTCACTCACCAAAACGGAAAAGGGGACGTCCTCGTAAAGATTCCACCACAACTACAGGCTCACCCCCATCTTCACCCTCTGCTGGTGCTCCTTCATCCCAAGAGCCTAATTTGTCAAGGTCTAATGTCATGCCTGAGACTTTGCCTACTGACAGTAAAATTTCACCAATAAGCTCTCCAACACTCTGCCCCACTTCACCCTTAAATGCTGCTGAAGTGTCCTCACTTCCAAAACCAGATTCTGAAATAATTCAGACCACTACATCGGTTTTACTGTCCACATCTCCATCAGAAACTGGTGTAGACTCGCATGGTGATACTTACGCCAGTCTGAACACCATAAGTTCATGCAATGACTCTGACAACAGTACACTTGTATCTTTACCACACAGCACCTCTACAGCAGCACCATATGAAACTTGTACTGATTCTTCTCCTACACTA[C/T]AGTTTACATATTCTTTCAGAGAGCCTCCAGTTACTACTGTTTCAATCTGTGCTGAGGAAATTGCCCACACGTCTGTACTTTCTGATGCCAGTGAAATCACTGCTTATTCAGAATCTTTAACTGTCTCAACGGCTGCAGTAGAAGCCGAGGAAAATTCAGTCACGGATAATCAGCAAGTAAATAATTTGCAGCCTTCAAATACATCGACTCAAGTCACTTCACAATGCGTAGATGAAACCGATCCAACTACAGACCTGCCACAAACCACTTTAGAGCCAATATACAGTGTAGCTGAATCTTCTACTCCCACTGATCAGCCATCCATCCAACCTAGTTCTCCACCTGCTTTGACTTCTGAAATTGAACCTGAAGCATCTTCATCTATATTGGAGGCACCAGAAACATCTGCTGTACAGACTGTGTCAACAGTTCAAAGATCTTTACCTCAGTCTGAGCAAATTTCTCCTCCGTCACAACTTCAAACTACAGCAATGGAAGCA
Associated Phenotype:
Not determined