Busch Lab

ZMP

LOC100002543

Ensembl ID:
ENSDARG00000069608
Human Orthologues:
AKAP2, PALM2-AKAP2
Human Descriptions:
A kinase (PRKA) anchor protein 2 [Source:HGNC Symbol;Acc:372]
PALM2-AKAP2 readthrough [Source:HGNC Symbol;Acc:33529]
Mouse Orthologues:
AF064781, Akap2
Mouse Descriptions:
A kinase (PRKA) anchor protein 2 Gene [Source:MGI Symbol;Acc:MGI:1306795]
cDNA sequence AF064781 Gene [Source:MGI Symbol;Acc:MGI:3845895]

Alleles

There are 8 alleles of this gene:

Allele Name Consequence Status Availability
sa17580 Essential Splice Site Available for shipment Available now
sa6157 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa15545 Essential Splice Site Available for shipment Available now
sa31762 Nonsense Mutation detected in F1 DNA Not yet available
sa21643 Nonsense Mutation detected in F1 DNA Not yet available
sa34819 Nonsense Mutation detected in F1 DNA Not yet available
sa38773 Nonsense Mutation detected in F1 DNA Not yet available
sa34820 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa17580
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
A > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101431 Essential Splice Site 80 1266 4 12
Genomic Location (Zv9):
Chromosome 10 (position 4778660)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4774954
GRCz11 10 4775258
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAGCTGATGTTGATCAATGACCTSRTGGTAGAAAATRTTTCCGCCTTAC[A/C]GTCTAAAGCCATGAGGGAGAGRTGGCTTCTTCAGGGGACACCAGCGSCGC
Long Flanking Sequence:
AAAAGCCAACAAATAAAATAAACAAGTAATTAACAGGGTGAGAATGAACTACGTCATATCATTAATATCATTTAATATTTTTTAACTAATAATATTTAACAAAAACTTTTCTCCTTTCCCACAGCTGTTACAATTTCTAGCCAATAAATATTGATTATCTGGTTATCTCTATGATCATGGATCATTAAGATGTTTGTACAGTCGTACCTGTTTCAGACTAAATCTCTTTAAAGTGTTCTATTTCGCTCGTGTTTGCGCACTTCGCTCGAGTCCCAAAAAAAAAAAAAACATCACATTTGCCGCCCACACTCAACCAAACTAGCAGACACATTGAGTATAAACCAGACTCAAGGGGTAGAATTGGGATTGGGCCATAGATTATCATTGGATCTACCCTTGTAAGCAGTAATGTGTGGACAATTATTAATCTGAGTGCACTTTAAATAAGTCCCAGCTGATGTTGATCAATGACCTCATGGTAGAAAATGTTTCCGCCTTAC[A/C]GTCTAAAGCCATGAGGGAGAGATGGCTTCTTCAGGGGACACCAGCGGCGCTACAAGAGGAAGACGAAGACCGCAGGAAACAGGTTGAGCAAGATGAACTTCACATCAAAAGGCTAGAGGATACCATTCACAGGTACAGTGATGTTTTTGATGGTTATATATTTTACTGTTCAGTAAGTGGAAATGTATTCATTAAGAAGATGCGCCTAACTGACAAATTAAGAACTGCTCTGTGTGTGAAATATTACAAAGTGAAATTAAAACTGATATTTAAGTGCATGTTCTTTAAACCAATCACAATTAAACTACCCTCAATACTGGATTAAATCAATGTAGGCTCATTATGAAAAGCCCTATATACATTTCTGGAGATCAAATTATGTAGCCAGAGGTATGTATGGCCGCATTTCATCCTTAAAACAAACGATACGAGGCGGTAAAATGTCGTTGCTTTTCATACCTCAGTATGGACGAATTTTTCCGCTGTTACCAGTTTGTCCC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa6157
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101431 Essential Splice Site 203 1266 7 12
Genomic Location (Zv9):
Chromosome 10 (position 4806836)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4803130
GRCz11 10 4803434
KASP Assay ID:
554-5134.1 (used for ordering genotyping assays)
KASP Sequence:
CAAACTCCAGTCTCAGCTTCAGGGGATCATCAGCCGCCAAGAAAACCTGG[T/A]AGGTGGTTGTGKGGGCCGGTGGGAGGGGCTGGAGGGTCACGGGTTTGGAC
Long Flanking Sequence:
GTTACTTCCAAGGTACCAGCGCAATGGTAGATAGGCACTCTGGGTATATCTCTTTTGTAAAACAGGGGGTCCAACGTTAGCCTCTTGGACCATTTCCCTCTTGCCTCAGCTAGACTATTGAACTCCACACACACGCCAATGACTCTGCACTTTGTTCACCCTGATCCGTCTATTCAAAGGGAATCCAGTAACCCACAGCCACCATTGTTTTGCTCTTATTCATTTGCACTGTTTTTGCTGTCTAAGCAATGATCTGCTTCACGGGGAAAAAAAAAAAGGGGGGGGCGAGAGAGAAAGTCAGTTTAGTGAGGGGGATTGGAAGGGGAGGGAGCCAATTCGGTGGGCTCTTGAGCACAGGAATCAAGTTTTAGTTTCTCTTCTGCTCTCCACCGGACAGATGCGGTGAATTACAACTGCTCGCAGATCCCTGGTCTCCCAGAACTGAACTCCCAAACTCCAGTCTCAGCTTCAGGGGATCATCAGCCGCCAAGAAAACCTGG[T/A]AGGTGGTTGTGGGGGCCGGTGGGAGGGGCTGGAGGGTCACGGGTTTGGACCAGAGCCAAAGAGAGGGAACATGATGTAGATGGCGCAGTTACTCACATGTTCTGAGTAAGGGTTGTTTTACATGACAACGTTTTCAGCCCAAAATAGGAACCTGTTGATATGATTTGCCTGATCGTGGAAGTTTTTGAAAATGCCGCCATTGTTGTTTCCGTGTAAACACACAAAGTCATATAAAACGATCTTGTCGTTCATGTGTTTAAGGAAATGCAGACTAAAAGCAAGCACAATCAAACACACACCAATGGCGGAGTCATATTTTGTTGCTCAAGTTTTAGCTAGCGCTTCAGCAGCAAAGTGTCGATTTACTTCACATTGCAGCAAAAGCGAAGATGCATCGTACACATTTACAATAATACAAAGCCATAAGCACCAAGCTGACGTCACTCCCTTACAAGTACTGTCTGTTAACTAATATGTTGACAGTGCCTGCGCAAATGTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa15545
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000101431 Essential Splice Site 203 1266 8 12
Genomic Location (Zv9):
Chromosome 10 (position 4811303)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4807597
GRCz11 10 4807901
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCCACCCSGAGTAGACAYTAACCCACAATCATCTGCACTCTTCCCCAA[G/A]CATTATAYGCCATGGAGATCAATGTGGAGAAGGACCGGAAAACGGGTGCC
Long Flanking Sequence:
TGGTTGGTTGCGTTTTATTTCTTGCATTTAATTTCCCCCTGCAGCCCTTAAGTTGCAAGCCACCAGTTTAGAGCCACTGGCTAGCATCAATCCTATTAGCTGTATCAGAAACAGCTTTGGGTGTTTTTACATTTTTCCTAGCAGATTTCTTTTCAGCGGAAGCTGTTATTAATAACTCGAAAACAAAATTGCAAATCCGTCACCTATAATATAAGAGTAATGGTGCATTTCCATGAAAAATTCAAGAGTTGGTCGTCAACTAAGCTTACATCAGCATACAGCGGTTACTGGCAACAGCGTAATAACAGAGCAAAGGGTAGGTTGAATTTGTTTTTTTCGGCTCTGATTTTAATGCCAGTTATGAAACTGTACAAATATTGCATGGACATAGAGGCATCACTGAAAAAATCCCATTAATATCAAGCATGCCACTTTTTAGTAATGCATGATAGGCCACCCGGAGTAGACATTAACCCACAATCATCTGCACTCTTCCCCAA[G/A]CATTATACGCCATGGAGATCAATGTGGAGAAGGACCGGAAAACGGGTGCCACCAAGATCCTCTCAGCCTCGGCCGTCAGCCCGCAGGACGCTCACCAGAGGGGCGTCAAGGTCTACGACGATGGCCGAAAAGTGATCTACGAGGTGCGTTCTGGGGGATCGACTACAATGGAGAACGGCACGCATGCCTGGAGTCCCGGAGAGATGAACCAACTCATGCAACAAGTCGGCGGGAAGCAACAACCAAGTGACGGAGCACGGGTGACCGTCACGCCAGCGGAGCCACAGCAAACAGGAGGACAGCTGAGCGCCAAAGAGCCCAAGCAGGACAAGAAACAAAACCATAGCAAAGGCTACGAGGGGGAGGTCACGGAGACTCCGAAGGCCTCCGCTGACAAACCCGTCACCATGATCTTCATGGGATACCACAGCATTGAAGACGAAGAGGAGTCCAAGAAGCTGCTAGGCTTTGATGGCACCATCAAGGCCGAGATTGTCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31762
Status:
Mutation detected in F1 DNA
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
ENSDART00000101431 Nonsense 226 1266 8 12
Genomic Location (Zv9):
Chromosome 10 (position 4811373)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4807667
GRCz11 10 4807971
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATGTGGAGAAGGACCGGAAAACGGGTGCCACCAAGATCCTCTCAGCCT[C/A]GGCCGTCAGCCCGCAGGACGCTCACCAGAGGGGCGTCAAGGTCTACGACG
Long Flanking Sequence:
GAGCCACTGGCTAGCATCAATCCTATTAGCTGTATCAGAAACAGCTTTGGGTGTTTTTACATTTTTCCTAGCAGATTTCTTTTCAGCGGAAGCTGTTATTAATAACTCGAAAACAAAATTGCAAATCCGTCACCTATAATATAAGAGTAATGGTGCATTTCCATGAAAAATTCAAGAGTTGGTCGTCAACTAAGCTTACATCAGCATACAGCGGTTACTGGCAACAGCGTAATAACAGAGCAAAGGGTAGGTTGAATTTGTTTTTTTCGGCTCTGATTTTAATGCCAGTTATGAAACTGTACAAATATTGCATGGACATAGAGGCATCACTGAAAAAATCCCATTAATATCAAGCATGCCACTTTTTAGTAATGCATGATAGGCCACCCGGAGTAGACATTAACCCACAATCATCTGCACTCTTCCCCAAGCATTATACGCCATGGAGATCAATGTGGAGAAGGACCGGAAAACGGGTGCCACCAAGATCCTCTCAGCCT[C/A]GGCCGTCAGCCCGCAGGACGCTCACCAGAGGGGCGTCAAGGTCTACGACGATGGCCGAAAAGTGATCTACGAGGTGCGTTCTGGGGGATCGACTACAATGGAGAACGGCACGCATGCCTGGAGTCCCGGAGAGATGAACCAACTCATGCAACAAGTCGGCGGGAAGCAACAACCAAGTGACGGAGCACGGGTGACCGTCACGCCAGCGGAGCCACAGCAAACAGGAGGACAGCTGAGCGCCAAAGAGCCCAAGCAGGACAAGAAACAAAACCATAGCAAAGGCTACGAGGGGGAGGTCACGGAGACTCCGAAGGCCTCCGCTGACAAACCCGTCACCATGATCTTCATGGGATACCACAGCATTGAAGACGAAGAGGAGTCCAAGAAGCTGCTAGGCTTTGATGGCACCATCAAGGCCGAGATTGTCCTTATCGACGAGGATGATGAGAAATCTCTGCGGGAGAAGACGGTCACTGATATCTCCACCATCGACGGCAATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa21643
Status:
Mutation detected in F1 DNA
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
ENSDART00000101431 Nonsense 241 1266 8 12
Genomic Location (Zv9):
Chromosome 10 (position 4811419)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4807713
GRCz11 10 4808017
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCGGCCGTCAGCCCGCAGGACGCTCACCAGAGGGGCGTCAAGGTCTA[C/A]GACGATGGCCGAAAAGTGATCTACGAGGTGCGTTCTGGGGGATCGACTAC
Long Flanking Sequence:
TTGGGTGTTTTTACATTTTTCCTAGCAGATTTCTTTTCAGCGGAAGCTGTTATTAATAACTCGAAAACAAAATTGCAAATCCGTCACCTATAATATAAGAGTAATGGTGCATTTCCATGAAAAATTCAAGAGTTGGTCGTCAACTAAGCTTACATCAGCATACAGCGGTTACTGGCAACAGCGTAATAACAGAGCAAAGGGTAGGTTGAATTTGTTTTTTTCGGCTCTGATTTTAATGCCAGTTATGAAACTGTACAAATATTGCATGGACATAGAGGCATCACTGAAAAAATCCCATTAATATCAAGCATGCCACTTTTTAGTAATGCATGATAGGCCACCCGGAGTAGACATTAACCCACAATCATCTGCACTCTTCCCCAAGCATTATACGCCATGGAGATCAATGTGGAGAAGGACCGGAAAACGGGTGCCACCAAGATCCTCTCAGCCTCGGCCGTCAGCCCGCAGGACGCTCACCAGAGGGGCGTCAAGGTCTA[C/A]GACGATGGCCGAAAAGTGATCTACGAGGTGCGTTCTGGGGGATCGACTACAATGGAGAACGGCACGCATGCCTGGAGTCCCGGAGAGATGAACCAACTCATGCAACAAGTCGGCGGGAAGCAACAACCAAGTGACGGAGCACGGGTGACCGTCACGCCAGCGGAGCCACAGCAAACAGGAGGACAGCTGAGCGCCAAAGAGCCCAAGCAGGACAAGAAACAAAACCATAGCAAAGGCTACGAGGGGGAGGTCACGGAGACTCCGAAGGCCTCCGCTGACAAACCCGTCACCATGATCTTCATGGGATACCACAGCATTGAAGACGAAGAGGAGTCCAAGAAGCTGCTAGGCTTTGATGGCACCATCAAGGCCGAGATTGTCCTTATCGACGAGGATGATGAGAAATCTCTGCGGGAGAAGACGGTCACTGATATCTCCACCATCGACGGCAATGCAGCAGACCTGGTGTCGGGACGGCCTTTGTCCGACACCACTGAACT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34819
Status:
Mutation detected in F1 DNA
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
ENSDART00000101431 Nonsense 299 1266 8 12
Genomic Location (Zv9):
Chromosome 10 (position 4811591)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4807885
GRCz11 10 4808189
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACCAAGTGACGGAGCACGGGTGACCGTCACGCCAGCGGAGCCACAG[C/T]AAACAGGAGGACAGCTGAGCGCCAAAGAGCCCAAGCAGGACAAGAAACAA
Long Flanking Sequence:
TGGCAACAGCGTAATAACAGAGCAAAGGGTAGGTTGAATTTGTTTTTTTCGGCTCTGATTTTAATGCCAGTTATGAAACTGTACAAATATTGCATGGACATAGAGGCATCACTGAAAAAATCCCATTAATATCAAGCATGCCACTTTTTAGTAATGCATGATAGGCCACCCGGAGTAGACATTAACCCACAATCATCTGCACTCTTCCCCAAGCATTATACGCCATGGAGATCAATGTGGAGAAGGACCGGAAAACGGGTGCCACCAAGATCCTCTCAGCCTCGGCCGTCAGCCCGCAGGACGCTCACCAGAGGGGCGTCAAGGTCTACGACGATGGCCGAAAAGTGATCTACGAGGTGCGTTCTGGGGGATCGACTACAATGGAGAACGGCACGCATGCCTGGAGTCCCGGAGAGATGAACCAACTCATGCAACAAGTCGGCGGGAAGCAACAACCAAGTGACGGAGCACGGGTGACCGTCACGCCAGCGGAGCCACAG[C/T]AAACAGGAGGACAGCTGAGCGCCAAAGAGCCCAAGCAGGACAAGAAACAAAACCATAGCAAAGGCTACGAGGGGGAGGTCACGGAGACTCCGAAGGCCTCCGCTGACAAACCCGTCACCATGATCTTCATGGGATACCACAGCATTGAAGACGAAGAGGAGTCCAAGAAGCTGCTAGGCTTTGATGGCACCATCAAGGCCGAGATTGTCCTTATCGACGAGGATGATGAGAAATCTCTGCGGGAGAAGACGGTCACTGATATCTCCACCATCGACGGCAATGCAGCAGACCTGGTGTCGGGACGGCCTTTGTCCGACACCACTGAACTGTCCTCAGAAGGCAAAGAGGAAAGCTCGACCAAGGAACTGCCATCTACAGGTATTGAAAAGAAAAAACGCTGCCAGTGCTGTGCTGTCATGTGACCTATCTCCCGCAACTTCTCTTTCCTGGAGCATATTCACCAAGGCTCTGCCTTCCTCACAAACAAATCTCACCCTCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38773
Status:
Mutation detected in F1 DNA
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
ENSDART00000101431 Nonsense 431 1266 9 12
Genomic Location (Zv9):
Chromosome 10 (position 4831965)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4828259
GRCz11 10 4828563
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGTGACTAGTGTTGTTGTTGTTTTTTGCAGGCAGTGAGAAGGCGCGTT[C/A]AGTCCTGCTGACGGCAGAGAACGGACTCTATCCATCAGCGACTGCACGAT
Long Flanking Sequence:
AATCATAAATCTCTTTCAGGTTCATTGAAGAGAAAGCTGTTCTTGCATTATAGAGATGACCTAGGGGTTGTTTTACAAAAATAATCATATCAAGAAAGCAACAAGACACACCGTAAAAAAGTGTCCACTTAAAGAAAATGACTCCAACGTTTTTAACCTAAAATAATTAAGTAATTTCAACTTAATTTATTGCAGTTTTCAGCAATAAATTACAGTAAGTAAAAAAAAAACAATTCTAAATGTAGTTAAATGTATATTTAGACTTTTAGATTTAACTGGATTATCAAGTAAGACTTCTCTATTTGTTGATTTCGCTGCGTGATTTCTGCTGCTAGTTGTGTATAGGAAACAGAGCAGGTTCATTGTTTTCCTGCAACTCCACCAGGACAGTGTGGAGGATGAATAAATTGATGGATGGTTGCTTAAAGCTCTGATACTGCACTTCATGAATGAGTGACTAGTGTTGTTGTTGTTTTTTGCAGGCAGTGAGAAGGCGCGTT[C/A]AGTCCTGCTGACGGCAGAGAACGGACTCTATCCATCAGCGACTGCACGATTTTCAGACCCTCAGGTGAGTCTAACGGTGATCATATTCGCAGGGCCGGTCTCCTGTTATTTCGGTCTGCTTGAGAAGGTTCATAAGGTGTCTTTAAATTTAAGCCGGGAAACAGTCATAACTCAGAATTGTAGTTTTGTTTAATTTTTAAATGTAGTACATGTGACAGACATGTAACGCAGGATTCATATGTTTTTGATTATTTGTGTGTCTGGAAAATGTTTCTGTTGTCTGTTTCTTATTATTGGACTATAATTACAATTTACTTGTGTCGAGTTCAGACTGGATGATTTTAAAGAAGTCGTGTCACGGATGTTTTCACACTGCATGGCTATCTGGGTTAGCGCTCTGTCGGTGCTGTGTTTACACTGTAGGATGGATCGGCGACAGGAGAGTTCACACTGCATGACTTTAAAATAGGAAGAATCACAGACAACTTTGTCCAAATTAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34820
Status:
Mutation detected in F1 DNA
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
ENSDART00000101431 Nonsense 810 1266 10 12
Genomic Location (Zv9):
Chromosome 10 (position 4892437)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 4888731
GRCz11 10 4889035
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTCGTGCGGTTCTGTCACTGTTGCCAATCAGGAAGGGGTCACATCCTA[C/A]GATGGAAGTGAAGTTACAACAGTCAAAGCTGAAAAGATTTACTGCTGCTC
Long Flanking Sequence:
GAGAAAGAAATTCGGGTGAAGAAAGTGAGACCCTCAGAAGAGGTCGCAGAGCTAGAGAGGGAAAGGCTGGAACTCATCCGGGGACAGGCAGTCAAGAAAAACCCTGGCATTGCAGCAAAATGGTGGAACCCACCTCAGGAAAAGACACTGGAAGAGGAGCTGGAACCAGAGCAGCTGGAGTCGCTTCGAAAGTATGAGGAGAGGAAGCAAAGGAAACCAGAAACCAACCGTATGCCGCAAGCTGCACCCAGACAGACTACCACCTTCATCCAACCTGAAATAGCAAATAAGGAGGACGTTGTCATGGAAGAGATTGACTTTTCTGCAGCTCGCAAGCAATTTCTGCAGATGGAACAAAGCAAGCATCCCACGGTCCCTAAGAGGAATGTGGCACCACAGCTTTACTCAGCCAAACCTTTCTTCAGGACTCCAGAGGTCACGCATGTAGAGAGGTCGTGCGGTTCTGTCACTGTTGCCAATCAGGAAGGGGTCACATCCTA[C/A]GATGGAAGTGAAGTTACAACAGTCAAAGCTGAAAAGATTTACTGCTGCTCTGGAGAATCCTTCATACCCACGAAAGATGGATTATCTCAGAACGAGATGAAGGATGATGACTTTACTTGTGCCCGGGCAGTGATGACCATAGTGAAGGATGAGGATGTCGATTTGTGTCAACGTTCTTTCAACAGCTCCCACCACACAGAAGAAATCGACTCTGGGTTGGATGATCTATCACTACGGTCTCAGGACACCACTGTACTTGAGACGCTCTCCAATGACTTCAGTATGGATAACATAAGTGACAGCGGTGCATCAAATGAGACTATGAGTGCCTACTTGGAAAACTCTCTTGGGGAGTACTCTTTTCCCTCAACCCCGATGGCAACTACACCAATCAATGGAAAACACGAAATCAGTATCAAATCTCCAGGGGATCAGATTGGGACTTATCAGGGAGATGGTTTAACAGAAGAAGAGTTGGAATATCATGCTGGTATTCTTGT
Associated Phenotype:
Not determined