celsr1a

Ensembl ID:

ENSDARG00000069185

ZFIN ID:

ZDB-GENE-030616-78

Description:

SI:bZ6L08.1 (Novel protein similar to human cadherin, EGF LAG seven-pass G-type receptor (CELSR)) [S

Human Orthologues:

CELSR1, CELSR2, CELSR3

Human Descriptions:

cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac
cadherin, EGF LAG seven-pass G-type receptor 2 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac
cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila) [Source:HGNC Symbol;Ac

Mouse Orthologues:

Celsr1, Celsr2, Celsr3

Mouse Descriptions:

cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo
cadherin, EGF LAG seven-pass G-type receptor 2 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo
cadherin, EGF LAG seven-pass G-type receptor 3 (flamingo homolog, Drosophila) Gene [Source:MGI Symbo

Allele Name	Consequence	Status	Availability
sa7553	Missense	Mutation detected in F1 DNA	Not yet available
sa18077	Nonsense	Available for shipment	Available now
sa26316	Nonsense	Mutation detected in F1 DNA	Not yet available
sa33484	Nonsense	Available for shipment	Available now
sa26315	Nonsense	Mutation detected in F1 DNA	Not yet available
sa31402	Essential Splice Site	Available for shipment	Available now
sa30853	Nonsense	Mutation detected in F1 DNA	Not yet available
sa6951	Nonsense	Mutation detected in F1 DNA	Not yet available

Allele Name:

sa7553

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 > G

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000187	Missense	26	1767	1	34
ENSDART00000043737	None	None	1224	None	26
ENSDART00000123617	None	None	1664	None	35

Genomic Location (Zv9):

Chromosome 4 (position 27589314)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28289591
GRCz11	4	28278879

KASP Assay ID:

554-4345.1 (used for ordering genotyping assays)

KASP Sequence:

CTGTACTCTCCGTGTCACCATCATCACTGATGAGATGCTAACAAACAGCA[T/G]CACAGTCCGTCTGGAGAACATGTCCCAGGAACGCTTCCTATCCCCACTAC

Long Flanking Sequence:

GATCTTGAAAGCGCCTGCATGGTATACATTGGCAATAAGCATGTGAAACACTGTAGTCATGCAAGGTCATGCACAATCCCATAACAAGCATTTCAATCCTTTTTGTACTTTTGTGTCAGAAAGCATTTACTGTGTTTTACGGTTGTCAAGTCTCCATTGCTGAGTTTTTAATACCATTAGTTTCAACAGAGAAGACAAGAGTGTGTCCTGAAGCAAGAAACCAAGTGATCTGTGTAATTGTGGTGCAACTGTGTAGTAATCCTATCTGTTAACATGCTTTCTTCTCCAAACCAAAACAGCATTCCGTCTTTCTCAGTGTGAAAAGTGTGAATCTTACAGAAGCTACCTGAAACAATCTAGTGCTTTAATAATAAGGTTGTGTTTTCATGACGTTTTTAACAGTAAGTTGTTTCTATATTTTTCAGATGGGATCCACCAAGTCACTGCCTTCTGTACTCTCCGTGTCACCATCATCACTGATGAGATGCTAACAAACAGCA[T/G]CACAGTCCGTCTGGAGAACATGTCCCAGGAACGCTTCCTATCCCCACTACTCTCCTTGTTCGTCAAAGGTGTAGCAGCTGTCCTCTCAACTAGTCGCGAAGGAGTTTTCATCTTCAATGTCCAGAACGACACGGACGTCAGTGGAAACATCCTCAATGTCACCTTCTCCGCCTTGCTCCCAGGAGGAGTTCCGGATCGCTACTTTCCTTCGGAGGAGCTTCAGGAGCAGATCTACCTGAACCGTACTCTGTTACAGGAAATCTCCAGCCAAAACGTCCTACCATTCGATGACAACATCTGCCTAAGGGAACCTTGCGAGAACTACATGAAATGCGTCTCTGTATTAAAGTTCGACAGCTCTCCACCTTTCATAGCTTCTGATACTGTTCTCTTCAGACCAATACATCCTATTAATGGTCTTCGCTGCCGTTGTCCGGCCGGCTTCACTGGAGACTACTGTGAGACTGAGATTGACCTGTGTTACTCAGGGCCATGCCGCA

Associated Phenotype:

Not determined

Allele Name:

sa18077

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000187	None	None	1767	None	34
ENSDART00000043737	None	None	1224	None	26
ENSDART00000123617	Nonsense	284	1664	6	35

Genomic Location (Zv9):

Chromosome 4 (position 27543073)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28243350
GRCz11	4	28232638

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGCATGAGRAACCTGACAATTGACAGTAAATCARTTGACATGGCCAGTTA[C/A]ATTGCCAACAAWGGCACTACCGAAGGTTAGCCACAAATCATTACATTGCT

Long Flanking Sequence:

AAACTGTGTACCTGTTTATAATTTATTTGTACTGCAAAAACTTTAAGAAATTACCTGTTTTATTATATAATATATCAATAAATCACCCAATGAGGTAAACAAAATAATCATATGTCAAAAGAAAAAACAATTATAATTTTGCTTACCCAATTGGTTGATTATTTTGTTTGTTTTAAGGAAAAACTCTCCTAATTGTGGCATATTATTTTTTTAAGACAAGACAATATTTTTGCTTGTCTAAAAACACTTCTTGATTTAAGAACTTGTAGAAATTGGGACTACAAAAAAGACAAAAAGTAAGAAAAGCTTTTTTTTTTTGCAGTGTACTATGGTGGATATTTAAGTGTTTCATCTCTCTTCAGGTCTTTGGATCTCACTGGACCACTTTTACTTGGCGGTGTTCCAAATCTTCCGGAGGATTTCCCCATACGGAACCGGGACTTCGTGGGTTGCATGAGGAACCTGACAATTGACAGTAAATCAGTTGACATGGCCAGTTA[C/A]ATTGCCAACAATGGCACTACCGAAGGTTAGCCACAAATCATTACATTGCTTGCTGATCAACTTTCGAATAGTTGTAATTCCTTAACTCTTGTATTCTGATTTTGAGGCTTTGGCCACAGCTTTCACAGTGTTTCAGCAAATAGACTAATTGTTTATGACACAGATTTTGTGAAAATGCTTTGGAATTTTTAAAAACTCAACAATACACTCAGGGTAAATTGTATTCTAGTGGTTGTTTTTGCTCTTTTTACTTTCATTATAATGACTTTTTTTTTCAAAGCAGTGACACTATATAGTCGTGCATTCTTGATTGTTGGTGGTTTGGAGGTACACTTTATCATTTTACTGTTGATCAGCAGTTACAGTGCTAAATAAAGCGTATTTTCTGGGTTTTATAAGCATTATAGTGTGAGTGTAAGAGAGTGTAAGAGTGCACACCTACCTTGAAATGTTTGAGAAAATCAAAAATAAGCAACTCTTAGAACATGGTAAACATAGTA

Associated Phenotype:

Not determined

Allele Name:

sa26316

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000187	None	None	1767	None	34
ENSDART00000043737	Nonsense	62	1224	2	26
ENSDART00000123617	Nonsense	397	1664	9	35

Genomic Location (Zv9):

Chromosome 4 (position 27533171)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28233448
GRCz11	4	28222736

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AACTATATGTTTATATACCATGATTTTTTTTTTAAGATAAGAGACAAGTA[T/A]GTGCAGTTTGAAGTGCTTCTCGGAGAGCAGAAGGTGGCCGTGCTGGATTT

Long Flanking Sequence:

GTAAAATAATTCATTATTTTGATAAATTGATCATTTTAAAGGGGGCAGTCATAAAAAAAAAAAAAAAAAAAAAAATATATATATATATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTTTTTTTTTTTGATAATTTTTCAGATTATTTTTTTATTTTAAGCAAGATGCTGATGGGCTAATTTGATTCAATGGTTTATGCTAAGGTAAGCTAAAATTGCTCCGGCCAGACCTGGAGACTGGCTGAATGTATAAAAAAAAATGTAAATCTTTTGTTAGTTTTTTTTTGGAGTAAGATGCTAATAGTGTAATCTGATTCAATGATCTATGCTAGGATAAGATAAAAGGGCTCCCGTCAGACCTGGGATTGGCTGAATGGGTTAAAAAAATGTAAATATAAAAAGGTAGTGTTTCTTTAACGCAATGTTTTGGTTTTTAAACTATATGTTTATATACCATGATTTTTTTTTTAAGATAAGAGACAAGTA[T/A]GTGCAGTTTGAAGTGCTTCTCGGAGAGCAGAAGGTGGCCGTGCTGGATTTCACAGATGTCCGAGTGAATGACGGGGAATGGCATCACCTGCTCGTGGAGCTGAGGAGCAGCAAAGATGGGAAGGACACAAAGTACATGGCACAGGTGCTTCTGGACTACGACATGTTCAAGGTCAGTTCTGCAGCACACCAGCTCAACAAATCAAAGCAGTTCTTGTATAAAACCTGCATAATATGGTGCTTTTGTGTGTTTTACAGAAGTCAGTAGAGATAGGAAATGAGCTTCCTGGACTCAAACTGAAGAGTTTTTTCATTGGTGGACTTCAGGGCCAGCGTGACATTGTCCAGCAGGGGTTTAAGGGATGCATGCAGGTGAGGCCAAAATATTTAGTAGCAGTTGTGAATTAAATTTAAAGTGTAATAAGCTGATTTTTGATGGTAAAAGAAGTATATAGTTTATTCAAGTTCGTTAAATACATGTTTTGTTTTGAAATTTAATAA

Associated Phenotype:

Not determined

Allele Name:

sa33484

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

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000187	Nonsense	750	1767	14	34
ENSDART00000043737	Nonsense	320	1224	7	26
ENSDART00000123617	Nonsense	655	1664	14	35

Genomic Location (Zv9):

Chromosome 4 (position 27527707)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28227984
GRCz11	4	28217272

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTATCAGCCAAAAGACAGTGACACCTGTTTCCCCTGTGACTGCTTTCATT[T/A]GGGCGCCAACTCGCGAACATGTGACCCAGAGACGGGACAGTGCCCTTGCA

Long Flanking Sequence:

GAATGAGATTAAAGTTTTTCGATTGTCCAACAGGCTGCAGAAGATGTTCTCAACCTTACACCACATTCTGTCTTTATATTACGCACTTAGCCATAAAGTGCTCTGCGTTGTGAGACAAAGGGGGAAAAAAAAAACTCTCAAAAAAAACTCTTTTTGGGACAACTTGAATGTTCTATGTGCCTTCCACATGAATTTGTAAAAATGCTTTCTTACAAAAGTCAACTTAAATGATTTGTGTTGGCACAACATGAAGGTATTATGTGGAACACTTGCTACTTCTAAAAAAAAAGCAAAAGAAAAAAAAAACAATTTTTTTTTCATTTACATAAACGAAAGTGTCAGAGGTAAACGTGTAAATGTAAATGTGGTTGACTCAACATGAAGTCAAATTTATTTTGAACTTTAGAGATTGTTACATTACTACAGTGTTTCTTTCACACAGGACAACTACTATCAGCCAAAAGACAGTGACACCTGTTTCCCCTGTGACTGCTTTCATT[T/A]GGGCGCCAACTCGCGAACATGTGACCCAGAGACGGGACAGTGCCCTTGCAAGGCGGGTGTGATTGGGCGACAGTGCAACCGCTGTGACAACCCTTTCTCTGAAGTGACTAGCACCGGCTGTGAGGGTATGTACCAATTTTTGTTCATTCAAGTATCTTTTTGCAGAAATTATATATATAAAGTACCAACATAATGTTTTCTGTGTTGTTACCTACTAGTTGGATATGAGGGCTGTCCAAAAGCCTTTGATTCTGGAATCTGGTGGCCCAGGACTAATTTTGGTTTCCCTGTGGCAATGAATTGCCCCAAGGGATCTATTGGTGAGTGAAACAGGCCTTTTTATCTTCACAAAATTATTGTATTTAAGCTAAAGAACAAAAATGACAGACACATTTGAGGTTTAATCAATAACTTTTTGTATTTTATTTTAGGCTTCAACTTTTTATATGTTATGTGGTGCATCAATTATTTTATTTCAACCATTATGCTATTATTCGGTT

Associated Phenotype:

Not determined

Allele Name:

sa26315

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000187	Nonsense	822	1767	15	34
ENSDART00000043737	Nonsense	392	1224	8	26
ENSDART00000123617	Nonsense	727	1664	15	35

Genomic Location (Zv9):

Chromosome 4 (position 27527399)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28227676
GRCz11	4	28216964

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTGGTGGCCCAGGACTAATTTTGGTTTCCCTGTGGCAATGAATTGCCCC[A/T]AGGGATCTATTGGTGAGTGAAACAGGCCTTTTTATCTTCACAAAATTATT

Long Flanking Sequence:

ATTTTTTTTTCATTTACATAAACGAAAGTGTCAGAGGTAAACGTGTAAATGTAAATGTGGTTGACTCAACATGAAGTCAAATTTATTTTGAACTTTAGAGATTGTTACATTACTACAGTGTTTCTTTCACACAGGACAACTACTATCAGCCAAAAGACAGTGACACCTGTTTCCCCTGTGACTGCTTTCATTTGGGCGCCAACTCGCGAACATGTGACCCAGAGACGGGACAGTGCCCTTGCAAGGCGGGTGTGATTGGGCGACAGTGCAACCGCTGTGACAACCCTTTCTCTGAAGTGACTAGCACCGGCTGTGAGGGTATGTACCAATTTTTGTTCATTCAAGTATCTTTTTGCAGAAATTATATATATAAAGTACCAACATAATGTTTTCTGTGTTGTTACCTACTAGTTGGATATGAGGGCTGTCCAAAAGCCTTTGATTCTGGAATCTGGTGGCCCAGGACTAATTTTGGTTTCCCTGTGGCAATGAATTGCCCC[A/T]AGGGATCTATTGGTGAGTGAAACAGGCCTTTTTATCTTCACAAAATTATTGTATTTAAGCTAAAGAACAAAAATGACAGACACATTTGAGGTTTAATCAATAACTTTTTGTATTTTATTTTAGGCTTCAACTTTTTATATGTTATGTGGTGCATCAATTATTTTATTTCAACCATTATGCTATTATTCGGTTGTTGATCTATCATCCATTTTTGAATCGCTACTTTTTTCTACAACTTTTAGATGTTTACAATTAGGCCTGTCACAGTAATCAATACATCGACTTATCGTACAATGCTCATTTTTAATGACTCAATATATGCTGGCCATCAGGCCATTATGAGTGGGCATCTGCTACGTTTTAGCTGATTGCACTATGAGTTTAACCTCTGTTGGACAACTACAATGCTTACCAGCAAGAAAGGGAGAATTTTCACATTTTACTGAAAAATAGCTACAGTCCATATGAGAAACGATTAACAATGAACATTAAAGTCCGTT

Associated Phenotype:

Not determined

Allele Name:

sa31402

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

Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000187	Essential Splice Site	989	1767	18	34
ENSDART00000043737	Essential Splice Site	559	1224	11	26
ENSDART00000123617	Essential Splice Site	894	1664	18	35

Genomic Location (Zv9):

Chromosome 4 (position 27523854)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28224131
GRCz11	4	28213419

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGAGGAAGACTTACCTGAAACCCTTCATCATCGTAACAGAGAATATGGG[T/A]GAGCATTGCTAAAAGTATCTTGCGTAGAACTTAAATGTAGTTTTAAGCAT

Long Flanking Sequence:

TTTAGGGGGATTTTTCTGTTGGTCTTTGCTGGGCTTGAAAAAAAAGTCTTTAGCAGCCCAAAATTGCATGCTTTTAGTGGTTTAGCAGATTAGTGTAAATAACACAGTGTATAGTGACTACTGTCATGAGAACGAAAACGCCCACGTTTAAAGCGCATCTGGCAACATGAACATGCTTATCATGATACATGGTTTTAGGATAAGGATGCGTTTTAGGGCCGCATTCATTATGTCTAGCCTTGGAACAGATTCAGACTTCTAATGGCTCTCAAATGTCCAGAATTTGACCCTGAAATATGTTTCTGAATGCTGTAGAACCTAGTGAAGGCTGGCAGCGCAATCCTGGATGCCAGTAATAAAGAGCACTGGGATCAGATACAGAGAACAGAAGGGGGCACGGCAAATCTGCTCAAACACTTTGAGGAATATGCCAACACTCTGGCTCAGAACATGAGGAAGACTTACCTGAAACCCTTCATCATCGTAACAGAGAATATGGG[T/A]GAGCATTGCTAAAAGTATCTTGCGTAGAACTTAAATGTAGTTTTAAGCATGGTTTTGAAAACTGGACAGTTCTTTATTAACCTTTTTTTATGACAGTTTTTGCAGTGGATTACTTGGTCACTTATCCAGATGCAACAAAAGTACCCAATTTCCAAACTACTGACCAGGAGTGTCCCAAAGACCTCAAGTCTTCTGTACTTTTCCCAGAATTCAGCTTCAAATCATCAGAGCATAAAGGTAAAACTTACAATATGGCAACAAAAAGACATTGAATTTGGAATTTCTGTAATAAATATCTTCTAAATTGGACATGACAATATAAAATTAATGAGAATAAATATTATATTTCAATACATTTGTGTTCACTCTCGTATATACTTAATCACTAAAAAAAACTTGAGTTTTCCCACAAAAACTTTGTTTCCTAGAAATGTAGCATTTATTGTAAATATCATTAAACAAAATCTCTTATTATATTAAAAAGGTCTTAAAATGGCGAG

Associated Phenotype:

Not determined

Allele Name:

sa30853

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
ENSDART00000000187	Nonsense	1121	1767	21	34
ENSDART00000043737	Nonsense	654	1224	14	26
ENSDART00000123617	Nonsense	1038	1664	22	35

Genomic Location (Zv9):

Chromosome 4 (position 27521555)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28221832
GRCz11	4	28211120

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAGCGCAACTGTGTACAGTGAAGGTCAGCCATTGCACATTCCTCTGGAG[C/T]GACCAATCACACTGGACTATAACCTTCTGGAGACCGAGGAGAGAACCAAA

Long Flanking Sequence:

TAGTTGCTAGCATTAAAAATAATAATAATAGTCTGTGCTTTTCTGTATTATCGAGTCATCAAATTTAAAAATAGCCGGATGCAGAAATGCCACATTTTGCACATGAACACTCTTGCTCTAGTTTCACCTACAGATGATCCAGAATTTCAGATCAACTCTGATGAAGAGGAGAAGCAGGCTACAAACAAGAGAAAAAGGCATGTTGAGACCATTCCTCCATTTCCTGTGGCTTCAGTCATCATCTATAAAACTCTAGGCCAGTTTCTACCAGAGCACTACGACCCTGACCGCCGCAGCCTCCGGTACAGAGCGCTTGTTCATCTGTATAGTGCCTGTCCAAATATTTAGTCTTGGTGACATTCCACAGCCACTCTGTTGCCATGCTGAGAAAGTTTGTGTTTTTTTTTTTCCACAGGGTGCCCAATCGCCCAGTCATTAACACTCCCATCGTGAGCGCAACTGTGTACAGTGAAGGTCAGCCATTGCACATTCCTCTGGAG[C/T]GACCAATCACACTGGACTATAACCTTCTGGAGACCGAGGAGAGAACCAAACCTGTGTGCGTCTTCTGGAACCACTCCATCACGTGAGTCCTAAACAATAATTCACTTTTTATTCTTCAGTTATGAAACTAACAAAACAAACATTTCAGAAATCAGTTTAAAGGGGCAGTTCACCCAAAATACAATTCTGTCATCATTTACTCATCCTTCATTTCTTCAAAACCTGTTTGAGTTTCTTTCTTCTGTTTCCAAACAATATATTTTTAAAAAATGCTGGTTACTGGGACCAATTGACTTCCATATTAAGTTTTCAACCAGCTTTCTTCAAAATACCTCTTTTTTTAACTCAAAAATGTTTAAAAACACAGAAGGTAAACAAAATAATGAGGTAATTTCCATTTTTGGGTGAACTATCCCTTTAAGTAGCTGATTTGCACATAATTAACACCAGTTTGATATTTTTCTCCGTGTCAGTGTTGGTGGAGCAGGCGCTTGGTCATC

Associated Phenotype:

Not determined

Allele Name:

sa6951

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000000187	Nonsense	1333	1767	25	34
ENSDART00000043737	Nonsense	866	1224	18	26
ENSDART00000123617	Nonsense	1250	1664	26	35

Genomic Location (Zv9):

Chromosome 4 (position 27514114)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	28214391
GRCz11	4	28203679

KASP Assay ID:

554-5223.1 (used for ordering genotyping assays)

KASP Sequence:

CTGGCTGTGGGTTTGGATCCGCAAGGATATGGCAACCCTGACTTCTGCTG[G/A]CTGTCCGTCCACGACACCCTCATCYGGAGTTTTGCTGGACCCATCGCTGT

Long Flanking Sequence:

AATCTTAAGGGTAATTACAACCTTAATTCATCTGTTTTTATTCCTGCCAACCAAACATAATGAATACTTTCCAAAAGATCAACTATTTTAGTAAACACTGTGAAAATATCCATGCTATATGTTAAACCTCACTTGTGAAAAAGATGAGAAAAAAAATCAATGAGGGCTAATAGTCTTTTAGAAGCACAATTAAACACTCAAGAAAGTGTTTTACATTTAAAAAGTTAATACGATGTTAAAAAGAATATTGAATGCATAGAAACTTTTAAAAACGCCCTAGAATTTTCTCAGAATACCCAGGTAATGCCATAACAGGGCCCTGGCAATCAAGGACTTGGATGATAGTTACTTTATCCTAACTTATAACAGAAAATCCTGCTTTTTAAAGATAACGATAACAATCCTGCTTTTTGAATAACAAGTCATATTAATATTTGCATCACATCAGGTCTGGCTGTGGGTTTGGATCCGCAAGGATATGGCAACCCTGACTTCTGCTG[G/A]CTGTCCGTCCACGACACCCTCATCTGGAGTTTTGCTGGACCCATCGCTGTGGTGGTACTGGTGAGTCCATCCAGCAGTTATTTACTGAACCATTTAAAGCAGGGGTGCACAAATTCGGCCCTGGAGGGGCAGTGTCCTGCATATTTTAGTTCCAACCCCAATTAAACACACCTGTCAAAGGAATCTGGAGCTAAACTATGGAGGACACCGGCCACTCCTGGACACTCCTGATTTAAAGTAAGAAAACTGATAAAGTTGCCATCATTTACTCATTATTCGCTTGTCACTGTTTGAGTTTCTTTTTTCTATTAAACGTAAAAGATGTTATTTTAACCTTTAACTTCCATAGTATTTGTTTTCTCTACTTTGGAAGTCAGTTGTAACATTTCAACAGAATCAAGAAACTCATAAAAGTTTAAAACCACTAGTATGGGAGAGTAAATTTTTTTTAATTTTGAATGAACTATCCTTTTAACGTTCTCTCTATCCACATTAACGCA

Associated Phenotype:

Not determined

ZMP

Alleles

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details

Mutation Details