Grand Champion REAL WORLD MOSHI MOSHI

Similar documents
GENETIC ANALYSIS REPORT

An Overview of Feline Diseases & Traits

Basic color/pattern genetics. Heather R Roberts 3 November 2007

pattern, full albino AR Brown/red color variant MC1R Melanocortin receptor 1

The Rest of the Story. Fine Points of Mendelian Genetics. Alleles don t necessarily come in two forms only! The Rest of the Story 3/9/11

Cat Breeds & Types. I. Cat Categories. II. Breed Registries. Kolts & Kitties Combined Cat Info

Studying Gene Frequencies in a Population of Domestic Cats

GENETIC ANALYSIS REPORT

SIBERIAN SUNSHINE. The new colour which came in from the cold? Eleonora Ruggiero Silvia Perego v.2017

No tail (Manx) is a dominant trait and its allele is represented by M The presence of a tail is recessive and its allele is represented by m

GCCF REGISTRATION POLICY FOR BRITISH SHORTHAIR CATS. Final Document V.1.7 (rev 5 March, 18)

The International Cat Association, Inc. Scan this QR tag from your Smartphone or Tablet to find out more about TICA.

AGREEMENT PROTOCOL. between the Parties

Exceptions to Mendel's Rules of Genetics

BRITISH SHORTHAIR GROUP COMMITTEE

Genetics Practice Problems. 1. For each genotype, indicate whether it is heterozygous (HE) or homozygous (HO) AA Bb Cc Dd.

Non-Mendelian Genetics

The TONKINESE BREEDING POLICY

GCCF REGISTRATION POLICY FOR BRITISH SHORTHAIR CATS. Proposal for Revision 2012

Eastern Regional High School

Here are some ground rules that you should ALWAYS follow when tackling an Inheritance Problem:

SUNSHINE COLOUR IN SIBERIAN CATS

The Governing Council of the Cat Fancy of Ireland

Sample Size Adapted from Schmidt, et al Life All Around Us.

Genetics Intervention

Incomplete Dominance, Co-Dominance, and Sex-linked dominance NON-MENDELIAN GENETICS

Complex Patterns of Inheritance Puzzle Stations Station #1: Multiple alleles, blood types

A cat that has two colours (or three in the case of torties) i.e. white and any other solid (or tortoiseshell) colour.

Visit for Videos, Questions and Revision Notes.

1. For each genotype, indicate whether it is heterozygous (HE) or homozygous (HO) Ii Jj kk Ll

Two-Factor Crosses. All of the resulting F 1 offsrping had round yellow peas (RrYy).

CAIRN TERRIER DNA test Results sent direct to KC Owner submission to KC Not recorded by the Kennel Club AB required AB rec'd Patent Genindexe

Genetics and Heredity Project

Station 1. Using the cards, match the vocabulary word with its definition. If there are any words you do not know, write them down if you have time!

THE TRADITIONAL CAT ASSOCIATION, INC. 1987

Non-Mendelian Genetics

B- indicates dominant phenotype

Patterns of Inheritance. What are the different ways traits can be inherited?

MERSEYSIDE CAT CLUB. SCHEDULE of the THIRTY-SIXTH ALL BREEDS CHAMPIONSHIP SHOW OPEN TO ALL. (Under Licence and Rules)

1 st Type basic vocabulary and setting up Punnett Squares:

GENETICS PRACTICE 1: BASIC MENDELIAN GENETICS

MERSEYSIDE CAT CLUB. SCHEDULE of the THIRTY-FIFTH ALL BREEDS CHAMPIONSHIP SHOW OPEN TO ALL. (Under Licence and Rules)

Biology 3201 Sex Linked Review Mr.Gillam Name:

THE IMPORTANCE OF CLINICAL GENETICS (Part II)

Colour and Pattern Guide for Domestic Cats

Homework Packet. Interactive Notebook. Unit Assessments. Exam-Genetics 100. Lab-Baby Reebops 25. Project: Genetic Disorders Planner 35

List of breeds, which are recognized and admitted by the WCF

GENETICS 310 PRACTICE EXAM I-1 ANSWERED

This information was gained from some research and a lot of personal experience. Lean and muscular bodies, large almondshaped

Step 4: All of the offspring will be rw. So the genotypic ratio is: 4 : 0 : 0 rw ww rr

AP Biology Genetics Practice Alternative Modes of Inheritance

Genetics #2. Polyallelic Traits. Genetics can be very complicated.

Manx Breeding, Registration policy and Standard of Points - suggested amendments Karen Kempsell - 16 th February 2013

Sex-linked Inheritance

Biology 120 Lab Exam 2 Review

What is Codominance?

The Governing Council of the Cat Fancy of Ireland

A Guide to Physical Characteristics of Cats

Marking the Judge s Book and Show Mechanics

Sex-linked/incomplete dominance/codominance quiz

S t r a y. The Cat Sourcebook for USCMC sorensen/crane

PERSIAN [PER] (Standard Source: FIFe 1987)

Welcome to Jeopardy! Genetics. Please get your blood typing lab out for me to check. Come up to my desk with your partner

BREED CODE MCO: MAINE COON GENERAL TYPE STANDARD

Balinese Breeding Policy

Genetics Lab #4: Review of Mendelian Genetics

Test results - Known disorders in the breed

Genetics Lab #4: Review of Mendelian Genetics

Cat Round Robin Questions. 1. What do you call an intact male cat? An intact female? A baby? (A Tom, a Queen, a kitten)

AYCI: Do NOT use your notes. This fish picture is an example of codominance. IN YOUR OWN WORDS, write an explanation of codominance based on what you

1 This question is about the evolution, genetics, behaviour and physiology of cats.

Heredity and Genetics Noteguide (Spring Semester)

MERSEYSIDE CAT CLUB. SCHEDULE of the THIRTY-FIRST ALL BREEDS CHAMPIONSHIP SHOW OPEN TO ALL. (Under Licence and Rules) TO BE HELD ON

TICA ELECTION Christine Lupo TICA Ragdoll Breed Committee

Genetics Extra Practice Show all work!

Biology 120 Lab Exam 2 Review

Name Period G eni G ames Worksheet Packet 1

Feline Genetics: a Combinatorial Approach Massimo Picardello

8.2- Human Inheritance

The Devon Rex. CFA Judges Workshop

Questions from last week. You have a mouse with red eyes and a mouse with blue eyes. How could you determine which is the dominant trait?

Different versions of a single gene are called allleles, and one can be dominant over the other(s).

Beauties and the Beasts

Incomplete Dominance and Codominance

NON MENDELIAN INHERITANCE PART III

SCOTTISH FOLD. Breed Council Secretary: Bruce Russell Cambridge, Ontario Total Members: 29 Ballots Received: 16

Mendelian Genetics Part 4: Dihybrid Cross

Genetics. What s Genetics? An organism s heredity is the set of characteristics it receives from its parents.

Biology 120 Structured Study Session Lab Exam 2 Review

Name: Project RECEIVED: Project DUE: Project is worth total points

Proceedings of the 33rd World Small Animal Veterinary Congress

Sponsored by HAPPY CAT, Naturally Healthier SCHEDULE OF THE. (Held under License & Rules of the GCCF)

NATIONAL CAT CLUB 9 th DECEMBER 2017 MRS GILLIAN CORNISH

Level 1 Science, 2011

SIAMESE [SIA] (Standard Source: FIFe 1987)

Karyotypes Pedigrees Sex-Linked Traits Genetic Disorders

Beyond Mendel. Extending Mendelian Genetics. Incomplete Dominance. Think about this. Beyond Mendel. Chapter 12

UNICORN GENETICS Understanding Inheritance

Station 1 Background Information: Punnett Square Problem: Questions:

Maine Coon American Longhair

Transcription:

Grand Champion REAL WORLD MOSHI MOSHI Gene Inheritance Probabilities Based On 4 Generations of Ancestors Category: All Genes, Alleles Present Sire: CH REAL WORLD BILLY BOY OF ARROW Full Breed Desc.: Copper-Eyed White Persian Breed Genotype: ll Pattern Genotype: aa Colour Genotype: Ww Disease Genotype: pkdpkd Phenotype: White Carried Traits: non-agouti + classic tabby Dam: REAL WORLD DIVA Full Breed Desc.: Red Persian Breed Genotype: ll Pattern Genotype: aa Colour Genotype: OO ww Dd Phenotype: Red Classic Tabby Carried Traits: dilute Gene A - Agouti (A- Agouti, a- Non-Agouti) Assumed background allele frequencies: A=50.00% a=50.00% 0.00% probability of A present 100.00% probability of a present Gene C - Albino (C- Full Color, cb- Burmese, cs- Colorpoint, ca- Blue-Eyed Albino, c- Pink-Eyed Albino) Assumed background allele frequencies: C=100.00% cb=0.00% cs=0.00% ca=0.00% c=0.00% 100.00% probability of C present Gene B - Chocolate (B- Black, b- Chocolate, bl- Cinnamon) Assumed background allele frequencies: B=50.00% b=50.00% bl=0.00% 98.44% probability of B present 29.69% probability of b present Gene D - Blue Dilution (D- Undiluted, d- Dilute) Assumed background allele frequencies: D=50.00% d=50.00% 100.00% probability of D present 100.00% probability of d present Gene S - White Spotting (S- High-Grade White Spotting, s- No White Spotting) Assumed background allele frequencies: S=0.00% s=100.00% 100.00% probability of s present Gene W - Dominant White (W- White, w- Not White) Assumed background allele frequencies: W=0.00% 100.00% probability of W present 100.00% probability of w present Gene L - Longhair (L- Shorthair, l- Longhair) Assumed background allele frequencies: L=0.00% w=100.00% l=100.00% Feb 18 2012, 22:06 1

100.00% probability of l present Gene Re - Devon Rex (Re- Not Devon Rex/Sphynx, re- Devon Rex, hr- Sphynx) Assumed background allele frequencies: Re=100.00% re=0.00% 100.00% probability of Re present Gene R - Cornish Rex (R- Not Cornish Rex, r- Cornish Rex, rg- German Rex) Assumed background allele frequencies: R=100.00% r=0.00% 100.00% probability of R present hr=0.00% rg=0.00% Gene Ro - Oregon Rex (Ro- Not Oregon Rex, ro- Oregon Rex) Assumed background allele frequencies: Ro=100.00% ro=0.00% 100.00% probability of Ro present Gene Se - Selkirk Rex (Se- Selkirk Rex, se- Not Selkirk Rex) Assumed background allele frequencies: Se=0.00% 100.00% probability of se present Gene Wh - Wirehair (Wh- Wirehaired, wh- Not Wirehaired) Assumed background allele frequencies: Wh=0.00% 100.00% probability of wh present se=100.00% wh=100.00% Gene Mc - Mackerel/Classic Tabby (Mc- Mackerel Tabby, mc- Classic Tabby) Assumed background allele frequencies: Mc=25.00% mc=75.00% 38.96% probability of Mc present 95.21% probability of mc present Gene Ta - Ticked Tabby (Ta- Ticked Tabby, ta- Unticked Tabby) Assumed background allele frequencies: Ta=0.00% 100.00% probability of ta present Gene Sp - Spotted Tabby (Sp- Spotted Tabby, sp- Unspotted Tabby) Assumed background allele frequencies: Sp=0.00% 100.00% probability of sp present Gene Dm - Dilute Blue Modifier (Dm- Dilute Modified, dm- Not Dilute Modified) Assumed background allele frequencies: Dm=0.00% 100.00% probability of dm present Gene I - Inhibitor of Melanin (I- Silver, i- Unsilvered) Assumed background allele frequencies: I=0.00% 100.00% probability of i present ta=100.00% sp=100.00% dm=100.00% i=100.00% Gene O - Red (O- Red, o- Black) Assumed background allele frequencies: O=50.00% o=50.00% 100.00% probability of O present 0.00% probability of o present Gene Rdg - Generalised PRA - PRA (Rdg- Not PRA, rdg- PRA) Assumed background allele frequencies: Rdg=99.00% rdg=1.00% 99.99% probability of Rdg present Feb 18 2012, 22:06 2

1.99% probability of rdg present Gene Rdy - Centralised PRA - CPRA (Rdy- CPRA, rdy- Not CPRA) Assumed background allele frequencies: Rdy=1.00% 1.99% probability of Rdy present 99.99% probability of rdy present rdy=99.00% Gene Gcl - Globoid Cell Leukodystrophy - GCL (Gcl- Not GCL, gcl- GCL) Assumed background allele frequencies: Gcl=99.00% gcl=1.00% 99.99% probability of Gcl present 1.99% probability of gcl present Gene Ga1 - Gangliosidosis GM1 - G-GM1 (Ga1- Not G-GM1, ga1- G-GM1) Assumed background allele frequencies: Ga1=99.00% ga1=1.00% 99.99% probability of Ga1 present 1.99% probability of ga1 present Gene Ga2 - Gangliosidosis GM2 - G-GM2 (Ga2- Not G-GM2, ga2- G-GM2) Assumed background allele frequencies: Ga2=99.00% ga2=1.00% 99.99% probability of Ga2 present 1.99% probability of ga2 present Gene Spi - Sphingomyelinosis - SPI (Spi- Not SPI, spi- SPI) Assumed background allele frequencies: Spi=99.00% spi=1.00% 99.99% probability of Spi present 1.99% probability of spi present Gene M - Manx Tailed (M- Manx, m- Not Manx) Assumed background allele frequencies: M=1.00% 1.99% probability of M present 99.99% probability of m present m=99.00% Gene No - Neuroaxonal Dystrophy - NO (No- Not NO, no- NO) Assumed background allele frequencies: No=99.00% no=1.00% 99.99% probability of No present 1.99% probability of no present Gene Clp - Cleft Lip/Palate (Clp- Not Cleft Lip/Palate, clp- Cleft Lip/Palate) Assumed background allele frequencies: Clp=99.00% clp=1.00% 99.99% probability of Clp present 1.99% probability of clp present Gene Aos - Aortic Stenosis - AOS (Aos- AOS, aos- Not AOS) Assumed background allele frequencies: Aos=1.00% 1.99% probability of Aos present 99.99% probability of aos present Gene Cut - Cutaneous Asthenia - CUT (Cut- CUT, cut- Not CUT) Assumed background allele frequencies: Cut=1.00% 1.99% probability of Cut present 99.99% probability of cut present aos=99.00% cut=99.00% Gene Hma - Hemophilia A - HMA Feb 18 2012, 22:06 3

(Hma- HMA, hma- Not HMA) Assumed background allele frequencies: Hma=99.00% hma=1.00% 99.00% probability of Hma present 1.00% probability of hma present Gene Hmb - Hemophilia B - HMB (Hmb- HMB, hmb- Not HMB) Assumed background allele frequencies: Hmb=99.00% hmb=1.00% 99.00% probability of Hmb present 1.00% probability of hmb present Gene Ch - Chediak-Higashi Syndrome - CHS (Ch- Not CHS, ch- CHS) Assumed background allele frequencies: Ch=99.00% ch=1.00% 99.99% probability of Ch present 1.99% probability of ch present Gene Ew - Episodic Weakness - EW (Ew- Not EW, ew- EW) Assumed background allele frequencies: Ew=99.00% ew=1.00% 99.99% probability of Ew present 1.99% probability of ew present Gene Fck - Flat-Chested Kitten Syndrome - FCK (Fck- Not FCK, fck- FCK) Assumed background allele frequencies: Fck=99.00% fck=1.00% 99.99% probability of Fck present 1.99% probability of fck present Gene Dp - Four-Ears (Dp- Not Four-Ears, dp- Four-Ears) Assumed background allele frequencies: Dp=99.00% dp=1.00% 99.99% probability of Dp present 1.99% probability of dp present Gene Hy - Hydrocephalus (Hy- Not Hydrocephalus, hy- Hydrocephalus) Assumed background allele frequencies: Hy=99.00% hy=1.00% 99.99% probability of Hy present 1.99% probability of hy present Gene Ho - Hyperoxaluria (Ho- Not Hyperoxaluria, ho- Hyperoxaluria) Assumed background allele frequencies: Ho=99.00% ho=1.00% 99.99% probability of Ho present 1.99% probability of ho present Gene Hce - Hyperchylomicronemia - HCMN (Hce- Not HCMN, hce- HCMN) Assumed background allele frequencies: Hce=99.00% hce=1.00% 99.99% probability of Hce present 1.99% probability of hce present Gene Ht - Hypothyroidism (Ht- Not Hypothyroidism, ht- Hypothyroidism) Assumed background allele frequencies: Ht=99.00% ht=1.00% 99.99% probability of Ht present 1.99% probability of ht present Gene Man - Mannosidosis (Man- Not Mannosidosis, man- Mannosidosis) Assumed background allele frequencies: Man=99.00% man=1.00% 99.99% probability of Man present Feb 18 2012, 22:06 4

1.99% probability of man present Gene Mec - Meningoencephalocele - MEC (Mec- Not MEC, mec- MEC) Assumed background allele frequencies: Mec=99.00% mec=1.00% 99.99% probability of Mec present 1.99% probability of mec present Gene Mps1 - Mucopolysaccharidosis 1 - MPS1 (Mps1- Not MPS1, mps1- MPS1) Assumed background allele frequencies: Mps1=99.00% mps1=1.00% 99.99% probability of Mps1 present 1.99% probability of mps1 present Gene Mps6 - Mucopolysaccharidosis 6 - MPS6 (Mps6- Not MPS6, mps6- MPS6) Assumed background allele frequencies: Mps6=99.00% mps6=1.00% 99.99% probability of Mps6 present 1.99% probability of mps6 present Gene Sf - Sparse-Fur (Sf- Not Sparse-Fur, sf- Sparse-Fur) Assumed background allele frequencies: Sf=99.00% sf=1.00% 99.99% probability of Sf present 1.99% probability of sf present Gene Spt - Spasticity (Spt- Not Spasticity, spt- Spasticity) Assumed background allele frequencies: Spt=99.00% spt=1.00% 99.99% probability of Spt present 1.99% probability of spt present Gene Si - Spheroid Lysosomal Disease - SLD (Si- Not SLD, si- SLD) Assumed background allele frequencies: Si=99.00% si=1.00% 99.99% probability of Si present 1.99% probability of si present Gene Tr - Tremor (Tr- Not Tremor, tr- Tremor) Assumed background allele frequencies: Tr=99.00% tr=1.00% 99.99% probability of Tr present 1.99% probability of tr present Gene Mk - Hypochondroplastic Dwarfism (Mk- Munchkin, mk- Not Munchkin) Assumed background allele frequencies: Mk=1.00% 1.99% probability of Mk present 99.99% probability of mk present Gene Cu - Curled Ears (Cu- Curled Ears, cu- Not Curled Ears) Assumed background allele frequencies: Cu=0.00% 100.00% probability of cu present Gene Hcm - Hypertrophic Cardiomyopathy - HCM (Hcm- HCM, hcm- Not HCM) Assumed background allele frequencies: Hcm=1.00% 1.99% probability of Hcm present 99.99% probability of hcm present mk=99.00% cu=100.00% hcm=99.00% Gene Ph - Pelger-Huet Anomaly - PHA (Ph- PHA, ph- Not PHA) Feb 18 2012, 22:06 5

Assumed background allele frequencies: Ph=1.00% 1.99% probability of Ph present 99.99% probability of ph present Gene Pkd - Polycystic Kidney Disease - PKD (Pkd- PKD, pkd- Not PKD) Assumed background allele frequencies: Pkd=1.00% 0.00% probability of Pkd present 100.00% probability of pkd present Gene Po - Porphyria (Po- Porphyria, po- Not Porphyria) Assumed background allele frequencies: Po=1.00% 1.99% probability of Po present 99.99% probability of po present Gene Sh - Split-Foot (Sh- Split-Foot, sh- Not Split-Foot) Assumed background allele frequencies: Sh=1.00% 1.99% probability of Sh present 99.99% probability of sh present Gene Jb - Japanese Bobtail (Jb- Bobtail, jb- Not Bobtail) Assumed background allele frequencies: Jb=0.00% 100.00% probability of jb present ph=99.00% pkd=99.00% po=99.00% sh=99.00% jb=100.00% Gene Fd - Folded Ears - FD (Fd- Folded Ears(homozygous), fd- Not Folded Ears) Assumed background allele frequencies: Fd=0.00% fd=100.00% 100.00% probability of fd present Gene Hag - Hageman Factor - HF (Hag- HF(Homozygous), hag- Not HF) Assumed background allele frequencies: Hag=1.00% 1.99% probability of Hag present 99.99% probability of hag present hag=99.00% Gene Bg - Blood Group (Bga- Blood-A, bgab- Blood-AB, bgb- Blood-B) Assumed background allele frequencies: Bga=49.50% bgab=1.00% 74.50% probability of Bga present 1.99% probability of bgab present 74.50% probability of bgb present bgb=49.50% Gene Pd - Polydactyly (Pd- Polydactyly(Homozygous), pd- Not Polydactyly) Assumed background allele frequencies: Pd=1.00% pd=99.00% 1.99% probability of Pd present 99.99% probability of pd present ---- Produced using Breeders Assistant for Cats software (www.tenset.co.uk, tel: +44 1223 290291). Feb 18 2012, 22:06 6